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1.
δ87Sr values and Ca/Sr ratios were employed to quantify solute inputs from atmospheric and lithogenic sources to a catchment in NW Germany. The aquifer consists primarily of unconsolidated Pleistocene eolian and fluviatile deposits predominated by >90% quartz sand. Accessory minerals include feldspar, glauconite, and mica, as well as disperse calcium carbonate in deeper levels. Decalcification of near-surface sediment induces groundwater pH values up to 4.4 that lead to enhanced silicate weathering. Consequently, low mineralized Ca–Na–Cl- and Ca–Cl-groundwater types are common in shallow depths, while in deeper located calcareous sediment Ca–HCO3-type groundwater prevails. δ87Sr values and Ca/Sr ratios of the dissolved pool range from 7.3 to −2.6 and 88 to 493, respectively. Positive δ87Sr values and low Ca/Sr ratios indicate enhanced feldspar dissolution in shallow depths of less than 20 m below soil surface (BSS), while equilibrium with calcite governs negative δ87Sr values and elevated Ca/Sr ratios in deep groundwater (>30 m BSS). Both positive and negative δ87Sr values are evolved in intermediate depths (20–30 m BSS). For groundwater that is undersaturated with respect to calcite, atmospheric supplies range from 4% to 20%, while feldspar-weathering accounts for 8–26% and calcium carbonate for 62–90% of dissolved Sr2+. In contrast, more than 95% of Sr2+ is derived by calcium carbonate and less than 5% by feldspar dissolution in Ca–HCO3-type groundwater. The surprisingly high content of carbonate-derived Sr2+ in groundwater of the decalcified portion of the aquifer may account for considerable contributions from Ca-containing fertilizers. Complementary tritium analyses show that equilibrium with calcite is restricted to old groundwater sources.  相似文献   

2.
Several kinds of geochemical anomaly before strong earthquakes have been observed in China since 1966. They include changes in groundwater radon levels, ion content of water (Ca+2, Mg+2, Cl–, SO 4 –2 , F–), dissolved gases (H2, CO2), and gases escaping from the aeration zone through abandoned dry wells (Ar, N2, CO2). The radon anomalies may be grouped as long-term and short-term anomalies. Most of the geochemical anomalies observed are characterized by a pattern of increase. The largest amplitude recorded was 37 times the base level. Preliminary study indicates that the types of seismogeochemical anomaly observed prior to strong earthquakes depend on tectonic, geologic, lithologic, and hydrogeological conditions at the monitoring station. Results obtained from modelling experiments on the mechanisms of some anomalies are given.  相似文献   

3.
Hydrogeochemical investigations along an E–W transect in the middle Meghna basin show groundwater chemistry and redox condition vary considerably with the change in geology. Groundwater in the Holocene shallow (<150 m bgl) alluvial aquifer in western part of the transect is affected by high arsenic concentration (As > 10 μg/l) and salinity. On the other hand, groundwater from the Pliocene Dupi Tila sandy aquifer in the eastern part is fresh and low in As (<10 μg/l). The Holocene shallow aquifers are high in dissolved As, , Fe and dissolved organic carbon (DOC), but generally low in and . High concentrations (250–716 mg/l) together with high DOC concentrations (1.4–21.7 mg/l) in these aquifers reflect active sources of degradable natural organic matter that drives the biogeochemical process. There is generally de-coupling of As from other redox-sensitive elements. In contrast, the Pliocene aquifers are low in As, and DOC. Molar ratio of /H4SiO4 suggests that silicate weathering is dominant in the deeper Holocene aquifers and in the Pliocene aquifers. Molar ratios of Cl−/ and Na+/Cl− suggest mixing of relict seawater with the fresh water as the origin of groundwater salinity. Speciation calculations show that saturation indices for siderite and rhodochrosite vary significantly between the Holocene and Pliocene aquifers. Stable isotopes (δ2H and δ18O) in groundwater indicate rapid infiltration without significant effects of evaporation. The isotopic data also indicates groundwater recharge from monsoonal precipitation with some impact of altitude effect at the base of the Tripura Hills in the east. The results of the study clearly indicate geological control (i.e. change in lithofacies) on groundwater chemistry and distribution of redox-sensitive elements such as As along the transect.  相似文献   

