加拿大和美国高放废物地质处置研究概况

本文主要介绍了作者2000年对加拿大和美国进行科学访问时实地考察所了解到的加拿大的核素在裂隙和孔隙介质中的迁移模式，地下实验室，白壳实验室（Whiteshell Labs)，高放废物处置库场地预选和美国拟作为高放废物处置库的尤卡山场地和已投入运行的军用超铀废物处置库的废物镉离实验工厂；着重论述了这两个国家的高放废物地质处置研究现状、经验和所取得的成果。     

真空堆载联合预压加固软基中孔隙水压力消散规律研究

通过实测资料分析了真空堆载联合预压中不同深度的孔隙水压力、超孔隙水压力、相对超孔隙水压力随时间的变化规律,并对孔压变化的原因进行了微观解释。结果表明:(1)处理区外侧,孔压变化主要由地下水位下降引起,受真空影响较小;(2)在处理区内,孔压变化受真空负压、土体渗透性和堆载荷载的影响。真空作用下的渗流是孔压消散的主要方式,土体渗透性的强弱影响着孔压消散的速度,消散的孔压转化成有效应力,促使土颗粒移动,对孔隙水产生挤压,这使孔压消散呈脉动性特征。     

沙质海床对波浪的响应及其稳定性研究的回顾

本文简要回顾了前人关于沙质海床在波浪作用下的响应，液化和稳定性等方面问题和研究状况。对各研究中所采用的计算模型、计算方法、应用范围以及存在的问题作了较为系统的评述。此外对各问题的最新研究成果也作了简要的介绍，最后讨论了该领域中有待于进一步研究的问题。     

静动力排水固结法中孔压、土压的响应特征及应用研究

在静动力排水固结法处理饱和软黏土地基处理的场地进行现场的数据测试,分析了该条件下的孔隙水压力和土压力的响应规律,提供在一定的施工条件下沉降规律及与孔压、土压响应关系的求解方法,为静动力排水固结法加固淤泥类软土地基的研究和工程实践提供了一定的参考依据。     

用切比雪夫多项式标准化GPS卫星轨道

根据精密星历提供的等时间间隔点上的卫星坐标,采用切比雪夫多项式拟合的方法,选用达到精度要求的最佳拟合多项式阶数,对GPS卫星轨道进行标准化,从中得出:选用不同的多项式阶数直接影响到拟合的精度。     

《测绘科学技术学报》荣获教育部科学技术司“第二届中国高校优秀科技期刊”奖

由教育部科学技术司组织的“第二届中国高校精品·优秀·特色科技期刊”评比活动於2008年10月20日结束。此次评比活动共评出精品科技期刊76种,优     

淮南煤田同变质程度不同煤层煤的成烃作用和储气性研究

本文从煤岩学、有机地球化学及煤的储气性原理出发,研究了淮南煤田同变质程度不同煤层煤(B_11b、B₁₀)在成烃母质、富烃特征、成烃作用和储气性等方面的差异性。B_11b煤层中含有较多的似石油物质、渗出体、显微组分等的荧光浸渍现象、油滴和油膜、微粒体等,它们是煤成烃作用的直接光学标志。B_11b煤层的地化参数指出较强的还原环境将有利于成烃作用。B_11b煤层的孔隙性（孔容、孔径分布、孔隙结构）说明它不仅有较好的储气性能,而且还具有较有利于煤层气体运移的物性条件。而上述特征是B₁₀煤层所不具备的。     

Geochemistry of porewater and sulfate-reducing bacteria in sediment cores from the Chianan Plain, Taiwan

High concentrations of arsenic and humic substances in groundwater from the southwestern coastal plain of Taiwan were well known for their probable relationships with black-foot disease. In order to realize the relationships between the concentrations of humic substances and arsenic in this area, 24 well water samples were analyzed. After filtered through 0.45 μm glass fiber membrane in the field, samples were kept in the dark at 4℃ and then separated into six fractions with varying range of molecular weight （〈0.5, 0.5-1, 1-5, 5-10, 10-50 and 〉50 k Da） by ultrafiltration apparatus （Molecular/Por Stirred Cell system） in the lab. Concentrations of humic substances were measured by fluorescence spectrometer （HITACHI F-2000, ex=370, em=445） and arsenic by FIAS-AA （Perkin Elmer AAnalyst 100, FIAS-400）. On average, only 6.2% of the total arsenic in water existed in the fraction of 〉0.5 k Da. and the others were complexed with humic substances （including humic acid and fulvic acid）. The results demonstrated a distinct positive correlation between the concentrations of humic substances and arsenic.     

High resolution profiles of trace metals in pore waters of marine and riverine sediments assessed by DET and DGT

In polluted aquatic systems, toxic metals are often accumulated in bottom sediments. They are, however, not necessarily stored definitively because diagenetic processs can modify redox, pH and even the amount of complexing ligands, releasing the trace metals back into the pore waters and the water column. Especially the labile metal fraction in the pore waters is important since this is the bioavailable fraction determining the bio-toxicity of the sediments. The goal of our study was therefore to assess, with novel sampling techniques, this bioavailable metal fraction in the pore waters as well as the flux towards the overlying water column. High-resolution profiles of trace metals in pore waters of marine and riverine sediments were assessed by DET （diffusive equilibrium in thin films） and DGT （diffusive gradients in thin films） gel techniques. The DET technique uses a diffusive gel layer that equilibrates with the aquatic system and with this technique the concentrations of total dissolved trace metals are obtained directly. The DGT technique uses an acrylamide diffusive gel backed by a resin gel （Chelex） which binds trace metals. With the DGT technique only labile species of selected metals can be captured. According to the redox potential measurements, the marine sediments were suboxic （200 mV to -220 mV versus Ag/AgCl electrode）, while the riverine sediments were completely anoxic （-160 mV to -220 mV versus Ag/AgCl electrode）. This redox potential was apparently controlling the trace metals species in the pore waters： for example a strong correlation between Mn and Co was found in the riverine sediments （for DET and DGT sampling）, while in the marine sediments trace metals presented various behaviors.