Molecular and bulk isotopic analyses of organic matter in marls of the Mulhouse Basin (Tertiary, Alsace, France)

Contents of 13C in kerogens and carbonates in 21 samples from a core of the MAX borehole, Mulhouse Evaporite Basin, range from -27.3 to -23.5 and -3.7 to -1.8% vs PDB, respectively. Organic nitrogen in the same samples is enriched in 15N relative to atmospheric N2 by 12.2-15.7%. Hydrogen indices and delta values for kerogens vary systematically with facies, averaging 493 mg HC/g Corg and -25.7% in the most saline facies (dominated by inputs from aquatic sources) and 267 mg HC/g Corg and -23.7% in the least saline facies (50/50 aquatic/terrigenous). Values of delta were measured for individual aliphatic hydrocarbons from three samples representing three different organic facies. For all samples, terrigenous inputs were unusually rich in 13C, the estimated delta value for bulk terrigenous debris, apparently derived partly from CAM plants, being -22.5%. In the most saline facies, isotopic evidence indicates the mixing of 13C-depleted products of photosynthetic bacteria with 13C-enriched products of halotolerant eukaryotic algae. At lower salinities, a change in the producer community is marked by a decrease in the 13C content of algal lipids. The content of 13C in algal lipids increases in the least saline facies, due either to succession of different organisms or to decreased concentrations of dissolved CO2.     

Molecular indicators for palaeoenvironmental change in a Messinian evaporitic sequence (Vena del Gesso, Italy). II: High-resolution variations in abundances and 13C contents of free and sulphur-bound carbon skeletons in a single marl bed

The extractable organic matter of 10 immature samples from a marl bed of one evaporitic cycle of the Vena del Gesso sediments (Gessoso-solfifera Fm., Messinian, Italy) was analyzed quantitatively for free hydrocarbons and organic sulphur compounds. Nickel boride was used as a desulphurizing agent to recover sulphur-bound lipids from the polar and asphaltene fractions. Carbon isotopic compositions (delta vs PDB) of free hydrocarbons and of S-bound hydrocarbons were also measured. Relationships between these carbon skeletons, precursor biolipids, and the organisms producing them could then be examined. Concentrations of S-bound lipids and free hydrocarbons and their delta values were plotted vs depth in the marl bed and the profiles were interpreted in terms of variations in source organisms, 13 C contents of the carbon source, and environmentally induced changes in isotopic fractionation. The overall range of delta values measured was 24.7%, from -11.6% for a component derived from green sulphur bacteria (Chlorobiaceae) to -36.3% for a lipid derived from purple sulphur bacteria (Chromatiaceae). Deconvolution of mixtures of components deriving from multiple sources (green and purple sulphur bacteria, coccolithophorids, microalgae and higher plants) was sometimes possible because both quantitative and isotopic data were available and because either the free or S-bound pool sometimes appeared to contain material from a single source. Several free n-alkanes and S-bound lipids appeared to be specific products of upper-water-column primary producers (i.e. algae and cyanobacteria). Others derived from anaerobic photoautotrophs and from heterotrophic protozoa (ciliates), which apparently fed partly on Chlorobiaceae. Four groups of n-alkanes produced by algae or cyanobacteria were also recognized based on systematic variations of abundance and isotopic composition with depth. For hydrocarbons probably derived from microalgae, isotopic variations are well correlated with those of total organic carbon. A resistant aliphatic biomacromolecule produced by microalgae is, therefore, probably an important component of the kerogen. These variations reflect changes in the depositional environment and early diagenetic transformations. Changes in the concentrations of S-bound lipids induced by variations in conditions favourable for sulphurization were discriminated from those related to variations in primary producer assemblages. The water column of the lagoonal basin was stratified and photic zone anoxia occurred during the early and middle stages of marl deposition. During the last stage of the marl deposition the stratification collapsed due to a significant shallowing of the water column. Contributions from anaerobic photoautotrophs were apparently associated with variations in depth of the chemocline.     