4.
Krainov  S. R.  Ryzhenko  B. N.  Pavlov  Yu. S. 《Water Resources》2003,30(2):154-176
Synthesis of empirical natural materials and thermodynamic computer modeling of geochemical processes in water–rock systems at different boundary conditions (solid-to-liquid ratio, , T) were used to determine the genetic causes of the inverse geochemical zonality that forms in deep horizons of oil-and-gas bearing structures. The geochemical pattern of inversion water was found to form chiefly because of changes in the Eh–pH-conditions of the original groundwater under the effect of organic components of rocks and because of an increase in temperature to 100°C at low values of solid-to-liquid ratios and at no higher than 10–2 bar.  相似文献   

5.
For 25 years, a plant in Israel manufacturing ammonium perchlorate disposed of untreated wastewater in four unlined ponds. This study explores the transport mechanisms of perchlorate infiltrated from 1965 to 1990 from one of these active storage ponds into a deep (40 m) layered vadose zone and the underlying Israeli coastal aquifer. Perchlorate migration from 1990, when wastewater disposal ceased, until today, with infiltration due only to natural rain (500 mm y−1), was also studied. Several indirect methods were used, including: mass balance in the unsaturated zone profile, δ18O and δ2H profiles below the pond, and a comparison of the same sediment profiles in 2005 and 2007. The isotopic composition of the pore water could be divided into two separate groups: lighter (depleted) and heavier (enriched) samples. All samples in the lighter group were from the shallow vadose zone, above two clayey layers, and represent natural infiltration of rainwater. The enriched samples were from the deeper section of the unsaturated zone (20–40 m) and represent water used for perchlorate manufacturing 14 years prior to drilling. Consequently, the overall maximum infiltration rate was estimated to be 1.4 m y−1. Below the clayey layer almost identical perchlorate concentrations were found along the sediment profile in 2005 and 2007 (two boreholes, 3 m apart). Very different perchlorate profiles were observed above the clayey layers. This suggests that perchlorate below the clay layers (20–40 m) is practically stagnant under the current natural conditions. The reduction in perchlorate concentration in groundwater below the ponds vs. its increased concentration further downgradient supports the contention that the current migration of perchlorate from the vadose zone to the groundwater is very small. We estimate that perchlorate concentration in the groundwater under the infiltration pond, which was 187 mg l−1 in 2004, will reach 10 μg l−1 within about 14 years. The existence of a clayey layer crossing the thick vadose zone was thus found to significantly change the infiltration rate when ponded conditions were replaced with natural precipitation.  相似文献   

6.
Groundwater is a very significant water source used for irrigation and drinking purposes in the karst region, and therefore understanding the hydrogeochemistry of karst water is extremely important. Surface water and groundwater were collected, and major chemical compositions and environmental isotopes in the water were measured in order to reveal the geochemical processes affecting water quality in the Gaoping karst basin, southwest China. Dominated by Ca2+, Mg2+, HCO3? and SO42?, the groundwater is typically characterized by Ca? Mg? HCO3 type in a shallow aquifer, and Ca? Mg? SO4 type in a deeper aquifer. Dissolution of dolomite aquifer with gypsiferous rocks and dedolomitization in karst aquifers are important processes for chemical compositions of water in the study basin, and produce water with increased Mg2+, Ca2+ and SO42? concentrations, and also increased TDS in surface water and groundwater. Mg2+/Ca2+ molar ratios in groundwater decrease slightly due to dedolomitization, while the mixing of discharge of groundwater with high Mg2+/Ca2+ ratios may be responsible for Mg2+/Ca2+ ratios obviously increasing in surface water, and Mg2+/Ca2+ ratios in both surface water and groundwater finally tending to a constant. In combination with environmental isotopic analyses, the major mechanism responsible for the water chemistry and its geochemical evolution in the study basin can be revealed as being mainly from the water–rock interaction in karst aquifers, the agricultural irrigation and its infiltration, the mixing of surface water and groundwater and the water movement along faults and joints in the karst basin. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

