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1.
Measured concentrations of environmental tracers in spring discharge from a karst aquifer in the Shenandoah Valley, USA, were used to refine a numerical groundwater flow model. The karst aquifer is folded and faulted carbonate bedrock dominated by diffuse flow along fractures. The numerical model represented bedrock structure and discrete features (fault zones and springs). Concentrations of 3H, 3He, 4He, and CFC-113 in spring discharge were interpreted as binary dilutions of young (0–8  years) water and old (tracer-free) water. Simulated mixtures of groundwater are derived from young water flowing along shallow paths, with the addition of old water flowing along deeper paths through the model domain that discharge to springs along fault zones. The simulated median age of young water discharged from springs (5.7  years) is slightly older than the median age estimated from 3H/3He data (4.4  years). The numerical model predicted a fraction of old water in spring discharge (0.07) that was half that determined by the binary-dilution model using the 3H/3He apparent age and 3H and CFC-113 data (0.14). This difference suggests that faults and lineaments are more numerous or extensive than those mapped and included in the numerical model.  相似文献   

2.
This paper presents new data on chromium mineralization in a fenitized xenolith in Mt. Kaskasnyunchorr in the Khibiny alkaline massif (Kola Peninsula, Russia) and summarizes data on Cr mineralogy in the Khibiny Mountains. Protolith silicates that contained Cr3+ admixture are believed to be the source of this element in the fenite. Cr-bearing (maximum Cr2O3 concentrations, wt %, are in parentheses) aegirine (5.8), crichtonite-group minerals (2.1), muscovite (1.3), zirconolite (1.1), titanite (1.0), fluorine-magnesioarfvedsonite (0.8), biotite (0.8), ilmenite (0.6), and aenigmatite (0.6) occur in the fenite. The late-stage spinellides of the FeTi-chromite-CrTi-magnetite series, which are very poor in Mg and Al and which formed after Crrich aegirine and ilmenite, are the richest in Cr (up to 42% Ct2O3). Cr concentrations grew with time during the fenitization process. Unlike minerals in the Khibiny ultramafic rocks where Cr is associated with Mg, Al (it is isomorphic with Cr), and with Ca, chromium in the fenites is associated with Fe, Ti, and V (with which Cr3+ is isomorphic) and with Na in silicate minerals. Cr3+ Mobility of Cr3+ and the unique character of chromium mineralization in the examined fenites were caused by high alkalinity of the fluid.  相似文献   

3.
Ayadi  Rahma  Trabelsi  Rim  Zouari  Kamel  Saibi  Hakim  Itoi  Ryuichi  Khanfir  Hafedh 《Hydrogeology Journal》2018,26(4):983-1007

Major element concentrations and stable (δ18O and δ2H) and radiogenic (3H and 14C) isotopes in groundwater have proved useful tracers for understanding the geochemical processes that control groundwater mineralization and for identifying recharge sources in the semi-arid region of Sfax (southeastern Tunisia). Major-ion chemical data indicate that the origins of the salinity in the groundwater are the water–rock interactions, mainly the dissolution of evaporitic minerals, as well as the cation exchange with clay minerals. The δ18O and δ2H relationships suggest variations in groundwater recharge mechanisms. Strong evaporation during recharge with limited rapid water infiltration is evident in the groundwater of the intermediate aquifer. The mixing with old groundwater in some areas explains the low stable isotope values of some groundwater samples. Groundwaters from the intermediate aquifer are classified into two main water types: Ca-Na-SO4 and Ca-Na-Cl-SO4. The high nitrate concentrations suggest an anthropogenic source of nitrogen contamination caused by intensive agricultural activities in the area. The stable isotopic signatures reveal three water groups: non-evaporated waters that indicate recharge by recent infiltrated water; evaporated waters that are characterized by relatively enriched δ18O and δ2H contents; and mixed groundwater (old/recent) or ancient groundwater, characterized by their depleted isotopic composition. Tritium data support the existence of recent limited recharge; however, other low tritium values are indicative of pre-nuclear recharge and/or mixing between pre-nuclear and contemporaneous recharge. The carbon-14 activities indicate that the groundwaters were mostly recharged under different climatic conditions during the cooler periods of the late Pleistocene and Holocene.

