Isotopes in the Hueco Bolson aquifer, Texas (USA) and Chihuahua (Mexico): local and general implications for recharge sources in alluvial basins

Stable isotope data for the Hueco Bolson aquifer (Texas, USA and Chihuahua, Mexico) distinguish four water types. Two types relate to recharge from the Rio Grande: pre-dam (pre-1916) river water with oxygen-18 and deuterium (δ¹⁸O, δD, ‰) from (?11.9, ?90) to (?10.1, ?82), contrasts with present-day river water (?8.5, ?74) to (?5.3, ?56). Pre-dam water is found beneath the Rio Grande floodplain and Ciudad Juárez, and is mixed with post-dam river water beneath the floodplain. Two other types relate to recharge of local precipitation; evidence of temporal change of precipitation isotopes is present in both types. Recharge from the Franklin and Organ Mountains plots between (?10.9, ?76) and (?8.5, ?60) on the global meteoric water line (GMWL), and is found along the western side of the Hueco Bolson, north of the Rio Grande. Recharge from the Diablo Plateau plots on an evaporation trend originating on the GMWL near (?8.5, ?58). This water is found in the southeastern Hueco Bolson, north of the river; evaporation may be related to slow recharge through fine-grained sediment. Pre-dam water, recognizable by isotope composition, provides information on groundwater residence times in this and other dammed river basins.     

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.

     

Groundwater salinization of the Sfax superficial aquifer,Tunisia

Groundwater salinization has become a crucial environmental problem worldwide and is considered the most widespread form of groundwater contamination. The origin of salinity in the coastal aquifer of the Sfax Basin, Tunisia was investigated by means of chemical analyses of groundwater samples from 65 wells. The groundwater samples present a clear gradation from calcium sulphate salinization to that of sodium chloride. The saturation indices for calcite and gypsum, and binary diagrams of different ions, together with multivariate analysis, indicate the existence of various salinization processes such as: dissolution of gypsum and calcite dispersed through the reservoir rock; ion exchange; intensive agricultural practices that produce effluents that infiltrate to the saturated zone; and sea-water intrusion, enhanced by excessive withdrawal of groundwater.     

Hydrochemical tracers in the middle Rio Grande Basin,USA: 1. Conceptualization of groundwater flow

Chemical and isotopic data for groundwater from throughout the Middle Rio Grande Basin, central New Mexico, USA, were used to identify and map groundwater flow from 12 sources of water to the basin, evaluate radiocarbon ages, and refine the conceptual model of the Santa Fe Group aquifer system.Hydrochemical zones, representing groundwater flow over thousands to tens of thousands of years, can be traced over large distances through the primarily siliciclastic aquifer system. The locations of the hydrochemical zones mostly reflect the modern predevelopment hydraulic-head distribution, but are inconsistent with a trough in predevelopment water levels in the west-central part of the basin, indicating that this trough is a transient rather than a long-term feature of the aquifer system. Radiocarbon ages adjusted for geochemical reactions, mixing, and evapotranspiration/dilution processes in the aquifer system were nearly identical to the unadjusted radiocarbon ages, and ranged from modern to more than 30 ka. Age gradients from piezometer nests ranged from 0.1 to 2 year cm^–1 and indicate a recharge rate of about 3 cm year^–1 for recharge along the eastern mountain front and infiltration from the Rio Grande near Albuquerque. There has been appreciably less recharge along the eastern mountain front north and south of Albuquerque.

