Application of environmental groundwater tracers at the Sulphur Bank Mercury Mine, California, USA

Boron, chloride, sulfate, δD, δ¹⁸O, and ³H concentrations in surface water and groundwater samples from the Sulphur Bank Mercury Mine (SBMM), California, USA were used to examine geochemical processes and provide constraints on evaporation and groundwater flow. SBMM is an abandoned sulfur and mercury mine with an underlying hydrothermal system, adjacent to Clear Lake, California. Results for non-³H tracers (i.e., boron, chloride, sulfate, δD, and δ¹⁸O) identify contributions from six water types at SBMM. Processes including evaporation, mixing, hydrothermal water input and possible isotopic exchange with hydrothermal gases are also discerned. Tritium data indicate that hydrothermal waters and other deep groundwaters are likely pre-bomb (before ~1952) in age while most other waters were recharged after ~1990. A boron-based steady-state reservoir model of the Herman Impoundment pit lake indicates that 71–79% of its input is from meteoric water with the remainder from hydrothermal contributions. Results for groundwater samples from six shallow wells over a 6–month period for δD and δ¹⁸O suggests that water from Herman Impoundment is diluted another 3% to more than 40% by infiltrating meteoric water, as it leaves the site. Results for this investigation show that environmental tracers are an effective tool to understand the SBMM hydrogeologic regime.

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Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.

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Résumé Les concentrations en bore, chlorure, sulfate, δD, δ¹⁸O, et ³H d’échantillons d’eaux de surface et souterraine prélevés dans le banc de soufre de la mine de mercure (SBMM en anglais) en Californie, USA, ont été utilisées pour étudier les processus géochimiques et pour fournir des contraintes à l’évaporation et à l’écoulement des eaux souterraines. La SBMM est une mine de soufre et de mercure abandonnée, adjacente au lac Clear en Californie et sous laquelle se trouve un système hydrothermal.Les résultats des traceurs autres que le tritium (bore, chlorure, sulfate, δD, et δ¹⁸O) ont permis d’identifier des contributions de six types d’eaux à SBMM. Des processus tels que l’évaporation, le mélange, l’entrée d’eau hydrothermale et de possibles échanges isotopiques avec des gaz hydrothermaux ont également été identifiés. Les données de tritium montrent que les eaux hydrothermales et d’autres eaux profondes sont probablement d’age antérieure à la bombe (avant ~1952), alors que la plupart des autres eaux sont issues de la recharge après ~1990. Un modèle de réservoir représentant le lac situé dans la partie Herman Impoundment de l’ancienne mine, en régime permanent et basé sur le bore, montre que 71–79% de l’eau provient des précipitations, le reste provenant de contributions hydrothermales. Les résultats de δD et δ¹⁸O pour des échantillons d’eau souterraine de six puits peu profonds sur une période de 6 mois suggèrent que l’eau de Hermann Impoundment est encore diluée entre 3% jusqu’à plus de 40% lorsqu’elle quitte le site du fait de l’infiltration d’eau météorique. Les résultats de cette étude montrent que les traceurs environnementaux constituent un outil efficace pour comprendre le régime hydrogéologique de la SBMM.

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Resumen Se han utilizado datos de concentraciones de boro, cloruros, sulfatos, δD, δ¹⁸O, y ³H en muestras de aguas superficiales y subterráneas procedentes de la Mina de Mercurio Sulphur Bank (SBMM), California, USA, para estudiar los procesos geoquímicos y caracterizar la evaporación y el flujo del agua subterránea. SBMM es una mina abandonada de azufre y mercurio con un sistema hidrotermal subyacente, cercano al Lago Clear, California.Los resultados de los trazadores que no son ³H (por ejemplo, boro, cloruros, sulfatos δD, y δ¹⁸O) identifican las contribuciones de seis tipos de agua en la SBMM. Se han identificado diversos procesos, como evaporación, mezcla, entrada de agua hidrotermal y la posibilidad de intercambios isotópicos con gases hidrotermales. Los datos de tritio indican que las aguas hidrotermales y otras aguas subterráneas profundas son probablemente pre-bombas (previas a ~1952) en edad mientras que la mayoría de las otras aguas se han recargado después de ~1990. Un modelo estacionario basado en el boro de la fosa del lago Herman Impoundment indica que el 71–79% de su entrada procede de agua meteórica con restos de contribución hidrotermal. Los resultados para las muestras de aguas subterráneas procedentes de seis pozos superficiales en un periodo de 6 meses para δD y δ¹⁸O sugieren que el agua procedente de Herman Impoundment se diluye en otro 3% hasta más del 40% debido a la infiltración de agua meteórica., que sale del sitio. Los resultados de esta investigación muestran que los trazadores ambientales son una herramienta efectiva para entender el régimen hidrogeológico de la SBMM.