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4.
The Silver Springs Group, Florida (USA), forms the headwaters of the Silver River and supports a diverse ecosystem. The 30 headwater springs divide into five subgroups based on chemistry. Five selected spring vents were sampled in 2007 to better understand the contaminant sources and groundwater flow system. Elevated nitrate-N concentrations (>0.8 mg/L) in the five spring vents likely originate from inorganic (fertilizers) and organic sources, based on nitrogen and oxygen isotope ratios of nitrate. Evidence for denitrification in the Lost River Boil spring includes enriched δ15N and δ18O, excess N2 gas, and low dissolved O2 concentrations (<0.5 mg/L). Multiple age-tracer data (SF6, 3H, tritiogenic 3He) for the two uppermost springs (Mammoth East and Mammoth West) indicate a binary mixture dominated by recent recharge water (mean age 6–7 years, and 87–97% young water). Tracer data for the three downstream spring vents (Lost River Boil, Catfish Hotel-1, and Catfish Conventional Hall-1) indicate exponential mixtures with mean ages of 26–35 years. Contamination from non-atmospheric sources of CFCs and SF5CF3 precluded their use as age tracers here. Variations in chemistry were consistent with mean groundwater age, as nitrate-N and dissolved O2 concentrations were higher in younger waters, and the Ca/Mg ratio decreased with increasing mean age.  相似文献   

5.
Tritium/helium-3 (3H/3He) and chlorofluorocarbon (CFCs, CFC–11, CFC–12, CFC–113) data are used to date the young fraction in groundwater mixtures from a karstic limestone aquifer near Valdosta, Georgia, where regional paleowater in the Upper Floridan aquifer receives recharge from two young sources—the flow of Withlacoochee River water through sinkholes in the river bed, and leakage of infiltration water through post-Eocene semi-confining beds above the Upper Floridan aquifer. In dating the young fraction of mixtures using CFCs, it is necessary to reconstruct the CFC concentration that was in the young fraction prior to mixing. The 3H/3He age is independent of the extent of dilution with older (3H-free and 3Hetrit-free) water. The groundwater mixtures are designated as Type-1 for mixtures of regional paleowater and regional infiltration water and Type-2 for mixtures containing more than approximately 4% of river water. The fractions of regional paleowater, regional infiltration water, and Withlacoochee River water in the groundwater mixtures were determined from Cl− and δ18O data for water from the Upper Floridan aquifer at Valdosta, Georgia.The chlorofluorocarbons CFC–11 and CFC–113 are removed by microbial degradation and/or sorption processes in most anaerobic (Type-2) groundwater at Valdosta, but are present in some aerobic Type-1 water. CFC–12 persists in both SO4-reducing and methanogenic water. The very low detection limits for CFCs (approximately 0.3 pg kg−1) permitted CFC–11 and CFC–12 dating of the fraction of regional infiltration water in Type-1 mixtures, and CFC-12 dating of the river-water fraction in Type-2 mixtures. Overall, approximately 50% of the 85 water samples obtained from the Upper Floridan aquifer have CFC–12-based ages of the young fraction that are consistent with the 3H concentration of the groundwater. Because of uncertainties associated with very low 3H and 3He content in dilute mixtures, 3H/3He dating is limited to the river-water fraction in Type-2 mixtures containing more than about 10% river water. Of the 41 water samples measured for 3H/3He dating, dilution of 3H and low 3He concentration limited 3H/3He dating to 16 mixtures in which 3H/3He ages are defined with errors ranging from ±2 to ±7.5 a (1 σ). After correction for dilution with (assumed) CFC-free regional infiltration water and regional paleowater in the Upper Floridan aquifer, adjusted CFC–12 ages agree with 3H/3He ages within 5 a or less in 7 of the 9 co-dated Type-2 mixtures.Tritium data and dating based on both CFC–11 and CFC–12 in Type-1 mixtures indicate that travel times of infiltration water through the overlying Post-Eocene semi-confining beds exceed 35 a. The CFC and 3H/3He dating indicate that the river fraction in most groundwater entered the groundwater reservoir in the past 20 to 30 a. Few domestic and municipal supply wells sampled intercept water younger than 5 a. Calculated velocities of river water in the Upper Floridan aquifer downgradient of the sinkhole area range from 0.4 to 8.2 m/d. Radiocarbon data indicate that ages of the regional paleowater are on the 10 000-a time scale. An average lag time of approximately 10 to 25 a is determined for discharge of groundwater from the surficial and intermediate aquifers above the Upper Floridan aquifer to the Withlacoochee River.  相似文献   