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Resumen Se utilizaron datos químicos e isotópicos de agua subterránea a lo largo de la cuenca central del río Grande, Nuevo México, EEUU, para identificar y mapear el flujo de agua subterránea de 12 fuentes de agua a la cuenca para evaluar edades por medio de radio carbon y para refinar el modelo conceptual del sistema acuífero del Grupo Santa Fé. Se puede establecer zonas hidrotérmicas que representan el flujo de agua subterránea a lo largo de miles a miles de decenas de años en grandes distancias a través del sistema acuífero principalmente siliclástico. Las ubicaciones de las zonas hidroquímicas mayormente reflejan la distribucion de la cabeza hidráulica pre-desarollo moderna pero son inconsistentes con una depresión en los niveles de agua pre-desarollo en la zona central oeste de la cuenca. Esto indica que esta depresión es un rasgo transitorio y no un rasgo de largo plazo del sistema acuífero. Las edades de radio carbon ajustadas para los procesos de reaciones geoquímicas, de mezclado y de evapotranspiración-dilución son casi idénticas a los edades de radio carbon no ajustadas oscilan en un rango desde la modernidad a 30 mil años. Las gradientes de edad de nidos de piezometros van de 0.1 a 2 años cm^–1 e indican un sitio de recarga de aproximadamente 3 cm/yr para la recarga a lo largo del frente montañoso oriental e infiltración del río Grande cerca de Albuquerque. Se aprecia una recarga menor a lo largo del frente oriental de montañas al norte y al sur de Albuquerque.

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Résumé Des données sur les éléments chimiques et les isotopes présents dans leau souterraine prélevée à divers endroits dans le bassin moyen du Rio Grande, au centre du Nouveau-Mexique (É-U), ont permis de déterminer lexistence et létendue de douze sources deau régionales dans le bassin, dévaluer les âges radiocarbones et de raffiner le modèle conceptuel du système aquifère du groupe de Santa Fe. Des zones hydro-chimiques qui représentent lécoulement de leau souterraine depuis des dizaines de milliers dannées peuvent être suivies sur de longues distances à travers laquifère principalement siliclastique. La position des zones hydro-chimiques reflète principalement la distribution moderne des charges hydrauliques mais est incohérente avec une dépression dans le niveau deau dans la partie centre-ouest du bassin, ce qui indique que cette dépression est un élément transitoire du système aquifère plutôt quun élément à long terme. Les âges radiocarbones ajustés aux réactions géochimiques et aux processus de mélange et dévapotranspiration/dilution qui ont lieu dans laquifère sont presque identiques aux âges non ajustés et varient de la période moderne jusquà 30 ka. Les gradients dâge établis à partir des nids de piézomètres sétendent de 0.1 à 2 a cm^–1 et suggèrent un taux de recharge denviron 3 cm a^–1 le long du front des montagnes à lest et pour linfiltration provenant du Rio Grande près dAlbuquerque. Il y a eu substantiellement moins de recharge le long du front des montagnes à lest, au nord et au sud dAlbuquerque.

     

Using turbidity dynamics and geochemical variability as a tool for understanding the behavior and vulnerability of a karst aquifer

In a karst system, the characterization of transport properties is based on the comparison of natural tracers observed at the inlet (a swallow hole on the karst plateau) and the outlets of the system (a spring and a well). At Norville, northwest France, electrical conductivity (EC) and turbidity (T) were used as natural tracers for characterizing dissolved elements (surface water geochemistry) and particulate matter transport, respectively. Two methods were used for this study: (1) a comparison of the relations between EC, T and spring discharge (Q) by means of normalized EC–T–Q curves, and (2) a principal component analysis (PCA) including water geochemistry data in addition to EC, T and Q. Three different characteristic flood events have been chosen for the analyses. EC–T–Q curves highlighted the direct transfer, resuspension and deposition of particles during their transport in the karst network. Transport from the swallow hole to both the spring and the well appeared to be dominated by karst-conduit flow. On the other hand, PCA results showed a diffuse source of contamination of groundwaters by nitrate and a point-source contamination of groundwaters by streaming/runoff surface waters with high turbidity and phosphate concentration infiltrated at the swallow hole.     

Deep groundwater flow and geochemical processes in limestone aquifers: evidence from thermal waters in Derbyshire, England, UK

