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1.
Regularities in the formation of mining water chemistry in Eastern Donbass were established and described for the 100-year period from the 1920s to 2010. The total of more than 1500 analyses were used. The changes in the chemistry were largest in the 1940s–1950s in the mines that had been recovered during World War II and after the mass abandonment of mines in the region (2002–2010). The size of groundwater resources acceptable for drinking water supply had decreased considerably; and the volumes of polluted surface water had increased abruptly. The export of dissolved substances by mining waters onto land surface reached its maximum (426 thousand t/year) in 2010. Four main lines of transformation of mine water chemistry were identified and their genesis was interpreted.  相似文献   

2.
Krainov  S. R.  Belousova  A. P.  Ryzhenko  B. N. 《Water Resources》2001,28(5):491-501
Generalized observational data on groundwater chemistry and the results of modeling geochemical processes allowed us to establish that the formation of high-carbonate alkaline waters follows two ways, i.e., calcium and soda. It is shown that the formation of alkaline waters in semiarid and arid zones can be facilitated by acid atmospheric precipitation, which forms the concentration of Ca in groundwater sufficiently high to initiate ion exchange processes resulting in the formation of H2CO3–Na waters. Ion exchange is shown to be a boundary process, which facilitates the transition from calcium to soda way of groundwater metamorphization with subsequent increase in the carbonate content and alkalinity of groundwater.  相似文献   

3.
Spatial distribution (horizonal and vertical) of groundwater microbial communities and the hydrogeochemistry in confined aquifers were studied approximately along the groundwater flow path from coteau to plain in the Nomhon area, Qinghai‐Tibet plateau, China. The confined groundwater samples at different depths and locations were collected in three boreholes through a hydrogeological section in this arid and semi‐arid area. The phylogenetic analysis of 16S rRNA genes and multivariate statistical analysis were used to elucidate similarities and differences between groundwater microbial communities and hydrogeochemical properties. The integrated isotopic geochemical measurements were applied to estimate the source and recharge characteristics of groundwater. The results showed that groundwater varied from fresh to saline water, and modern water to ancient water following the flowpath. The recharge characteristics of the saline water was distinct with that of fresh water. Cell abundance did not vary greatly along the hydrogeochemical zonality; however, dissimilarities in habitat‐based microbial community structures were evident, changing from Betaproteobacteria in the apex of alluvial fan to Gammaproteobacteria and then to Epsilonproteobacteria in the core of the basin (alluvial‐lacustrine plain). Rhodoferax, Hydrogenophaga, Pseudomonas, and bacterium isolated from similar habitats unevenly thrived in the spatially distinct fresh water environments, while Sulfurimonas dominanted in the saline water environment. The microbial communities presented likely reflected to the hydrogeochemical similarities and zonalities along groundwater flowpath.  相似文献   

4.
An integrated study with the use of uranium-isotope and microelement hydrogeochemical methods showed the possibility of studying changes in the dynamics and geoenvironmental condition of groundwater in an urban area by the indicator modeling of groundwater formation and circulation, as well as interaction of waters from different horizons, including water ingress from deeper aquifers.  相似文献   

5.
Groundwater chemistry in the northwestern Bol’shekhetskaya Megasyneclise is considered, and the predominance of inversion hydrogeochemical zonality is identified. The analysis of the hydrogeochemistry and genetic coefficients enabled the tentative identification of infiltrogenic, sedimentogenic, lithogenic, and condensatogenic types of waters. The implemented paleohydrogeochemical reconstructions confirmed the predominance in the cross-section of ancient infiltrogenic and slightly saline sedimentogenic water at all development stages of the sedimentary basin.  相似文献   

6.
The impacts of long-term pumping on groundwater chemistry remain unclear in the Manas River Basin, Northwest China. In this study, major ions within five surface water and 105 groundwater samples were analyzed to identify hydrogeochemical processes affecting groundwater composition and evolution along the regional-scale groundwater flow paths using the multivariate techniques of hierarchical cluster analysis (HCA) and principal components analysis (PCA) and traditional graphical methods for analyzing groundwater geochemistry. HCA classified the groundwater samples into four clusters (C1 to C4). PCA reduced the dimensionality of geochemical data into three PCs, which explained 86% of the total variance. The results of HCA and PCA were used to identify three zones: “recharge,” “transition,” and “discharge.” In the recharge zone the groundwater type is Ca-HCO3-SO4 and is primarily impacted by the dissolution of calcite and silicate weathering. In the transition zone the groundwater type is Ca-HCO3-SO4-Cl and is impacted by rock dissolution and reverse ion exchange. In the discharge zone the groundwater type is Na-Cl and is impacted by evaporation and reverse ion exchange. In addition, anthropogenic activities impact the groundwater chemistry in the study area. The groundwater type generally changes from Ca-HCO3-SO4 in the recharge area to Na-Cl in the discharge area along the regional-scale groundwater flow paths. This study provides a process-based knowledge for understanding the interaction of groundwater flow patterns and geochemical evolution within the Manas River Basin.  相似文献   

