The utilization of boron and strontium isotopes for the assessment of boron contamination of the Cecina River alluvial aquifer (central-western Tuscany,Italy)

The groundwater B concentration in the alluvial aquifer of the upper Cecina River basin in Tuscany, Italy, often exceeds the limit of 1 mg L⁻¹ set by the European Union for drinking water. On the basis of hydrogeological and geochemical observations, the main source of the B contamination of groundwater has been attributed to past releases into streams of exhausted, B-rich geothermal waters and/or mud derived from boric acid manufacturing in Larderello. The releases were discontinued 25–30 years ago.This study confirms that the B dissolved in groundwater is anthropogenic. In fact, the δ¹¹B values of groundwater B match the range −12.2‰ to −13.3‰ of the Turkish B mineral (colemanite) processed in boric acid manufacturing, in the course of which no significant isotopic effects have been observed. This isotopic tracing of the Cecina alluvial aquifer occurs just below the confluence of the Possera Creek, which carries the B releases from Larderello. Strontium isotope ratios support this conclusion.At about 18 km from the Possera Creek confluence, the groundwater δ¹¹B drops to much more negative values (−22‰ to −27‰), which are believed to be produced by adsorption–desorption interactions between dissolved B and the aquifer matrix. The δ¹¹B of B fixed in well bottom sediments shows a similar variation. At present, desorption is prevailing over adsorption because the releases of B-rich water have ceased. A theoretical model is suggested to explain the isotopic trends observed.Thus, B isotopes appear to be a powerful tool for identifying the origin of B contamination in natural waters, although isotopic effects associated with adsorption–desorption processes may complicate the picture, to some extent.     

A study of234U/238U ratios in groundwaters of Taiyuan area,Shanxi Province

Uranium contents and²³⁴U/²³⁸U ratios have been determined on 29 water samples from the Taiyuan area, Shanxi Province. The results show that the same artesian aquifer has similar uranium contents and²³⁴U/²³⁸U activity ratios, and the deeper aquifers have higher A. R. values but lower uranium contents. The A. R. values increase slightly towards groundwater flow in the artesian aquifers dominated by oxidizing ground waters. The Lancun Spring and the famous Jinci Spring belong to two different karst groundwater systems, i.e., the east and west karst groundwater systems. The recharge area of the Lancun Spring should cover the wide limestone outcrops of middle Ordovician in the northeast. The Ordovician fissure-karst ground water to the Jinci Spring is extensively mixed with fissure water in Carboniferous-Jurassic formations and seepage water from the Fenhe River.     

Hydrogeology of a montane headwater groundwater system downgradient of a coal-mine waste rock dump: Elk Valley,British Columbia,Canada

Steelmaking-coal waste rock placed in mountain catchments in the Elk Valley, British Columbia, Canada, drain constituents of interest (CIs) to surface water downgradient of the waste rock dumps. The role of groundwater in transporting CIs in the headwaters of mountain catchments is not well understood. This study characterizes the physical hydrogeology of a portion of a 10-km² headwater catchment (West Line Creek) downgradient of a 2.7-km² waste rock dump placed over a natural headwater valley-bottom groundwater system. The study site was instrumented with 13 monitoring wells. Drill core samples were collected to determine subsurface lithology and geotechnical properties. The groundwater system was characterized using field testing and water-level monitoring. The valley-bottom sediments were composed of unconsolidated glacial and meltwater successions (<64 m thick) deposited as a series of cut and fill structures overlying shale bedrock. An unconfined basal alluvial aquifer located above fractured bedrock was identified as the primary conduit for groundwater flow toward Line Creek (650 m from the toe of the dump). Discharge through the basal alluvial aquifer was estimated using the geometric mean hydraulic conductivity (±1 standard deviation). These calculations suggest groundwater discharge could account for approximately 15% (ranging from 2 to 60%) of the total water discharged from the watershed. The residence time from the base of the waste rock dump to Line Creek was estimated at <3 years. The groundwater system was defined as a snowmelt (i.e., nival) regime dominated by direct recharge (percolation of precipitation) across the catchment.     