Thermal waters potentially provide information on geochemical processes acting deep within aquifers. New isotopic data on groundwater sulphate, inorganic carbon and strontium in thermal and non-thermal waters of a major limestone aquifer system in Derbyshire, England, UK, are used to constrain sulphate sources and groundwater evolution. Shallow groundwaters gain sulphate from oxidation of sulphide minerals and have relatively ¹³C-depleted dissolved inorganic carbon (DIC). Thermal waters have relatively high Sr/Ca and more ¹³C-enriched DIC as a result of increased water–rock interaction. In other respects, the thermal waters define two distinct groups. Thermal waters rising at Buxton have higher Mg, Mn and ⁸⁷Sr/⁸⁶Sr and lower Ca and SO₄, indicating flow from deep sandstone aquifers via a high permeability pathway in the limestone. By contrast, Matlock-type waters (97% of the thermal flux) have elevated sulphate concentrations derived from interaction with buried evaporites, with no chemical evidence for flow below the limestone. About 5% of the limestone area's groundwater flows to the Matlock group springs via deep regional flow and the remainder flows via local shallow paths to many non-thermal springs. Gypsum dissolution has produced significant tertiary porosity and tertiary permeability in the carbonate aquifer and this is an essential precursor to the development of karstic drainage.

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Resumen Las aguas termales potencialmente proporcionan información sobre procesos geoquímicos que actúan a profundidad en acuíferos. Nuevos datos isotópicos de sulfatos, carbón inorgánico y estroncio en aguas termales y no-termales de un acuífero importante de caliza en Derbyshire, Inglaterra se utilizan para delinear las fuentes de sulfato y la evolución de aguas subterráneas.Las aguas subterráneas no muy profundas adquieren sulfato a través de la oxidación de minerales de sulfuro y poseen carbón inorgánico disuelto (DIC) relativamente deplatado de ¹³C. Las aguas termales muestran un ratio Sr/Ca relativamente alto y poseen (DIC) más enriquecido en¹³C, como resultado de la mayor interacción de roca-agua. En otros aspectos, los aguas termales definen dos grupos distintivos. Las aguas termales que ascienden en Buxton tienen mas Mg, Mn y ⁸⁷Sr/⁸⁶Sr y menos Ca and SO₄, indicando flujo de acuíferos de areniscas profundas por un sendero de alta permeabilidad en la caliza.En contraste el tipo de agua - Matlock (97% del flujo termal) posee altas concentraciones de sulfato, derivado por interacción con evaporitas enterradas, sin evidencia química de flujo debajo de la caliza. Aproximadamente 5% del agua del área de la caliza se fluye al grupo de manantiales de Matlock a través de un flujo regional profundo y el resto fluye por senderos locales poco profundos a muchos de los manantiales no-termales. La disolución de yeso ha producido porosidad terciaria importante así como permeabilidad en el acuífero de carbonato y este es un precursor esencial del desarrollo de drenaje kárstico.

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Résumé Les eaux thermales peuvent apporter des informations sur les processus géochimiques dans les aquifères profonds. De nouvelles données isotopiques sur les sulfates présents dans les eaux souterraines, le carbone inorganique et le strontium dans les eaux thermales et non thermales d'un système aquifère calcaire majeur dans le Derbyshire, Angleterre, Royaume Uni, sont utilisées pour comprendre les sources de sulfates et l'évolution des eaux souterraines. Les eaux souterraines phréatique s'enrichissent en sulfate via l'oxydation des minéraux sulfatés et ont un Carbone Inorganique Dissous (DIC) relativement appauvri en¹³C. Les eaux thermales ont un rapport Sr/Ca relativement plus élevé et un DIC plus enrichi en¹³C, du fait de l'interaction accrue des eaux avec les roches. En d'autres mots, les eaux thermales définissent deux groupes distincts. Les eaux thermales remontant à Buxton ont un Mg, un Mn et un rapport ⁸⁷Sr/⁸⁶Sr plus hauts, mais un Ca et SO₄ plus faible, indiquant un écoulement à travers les zones perméables des aquifers gréseux. Par contraste, les eaux du type de Matlock (97% du flux thermique), possèdent des concentrations élevées en sulfates, provenant de l'interaction des eaux avec les évaporites enfouies, tandis qu'il n'existe aucune évidence chimique d'un écoulement sous les calcaires. Sur environ 5% de la surface des calcaires, les eaux souterraines alimentent des sources non-thermales. La dissolution du Gypse a produit une porosité tertiaire significative et une perméabilité dans les aquifères calcaires, et ceci est un précurseur essentiel au développement du drainage karstique.

     

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.

