GROUNDWATER QUALITY AND CONTAMINATION INDEX MAPPING IN CHANGCHUN CITY, CHINA

1INTRODUCTIONGroundwater in Changchun City assures about 45% of total water supply. Drinking water supply of Chang-chun City was mostly served by surface water from Shitoukoumen and Xinlicheng reservoirs located in the east and south of the city (ZHANG, 1993). However, with the development of urban construction the ground-water especially from deep boreholes is also used for drinking purpose in suburban areas. The urbanization process in Changchun City threatens the groundwater quali…     

Coal seam gas distribution and hydrodynamics of the Sydney Basin,NSW, Australia

This paper reviews various coal seam gas (CSG) models that have been developed for the Sydney Basin, and provides an alternative interpretation for gas composition layering and deep-seated CO₂ origins. Open file CSG wells, supplemented by mine-scale information, were used to examine trends in gas content and composition at locations from the margin to the centre of the basin. Regionally available hydrochemistry data and interpretations of hydrodynamics were incorporated with conventional petroleum well data on porosity and permeability. The synthesised gas and groundwater model presented in this paper suggests that meteoric water flow under hydrostatic pressure transports methanogenic consortia into the subsurface and that water chemistry evolves during migration from calcium-rich freshwaters in inland recharge areas towards sodium-rich brackish water down-gradient and with depth. Groundwater chemistry changes result in the dissolution and precipitation of minerals as well as affecting the behaviour of dissolved gases such as CO₂. Mixing of carbonate-rich waters with waters of significantly different chemistries at depth causes the liberation of CO₂ gas from the solution that is adsorbed into the coal matrix in hydrodynamically closed terrains. In more open systems, excess CO₂ in the groundwater (carried as bicarbonate) may lead to precipitation of calcite in the host strata. As a result, areas in the central and eastern parts of the basin do not host spatially extensive CO₂ gas accumulations but experience more widespread calcite mineralisation, with gas compositions dominated by hydrocarbons, including wet gases. Basin boundary areas (commonly topographic and/or structural highs) in the northern, western and southern parts of the basin commonly contain CO₂-rich gases at depth. This deep-seated CO₂-rich gas is generally thought to derive from local to continental scale magmatic intrusions, but could also be the product of carbonate dissolution or acetate fermentation.     

Isotopes and geochemistry in a managed aquifer recharge scheme: a case study of fresh water injection at the Damascus University Campus,Syria

A combination of stable isotopes (¹⁸O and ²H) and hydrochemistry has been applied to investigate storage processes in relation to aquifer storage and recovery (ASR) of the shallow alluvial Quaternary aquifer in Damascus basin. The stored water, entirely taken from the Figeh springs during flood periods, was injected in a single well having a brackish groundwater. Water samples were collected from four observation wells drilled in the Damascus University Campus (DUC) site during a 3‐year period (2006–2008). The injectant water, which deviates in its chemical and isotopic signatures from that of the ambient groundwater, shows that the stored water plume remains within close proximity to the injection well (IW) (<≈ 100 m). Thus, only two wells (W13 and W14) located at a distance less than 80 m from the injection point were affected by this injection. The observation wells located at longer distances from the IW (≈145 m and ≈ 600 m for wells W15 and WHz, respectively) were completely unaffected by the injection. Although most of the chemical and isotopic parameters usefully reflected the mixing process that occurs between the injectant water and ambient groundwater, the stable isotope (¹⁸O) and chloride (Cl⁻) were the most sensitive parameters that quickly reflect this signature. Using a simple mass balance, the calculated proportion of injectant water reaching the well W13 was in the range of 50–90%. This proportion was even lower (30–55%) in the case of well W14. Although the drought event prevailing during this study did not much help to inject further amounts of water, higher than the injected volume (0·2416 M m³) and also not favourable to better evaluate the fate and subsurface hydrological processes, these findings offer encouragement to continue the ASR activities, as an alternative way for better management of water resources in this basin facing intensive problems. Copyright © 2010 John Wiley & Sons, Ltd.     