     

Hydrochemical and isotopical tracers in the lacustrine aquifer of the Cerro Prieto area, Baja California, México

A series of patterns in the chemical and isotopic composition of the groundwater of the Cerro Prieto area have been recognized. These patterns were used to define four hydrochemical and isotopical zones in the area. One of these areas located at the east side was found to be the source of recharge, while another in the central part is where an older aquifer exist in lacustrine deposits. The low permeability of the area causes the aquifer to act as an aquitard, which at least is partly surrounded by an interface zone where mixing of waters occurs. Tritium and radiocarbon method revealed that the aquitard is an isolate system whose residence time is of 32 ka.     

Chemical characteristics of groundwater in parts of mountainous region, Alvand, Hamadan, Iran

Eighty-seven groundwater samples have been collected from a mountainous region (Alvand, Iran) for hydrochemical investigations to understand the sources of dissolved ions and assess the chemical quality of the groundwater. Most water quality parameters are within World Health Organization acceptable limits set for drinking water. The least mineralized water is found closest to the main recharge zones and the salinity of water increased towards the north of the basin. The most prevalent water type is Ca–HCO₃ followed by water types Ca–NO₃, Ca–Cl, Ca–SO₄ and Mg–HCO₃. The Ca–NO₃ water type is associated with high nitrate pollution. Agricultural and industrial activities were associated with elevated level of NO₃⁻. Mineral dissolution/weathering of evaporites dominates the major element hydrochemistry of the area. Chemical properties of groundwater in Alvand region are controlled both by natural geochemical processes and anthropogenic activities.     

浅谈水化数字观测仪器的使用

以朝阳地震台水化观测实践为基础，对使用水化数字仪器遇到的问题进行了详细讨论。     

Isotopic and geochemical characterization of salinization in the shallow aquifers of a reclaimed subsiding zone: The southern Venice Lagoon coastland

The coastal plain bordering the southern Venice Lagoon is a reclaimed lowland characterized by high subsidence rate, and ground level and water-table depth below sea level. In this agricultural region, where the surface hydrologic network is entirely artificially controlled by irrigation/drainage canals, salinization problems have long been encountered in soils and groundwaters. Here we use isotopic and geochemical tracers to improve our understanding of the origin of salinization and mineralization of the semi-confined aquifer (0–40 m), and the freshwater inputs to this hydrological system. Water samples have been collected at different seasons in the coastal Adriatic Sea, lagoon, rivers and irrigation canals, as well as in the semi-confined aquifer at depths between 12 and 35 m (14 boreholes), and in the first confined aquifer (three boreholes drilled between 40 and 80 m depth). Stable isotopes (δ¹⁸O and δD) and conductivity profiles show that direct saline intrusion from the sea or the lagoon is observed only in a restricted coastal strip, while brackish groundwaters are found over the entire topographic and piezometric depression in the centre of the study area. Fresh groundwaters are found only in the most western zone. The sharp isotopic contrast between the western and central regions suggests disconnected hydrological circulations between these two parts of the shallow aquifer. The border between these two regions also corresponds to the limits of the most strongly subsiding zone.Our results can be interpreted in terms of a four end-member mixing scheme, involving (1) marine water from the lagoon or the open sea, (2) alpine and pre-alpine regional recharge waters carried either by the main rivers Adige, Bacchiglione and Brenta (irrigation waters) or by the regional groundwater circulation, (3) local precipitation, and (4) evaporated waters infiltrated from the surface. Infiltration from the surface is also revealed by the stratification of the electrical conductivity profiles, showing that the brackish groundwaters are overlain by a shallow layer of less saline water all over the central depression. In the first confined aquifer, the groundwaters have isotopic compositions similar to the deep groundwaters of the Venetian confined aquifers (40–400 m depth). The isotopic data and the Br/Cl ratio show that the origin of the salinization of the phreatic aquifer can be ascribed to seawater intrusion alone, with no indication of the involvement of deep brines (identified at 450 m depth) in the process.The chemical composition of the saline and brackish groundwaters is characterized by an excess of sodium and a deficit of calcium compared to conservative mixing between fresh groundwaters and seawater. This suggests that the phreatic aquifer is progressively freshening, as a consequence of the beneficial influence of the extensive irrigation/drainage network, including raised canals acting as a hydraulic barrier along the coast. This freshening tendency may have been lasting since the reclamation in the mid-twentieth century, and has probably been accelerated by the ban on groundwater abstraction since the 1970s.     