Distribution of terminal electron-accepting processes in an aquifer having multiple contaminant sources

Concentrations of electron acceptors, electron donors, and H₂ in groundwater were measured to determine the distribution of terminal electron-accepting processes (TEAPs) in an alluvial aquifer having multiple contaminant sources. Upgradient contaminant sources included two separate hydrocarbon point sources, one of which contained the fuel oxygenate methyl tertbutyl ether (MTBE). Infiltrating river water was a source of dissolved NO₃, SO₄ and organic carbon (DOC) to the downgradient part of the aquifer. Groundwater downgradient from the MTBE source had larger concentrations of electron acceptors (dissolved O₂ and SO₄) and smaller concentrations of TEAP end products (dissolved inorganic C, Fe²⁺ and CH₄) than groundwater downgradient from the other hydrocarbon source, suggesting that MTBE was not as suitable for supporting TEAPs as the other hydrocarbons. Measurements of dissolved H₂ indicated that SO₄ reduction predominated in the aquifer during a period of high water levels in the aquifer and river. The predominant TEAP shifted to Fe³⁺ reduction in upgradient areas after water levels receded but remained SO₄ reducing downgradient near the river. This distribution of TEAPs is the opposite of what is commonly observed in aquifers having a single contaminant point source and probably reflects the input of DOC and SO₄ to the aquifer from the river. Results of this study indicate that the distribution of TEAPs in aquifers having multiple contaminant sources depends on the composition and location of the contaminants and on the availability of electron acceptors.     

Delineation of recharge patterns and contaminant transport using 3H–3He in a shallow aquifer contaminated by chlorinated solvents in South Korea

Stable isotopes of water and ³H–³He were used to delineate recharge patterns and contaminant transport for a granitic regolith aquifer in an industrial complex in Wonju, South Korea, that has historically been contaminated with chlorinated solvents including trichloroethene (TCE) and carbon tetrachloride (CT). Groundwater recharge mainly occurred in upgradient forested areas while little recharge occurred in the downgradient industrial areas covered with extensive sections of impermeable pavement and paddy fields. δ¹⁸O and δD data indicated that groundwater was mainly derived from summer precipitation. The apparent groundwater ages using ³H–³He ranged from 1 to 4 yrs in the upgradient area and from 9 to 10 yrs in the downgradient area. Comparison of groundwater flow velocities based on Darcy’s law and those calculated with simple mass balance models and groundwater age supported the presence of preferential pathways for TCE movement in the study area. Measureable TCE was observed in groundwater irrespective of groundwater age. Considering the 3-yr duration of the TCE spill, 14 yrs before sampling, this indicates that TCE plumes were continuously fed from sources in the unsaturated zone after the spill ended and moved downgradient without significant degradation in the aquifer.     

234U/238U evidence for local recharge and patterns of ground-water flow in the vicinity of Yucca Mountain,Nevada, USA

Uranium concentrations and ²³⁴U/²³⁸U ratios in saturated-zone and perched ground water were used to investigate hydrologic flow and downgradient dilution and dispersion in the vicinity of Yucca Mountain, a potential high-level radioactive waste disposal site. The U data were obtained by thermal ionization mass spectrometry on more than 280 samples from the Death Valley regional flow system. Large variations in both U concentrations (commonly 0.6–10 μg l⁻¹) and ²³⁴U/²³⁸U activity ratios (commonly 1.5–6) are present on both local and regional scales; however, ground water with ²³⁴U/²³⁸U activity ratios from 7 up to 8.06 is restricted largely to samples from Yucca Mountain. Data from ground water in the Tertiary volcanic and Quaternary alluvial aquifers at and adjacent to Yucca Mountain plot in 3 distinct fields of reciprocal U concentration versus ²³⁴U/²³⁸U activity ratio correlated to different geographic areas. Ground water to the west of Yucca Mountain has large U concentrations and moderate ²³⁴U/²³⁸U whereas ground water to the east in the Fortymile flow system has similar ²³⁴U/²³⁸U, but distinctly smaller U concentrations. Ground water beneath the central part of Yucca Mountain has intermediate U concentrations but distinctive ²³⁴U/²³⁸U activity ratios of about 7–8. Perched water from the lower part of the unsaturated zone at Yucca Mountain has similarly large values of ²³⁴U/²³⁸U. These U data imply that the Tertiary volcanic aquifer beneath the central part of Yucca Mountain is isolated from north-south regional flow. The similarity of ²³⁴U/²³⁸U in both saturated- and unsaturated-zone ground water at Yucca Mountain further indicates that saturated-zone ground water beneath Yucca Mountain is dominated by local recharge rather than regional flow. The distinctive ²³⁴U/²³⁸U signatures also provide a natural tracer of downgradient flow. Elevated ²³⁴U/²³⁸U in ground water from two water-supply wells east of Yucca Mountain are interpreted as the result of induced flow from 40 a of ground-water withdrawal. Elevated ²³⁴U/²³⁸U in a borehole south of Yucca Mountain is interpreted as evidence that natural downgradient flow is more likely to follow southerly paths in the structurally anisotropic Tertiary volcanic aquifer where it becomes diluted by regional flow in the Fortymile system.     