6.
The geochemical and isotopic composition of surface waters and groundwater in the Velenje Basin, Slovenia, was investigated seasonally to determine the relationship between major aquifers and surface waters, water–rock reactions, relative ages of groundwater, and biogeochemical processes. Groundwater in the Triassic aquifer is dominated by HCO3 –, Ca2+, Mg2+ and δ13CDIC indicating degradation of soil organic matter and dissolution of carbonate minerals, similar to surface waters. In addition, groundwater in the Triassic aquifer has δ18O and δD values that plot near surface waters on the local and global meteoric water lines, and detectable tritium, likely reflecting recent (<50 years) recharge. In contrast, groundwater in the Pliocene aquifers is enriched in Mg2+, Na+, Ca2+, K+, and Si, and has high alkalinity and δ13CDIC values, with low SO4 2– and NO3 – concentrations. These waters have likely been influenced by sulfate reduction and microbial methanogenesis associated with coal seams and dissolution of feldspars and Mg-rich clay minerals. Pliocene aquifer waters are also depleted in 18O and 2H, and have 3H concentrations near the detection limit, suggesting these waters are older, had a different recharge source, and have not mixed extensively with groundwater in the Triassic aquifer.  相似文献   

7.
The Pampa region in Argentina includes vast unconfined–semiconfined aquifers that local economies depend upon, but detailed knowledge of the associated water resources is still lacking. The Pampeano aquifer in the Pampa plain of Argentina covers around 1.5 million km2. In order to achieve a better understanding of the hydrogeological system through the estimation of mean residence times (MRT), water samples were taken from 12 monitoring wells, drilled at different depths in four locations, and analyzed for environmental tracers. The concentrations of 3H, tritiogenic 3He and chlorofluorocarbons (CFCs) can be explained by mixtures of young waters adjusted to exponential piston flow models (EPM) or dispersion models (DM), and different proportions of tracer-free waters (dead water). The sampling site located very close to the water divide shows a dominance of young waters: 85 % of water best represented by a DM model with a MRT of 3 years. For the shallow wells at other sites, best-fitting models result in a DM with MRT between 20 and 35 years, and proportions of dead water between 40 and 60 %. These results lead to important updates in the conceptual model of the Pampeano aquifer. Large proportions of dead water at a few meters depth can be the consequence of upward flows in a multilayered aquifer or diffusive retardation in the inter-bedded clay layers.  相似文献   

8.
Conjoint consideration of distribution of major, rare earth elements (REE) and Y (combined to REY) and of H, O, C, S, Sr isotopes reveals that four types of groundwater are distinguishable by their chemical composition presented by spider patterns. REY patterns indicate thermo-saline deep water and two types of shallow saline groundwaters. Presence of connate waters is not detectable. Sr isotope ratios distinguish three sources of Sr: fast and slow weathering of biotite and K-feldspar in Pleistocene sediments, respectively, and dissolution of limestones. δ13C(DIC) indicate dissolution of limestone under closed and open system conditions. Numerous samples show δ13C(DIC) > 13‰ which is probably caused by incongruent dissolution of calcite and dolomite. The brines from below 1,000 m represent mixtures of pre-Pleistocene seawater or its evaporation brines and infiltrated post-Pleistocene precipitation. The shallow waters represent mixtures of Pleistocene and Recent precipitation salinized by dissolution of evaporites or by mixing with ascending brines. The distribution of water types is independent on geologic units and lithologies. Even the Tertiary Rupelian aquiclude does not prevent salinization of the upper aquifer.  相似文献   

