利用Lageos 1 SLR资料解算1990-2001年的地球定向参数

利用 12年的Lageos 1卫星激光测距资料 (1990 - 2 0 0 1)解算得到了地球定向参数 (EOP) ,将该序列的结果与同期的EOP(IERS)C0 4进行比较 ,其外符精度为 :极移XP— 0 .4 0mas,YP— 0 .4 2mas ,日长变化Dr— 0 .0 35ms。     

对月日潮汐摩擦耗散的估计

月日潮汐摩擦和地球惯量矩变化是日长长期变化的主要原因．在本文中，利用最新的地球物理和古生物钟数据，对过去15亿年以来的月日潮汐摩擦、地球惯量矩变化和日长长期变化等作了数值对比研究．由此得到二个重要结论：一是仅利用地球的自转形变不能解释J2的变化，这说明地球的重力分异现象至今仍存在着；其二是在几亿年前的潮汐摩擦比现在大得多，若取潮汐耗散与距离的立方成反比时，理论结果与由古生物钟得到的回归年日数和朔望月日数数据较为符合。     

围绕中心强化服务努力拓展测绘工作新视野

测绘，顾名思义，就是测而绘之，是测量与绘图的总称，就是采用科学技术手段获取、处理、管理和分发地球上各种与地理位置有关的自然、社会和人文的空间信息，从而为经济建设和社会发展服务。测绘科学是在人类与自然斗争的实践中逐步发展起来的。随着科学技术和生产实践的不断发展，测绘由简单的测量绘图转变为科学测绘，     

CHARACTERIZATION OF LACTATE DEHYDROGENASE ISOZYME PATTERN AND MORPHOLOGY OF THREE MARINE FISH CELL LINES

Three continuous marine fish cell lines of FG (i. e., Hounder Gill) from flounder (Paralichthys olivaceus) gill, SPH (i. e. , Sea Perch Heart) from sea perch (Lateolabrax japonicus) heart and RSBF (i.e., Red Sea Bream Fin) from red sea bream (Pagrosomus major) fin, were characterized by lactate dehydrogenase (LDH) isozyme and morphological analysis. The LDH isozyme patterns of these three cell lines and their corresponding tissues of origin were investigated and compared. The results showed: (1) No difference was found in the LDH isozyme patterns of FG and flounder gill tissue. However, the LDH isozyme patterns of SPH and RSBF were significantly different from their corresponding tissues of origin; (2) LDH isozyme patterns of FG, SPH and RSBF were markedly different from each other and could serve as genetic markers for species identification and detection of cross contamination. Morphological change analysis of these three cell lines in comparison to their original tissues indicated that FG cells still appeared epithelioid without morphological transformation. However, morphological changes were found in SPH and RSBF compared to their original tissues. Therefore, the cellular morphology was still plastic in the relatively stable culture conditions, and it was possible that change of LDH patterns wasrelated to morphological changes of fish cells in vitro.