基于Hough变换识别单周期正弦曲线图像的算法及实现     

吴志芳 《仲恺农业技术学院学报》2006,19(3):43-46

手工识别成像测井中的裂缝具有一定的主观性，不同的人可能会有不同的解释结果．作者介绍利用Hough变换自动识别裂缝的原理及其算法，并通过实例分析了其应用效果，结果表明，这种算法计算裂缝参数不仅精度可靠，还保证了裂缝参数拾取的唯一性，对实现井壁裂缝参数的完全自动解释有重要意义．  相似文献   

标准差在单粒播种机试验中的应用     

范东方  罗林海  刘显耀 《农机化研究》2004,(3):191-192

单粒播种机试验方法中的标准差与众不同,有很多专业特点,研究它利于提高试验水平,进而利于产品质量的提高。为此,探讨了标准差在单粒播种机试验中的应用。  相似文献   

Quantitative capillary reversed passive latex agglutination test for C-reactive protein (CRP) in the dog     

K. Tagata  S. Yokoyama  T. Ginbo  M. Honda  T. Okimura  M. Odakura  M. Nomura  S. Yamamoto 《Veterinary research communications》1996,20(1):21-30

A capillary reversed passive latex agglutination test (capillary RPLA) was developed which allows quantification of serum C-reactive protein (CRP) within approximately 15 min. The logarithmic regression line (calibration curve) obtained after measuring each CRP concentration three times in twofold dilutions of a standard canine serum containing 222 g/ml of CRP was y=6.394+0.030x (r=0.995). Capillary RPLA permitted quantification of CRP in the range 6.9–222 g/ml. The coefficients of variation ranged from 10.28% to 12.40%. The recovery rates (percentage recovery) of CRP by capillary RPLA were within the range 87% to 106%. On measuring the CRP concentrations in sera from 78 dogs by capillary RPLA, single radial immunodiffusion (SRID) and enzyme-linked immunosorbent assay (ELISA), close correlations were demonstrated between SRID and capillary RPLA (y=7.250+1.109x, r=0.978), between SRID and ELISA (y=3.042+1.059x, r=0.967), and between capillary RPLA and ELISA (y=1.778+0.929x, r=0.962). Capillary RPLA may be considered useful as a routine biochemical technique for measurement of serum CRP concentration in the dog.Abbreviations CRP C-reactive protein - ELISA enzyme-linked immunosorbent assay - RPLA reversed passive latex agglutination test - SRID single radial immunodiffusion  相似文献   

小水电科技发展领域的系统分析     

李卫国 《中国农村水利水电》1992,(12)

该文用层次分析法(AHP)和德尔菲法(Delphi)相结合的系统分析法,对江西省上饶地区小水电科技发展领域分析模型作了探索,提出了小水电科技发展领域的优先度及重点,为“八五”、“九五”小水电科技规划的制定提供了依据,同时也为水利水电同行在科技规划中提供一点参考。  相似文献   

黑木耳烘干控制系统的研究     

齐怀琴  李春林 《中国食用菌》2005,24(6):49-51

黑木耳烘干控制系统，采用压缩式热泵，AT89C51单片机、SHT75型温湿度传感器、加热器等组成温湿度控制电路。控制干燥室内的温湿度，完成对干燥室内的黑木耳进行低温、高效率的去湿干燥。  相似文献   

马铃薯渣酶法水解液制备单细胞蛋白饲料的研究   总被引：1，自引：0，他引：1  

王文侠 《中国饲料》2005,(6):33-36

本文研究了酶法水解马铃薯渣制备膳食纤维后的滤液制备单细胞蛋白的可行性。试验结果表明,单细胞蛋白边糖化边发酵的摇瓶培养的较优工艺条件为:底物浓度为8%(添加8%的麸皮水)、初始pH值为4.5、接种量为15%、葡萄糖淀粉酶加入量为100U/g(原料中淀粉)、青霉素加入量为80U/g(原料)、培养温度为28℃、培养时间为6h、转速为250r/min。在此条件下,干酵母产量最高为19.920g/L,单细胞蛋白中的蛋白质含量达12.27%。  相似文献   

酵母蛋白饲料培养条件的研究   总被引：4，自引：0，他引：4  

于荣  董颖超  秦玉昌 《中国饲料》2005,(18):20-21

对啤酒酵母进行发酵试验,结果表明:该酵母最优的培养条件是麦芽汁培养基稀释倍数2.5,培养时间20h,蔗糖添加量10Brix,尿素添加量0.02%,且酵母菌耐酸耐铜的性能好。  相似文献   

Engineering of a Single Chain Variable Fragment Antibody Specific for the Citrus tristeza virus and its Expression in Escherichia coli and Nicotiana tabacum     

P. Galeffi  G. Giunta  S. Guida  C. Cantale 《European journal of plant pathology / European Foundation for Plant Pathology》2002,108(5):479-483

Citrus tristeza virus (CTV) is one of the most destructive citrus virus diseases in the world. The construction of an engineered antibody, EMBL accession number AJ278109, able to specifically recognize its antigen, i.e. the coat protein of CTV, directly on infected plant material without any purification or manipulation of the entire woody plant. The potential uses of this engineered antibody are discussed.  相似文献   

单对汰选方法在加速抗高效氯氟氰菊酯棉铃虫品系汰选中的应用   总被引：1，自引：0，他引：1  

卢美光  范贤林 《农药学学报》2002,4(2):89-92

通过设计杂合种群单对杂交方式,研究了加速获得抗性品系的方法。以高效氯氟氰菊酯群体汰选后抗性倍数为4.9倍的棉铃虫种群及其同源对照种群为材料,同时设置常规群体汰选方法与单对汰选方法,研究单对汰选方法在加速抗高效氯氟氰菊酯棉铃虫品系汰选中的作用。结果表明,群体汰选两代后抗性倍数由4.9倍提高到7.4倍, 而单对汰选两代后抗性倍数由4.9倍提高到27.3倍。表明在常规群体汰选中穿插几代单对汰选方法可明显加快棉铃虫种群对高效氯氟氰菊酯的抗性汰选进程。  相似文献   

Identification of ALS inhibitor‐resistant Amaranthus biotypes using polymerase chain reaction amplification of specific alleles     

J Wagner  H U Haas  K Hurle 《Weed Research》2002,42(4):280-286

Summary Polymerase chain reaction (PCR) amplification of specific alleles (PASA) was adapted as a molecular marker‐based method for the rapid detection of point mutations in Amaranthus retroflexus and Amaranthus rudis leading to ALS inhibitor resistance. Two pairs of primers were designed for the specific amplification of alleles of the ALS gene of susceptible and resistant biotypes. The allele‐specific primer matched the desired allele, but mismatched the different allele at its 3′ end. Differentiation was carried out by comparison of the amplified DNA fragments in gel electrophoresis after PASA‐PCR. In A. rudis, differentiation was possible with one PCR and genomic DNA as probe. A ‘nested’ PCR was necessary for the differentiation of sensitive and resistant A. retroflexus. PASA is useful for the identification of resistant weed biotypes and also as a monitoring tool to map resistance occurrence and distribution. Advantages include the fast and clear separation of those plants with and without mutations at an early stage of development, its easy and consistent performance and quick results compared with existing resistance detection tests. These advantages, when combined with management strategies, enable further activities to reduce herbicide resistance.  相似文献