9.
《Applied Geochemistry》2003,18(3):339-351
Water inflows in 9 tunnels and galleries through the Alpine crystalline massifs have been analysed for their 3H activities and δ18O contents. Tritium provides information on water transit times and the dynamics of deep water circulation, whereas δ18O contributes to understanding the origin and flow paths of water in such mountainous regions. Owing to ambiguities arising from the irregularity of the historical 3H input function since 1945, a unequivocal and straightforward interpretation of water transit times in Alpine tunnels is not possible. Nevertheless, the ambiguity can be resolved by considering the 3H data in combination with (a) the generalized hydraulic conductivity of the massif obtained from discharge data, and (b) the Na and silica content of the water as an indication of the extent of rock-water interaction. When the data are resolved in this way, the waters that were sampled in the tunnels/galleries can be divided into 3 age groups, i.e. <15, 15–40 and >40 a. In general, water beneath a rock-cover thickness of <500 m is less than 15 a old, which confirms the active circulation of groundwater in a “decompressed zone” (i.e. a zone of unloading fractures that is expected to have a depth of this magnitude). Moreover, tunnel excavation can radically alter the hydrology, as is shown by the 3H content of a water inflow in the Gothard gallery. Oxygen-18 data primarily reflect the recharge altitude, which can be predicted a priori by considering the large-scale geological structures of each massif and the extent to which they control the subvertical paths followed by the groundwater. Anomalous δ18O data may reflect local or general departures from this interpretation. A general pattern is that downslope flow in the better jointed “decompressed zone”, which parallels the topography, may divert recharge from a higher to lower altitude before it follows the structural pathways into the tunnel. This results in a somewhat lower δ18O value than would be predicted from structure alone, but tends to confirm the existence and role of the “decompressed zone” indicated by the 3H. More local δ18O anomalies reflect recharge from rivers or lakes entering the tunnels, and are illustrated by examples in this paper. Results show that environmental isotopes contribute to a better understanding of the hydrogeology of mountain massifs and of the interactions between tunnels/galleries and groundwater. They provide information not given by other tracing methods and are thus a precious tool for tunnelling engineers and geologists.  相似文献   

10.
The West Coast belt, consisting of nearly 60 thermal springs, is one of the most diversified geothermal fields in India. The present work describes the multi-isotopic (O, H, C, S, B and Sr) characterization of thermal waters carried out in the Tural-Rajwadi geothermal field, situated in southern sector of the west coast geothermal area. The aim of this study is to delineate the origin of thermal water as well as to ascertain the sources of carbon, sulphur, boron and strontium dissolved in those thermal springs. The stable isotopes (δ2H and δ18O) and tritium data indicate that these thermal springs are not recently recharged rain water rather, it contains very old component of water. Oxygen-18 shift is observed due to rock-water interaction over a long period of time. Carbon isotopic composition of DIC points out to the silicate weathering with soil CO2 coming from C3 type of plants whereas δ34S of dissolved sulphate confirms the marine origin of sulphate. This marine signature is basically derived from paleo-seawater possibly entrapped within the flows. Boron isotopic data reveals that both the seawater and rock dissolution are the sources of boron in the thermal waters whereas high 87Sr/86Sr ratios (0.7220–0.7512) of the thermal waters conclusively establishes that archean granitic basement is the predominant rock source of strontium, not the Deccan flood basalts. In addition, like strontium, concentrations of lithium, rubidium and caesium are also governed by the rock-water interaction. Thus, the combined use of this multi-isotope technique coupled with trace element concentrations proves to be an effective tool to establish the sources of solutes in the thermal water.  相似文献   

