Tracking selenium in the Chalk aquifer of northern France: Sr isotope constraints

Groundwater at the southern and eastern edges of France’s Paris Basin has a selenium content that at times exceeds the European Framework Directive’s drinking-water limit value of 10 μg/L. To better understand the dynamics of the Chalk groundwater being tapped to supply the city of Lille and the Se origins, we used a combination of geochemical and isotopic tools. Strontium isotopes, coupled with Ca/Sr, Mg/Sr and Se/Sr ratios, were used to identify the main groundwater bodies and their mixings, with the Mg/Sr and Se/Sr ratios constraining a ternary system. Groundwater in the agricultural aquifer-recharge zone represents a first end-member and displays the youngest water ages of the catchment along with the highest Sr isotopic signature (0.70842) and low Se contents. Anaerobic groundwater constitutes a second major end-member affected by water-rock interactions over a long residence time, with the lowest Sr isotopic signature (0.70789) and the lowest Se content, its low SF6 content confirming the contribution of old water. Se-rich groundwater containing up to 30 μg/L of Se represents a third major end-member, with an intermediate Sr isotopic ratio (0.70826), and is mainly constrained by the clayey Se-rich formation overlying the Chalk aquifer. The spatial and temporal Se variability in the groundwater is clearly linked to the presence of this formation identified as Tertiary and also to the hydrological conditions; saturation of the Se-rich clays by oxygenated groundwater enhances Se mobility and also Sr adsorption onto the clays. This multi-tool study including Sr isotopes successfully identified the Se origins in the aquifer and has led to a better understanding of the regional mixing and processes affecting the Chalk groundwater.     

Geochemical evolution of uraniferous soda lakes in Eastern Mongolia

Extremely high concentrations of uranium (U) were discovered in shallow, groundwater-fed hyperalkaline soda lakes in Eastern Mongolia. A representative groundwater sample in this area is dilute and alkaline, pH = 7.9, with 10 mM TIC and 5 mM Cl⁻. In contrast, a representative lake water sample is pH ~ 10 with TIC and Cl⁻ each more than 1,000 mM. Groundwater concentrations of U range from 0.03 to 0.43 μM L⁻¹. Lake water U ranges from 0.24 to >62.5 μM, possibly the highest naturally occurring U concentrations ever reported in surface water. Strontium isotopes ⁸⁷Sr/⁸⁶Sr varied in groundwaters from 0.706192 to 0.709776 and in lakes ⁸⁷Sr/⁸⁶Sr varied from 0.708702 to 0.709432. High concentrations of U, Na, Cl⁻, and K correlate to radiogenic Sr in lake waters suggesting that U is sourced from local Cretaceous alkaline rhyolites. Uranium-rich groundwaters are concentrated by evaporation and U(VI) is chelated by CO₃⁻² to form the highly soluble UO₂(CO₃)₃⁻⁴. Modeled evaporation of lakes suggests that a U-mineral phase is likely to precipitate during evaporation.     

Hydrochemistry and isotope compositions of groundwater from the Shihongtan sandstone-hosted uranium deposit, Xinjiang, NW China

Groundwaters and surface water in the Shihongtan sandstone-hosted U ore district, Xinjiang, NW China, were sampled and analyzed for their major-, and trace element concentrations and oxygen, hydrogen, boron and strontium isotope compositions in order to assess the possible origins of the waters and water–rock interactions that occurred in the deep aquifer system. The waters in the study district have been grouped into three hydrochemical facies: Facies 1, potable spring-water, is a pH neutral (7.0), Na–Ca–HCO₃ type water with low total dissolved solids (TDS; 0.2 g/l, fresh) and has δ¹⁸O of − 8.3‰, δD of − 48.2‰,δ¹¹B of 1.5‰, and ⁸⁷Sr/⁸⁶Sr of 0.70627. Facies 2 groundwaters are mildly acidic to mildly alkaline (pH of 6.5–8.0, mean 7.3), Na–Ca–Mg–Cl–SO₄ type waters with moderate TDS (8.2 g/l–17.2 g/l, mean 9.3 g/l, brackish) and haveδ¹⁸O values in the − 5.8‰ to − 9.3‰ range (mean − 8.1‰), δD values in the − 20.8‰ to − 85.5‰ range (mean − 47.0‰),δ¹¹B values in the + 9.5‰ to + 39.1‰ range (mean + 17.1‰), and ⁸⁷Sr/⁸⁶Sr values in the 0.70595 to 0.70975 range (mean 0.70826). Facies 3, Aiting Lake water, is a mildly alkaline (pH = 7.4), Na–Ca–Mg–Cl–SO₄ type water with the highest TDS (249.1 g/l, brine) and has δ¹⁸O of − 2.8‰, δD of − 45.8‰,δ¹¹B of 21.2‰, and ⁸⁷Sr/⁸⁶Sr of 0.70840. The waters from the study district show a systematic increase in major, trace element and TDS concentrations and δ¹¹B values along the pathway of groundwater migration which can only be interpreted in terms of water–rock interaction at depth and strong surface evaporation. The hydrochemical and isotopic data presented here confirm that the groundwaters in the Shihongtan ore district are the combined result of migration, water–rock interaction and mixing of meteoric water with connate waters contained in sediments.     