7.
Enhanced production of unconventional hydrocarbons in the United States has driven interest in natural gas development globally, but simultaneously raised concerns regarding water quantity and quality impacts associated with hydrocarbon extraction. We conducted a pre‐development assessment of groundwater geochemistry in the critically water‐restricted Karoo Basin, South Africa. Twenty‐two springs and groundwater samples were analyzed for major dissolved ions, trace elements, water stable isotopes, strontium and boron isotopes, hydrocarbons and helium composition. The data revealed three end‐members: a deep, saline groundwater with a sodium‐chloride composition, an old, deep freshwater with a sodium‐bicarbonate‐chloride composition and a shallow, calcium‐bicarbonate freshwater. In a few cases, we identified direct mixing of the deep saline water and shallow groundwater. Stable water isotopes indicate that the shallow groundwater was controlled by evaporation in arid conditions, while the saline waters were diluted by apparently fossil meteoric water originated under wetter climatic conditions. These geochemical and isotopic data, in combination with elevated helium levels, suggest that exogenous fluids are the source of the saline groundwater and originated from remnant seawater prior to dilution by old meteoric water combined with further modification by water‐rock interactions. Samples with elevated methane concentrations (>14 ccSTP/kg) were strongly associated with the sodium‐chloride water located near dolerite intrusions, which likely provide a preferential pathway for vertical migration of deeply sourced hydrocarbon‐rich saline waters to the surface. This pre‐drill evaluation indicates that the natural migration of methane‐ and salt‐rich waters provides a source of geogenic contamination to shallow aquifers prior to shale gas development in the Karoo Basin.  相似文献   

8.
Popov  V. G. 《Water Resources》2002,29(4):396-403
The main types of mass transfer in the subsurface hydrosphere are considered. Specific features of vertical hydrogeochemical zonality in the Volga–Ural Artesian Basin are discussed, and the history of its hydrogeological development is considered. The principal role in the formation of the zone of different-composition brines, dominating in the sedimentary cover, is shown to belong to the processes of halogenesis in the Early Permian and density-driven convection of mother brine from evaporite paleoreservoirs into underlying terrigenous–carbonate Paleozoic strata. The problems regarding the mechanism and lithologic–hydrogeochemical consequences of the density-driven convection in the subsurface hydrosphere in a sedimentary basin are considered.  相似文献   

9.
Hydrochemical, inverse geochemical modelling and isotopic approaches are used to assess the hydrogeochemical evolution of groundwater from the basement aquifers in the southeastern part of the Plateaux Region, Togo. Groundwater originates from present-day rainwater infiltration and is mostly fresh and slightly acidic to neutral. Hydrochemical facies are predominantly mixed cations-HCO3 associated with Ca/Mg-Cl, Na-HCO3 and Na-Cl water types in equilibrium with kaolinite and Ca/Mg-smectites. They are related to silicates hydrolysis, anthropogenic contamination, nitrification/denitrification, mixing along flowpaths and dissolution/precipitation of secondary minerals. The pattern of flow paths is in accordance with an increasing trend in total dissolved solids (TDS) toward the potentiometric depression located in the central and southern parts of the aquifer system. Inverse geochemical modelling using the NETPATH-WIN model showed the relative importance of biotite, plagioclase and amphibole weathering and dissolution of secondary carbonate minerals along the flowpath, suggesting that an abundance of minerals is not necessarily the main factor controlling the groundwater chemistry evolution.  相似文献   

10.
Principal-Component Method is used to identify the major factors governing the long-term variations of water chemistry in the transboundary rivers of Selenga and Kiran. Their preliminary interpretation was made. Water chemistry formation in both large (Selenga) and small (Kiran) rivers is shown to be mostly governed by natural-climatic factors. Thus, an increase in water abundance has a dual effect on water chemistry: on the one hand, water is enriched with substances increasingly entering it because of the more intense erosion and dissolution of solid rocks, and, on the other hand, the concentrations of chemicals of anthropogenic origin decrease because of their greater dilution. A conclusion was made regarding a relationship between a positive trend in water temperature and an increase in the concentration of chlorine ion in water. A preliminary estimate is given to the effect of municipal and industrial wastes, as well as surface and subsurface waters of various genesis on long-term variations of river water chemistry. Trends in changes in water chemistry were studied by using approximations of long-term series of the variables that determine the interpretation of principal factors with the help of a slow trend by “caterpillar” method.  相似文献   