7.
Since the March–April 1982 eruption of El Chichòn volcano, intense hydrothermal activity has characterised the 1-km-wide summit crater. This mainly consists of mud and boiling pools, fumaroles, which are mainly located in the northwestern bank of the crater lake. During the period 1998–2000, hot springs and fumaroles discharging inside the crater and from the southeastern outer flank (Agua Caliente) were collected for chemical analyses. The observed chemical fluctuations suggest that the physico-chemical boundary conditions regulating the thermodynamic equilibria of the deep rock/fluid interactions have changed with time. The chemical composition of the lake water, characterised in the period 1983–1997 by high Na+, Cl−, Ca2+ and SO42− contents, experienced a dramatic change in 1998–1999, turning from a Na+–Cl−- to a Ca2+–SO42−-rich composition. In June 2000, a relatively sharp increase in Na+ and Cl− contents was observed. At the same time, SO2/H2S ratios and H2 and CO contents in most gas discharges increased with respect to the previous two years of observations, suggesting either a new input of deep-seated fluids or local variations of the more surficial hydrothermal system. Migration of gas manifestations, enhanced number of emission spots and variations in both gas discharge flux and outlet temperatures of the main fluid manifestations were also recorded. The magmatic-hydrothermal system of El Chichòn is probably related to interaction processes between a deep magmatic source and a surficial cold aquifer; an important role may also be played by the interaction of the deep fluids with the volcanic rocks and the sedimentary (limestone and evaporites) basement. The chemical and physical changes recorded in 1998–2000 were possibly due to variations in the permeability of the conduit system feeding the fluid discharges at surface, as testified by the migration of gas and water emanations. Two different scenarios can be put forward for the volcanic evolution of El Chichòn: (1) build-up of an infra-crater dome that may imply a future eruption in terms of tens to hundreds of years; (2) minor phreatic–phreatomagmatic events whose prediction and timing is more difficult to constrain. This suggests that, unlike the diminished volcanic activity at El Chichòn after the 1982 paroxistic event, the volcano-hydrothermal fluid discharges need to be more constantly monitored with regular and more frequent geochemical sampling and, at the same time, a permanent network of seismic stations should be installed.  相似文献   

8.
ABSTRACT

Five-year monitoring of physicochemical parameters was performed with two campaigns in low and high water periods of the Lower Soummam catchment. Data from 18 wells were processed by multivariate statistical tools in order to identify the principal factors influencing groundwater chemistry. Two matrices of 14 and 8 physicochemical parameters with 18 groundwater samples collected in wells were obtained. The correlation matrix showed strong associations between nine variables: K+, Ca2+, Na+, SO42?, Cl?, Mg2+, NO2?, Zn2+ and Sr2+. Principal component analysis and factor analysis showed that the cumulated variance of high and low water periods was of 83.19% and 78.55%, respectively. The variables assigned to the mineralization effect or to pollution indicators were presented by the factor analysis. The bivariate plots confirmed a mineralization model, ascribed to dissolution of geological materials, and to high levels of saline contamination attributed to leakages from sanitary systems. They also showed an increase “upstream to downstream” of the mineralization, visualization of temporal variations, and a dilution process identification of the natural mineralization during the recharge of the aquifer.
EDITOR D. Koutsoyiannis; ASSOCIATE EDITOR X. Chen  相似文献   

9.
In this paper the chemistry of major and trace elements and, for the first time, strontium isotopic ratios measured in running waters from the Arno River Basin (Tuscany, central-northern Italy) and thermal springs discharging in the same hydrographic system are presented and discussed. Classical graphical methods (e.g. mixing diagrams) have here been improved to identify, in a correct statistical sample space, extreme chemical compositions attributable to the action of geochemical processes and/or inherited from specific lithologies (namely contributions or components 1, 2 and 3) to be used in inverse modeling procedures, due to the absence of clear end-members. A linear least squares problem, with non-negativity constraints and distances, as required for compositional data (convex linear mixing) was solved by considering the contribution of the most discriminant variables given by the 87Sr/86Sr isotopic ratios and the concentration of Ca2+, Mg2+, Sr and Rb. Following such approach, it can be assumed (p < 0.05) that component 1, characterized by a Ca2+(Mg2+)– radiogenic-rich (87Sr/86Sr = 0.71274; Rb/Sr = 0.039), represents a dominant feature at basin scale, with a weight ranging from 69% to 100%. Much lower percentages are related to component 2, represented by a Ca2+(Mg2+)– facies with intermediate 87Sr/86Sr (0.70874) and low Rb/Sr (2.8 × 10−4) ratios and component 3, identified by Ca2+– facies with less radiogenic 87Sr/86Sr (0.70827) and low Mg2+/Ca2+ (0.011) ratios. These components are mainly dominated by the dissolution of evaporitic rocks and/or mixing with thermal waters in the southern part of the Arno River Basin and by dissolution of the carbonatic fraction, kinetically favored with respect to that of the silicatic minerals, in the upper reaches of the main course and its tributaries, respectively.  相似文献   