11.
In this study a typical coastal karst aquifer, developed in lower Cretaceous limestones, on the western Mediterranean seashore (La Clape massif, southern France) was investigated. A combination of geochemical and isotopic approaches was used to investigate the origin of salinity in the aquifer. Water samples were collected between 2009 and 2011. Three groundwater groups (A, B and C) were identified based on the hydrogeological setting and on the Cl− concentrations. Average and maximum Cl− concentrations in the recharge waters were calculated (ClRef. and ClRef.Max) to be 0.51 and 2.85 mmol/L, respectively). Group A includes spring waters with Cl− concentrations that are within the same order of magnitude as the ClRef concentration. Group B includes groundwater with Cl− concentrations that range between the ClRef and ClRef.Max concentrations. Group C includes brackish groundwater with Cl− concentrations that are significantly greater than the ClRef.Max concentration. Overall, the chemistry of the La Clape groundwater evolves from dominantly Ca–HCO3 to NaCl type. On binary diagrams of the major ions vs. Cl, most of the La Clape waters plot along mixing lines. The mixing end-members include spring waters and a saline component (current seawater or fossil saline water). Based on the Br/Clmolar ratio, the hypothesis of halite dissolution from Triassic evaporites is rejected to explain the origin of salinity in the brackish groundwater.Groundwaters display 87Sr/86Sr ratios intermediate between those of the limestone aquifer matrix and current Mediterranean seawater. On a Sr mixing diagram, most of the La Clape waters plot on a mixing line. The end-members include the La Clape spring waters and saline waters, which are similar to the deep geothermal waters that were identified at the nearby Balaruc site. The 36Cl/Cl ratios of a few groundwater samples from group C are in agreement with the mixing hypothesis of local recharge water with deep saline water at secular equilibrium within a carbonate matrix. Finally, PHREEQC modelling was run based on calcite dissolution in an open system prior to mixing with the Balaruc type saline waters. Modelled data are consistent with the observed data that were obtained from the group C groundwater. Based on several tracers (i.e. concentrations and isotopic compositions of Cl and Sr), calculated ratios of deep saline water in the mixture are coherent and range from 3% to 16% and 0% to 3% for groundwater of groups C and B, respectively.With regard to the La Clape karst aquifer, the extension of a lithospheric fault in the study area may favour the rise of deep saline water. Such rises occur at the nearby geothermal Balaruc site along another lithospheric fault. At the regional scale, several coastal karst aquifers are located along the Gulf of Lion and occur in Mezosoic limestones of similar ages. The 87Sr/86Sr ratios of these aquifers tend toward values of 0.708557, which suggests a general mixing process of shallow karst waters with deep saline fossil waters. The occurrence of these fossil saline waters may be related to the introduction of seawater during and after the Flandrian transgression, when the highly karstified massifs invaded by seawater, formed islands and peninsulas along the Mediterranean coast.  相似文献   

12.
The interaction of natural and industrial waters with the rocks and apatite ores of the Khibiny alkaline massif was studied to estimate the extent of anthropogenic influence on natural processes. The abundance of the major rock-forming elements of the nepheline syenites and foidolites in the natural waters indicates that dissolution of nepheline and feldspathoids in natural water plays a significant role under the conditions of slow weathering in the Far North. Experiments showed that fine nepheline particles are transformed into amorphous phases at a fixed water volume at 18–20°C and pH 7.5–8.1. This process became observable already within the first day and continued for months. It is possible in stagnant reservoirs of natural waters and clearly expressed in industrial settling tanks. This is supported by the high content of amorphous phases enriched in Na, K, Al, and Si in the top layer of lacustrine sediments at the zone affected by the sewage of a concentrating mill.  相似文献   

13.
This paper reviews the geochemical, isotopic (2H, 18O, 13C, 3H and 14C) and numerical modelling approaches to evaluate possible geological sources of the high pH (11.5)/Na–Cl/Ca–OH mineral waters from the Cabeço de Vide region (Central-Portugal). Water–rock interaction studies have greatly contributed to a conceptual hydrogeological circulation model of the Cabeço de Vide mineral waters, which was corroborated by numerical modelling approaches. The local shallow groundwaters belong to the Mg–HCO3 type, and are derived by interaction with the local serpentinized rocks. At depth, these type waters evolve into the high pH/Na–Cl/Ca–OH mineral waters of Cabeço de Vide spas, issuing from the intrusive contact between mafic/ultramafic rocks and an older carbonate sequence. The Cabeço de Vide mineral waters are supersaturated with respect to serpentine indicating that they may cause serpentinization. Magnesium silicate phases (brucite and serpentine) seem to control Mg concentrations in Cabeço de Vide mineral waters. Similar δ2H and δ18O suggest a common meteoric origin and that the Mg–HCO3 type waters have evolved towards Cabeço de Vide mineral waters. The reaction path simulations show that the progressive evolution of the Ca–HCO3 to Mg–HCO3 waters can be attributed to the interaction of meteoric waters with serpentinites. The sequential dissolution at CO2 (g) closed system conditions leads to the precipitation of calcite, magnesite, amorphous silica, chrysotile and brucite, indicating that the waters would be responsible for the serpentinization of fresh ultramafic rocks (dunites) present at depth. The apparent age of Cabeço de Vide mineral waters was determined as 2790 ± 40 a BP, on the basis of 14C and 13C values, which is in agreement with the 3H concentrations being below the detection limit.  相似文献   

