精密光机系统多敏感轴装配精度分析与装配工艺优化

精密光机系统是对地、空、海探测与制导装备中的核心部件,其光轴、惯导轴、机械轴等多敏感轴的精密装配是影响系统最终性能的关键环节之一。以某型装备为研究对象,通过分析该类精密光机系统的装配特点,将多敏感轴的精密装配问题转换为舱体对接时的角偏问题,并进行了阐述和定义;在此基础上,建立了多敏感轴装配过程的角偏误差累积模型,并推导了加工误差与角偏分布之间的关系;基于该模型对当前的直接对接法进行建模,分析了该方法导致装配一次性合格率较低的原因,并提出了一种基于装配方向调整的逐工序优化装配方法,该方法优化了现有的多敏感轴精密装配工艺。仿真结果表明,与直接对接法相比,所提方法能够有效保证各敏感轴线之间的装配精度。     

基于振动的土壤挖掘阻力与耗能特性试验研究

为了研究振动频率、振动方向等参数对振动式土壤挖掘降阻特性和耗能特性的影响,设计开发了振动式土壤挖掘阻力试验台。经理论分析、计算确定了振动挖掘机构运动参数。在土壤平均相对湿度为27%、平均土壤坚实度为2.2MPa条件的室内土槽系统中,在挖掘深度150mm、前进速度0.15~1.00m/s、振动频率2~20Hz的因素条件下,利用该试验台开展了土壤振动挖掘阻力和耗能特性试验研究。结果表明,振动式土壤挖掘能够有效降低工作阻力,其降阻率先随着振动频率增大而增大,在2~20Hz频率段,前后方向振动和垂向振动振幅分别为13mm和10mm时,其最大降阻率分别可达到21%和25%。降阻率在10~14Hz后增长速度变缓,表明该区间处于土壤的自振频率区间。前后方向振动下土壤挖掘降阻率和振动速度与前进速度的比值有关,当振动速度小于前进速度时,降阻率比较小,随着振动频率增加而缓慢增大;当振动速度大于前进速度后,在对应的频率点其降阻率会迅速上升,之后增长速度逐渐变缓。由于需要额外激振能量输入,两种振动方向的强迫振动式土壤挖掘综合耗能并不减少,在振动频率低于10Hz下,耗能比范围在1~1.07,但超过10Hz后,耗能比会随着振动频率增大以较快速度增加。振幅的增大能够使土壤挖掘阻力获得一定的降低,但同时振动挖掘耗能有较大的增加。     

基于部分亲和场的行走奶牛骨架提取模型

在奶牛关键点预测的基础上,通过点、线重构奶牛骨架结构,可为奶牛跛行检测、发情行为分析、运动量估测等提供重要参考。本研究基于部分亲和场,以养殖场监控摄像头拍摄的视频为原始数据,使用1 600幅图像训练了奶牛骨架提取模型,实现了奶牛站立、行走状态下关键点信息和部分亲和场信息的预测,并通过最优匹配连接对奶牛骨架结构进行准确提取。为了验证该模型的性能,采用包含干扰因素的100幅单目标奶牛和100幅双目标奶牛图像进行了测试。结果表明,该模型对单目标行走奶牛骨架提取的置信度为78.90%,双目标行走奶牛骨架提取的置信度较单目标下降了10.96个百分点。计算了不同关键点相似性(Object keypoint similarity,OKS)下的模型准确率,当OKS为0.75时,骨架提取准确率为93.40%,召回率为94.20%,说明该模型具有较高的准确率。该方法可以提取视频中奶牛骨架,在无遮挡时具有高置信度和低漏检率,当遮挡严重时置信度有所下降。该模型的单目标和双目标图像帧处理速度分别为3.30、3.20 f/s,基本相同。本研究可为多目标奶牛骨架提取提供参考。     

阔叶猕猴桃果实GalDH cDNA 克隆及其在大肠杆菌中的表达

 以猕猴桃属植物中果实维生素C含量最高的阔叶猕猴桃(Actinidia latifolia Merr. ) 果实为试 材, 经RT2PCR扩增获得约110 kb的L - 半乳糖脱氢酶cDNA片段。生物信息学分析表明, 该cDNA片段长为997 bp, 最大开放阅读框为960 bp, 可编码319 个氨基酸残基, 命名为A lGalDH, GenBank登录号为EU525846, 核苷酸序列及其推导的氨基酸序列与已知其它植物GalDH核苷酸、氨基酸序列间的同源性分别在76%和70%以上, 且具有醛酮还原酶的保守结构域。构建了其原核表达载体pET-A lGalDH并转化大肠杆菌BL21, 经0.1 mmol·L ^{- 1} IPTG诱导, 获得具有较高活性的表达融合蛋白6 ×His-AlGalDH。经Ni-His亲和磁珠分离纯化, 获得单一的融合目的蛋白条带, 测定其酶活为120 pmol·min^{- 1} ·mg^{- 1}。     

樱桃透光和郁闭树冠相对光照强度及其果实品质和产量的差异

 以13年生‘红灯’甜樱桃（Prunus avium L.）为试材,应用树冠分格方法,研究了树冠透光和郁闭两种冠型内相对光照强度及其果实品质和产量的差异,以及相对光照强度与果实产量品质的关系。结果表明,两种树冠内相对光照强度均自下而上逐渐增高,透光和郁闭树冠小于30%的相对光照区域分别占树冠总体积的25.23%和52.78%。透光树冠果实分布均匀,主要集中在树冠1.5～2.5 m的高度;而郁闭树冠果实分布差异较大,主要在树冠的外围和上部;产量分别是9.02t.hm-2和3.53t.hm-2。果实品质因素与相对光照强度的回归分析表明樱桃单果质量、果实硬度、果实可溶性固形物含量、可滴定酸含量、固酸比最佳的相对光照强度值分别为76.52%、46.84%、100.00%、41.63%和75.77%。     