10.
Abstract

Comprehensive geological, hydrogeological and hydrogeochemical investigations were carried out in the south of Hodh El Chargui (southeast Mauritania). Obtaining a hydrogeological conceptual model is crucial for groundwater resources development and management. This is especially true in developing countries and in the rural areas of sub-Saharan Africa. The chosen areas are represented by lithologies referring to a long geological time frame, dating from the Upper Neoproterozoic to the Quaternary age. We developed a methodology in order to identify sites that were suitable for the realization of productive, protected and correct wells to supply safe water to the rural community. A multicriteria approach to studying hydrogeology was used in the project area. In order to identify some main areas in which to carry out pilot interventions, criteria relating to water accessibility and availability, and to hydrogeological and water quality, were considered. Moreover, during the project, it was possible to transfer know-how and hand over responsibilities to the local population and bodies.

Citation Ghiglieri, G. & Carletti, A. (2010 Ghiglieri, G., Balia, R., Oggiano, G. and Pittalis, D. 2010. Prospecting for safe (low fluoride) groundwater in the Eastern African Rift: the Arumeru District (Northern Tanzania). Hydrol. Earth System Sci., 14: 1081–1091.  [Google Scholar]) Integrated approach to choosing suitable areas for the realization of productive wells in rural areas of sub-Saharan Africa. Hydrol. Sci. J. 55(8), 1357–1370.  相似文献   

11.
《水文科学杂志》2013,58(3):526-537
Abstract

The study of the Continental Intercalaire aquifer system of southern Tunisia, based on the interpretation of geochemical (major elements) and isotopic (18O, 2H, 13C and 14C) data, has aided the understanding of the hydrodynamics of this multi-layer aquifer system, which is greatly influenced by tectonics. The determination of the origin of groundwater salinization and the understanding of the hydrogeological and geochemical behaviour of this aquifer were achieved by studying the correlation between the major elements and total mineralization (TDS). By using isotopic tools, it was shown that the water of this aquifer has been recharged under cooler, palaeoclimatic conditions. The technique also made it possible to better understand the hydrodynamic functioning of the aquifer system: it showed that the relatively recent recharge of the aquifer has been by direct infiltration from carbonate and sandy outcrops of the Cretaceous and Miocene, respectively, located in the eastern and northeastern parts of the aquifer. The 18O content was used to calculate the altitude of recharge basins. The isotopic gradient defined in this study is ?0.5 δ18O ‰/100 m.  相似文献   

