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A Multistate Investigation of Antibiotic‐Resistant Salmonella enterica Serotype I 4,[5],12:i:‐ Infections as Part of an International Outbreak Associated with Frozen Feeder Rodents 下载免费PDF全文
E. J. Cartwright T. Nguyen C. Melluso T. Ayers C. Lane A. Hodges X. Li J. Quammen S. J. Yendell J. Adams J. Mitchell R. Rickert R. Klos I. T. Williams C. Barton Behravesh J. Wright 《Zoonoses and public health》2016,63(1):62-71
While most human Salmonella infections result from exposure to contaminated foods, an estimated 11% of all Salmonella infections are attributed to animal exposures, including both direct animal handling and indirect exposures such as cleaning cages and handling contaminated pet food. This report describes the epidemiologic, environmental and laboratory investigations conducted in the United States as part of the response to an international outbreak of tetracycline‐resistant Salmonella enterica serotype I 4,[5],12:i:‐ infections with over 500 illnesses occurring from 2008 to 2010. This investigation found that illness due to the outbreak strain was significantly associated with exposure to pet reptiles and frozen feeder rodents used as food for pet reptiles. Salmonella isolates indistinguishable from the outbreak strain were isolated from a frozen feeder mice‐fed reptile owned by a case patient, as well as from frozen feeder mice and environmental samples collected from a rodent producing facility (Company A). An international voluntary recall of all Company A produced frozen feeder animals sold between May 2009 and July 2010 occurred. Only 13% of cases in our investigation were aware of the association between Salmonella infection and mice or rats. Consumers, the pet industry, healthcare providers and veterinarians need to be aware of the potential health risk posed by feeder rodents, whether live or frozen. Frozen feeder rodent producers, suppliers and distributors should follow the animal food labelling requirements as described in 21 CFR §501.5, and all packages of frozen feeder rodents should include safe handling instructions. Persons should wash their hands thoroughly with soap and water after handling live or frozen feeder rodents, as well as reptiles or anything in the area where the animals live. Continued opportunities exist for public health officials, the pet industry, veterinarians and consumers to work together to prevent salmonellosis associated with pet food, pets and other animals. 相似文献
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各国奶牛群体的选育目标建立之后,选育目标一直在不断发展,选择指数中性状的组成、定义和权重等都在不断变化。奶牛的选育是从关注产奶性能而开始,随后增加了体型外貌性状。由于奶牛的健康和繁殖问题的增加以及社会对动物福利的不断关注,20世纪末,世界范围内平衡育种理念在奶牛育种中逐渐形成,一些重要的功能性状加入各国的选择指数中;进入21世纪后,随着奶牛养殖业和社会的发展,育种家们开始关注和研究更多的性状,部分新性状已经开始在育种实践中选育应用。本文通过整理奶牛育种中有关新性状的研究并收集各国奶牛选育方案中的相关信息,综述了近十年奶业发达国家在奶牛遗传选育中正在研究或已经开始应用的新性状,并将这些新性状分为生产效率相关的新性状、应对环境挑战的新性状、健康福利相关的新性状、产品和加工相关的新性状及管理相关的新性状五大类,总结了这些性状的选育背景、定义方法、遗传基础和选育应用情况等,最后还总结了奶牛育种中新性状的研究应用过程,以期为我国奶牛遗传育种研究和育种目标完善提供一定的借鉴。 相似文献
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紫花苜蓿人工草地施肥试验 总被引:1,自引:0,他引:1
在辽宁西部坡地上进行紫花苜蓿不同施肥处理试验,经过1年的研究结果表明,在苜蓿人工草地上无论是单一施用氮肥还是复合肥,均可有效地提高牧草产量并取得较为明显的经济效益,其中以每亩施用尿素15 kg和25 kg效果最好,效益最高,每亩可增经济效益分别是40.74元和40.63元。 相似文献
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The present study was to investigate the feasibility and efficiency of the DNA vaccine to protect chickens against very virulent infectious bursal disease virus (vvIBDV) infection. A plasmid DNA carrying VP2‐4‐3 genes of vvIBDV SH95 and a plasmid DNA carrying chicken interleukin‐6 (ChIL‐6) genes were constructed and designated as pALTER‐MAX‐VP2‐4‐3 and pALTER‐MAX‐ChIL‐6 respectively. Several DNA vaccination experiments were performed: 1‐week‐old chickens were intramuscularly injected with only plasmid pcDNA3‐VP2, pALTER‐MAX‐VP2‐4‐3 or mixture with pALTER‐MAX‐ChIL‐6. The chickens at 4 weeks old were orally inoculated with vvIBDV SH95. The results showed that immunization with the mixture of pALTER‐MAX‐VP2‐4‐3 and pALTER‐MAX‐ChIL‐6 three times conferred protection for 90% of chickens. Enzyme‐linked immunosorbent assay (ELISA) antibody titres in chickens immunized together with pALTER‐MAX‐ChIL‐6 were higher than those immunized simply with plasmid pcDNA3‐VP2 or pALTER‐MAX‐VP2‐4‐3. IBDV was not detected in the bursa of the protected chickens at 8 days after challenge by RT‐PCR. The results indicate that protection against vvIBDV can be achieved by using the VP2‐4‐3 gene of vvIBDV as a DNA vaccine. Furthermore, the simultaneous injection of ChIL‐6 plasmid significantly increased the protection after challenge with the very virulent strain. 相似文献