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1.
The water system in a rural area of Lanmuchang in Southwest Guizhou is facing a risk of thallium (Tl) contamination due to Tl mineralization around the area. The major trace elements and Tl in the water system are studied to understand the hydrogeochemical processes of Tl constrained by Tl mineralization. The results showed that the dispersion pattern of Tl follows a descending order in concentration from mine groundwater (deep groundwater) →stream water→shallow groundwater→background water, reflecting the impact of Tl mineralization on the hydrogeochemical composition. Tl concentrations in stream water in both regimes are remarkably higher (2-30 fold) downstream than up- and mid-streams, probably caused by the unidentified discharge of deep groundwater. Low Tl levels are detected in the current drinking water, however, the highly elevated Tl in stream water and ground water may pose a potential environmental risk through daily washing and agricultural irrigation. This study suggests that human activities, such as agricultural irrigation, could intensify the environmental risk of Tl.  相似文献   

2.
Mercury as a toxic element poses environmental concerns, especially in historically Hg-mined districts. The Wanshan Hg mine located in the eastern part of Guizhou Province, southwestern China, ranks the largest Hg-producing district in China. Mining at Wanshan was initiated in 221 B.C., but ceased in 2001. Approximately 22000 tons of Hg, 6000 tons of cinnabar and large quantities of mine-wastes had been produced at Wanshan. Significant quantities of calcines, which were piled irregularly near the old mine processing sites and retorts, continue to impact the local environments in the Wanshan area. In this study, a regional contamination of mercury in surface waters collected from the Meizixi, Dashuixi, Huandao and Gaolouping rivers, whose upstreams or branches originate from the hilly karstic area and receive drainage arising from the calcines, was investigated by determining all Hg species in a base-flow and a flood-flow season. Reactive, dissolved, particulate, and total Hg concentrations in surface water varied from 0.60 to 400 ng/L, 11 to 430 ng/L, 1.4 to 9210 ng/L, and 15 to 9260 ng/L, respectively. Total methylmercury in water samples ranges from 0.31 to 25 ng/L. The concentrations of total Hg and particulate Hg in water samples collected during the flood season are higher than those in the base-flow season, whereas, the concentrations of dissolved and reactive Hg are lower with the peak values observed in water samples collected in the base-flow season. A strong positive correlation between total Hg and particulate Hg is noticed in the water samples collected from Hg-mined areas with the proportion higher than 80%.  相似文献   

3.
黔西南Au-As-Hg-Tl矿化区毒害金属元素的水地球化学   总被引：19，自引：3，他引：16  
研究了黔西南典型Ａｕ－Ａｓ－Ｈｇ－Ｔｌ矿化区内毒害金属元素在采矿活动和自然状态影响下的水地球化学特征及其环境效应。结果表明,已开采的Ｈｇ－Ｔｌ矿区地下水和地表水中均有很高的毒害金属元素,煤采区地下水中亦表现出类似的特征,而Ｈｇ－Ｔｌ矿区外围地下水中金属元素保持在较低的水平。Ｈｇ－Ｔｌ矿区地素水中Ａｓ和Ｔｌ的分布模式表明,其含量的变化受矿区地下水排泄和尾矿淋滤作用的控制。在尚未开采的金矿区,浅层地下  相似文献   

4.
Significant upward movement of mineralized water takes place in the Puebla aquifer system. Preferential groundwater flow paths related to the geological structure and the lowering of the potentiometric surface are suspected to be the prime factors for this intrusion. A combined approach of geochemical and isotope analyses was used to assess the sources of salinity and processes that are controlling the changes in groundwater chemical composition in the Puebla aquifer. Geochemical and isotope data indicate that the likely source of increased solutes is mineralized water from the dissolution of evaporites of the Cretaceous age at the base of the Upper deep aquifer, which is deeper than the intakes of the shallow wells. Dedolomitization and cation exchange seems also to occur along flow paths where sulphate concentrations tend to increase. The deep regional flow paths controls the chemical stratification of groundwater in response to decreased heads through interconnecting vertical and horizontal pathways, such as in the Fosa Atlixco. The results also suggest that high sulphate concentrations originating in the Lower deep aquifer are currently affecting shallow production wells. It is concluded that hydrodynamic aspects together with hydrogeochemical characteristics need to be taken into account to correctly explain the hydrochemical evolution in the stratified aquifer.  相似文献   

