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Infection of Prunus spp. by Plum pox virus (PPV) is characterized by an uneven distribution of the virus within the tree and branches. In order to gain a better understanding of this distribution, a method for modelling tree growth was used. PPV spread was followed within susceptible Mariana plum clone GF 8-1 shoots for 4 months after inoculation. Shoot growth was unaffected by the presence of the virus. Symptoms appeared on leaves produced in the most actively growing parts of the shoots, i.e. at the beginning of the season. PPV was detected in leaves other than those showing symptoms. The proportion of leaves with detectable virus decreased from the zone showing symptoms, with 100% ELISA-positive responses, to the shoot tip with no detectable virus in leaves produced between 111 and 127 days after inoculation. Furthermore, a higher proportion of positive ELISA results was obtained below the zone showing symptoms (77%) compared with 50% above. PPV was detected in 95% of the most vigorous shoots 71 days after inoculation compared with 37% of slower-growing, later-produced shoots. 相似文献
23.
晋南冬麦区大麦黄矮病毒流行株系监测及防治策略探讨 总被引:2,自引:0,他引:2
连续5年(1996~2000年)采集晋南冬麦区小麦黄矮病标样,采用生物学和血清学(酶联免疫吸附法)相结合的诊断方法对该地区的大麦黄矮病毒流行株系进行了鉴别。结果表明,该小麦黄矮病流行区近五年以GAV株系为主流株系,兼有少量GPV、PAV和混合株系存在。同时对小麦抗黄矮病新品种“临抗1号”进行了GPV和GAV两种株系的抗性测定,明确了该品种兼抗GPV和GAV两种株系。根据小麦黄矮病发生现状,提出了一套以选育推广抗耐病品种为主,以药剂防治为辅的综合防治措施。以期为当地小麦生产服务。 相似文献
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梨火疫细菌实时荧光PCR和诱捕PCR-ELISA检测方法的建立 总被引:8,自引:1,他引:8
根据梨火疫细菌中独特而保守存在的质粒pEA29,设计了1对引物和3条探针,建立了实时荧光PCR检测方法和诱捕PCR-ELISA检测方法。实时荧光PCR采用带荧光标记的核酸杂交探针,边扩增边检测,步骤简单,不需PCR后处理,可避免假阳性和交叉污染;诱捕PCR-ELISA检测方法只需简单处理的样品就能检测,减少了核酸不纯出现的漏检,由于增加了核酸杂交探针,可不需凝胶电泳EB染色检测,不会出现假阳性问题。 相似文献
27.
D. Boscia H. Zeramdini M. Cambra O. Potere M.T. Gorris A. Myrta B. Di Terlizzi V. Savino 《European journal of plant pathology / European Foundation for Plant Pathology》1997,103(5):477-480
A monoclonal antibody to an Albanian isolate of plum pox potyvirus (PPV) was obtained (MAbAL), that specifically recognized strain M of this virus. The specificity of MAbAL, assessed by comparative ELISA on 130 PPV isolates of different geographical origin, 22 of which were also tested by comparative IC-PCR, gave consistent and highly reproducible results. MAbAL seems to be elicited by a stable surface determinant that makes it particularly suitable for successful use under a wide range of conditions. MAbAL is an useful addition to the panel of PPV-specific MAbs available to date. 相似文献
28.
Y. Antignus M. Lapidot N. Ganaim J. Cohen O. Lachman M. Pearlsman B. Raccah A. Gera 《Phytoparasitica》1997,25(4):319-330
Received April 24, 1997; received in final form June 29, 1997. Symptoms resembling tomato spotted wilt virus (TSWV) infections
were documented among ornamental and vegetable crops in commercial greenhouses and open fields in Israel. Plants exhibiting
these symptoms were collected from January 1992 to December 1996. Among cultivated plants analyzed for TSWV by enzyme-linked
immunosorbent assay (ELISA), 19 species representing five families were found to be infected; natural infection was also recorded
in six plant species of weeds. Virus identity was characterized by host range, serology and electron microscopy. Serological
reaction with the isolates, found in Israel, using antisera from different sources as well as the sequence analysis of the
nucleocapsid gene, demonstrated that the Israeli isolates of TSWV are a member of tospovirus serogroup I, type I (BR-01 strain).
No virus transmission was found in seeds collected from virus-infected vegetable and ornamental crops. A non-radioactive molecular
probe derived from the cloned nucleocapsid isolate enables specific detection of the virus in crude sap from infected plants.
The detection of TSWV in Israel constitutes a severe potential threat to the ornamental and vegetable industry. 相似文献
29.
动物组织中四环素类抗生素残留的ELISA检测研究——土霉素抗体的制备 总被引:3,自引:0,他引:3
四环素类抗生素属小分子半抗原物质 ,必须与大分子物质结合才能产生免疫原性。本试验采用重氮化法合成土霉素 牛血清白蛋白 (BSA OTC)及土霉素 鼠血清白蛋白 (RSA OTC)人工抗原 ,用紫外扫描对其进行鉴定。以BSA OTC免疫家兔制备抗血清 ,以RSA OTC为包被抗原 ,采用双向免疫扩散法和ELISA方法对抗血清进行鉴定。结果表明用重氮化法合成的人工抗原对四环素类药物有特异的抗原抗体反应 ,抗血清效价达 1 2 8× 1 0 5,完全能够满足四环素类药物残留的ELISA检测要求 相似文献
30.
PRRS ELISA试剂盒检测猪繁殖与呼吸综合征病毒抗体的应用 总被引:2,自引:0,他引:2
利用重组杆状病毒表达的PRRSV核衣壳蛋白作抗原制成ELISA诊断试剂盒,检测人工感染PRRSV猪血清、疫苗免疫抗体和田间血清,并与IDEXX公司生产的试剂盒进行比较。结果表明,该试剂盒在PRRSV感染后8天内就可检出感染性抗体,而用IDEXX公司生产的试剂盒在感染后的18天才检测到感染性抗体,对弱毒疫苗的免疫检测也基本能反映出疫苗的免疫应答状况。对华东地区PRRSV流行病学调查结果表明,PRRSV在国内普遍存在,同时也证明研制的试剂盒,是客观科学调查我国PRRS流行情较理想的检测工具。 相似文献