塔里木盆地塔中低凸起地层水化学特征对不整合的响应

对塔中低凸起地层水化学特征与不整合之间关系的研究结果表明,地层水化学特征对不整合具有很好的响应。在遭受强烈抬升和剥蚀、之间形成不整合的奥陶系和志留系,以及紧靠不整合面附近的石炭系CⅢ油组,其地层水具有矿化度、Cl-含量、K Na 含量和r(Cl-Na)/rMg值相对较小,而HCO3-含量、rNa/rCl值和rSO42-×100/rCl值相对较大的特点,反映出地质历史时期大气降水的影响。在志留系与石炭系之间以及志留系与奥陶系之间的不整合面附近,地层水的矿化度、r(Cl-Na)/rMg值和B3 含量变小,而rNa/rCl值和rSO24-×100/rCl值变大,具有典型的遭受大气淋滤的地层水化学基本特征。     

廊坊市地下水化学特征变化研究

为揭示廊坊市地下水水化学特征的形成机理,收集并检测了39个地下水样本。采用相关性分析法、水化学方法和离子比系数法研究了其水化学特性、影响因素和变化原理。研究结果表明:影响浅层地下水盐渍化的主要化学离子为SO42-、NO3-、Cl-和K+。SO42-、NO3-和Cl-的含量差异很大,其他指标相对稳定。γNa/γCl的比值表明在径流形成过程中Na+从土壤含水层中释放出来;水中的Ca2+与土壤中的Na+之间存在交换,导致γNaγCl;γNa/(γNa+γCl)的比值表明,随着地下水深度的增加,阳离子交换水平增强,导致主要阳离子从Na+转变为Ca2+;γHCO3+γSO4/γCa+γMg的比值表明浅层地下水主要来自大气降水,阳离子交换对深层地下水的影响更为明显。廊坊市浅层地下水类型主要为HCO3·SO4-Ca,其分类较复杂,而深层地下水主要为HCO3-Na,地下水的类别较简单。     

河南省永城市浅层地下水化学特征及形成机制

地下水是河南省永城市重要的供水水源,浅层地下水水质污染严重制约了该市经济发展和居民生活质量的提高.在实地调查采样分析的基础上,运用水化学图解法、数理统计法、地球化学模拟法等方法综合分析了永城市浅层地下水的水化学特征和形成机制,探讨了该市浅层地下水污染来源和主要影响因素.结果表明:随含水介质和人类活动影响强度的变化,浅层地下水中K+、Ca2+、NO₃-、Cl-、SO₄2-的浓度和COD（chemical oxygen demand）随深度增加而减少,而Na+、F-、Mg2+、HCO₃-的浓度和TDS（total dissolved solids）随深度增加而上升.在煤矿区及煤化工区浅层地下水中SO₄2-浓度大于250 mg/L,远远高于其他区域的SO₄2-浓度,而在农业区浅层地下水中NO₃-浓度大于30 mg/L,远远高于其他区域的NO₃-浓度.综合分析表明:煤矿及其化工业废水和生活污水排放、过量使用化肥农药是永城市浅层地下水污染的主要因素.      

河北省任丘市浅层地下水化学特征及形成机制

浅层地下水是任丘市重要的水资源之一,为研究其水化学特征及其形成机制,本文在实地调查取样分析化验的基础上,以水文地球化学理论为指导,借助多元数理统计的方法,从多个角度揭示了研究区浅层地下水的形成演化过程：① 通过离散分析,认为研究区各主要离子变异系数较大,说明研究区浅层地下水受人为影响明显,水化学特征复杂。 ② 通过相关分析,认为Na+、Ca2+、Mg2+、Cl-、以及SO2-4为研究区原始浅层地下水主要离子,而HCO-3与NO-3为外来离子且异源;③ 通过聚类分析,可将研究区浅层地下水分为A、B、C三类,其中A类处于Gibbs图中岩石风化端元,矿化度较低,为微咸水或淡水,含HCO-3和NO-3,受农业灌溉水影响;B类处于Gibbs图中岩石风化端元向蒸发浓缩端元过渡,矿化度居中,为微咸水,NO-3含量相对较高,受生活污水影响;C类地下水处于Gibbs图中蒸发浓缩端元,矿化度较高,以咸水为主,与地表水体连通性差,接近原始浅层地下水化学类型。④ 通过主成分分析,认为研究区原始地下水化学类型为SO2-4·Cl-—Na+型及SO2-4·Cl-—Na+·Ca2+型,受干旱环境下蒸发和海水入侵双重影响。     