14.
Environmental tracers (CFCs, stable isotopes 18O, 2H, and 3H) and major ions were employed to study river infiltration and groundwater recharge in the aquifer system in the basin of the Lower Heihe River, Northwest China. Three groups of waters have been recognized: (1) young groundwater, connected to the river, with large variation of CFC apparent ages ranging from <10 a to 40 a, and δ18O and δ2H values which are similar to the river water; (2) regional background water, unaffected by the river, having CFC apparent ages >40 a, and being depleted in 18O and 2H compared with the river water; and (3) groundwater in Gurinai, a grassland located about 100 km from the river, in which the predominant discharge is from the Badain Jaran desert, with CFC apparent ages ranging from 25 to >50 a and being enriched in 18O and 2H compared to the river water. The groundwater along the river contains CFCs and 3H down to depths of about 120 m, and the shallow groundwater exhibits CFC apparent ages in a wide range which are not dependent on the well depth. Groundwaters along the river show a similar trend of enrichment in 18O and 2H as the river water whereas groundwaters in depression cones are depleted in heavier isotopes, and have low CFC and 3H concentrations. The CFC apparent age of the groundwater increases with increasing distance downstream, indicating that the dominant part of the groundwater is from infiltration of river water in the upper reaches. Modifications of groundwater recharge are reflected in variations of stable isotope compositions, as well as CFC and 3H concentrations in the groundwater that was recharged from the river over the last decades. Despite recharging from river water, groundwater abstraction has induced a water balance deficit. The riparian ecosystem in the Ejina Oasis is constrained by both decreased river flow and increased groundwater abstraction. The vegetation degradation in the Ejina Oasis is controlled not only by natural aridification but also worsened by heavy groundwater abstraction and decreased river flow.  相似文献   

15.
New major, trace and isotopic geochemical results from a regional study of springs discharging from the major carbonate rock aquifer in the Interlake Region of Manitoba, Canada, are used to understand water–rock reactions, timing of recharge/discharge, tufa formation processes, and as baseline data. Spring waters are fresh with total dissolved solids (TDS) concentrations ranging from 150 to 880 mg/L. Waters discharging in the northern part of the study area have lower TDS, are dominantly Ca–Mg–HCO3 waters with low SO4 concentrations (<< 50 mg/L), and appear to have interacted primarily with Silurian carbonate lithologies. In contrast, waters in the southeastern part of the study area have higher TDS and have elevated SO4 concentrations (up to 210 mg/L). Spring waters have elevated Mg/Camolar (1.23 ± 0.23), typically greater than congruent dissolution of dolomite. Ca and Mg concentrations and Mg/Camolar indicate that groundwater residence times were sufficient to allow equilibration with bedrock dolomite lithologies; elevated tritium in northern waters indicates a significant recharge component in the 1960's and 1970's. Tufa precipitates that have formed from many of the spring waters are low-Mg calcite (MgO = 1.70 to 5.80 wt.%). Sr concentrations are variable (57 to 657 ppm) and tufa Sr/Camolar ratios appear to be entirely controlled by spring water Sr/Camolar. Empirically determined Sr distribution coefficients (DSr = 0.389 ± 0.083) indicate rapid crystallization following CO2 degassing, consistent with heavier δ13CVPDB compared to spring waters. Sulfate concentrations are generally too low for calcitization (dedolomitization) reactions driven by anhydrite dissolution to be the dominant control on the elevated groundwater Mg/Camolar, implying either extensive sulfate reduction along the flow paths (however, δ13CDIC suggests the elevated SO4 is more consistent with Fe-sulfide oxidation), or that other processes are involved. Major ion ratios suggest that the waters in the southern part of the study area are more consistent with interaction with siliciclastic rocks than with anhydrite dissolution. We suggest that calcitization (dedolomitization) reactions driven by anhydrite dissolution may not dominate all carbonate aquifers and that mixing of waters in karst conduits combined with ion exchange reactions are important controls on water chemistry in these systems.  相似文献   