5.
In order to identify the origin of the main processes that affect the composition of groundwater in a karstic aquifer, a hydrogeochemical and isotopic study was carried out of water from numerous observation wells located in Sierra de Gador, a semiarid region in SE Spain. Several natural and anthropogenic tracers were used to calculate groundwater residence time within this complex aquifer system. Analysis of major ions enabled the principal geochemical processes occurring in the aquifer to be established, and the samples were classified into four distinctive solute groups according to this criterion. Dissolution of carbonate rocks determines the chemical composition of less mineralized water. In another group, the concurrent dissolution of dolomite and precipitation of calcite in gypsum-bearing carbonate aquifer, where the dissolution of relatively soluble gypsum controls the reaction, are the dominant processes. Marine intrusion results in highly mineralized waters and leads to base exchange reactions. The groundwater enrichment of minor and trace elements allowed classification of the samples into two classes that are linked to different flow patterns. One of these classes is influenced by a slow and/or deep regional flow, where the temperature is generally elevated. The influence of sulphate reduces by up to 40 % the barium concentration due to the barite precipitation. Isotope data (T, 14C) confirm the existence of recent local flows, and regional flow system, and ages of ground water may reach 8000 years. The importance of gypsum dissolution in this aquifer is proved by the δ34S content.  相似文献   

6.
Arsenic occurrence in groundwater near the Cimino-Vico volcanoes (central Italy) was analysed considering the hydrostratigraphy and structural setting and the shallow and deep flows interacting within the Quaternary volcanics. Groundwater is the local source of drinking water. As documented in the past, arsenic in the groundwater has become a problem, and the European maximum allowable contaminant level was recently lowered to 10 μg/L. Chemical analyses of groundwater were conducted, sampled over an area of about 900 km2, from 65 wells and springs representative of the volcanic aquifer and thermal waters. Considering the type of aquifer, the nature of the aquifer formation and its substratum, the hydrochemical data highlight that the arsenic content of the groundwater is mainly connected with the hydrothermal processes in the volcanic area. Thermal waters (54–60°C) fed from deep-rising fluids show higher arsenic concentrations (176–371 μg/L). Cold waters sampled from the volcanic aquifer are characterized by a wide variability in their arsenic concentration (1.6–195 μg/L), and about 62% exceed the limit of 10 μg/L. Where the shallow volcanic aquifer is open to deep-rising thermal fluids, relatively high arsenic concentrations (20–100 μg/L) are found. This occurs close to areas of the more recent volcano-tectonic structures.  相似文献   

7.
《Applied Geochemistry》2001,16(6):583-596
Nitrate concentrations monitored for 2.5 a in the stream water and groundwater of a small catchment, 86.5% of which is devoted to intensive agriculture, show temporal variations with a maximum during winter (as much as 200 mg l−1 in groundwater and 100 mg l−1 in stream water) and a minimum at the end of summer/beginning of autumn. Variations were also observed in the stream water and shallow groundwater after rainfall. The processes involved to explain these variations, determined mainly from NO3− Cl−, SO42−, piezometric and streamflow data, are: (a) variability of the relative contributions to stream water and shallow groundwater by upward fluxes of deeper groundwater which, as demonstrated previously, is denitrified mainly as a result of reaction with pyrite. (b) Denitrification of shallow groundwater during summer with organic matter acting as the electron donor. (c) Dilution by rain water. Nitrate concentrations in both stream water and shallow groundwater depend on the amount of precipitation, with an increased contribution from deep denitrified groundwater during dry periods. The temporal variations in NO3− concentration observed several metres below the water table are related to the preferential and rapid movement of NO3−-polluted water through fractures and large fissures, which has been estimated at 1 m day−1. Nitrate pollution in the catchment, because of the interaction with pyrite, also increases the net chemical weathering rate to values exceeding the world average.  相似文献   