Environmental isotopic and hydrochemical study of groundwater in the Ejina Basin,northwest China

The study investigates the groundwater evolution and its residence time in the Ejina Basin, northwest China according to isotope and hydrochemical analyses results. The groundwater chemistry is mainly controlled by the dissolution of halite, Glauber’s salt, gypsum, dolomite and calcite, also influenced by other processes such as evaporation, ion exchange, and deposition. Based on tritium content in atmospheric precipitation and by adopting a model with exponential time distribution function, the mean residence time of the unconfined aquifer groundwater with fairly high tritium activities (21–49 TU) is evaluated. The results show that these groundwaters have low residence time (5–120 years) and are renewable. In contrast, the deep confined groundwaters are tritium-free and radiocarbon values range from 18.3 to 26.7 pmc. According to the most commonly used ¹⁴C correction models, the radiocarbon groundwater ages were calculated which yield ages of approximately 4,087–9,364 years BP. Isotopic signatures indicate formation of deep confined groundwaters in a colder and wetter climate during the late Pleistocene and Holocene. It is suggested that long-term, rational water usage guide should be set up for the Heihe River Basin as a whole to permit a considerable discharge to the Ejina Basin.     

Effect of agricultural land use on the chemistry of groundwater from basaltic aquifers, Jeju Island, South Korea

Geochemical processes were identified as controlling factors of groundwater chemistry, including chemical weathering, salinization from seawater and dry sea-salt deposition, nitrate contamination, and rainfall recharge. These geochemical processes were identified using principal component analysis of major element chemistry of groundwater from basaltic aquifers in Jeju Island, South Korea, a volcanic island with intense agricultural activities. The contribution of the geochemical processes to groundwater chemistry was quantified by a simple mass-balance approach. The geochemical effects due to seawater were considered based on Cl contributions, whereas the effects due to natural chemical weathering were based on alkalinity. Nitrogenous fertilizers, and especially the associated nitrification processes, appear to significantly affect groundwater chemistry. A strong correlation was observed between Na, Mg, Ca, SO₄ and Cl, and nitrate concentrations in groundwater. Correspondingly, the total major cations, Cl, and SO₄ in groundwater were assessed to estimate relative effect of N-fertilizer use on groundwater chemistry. Cl originates more from nitrate sources than from seawater, whereas SO₄ originates mostly from rainwater. N-fertilizer use has shown the greatest effect on groundwater chemistry, particularly when nitrate concentrations exceed 6–7 mg/L NO₃–N. Nitrate contamination significantly affects groundwater quality and 18% of groundwater samples have contamination-dominated chemistry.     

Mineralogy of suspended sediment in three karst springs

Springs in karstic carbonate rocks frequently carry a sediment load as well as a dissolved load. Analysis of morphology and mineralogy of suspended sediment from three contrasting karst springs reveals a suite of clastic particles that reflect both source areas and processes that take place within the aquifer. Nolte Spring in Lancaster County, Pennsylvania, USA, discharges sediment of apparently precipitated calcite, indicating that at some point in the aquifer or vadose zone, water exceeds saturation with respect to calcite. Sediment morphologies and chemical conditions in the aquifer point to two different scenarios for this precipitation. The other two springs, Arch Spring in Blair County, Pennsylvania and Bushkill Spring in Northampton County, Pennsylvania, show no evidence of calcite precipitation. Arch Spring discharges mainly layer silicates, while Bushkill Spring discharges mainly silica.

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Resumen Los manantiales en rocas carbonatadas karstficadas tienen frecuentemente una carga de sedimentos y de sólidos disueltos. Los análisis de la morfología y mineralogía de los sedimentos suspendidos de tres manantiales kársticos contrastados revela un conjunto de partículas clásticas que reflejan ambas áreas fuente y los procesos que tienen lugar dentro del acuífero. Nolte Spring en el Condado de Lancaster, Pennsylvania, USA, descarga sedimento de calcita aparentemente precipitada indicando que en cierto punto del acuífero o en la zona vadosa, el agua supera la saturación con respecto a la calcita. La morfología de los sedimentos y las condiciones químicas en el acuífero apuntan a dos escenarios diferentes para esta precipitación. Los otras dos manantiales, Arch Spring en el Condado de Blair, Pennsylvania y Bushkill Spring en el Condado de Norhtampton, Pennsylvania, no muestran evidencia de precitación de calcita. Arch Spring descarga principalmente filosilicatos mientras que Bushkill Spring descarga fundamentalmente Sílice.

