青藏高原草地退化原因述评

导致青藏高原草地退化的因子很多,主要有气候、野生动物和人类活动等。在气候因素中以气温和降水的影响为主,短期内气候的变化不会成为草地退化的主导因素,从长期来看,气候变化与草地退化之间的相互作用可引起草地生态系统的退化;野生动物因素中主要以植食性小哺乳动物的影响为主,其危害程度取决于其种群数量的高低,同时大型野生草食动物对草地退化的影响也不容忽视;人类活动因素中主要以家畜过度放牧为主,在一定程度上,家畜放牧强度的高低直接决定草地的退化程度;草地退化是多种因素综合作用的结果。不同地区导致草地退化的主要因素不尽相同,导致青藏高原草地退化最主要的因子是过度放牧和植食性小哺乳动物种群爆发。针对退化的原因,提出了青藏高原退化草地恢复与管理过程中应注意的事项。     

佛山市高明区生态安全格局和建设用地扩展预案

城市生态环境问题已上升到生态安全的层面.以人类生存安全和理想人居环境为目标,基于空间数据和统计资料,利用景观安全格局原理和地理信息系统空间分析方法,构建了包含基本保障格局-缓冲格局-最优格局3个级别的水安全格局、地质灾害安全格局、大气安全格局、生物保护安全格局和农田安全格局,叠加得到高明区综合生态安全格局,在此基础上提出了高明区建设用地扩展最优方案和生态功能分区.结果显示,并非生态安全格局水平越高,城乡发展模式越优,缓冲生态安全格局下的高明区建设用地扩展模式,最可能实现生态安全保护与城镇扩展的和谐发展.综合生态安全格局明确了区域的生态环境敏感区和生态服务功能重要区,为区域生态功能分区提供了新的思路.     

基于GIS的那坡县林地景观格局分析

运用ARCGIS软件的扩展模块Patch Analyst,以那坡县林地保护利用规划的基准年(2009)数据为基础数据,基于10个林地景观类型,计算其景观形状特征指数、景观破碎化指数、多样性指数;按优势树种将森林景观划分为14个景观,并计算其多样性指数。结果表明:景观形状指数特征表明林地景观的斑块边界褶皱程度不高,乔木林景观受人为活动干扰程度较小;景观破碎化特征表明乔木林景观在林地景观中占主导地位,其受人为干扰的程度较低;林地地类与森林景观类型的多样性与其最大多样性指数相差较大,说明各分类所占面积比例差距较明显。     

靶向S基因外源性microRNA抑制TGEV增殖效果的研究

应用生物信息学软件对猪传染性胃肠炎病毒(TGEV)S基因进行分析,筛选出可能与S基因有相互作用的外源miRNA:amiRNA-S-28035,amiRNA-S-28038,amiRNA-S-28165。之后,利用脂质体将构建好的相应的表达载体瞬时转染至PK-15细胞;通过Q-PCR和间接免疫荧光方法检测其对S基因的抑制作用;CPE分析和TCID50测定检测其对TGEV增殖的抑制效果。结果发现,3个外源性miRNA均降低了S基因mRNA的转录和蛋白的表达,其中amiRNA-S-28038对TGEV mRNA的平均抑制率可达64.6%,最高可达69.9%,表明外源性microRNA可以通过靶向TGEV基因组来抑制TGEV的复制。研究结果为猪传染性胃肠炎的预防和治疗提供了新的思路。     

高山草原绵羊放牧生态及消化代谢的研究：Ⅰ放牧绵羊嗜食性研究

利用植物显微技术镜检法和食道瘘管法对放牧绵羊采食的高山草原植物成分与嗜食性指数进行分析。结果表明，绵羊在黄草期采食植物成分比青草期多，其嗜食性指数在不同时期变幅较大，随着冬季来临，绵羊对草地植物的嗜食性不如青草期强烈，至某些植物嗜食性是相对稳定的。     

5种花梨木的红外光谱比较分析

为了提供识别花梨木品种的新思路和新方法,采用红外光谱分析方法,对越柬紫檀、刺猬紫檀、印度紫檀、大果紫檀、鸟足紫檀5种花梨木的一维红外光谱(FTIR)、二阶导数光谱(SDIR)、二维相关红外光谱(2DIR)进行对比分析。结果表明:1)在FTIR谱图中,5种花梨木在781 cm-1处的差异可以把越柬紫檀和刺猬紫檀与其他3种花梨木区分开;2)在SDIR 谱图中,刺猬紫檀在1 179 cm-1处存在1个吸收峰;大果紫檀在781 cm-1处存在吸收峰;鸟足紫檀在1 351、1 299、1 147、1 131、938 cm-1处都有明显的吸收峰,而印度紫檀没有吸收峰;3)在2DIR谱图中,1 100、1 150、1 258 cm-1处的差异可以将刺猬紫檀与其他4种花梨木区分开,1 467、1 518 cm-1处的差异可以把越柬紫檀、刺猬紫檀与鸟足紫檀区分开来。单独使用2DIR识别方法并不能把5种花梨木完全区分,但将FTIR、SDIR、2DIR这3种方法结合可以实现5种花梨木的区分,也有助于红木树种的无损识别。      

内燃机空气滤清器试验台的研究

空气滤清器的性能优劣对发动机的性能有着重要的影响,为此建立内燃机空气滤清器试验台有着至关重要的作用.根据待测的空气滤清器的主要性能指标确定了空气滤清器试验台的基本配置及功用,并在此基础上以虚拟仪器技术作为控制核心初步构建了用以检测空气滤清器性能的试验系统.     