8.
河南荥巩矿区岩溶水发育规律研究   总被引：1，自引：0，他引：1  
通过对矿区地层、构造以及水文地质条件的分析,认为寒武-奥陶系岩溶裂隙含水层是矿区的主要含水层。岩溶水受地层岩性、构造的作用明显,岩溶发育程度在矿区呈现出西弱东强,浅部强、深部弱的发育规律。岩溶水动态受大气降水和矿井排水的双重控制,大气降水是岩溶水的主要补给来源,矿井排水是主要排泄方式,水位动态属于降水-矿排型。在天然状态下,岩溶水主要接受南部露头区大气降水的补给,然后自南向北、自西向东径流,经过新中-三李一带的岩溶水强径流带,在三李一带以岩溶大泉的方式向外排泄。  相似文献   

9.
广东三坑地热田位于吴川－四会深大断裂带的东北侧,三坑向斜岩溶盆地内。地下热水主要赋存于ＮＥ与ＮＷ向断裂构造及其交汇部位的岩溶裂隙发育带中。根据地热地质条件及水热对流系统分析,地下热水是在水热对流系统中由深循环高温构造裂隙水与浅循环８常温岩溶水混合而成。三坑地热田热水资源具有水温适中、水量丰富、水质良好、动态稳定等特点。开发潜力很大。  相似文献   

10.
Groundwater abstraction has resulted in spring flow and groundwater base-flow declines in the Hillsborough River system of central Florida, USA. These declines have resulted in reduction of inflows to the Tampa city reservoir as well as likely adverse environmental effects on riverine and estuarine biota. Causes evaluated for the declines include effects of groundwater development, reduced rainfall, and land alterations. The karstic, heterogeneic nature of the area renders groundwater flow modeling an ineffective method for overall evaluation. Therefore, the evaluation of these declines is accomplished through the systematic use of parametric and nonparametric statistical techniques. These techniques include contingency table analysis, linear regression, Kendall-Theil and Mann-Kendall trend analysis, locally weighted regression, Pearson correlation, Kendall-tau correlation, Spearman correlation, runs test, Student’s t test, and the Kruskall-Wallis test. Data evaluated include groundwater withdrawals, rainfall, base flow, streamflow, stream stage, spring flow, and groundwater levels. Additional methods used include double mass analysis, base flow separation, a low-stage trend analysis, data visualization techniques, and water level change maps. The methodical application of these analyses and techniques to the hydrologic and climatic data yields the conclusion that the primary factor causing the spring flow and base-flow declines is lowered groundwater levels caused by over-abstraction.  相似文献   

11.
地下热水的形成和化学组分特征常受断裂构造和热储地层岩性的影响。川西南喜德地热田内出露的冷泉水和地热水严格受断裂控制,前者为主断裂控制的浅循环型碎屑岩或岩溶裂隙孔隙水;后者则为次级断裂所控制的深循环型裂隙水,其热储层为碳酸盐岩。基于喜德热田形成的地质构造背景,通过开展热田内地热水和冷泉水水化学指标的测试和分析及水岩相互作用模拟,对该热田水文地球化学特征进行了研究。结果表明：喜德热田地热水和冷泉水水源均为大气降水,补给高程分别为2 874~3 092 m和2 584~2 818 m。受温度、含水层矿物类型、水岩相互作用的影响,地热水和冷泉水水化学类型和各组分差别较大,前者为HCO3·SO4-Ca·Mg型水,后者为HCO3-Ca·Mg型水。水岩相互作用模拟表明碳酸盐岩矿物、石膏矿物的溶解和沉淀及阳离子交换过程是导致地热水和冷泉水水化学组分差别较大的主要原因。此外,采用二氧化硅类温标计算喜德热田热储温度为56~90 ℃,循环深度为1 422~2 558 m。研究结果对阐明喜德热田的成因模式,地热水的进一步开发和热水资源的可持续利用具有重要意义。  相似文献   

