Cenozoic sedimentary basins of southern Turkey: an introduction     

《Sedimentary Geology》2005,173(1-4):1-13

  相似文献   

土壤中氟的形态分析   总被引：11，自引：3，他引：8  

桂建业  韩占涛  张向阳  刘福亮 《岩矿测试》2008,27(4):284-286

以宁夏盐池地区高氟土壤为例,采用连续提取法对土壤样品中各形态氟进行提取,离子色谱法测定各形态氟的含量。根据研究目的及土壤特点将氟的形态划分为水溶态、离子交换态、可还原态、可氧化态及残渣态5种形态;对各种形态连续提取过程中使用的提取液进行了选择。采用建立的方法获得提取土壤中F-的检出限为0.76μg/g;方法精密度(RSD,n=7)各形态氟为水溶态氟11.3%,离子交换态氟13.5%,可还原态氟10.7%,可氧化态氟8.9%。  相似文献   

地下水封储油库库址的水文地质工程地质问题   总被引：5，自引：1，他引：4  

刘琦  卢耀如  张凤娥 《水文地质工程地质》2008,35(4):1-5

将石油储存于地下水封洞库是建设大型石油储备基地的重要发展方向。由于建设地下水封储油洞库的地质条件、设计和施工的复杂性,为满足建设的安全性和经济性,需要综合考虑水文地质、工程地质、环境地质问题。文章考虑了建设地下水封油库的原则和外部依托条件,特别针对库址选择时应注意的水文地质、工程地质问题,提出了相应的认识。  相似文献   

华北东部平原深层抽水井水跃值计算方法及其规律研究   总被引：1，自引：1，他引：0  

吴庆华  高业新  蔺文静  张薇  靳晓颖  韩玉英  王贵玲 《水文地质工程地质》2008,35(6):29-32

文章分析了目前常用的几种水跃值计算方法的适用性与不足,认为在华北东部平原地下水位变化强烈的漏斗区,这些方法均难以应用。同时提出了C—G法,即一次定流量抽水同步观测抽水井和观测井的水位,合理地解决了区域背景水位对水跃值计算的影响。研究表明,与修正后的多次定流量试验法——两次定流量抽水法相比,C—G法计算结果可靠。然后探讨了如何间接获取抽水期间抽水层区域背景水位动态资料的方法,校正背景水位波动对抽水水位的影响,采用自动水位计(DIVER)同步监测井中大气压对地下水位的影响。最后分析水跃值随时间和抽水井水位降深的变化规律。  相似文献   

快速城镇化进程中珠江三角洲高铵地下水赋存环境及驱动因素          下载免费PDF全文

吕晓立  刘景涛  韩占涛  朱亮  杨明楠  李海军 《中国地质》2021,48(6):1770-1780

地下水中高浓度的铵态氮对生活饮用水安全及生态环境存在潜在威胁。相比较硝态氮，高浓度的铵态氮不仅有各种人为来源，天然沉积环境更是造成高铵地下水的主要成因。本文以城镇化快速发展的珠江三角洲为研究区，运用数理统计、主成分分析等方法深入探讨了研究区高铵地下水的赋存环境特征及驱动因素。结果表明，研究区地下水中NH₄⁺质量浓度介于未检出~180 mg/L。研究区1539组地下水样品中，NH₄⁺质量浓度大于10 mg/L的高铵地下水69组，其中含NH₄⁺质量浓度大于30 mg/L的高铵"肥水"23组。对比2005-2008年历史水化学数据，2009-2018年新增建设用地孔隙含水层高铵地下水样品比例增加25%。高铵地下水呈斑块状分布于三角洲平原区第四系底部低洼的基底、洼地等退积层序发育的淤泥质含水层中。淤泥层等富含有机质和总有机碳的沉积层是珠江三角洲地区的"生铵层"，有机氮的矿化是三角洲平原区城市化孔隙含水层中高铵地下水的主要驱动力。城镇化扩张引起生活污水及富铵工业废水的泄漏入渗是城乡结合部高铵地下水铵氮的重要来源。三角洲平原区中性至弱碱性富含有机质的还原环境是高铵地下水的主要成因。风化溶滤、阳离子交换吸附、海陆交互作用是珠江三角洲高铵地下水质演变的主要水文地球化学过程。  相似文献   

Use of chemical tracing to study acquisition modalities of the mineralization and behaviour of unconfined groundwaters under a semi-arid climate: the case of the Souss plain (Morocco)     

Y. Hsissou  L. Bouchaou  J. Mudry  J. Mania  P. Chauve 《Environmental Geology》2002,42(6):672-680

The chemical content of the Souss unconfined groundwater displays spatial variations in conductivity (between 400 and 6,000 µS cm^-1). The chemical tracers (Cl^-, SO₄^2-, Sr²⁺, Br^-), which characterize the different components of the groundwater, allowed the determination of the origin of water salinity. Cl^- and SO₄^2-, reaching respectively 2,000 and 1,650 mg L^-1, display localized salinity anomalies. Br^-/Cl^- ratio distinguishes marine-influenced impoverished zones versus the oceanic domain. Thus, salinity anomalies can be attributed: (1) downstream, to a currently existing salt-encroachment (with added waste water) and sedimentary palaeosalinity, (2) in the middle-Souss, to High Atlas evaporites and to irrigation water recycling. Sr²⁺/Ca²⁺ ratio (evaporites if >1‰), confirms the evaporitic origin of the anomalies along the right bank of oued Souss. Furthermore, it facilitates the distinction between the different aquifer contributions (Cretaceous, Jurassic and Triassic), and it highlights leakage from deep Turonian limestones in the groundwater recharge system. To the south, recharge is from the Anti Atlas (evaporite-free) waters. Oxygen-18 measurements confirm the groundwater recharge from the High and Anti Atlas as piezometric maps and chemical tracers suggested, plus from leakage from the Turonian and the marine aquifers.  相似文献   