Identifying the Sources of Solutes in Karst Groundwater in Chongqing,China: a Combined Sulfate and Strontium Isotope Approach

Groundwater from karst subterranean streams is among the world’s most important sources of drinking water supplies, and the hydrochemical characteristics of karst water are impacted by both natural environment and people. Therefore, the study of hydrochemistry and its solutes’ sources is very important to ensure the normal function of life support systems. In this paper, thirty?five representative karst groundwater samples were collected from different aquifers (limestone and dolomite) and various land use types in Chongqing to trace the sources of solutes and relative hydrochemical processes. Hydrogeochemical types of karst groundwater in Chongqing were mainly of the Ca?HCO3 type or Ca (Mg)?HCO3 type. However, some hydrochemical types of karst groundwater were the K+Na+Ca?SO4 type (G25 site) or Ca?HCO3+SO4 type (G26 and G14 site), indicating that the hydrochemistry of these sites might be strongly influenced by anthropogenic activities or unique geological characteristics. The dissolved Sr concentrations of the studied groundwater ranged from 0.57 to 15.06 μmmol/L, and the 87Sr/86Sr varied from 0.70751 to 0.71627. The δ34S?SO42? fell into a range of ?6.8‰?21.5‰, with a mean value of 5.6‰. The variations of both 87Sr/86Sr and Sr values of the groundwater samples indicated that the Sr element was controlled by the weathering of limestone, dolomite and silicate rock. However, the figure of 87Sr/86Sr vs. Sr2+/[K++Na+] showed that the anthropogenic inputs also obviously contributed to the Sr contents. For tracing the detailed anthropogenic effects, we traced the sources of solutes collected karst groundwater samples in Chongqing according to the δ34S value of potential sulfate sources. The variations of both δ34S and 1/SO42? values of the groundwater samples indicated that the atmospheric acid deposition (AAD), dissolution of gypsum (GD), oxidation of sul?de mineral (OS) or anthropogenic inputs (SF: sewage or fertilizer) have contributed to solutes in karst groundwater. The influence of oxidation of sul?de mineral, atmospheric acid deposit and anthropogenic inputs to groundwater in Chongqing karst areas was much widespread.     

Environmental isotopes (18O, 2H, and 87Sr/86Sr) as a tool in groundwater investigations in the Keta Basin, Ghana

Analyses of environmental isotopes (¹⁸O, ²H, and ⁸⁷Sr/⁸⁶Sr) are applied to groundwater studies with emphasis on saline groundwater in aquifers in the Keta Basin, Ghana. The ⁸⁷Sr/⁸⁶Sr ratios of groundwater and surface water of the Keta Basin primarily reflect the geology and the mineralogical composition of the formations in the catchments and recharge areas. The isotopic compositions of ¹⁸O and ²H of deep groundwater have small variations and plot close to the global meteoric water line. Shallow groundwater and surface water have considerably larger variations in isotopic compositions, which reflect evaporation and preservation of seasonal fluctuations. A significant excess of chloride in shallow groundwater in comparison to the calculated evaporation loss is the result of a combination of evaporation and marine sources. Groundwaters from deep wells and dug wells in near-coastal aquifers are characterized by relatively high chloride contents, and the significance of marine influence is evidenced by well-defined mixing lines for strontium isotopes, and hydrogen and oxygen stable isotopes, with isotopic compositions of seawater as one end member. The results derived from environmental isotopes in this study demonstrate that a multi-isotope approach is a useful tool to identify the origin and sources of saline groundwater. Electronic Publication     