11.
Transient hydrogeochemical anomalies were detected in a granite-hosted aquifer, which is located at a depth of 110 m, north of the Shillong Plateau, Assam, India, where groundwater chemistry is mainly buffered by feldspar alteration to kaolinite. Their onsets preceded moderate earthquakes on December 9, 2004 (MW = 5.3) and February 15, 2005 (MW = 5.0), respectively, 206 and 213 km from the aquifer. The ratios [Na+K]/Si, Na/K and [Na+K]/Ca, conductivity, alkalinity and chloride concentration began increasing 3–5 weeks before the MW = 5.3 earthquake. By comparison with field, experimental and theoretical studies, we interpret a transient switchover between source aquifers, which induced an influx of groundwater from a second aquifer, where groundwater chemistry was dominantly buffered by the alteration of feldspar to smectite. This could have occurred in response to fracturing of a hydrological barrier. The ratio Ba/Sr began decreasing 3–6 days before the MW = 5.0 earthquake. We interpret a transient switchover to anorthite dissolution caused by exposure of fresh plagioclase to groundwater interaction. This could have been induced by microfracturing, locally within the main aquifer. By comparison with experimental studies of feldspar dissolution, we interpret that hydrogeochemical recovery was facilitated by groundwater interaction and clay mineralization, which could have been coupled with fracture sealing. The coincidence in timing of these two hydrogeochemical events with the only two MW ≥ 5 earthquakes in the study area argues in favor of cause-and-effect seismic-hydrogeochemical coupling. However, reasons for ambiguity include the lack of similar hydrogeochemical anomalies coupled with smaller seismic events near the monitoring station, the >200 km length scale of inferred seismic-hydrogeochemical coupling, and the potential for far-field effects related to the Great Sumatra–Andaman Islands Earthquake of December 26, 2004.  相似文献   

12.
The Jiangcang Basin is an important mining area of the former Qilian Mountain large coal base in Qinghai Province, and understanding the groundwater circulation mechanism is the basis for studying the hydrological effects of permafrost degradation in alpine regions. In this study, hydrogeochemical and multiple isotope tracer analysis methods are used to understand the chemical evolution and circulation mechanisms of the groundwater in the typical alpine region of the Jiangcang Basin. The diversity of the groundwater hydrochemistry in the study area reflects the complexity of the hydrogeochemical environment in which it is located. The suprapermafrost water and intrapermafrost water are recharged by modern meteoric water. The groundwater is closely hydraulically connected to the surface water with weak evaporation overall. The high δ34S value of deep groundwater is due to SO4 reduction, and SO42−-rich snow recharge with lixiviated sulfate minerals are the main controlling factor for the high SO42− concentration in groundwater. According to the multivariate water conversion relationships, it reveals that the river receives more groundwater recharge, suprapermafrost water is recharged by the proportion of meteoric water, which is closely related to the mountainous area at the edge of the basin, while intrapermafrost water is mainly recharged by the shallow groundwater. This study provides a data-driven approach to understanding groundwater recharge and evolution in alpine regions, in addition to having significant implications for water resource management and ecological environmental protection in coal bases of the Tibetan Plateau.  相似文献   

13.
ABSTRACT

Multivariate statistical analysis and inverse geochemical modelling techniques were employed to deduce the mechanism of groundwater evolution in the hard-rock terrain of Telangana, South India. Q-mode hierarchical cluster analysis (HCA) and principal component analysis (PCA) were used to extract the hydrogeochemical characteristics and classify the groundwater samples into three principal groups. Use of thermodynamic stability diagrams and inverse geochemical modelling in PHREEQC identified the chemical reactions controlling hydrogeochemistry of each of the groups obtained from statistical analysis. The model output showed that a few phases are governing the water chemistry in this area and the geochemical reactions responsible for evolution of groundwater chemistry along the flow path are (i) dissolution of evaporite minerals (dolomite, halite); (ii) dissolution of primary silicate minerals (albite, anorthite, K-feldspar, biotite); (iii) precipitation of secondary silicate minerals (kaolinite, quartz, gibbsite, Ca-montmorillonite) along with anhydrite and calcite; and (iv) reverse ion exchange processes.  相似文献   