Hydrogeologic characteristics of the alluvial tuff aquifer of northern Sahand Mountain slopes, Tabriz, Iran

The Tabriz area is a densely populated area of northwestern Iran (more than 1.5 million in population) with a large proportion of its drinking, domestic, industrial and agricultural water supplied from groundwater resources. The average rate of drinking and industrial water use in the city of Tabriz is about 3.45 m³ s^–1. The Plio-Pleistocene unconfined alluvial tuff aquifer (about 1,275 km²), the most important aquifer in the area, has been known for many years as a reliable resource. The greatest estimated thickness of the alluvial tuff lies in the Saidabad area, with 350 m thickness. There are 994 deep and 284 shallow active pumping wells and 83 qanats operate in the alluvial tuff aquifer. The total water withdrawal from all these artificial discharge points has been measured at 72, 3.8 and 17 million m3/year, respectively. Analytical and numerical methods have been applied to the constant rate pumping test data from the Saidabad wellfield (eight pumping and three observation wells). The values of electrical conductivity in the groundwater of alluvial tuff aquifer range from 203 to 960 μS cm^–1 and bicarbonate type water dominates.     

Assessment of naturally occurring arsenic contamination in the groundwater of Sarkisla Plain (Sivas/Turkey)

High arsenic levels in groundwater of the aquifers, belonging to the Pliocene terrestrial layers and Quaternary alluvial sediments, have become a significant problem for the inhabitants living in Sarkisla (Turkey). The main objective of this study was to determine the origin and arsenic contamination mechanisms of the Sarkisla drinking water aquifer systems. The highest arsenic concentrations were found in Pliocene layers and alluvial sediments with concentrations ranging from 2.1 to 155 mg/kg. These rocks are the main aquifers in the study area, and most of the drinking groundwater demand is met by these aquifers. Groundwater from the Pliocene aquifer is mainly Ca-HCO₃ and Ca-SO₄ water type with high EC values reaching up to 3,270 μS/cm, which is due to the sulfate dissolution in some parts of the alluvial aquifer. Stable isotope values showed that the groundwater was of meteoric origin. Tritium values for the groundwater were between 8.31 and 14.06 TU, representing a fast circulation in the aquifer. Arsenic concentrations in the aquifers were between 0.5 and 345 μg/L. The highest arsenic concentrations detected in the Pliocene aquifer system reached up to 345 μg/L with an average value of 60.38 μg/L. The arsenic concentrations of the wells were high, while the springs had lower arsenic concentrations. These springs are located in the upper parts of the study area where the rocks are less weathered. The hydrogeochemical properties demonstrated that the water–rock interaction processes in sulfide-bearing rocks were responsible for the remarkably high groundwater arsenic contamination in the study area. In the study area, the arsenic levels determined in groundwater exceeded the levels recommended by the WHO. Therefore, it is suggested that this water should not be used for drinking purposes and new water sources should be investigated.     