Strontium-isotope studies of “brown water” (organic-rich groundwater) from Denmark

 Groundwater from some Quaternary and upper Tertiary aquifers in western Jutland, Denmark, is heavily influenced by "brown water", i.e., groundwater with a high content of naturally occurring dissolved organic matter. Stable-isotope analyses (¹⁸O/¹⁶O and D/H) indicate that both Quaternary and upper Tertiary aquifers are dominated by meteoric water. However, strontium-isotope analyses make it possible to distinguish between water samples from Quaternary and Miocene aquifers. Relatively low ⁸⁷Sr/⁸⁶Sr ratios, i.e., ∼0.7083, in Sr-rich water samples indicate that the majority of dissolved Sr in groundwater from Miocene as well as Quaternary strata is probably derived from Miocene marine skeletal carbonate matter in the subsurface. This situation is probably the result of Quaternary glacial reworking of upper Tertiary material and/or hydraulic contact between Quaternary and Miocene aquifers. A positive correlation between Sr contents and non-volatile organic carbon indicates that the remarkably high contents of organic matter recorded in these aquifers almost certainly are derived from Miocene sources as well. Received, February 1999 / Revised, July 1999 / Accepted, July 1999     

Controls on stable isotope profiles in the Chalk aquifer of north-east Norfolk, UK, with special reference to dissolved sulphate

Groundwater samples were collected at a site in N Norfolk, UK, comprising a borehole penetrating Upper Chalk and piezometers open within the overlyinf glacial deposits and intervening, weathered Putty Chalk. The samples were analyzed for δ¹⁸O (water), δ³⁴S and δ¹⁸O(SO₄) and δ¹³_C(HCO₃) as well as major ions. Variations in solute concentration and isotopic composition with depth were found to be caused by limited groundwater circulation at the site and incomplete flushing of old groundwater. The isotopic data prove the existence of a mineralized palaeowater at depth, which has undergone SO₄ reduction and is being slowly modified by mixing with recent groundwater circulating at a shallow depth in a more transmissive Chalk horizon. One measured δ¹⁸O (H₂O) value of −8.25‰_vsmow represents the lightest value reported for the Norfolk Chalk aquifer and is evidence for a component of Late Pleistocene recharge trapped at depth.The wide range of observed isotope ratios at the site, e.g.δ³⁴S and δ¹⁸O SO₄ between 7.8 to 27.8‰_cdt and 5.2 to 20.0‰_ovsmow respectively, demonstrates the importance of vertical stratification of solutes and the implications this has for interpreting spatial hydrochemical surveys of groundwater.     

Assessment of groundwater quality and hydrochemical characteristics in Farashband plain,Iran

Groundwater in Farashband plain, Southern Iran, is the main source of water for domestic and agricultural uses. This study was carried out to assess the overall water quality and identify major variables affecting the groundwater quality in Farashband plain. The hydrochemical study was undertaken by randomly collecting 84 groundwater samples from observation wells located in 13 different stations covering the entire plain in order to assess the quality of the groundwater through analysis of major ions. The water samples were analyzed for various physicochemical attributes. Groundwater is slightly alkaline and largely varies in chemical composition; e.g., electrical conductivity (EC) ranges from 2314 to 12,678 μS/cm. All the samples have total dissolved solid values above the desirable limit and belong to a very hard type. The abundance of the major ions is as follows: Na⁺ > Ca²⁺ > Ma²⁺ > K⁺ and Cl^? > SO₄ ^2– > HCO₃ ^?. Interpretation of analytical data shows three major hydrochemical facies (Ca–Cl, Na–Cl, and mixed Ca–Mg–Cl) in the study area. Salinity, total dissolved solids, total hardness, and sodium percentage (Na%) indicate that most of the groundwater samples are not suitable for irrigation as well as for domestic purposes and far from drinking water standard. A comparison of groundwater quality in relation to drinking water standards showed that most of the water samples are not suitable for drinking purposes. Based on the US salinity diagram, most of samples belong to high salinity and low to very high sodium type.     