Effect of atorvastatin on neointimal hyperplasia of venous autografts in rats

AIM: To investigate the effect of atorvastatin on neointimal hyperplasia of autogenous vein graft in rats. METHODS: The model of autogenous vein graft was prepared by transplanting the external jugular vein into aorta in Wistar rats. The rats were divided into three groups: sham operation group, graft control group and graft experimental group. From three days after transplantation, the rats of autograft experimental group were treated by atorvastatin at a dosage of 5 mg·kg-1·d-1. Four weeks after treatment, venous autografts were removed at autopsy and cut into 4 μm sections. Histopathological examination was carried out to analysis the neointimal hyperplasia of grafted veins. Immunohistochemical staining was conducted to evaluate SMα-actin and PCNA expression of neointimal cells in venous autografts. RESULTS: In venous autograft control and experimental groups, SMα-actin-positive smooth muscle cells were proliferated and accumulated excessively in venous autografts, which resulted in significant neointimal formation and vascular lumen narrowing. Neointima quantitative assay revealed that the neointimal hyperplasia of venous autografts was suppressed obviously in graft experimental group, and its neointimal area and NIA/MA ratio of venous autografts were significantly lower than those in graft control group (P<0.01). Immunohistochemical assay indicated that the PCNA labeling index of neointimal cells was significantly lower in graft experimental group than that in graft control group (P<0.01). CONCLUSION: Atorvastatin significantly inhibits the proliferation of neointimal smooth muscle cells and the development of neointimal hyperplasia of venous autografts in rats. Atorvastatin is a powerful inhibitor of restenosis after vascular reconstructive operation with a potential for therapeutic use.     

In vitro differentiation of exocrine pancreatic cells from mouse embryonic stem cells

AIM: To explore the effects of sodium butyrate, activin A and dexamthasone on inducing mouse embryonic stem (ES) cells to differentiate into exocrine pancreatic cells in vitro. METHODS: E14 mouse ES cells were cultured in suspension to form embryonic bodies (EBs). The EBs were cultured with differentiating medium containing different concentrations of sodium butyrate, and the spontaneously differentiated ES cells were used as control. Exocrine pancreatic genes such as amylase, chymotrypsinogen, elastase 1, elastase 2 and carboxypeptidase were detected by RT-PCR at different time points to determine the optimal concentration and exposure time of sodium butyrate. Furthermore, activin A or dexamthasone was also used to explore the effects on exocrine differentiation. After that, the combination of sodium butyrate, activin A and dexamthasone was used to promote the differentiation of exocrine pancreatic cells from ES cells. During the differentiation course, the gene expressions of amylase, chymotrypsinogen, elastase 1, elastase 2 and carboxypeptidase were detected by RT-PCR. Morphological changes were investigated by phase contrast microscopy. Amylase expression was examined by immunofluorescence staining. RESULTS: Exocrine pancreatic gene expressions such as amylase, chymotrypsinogen, elastase 1, elastase 2 and carboxypeptidase were detected in spontaneously differentiated EBs. A relatively lower concentration of sodium butyrate with a shorter exposure time significantly promoted those above gene expressions as compared to that of spontaneously differentiated EBs. Activin A and dexamethasone induced upregulation of exocrine gene expression. The combination of activin A, sodium butyrate and dexamethasone significantly enhanced the mRNA levels of amylase, chymotrypsinogen, elastase 1, elastase 2 and carboxypeptidase. Under the treatment of activin A, sodium butyrate and dexamethasone, differentiated cells were polygonal in shape with large, round, and center-situated nuclei. According to the observation of immunofluorescence staining, amylase was positive expressed at the final stage. CONCLUSION: These data indicate that exocrine pancreatic differentiation of ES cells is induced by sodium butyrate, activin A and dexamethasone. The combination of pancreatic inducing factors improves the differentiating efficiency.     

黄连、黄芩提取液与二氧化氯复配对结球甘蓝种传黑斑病的抑菌效果研究

采用三元二次回归正交旋转组合设计方法,确立了黄连、黄芩提取液与二氧化氯对甘蓝链格孢菌抑制效果最佳的复配组合:黄连提取液13.48%、黄芩提取液15.56%、二氧化氯0.14%.用此复配剂浸种,芸苔链格孢菌和甘蓝链格孢菌的侵染率分别降低了97.33%和94.85%,且提高了种子发芽势及萌发相关酶活性.     

山东省沙地葡萄茎痘相关病毒的检测

为明确沙地葡萄茎痘相关病毒(GRSPaV)在山东省发生的情况,2006-2007年在葡萄主栽区和葡萄品种资源圃进行了田间调查、样品采集和病原检测。应用GRSPaV外壳蛋白基因表达获得的多克隆抗体,经间接酶联免疫吸附试验(PTA-ELISA)和斑点酶联免疫吸附试验(Dot-ELISA)检测,在2a采集的298个样品中,125个样品为阳性反应,阳性率41.95%。125个阳性样品涉及43个品种,品种被侵染率74.14%。研究对检测的样品用RT-PCR法验证,有3对引物均扩增出了预期片段,分别为解旋酶基因340bp片段、外壳蛋白(CP)基因842bp片段和RNA聚合酶(RdRp)基因499bp片段。     

东方红-YZDZ80C液压自行式移动电站

介绍东方红-YZDZ80C液压自行式移动电站的主要技术参数和主要部件结构性能特点。