14.
Analyses are presented of anion chemistry and sulphur isotopic compositions of sulphate in sinking streams and groundwaters in a mixed allogenic–autogenic karst catchment. Using the sulphur isotopic data, sources of sulphate from agriculture and the effects of sulphate reduction arising from slurry application can be distinguished from natural rock weathering sources. Within the aquifer, sulphate in known autogenic waters has isotopic compositions distinct from allogenic waters, the autogenic waters being dominated by sulphate from rainfall and rock weathering in these low agricultural intensity catchments. On this basis, water rising at low flow from Whirlpool Rising, Speedwell Cavern, has been identified as dominantly autogenic. Groundwater flow between the sinks and risings in Speedwell Cavern is believed to be along conduits following mineralized faults (rakes). During transit SO42−/Cl− in the water increases. Isotopic mass balance shows that this must be due to addition of sulphate from the oxidation of ore minerals by groundwater. Mass balance considerations show that the present rate of sulphide oxidation must be the result of enhancement by lead mining operations on the rakes. Copyright © 2000 John Wiley & Sons, Ltd.  相似文献   

15.
ABSTRACT

Groundwater is used by 3?million inhabitants in the coastal urban city of Douala, Cameroon, but comprehensive data are too sparse for it to be managed in a sustainable manner. Hence this study aimed to (1) assess the potability of the groundwater; (2) evaluate the spatial variation of groundwater composition; and (3) assess the interaction and recharge mechanisms of different water bodies. Hydrogeochemical tools and methods revealed the following results in the Wouri and Nkappa formations of the Douala basin, which is beneath Douala city: 30% of water samples from hand-dug wells in the shallow Pleistocene alluvium aquifer were saline and highly mineralized. However, water from boreholes in the deeper (49–92 m depth) Palaeocene aquifer was saline-free, less mineralized and potable. Water in the shallow aquifer (0.5–22 m depth) was of Na+-K+-Cl?-NO3? type and not potable due to point source pollution, whereas Ca+-HCO3? unpolluted water dominates in the deeper aquifer. Water in the deep and shallow aquifers indicates the results of preferential flow pass and evaporative recharge, respectively. Possible hydrogeochemical processes include point source pollution, reverse ion exchange, remote recharge areas and mixing of waters with different chemical signatures.
EDITOR D. Koutsoyiannis ASSOCIATE EDITOR M.D. Fidelibus  相似文献   

16.
Hui-Long  Xu  Jian-Wei  Shen Xue-Wu  Zhou 《Island Arc》2006,15(1):199-209
Abstract   Geothermal waters in the Niigata Sedimentary Basin, central Japan, are divided into four groups based on their chemical composition (i.e. Na-SO4-type, Na-SO4-Cl-type, Na-Cl-type and Na-Cl-HCO3-type). The Na-SO4-type geothermal water forms as a consequence of water–rock interaction and generally occurs in the outer part of the basin. The Na-Cl-type geothermal water is further subdivided into the original Na-Cl-type geopressured thermal water and the mixed Na-Cl-type geothermal water, in terms of its geochemical and isotopic composition. The original Na-Cl-type geopressured thermal water originates from a geopressured hydrothermal system containing the altered fossil formation waters that are sealed at depth. It moves up to the upper part of the depositional succession or the ground, and generally does not mix with groundwater that is of meteoric origin. This type of water is cooled by heat conduction. The concentration of Cl– in this type of thermal water is very similar to that in seawater. The δD and δ18O values are approximately constant and independent of temperature. The original Na-Cl-type geopressured thermal water is distributed mainly along anticlinal axes in folded Neogene formations. The mixed Na-Cl-type geothermal water is related to the expulsion activity of the geopressured hydrothermal system and occurs mostly along active faults. It is formed by shallow groundwater of meteoric origin being mixed with geopressured hydrothermal water when the geopressured hydrothermal system was expulsed along active faults by paroxysmal tectonic events.  相似文献   