Hydrogeochemical processes,mixing and isotope tracing in hard rock aquifers and surface waters from the Subarnarekha River Basin, (east Singhbhum District,Jharkhand State,India)

Geochemical observations, including major ion and trace element analysis, and isotopic tracing have been carried out in the Subarnarekha River system (northeastern India) during a surface-water- and groundwater-monitoring program aimed at evaluating impacts of mining. The aquifer is of fracture type. Groundwater flow conditions and pollutant transfer were observed through a network of 69 wells. δ¹⁸O and δ²H results suggest that transfer from rainfall towards groundwater storage through soils and the unsaturated zone is fast, without any major transformation like evaporation. The scatter of ⁸⁷Sr/⁸⁶Sr signatures in surface water and groundwater are explained by three end-members. One is compatible with rainwater inputs. The most mineralised end-member represents anthropogenic inputs (agricultural practices and ore processing). The third end-member, characterised by a high ⁸⁷Sr/⁸⁶Sr signature, is believed to be controlled by natural geochemical processes, although affected by human activities (e.g. drainage of mine waste). Potential flow paths, investigated north of the area, reveal that all groundwater types seem to evolve more in pockets than along a flow path. The limited extent of transfer and the predominance of natural phenomena help to explain the moderate level of groundwater contamination and the characteristics of surface water contamination by mining and the metallurgy industry.     

Chemical and Sr isotopic characterization of North America uranium ores: Nuclear forensic applications

This study reports major, minor, and trace element data and Sr isotope ratios for 11 uranium ore (uraninite, UO_2+x) samples and one processed uranium ore concentrate (UOC) from various U.S. deposits. The uraninite investigated represent ores formed via different modes of mineralization (e.g., high- and low-temperature) and within various geological contexts, which include magmatic pegmatites, metamorphic rocks, sandstone-hosted, and roll front deposits. In situ trace element data obtained by laser ablation-ICP-MS and bulk sample Sr isotopic ratios for uraninite samples investigated here indicate distinct signatures that are highly dependent on the mode of mineralization and host rock geology. Relative to their high-temperature counterparts, low-temperature uranium ores record high U/Th ratios (>1000), low total rare earth element (REE) abundances (<1 wt%), high contents (>300 ppm) of first row transition metals (Sc, Ti, V, Cr, Mn, Co, Ni), and radiogenic ⁸⁷Sr/⁸⁶Sr ratios (>0.7200). Comparison of chondrite normalized REE patterns between uraninite and corresponding processed UOC from the same locality indicates identical patterns at different absolute concentrations. This result ultimately confirms the importance of establishing geochemical signatures of raw, uranium ore materials for attribution purposes in the forensic analysis of intercepted nuclear materials.     

Isotopic and noble gas study of Chalk groundwater in the London Basin, England

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.     

Enhanced pumping test using physicochemical tracers to determine surface-water/groundwater interactions in an alluvial island aquifer,river Rhône,France

Groundwater extracted from the Barthelasse Island aquifer, surrounded by the river Rhône (southeastern France), contributes to the drinking water supplies of 180,000 inhabitants. Owing to its location close to the river and the presence of two backwaters (oxbow lakes), the pumped groundwater is highly vulnerable to river pollution. A pumping test was conducted over 24 h to analyse and quantify the water exchange processes between the river, backwaters and groundwater. During the pumping test, isotopic (δ¹⁸O, δ²H and ²²²Rn), hydrochemical and hydrophysical monitoring of the groundwater was undertaken. Hydraulic heads were measured in pumping wells and at a piezometer located between the wells. Discrete water samples were collected at several observation points in the field, including the backwater and river. The results show mixing between three end-members, as defined by the deuterium excess and silica concentration, led by river Rhône water which had been affected by water–rock interactions over time and mixing with surface evaporated waters. The pumped water resulted from mixing between three end-members, all of which depended on the river Rhône but differed in terms of residence time in the system. Although the groundwater pumping wells are close to each other (<70 m) and have similar depths, the changes in the contributions from end-member waters at each well were different during the pumping test. Comparing isotopic tracers and geochemistry made it possible to quantify the different hydrological compartments that contribute to the groundwater pumped from the boreholes, which is critical in constructing a conceptual flow model.