12.
The Ischia geothermal system is hosted by silicic rocks of the Quaternary Potassic Roman Province, in southern Italy. Exploration drilling down to 1156 m depth in the mid-1950s provided information on boiling profiles (up to 250°C) and on the depth and permeability of the potential reservoirs. Discharge fluid samples were collected and analyzed to define the inflow of surrounding seawater (C1 ranges from 2.5 to 20 g/kg) into the system.Analyses of samples from surface manifestations and shallow wells collected during 1983 and 1988 point to the existence of three distinct mixing regimes, involving three water components. A dishomogeneous body of diluted water (Cl less than 2.5 g/kg), that occurs at depths > 700 m and reequilibrates at 240°C at least, is overlain by an aquifer of groundwater variably mixed with variably seawater (Cl from 4 to 10 g/kg), which tends to reequilibrate at 160°C. Steam-heated waters locally develop and act as dilutants of the rising geothermal fluids.Dilution, mixing, and evaporation of the ascending chloride fluids are supported by oxygen and hydrogen isotopic data the thermal waters being enriched in 18O and D with respect to local meteoric water by up to 7 and 30‰, respectively. The relative composition of the major cations in thermal solutions was used to discriminate the two main groups of thermal waters, the reservoir temperatures of which are estimated from the Na/K-gethermometer. K-Mg geothermometer indicates reequilibration in near-surface conditions.The isotopic composition of the fumarolic steam varies from −7 to −12‰ in ∂8O and from − 35 to − 70‰ in ∂D, in agreement with a deep mixed fluid that boils adiabatically from 240 to 80°C. The deuterium content of the H2O-H2 pair gives enrichment factor of about 830‰, corresponding to equilibrium temperature conditions slightly higher than the surface boiling temperatures. The ∂13C of CO2is almost constant at −4.5‰ (1δ=0.4), suggesting an important magmatic contribution, and the ∂18O values of CO2appears to in equilibrium with accompanying steam at the measured temperatures.The CO2/Ar and H2/Ar chemical ratios have been used to derive aquifer temperatures, the values obtained being consistent with those of solute geothermometers.  相似文献   

13.
Groundwater samples were collected along a flow path in a shallow, fractured tuffaceous aquifer from the Oasis Valley–Beatty Wash region of southern Nevada, USA, and analyzed for a number of oxyanion-forming trace elements including arsenic (As), antimony (Sb), selenium (Se), molybdenum (Mo), and tungsten (W). In addition, ancillary geochemical parameters, including pH, major solute compositions, dissolved silica, dissolved oxygen, and iron and manganese concentrations were quantified in the groundwaters. Arsenic concentrations range from 70 nmol/kg up to 316 nmol/kg in groundwaters of the Oasis Valley–Beatty Wash flow system, and generally exhibit increasing concentrations with flow down-gradient along the flow path. Antimony, W, and to a lesser extent, Mo, exhibit similar increasing concentration trends with flow down-gradient in the aquifer, albeit, at lower concentrations levels (e.g., mean ± SD for Sb, W, and Mo are 2.3 ± 0.9 nmol/kg, 7.4 ± 3.7 nmol/kg, and 101 ± 19 nmol/kg, respectively). Selenium concentration, which range between 4 and 11 nmol/kg, generally decrease in groundwaters with flow down-gradients in the Oasis Valley–Beatty Wash groundwater flow systems. Inverse modeling of groundwater chemistry evolution from the lower reaches of the Oasis Valley flow path using PHREEQC indicate that the groundwater composition is consistent with mixing of nearly equal proportions of groundwater from upper reaches of Oasis Valley and Beatty Wash groundwater, along with dissolution of volcanic glass, potassium feldspar, and gypsum, followed by calcite precipitation, and formation of secondary zeolites (analcime), clay minerals (Ca-montmorillonite), and cristobalite. The geochemical modeling indicates that the concentrations of As and the other oxyanion-forming trace elements are controlled by dissolution of volcanic glass, water–rock interaction with mineralized zones within the aquifer (i.e., sulfide oxidation), desorption from aquifer surface sites, and mixing of Oasis Valley and Beatty Wash groundwaters.  相似文献   

