奶牛乳房炎多联苗(B)的临床免疫试验

用奶牛乳房炎多联苗 (B)免疫家兔 ,14 d血清中金黄色葡萄球菌抗体效价可达 1∶ 8,2 8d抗体水平明显升高 ,可达 1∶ 32 ,注苗后 35 d攻毒 ,攻毒后 2 d保护率为 93.3% (14 /15 ) ,自然保护率为 2 0 % (1/5 ) ,10 d保护率为 6 6 .6 % (10 /15 ) ,自然保护率为 2 0 % (1/5 ) ;用多联苗 (B)臀部肌肉注射免疫泌乳牛 ,试验期间 4个月内 ,3ml剂量组临床型乳房炎月平均发病率为 11.0 9% ,其对照组为 2 0 .19% ,发病率降低 4 5 .2 9% ,差异极显著 (P<0 .0 1) ;5 m l剂量组月平均发病率为 13.0 1% ,其对照组为 31.36 % ,发病率降低 5 8.5 1% ,差异极显著 (P<0 .0 1) ;3ml剂量组与 5 m l剂量组之间发病率无明显差异 (P>0 .0 5 ) ;注苗后泌乳牛血清抗体水平可持续 4个月 ,且 30 d时效价水平最高。     

体外循环对血液有形成份的影响（附34例观察）

观察３４例心内直视手术体外循环前后对血液有形成份的影响，发现体外循环后血红蛋白、红细胞与血小板有显著降低，而白细胞显著增高，这可能与机械损伤、血液稀释和机体反应有关。因此选用接近人体生理循环的人工心肺机，改进手术吸引装置、缩短体外循环时间及提高手术质量，可能有助于减少体外循环对血液有形成份的影响。     

催干剂对氨基环氧树脂阴极电泳漆的影响

以氨基环氧树脂为基体树脂，Co^2 ,Pb^2 盐为催干剂合成了阴极电泳漆，并对膜性能进行考察，结果表明，所合成的阴极电泳涂料在PH值为6－7、电泳时间2min的条件下。加入不同的催干剂，在不同的烘干温度下，得到性能不同的漆膜。经过膝膜综合性能试验，结果表明，加入钴和铅复合催化剂，在160℃左右烘干20min，可得到完全固化，硬度较高、耐潮、耐盐、耐酸碱性较好的漆膜。     

豫西山区森林群落结构与物种多样性研究

对栾川、卢氏两地不同森林群落的类型、种类组成与结构,以及物种多样性等进行了分析,结果表明:群落的物种组成比较丰富,在生活型组成上以地上芽植物所占比例较大,物种多样性指数的顺序是阔叶林>混交林>针叶林,通过多样性指数和均匀度指数的分析可以较为客观的评价群落的稳定性。     

ERP系统中设备维修计划的研究

在制造企业设备的使用过程中,设备维修计划成了各种设备管理系统所公认的管理重点,这就更需要设备维修活动在企业内部能形成一个有计划、有步骤的活动。为此,简要介绍了作为ERP管理系统中的子系统一设备管理系统的主要目标,着重讨论了设备管理系统的管理重点一维修计划新思想的形成以及制定维修计划的步骤。     

民国时期美术教育发展模式研究分析

从1911年至1949年,中国近代美术教育是在初期的社团、师范学堂、私立、公立美术教育的基础上,形成了后期的国统区与延安鲁艺的美术教育,教育理念借鉴与效法“新式”、“兼容并包”、“通才”、“理论和实践相结合”的人才培养模式。     

Reproduction and Development of the Released Przewalski’s Horses (Equus przewalskii) in Xinjiang,China

In China, the first Przewalski’s horse (Equus przewalskii) group was released in Kalamaili Ungulate Protected Area in Xinjiang, in August 2001. The objective of this study was to investigate reproduction and development of released Przewalski’s horses in Xinjiang, China from 2002 to 2006. Twenty-four descendants were naturally born, average reproduction rate was 38.7%, and average survival rate of foals was 69.1% in this interim. Frequent alternation of the leading stallion and infertility in female horses due to environmental factors were main causes for the low reproduction rate. The infant mortality rate of released Przewalski’s horses was 25.0%, and 83.3% of death in infants was due to the leading stallion infanticide. The released Przewalski’s horses exhibited seasonal breeding, 70.8% of infants were born in May and June. The fertility rates were 8.3% in April and 37.5% in May, which were lower compared to those of the captive Przewalski’s horse groups (18.3% and 44.3%, respectively). Furthermore, the fertility rate in June was 33.3% and higher than the captive groups (18.3%). These findings showed that the breeding peak of the released Przewalski’s horse groups was later than the captive groups, and suggested that the altered survival environment and food supplies were the main reasons contributing to the delayed breeding peak.     

部分桂花栽培品种的AFLP分析

 从22对AFLP引物中筛选出6对用来检测22个桂花品种和木犀属3个种的多态性位点,共检测到171个位点,其中多态性位点104个,占60.8%。利用DPSv 3.11软件计算25个样品之间的Nei遗传距离,并按照非加权算术平均数聚类方法（UPGMA）,构建树状分支图。AFLP分析结果表明：桂花花色较深的品种之间和花色较浅的品种之间分别存在着较近的亲缘关系,而花色深浅不同的两类品种之间亲缘关系较远。从聚类图上看,22个桂花品种中最后聚在一起的分别是3个银桂品种（遗传距离0.19处）和3个四季桂品种（遗传距离0.21处）,说明四季桂类和银桂类中的部分品种与金桂品种群和丹桂品种群有较远的亲缘关系。从分类上看,AFLP分析结果与传统的以形态特征为基础的分类结果并不完全一致。     

Response of CREG1 promoter to serum starvation in human vascular cells

AIM: In order to explore the regulatory mechanisms of the human cellular repressor of E1A-stimulated genes (hCREG1) in vascular smooth muscle cells (VSMCs)-HITASY and in human umbilical vein endothelial cells (HUVECs), we clone and construct hCREG1 promoter vector to detect its expression in different vascular cells. METHODS: With the results of biological information, the fragments including -3 677 bp, -2 310 bp and -945 bp upstream sequences of hCREG1 were amplified respectively using human genomic DNA template by PCR. The products were inserted into pMD18-T vector, and then were subcloned into pEGFP-1 report vector to obtain the pEGFP-hCREG1-promoter vectors. The pEGFP-hCREG1-P3677, pEGFP-hCREG1-P2310 and pEGFP-hCREG1-P945 vectors were transfected into HITASY cells and HUVECs transiently and the expression of green fluorescent protein (GFP) was detected respectively by Western blotting and fluorescent microscope. RESULTS: It was confirmed that all three PCR fragments inserted into vectors were corrected by sequencing analysis. However, the expression of GFP was different significantly in both types of vascular cells. The expression of GFP in HUVECs was higher than that in HITASY cells. Meanwhile, the expression of GFP in HITASY cells with 0.5% FBS was increased obviously compared to that in HITASY cells with 10% FBS. CONCLUSION: The reporter vectors of hCREG1 promoter are constructed successfully in which the core promoter region might be located in -945 bp-0 bp of 5′ upstream sequences. This study will provide an experimental basis for exploring the regulation of hCREG1 expression.