     

Improvement of groundwater quality due to fresh water ingress in Potharlanka Island, Krishna delta, India

Hydrochemical study had been carried out on the groundwater resources of Potharlanka Island, Krishna delta, India. Groundwater samples were collected and analyzed at 42 sites in December 2001 and October 2006. A comparative study of hydrochemical data indicates: groundwater is mildly alkaline with a pH of 7.0–8.2; electrical conductivity (EC) varies from 605 to 5,770 μS/cm in December 2001, and 652–5,310 μS/cm in October 2006. More than 62% of the groundwater samples in 2006 have TDS value <2,000 mg/l, which is within permissible limit of potable water, but 57% of the samples in 2001, are higher than the maximum permissible limit. Extremely low HCO₃/Cl and variable high Mg/Ca (molar ratios) had been indicated the transformation of the fresh groundwater aquifer systems to saline in 2001. Groundwater of this Island is mainly classified as Na–Cl and mixed types. A high percentage of Na–Cl type of these waters indicates the possibility of seawater ingression/intrusion process during 2001 and comparatively mixed water type indicates the dilution activities of groundwater. Excessive withdrawal of groundwater has caused the increase of saline water intrusion. Improvement of groundwater quality in this Island due to artificial recharge structures made by NGRI under RGNDWM project and affects of the flood due to heavy rainfall of the months of September–October 2005 are discussed in this paper.     

Use of 234U and 238U isotopes to evaluate contamination of near-surface groundwater with uranium-mill effluent: a case study in south-central Colorado, U.S.A.

The ²³⁴U/²³⁸U alpha activity ratio (AR) was determined in 47 samples of variably uraniferous groundwater from the vicinity of a uranium mill near Cañon City, Colorado. The results illustrate that uranium isotopes can be used to determine the distribution of uranium contamination in groundwater and to indicate processes such as mixing and chemical precipitation that affect uranium concentrations. Highly to moderately contaminated groundwater samples collected from the mill site and land immediately downgradient from the mill site contain more than 100?μg/l of dissolved uranium and typically have AR values in the narrow range of 1.0–1.06. Other samples from the shallow alluvial aquifer farther downgradient from the mill contain 10–100?μg/l uranium and plot along a broad trend of increasing AR (1.06–1.46) with decreasing uranium concentration. The results are consistent with mixing of liquid mill waste (AR≈1.0) with alluvial groundwater of small, but variable, uranium concentrations and AR of 1.3–1.5. In the alluvial aquifer, the spatial distribution of wells with AR values less than 1.3 is consistent with previous estimates of the probable distribution of contamination, based on water chemistry and hydrology. Wells more distant from the area of probable contamination have AR values that are consistently greater than 1.3 and are indicative of little or no contamination. The methodology of this study can be extended usefully to similar sites of uranium mining, milling, or processing provided that local geohydrologic settings promote uranium mobility and that introduced uranium contamination is isotopically distinct from that of local groundwater.     

Sources of Sr and implications for weathering of limestone under tallgrass prairie, northeastern Kansas

