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Specific and sensitive TaqMan real-time PCR assays were developed targeting chromosomal DNA of Erwinia amylovora ( ams C gene and ITS region). These assays increased the reliability of detection of E. amylovora strains, regardless of their plasmid profile, and have the ability to differentiate between Erwinia spp. strains from Hokkaido, Erwinia pyrifoliae and Erwinia spp. isolated from necrotic pear blossoms in Spain. The assays were used for testing the efficiency of three different extraction methods to remove plant-based PCR inhibitors. Combined with an automated DNA-extraction method based on magnetic beads (QuickPick™), the real-time PCR assays reliably detected at least 103 cells mL−l ( c. four cells per reaction) of the pathogen from blighted woody plant material. In testing of symptomless samples, absolute quantification of E. amylovora before and after enrichment in liquid media provided proof of E. amylovora viability and its ability to multiply, including in cases when subsequent isolation in pure culture was unsuccessful. 相似文献
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赵昌普 《拖拉机与农用运输车》2009,36(6):1-5
论述了在内燃机缸内速度测量、喷雾粒子粒度测量及燃烧过程温度和组分浓度测量中常用的激光诊断技术和测试方法,并对其工作原理、适用范围与场合、优缺点等进行了比较和分析。相位多谱勒粒子测速(PDPA)技术比较适合于单点速度、粒子尺寸及其分布的测量;粒子图像测速(PIV)技术适合于缸内二维平面速度场的测量;激光全息术是分析喷雾特性的有效途径和测量喷雾液滴尺寸的标准方法;平面激光诱导荧光(PLIF)法已成为喷雾、燃烧过程组分浓度及火焰结构研究的重要工具。 相似文献
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Ioannis E. Tzanetakis 《International Journal of Fruit Science》2016,16(4):142-147
ABSTRACTStrawberry is susceptible to several systemic pathogens and, in particular, viruses. There are several examples of disease epidemics that resulted from virus-infected propagation material and led to losses estimated in the tens of millions of dollars. This communication focuses on actions needed to minimize the risk of similar outbreaks by developing a systems-based approach from breeding to the commercial field. This includes the development of molecular biology and bioinformatic tools that allow for the detection of all known viruses infecting strawberry but most importantly for the discovery of viruses that circulate in the system undetected and may have contributed to past epidemics. Surveys in commercial fields have yielded a map of the most prevalent viruses in strawberry production areas across the United States, knowledge that will be used in the nascent National Certification Program for Strawberry. 相似文献
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M Dorsch B Meehan WP Michalski HG Heine AJ Foord G Carlile J Wang S McCullough K Zuelke 《Australian veterinary journal》2016,94(3):64-66
In this study, we explored the potential utility of the human‐focused FilmArray® Respiratory Panel for the diagnosis of a broad range of influenza viruses of veterinary concern as compared with the standard portfolio of recommended TaqMan®‐based diagnostic tests. In addition, we discuss some potential operational advantages associated with the use of such integrated sample extraction, amplification and analysis devices in the context of a future long‐term, dual‐role strategy for the detection of emergency diseases of both human and veterinary concern. 相似文献
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肉毒中毒症是一种潜在的致死性瘫痪疾病,快速准确的诊断对该病的治疗显得尤为必要。本文综述了肉毒中毒症毒素检测、细菌培养、分子检测、遗传鉴定等实验室诊断的进展情况,以期对本病的快速诊断有所启示。 相似文献
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Molecular diagnostics of some trichodorid nematodes and associated Tobacco rattle virus 总被引:1,自引:1,他引:1
K. Boutsika M. S. Phillips S. A. MacFarlane D. J. F. Brown R. C. Holeva V. C. Blok † 《Plant pathology》2004,53(1):110-116
Several Paratrichodorus and Trichodorus (trichodorid) nematode species are natural vectors of Tobacco rattle virus (TRV) and cause economically important diseases, especially in potato and ornamental bulbous crops. Identification of trichodorid species based on morphological characters is laborious, time-consuming, and requires the services of highly trained personnel. Molecular diagnostics for trichodorid nematodes, using the ribosomal DNA repeat unit, were successfully developed to distinguish two Paratrichodorus and two Trichodorus species. The complete sequences of the 18S genes and the ITS-1 regions for these species were obtained and species-specific primers successfully designed for them. An RT-PCR assay was developed utilizing isolate-specific primers that amplify serologically distinguishable strains of TRV in individual trichodorid nematodes. The primers were based on the highly conserved RNA-1 segment of the bipartite genome and also on different parts of the RNA-2 segment of the virus genome. 相似文献