阳离子交换系数及其在地下水Pb污染研究中的应用

本文首先计算了地下水中常见阳离子与被吸附Pb^2＋的交换系数，在此基础上利用实际地下水水质资料计算了天津市浅层地下水含水介质吸附最离子的当量分数，并利用吸附Pb^2 的当量分数估算了含水介质吸附Pb^2＋的量及地下咸水中Pb^2 的浓度的增大量。     

天津滨海地区土壤剖面盐渍化特征及其影响因素

土壤盐渍化是由自然或人类活动引起的一种环境风险,对工农业生产具有重要影响。本次研究在天津滨海地区布置了6条具有代表性的土壤盐渍化剖面,选取其中4个剖面进行了为期两年的按月采样监测。研究发现,除了BHY6土壤剖面由于长年耕种,表现为平衡型土壤剖面形态之外,其余基本表现为底聚型土壤盐渍化剖面形态;从剖面中下部直到底部浅层地下水位附近,土壤中阳离子以Na+为主,阴离子以Cl-或Cl-+HCO-3为主,尤其在浅层地下水矿化度显著偏高(达盐水程度)的地区,土壤中Na+、Cl-所占比例具有绝对优势,具有滨海盐土的基本发生特征;气候因素、浅层地下水矿化度及埋深、表层土壤植被都是滨海地区土壤盐渍化的重要影响因素。表层土壤表现出春季积盐、夏季脱盐、秋冬季缓慢积盐的特征,浅层地下水矿化度越高、埋深越浅,其土壤剖面含盐量越高;果林地和长期耕种的土地可以降低土壤盐分的活性,有效抑制盐分的累积,降低滨海地区土壤盐渍化程度,保护和改良土壤。     

沉积环境和人类活动对苏锡常地区浅层地下水的水质效应

为指导苏锡常地区浅层地下水科学合理地开发利用,笔者从地质历史的角度分析了沉积环境对浅层地下水水质分布的影响;充分利用研究区域浅层地下水的历史水质资料,分析人类活动影响下的水质演化规律。结果表明:沉积环境对研究区的浅层地下水水质的空间分布特征具有控制作用,而人类活动对浅层地下水的水质演化具有污染和开采淡化的双重效应。     

新疆喀什噶尔河流域高氟地下水富集因素分析

以新疆喀什噶尔河流域地下水中的氟为研究对象,依据地下水污染调查数据,分析研究区地下水中氟的富集因素。研究结果表明,地下水主导阴离子为SO42-和Cl-,主导阳离子为Na+和Ca2+,水化学类型以SO4·Cl型和Cl·SO4型水为主。地形及水文地质条件是影响浅层地下水中氟富集的主要外在因素,水文地质条件是影响深层地下水的主要外在因素。水化学环境也是影响地下水中F-富集的重要因素,地下水的弱碱性环境对F-含量具有一定的富集作用,同时,高TDS、高TH、高Cl-、高HCO3-、高Ca2+和高Na+均有利于F-的富集。     

保定平原区地下水化学特征及演化

为揭示保定平原地下水水化学特征及演化规律,本文以保定平原为研究对象,对216组地下水样水化学特征进行了分析。综合运用Piper三线图、Gibbs图、相关离子分析等方法,研究了保定平原区深浅层地下水化学组成及水化学类型空间分布特征,识别了水化学形成机制与控制作用,在此基础上分析了水化学演化的成因。结果表明：沿地下水径流方向,浅层地下水与深层地下水主要离子含量呈现明显的递变规律,TDS、Na+、Mg2+、Cl-、SO2-4、HCO-3含量逐渐升高,K+、Ca2+逐渐降低,地下水优势阳离子Ca2+主导地位逐渐被Na+代替,优势阴离子HCO-3主导地位逐渐向Cl-过渡。地下水化学特征主要受水岩作用、阳离子交替吸附作用以及人类活动共同影响,水岩作用以碳酸盐岩和铝硅酸盐岩共同溶滤作用为主;浅层地下水受人类活动影响较大,影响离子主要为NO-3,集中分布于补给区,除了与农业活动相关外,主要与山前平原岩性颗粒粗,具有较强的渗透性有关。     