Grasslands of north-central Kansas are underlain by carbonate aquifers and shale aquitards. Chemical weathering rates in carbonates are poorly known, and, because large areas are underlain by these rocks, solute fluxes are important to estimating global weathering rates. Grasslands exist where the amount of precipitation is extremely variable, both within and between years, so studies in grasslands must account for changes in weathering that accompany changes in precipitation. This study: (1) identifies phases that dominate chemical fluxes at Konza Prairie Biological Station (KPBS) and Long-Term Ecological Research Site, and (2) addresses the impact of variable precipitation on mineral weathering. The study site is a remnant tallgrass prairie in the central USA, representing baseline weathering in a mid-temperate climate grassland.Groundwater chemistry and hydrology in the 1.2 km² watershed used for this study suggest close connections between groundwater and surface water. Water levels fluctuate seasonally. High water levels coincide with periods of precipitation plus low evapotranspiration rather than during precipitation peaks during the growing season. Precipitation is concentrated before recharging aquifers, suggesting an as yet unquantified residence time in the thin soils.Groundwater and surface water are oversaturated with respect to calcite within limitations of available data. Water is more dilute in more permeable aquifers, and water from one aquifer (Morrill) is indistinguishable from surface water. Cations other than Ca co-vary with each other, especially Sr and Mg. Potassium and Si co-vary in all aquifers and surface water, and increases in concentrations of these elements are the best indicators of silicate weathering at this study site. Silicate-weathering indices correlate inversely to aquifer hydraulic conductivity.⁸⁷Sr/⁸⁶Sr in water ranges from 0.70838 to 0.70901, and it decreases with increasing Sr concentration and with increasing silicate-weathering index. Carbonate extracted from aquifer materials, shales, soil, and tufa has Sr ranging from about 240 (soil) to 880 ppm (Paleozoic limestone). ⁸⁷Sr/⁸⁶Sr ranges from 0.70834 ± 0.00006 (limestone) to 0.70904 ± 0.00019 (soil). In all cases, ⁸⁷Sr/⁸⁶Sr of aquifer limestone is lower than ⁸⁷Sr/⁸⁶Sr of groundwater, indicating a phase in addition to aquifer carbonate is contributing solutes to water.Aquifer recharge controls weathering: during periods of reduced recharge, increased residence time increases the total amount of all phases dissolved. Mixing analysis using ⁸⁷Sr/⁸⁶Sr shows that two end members are sufficient to explain sources of dissolved Sr. It is proposed that the less radiogenic end member is a solution derived from dissolving aquifer material; longer residence time increases its contribution. The more radiogenic end member solution probably results from reaction with soil carbonate or eolian dust. This solution dominates solute flux in all but the least permeable aquifer and demonstrates the importance that land-surface and soil-zone reactions have on groundwater chemistry in a carbonate terrain.     

Strontium isotope systematics of mixing groundwater and oil-field brine at Goose Lake in northeastern Montana,USA

Groundwater, surface water, and soil in the Goose Lake oil field in northeastern Montana have been affected by Cl⁻-rich oil-field brines during long-term petroleum production. Ongoing multidisciplinary geochemical and geophysical studies have identified the degree and local extent of interaction between brine and groundwater. Fourteen samples representing groundwater, surface water, and brine were collected for Sr isotope analyses to evaluate the usefulness of ⁸⁷Sr/⁸⁶Sr in detecting small amounts of brine. Differences in Sr concentrations and ⁸⁷Sr/⁸⁶Sr are optimal at this site for the experiment. Strontium concentrations range from 0.13 to 36.9 mg/L, and corresponding ⁸⁷Sr/⁸⁶Sr values range from 0.71097 to 0.70828. The local brine has 168 mg/L Sr and a ⁸⁷Sr/⁸⁶Sr value of 0.70802. Mixing relationships are evident in the data set and illustrate the sensitivity of Sr in detecting small amounts of brine in groundwater. The location of data points on a Sr isotope-concentration plot is readily explained by an evaporation-mixing model. The model is supported by the variation in concentrations of most of the other solutes.     

Hydrogeology of a coal-seam gas exploration area, southeastern British Columbia, Canada: Part 1. Groundwater flow systems

Discovery of high contents of methane gas in coals of the Mist Mountain Formation in the Elk River valley, southeastern British Columbia, Canada, has led to increased exploration activity for coal-seam gas (CSG). CSG production requires groundwater abstraction to depressurize the coal beds and to facilitate methane flow to the production wells. Groundwater abstraction will have hydrodynamic effects on the flow system, and an understanding of the groundwater flow system is needed to evaluate these effects. The purpose of this paper is to describe the groundwater flow system in the area by means of a groundwater flow model and interpretation of hydrochemical and isotopic analyses of groundwater and surface water. Groundwater flow for the Weary Creek exploration area is modeled in two vertical sections. The model domains, based on classic upland–lowland conceptual flow models, are approximately 10,000 m long and 4,000 m deep. Each consists of a fixed water-table boundary and no-flow boundaries along the traces of major faults. Steady-state groundwater flow is calibrated to hydraulic-head, streamflow, and groundwater-recharge data. Simulated steady-state velocity fields define regional and local flow components consistent with the conceptual model. The results are consistent with regional trends in δ²H, δ¹⁸O, tritium, and TDS, which define two distinct groundwater groups (A and B) and a third of intermediate composition. An active, shallow, local flow component (group A) is recharged in beds cropping out along subdued ridges; this component discharges as seeps along lower and mid-slope positions in the southern part of the study area. The waters are tritiated, relatively enriched in δ²H and δ¹⁸O, and have low TDS. A deeper regional flow component (group B), which originates at a higher altitude and which discharges to the Elk River valley bottom, is characterized by non-tritiated groundwater with relatively depleted δ²H and δ¹⁸O, and higher TDS. Groundwater contributes less than 10% of the total direct flow to the Elk River, as indicated by flow measurements and by the absence of group A and group B characteristics in the river water. Thus it is hypothesized that groundwater extraction during CSG production will have little impact on the river. The groundwater flow model developed in this work is used in a companion paper to further test this hypothesis. Electronic Publication     