Factors controlling the chemical evolution of travertine‐depositing rivers of the Barkly karst,northern Australia

Groundwaters feeding travertine‐depositing rivers of the northeastern segment of the Barkly karst (NW Queensland, Australia) are of comparable chemical composition, allowing a detailed investigation of how the rate of downstream chemical evolution varies from river to river. The discharge, pH, temperature, conductivity and major‐ion concentrations of five rivers were determined by standard field and laboratory techniques. The results show that each river experiences similar patterns of downstream chemical evolution, with CO₂ outgassing driving the waters to high levels of calcite supersaturation, which in turn leads to widespread calcium carbonate deposition. However, the rate at which the waters evolve, measured as the loss of CaCO₃ per kilometre, varies from river to river, and depends primarily upon discharge at the time of sampling and stream gradient. For example, Louie Creek (Q = 0·11 m³ s^?1) and Carl Creek (Q = 0·50 m³ s^?1) have identical stream gradients, but the loss of CaCO₃ per kilometre for Louie Creek is twice that of Carl Creek. The Gregory River (Q = 3·07 m³ s^?1), O'Shanassy River (Q = 0·57 m³ s^?1) and Lawn Hill Creek (Q = 0·72 m³ s^?1) have very similar gradients, but the rate of hydrochemical evolution of the Gregory River is significantly less than either of the other two systems. The results have major implications for travertine deposition: the stream reach required for waters to evolve to critical levels of calcite supersaturation will, all others things being equal, increase with increasing discharge, and the length of reach over which travertine is deposited will also increase with increasing discharge. This implies that fossil travertine deposits preserved well downstream of modern deposition limits are likely to have been formed under higher discharge regimes. Copyright © 2002 John Wiley & Sons, Ltd.     

常州市地下水化学特征与成因分析

常州市是长江三角洲地区典型的工业化城市,多年来的快速发展对地下水环境产生了系列影响,地下水化学组分受到天然条件和人为活动的双重因素控制,现状地下水化学成因和影响因素亟需深入研究。本文在地下水赋存条件分析的基础上,综合采用统计分析、离子比值、主成分分析法对常州各层地下水化学特征和成因开展分析。结果表明,区域潜水水化学类型以HCO₃^-—Ca²⁺·Mg²⁺、HCO₃^-—Ca²⁺和HCO₃^-·Cl^-—Na⁺·Ca²⁺型为主,第Ⅰ承压水以HCO₃^-—Na⁺·Ca²⁺和HCO₃^-—Ca²⁺型为主、第Ⅱ承压水以HCO₃^-—Na⁺     

黄河三角洲浅层地下水盐分来源及咸化过程研究

黄河三角洲地下水咸化已成为区域最突出的生态环境问题之一。识别地下水补给及盐分来源是有效控制和改善地下水咸化问题的关键。本研究采集了研究区浅层地下水、地表水和海水等不同类型水样,利用离子比、Piper三线图、吉布斯图等方法对八大离子浓度、δD和δ¹⁸O 组成、Br和Sr 浓度等进行地下水补给研究与盐分来源辨析。结果表明:(1)黄河三角洲浅层地下水以总溶解性固体(TDS)为338 g/L的咸水为主,地下水水化学类型较为单一,主要为Cl-Na型。(2)三角洲区域地下水以大气降水补给为主,并且在补给过程中经历了不同程度的蒸发作用的影响,黄河现行流路区域地下水主要来源于河水侧渗补给,但浅层地下水含水层水平渗透性较差限制了黄河侧渗补给范围。(3)海洋是黄河三角洲浅层地下水盐分的主要来源,黄河现行流路区域及近岸地下水盐分来源于海水混合,三角洲北部刁口河等古河道区域地下水盐分主要来源于海相蒸发盐淋滤溶解。     

