以专业实验室评估为契机积极推进学生素质教育

教育的目的就是为了全面提高人的素质，为适应素质教育的需要，积极推进专业实验室评估势在必行。本文就我院当前形势，结合专业实验室评估的实际工作，对以专业实验室评估为契机积极推进学生素质教育进行了深入的剖析。     

孤岛油田馆(1+2)地层划分对比与沉积模式

孤岛油田馆(1 2)砂层组属于河流相沉积，其纵向、横向相变迅速，砂体难以大面积追踪，本利用河流结构单元分析法、标准层与辅助标志层控制下的“旋回-厚度”对比法，很好地解决了馆(1 2)地层的划分对比问题，其中馆(1 2)砂层组内辅助标志层的发现为地层的划分对比提供了重要的保证．根据结构单元分析、砂体的岩性特征、粒度特征、河流砂体的空间展布形态以及河流曲率的计算，对馆(1 2)河流沉积的垂向旋回性及沉积模式进行了研究。对比Miall的16种河流分类方案，孤岛油田馆(1 2)砂层组属于细粒曲流河沉积．     

The essential bacterial cell-division protein FtsZ is a GTPase.

Cytokinesis defines the last stage in the division cycle, in which cell constriction leads to the formation of daughter cells. The biochemical mechanisms responsible for this process are poorly understood. In bacteria, the ftsZ gene product, FtsZ, is required for cell division, playing a prominent role in cytokinesis. The cellular concentration of FtsZ regulates the frequency of division and genetic studies have indicated that it is the target of several endogenous division inhibitors. At the time of onset of septal invagination, the FtsZ protein is recruited from the cytoplasm to the division site, where it assembles into a ring that remains associated with the leading edge of the invaginating septum until septation is completed. Here we report that FtsZ specifically binds and hydrolyses GTP. The reaction can be dissociated into a GTP-dependent activation stage that is markedly affected by the concentration of FtsZ, and a hydrolysis stage in which GTP is hydrolysed to GDP. The results indicate that GTP binding and hydrolysis are important in enabling FtsZ to support bacterial cytokinesis, either by facilitating the assembly of the FtsZ ring and/or by catalysing an essential step in the cytokinetic process itself.     

均匀细圆环和均匀薄圆盘对任意轴线的转动惯量

分别运用一般方法和投影法计算了均匀细圆环和均匀薄圆盘对任意轴线的转动惯量,在验证投影法计算结果正确性的基础上,对计算结果进行了讨论,可以用于对实际问题的分析研究.     

Male tarsal sex-comb teeth pattern in theDrosophila bipectinata complex

Summary Species within theD. bipectinata species complex pose problems experimentally because of their morphological similarity. By measuring the number of teeth in each row of the male tarsal sex-comb, an unknown specimen can be allocated to a hybrid or parental group by means of a discriminant function. This paper describes which rows of the sex-comb are the best discriminators for particular comparisons.Acknowledgments. We thank L. Anderson and P. Rowbury for technical and research assistance, Dr I. Bock for providing fly stocks and for his continued interest and helpful discussions, and the Australian Research Grants Scheme for financial assistance.     

Tumor-derived angiogenesis factors from rat Walker 256 carcinoma: an experimental investigation and review

Summary Angiogenesis, the process of developing a hemovascular network, is an essential feature of the growth of solid tumors, and is induced by factors secreted by tumor cells. Assay procedures suitable for the investigation of angiogenesis, and for the screening of angiogenesis factors during purification are reviewed; and a number of reports describing the purification of angiogenesis factors, primarily from the rat Walker 256 carcinoma as starting material, are discussed. Work from the authors' laboratory is also presented. Walker 256 cells grown in large-scale culture were the source of a reproducible and homogeneous source of angiogenic material. Factors secreted by these cells were isolated by a series of chromatographic steps. Ion exchange chromatography on carboxymethyl-Sephadex produced two active fractions, one of which was fractionated into several macromolecular species by lectin affinity and hydrophobic adsorption chromatography. The other gave a high mol.wt, active fraction that was resolved into a low mol.wt, active component and a non-angiogenic but possibly carrier molecule with a mol.wt of 140,000. While none of the angiogenic factors were identified chemically, the results demonstrate the existence of both high and low mol.wt tumor-secreted angiogenic substances, confirming the hypothesis for tumor-induced angiogenesis and predicting potential means to interfere with the process of tumor growth.This work was supported by funds from the Monsanto Company under Agreements with Harward University and from the U.S. Public Health Service, Contract No. N01-CB-43942. We are particularly indebted to Bernard S. Wildi and Monte C. Throdahl for their advice, cooperation, and encouragement. We also thank Dr Judah Folkman for the initial supply of male mouse submaxillary glands and rat Walker carcinoma conditioned medium, for help with the CAM assays, assays in the rabbit cornea, and many helpful discussions; and R. Bretton, A. Ehrlich, B. Evans, F. Fu, N. Hay and B. Tsokanis for excellent technical assistance.Author to whom correspondence should be addressed.