Correction to: Predation on glass eels of Japanese eel <Emphasis Type="Italic">Anguilla japonica</Emphasis> in the Tone River Estuary,Japan     

Yoichi Miyake  Aigo Takeshige  Hikaru Itakura  Hajime Itoh  Hiroaki Onda  Akira Yamaguchi  Akihito Yoneta  Kohma Arai  Yulina V. Hane  Shingo Kimura 《Fisheries Science》2018,84(6):1015-1016

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Alessandro Bonanno and Lawrence Busch (eds): Handbook of the international political economy of agriculture and food     

Marie Louise Ryan 《Agriculture and Human Values》2018,35(3):731-732

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高维Moebius变换的分类及类型判别     

周展 《湖南农业大学学报(自然科学版)》1990,17(1)

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阔叶红松林的生物量和营养元素含量的研究   总被引：6，自引：0，他引：6  

詹鸿振  刘传照 《林业科学》1990,26(1):80-85

一、研究内容和方法我们于1985—1987年对小兴安岭阔叶红松林的生物量进行了研究。生物量的测定是在凉水自然保护区的阔叶红松林内进行的。林龄220年,组成8红2椴,林分平均高23.1m,平均直径37.4cm。其中红松平均高27.2m,平均直径45.2cm,密度622株/ha,针  相似文献   

频域心电图对冠心病诊断价值的初步探讨     

梁海华  吴梅丽 《湛江医学院学报》1994,12(4):314-316

对５０例冠心病和５０例随机做平板运动试验（ＴＥＴ）者作频域心电图（ＦＣＧ）对比分析探讨ＦＣＧ对冠心病的诊断价值。结果表明：单纯根据ＦＣＧ异常诊断冠心病有较高假阳性（６５．２２％）。如将ＦＣＧ的阳性指标作综合判断，虽然敏感性降低（８８．００％降至７０．００％）。假阳性都明显降低（６５．２２％降至２６．００％）。认为ＴＥＴ的特异性较ＦＣＧ高。若两者均为阴性，则冠心病可能性很小。  相似文献   

两种塑料暖棚猪舍的应用效果观测   总被引：1，自引：0，他引：1  

侯正录  杨占魁 《家畜生态》2002,23(3):17-18

在青海省乌兰县舍外温度－6．30℃条件下，选用40头荣昌猪分作2组，每组20头，在自行设计的半开放－封闭式多用塑料暖棚猪舍与常用简易塑料暖棚猪舍内开展对比试验。结果表明，前者可显著提高舍内温度，降低舍内湿度，且育猪增重效果明显。  相似文献   

河蟹养殖技术之五提高成蟹养殖效益的措施     

詹松文 《中国水产》2005,(10)

据调查,不少养蟹户年初放养的蟹种,由于幼蟹品种不纯、放养密度过高、防病措施不力、养殖管理不善等原因,年终河蟹成活率低、规格偏小、品质较差、价值很低,结果严重影响河蟹养殖效益,甚至出现亏本现象.为了便于广大养蟹者提高养殖效益,现将培育大规格、优质蟹的高产高效技术措施综述如下:  相似文献   

多花黑麦草播期试验(1987～1988年)     

易克贤  詹爱民  刘斌  王贵兰  周省善  陈哲忠  肖小文  傅新如 《江西农业大学学报》1991,(6)

本试验研究了7个不同播期对多花黑麦草出苗、生产性能的影响.结果表明:在江西清江种草养畜试验站从8月中旬至11月中旬均可播种多花黑麦草,尤以9月中旬至10月中旬更为适宜.  相似文献   

桑蓟马田间种群消长规律的研究   总被引：2，自引：0，他引：2  

尹益寿  易富文 《江西农业大学学报》1994,16(2):124-129

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‘Plantibodies’: a flexible approach to design resistance against pathogens     

A. Schots  J. De Boer  A. Schouten  J. Roosien  J. F. Zil Verentant  H. Pomp  L. Bouwman-Smits  H. Overmars  F. J. Gommers  B. Visser  W. J. Stiekema  J. Bakker 《European journal of plant pathology / European Foundation for Plant Pathology》1992,98(2):183-191

Engineering resistance against various diseases and pests is hampered by the lack of suitable genes. To overcome this problem we started a research program aimed at obtaining resistance by transfecting plants with genes encoding monoclonal antibodies against pathogen specific proteins. The idea is that monoclonal antibodies will inhibit the biological activity of molecules that are essential for the pathogenesis. Potato cyst nematodes are chosen as a model and it is thought that monoclonal antibodies are able to block the function of the saliva proteins of this parasite. These proteins are, among others, responsible for the induction of multinucleate transfer cells upon which the nematode feeds. It is well documented that the ability of antibodies to bind molecules is sufficient to inactivate the function of an antigen and in view of the potential of animals to synthesize antibodies to almost any molecular structure, this strategy should be feasible for a wide range of diseases and pests.Antibodies have several desirable features with regard to protein engineering. The antibody (IgG) is a Y-shaped molecule, in which the domains forming the tips of the arms bind to antigen and those forming the stem are responsible for triggering effector functions (Fc fragments) that eliminate the antigen from the animal. Domains carrying the antigen-binding loops (Fv and Fab fragments) can be used separately from the Fc fragments without loss of affinity. The antigen-binding domains can also be endowed with new properties by fusing them to toxins or enzymes. Antibody engineering is also facilitated by the Polymerase Chain Reaction (PCR). A systematic comparison of the nucleotide sequence of more than 100 antibodies revealed that not only the 3′-ends, but also the 5′-ends of the antibody genes are relatively conserved. We were able to design a small set of primers with restriction sites for forced cloning, which allowed the amplification of genes encoding antibodies specific for the saliva proteins ofGlobodera rostochiensis. Complete heavy and light chain genes as well as single chain Fv fragments (scFv), in which the variable parts of the light (V_L) and heavy chain (V_H) are linked by a peptide, will be transferred to potato plants. A major challenge will be to establish a correct expression of the antibody genes with regard to three dimensional folding, assembly and intracellular location.  相似文献