16.
The assessment of groundwater quality in shallow aquifers is of high societal relevance given that large populations depend directly on these water resources. The purpose of this study was to establish links between groundwater quality, groundwater residence times, and regional geology in the St. Lawrence Lowlands fractured bedrock aquifer. The study focuses on a 4500 km2 watershed located in the St. Lawrence Lowlands of the province of Quebec in eastern Canada. A total of 150 wells were sampled for major, minor, and trace ions. Tritium (3H) and its daughter element, 3He, as well as radiocarbon activity (A14C) were measured in a subset of wells to estimate groundwater residence times. Results show that groundwater evolves from a Ca–HCO3 water type in recharge zones (i.e., the Appalachian piedmont) to a Na–HCO3 water type downgradient, toward the St. Lawrence River. Locally, barium (Ba), fluoride (F), iron (Fe), and manganese (Mn) concentrations reach 90, 2, 18, and 5.9 mg/L respectively, all exceeding their respective Canadian drinking water limits of 1, 1.5, 0.3, and 0.05 mg/L. Release of these elements into groundwater is mainly controlled by the groundwater redox state and pH conditions, as well as by the geology and the duration of rock–water interactions. This evolution is accompanied by increasing 3H/3He ages, from 4.78 ± 0.44 years upgradient to more than 60 years downgradient. Discrepancies between calculated 3H/3He and 14C water ages (the latter ranging from 280 ± 56 to 17,050 ± 3410 years) suggest mixing between modern water and paleo-groundwater infiltrated through subglacial recharge when the Laurentide Ice Sheet covered the study area, and during the following deglaciation period. A linear relationship between 3H activity and corrected 14C versus Mg/Ca and Ba support a direct link between water residence time and the chemical evolution of these waters. The Ba, F, Fe, and Mn concentrations in groundwater originate from Paleozoic rocks from both the St. Lawrence Platform and the Appalachian Mountains. These elements have been brought to the surface by rising hydrothermal fluids along regional faults, and trapped in sediment during their deposition and diagenesis due to reactions with highly sulfurous and organic matter-rich water. Large-scale flow of meltwater during subglacial recharge and during the subsequent retreat of the Laurentide Ice Sheet might have contributed to the leaching of these deposits and their enrichment in the present aquifers. This study brings a new and original understanding of the St. Lawrence Lowlands groundwater system within the context of its geological evolution.  相似文献   

17.
The chemical and isotopic composition of groundwater from 52 sites in the London (U.K.) area was determined as part of a project aimed at assessing the spatial variation in the age of Chalk groundwater, and in determining the relationship between fracture and matrix groundwater in this dual porosity system.Systematic changes in groundwater chemistry take place in the downgradient direction in response to several chemical processes. These processes include early concentration by evaporation and congruent dissolution of calcite followed by widespread incongruent dissolution and ion exchange in addition to local oxidation-reduction reactions, gypsum dissolution and saline intrusion. As a result of the above processes, Chalk groundwater follows an evolutionary path from Ca bicarbonate type to Na bicarbonate type.The age of Chalk groundwater was modelled using14C, δ13C,3H, δ2H and δ180. There is a general increase in the groundwater age in a downgradient direction with the oldest water found in N central areas of the basin. Groundwater in the unconfined zones and in areas S of the Greenwich fault is almost entirely of unevolved, modem composition. Carbon-14 modelling suggests that Chalk groundwater in the S basin is generally less than 10000 a old while that in the north is generally between 10000 and 25000 a old. The presence of3H in concentrations of up to 7 TU in groundwater which yields ages of several 1000 a, however, indicates that mechanisms exist for the rapid introduction of recent groundwater to the confined aquifer. Results of palaeorecharge temperature determinations using δ2H, δ180 and noble gas analytical results suggest that significant Devensian recharge did indeed occur in the aquifer.A model of the development of the Chalk recognizes that it is a classic dual porosity aquifer in which groundwater flow occurs predominantly in the fracture system. The upper 50 m of the aquifer was flushed with fresh water during the 2–3 × 106 a of the Quaternary and therefore meteoric water largely replaced the Tertiary and Cretaceous marine water that previously saturated the system. Most processes which control the chemistry of the groundwater occur in the matrix where the surface area is exceptionally high. Although fracture flow dominates the flow regime, diffusion from the matrix into the fracture porosity controls the chemistry of Chalk groundwater.  相似文献   