保定平原区地下水化学特征及演化

为揭示保定平原地下水水化学特征及演化规律,本文以保定平原为研究对象,对216组地下水样水化学特征进行了分析。综合运用Piper三线图、Gibbs图、相关离子分析等方法,研究了保定平原区深浅层地下水化学组成及水化学类型空间分布特征,识别了水化学形成机制与控制作用,在此基础上分析了水化学演化的成因。结果表明：沿地下水径流方向,浅层地下水与深层地下水主要离子含量呈现明显的递变规律,TDS、Na+、Mg2+、Cl-、SO2-4、HCO-3含量逐渐升高,K+、Ca2+逐渐降低,地下水优势阳离子Ca2+主导地位逐渐被Na+代替,优势阴离子HCO-3主导地位逐渐向Cl-过渡。地下水化学特征主要受水岩作用、阳离子交替吸附作用以及人类活动共同影响,水岩作用以碳酸盐岩和铝硅酸盐岩共同溶滤作用为主;浅层地下水受人类活动影响较大,影响离子主要为NO-3,集中分布于补给区,除了与农业活动相关外,主要与山前平原岩性颗粒粗,具有较强的渗透性有关。     

鲁西南地区高氟水分布规律与成因分析

地方性氟中毒是我国北方地区最为典型的地方病之一,查明高氟地下水的空间分布及其成因是除氟改水、防治氟害的前提。通过对鲁西南地区不同层位地下水水质分析结果及水文地质、地质条件等多个环境影响因素的综合分析,查明了鲁西南地区高氟水的空间分布规律,并分析了影响浅层和深层高氟水形成的环境因素。浅层高氟水呈片状分布于洼地、缓平坡地等地势较低的区域,占鲁西南地区总面积的47%,大部分地区高氟水氟离子含量为1.2～2.0 mg/L,局部大于4.0 mg/L,其形成受气候、地质环境、地形地貌特征及水化学环境等多个因素的影响,成因类型为溶滤-蒸发浓缩型。深层高氟水具有水平分带性,占鲁西南地区总面积的65%,大部分高氟水氟离子含量为2.0～4.0 mg/L,氟离子含量分布与晚更新世沉积相带呈现很好的相似性,推测其为地质历史时期形成的古地下水。     

Modeling of lithology induced chemical anomalies in the aquifer systems of the Kazan Trona deposit area, Ankara, Turkey

The study was carried out in order to investigate existing hydrogeochemical relationships between groundwater environment and geological units in the Kazan trona deposit area, Ankara, Turkey. Evaluations indicate that concentrations of alkalinity, boron, chloride and sodium in the upgradient groundwater of the Eocene sedimentary units gradually increase toward downgradient by the interactions of saline minerals (searlesite, shortite, northupite and pyrite) present in the secondary structures (microfractures and irregular voids) at various levels. Inverse modeling calculations suggest that the range of dissolved mass amounts in millimoles per kilogram of water for searlesite, shortite and northupite minerals are 0.05–28.67, 2.62–24.39 and 0.01–24.19, respectively, in the aquifer between the upgradient and downgradient locations. The ranges of accompanying calcite and dolomite precipitations are 4.54–48.71 and 2.16–24.08 mmol per kg of water, respectively. Chemical composition of the groundwater in the overlying Neogene sedimentary unit includes also higher concentrations of the major ions as measured in groundwater of the underlying units. However the lack of saline mineral zones in the Neogene unit indicates that upward groundwater mixing takes place from the underlying aquifer as also suggested by the measured upward gradient. The mixing percentage of the underlying groundwater as determined from the nested wells ranges from 2.7 to 48.3%, from upgradient to downgradient, respectively. The unconfined alluvium aquifer overlying the Neogene unit includes relatively dilute groundwater except in two locations, where high-ion concentrations detected in groundwater of the underlying units are also high in these locations, suggesting upward groundwater mixing from the underlying aquifer due to upward gradient. However, groundwater input investigations from the alluvium aquifer to the nearby Ova stream indicate that the detected high concentrations in these locations are diluted or sorbed by the aquifer material toward downgradient (Ova Stream).     