Investigation of the hydrogeochemical processes in an alluvial channel aquifer located in a typical Karoo Basin of Southern Africa

An investigation was conducted to assess the hydrogeochemical processes of an alluvial channel aquifer located in a typical Karoo Basin of Southern Africa. The investigation was aimed at identifying and describing the groundwater chemistry evolution and its contribution to the overall groundwater quality. X-ray fluorescent spectrometry (XRF) and X-ray diffractometry (XRD) analyses were performed on geological samples to identify and quantify the major element oxides and minerals. The study utilises the conventional Piper diagram, bivariate plots and PHREEQC hydrogeochemical model to analyse groundwater chemistry data obtained during the wet (February and May) and dry seasons (August and December) of 2011. The XRF and XRD results show that the channel deposits are dominated by SiO₂ element oxides and quartz minerals, thus elevated concentrations of silicon (Si⁴⁺) were found in the groundwater. Dolomite and calcite minerals were also detected in the unconsolidated aquifer sediments. The detailed study of the alluvial aquifer system has shown that dissolution of dolomite and calcite minerals and ion exchange are the dominant hydrogeochemical processes influencing the groundwater quality. The groundwater evolves from Ca²⁺–Mg²⁺–HCO₃ ^? recharge water that goes through ion exchange with Na⁺ in the clay-silt sediment to give a Na⁺–HCO₃ ^? water type. The groundwater is supersaturated with respect to quartz, dolomite and calcite minerals. The study shows the potential usefulness of simple bivariate plots as a complimentary tool to the conventional methods for analyzing groundwater hydrogeochemical processes.     

Geochemistry analysis and evolution of a bolson aquifer,basin and range province in the southwestern united states

This paper expands significantly on the major-ion geochemical characterization, evolution, and differentiation of groundwater in the Presidio-Redford Bolson (PRB) Aquifer of Texas as presented in Chowdhury et al. (2008). For 19 groundwater samples from the PRB Aquifer, the author calculated major cation–anion balance errors, equilibrium carbon dioxide partial pressure values and saturation indices for selected minerals. Comparison of major-ion analyses for groundwater from basin margin wells with those for basin center wells is documented and illustrated with ion-concentration maps and Piper and Stiff diagrams and reveals significant increases in concentrations of chloride, sulfate and sodium coupled with notable decrease of calcium in bolson-center well samples. These geochemical changes suggest dissolution of aquifer minerals and cation exchange as groundwater migrates downgradient to the bolson center. The US Geological Survey (USGS) computer code, NETPATH, was used to interpret probable net geochemical mass-balance reactions that potentially have occurred within the PRB Aquifer along groundwater flowpaths from bolson margin to bolson center. For all four upgradient–downgradient well pairs studied, at least three NETPATH models contain cation exchange values; calcium is being exchanged for sodium. The Rio Grande Alluvium Aquifer and Rio Grande River are notably minor sources of recharge to the PRB Aquifer, based on Chowdhury et al. (2008) and geochemical evaluations of this study.     

Hydrochemical characteristics of shallow groundwater in aquifer containing uranyl phosphate minerals, in the Köprübaşı (Manisa) area, Turkey

The concentrations of uranium, iron and the major constituents were determined in groundwater samples from aquifer containing uranyl phosphate minerals (meta-autunite, meta-torbernite and torbernite) in the Köprüba?? area. Groundwater samples from wells located at shallow depths (0.5–6 m) show usually near neutral pH values (6.2–7.1) and oxidizing conditions (Eh = 119–275 mV). Electrical conductivity (EC) values of samples are between 87 and 329 μS/cm^?1. They are mostly characterized by mixed cationic Ca dominating bicarbonate types. The main hydrogeochemical process is weathering of the silicates in the shallow groundwater system. All groundwater in the study area are considered undersaturated with respect to torbernite and autunite. PHREEQC predicted UO₂(HPO₄) ₂ ^2? as the unique species. The excellent positive correlation coefficient (r = 0.99) between U and PO₄ indicates the dissolved uranium in groundwater would be associated with the dissolution of uranyl phosphate minerals. The groundwater show U content in the range 1.71–70.45 μg/l but they are mostly lower than US EPA (2003) maximum contaminant level of 30 μg/l. This low U concentrations in oxic groundwater samples is attributed to the low solubility of U(VI) phosphate minerals under near neutral pH and low bicarbonate conditions. Iron closely associated with studied sediments, were also detected in groundwater. The maximum concentration of Fe in groundwater samples was 2837 μg/l, while the drinking water guidelines of Turkish (TSE 1997) and US EPA (2003) were suggested 200 and 300 μg/l, respectively. Furthermore, iron and uranium showed a significant correlation to each other with a correlation coefficient (r) of 0.94. This high correlation is probably related to the iron-rich sediments which contain also significant amounts of uranium mineralization. In addition to pH and bicarbonate controlling dissolution of uranyl phosphates, association of uranyl phosphates with iron (hydr) oxides seems to play important role in the amount of dissolved U in shallow groundwater.     