12.
《Applied Geochemistry》2000,15(3):311-325
Barium/Sr and Ca/Sr ratios have been used to model the relative importance of different sources of stream water. Major and trace element concentrations together with 87Sr/86Sr ratios were measured in precipitation, soil water, groundwater and stream water in a small (9.4 km2) catchment in northern Sweden. The study catchment is drained by a first order stream and mainly covered with podzolized Quaternary till of granitic composition. It is underlain by a 1.8 Ga granite. A model with mixing equations used in an iterative mode was developed in order to separate the stream water into 3 subsurface components: soil water, shallow groundwater, and deep groundwater. Contributions from precipitation are thus not included in the model. This source may be significant for the stream water generation, but it does not interfere with the calculations of the relative contributions from the subsurface components. The results show that the deep groundwater constitutes between 5 and 20% of the subsurface water discharge into the stream water. The highest values of the deep groundwater fraction occur during base flow. Soil water dominates during snowmelt seasons, whereas during base flow it is the least important fraction. Soil water accounts for 10–100% of the subsurface water discharge into the stream water. Shallow groundwater accounts for up to 80% of the subsurface water discharge with the lowest values at peak discharge during snowmelt seasons and the highest values during base flow. The validity of the model was tested by comparing the measured 87Sr/86Sr ratios in the stream water with the 87Sr/86Sr ratios predicted by the model. There was a systematic difference between the measured and modelled 87Sr/86Sr ratios which suggests that the fraction of soil water is overestimated by the model, especially during spring flood. As a consequence of this overestimation of soil water the amount of shallow groundwater is probably underestimated during this period. However, it is concluded that the differences between measured and predicted values are relatively small, and that element ratios are potentially effective tracers for different subsurface water flowpaths in catchments.  相似文献   

13.
The role of different minerals in base cation release and thus the increase of buffering capacity of groundwater against acid deposition is controversially discussed in the literature. The 87Sr/86Sr ratios and base cation concentration were investigated in whole rock leachates, mineral separates, precipitation, soil solution, groundwater and stream water samples in the Lehstenbach catchment (Germany) to identify the weathering sequence of the granite bedrock. Three different approaches were followed in parallel. It was assumed that the contribution of different minerals to base cation supply of the groundwater with increasing weathering intensity would be observed by investigating (1) unweathered rock leachates, deep groundwater and shallow groundwater, (2) groundwater samples from new groundwater wells, reflecting the initial weathering of the drilled bedrock, and groundwater from wells that were drilled in 1988, (3) stream water during baseflow, dominated by deep groundwater, and stream water during high flow, being predominantly shallow groundwater. Whereas the first approach yielded consistent patterns, there was some evidence that groundwater from the new wells initially reflected contamination by the filter gravel rather than cation release in an initial stage of weathering. Time series samples of stream water and groundwater solute concentrations and isotope ratios turned out to reflect varying fractions of soil water and precipitation water at baseflow and high flow conditions rather than varying contributions of different minerals that prevail at different stages of granite weathering.  相似文献   

14.
Groundwater residence time in the Kulnura–Mangrove Mountain aquifer was assessed during a multi-year sampling programme using general hydrogeochemistry and isotopic tracers (H2O stable isotopes, δ13CDIC, 3H, 14C and 87Sr/86Sr). The study included whole-rock analysis from samples recovered during well construction at four sites to better characterise water–rock interactions. Based on hydrogeochemistry, isotopic tracers and mineral phase distribution from whole-rock XRD analysis, two main groundwater zones were differentiated (shallow and deep). The shallow zone contains oxidising Na–Cl-type waters, low pH, low SC and containing 3H and 14C activities consistent with modern groundwater and bomb pulse signatures (up to 116.9 pMC). In this shallow zone, the original Hawkesbury Sandstone has been deeply weathered, enhancing its storage capacity down to ～50 m below ground surface in most areas and ～90 m in the Peats Ridge area. The deeper groundwater zone was also relatively oxidised with a tendency towards Ca–HCO3-type waters, although with higher pH and SC, and no 3H and low 14C activities consistent with corrected residence times ranging from 11.8 to 0.9 ka BP. The original sandstone was found to be less weathered with depth, favouring the dissolution of dispersed carbonates and the transition from a semi-porous groundwater media flow in the shallow zone to fracture flow at depth, with both chemical and physical processes impacting on groundwater mean residence times.