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Résumé Les sources situées en contexte carbonaté karstique charrient fréquemment, outre les matières dissoutes, une charge solide. La morphologie et la minéralogie des sédiments en suspension issus de trois sources karstiques de caractéristiques distinctes ont été analysées : une série de particules clastiques, reflétant à la fois les secteurs des sources et les processus internes de l’aquifère, en ressort. Les sédiments issus de Nolte Spring (Comté de Lancaster, Pennsylvanie, Etats-Unis) sont constitués de calcite apparemment précipitée: ceci indique que l’eau atteint la sursaturation vis-à-vis de la calcite à un certain point de l’aquifère ou de la zone non-saturée. La morphologie des sédiments et les conditions chimiques au sein de l’aquifère mènent à deux scénarii différents pour expliquer cette précipitation. Les deux autres sources, Arch Spring (Comté de Blair, Pennsylvanie) et Bushkill Spring (Comté de Northampton, Pennsylvanie), ne présentent aucun indice de précipitation de calcite. Arch Spring exporte essentiellement des phyllosilicates, alors que la silice est majoritaire à Bushkill Spring.

     

Hydrogeology of the Winnipeg Formation in Manitoba, Canada

The Winnipeg Formation is the basal sedimentary unit throughout much of southern and central Manitoba, Canada, where it forms a regional aquifer over most of its extent. This aquifer is an important source of water in southeastern Manitoba and in Manitoba’s Interlake area, but in most other areas, groundwater within the aquifer is saline. Chemical and isotopic evidence indicate the presence of groundwaters of three different origins: (1) basin brines; (2) modern meteoric recharge; and (3) subglacial recharge that occurred during the late Pleistocene. Hydraulic head and sedimentary facies distributions indicate that the flow system in parts of the area is not in a state of equilibrium and saline waters will encroach on areas currently occupied by freshwater in some areas, while in other areas, freshwater will replace saline water. These features must be considered in groundwater resource management, as groundwater withdrawals will likely hasten these processes.

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Resumen La Formación Winnipeg es la unidad sedimentaria basal en la mayor parte de Manitoba central, Canadá, donde forma un acuífero regional en la mayor parte de su extensión. Este acuífero es una fuente importante de agua en el Sureste de Manitoba y el área de entrelagos de Manitoba, pero en la mayoría de las otras zonas del acuífero, el agua es salina. Las evidencias químicas e isotópicas indican que existen aguas subterráneas de tres orígenes diferentes: (1) salmueras de cuenca; (2) recarga meteórica actual; y (3) recarga subglacial ocurrida durante el Pleistoceno Superior. Los niveles piezométricos y la distribución de las facies sedimentarias indican que el sistema de flujo no se encuentra en estado de equilibrio en parte del área y las aguas salinas irán invadiendo áreas actualmente ocupadas con aguas dulces, mientras que en otras zonas el agua dulce está reemplazando al agua salina. Estos hechos deben ser considerados en la gestión de las aguas subterráneas como recurso, ya que las extracciones de agua acelerarán probablemente estos procesos.

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Résumé La Formation de Winnipeg est l’unité sédimentaire de base sur la plus grande partie du Sud et du centre du Manitoba au Canada, où elle forme un aquifère régional sur pratiquement toute son extension. Cet aquifère représente une ressource en eau importante dans le Sud-Est du Manitoba et dans les zones d’entre les lacs, mais salée dans la plus part des autres zones. Les indications isotopiques et chimiques permettent de distinguer trois différentes origines des eaux souterraines: (1) les saumures de bassin; (2) la recharge météoritique moderne; (3) la recharge sub-glaciaire qui est apparue durant le Pléistocène récent. Les charges hydrauliques et la distribution des faciès sédimentaires indiquent que le système d’écoulement dans certaines zones n’est pas dans un état d’équilibre et que les eaux salées empièteront sur des zones d’eau douce, tandis que dans d’autres zones l’eau douce remplacera les eaux salées. Ces aspects doivent être considérés dans la gestion des ressources en eau souterraine, car le prélèvement des eaux souterraines pourrait accentuer ces processus.

     

Extension spatiale de la salinisation des ressources en eau et modèle conceptuel des sources salées dans la plaine des Triffa (Maroc nord-oriental)

The succession of drought years and excessive abstraction in the plain of Triffa caused deterioration in water quality and endangers future exploitation of groundwater resources. A combination of geophysical surveys, including electrical resistivity and hydrochemical data has been used to identify the geographical extension of salinization and identify its origin. Electrical conductivity measurements are used to show the history of salinization in space and time. In this paper, a first conceptual model of the brackish springs has been established. To cite this article: M. Boughriba et al., C. R. Geoscience 338 (2006).