Comparison of in situ uranium KD values with a laboratory determined surface complexation model

Reactive solute transport simulations in groundwater require a large number of parameters to describe hydrologic and chemical reaction processes. Appropriate methods for determining chemical reaction parameters required for reactive solute transport simulations are still under investigation. This work compares U(VI) distribution coefficients (i.e. K_D values) measured under field conditions with K_D values calculated from a surface complexation model developed in the laboratory. Field studies were conducted in an alluvial aquifer at a former U mill tailings site near the town of Naturita, CO, USA, by suspending approximately 10 g samples of Naturita aquifer background sediments (NABS) in 17-5.1-cm diameter wells for periods of 3 to 15 months. Adsorbed U(VI) on these samples was determined by extraction with a pH 9.45 NaHCO₃/Na₂CO₃ solution. In wells where the chemical conditions in groundwater were nearly constant, adsorbed U concentrations for samples taken after 3 months of exposure to groundwater were indistinguishable from samples taken after 15 months. Measured in situ K_D values calculated from the measurements of adsorbed and dissolved U(VI) ranged from 0.50 to 10.6 mL/g and the K_D values decreased with increasing groundwater alkalinity, consistent with increased formation of soluble U(VI)-carbonate complexes at higher alkalinities. The in situ K_D values were compared with K_D values predicted from a surface complexation model (SCM) developed under laboratory conditions in a separate study. A good agreement between the predicted and measured in situ K_D values was observed. The demonstration that the laboratory derived SCM can predict U(VI) adsorption in the field provides a critical independent test of a submodel used in a reactive transport model.     

Application of tritium in precipitation and in groundwater of the Kouris catchment (Cyprus) for description of the regional groundwater flow

The Kouris catchment is located in the south of the Troodos massif in Cyprus. It constitutes one of the biggest catchments of the island with important freshwater resources. Geologically, the catchment includes an ophiolitic complex outcropping in the north which is overlaid by sedimentary rocks in the south. The hydrology is driven by a Mediterranean climate, a mountainous topography, and a complex distribution of the hydrogeological properties resulting from the complex geology.To improve the understanding of groundwater hydrology of the Kouris catchment, 176 groundwater and precipitation samples were collected and their ³H contents were analyzed. The three-dimensional ³H transport in the groundwater was simulated by the PMPATH code. For numerical modelling, a regional input function of ³H in precipitation was constructed from a linear regression between data for Cyprus and for neighboring meteorological stations. The calculated residence times for the groundwaters in the sedimentary aquifer and Pillow Lavas were greater than 48 a and were considerably greater than those of the ophiolitic complex (14–30 a). The calibrated aquifer porosities were in a range of 0.05–0.06. The PMPATH model was applied for delineation of spring catchments that were represented by quite narrow zones of lengths up to 5 km.Another contribution resulting from the ³H analysis was a better understanding of the river–aquifer interactions. In most of the southern part, the lithified sediments received only negligible amounts of water from the rivers, while the alluvial aquifer contained mostly water infiltrated from rivers. The largest springs in the southern part, associated with the alluvial aquifer, also discharged water identical to that in the rivers.     