华北平原高氟地下水中稀土元素分布和分异特征

高氟地下水是世界各国研究者广泛关注的重大环境问题。尽管对高氟地下水的化学特征、形成机理和扩散机制等已有不少研究,但其稀土元素(REE)的含量和分异特征以及这些特征能否反映高氟地下水的形成和分布尚不清楚,这在一定程度上限制了REE在高氟地下水中的运用。本研究以地下水氟离子异常严重地区——华北平原为研究区,沿地下水流向采集浅层和深层地下水样,研究分析了水中氟离子和REE的地球化学特征。浓度分析结果表明地下水氟离子浓度介于0.28 mg/L和9.33 mg/L之间,其中55%超出我国饮用水标准规定值1.0 mg/L;PHREEQC计算结果反映地下水中氟以NaF、CaF⁺、MgF⁺和自由态F^-形式存在,其中自由态F^-含量占主导(85.42%99.39%);高氟地下水主要分布于中部冲积湖积平原以及东部冲积海积平原,60%高氟地下水样分布在180 m深度以下;水化学图件分析结果指示浅层高氟地下水的形成主要受蒸发浓缩作用的控制,而深层高氟地下水是水岩相互作用下的矿物溶解和离子竞争吸附共同作用的结果。研究区地下水REE含量处于pmol/L至nmol/L级别,PHREEQC模拟计算结果表明REE主要以碳酸络合物( {\mathrm{REECO}}_3^{+}和$REE(CO_{3})_{2}^{-})$的形式存在,与氟离子络合的稀土元素(REEF²⁺和 {\mathrm{REEF}}_2^{+})占01.18%;上陆壳(UCC)标准化结果显示,所有地下水均呈重REE(HREE)和中REE(MREE)相对于轻REE(LREE)富集的模式,且具有显著Ce负异常(0.11* = Ce_UCC/(La_UCC×Pr_UCC)^0.5<2.29)特性;地下水富HREE主要归因于HREE比LREE优先与碳酸根络合,并且形成更加稳定的碳酸络合物。沿地下水流向,深层地下水中总REE含量与地下水中氟浓度均呈现不断上升的变化趋势,同时高氟地下水比低氟地下水更易富集重稀土元素,说明稀土元素对深层含水层富氟行为具有一定的指示作用。     

我国北方新生代玄武岩地下水化学特征及其成因——以河北省张北县为例

为了进一步了解我国北方新生代玄武岩地下水的赋存规律和形成演化机理,以河北省张北县玄武岩地下水为研究对象,在野外采集地下水样、测定水化学和同位素组成的基础上,利用统计分析、离子比例系数、氢氧同位素、反向地球化学模拟等方法,对区内玄武岩地下水的水化学形成机制进行了研究。结果表明:沿地下水径流方向,研究区内玄武岩地下水中多数离子质量浓度呈现增大趋势,补给区的地下水化学类型以HCO₃-Ca·Mg为主,TDS质量浓度多小于500mg/L,排泄区地下水中阴离子以Cl^-和SO₄^2-为主,阳离子以Na⁺为主,TDS质量浓度多大于1 400mg/L;研究区地下水补给来源为当地大气降水;硅铝酸盐、岩盐、硫酸盐的风化溶解是地下水中离子的主要来源;溶滤作用、阳离子交替吸附作用和农业施肥等人类活动影响是控制地下水化学形成的主要作用。     

The influence of diurnal temperatures on the hydrochemistry of a tufa‐depositing stream

At‐a‐station diurnal variations in carbonate hydrochemistry were measured during four observation periods at Davys Creek, a tufa‐depositing stream in central NSW, Australia. Major ion concentrations and continuously logged measurements of specific conductivity, pH and temperature showed that changes in the amount of CaCO₃ deposited upstream of the study reach were directly related to changes in diurnal water temperatures, which control the rate of CO₂ efflux to the atmosphere. The greatest upstream losses occurred during the mid‐afternoon water temperature peak, whereas the lowest upstream losses occurred at sunrise, when water temperatures were at their lowest. Cloudy days at all times of the year produced small diurnal water temperatures ranges (c. 2–5°C) and, consequently, relatively small changes in upstream CaCO₃ loss (23–50 mg L^?1) through the day. Clear sunny days, especially during summer months, produced large diurnal water temperature changes (up to c. 11°C), which in turn triggered diurnal changes in upstream CaCO₃ loss of up to 100 mg L^?1. By implication, the active reach of tufa deposition must advance downstream and increase in length during the evening and vice versa during the day. Given that the temperature of Davys Creek waters are a function of insolation, changes in the reach of tufa deposition under baseflow conditions are a direct function of the prevailing weather. This has implications for the palaeoclimatic interpretation of fossil tufa deposits. Copyright © 2003 John Wiley & Sons, Ltd.     

赛里木湖水化学特征及水质现状评价

通过对赛里木湖天然水体化学成份的分析,确定了水化学类型及平面分布特征,湖水属中高度矿化水,硬度较大,pH偏碱,溶解氧丰富。水化学类型为硫酸盐镁组Ⅱ型（SⅡMg）。本文还对该湖水质及营养状况进行了综合评价,并得出以Ⅱ类水体为主,中度营养化的评价结论,基本符合景观、娱乐、渔业等多种用途的需要。