14.
A critical evaluation of literature values for the solubility products, K sp NBS = [Fe2+][HS–] Fe2+ HS– (H NBS + )–1, of various iron sulphide phases results in consensus values for the pKs of 2.95 ± 0.1 for amorphous ferrous sulphide, 3.6 ± 0.2 for mackinawite, 4.4 ± 0.1 for greigite, 5.1 ± 0.1 for pyrrhotite, 5.25 ± 0.2 for troilite and 16.4 ± 1.2 for pyrite.Where the analogous ion activity products have been measured in anoxic freshwaters in which there is evidence for the presence of solid phase FeS, the values lie within the range of 2.6–3.22, indicating that amorphous iron sulphide is the controlling phase. The single value for a groundwater of 2.65 (2.98 considering carbonate complexation) agrees. In seawater four values range between 3.85 to 4.2, indicating that mackinawite or greigite may be the controlling phase. The single low value of 2.94 is in a situation where particularly high fluxes of Fe (II) and S (–II) may result in the preferential precipitation of amorphous iron sulphide. Formation of framboidal pyrite in these sulphidic environments may occur in micro-niches and does not appear to influence bulk concentrations. Calculations show that the formation of Fe2S2 species probably accounts for very little of the iron or sulphide in most natural waters. Previously reported stability constants for the formation of Fe (HS)2 and (Fe (HS)3)– are shown to be suspect, and these species are also thought to be negligible in natural waters. In completely anoxic pore waters polysulphides also have a negligible effect on speciation, but in tidal sediments they may reach appreciable concentrations and lead to the direct formation of pyrite. Concentrations of iron and sulphide in pore waters can be controlled by the more soluble iron sulphide phase. The change in the IAP with depth within the sediment may reflect ageing of the solid phase or a greater flux of Fe (II) and S (–II) nearer the sediment surface. This possible kinetic influence on the value of IAPs has implications for their use in geochemical studies involving phase formation.  相似文献   

15.
Geochemical evaluation of the sources and movement of saline groundwater in coastal aquifers can aid in the initial mapping of the subsurface when geological information is unavailable. Chloride concentrations of groundwater in a coastal aquifer near San Diego, California, range from about 57 to 39,400 mg/L. On the basis of relative proportions of major‐ions, the chemical composition is classified as Na‐Ca‐Cl‐SO4, Na‐Cl, or Na‐Ca‐Cl type water. δ2H and δ18O values range from ?47.7‰ to ?12.8‰ and from ?7.0‰ to ?1.2‰, respectively. The isotopically depleted groundwater occurs in the deeper part of the coastal aquifer, and the isotopically enriched groundwater occurs in zones of sea water intrusion. 87Sr/86Sr ratios range from about 0.7050 to 0.7090, and differ between shallower and deeper flow paths in the coastal aquifer. 3H and 14C analyses indicate that most of the groundwater was recharged many thousands of years ago. The analysis of multiple chemical and isotopic tracers indicates that the sources and movement of saline groundwater in the San Diego coastal aquifer are dominated by: (1) recharge of local precipitation in relatively shallow parts of the flow system; (2) regional flow of recharge of higher‐elevation precipitation along deep flow paths that freshen a previously saline aquifer; and (3) intrusion of sea water that entered the aquifer primarily during premodern times. Two northwest‐to‐southeast trending sections show the spatial distribution of the different geochemical groups and suggest the subsurface in the coastal aquifer can be separated into two predominant hydrostratigraphic layers.  相似文献   

16.
Abstract

Knowledge of the processes that control nitrate migration and its geochemical evolution in the subsurface are fundamental for the regional management of polluted aquifers. In this paper, the spatial distribution and transient variations of nitrate concentrations, associated with manure fertilization, are used to depict hydrogeological dynamics within the sedimentary aquifer system of la Plana de Vic in the Osona region of Spain. Flow systems are identified from geological, hydraulic head, hydrochemical and isotopic data, and by considering nitrate itself as a tracer that indicates how flow paths are modified by human pressures. In this area, nitrates move through fractured aquitards in flows induced by groundwater pumping. Moreover, the lack of casing in the boreholes permits a mixing of groundwater from distinct layers inside the wells, which negates any benefits from the low-nitrate groundwater found in the deepest aquifer layers. Therefore, impacts on groundwater quality are related to intensive manure fertilization as well as to inadequate well construction and exploitation strategies.

Citation Menció, A., Mas-Pla, J., Otero, N. & Soler, A. (2011) Nitrate as a tracer of groundwater flow in a fractured multilayered aquifer. Hydrol. Sci. J. 56(1), 108–122.  相似文献   