Baseline geochemical conditions in the Chalk aquifer,Berkshire, U.K.: a basis for groundwater quality management

The Chalk aquifer is the most important British aquifer and is also important over much of northern Europe. Aquifer protection requires a sound knowledge of the baseline conditions and how these might vary, or have varied, with time. This detailed geochemical study of a representative area of Chalk in Berkshire, U.K., includes a consideration of several components: (1) the inputs from the atmosphere; (2) the interstitial water of the soil and the unsaturated zone; (3) the interstitial water in the confined and unconfined sections of the aquifer; and (4) the saturated, mainly fissure flow, along the hydraulic gradient which forms an important water supply of the Thames Valley region.Atmospheric inputs form an important source of some elements, but the dominant chemical characteristics of the Chalk groundwater are acquired during percolation through the soil and the upper unsaturated zone. During saturated flow downgradient the chemistry is modified mainly by incongruent reactions of the carbonate matrix and by redox reactions, and only to a minor extent by exchange reactions and mixing with residual saline connate water. The incongruent reaction of carbonate results in a marked increase in the Mg/Ca ratio and the Sr and ¹³C contents of the groundwater with increased residence time. Oxygen concentrations are reduced mainly by oxidation of Fe²⁺, and the onset of reducing conditions allows dissolved Fe²⁺ to increase and rapid denitrification to occur. The salinity profile through the confined Chalk confirms that residual connate water, up to one-fifth sea water concentration, still remains at depth, and this accounts for some salinity increase in the confined groundwater resulting from fissure water.pore water diffusional exchange.Timescales for groundwater movement have been established using tritium, radiocarbon, and indirectly using inert gas ratios and stable isotope ratios. On balance, it is concluded that all abstracted water is of Holocene age, although inert gas temperatures indicate cooler climatic conditions for recharge for some of the confined groundwater.The implications for development and aquifer protection are discussed, especially the prospect of natural in situ denitrification, problems of Fe solubility, and the recognition of groundwater of different maturities.     

Behaviour of boron and strontium isotopes in groundwater–aquifer interactions in the Cornia Plain (Tuscany,Italy)

The Cornia Plain alluvial aquifer, in Tuscany, is exploited intensely to meet the demand for domestic, irrigation and industrial water supplies. The B concentration of groundwater, however, is often above the European limit of 1 mg L⁻¹, with the result that exploitation of these water resources requires careful management. Boron and Sr isotopes have been used as part of a study on the origin and distribution of B dissolved in groundwater, and indirectly as a contribution to the development of appropriate water management strategies.The geochemistry of the Cornia Plain groundwater changes from a HCO₃ facies in the inland areas to a Cl facies along the coastal belt, where seawater intrusion takes place. The B concentration of groundwater increases towards the coastal areas, while the ¹¹B/¹⁰B ratio decreases. This indicates that there is an increasing interaction between dissolved B and the sediments forming the aquifer matrix, whose B content is in the order of 100 mg kg⁻¹. Adsorption–desorption exchanges take place between water and the sediment fine fraction rich in clay minerals, with a net release of B from the matrix into the groundwater, and a consequent δ¹¹B shift from positive to negative values. The aquifer matrix sediments therefore seem to be the major source of B dissolved in the groundwater.The groundwater–matrix interactions triggered by the ionic strength increase caused by seawater intrusion can also be detected in the Ca–Na ion exchanges. Dissolved Sr follows a trend similar to that of Ca, while the ⁸⁷Sr/⁸⁶Sr ratio is equal to that of the exchangeable Sr of the aquifer matrix and therefore does not change significantly.These results have helped to define a new strategy for groundwater exploitation, with the final objective of reducing B concentration in the water extracted from the aquifer.     

Comparison of two alluvial aquifers shows the probable role of river sediments on the release of arsenic in the groundwater of district Vehari,Punjab, Pakistan

The study was done to assess the effect of the river Sutlej on arsenic (As) contamination. Sampling was done from the alluvial plain with increasing distance from the river Sutlej in district Vehari and compared with the study done in the proximity of River Sutlej. Sixty (60) groundwater samples mostly from shallow depths were collected and analyzed for As concentrations. Multivariate statistical tools (PCA and CA), saturation index, piper plots and Gibbs diagrams were used to detect evidence about the interrelationship and sources of As and other water quality variables responsible for groundwater contamination. Results revealed that As concentration ranged from below detection limit to 156 µg/L indicating that 50% samples exceeding the WHO guidelines (10 µg/L) and 17% exceeding the Pakistan National Environmental Quality Standards (NEQS) limits (50 µg/L) Sutlej. The piper plot revealed that water chemistry of the study area was Ca–HCO₃^?, Ca–Mg–Cl, type. Correlations between As and HCO₃^? (r²?=?0.433) was positive, while negative correlations were observed between As–Mn²⁺ and As–Fe²⁺ (r²?=???0.102), (r²?=?0.107) respectively. Geochemical signatures of the groundwater in the study area showed that the As could be released by oxidative dissolution to some extent and elevated evaporation in the arid environment of the study area under the stimulus of alkaline water and high pH (range 7.1–8.4). Although the concentrations are exceeding the WHO limit in 50% of the water samples but, are less than the previous study done in Mailsi near River Sutlej. Further, the concentrations decreased as the distance from the River increased which shows the probable role of sediments deposited by the River Sutlej.     