17.
Major‐ion compositions of groundwater are employed in this study of the water–rock interactions and hydrogeochemical evolution within a carbonate aquifer system. The groundwater samples were collected from boreholes or underground tunnels in the Ordovician limestone of Yanzhou Coalfield where catastrophic groundwater inflows can be hazardous to mining and impact use of the groundwater as a water supply. The concentration of total dissolved solid (TDS) ranged from 961 to 3555 mg/l and indicates moderately to highly mineralized water. The main water‐type of the middle Ordovician limestone groundwater is Ca‐Mg‐SO4, with SO42‐ ranging from 537 to 2297 mg/l, and average values of Ca2+ and Mg2+ of 455.7 and 116.6 mg/l, respectively. The water samples were supersaturated with respect to calcite and dolomite and undersaturated or saturated with respect to gypsum. Along the general flow direction, deduced from increases of TDS and Cl‐, the main water–rock interactions that caused hydrogeochemical evolution of the groundwater within the aquifer were the dissolution of gypsum, the precipitation of calcite, the dissolution or precipitation of dolomite, and ion exchange. Ion exchange is the major cause for the lower mole concentration of Ca2+ than that of SO42‐. The groundwater level of Ordovician aquifer is much higher than that of C‐P coal‐bearing aquifers, so the potential flow direction is upward, and the pyrite in coal is not a possible source of sulfate; additional data on the stable sulfur and oxygen isotopic composition of the sulfate may be helpful to identify its origin. Although ion exchange probably accounts for the higher mole concentration of Na+ than that of Cl‐, the dissolution of aluminosilicate cannot be ruled out. The data evaluation methods and results of this study could be useful in other areas to understand flow paths in aquifers and to provide information needed to identify the origin of groundwater. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

18.
Trends in precipitation and surface water chemistry at a network of 15 small watersheds (< 10 km2) in the USA were evaluated using a statistical test for monotonic trends (the seasonal Kendall test) and a graphical smoothing technique for the visual identification of trends. Composite precipitation samples were collected weekly and surface water samples were collected at least monthly. Concentrations were adjusted before trend analysis, by volume for precipitation samples and by flow for surface water samples. A relation between precipitation and surface water trends was not evident either for individual inorganic solutes or for solute combinations, such as ionic strength, at most sites. The only exception was chloride, for which there was a similar trend at 60% of the sites. The smoothing technique indicated that short-term patterns in precipitation chemistry were not reflected in surface waters. The magnitude of the short-term variations in surface water concentration was generally larger than the overall long-term trend, possibly because flow adjustment did not adequately correct for climatic variability. Detecting the relation between precipitation and surface water chemistry trends may be improved by using a more powerful sampling strategy and by developing better methods of concentration adjustment to remove the effects of natural variation in surface waters.  相似文献   

19.
A simple mixing model demonstrates that chemical variations in Cascade surface waters reflect flow from three general zones: alpine areas, forested colluvial slopes, and seasonally saturated areas. The chemistry of weathering solutions in alpine portions of the Williamson Creek catchment (North Cascade Range) results from alteration of plagioclase, hornblende, and biotite to kaolinitic material and vermiculite. Surface and shallow groundwater in forested portions of the catchment reflect these reactions, dissolution of small quantities of carbonate, and biologic activity. Both at-a-point and downstream chemical variations are explained quantitatively by the volume of water that originates in each of the hydrogeochemical source areas. Water from the forested colluvial slopes is most significant on an annual basis. However, summer low-flow is a mixture of colluvial waters and dilute solutions from the alpine zone, whereas 10 to 30 per cent of peak flow in snowmelt and rainstorms is produced from seasonally saturated areas. Poor concentration/discharge (C/Q) correlations, typical of Cascade rivers, result from mixing of significant C/Q relations for water leaving each source area. Model predictions could be substantially improved by better data for the effects of temperature, water-contact time, and biologic cycling on the chemistry of soil water from forested zones.  相似文献   

20.
Seawater intrusion causes many problems for groundwater quality, whereas natural remediation is time consuming. However, in cases where groundwater replenishment is feasible, groundwater quality remediation is possible and rapid. The alluvial aquifer in the lowland of the Glafkos River basin, which extends south of Patras city, was for over 30 years the major water source supplying the broader area. Groundwater quality has been degraded due to seawater intrusion, caused by overpumping and generally by inappropriate groundwater management. During the last decade, groundwater quality has been remedied due to diminished groundwater abstractions. The remediation rate was further higher because of rapid discharge of the brackish groundwater, through wells with freely flowing water in the coastal area, where, however, groundwater quality remains low. This paper deals with the hydrogeochemical processes that take place in the area. It is ascertained that ion exchange and mineral dilution processes are dominant. The ion relations between chloride, bromide and iodide, as well as the distribution maps of their concentrations, were used to determine the spatial distribution of the seawater intrusion front. In the lower part of the area in a distance from 1000 and 1500 m from the coast, the rBr?/rCl? ratio showed low values (<2·5 × 10?3) similar to those of seawater. The rI?/rCl? ratio also presented low values (<7 × 10?5), with the lowest one (2·7 × 10?5) detected along the coastline. In the upper part of the area, a gradual change of those ratios was observed upstream, until they receive values similar to those of the surface waters of Glafkos River. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

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