0．7Ma以来的念青唐古拉山脉隆升过程——来自冰川剥蚀作用的证据

通过对念青唐古拉山冰碛地层划分及冰碛物同位素测年，发现最早一期冰碛物形成于0．7～0．6MaBP，指示自中更新世以来念青唐古拉山脉开始隆升，主峰地区发生了大规模的冰川剥蚀作用，形成了大面积分布的冰碛高平台；0．2～0．14MaBP念青唐古拉山又快速隆升，并堆积了刚刚伸出各大沟谷口的高侧碛；0．07～0．03MaBP念青唐古拉山再次小规模隆起，形成各大沟谷内的侧碛和终碛垄；0．01Ma BP还有小规模冰川活动。念青唐古拉山主峰地区的冰川剥蚀作用反映出的山脉隆升过程，可较好地与青藏高原的隆起过程相对比，它应是青藏高原隆升的响应。     

地震勘探中的炸药震源药量理论与实验分析

炸药由于具有良好的脉冲特性及高能量的特点而作为地震勘探中的主要震源，就炸药本身来说，在地震勘探中药量、井深等参数的选取对激发能量和激发频率有很大的影响。为此，本文运用炸药爆炸理论，从炸药作功角度来加以论述，并通过理论和实验分析得出选取一个最佳的药量和井深激发，既能提高炸药作功能力，又能增强激发能量，从而激发强能量的高频震源子波，达到指导野外地震采集和节约经济成本的目的。     

海原断裂带西段断层泥的分形研究

利用光学和电子显微镜研究了海原断裂带西段断层泥的粒径分布，５微米至１厘米的粒径段，断层泥具有自相似特征，断层面的粘滑摩擦的特征位移参数可由分维上限（约１厘米）确定。同时用分形理论分析了断层泥粒度分重量百分比的分形结构特征，探讨了粒度成分分维值与断层运动特征的关系。     

黑龙江省东部跃进山群中绿片岩的地球化学特征及地质意义

跃进山群出露位于佳木斯地块和那丹哈达地体之间，是完达山造山带的组成部分。它由大陆斜坡相沉积物、大洋中脊型玄武岩和洋岛型玄武岩组成，其中有镁铁－超镁铁质岩块体。它不是一个地层单位，而是与活动大陆边缘板块俯冲作用有关的蛇绿混杂岩     

安徽省江淮地区清水钻进的管井取水效果探讨

本文根据施工实践的结果，综合分析对比了清水钻进与泥浆钻进的管井取水效果，指出清水钻进成井工艺是在现有机具设备条件下提高管井单井取水量的一个重要技术措施。特别是在安徽江淮相对贫水地区，采用清水钻进工艺成井的地质效果尤为明显。     

吉林延边缝合带的性质与东北亚构造

根据近年的新进展，讨论了延边缝合带的性质，认为它是晚侏罗世兴凯地块与龙岗-冠帽地块联合的增生缝合带，属于东北亚中生代环太平洋构造带的一部分。中国东北与整个东北亚一样．中生代构造主要形成于晚侏罗世-早白垩世，其内带是大陆(包括大陆边缘)碎块的增生．外带主要是具有特提斯洋特征的洋壳和岛弧碎块的增生。     

近20年华北地电阻率异常空间演化及强震短期前兆判别标志研究

开展了华北地电阻率异常参数提取的研究，以1980—2001年的异常参数为输入进行了全时空扫描，并对其动态图像演化做全面分析，由此提取出华北地区5级以上地震的地电阻率短期前兆的判别标志。为了进行初步检验，本文依上述判别标志对华北近年地电阻率动态图像做了对比分析。     

石灰改良高液限土强度特性的函数模型研究

针对广西荔玉高速路基沿线产生的大量高液限土弃方问题,采用生石灰对高液限土进行改良处理。选取弃土场的高液限土,分别配制不同初始含水率、不同石灰掺量的试样进行侧限压缩试验和快剪试验,采用基本初等数学函数模型拟合不同饱和状态、不同初始含水率下石灰掺量对试件压缩特性和抗剪强度影响。结果表明:(1)高液限土的压缩系数随石灰掺量增加呈指数形式减小;(2)不同饱和状态试件的黏聚力和内摩擦角随石灰掺量增加呈二次函数形式变化;(3)高液限土具有水敏性,饱和素土试件最大抗剪强度对应的含水率较击实试验最大干密度对应的含水率高3%～6%;(4)当初始含水率不高于26.73%时,建议石灰掺量不低于6%,否则改良高液限土的石灰掺量不低于8%,可在满足经济性的前提下达到较好的改良效果。