Origin of groundwater salinity in the Fasa Plain,southern Iran,hydrogeochemical and isotopic approaches

The study area, the Fasa Plain, is situated in the semiarid region of Fars Province in the south of Iran. The Salloo diapir is a salt dome that crops out in the northwest of the study area. Isotopic and hydrochemical analyses were used to examine the water and how the origin of salinity and the diapir affect the quality of the groundwater quality in the study area. Groundwater was sampled from 31 representative pumping wells in alluvial aquifer and five springs in order to measure their stable isotope compositions, bromide ion concentration, and physical and chemical parameters. The alluvial aquifer was organized into two main groups based on the chemistry, with Group 1 consisting of low-salinity well samples (544–1744 µS/cm) with water type Ca–Mg–HCO₃–SO₄ which were taken in the center and north of the area, and Group 2 consisting of high-salinity samples (2550–4620 µS/cm) with water type Ca–Mg–Cl–SO₄ which were taken from the wells in the south and southwest of the area. A saline spring near the salt dome with an EC of 10,280 µS/cm has water type Na–Cl, while the compositions of the water in the other karstic springs is comparable to the fresh groundwater samples. All groundwater samples are undersaturated with respect to gypsum, anhydrite, and halite and are supersaturated with respect to calcite and dolomite. Stable isotopes (δ¹⁸O and δ²H) differentiated four water types: saline springs, freshwater spring, fresh groundwater, and saline groundwater. The results indicate that meteoric water is the main origin of these water resources. Halite dissolution from the salt dome was identified as the origin of salinity. The Na/Cl and Cl/Br ratios confirmed the results. Groundwater compositions in the southwestern part of the area are affected by the intrusion of saltwater from the salt dome. The average saltwater fraction in the some water wells is about 0.2%. In the south and southwestern part of the area, the saltwater fraction is positive in mixed freshwater/saltwater (Group 2). Different processes interact together to change the hydrochemical properties of Fasa’s alluvial aquifer. The main processes that occur in the aquifer are mixing, gypsum dissolution, and calcite precipitation.     

Changes in groundwater chemistry due to metallurgical activities in an alluvial aquifer in the Moa area (Cuba)

The aim of this work is to evaluate the changes in groundwater chemistry in an alluvial aquifer in the Moa area. Surface and ground water, metallurgical waste and various geological material samples were collected in order to evaluate groundwater composition. The results show that the alluvial aquifer is polluted with SO₄^2-, Mg²⁺and heavy metals. According to its major components in the alluvial aquifer, two types of groundwater are identified: magnesi-bicarbonated and sulphate-magnesic. Maximum SO₄^2– and Mg²⁺ contents are more than 1000 mg/L, and are four times higher than the acceptable levels for human consumption of water. The high values of Cr(VI), Ni(II), Mn(II) Fe_(total), SO₄^2– and Mg²⁺ in alluvial aquifers are due to polluted recharge from metallurgical waste from the tailing dam. This recharge is favoured by the preferential flow due to desiccation cracks in metallurgical waste. Geochemical modelling showed that potentially toxic heavy metals might exist largely in the forms of MSO₄^2– and M²⁺ in pore water of SAL metallurgical waste. All samples were supersaturated in goethite and hematite. Results from batch testing indicate that the heavy metals have two origins: natural, due to the existing ultramaphic rocks and laterites, and anthropogenic, by metallurgical waste rich in sulphate and (oxy)hydroxide minerals. These results highlight the need to locate and evaluate a new water source to supply the population of the city of Moa.     