山西省襄汾县陶寺遗址出土动物牙釉质的锶同位素比值分析

锶同位素分析技术已经成为国际考古学界用于探索人和动物迁移活动的主要方法.陶寺遗址位于山西省襄汾县陶寺镇,距今4500～3900年,是目前我国规模最大的、显现文明化程度最高的史前聚落遗址之一.文章通过热电离质谱分析方法对山西襄汾县陶寺镇陶寺遗址龙山晚期出土动物的14个动物牙釉质的锶同位素比值进行了测定.研究结果表明,5个...     

Assessment of groundwater quality of Lokoja basement area, North-Central Nigeria

The hydrochemical characteristics and quality of groundwater in Lokoja basement area have been evaluated based on different indices for assessing groundwater for drinking and irrigation purposes. Twenty groundwater samples were collected and analyzed for physicochemical parameters, major ions and heavy metals. The results revealed that the groundwater is slightly alkaline, with little variations in chemical composition. For example, electrical conductivity (EC) ranges from 242μS/cm to 1835μS/cm. The abundance of the major ions is in the order of Ca²⁺ >Na⁺>Mg²⁺>K⁺> Fe^2+/3+ = HCO₃ >Cl^? >NO₃ >SO₄ >PO₄. Based on the hydrochemical data, four hydrochemical facies were identified namely, Ca-Mg-HCO₃, Na-K-HCO₃, Na-K-Cl-SO₄ and Ca-Mg-Cl-SO₄ and these facies depict groundwater recharge zone, transition flow zone, deep flow zone and mixed water zone respectively. Groundwater from the area is unsuitable for drinking and domestic purposes as some of the ions and heavy metals of health concerns are well above the stipulated guideline values. Irrigation water quality indicators (salinity, Na % and Mg %), reveal that the groundwater is unsuitable for irrigation purposes. Interpreted statistical analysis reveals that the groundwater chemical compositions are controlled predominantly by weathering of litho units of the basement rocks and by drainage from domestic wastes.     

Groundwater mixing and mineralization processes in a mountain–oasis–desert basin,northwest China: hydrogeochemistry and environmental tracer indicators

Hydrogeochemistry and environmental tracers (²H, ¹⁸O, ⁸⁷Sr/⁸⁶Sr) in precipitation, river and reservoir water, and groundwater have been used to determine groundwater recharge sources, and to identify mixing characteristics and mineralization processes in the Manas River Basin (MRB), which is a typical mountain–oasis–desert ecosystem in arid northwest China. The oasis component is artificial (irrigation). Groundwater with enriched stable isotope content originates from local precipitation and surface-water leakage in the piedmont alluvial–oasis plain. Groundwater with more depleted isotopes in the north oasis plain and desert is recharged by lateral flow from the adjacent mountains, for which recharge is associated with high altitude and/or paleo-water infiltrating during a period of much colder climate. Little evaporation and isotope exchange between groundwater and rock and soil minerals occurred in the mountain, piedmont and oasis plain. Groundwater δ²H and δ¹⁸O values show more homogeneous values along the groundwater flow direction and with well depths, indicating inter-aquifer mixing processes. A regional contrast of groundwater allows the ⁸⁷Sr/⁸⁶Sr ratios and δ¹⁸O values to be useful in a combination with Cl, Na, Mg, Ca and Sr concentrations to distinguish the groundwater mixing characteristics. Two main processes are identified: groundwater lateral-flow mixing and river leakage in the piedmont alluvial–oasis plain, and vertical mixing in the north oasis plain and the desert. The ⁸⁷Sr/⁸⁶Sr ratios and selected ion ratios reveal that carbonate dissolution and mixing with silicate from the southern mountain area are primarily controlling the strontium isotope hydrogeochemistry.