     

Hydrochemistry of urban groundwater in Seoul, South Korea: effects of land-use and pollutant recharge

The ionic and isotopic compositions (δD, δ¹⁸O, and ³H) of urban groundwaters have been monitored in Seoul to examine the water quality in relation to land-use. High tritium contents (6.1–12.0 TU) and the absence of spatial/seasonal change of O–H isotope data indicate that groundwaters are well mixed within aquifers with recently recharged waters of high contamination susceptibility. Statistical analyses show a spatial variation of major ions in relation to land-use type. The major ion concentrations tend to increase with anthropogenic contamination, due to the local pollutants recharge. The TDS concentration appears to be a useful contamination indicator, as it generally increases by the order of forested green zone (average 151 mg/l), agricultural area, residential area, traffic area, and industrialized area (average 585 mg/l). With the increased anthropogenic contamination, the groundwater chemistry changes from a Ca–HCO₃ type toward a Ca–Cl(+NO₃) type. The source and behavior of major ions are discussed and the hydrochemical backgrounds are proposed as the basis of a groundwater management plan.     

Glacio-lacustrine stratigraphy,aquifer characterization and contaminant transport: a case study in South Lake Tahoe,California, USA

A hydrogeologic model that has been used by many researchers and consultants to describe an area of South Lake Tahoe, California, USA impacted by MTBE contamination describes a relatively homogeneous unconfined aquifer comprised of poorly sorted glacial outwash deposits, within which water-supply wells are able to exert significant alteration in natural groundwater flow. A re-examination of the area’s hydrogeology is presented, which supports a layered heterogeneous aquifer system constructed of alternating fine and coarser-grained glacio-lacustrine depositional units. This re-evaluation was accomplished through a review of lithologic logs across an area of approximately 1 km², combined with observations of significant hydraulic head differences and knowledge of the depositional environments controlled by Pleistocene Lake Tahoe high stands. Many of the fine-grained units observed at depths from 6 to 15 m, although relatively thin, are generally continuous and serve as significant barriers to groundwater flow. The vertical migration of contamination across these fine-grained units to deeper groundwaters was facilitated by cross-screened monitoring wells installed as part of site investigation activities. This conclusion highlights the importance of geologic characterization and proper monitoring well construction at contaminated site investigations.

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

Hydrogeochemistry and isotope analyses used to determine groundwater recharge and flow in low-gradient catchments of the province of Buenos Aires,Argentina

The region known as Pampa Plain, in Argentina, is a vast area characterized by slopes of less than 0.05%. The surface sediment is silty sand, mainly Aeolian, referred to as Pampean Loess, which is a phreatic aquifer unit of utmost importance for the water supply of the region. On account of the slight gradient, hydrogeological analyses using only hydraulic measurements are difficult to perform, often leading to confusing results. Thus, the study presented relies on hydrochemical modeling and isotopic determinations as well. The study area comprises three catchments in the inter-mountainous area corresponding to El Moro, Tamangueyú and Seco creeks, and covering 2,570 km² in the province of Buenos Aires. Measurements of piezometric levels and samples of groundwater, surface water and rainwater were carried out between January and March 2005. Major ion results were analyzed by means of hydrochemical graphs and hydrogeochemical modelling using NETPATH. The resulting data show that it is possible to identify local changes in recharge, flow direction and stream/groundwater relationship by using hydrochemical and isotopic information, which may become a useful and more precise tool for the study of particularly flat landscapes.     

Evaluation of groundwater in a three-aquifer system in Ramtha area, Jordan: recharge mechanisms, hydraulic relationship and geochemical evolution

The groundwater wells in the Ramtha region of Jordan are tapping three aquifers: the upper, intermediate and deep aquifers. The upper aquifer groundwater is tritiated and its stable isotopic composition varies over a wide range. This signifies short residence times and local recharge from an elevation around 600 m above sea level. The groundwater of the upper aquifer has an elevated level of , which is attributed to anthropogenic sources. The intermediate and deep aquifers are untritiated and have long residence times. The stable isotope results signify a recharge elevation for the intermediate aquifer higher than that for the upper aquifer. Stable isotopes in groundwater from both aquifers clustered along the eastern meteoric water line and demonstrate association with the dominant climate of Jordan. The groundwater of the intermediate aquifer is classified as Ca²⁺- , which reflects circulation through a carbonate aquifer. There is evidence that leakage from the upper aquifer has influenced the isotopic and chemical makeup of the groundwater in an intermediate aquifer well. The groundwater of the deep aquifer has the highest temperature in the basin and its isotopic composition is much more depleted than both the upper and intermediate aquifers and plots on the global meteoric water line.