氮同位素比（^15N／^14N）在地下水氮污染研究中的应用基础   总被引：25，自引：1，他引：25  

王东升 《地球学报》1997,18(2):220-223

华北地下水中硝态氮浓度和δ＾１５Ｎ值如下：在自然状态下为４．４≤＋５，来自下水道粪便污染者为２０－７０和＋１０－＋２０，受化肥污染者为３０－６０和－２－＋５。因此，氮同位素可用来识别氮污染来源和氮的迁移。  相似文献   

地质微生物地球化学作用的意义与展望     

张胜  张翠云  张云  李政红  张明 《地质通报》2005,(Z1)

概要论述了地质微生物学、地下水微生态学、微生物地球化学作用的基本概念、研究内容、研究现状、科学意义、关键问题、发展前景和在地下水环境保护中的作用。该研究领域不仅拓宽了整个地质科学的研究范畴,而且推动了地质科学的发展,具有一定的创新性。  相似文献   

Diffusive mass exchange of non‐reactive substances in dual‐porosity porous systems – column experiments under saturated conditions          下载免费PDF全文

Bastian Knorr  Piotr Maloszewski  Florian Krämer  Christine Stumpp 《水文研究》2016,30(6):914-926

Diffusive mass exchange into immobile water regions within heterogeneous porous aquifers influences the fate of solutes. The percentage of immobile water is often unidentified in natural aquifers though. Hence, the mathematical prediction of solute transport in such heterogeneous aquifers remains challenging. The objective of this study was to find a simple analytical model approach that allows quantifying properties of mobile and immobile water regions and the portion of immobile water in a porous system. Therefore, the Single Fissure Dispersion Model (SFDM), which takes into account diffusive mass exchange between mobile and immobile water zones, was applied to model transport in well‐defined saturated dual‐porosity column experiments. Direct and indirect model validation was performed by running experiments at different flow velocities and using conservative tracer with different molecular diffusion coefficients. In another column setup, immobile water regions were randomly distributed to test the model applicability and to determine the portion of immobile water. In all setups, the tracer concentration curves showed differences in normalized maximum peak concentration, tailing and mass recovery according to their diffusion coefficients. These findings were more pronounced at lower flow rates (larger flow times) indicating the dependency of diffusive mass exchange into immobile water regions on tracers' molecular diffusion coefficients. The SFDM simulated all data with high model efficiency. Successful model validation supported the physical meaning of fitted model parameters. This study showed that the SFDM, developed for fissured aquifers, is applicable in porous media and can be used to determine porosity and volume of regions with immobile water. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

Chemical and isotopic interpretation of major ion compositions from precipitation: a one-year temporal monitoring study in Wrocław,SW Poland     

M. Ciężka  M. Modelska  M. Górka  A. Trojanowska-Olichwer  D. Widory 《Journal of Atmospheric Chemistry》2016,73(1):61-80

The chemical compositions (Na⁺, NH₄ ⁺, K⁺, Mg²⁺, Ca²⁺, Cl^?, NO₂ ^?, NO₃ ^?, SO₄ ^2?, HCO₃ ^?) of wet precipitation and nitrogen isotope compositions δ¹⁵N(NH₄ ⁺) were studied from January to December 2010 in Wroc?aw (SW Poland). Results of a principle component analysis show that 82 % of the data variability can be explained by three main factors: 1) F1 (40 %) observed during vegetative season (electrical conductivity, HCO₃ ^?, NO₃ ^?, NO₂ ^?, NH₄ ⁺ and SO₄ ^2?), mainly controlling rainwater mineralization; 2) F2 (26 %) observed during vegetative and heating seasons (K⁺, Ca²⁺ and Mg²⁺), probably representing a combination of two processes: anthropogenic dusts and fertilizers application in agricultural fields, and 3) F3 (16 %) reported mainly during heating season (Na⁺ and Cl^?) probably indicating the influence of marine aerosols. Variations of δ¹⁵N(NH₄ ⁺) from ?11.5 to 18.5?‰ identify three main pathways for the formation of NH₄ ⁺: 1) equilibrium fractionation between NH₃ and NH₄ ⁺; 2) kinetic exchange between NH₃ and NH₄ ⁺; 3) NH₄ ⁺ exchange between atmospheric salts particles and precipitation. The coupled chemical/statistical analysis and δ¹⁵N(NH₄ ⁺) approach shows that while fossil fuels burning is the main source of NH₄ ⁺ in precipitation during the heating season, during the vegetative season NH₄ ⁺ originates from local sewage irrigation fields in Osobowice or agricultural fertilizers.  相似文献