The effect of Si and Al concentrations on the removal of U(VI) in the alkaline conditions created by NH3 gas

Remediation of uranium in the deep unsaturated zone is a challenging task, especially in the presence of oxygenated, high-carbonate alkalinity soil and pore water composition typical for arid and semi-arid environments of the western regions of the U.S. This study evaluates the effect of various pore water constituencies on changes of uranium concentrations in alkaline conditions, created in the presence of reactive gases such as NH₃ to effectively mitigate uranium contamination in the vadose zone sediments. This contaminant is a potential source for groundwater pollution through slow infiltration of soluble and highly mobile uranium species towards the water table. The objective of this research was to evaluate uranium sequestration efficiencies in the alkaline synthetic pore water solutions prepared in a broad range of Si, Al, and bicarbonate concentrations typically present in field systems of the western U.S. regions and identify solid uranium-bearing phases that result from ammonia gas treatment. In previous studies (Szecsody et al. 2012; Zhong et al. 2015), although uranium mobility was greatly decreased, solid phases could not be identified at the low uranium concentrations in field-contaminated sediments. The chemical composition of the synthetic pore water used in the experiments varied for silica (5–250 mM), Al³⁺ (2.8 or 5 mM), HCO₃⁻ (0–100 mM) and U(VI) (0.0021–0.0084 mM) in the solution mixture. Experiment results suggested that solutions with Si concentrations higher than 50 mM exhibited greater removal efficiencies of U(VI). Solutions with higher concentrations of bicarbonate also exhibited greater removal efficiencies for Si, Al, and U(VI). Overall, the silica polymerization reaction leading to the formation of Si gel correlated with the removal of U(VI), Si, and Al from the solution. If no Si polymerization was observed, there was no U removal from the supernatant solution. Speciation modeling indicated that the dominant uranium species in the presence of bicarbonate were anionic uranyl carbonate complexes (UO₂(CO₃)₂⁻² and UO₂(CO₃)₃⁻⁴) and in the absence of bicarbonate in the solution, U(VI) major species appeared as uranyl-hydroxide (UO₂(OH)₃⁻ and UO₂(OH)₄⁻²) species. The model also predicted the formation of uranium solid phases. Uranyl carbonates as rutherfordine [UO₂CO₃], cejkaite [Na₄(UO2)(CO₃)₃] and hydrated uranyl silicate phases as Na-boltwoodite [Na(UO₂)(SiO₄)·1.5H₂O] were anticipated for most of the synthetic pore water compositions amended from medium (2.9 mM) to high (100 mM) bicarbonate concentrations.     

Isotope hydrology of the Chalk River Laboratories site,Ontario, Canada

This paper presents results of hydrochemical and isotopic analyses of groundwater (fracture water) and porewater, and physical property and water content measurements of bedrock core at the Chalk River Laboratories (CRL) site in Ontario. Density and water contents were determined and water-loss porosity values were calculated for core samples. Average and standard deviations of density and water-loss porosity of 50 core samples from four boreholes are 2.73 ± 12 g/cc and 1.32 ± 1.24 percent. Respective median values are 2.68 and 0.83 indicating a positive skewness in the distributions. Groundwater samples from four deep boreholes were analyzed for strontium (⁸⁷Sr/⁸⁶Sr) and uranium (²³⁴U/²³⁸U) isotope ratios. Oxygen and hydrogen isotope analyses and selected solute concentrations determined by CRL are included for comparison. Groundwater from borehole CRG-1 in a zone between approximately +60 and −240 m elevation is relatively depleted in δ¹⁸O and δ²H perhaps reflecting a slug of water recharged during colder climatic conditions. Porewater was extracted from core samples by centrifugation and analyzed for major dissolved ions and for strontium and uranium isotopes. On average, the extracted water contains 15 times larger concentration of solutes than the groundwater. ²³⁴U/²³⁸U and correlation of ⁸⁷Sr/⁸⁶Sr with Rb/Sr values indicate that the porewater may be substantially older than the groundwater. Results of this study show that the Precambrian gneisses at Chalk River are similar in physical properties and hydrochemical aspects to crystalline rocks being considered for the construction of nuclear waste repositories in other regions.