Hydrochemistry and isotope geochemistry as tools for groundwater hydrodynamic investigation in multilayer aquifers: a case study from Lomellina, Po plain, South-Western Lombardy, Italy

A multicriteria approach in studying hydrodynamics of a multilayer aquifer system has been used in the Lomellina region (Northern Italy). It involves the reconstruction of the hydrogeological framework coupled to the definition of the hydrochemical and isotopic features of the aquifers. A shallow phreatic aquifer, reaching depths of about 60–80 m from the surface, and deeper aquifers containing confined groundwater, were distinguished. Groundwater generally shows mineralisation decreasing with depth; dissolved ions depict calcium-bicarbonate hydrochemical facies and stable isotopes define the recharge mechanisms, the origin of groundwater, and the hydraulic confinement of deep aquifers. The phreatic aquifer is fed by local infiltration and by streams and irrigation channels. Tritium and Carbon-14 groundwater dating indicate long residence times (on the order of thousands of years) for confined aquifers. The confined aquifers show essentially passive hydrodynamic conditions and maintain a higher piezometric level than the phreatic aquifer. This inhibits the possibility of recent water penetrating far below the surface. The hydrogeological setting of the Lomellina region displays features which are common to other sectors of the Po plain. As a consequence, the results of this study, although conducted on a restricted area, are highly illustrative of groundwater hydrodynamics in large sedimentary aquifers.     

长江中游故道区高碘地下水分布与形成机理

高碘地下水(碘浓度大于100μg/L)广泛分布于我国沿海地区和干旱内陆盆地,威胁近千万人口的饮水安全,但目前对湿润区河湖平原地下水中碘的分布与成因机制的认识还十分薄弱.通过采集长江中游故道区75组浅层地下水样品和7组地表水样品进行了水化学分析,查明了地下水中碘的空间分布特征,并运用主成分分析识别了碘富集的水环境要素和水...     

Dissolved noble gases and stable isotopes as tracers of preferential fluid flow along faults in the Lower Rhine Embayment,Germany

Groundwater in shallow unconsolidated sedimentary aquifers close to the Bornheim fault in the Lower Rhine Embayment (LRE), Germany, has relatively low δ²H and δ¹⁸O values in comparison to regional modern groundwater recharge, and ⁴He concentrations up to 1.7?×?10^?4 cm³ (STP) g^–1?±?2.2 % which is approximately four orders of magnitude higher than expected due to solubility equilibrium with the atmosphere. Groundwater age dating based on estimated in situ production and terrigenic flux of helium provides a groundwater residence time of ～10⁷ years. Although fluid exchange between the deep basal aquifer system and the upper aquifer layers is generally impeded by confining clay layers and lignite, this study’s geochemical data suggest, for the first time, that deep circulating fluids penetrate shallow aquifers in the locality of fault zones, implying  that sub-vertical fluid flow occurs along faults in the LRE. However, large hydraulic-head gradients observed across many faults suggest that they act as barriers to lateral groundwater flow. Therefore, the geochemical data reported here also substantiate a conduit-barrier model of fault-zone hydrogeology in unconsolidated sedimentary deposits, as well as corroborating the concept that faults in unconsolidated aquifer systems can act as loci for hydraulic connectivity between deep and shallow aquifers. The implications of fluid flow along faults in sedimentary basins worldwide are far reaching and of particular concern for carbon capture and storage (CCS) programmes, impacts of deep shale gas recovery for shallow groundwater aquifers, and nuclear waste storage sites where fault zones could act as potential leakage pathways for hazardous fluids.     