17.
The coupled spatial investigation of the geometrical and geochemical properties of a chalk karstic aquifer provides information on the degree to which geologic structure controls aquifer functioning and groundwater quality. Major ion concentrations in the chalk aquifer of the Haute-Normandie region (France) were measured at a high spatial resolution (more than 100 sampling sites over a 6000 km2 area) and mapped. The first observation is a continuity of the geochemical properties, in spite of the karstic properties of the aquifer principal components analysis of geochemical maps revealed two types of spatial distributions: ions with an autochthonous origin (Ca2+, HCO3), and ions with a principally allochthonous origin (Cl−, Na+, , ). Mg2+ was categorised as both autochthonous (chalk dissolution) and allochthonous (brought in by infiltration of Tertiary deposits). To better understand the spatial distribution of the geochemistry, the aquifer geochemistry was compared to the physical properties of the aquifer, in particular aquifer thickness (representing aquifer geometry) and piezometric level (representing aquifer flow). Use of spatial correlation between the geochemical and the geometrical properties provided insight regarding the directional structure of the data and give evidence of directional relations between geochemical and geometrical properties. The degree of mineralisation (principally composed of Ca2+ and ions) increased along the direction of flow, corresponding to an increase in chalk dissolution rate along the flowpath. The steepest mineralisation gradients were related to an increase in the Mg/Ca ratio, evidence of longer residence times and corresponding to zones where aquifer flow capacity is limited because of a decrease of the thickness of the flow section (anticlines or faults). These results highlight the dominant role played by the geometry and the structural context in controlling aquifer geochemistry.  相似文献   

18.
We consider 3D steady flow of fresh water over a salt water body in a confined aquifer of constant thickness D, with application to a pumping well in a coastal aquifer. With neglect of mixing, a sharp interface separates the two fluid bodies and an existing analytical solution, based on the Dupuit assumption, is adopted. The aim is to solve for the mixing between the fresh and salt waters for αT/D  1 (αT transverse dispersivity), as field studies indicate that αT = O(10−3 − 10−2 m). The mixing zone around the interface is narrow and solutions by existing codes experience numerical difficulties. The problem is solved by the boundary layer (BL) approximation, extending a method, applied previously to two-dimensional flows. The BL equations of variable-density flow are solved by using the Von Karman integral method, to determine the BL thickness and the rate of entrainment of salt water along the interface. Application to the pumping well problem yields the salinity of the pumped water, as function of the parameters of the problem (well discharge, seaward discharge, well distance from the coast and density difference).  相似文献   

19.
A combined analysis of lineament length density from radar imagery and surface resistivity data is used to assess the hydrogeological conditions in the Oban massif, Nigeria. The results show that the data guided the qualitative and quantitative estimation of some aquifer parameters. These include resistivity of the water bearing formations (280–740 ω m), thickness (5–140 m), limited hydraulic conductivity (8.53-13.18 m/day) and transmissivity (410.65–725.88 m2/day) data. In addition, the lineament length density for the area ranged between less than 0.2 to slightly more than 0.4. Site evaluation for the location of productive boreholes/wells using a groundwater potential index (GWPI) indicates that areas with a GWPI of greater than 35 are consistent with relatively high yield.  相似文献   

20.
Studies on the hydrogeological conditions of the Mesogea basin in east Attica reveal that the aquifers developed on the post‐alpine formations at the inner part of the coastal brackish zone exhibit positive hydraulic head. These Neogene and Quaternary deposits present high salt concentrations. Selected points were sampled (total 85: 51 wells and 34 boreholes) in order to obtain hydrogeological and hydrochemical data for a better understanding of the structure, operation and dynamics of the aquifer of the area. Statistical methods, R‐mode factor analysis and scatter‐plot diagrams were used for the hydrochemical analysis and presentation of the data. The groundwater resources are relatively weak and there is significant quality degradation due to the geological structure of the greater area, as well as the bad management of the aquifer and anthropogenic activities. Groundwater is characterized by high salt concentrations. Electrical conductivity values range between 260 and 6970 µS cm?1. High salt concentrations at the coastal aquifers are due to sea intrusion, whereas they are attributed to the dissolution of minerals of the geological environment in the inland area. The groundwaters of the study area can be classified into five water types: Ca–HCO3, Mg–HCO3, Na–HCO3, Na–Cl and Mg–Cl. They are saturated in dolomite and calcite, whereas they are unsaturated in anhydrite. High ion concentrations, e.g. ] (0‐221 mg l?1), ] (0·01‐1·88 mg l?1), ] (0·01‐6·75 mg l?1), as well as high heavy metals concentrations are attributed to anthropogenic impacts. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

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