Detailed temporal and spatial sampling of groundwater revealed important inter-annual variations driven by groundwater extraction showing a progressive influx of modern groundwater found at >100 m in the Peats Ridge area. The progressive modernisation has exposed deeper parts of the aquifer to increased NO3? concentrations and evaporated irrigation waters. The change in chemistry of the groundwater, particularly the lowering of groundwater pH, has accelerated the dissolution of mineral phases that would generally be inactive within this sandstone aquifer triggering the mobilisation of elements such as aluminium in the aqueous phase.  相似文献   

15.
The Complex Terminal (CT) confined aquifer of the Djerid basin, southwestern Tunisia, was studied using major ion concentrations and stable isotope contents in order to (1) investigate the changes on its hydrodynamic functioning due to the long-term over-pumping and the large-scale flood irrigation practices, (2) determine the principal mineralization processes of its fossil groundwater, and (3) examine the mode of recharge of this aquifer and whether it contains part of modern hydrological regime. The observed geochemical patterns indicated that the main mineralization processes affecting the CT groundwater water/rock interactions and mixing. The native Na > Cl and Cl > SO4 > Ca > Na waters, resulting from the dissolution of halite and gypsum and from pyrite oxidation, interacted with those of the underlying and the overlying aquifers without changing their chemical facies. Stable isotope data provided evidences about upward and downward leakage into the CT aquifer and their relationships with anthropogenic activities. They demonstrated that the long-term over-pumping of the CT aquifer, which contributed to the loss of its potentiometric pressure, favored the upward leakage of the artesian deep groundwater along parts of the major faults. Moreover, the large-scale flood irrigation practices in the oases domain, which ensured the recharge of the shallow water table by return flow, enhanced the downward leakage toward the CT aquifer.  相似文献   

16.
Studies of hot springs have focused mainly on the properties of fluids and solids. Fewer studies focus on the relationship between the hot springs and groundwater/surface-water environments. The differences in temperature and dissolved solids between hot-spring water and typical surface water and groundwater allow interactions to be traced. Electromagnetic terrain (EMT) conductivity is a nonintrusive technique capable of mapping mixing zones between distinct subsurface waters. These interactions include zones of groundwater/surface-water exchange and groundwater mixing. Herein, hydrogeological techniques are compared with EMT conductivity to trace hot-spring discharge interactions with shallow groundwater and surface water. Potentiometric-surface and water-quality data determined the hydrogeochemistry of two thermally influenced areas in Yellowstone National Park, Wyoming (USA). Data from the sites revealed EMT conductivity contrasts that reflected the infiltration of conductive hot-spring discharge to local groundwater systems. The anomalies reflect higher temperatures and conductivity for Na+–Cl?-rich hydrothermal fluids compared to the receiving groundwater. EMT conductivity results suggested hot springs are fed by conduits largely isolated from shallow groundwater; mixing of waters occurs after hot-spring discharge infiltrates groundwater from the surface and, generally, not by leakage in the subsurface. A model was proposed to explain the growth of sinter mounds.  相似文献   

17.
The Central West Bank aquifer (CWB) is one of the most important resources of fresh groundwater of Palestine. The geology of the area consists mainly of karstic and permeable limestones and dolomites interbedded with argillaceous beds of late Albian–Turonian age. Exploitation of the CWB aquifer, combined with lack of information required to understand the groundwater pattern, represents a challenge for reservoir management. The present work reports hydrogeochemistry, microbiology and environmental isotope data from spring water samples, which were utilized to understand recharge mechanisms, geochemical evolution and renewability of groundwater in CWB aquifer. Besides the major chemical compositions, ionic ratios were used to delineate mineral-solution reactions and weathering processes. Interpretation of chemical data suggests that the chemical evolution of groundwater is primarily controlled by (1) water–rock interactions, involving dissolution of carbonate minerals (calcite and dolomite), and (2) cation exchange processes. The measured equation of the local meteoric water line is δD?=?5.8 δ18O?+?9.9. Stable isotopes show that precipitation is the source of recharge to the groundwater system. The evaporation line has a linear increasing trend from south to north direction in the study area. All analyzed spring waters are suitable for irrigation, but not for drinking purposes. The results from this study can serve as a basis for decision-makers and stakeholders, with the intention to increase the understanding of sustainable management of the CWBs.  相似文献   

