胶束分光光度法测定环境样品中的痕量锰     

陈同森  张建云 《湖南农业大学学报(自然科学版)》1993,20(4)

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氧漂期间桦木硫酸盐纸浆表面性质变化的探讨     

金广林  王凤君 《东北林业大学学报》1993,21(4):53-58

尝试性地应用ESCA对桦木硫酸盐浆氧漂期间表面性质的变化进行了初步分析。结果表明:桦木硫酸盐浆氧漂期间氧碳比逐渐增加,碳价态发生了显著的变化。这对于指导纸浆氧漂工艺条件的合理制定,预测或控制纸浆的宏观质量有非常重要作用。ESCA可为研究纸浆漂白提供新的有效手段。  相似文献   

改进芳草A系原种产卵性的试验     

靳远祥  杨明观  陈玉银 《蚕桑通报》2001,32(1):19-23

本试验采取母蛾延迟交配，拆对后冷藏、改变交配时间和产卵室保护温度等技术措施来探讨改善芳草A系原种产卵性的方法。结果表明，这些措施对产卵性能的改进有一定的效应，但由于性状间存在相关关系，对某一性状的促进效应往往同时也对另一产卵性状产生负向影响。  相似文献   

电机护环钢在硝酸盐溶液中应力腐蚀开裂的控制过程研究     

靳九成  李建明 《湖南农业大学学报(自然科学版)》1993,20(6)

本文在文献［１］基础上，运用金相，电化学方法研究了５０Ｍｎ１８Ｃｒ４电机护环钢依照ＱＨＪ－７９试验标准在硝酸盐介质中应力腐蚀开裂（即ＳＣＣ）的性质，结果指出，此体系中ＳＣＣ的控制过程为阳极溶解。  相似文献   

鸡白血病病毒抗原ELISA试剂盒的研制和应用   总被引：5，自引：2，他引：3  

黄进  陈德威 《中国兽医杂志》1994,20(4):3-5

以双抗体夹心酶联免疫吸附试验（ＤＡＳ－ＥＬＩＳＡ）为基本原理，成功地研制出鸡白血病病毒抗原ＥＬＩＳＡ试剂盒，该试剂盒与国外同类试剂盒相比，具备相同的特异性和敏感性，对ＲＡＶ－１纯化样品的最小检出量可达０．７８ｕｇ／ｍｌ，且敏感性高于直接补体结合试验。经初步应用发现，我国商品种鸡群ＡＬＶ阳性率为０．７－１４％，在部分ＳＰＦ鸡群中未检出阳性鸡。  相似文献   

红虹木业，“顶端优势”之我见     

施金 《国际木业》2005,35(8):5-6

《国际木业》：上海红虹木业有限公司作为一家拥有悠久历史的家族企业，自从事木材行业至今已发展为在北美、欧洲、东南亚等地区都有力量分布的规模供应商，整个过程中企业对自己的理念和战略有怎样的发展？  相似文献   

深基坑锻锤基础冬期施工     

金虹  张军 《林业科技情报》2004,36(2):18-18

在冬期施工，对于土方开挖、钢筋绑扎、人员的通行、砼的浇铸、砼的温度控制，基坑的保温等都带来一定困难，为此提出了深基坑锻锤基础才是最佳实践应用。  相似文献   

黑杨无性系日CO2固定总量的测定及与苗木生产潜势的相关性研究   总被引：1，自引：0，他引：1  

滕小锘  赵凤君  韩锦  沈应柏 《河北林果研究》2005,20(1):21-26

通过对不同基因型黑杨无性系植株净光合速率日变化曲线与光合主体叶面积在时间和光强上进行累计积分来计算植株日CO2固定总量P。由于净光合速率日变化曲线不易准确测得，故以光响应曲线和光强的日变化来推测净光合速率日变化。对P值和生物量的相关性研究表明，二者的相关性很高。且认为可以用计算出的P值作为评估苗木生产潜势的指标之一，这为育种中生产力的早期选择提供了有力的证据。  相似文献   

粟品种对粟瘟病的抗病性初步观察     

朱羣 《植物保护学报》1964,3(4):413-413

近年来,粟瘟病在山西省中部及东南部严重发生危害,輕者减产,重者籽粒不收。作者于1962—1963年进行了粟品种間抗病性的初步观察,簡报如下: 在本所試驗地和山西省晋东南区各县良种繁殖場谷子品种区域試驗地共調查品种520个。調查时期:重点品种分苗期、拔节期、拔节末期、抽穗盛期、乳熟期进行;一般品种只在发病盛期(即抽穗盛期)进行。在自然条件下未感染粟瘟病的品种,再在溫室中种植,进行人工接种。抗病性鑑定結果如下: (一)尚未发現有免疫品种。 (二)不同品种对栗瘟病的抗病性有显著差异:在发病盛期調查,高度抗病品种61个,占总数12％,发病指数为0.1—10;抗病品种149个,占总数28.7％,发病指数为10.1—20.0;輕度感病品种128个,占总数24.6％;发病指数为20.1—  相似文献   

‘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