Influence of murine cytomegalovirus infection on the differentiation and the differentiation genes expression in neural stem cells

AIM: The influence of MCMV infection on differentiation and differentiation gene expression in neural stem cells(NSCs) in vitro were investigated for studying the mechanisms of brain abnormalities caused by congenital cytomegalovirus infection.METHODS: NSCs were separated from fetal BALB/C mouse, and cultured and identified in vitro. The differentiation potency of NSCs was observed by immunofluorescence. The NSCs infected by MCMV at dosage of MOI(multiplicity of infection) equaled to 5, 1 and 0.1,respectively, were cultured in differentiation medium. The morphological changes of infected cells were observed under inverted microscope. The ratios of NSCs and its differentiated cells were detected by flow cytometry. The expressions of nestin, GFAP and NSE, markers of NSCs and its differentiated cells, were studied by immunofluorescence(MOI=1). The expression of early antigen(EA) of MCMV was detected to observe the infection process. Real-time RT-PCR method was employed to measure the expression levels of the key genes Neurog2, Myc and Ccnd1 in Wnt signal pathway of NSCs at early stage of differentiation culture.RESULTS: NSCs isolated from embryonic mouse brains proliferated to form neurospheres, strongly expressed nestin and differentiated into NF-200 positive neurons or GFAP positive astrocytes. The infected NSCs did not adhere to the wall and appeared differentiation growths, but showed swollen gradually after differentiation culture. The nestin expression in the infected cells downregulated slowly and was higher than that in control groups(P<0.05). The GFAP and NSE expressions of the infected cells were lower than those in control groups(P<0.05). The early antigen(EA) of MCMV was always detected in the cells in infected groups. The ratios of nestin positive cells in infected groups were higher than those in control groups, but the ratios of GFAP and NSE positive cells of former were lower than that of the latter from 3rd to 9th d after differentiation culture(P<0.05). The levels of Neurog2 mRNA and Myc mRNA in infected groups were markedly lower than those in normal control groups on 1st d and from 1st to 4th d after differentiation culture, respectively(P<0.05). The levels of Ccnd1 mRNA of infected groups were obviously lower than those in normal control groups from 12th h to 1st d(P<0.05). These changes in infected groups became more obvious as MCMV MOI increased.CONCLUSION: MCMV significantly inhibits differentiation of NSCs to neurons and astrocytes, and leads to the decrease in differentiated cells. MCMV inhibits or interferes with the gene expression of Neurog2, Myc and Ccnd1 in Wnt signal pathway of NSCs. The effect that MCMV inhibits the expressions of differentiation and the differentiation genes in NSCs shows dose-dependent with MCMV MOI. The inhibitory effect of MCMV on the differentiation of NSCs might be induced by interfering with the expression of differentiation gene in NSCs, which is possibly the one of primary causes of brain development disorders induced by congenital CMV infection.     

高铜日粮对肉鸡肝细胞线粒体呼吸链复合物活性的影响

在对照组（Cu 11mg／kg，A组）基础上设高铜组3个（110mg／kg、220mg／kg和330mg／kg，分别对应为试验组B、C、D），试验期为60d，在12、24、36、48、60日龄采集肝组织，提取线粒体，测定线粒体复合物Ⅰ、Ⅱ、Ⅲ、Ⅳ和Ⅴ的活性变化。结果表明，11mg／kg和110mg／kg铜日粮添加组线粒体复合物Ⅰ、Ⅱ、Ⅲ、Ⅳ、Ⅴ的活性呈增加趋势。220mg／kg和330mg／kg铜日粮添加组肉鸡肝细胞线粒体复合物Ⅰ、Ⅱ、Ⅲ、Ⅳ、Ⅴ活性减弱，但主要在试验后期，尤其是48日龄之后，比对照组和各组内的试验前期下降明显（P〈0．05）。说明高铜日粮在一定程度上对线粒体复合物活性是有利的，但过高的铜添加到日粮中（≥220mg／kg）可降低肉鸡肝细胞线粒体呼吸链复合物的功能活性。据此可以推测，线粒体是机体铜过量状态下侵害的靶部位之一，而且能作用于线粒体各个复合物，造成线粒体呼吸功能减弱，呼吸链中电子传递发生故障，从而影响线粒体功能的正常发挥。