18.
Large karstic springs in east-central Florida, USA were studied using multi-tracer and geochemical modeling techniques to better understand groundwater flow paths and mixing of shallow and deep groundwater. Spring water types included Ca–HCO3 (six), Na–Cl (four), and mixed (one). The evolution of water chemistry for Ca–HCO3 spring waters was modeled by reactions of rainwater with soil organic matter, calcite, and dolomite under oxic conditions. The Na–Cl and mixed-type springs were modeled by reactions of either rainwater or Upper Floridan aquifer water with soil organic matter, calcite, and dolomite under oxic conditions and mixed with varying proportions of saline Lower Floridan aquifer water, which represented 4–53% of the total spring discharge. Multiple-tracer data—chlorofluorocarbon CFC-113, tritium (3H), helium-3 (3Hetrit), sulfur hexafluoride (SF6)—for four Ca–HCO3 spring waters were consistent with binary mixing curves representing water recharged during 1980 or 1990 mixing with an older (recharged before 1940) tracer-free component. Young-water mixing fractions ranged from 0.3 to 0.7. Tracer concentration data for two Na–Cl spring waters appear to be consistent with binary mixtures of 1990 water with older water recharged in 1965 or 1975. Nitrate-N concentrations are inversely related to apparent ages of spring waters, which indicated that elevated nitrate-N concentrations were likely contributed from recent recharge.The online version of the original article can be found at  相似文献   

19.
Arsenic (As) contamination in groundwater in mineralized areas typically results from the oxidation of As-rich sulfide minerals in aquifers, from hydrothermal alteration of geothermal systems, or as a result of anthropogenic influences such as mining activity. The primary goal of this study was to determine the spatial and temporal variance in As concentrations in shallow groundwater in a mineralized area and to identify the main As source controlling the concentration patterns. To this end, a combination of a geostatistical technique for space–time modeling of As concentrations and a numerical simulation, which models the transport of As in groundwater, is implemented. A study site in North Sulawesi, Sulawesi Island, Indonesia was selected as it was suitable for investigating the importance of fault lines and metal mining on As contamination. Initially, stable isotope analysis was used to ascertain the groundwater source and the mixing mechanism of the shallow and deep groundwater. Geostatistical modeling revealed consistent general patterns of As concentrations during the past 10 years, with high concentrations found along a NW–SE axis. By matching the geostatistical results with the distributions of As concentrations obtained through transport modeling, the deep-seated hydrothermal system along the fault zone was found to be the major As source. Wastewater from the mine was also observed to be a local As source. Another important influence on the As concentration pattern was a river, which acted as a boundary to separate the groundwater systems into two regions.  相似文献   

20.
Large karstic springs in east-central Florida, USA were studied using multi-tracer and geochemical modeling techniques to better understand groundwater flow paths and mixing of shallow and deep groundwater. Spring water types included Ca–HCO3 (six), Na–Cl (four), and mixed (one). The evolution of water chemistry for Ca–HCO3 spring waters was modeled by reactions of rainwater with soil organic matter, calcite, and dolomite under oxic conditions. The Na–Cl and mixed-type springs were modeled by reactions of either rainwater or Upper Floridan aquifer water with soil organic matter, calcite, and dolomite under oxic conditions and mixed with varying proportions of saline Lower Floridan aquifer water, which represented 4–53% of the total spring discharge. Multiple-tracer data—chlorofluorocarbon CFC-113, tritium (3H), helium-3 (3Hetrit), sulfur hexafluoride (SF6)—for four Ca–HCO3 spring waters were consistent with binary mixing curves representing water recharged during 1980 or 1990 mixing with an older (recharged before 1940) tracer-free component. Young-water mixing fractions ranged from 0.3 to 0.7. Tracer concentration data for two Na–Cl spring waters appear to be consistent with binary mixtures of 1990 water with older water recharged in 1965 or 1975. Nitrate-N concentrations are inversely related to apparent ages of spring waters, which indicated that elevated nitrate-N concentrations were likely contributed from recent recharge.An erratum to this article can be found at  相似文献   

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