Petroleum geochemistry of oil samples from shallow boreholes at Sakran site,western Iraq

Findings of the oil source affinity for oil sample collected from shallow borehole already drilled for ground water purposes at the Sakran area, NE Haditha city, western Iraq, is performed in this study by biomarker studies with addition to the analysis of gravity map. Petroleum geochemistry study is carried out on oil sample. The terpane and sterane biomarker distributions, as well as the stable isotope values, are used for determining the validity of oil to correlate its source. The results showed that the oil belongs to the Jurassic age, with high sulfur content (2.75 %) and value of C28/C29 up to 0.75. The tricyclic terpanes values as well as hopanes indicated a source rock affinity of carbonates, whereas the pristine/phytane ratio indicated marine algal source of kerogen type II. All these information could confirm that the source rock affinity was the Sargelu Formation (Jurassic), in which their age’s equivalent to the source in East Baghdad Oil Field and Tikrit Oil Field, with a difference from the oil family near the Akkas field, located to the west of the area. Chemical analyses of water sample collected from the borehole showed the following results: TDS?=?12,700 mg/l, EC?=?215,900 μs/cm, pH?=?6.8, DO?=?28 mg/l, and temperature?=?24 °C. Hydrochemical functions such as rNa/rCl (<1), (rNa–rCl)/rSO₄ (<0) and rSO₄/rCl (<1) indicate that the water is of marine origin, partially mixed with meteoric water. Analysis of the gravity map revealed two anomalous areas; the western one represents large anomaly with EW trend similar to the Anah graben to the north. The second one consists of many anomalies trending N–NW direction. The main local anomaly is identical with the seeps from the drilled borehole covering large area. The boundaries and trends of the main geological structures have been defined by gradient analysis procedure to the gravity data. The closed gravity anomalies with their large extensions reflect the importance of the results for further studies and promising area for oil reservoirs.     

Evaluating shallow flow-system response to climate change through analysis of spring deposits in southwestern Wisconsin,USA

Tufa-depositing springs in the southern Driftless Area of Wisconsin, USA, are used to inform the response of shallow and local groundwater flow systems to changes in climate over the last 3,000 years. The springs emanate from a shallow, unconfined, sedimentary bedrock aquifer and at stratigraphic positions similar to a shallow, perched aquifer that was identified in the eastern Driftless Area. The perched aquifer was shown to be stable under current climate conditions and over decadal time scales. This study provides further evidence of the significance of the stratigraphic interval in controlling shallow groundwater flow patterns in the region and in the stability of shallow and local groundwater flow systems over thousands of years. The tufa carbonates in three cores collected from the mounds adjacent to the springs show variations in stable isotope (δ¹³C, δ¹⁸O) and elemental (Mg/Ca) values that agree with well-established paleoclimate records for the region, suggesting that the springs were active and depositing tufa in the past, during climate conditions that were similar to the present and during conditions that were drier than the present.     

天津市宁河北奥陶系灰岩水源地的水文地球化学模拟

天津市宁河北水源地属埋藏型地下水源地,其开采层奥陶系灰岩含水层呈北东向的向斜展布,隐伏于石炭系-二叠系砂页岩之下,并被新近系覆盖,仅在东北部与第四系含水层有水力联系,地下水的补给主要来自浅层第四系含水层的越流补给。应用水文地球化学模拟方法,研究从第四系含水层到奥陶系含水层地下水经历的水-岩作用,包括方解石、白云石、萤石和硬石膏的溶解或沉淀、二氧化碳气体的溶解或逸出等,地下水硬度、矿化度总体上有下降趋势,这是由于含Ca²⁺、Mg²⁺和HCO^-₃的矿物相发生溶解,迁入溶液的比率要小于发生沉淀迁出溶液的比率,具体表现在从第四系含水层到奥陶系含水层Ca²⁺、和HCO^-₃浓度的降低幅度较大。通过模拟计算,可以定量确定从补给区到研究区沿水流路径上的水-岩相互作用及质量交换,有助于揭示该区地下水化学环境的演化机制。