18.
A study of tritium content and some physicochemical parameters has been performed in order to investigate interconnection between surface and atmospheric waters and underground waters in Belgrade area. Samples of the precipitation at Zeleno Brdo-Belgrade meteorological station, the Danube and the Sava river water, and underground water (Ranney wells and piezometers) have been analyzed. The3H content, the content of dissolved ions, total hardness, and electrical conductivity have been measured. The tritium data show existence of two water strata in the aquifer. The upper stratum (about 16 m thick) contains older water (mean monthly3H concentration of 17 TU) and has weak interaction with the river and the precipitation. Below this stratum lies the principal water bearing stratum, strongly connected with the river with the3H concentration similar to that of surface water (mean monthly3H concentration of 50 TU) and spreading out through the entire aquifer. The contribution of the Sava river water and the two water layers at the Ranney well are calculated starting with the hydrological aquifer model, which supposes that three water components are mixed in the pumped Ranney well water. According to calculation results using the3H concentration and physicochemical characteristics as parameters, more than 70 percent of the water pumped by the Ranney well (in 1983) comes from the Sava with a time delay of less that 15 days.Properties of tritium distribution in precipitation, river waters, and underground water in the Belgrade region are established from the results of measurements of3H concentrations in the period 1976–1983.  相似文献   

19.
This paper presents results from the numerical modelling of the transport of atmospheric noble gases (He, Ne, Ar, Kr, Xe), tritiated water and 3He produced by radioactive decay of 3H, in unconsolidated lacustrine sediment. Two case studies are discussed: (1) the evolution of 3H and 3He concentrations in the sediment porewater of Lake Zug (Switzerland) from 1953 up to the present; and (2) the response of dissolved atmospheric noble gas concentrations in the sediment porewater of a subtropical lake to an abrupt climatic change that occurred some 10 kyr before the present. (1) Modelled 3H and 3He porewater concentrations are compared with recent data from Lake Zug. An estimate of the effective diffusion coefficients in the sediment porewater is derived using an original approach which is also applicable also to lakes for which the historical 3H and 3He concentrations in the water column are unknown. (2) The air/water partitioning of atmospheric noble gases is sensitive to water temperature and salinity, and thus provides a mechanism by which these environmental variables are recorded in the concentrations of atmospheric noble gases in lakes. We investigate the feasibility of using noble gas concentrations in the porewater of lacustrine sediments as a proxy for palaeoenvironmental conditions in lakes. Numerical modelling shows that heavy noble gases in sediment porewater, because of their comparatively small diffusion coefficients and the strong temperature sensitivity of their equilibrium concentrations, can preserve concentrations corresponding to past lake temperatures over times on the order of 10 kyr. Noble gas analysis of sediment porewaters therefore promises to yield valuable quantitative information on the past environmental states of lakes.  相似文献   

20.
The Oylat spa is located 80 km southeast of Bursa and 30 km south of Ineg?l in the Marmara region. With temperature of 40°C and discharge of 45 l/s, the Oylat main spring is the most important hot water spring of the area. Southeast of the spa the Forest Management spring has a temperature of 39.4°C and discharge of 2 l/s. The G?z spring 2 km north of the spa, which is used for therapy of eye disease, and cold waters of the Saadet village springs with an acidic character are the further important water sources of the area. EC values of Main spring and Forest Management hot spring (750–780 μS/cm) are lower than those of Saadet and G?z spring waters (2,070–1,280 μS/cm) and ionic abundances are Ca > Na + K > Mg and SO4 > HCO3 > Cl. The Oylat and Sızı springs have low Na and K contents but high Ca and HCO3 concentrations. According to AIH classification, these are Ca–SO4–HCO3 waters. Based on the results of δ18O, 2H and 3H isotope analyses, the thermal waters have a meteoric origin. The meteoric water infiltrates along fractures and faults, gets heated, and then returns to surface through hydrothermal conduits. Oylat waters do not have high reservoir temperatures. They are deep, circulating recharge waters from higher enhanced elevations. δ13CDIC values of the Main spring and Forest Management hot spring are −6.31 and −4.45‰, respectively, indicating that δ13C is derived from dissolution of limestones. The neutral pH thermal waters are about +18.7‰ in δ34S while the sulfate in the cold waters is about +17‰ (practically identical to the value for the neutral pH thermal waters). However, the G?z and Saadet springs (acid sulfate waters) have much lower δ34S values (~+4‰).  相似文献   

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