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Résumé  Les puits de la région de Ramtha en Jordanie captent trois aquifères : les aquifères supérieur, intermédiaire et profond. L’eau de l’aquifère supérieur est tritiée et sa composition en isotopes stables varie dans un large intervalle. Ceci signifie des temps de séjour courts et une recharge locale à une altitude d’environ 600 mètres au-dessus du niveau de la mer. L’eau de l’aquifère supérieur a une teneur en élevée, qui est attribuée à des origines anthropiques. Les aquifères intermédiaire et profond ne sont pas tritiés et ont des temps de séjour longs. Les valeurs des isotopes stables indiquent une altitude de recharge pour l’aquifère intermédiaire plus élevée que pour l’aquifère supérieur. Les isotopes stables de l’eau des deux aquifères groupés le long de la droite des eaux météoriques orientale démontrent une relation avec le climat prédominant en Jordanie. L’eau de l’aquifère intermédiaire est de type Ca²⁺-, ce qui traduit une circulation dans un aquifère carbonaté. Il est évident qu’un apport de l’aquifère supérieur a influencé la composition isotopique et chimique da l’eau d’un puits dans l’aquifère intermédiaire. L’eau de l’aquifère profond a la température la plus élevée dans le bassin et sa composition isotopique est bien plus déprimée que dans les deux aquifères supérieur et intermédiaire et se situe sur la droite globale de l’eau météorique.

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Resumen  Las perforaciones en la región de Ramtha de Jordania atraviesan tres acuíferos: los acuíferos superior, intermedio y profundo. El agua del acuífero superior contiene tritio y su composición isotópica varía en un rango amplio. Esto se interpreta como aguas de corto período de residencia recargadas localmente en una zona elevada a unos 600 m sobre el nivel del mar. El agua del acuífero superior posee elevadas concentraciones de , de origen antropogénico. Las aguas de los acuíferos intermedio y profundo no contienen tritio y su período de residencia es largo. Los resultados de las concentraciones de isótopos estables sugieren que la recarga del acuífero intermedio proviene de alturas mayores que las correspondientes al acuífero superior. Los datos de isótopos estables de ambos acuíferos se agrupan a lo largo de la Línea Meteórica Este, y demuestra su asociación con el clima predominante en Jordania. El agua subterránea del acuífero intermedio se clasifica como Ca²⁺-, lo que refleja su circulación a través de un acuífero carbonático. Hay evidencias que las filtraciones desde el acuífero superior han influenciado las características químicas e isotópicas del acuífero intermedio. Las aguas del acuífero profundo son las de mayor temperatura en la cuenca, su composición isotópica es más reducida que aquella de los acuíferos superior e intermedio, y su posición gráfica se aproxima a la Línea Meteórica Mundial.

     

Groundwater recharge and chemical evolution in the southern High Plains of Texas, USA

The unconfined High Plains (Ogallala) aquifer is the largest aquifer in the USA and the primary water supply for the semiarid southern High Plains of Texas and New Mexico. Analyses of water and soils northeast of Amarillo, Texas, together with data from other regional studies, indicate that processes during recharge control the composition of unconfined groundwater in the northern half of the southern High Plains. Solute and isotopic data are consistent with a sequence of episodic precipitation, concentration of solutes in upland soils by evapotranspiration, runoff, and infiltration beneath playas and ditches (modified locally by return flow of wastewater and irrigation tailwater). Plausible reactions during recharge include oxidation of organic matter, dissolution and exsolution of CO₂, dissolution of CaCO₃, silicate weathering, and cation exchange. Si and ¹⁴C data suggest leakage from perched aquifers to the High Plains aquifer. Plausible mass-balance models for the High Plains aquifer include scenarios of flow with leakage but not reactions, flow with reactions but not leakage, and flow with neither reactions nor leakage. Mechanisms of recharge and chemical evolution delineated in this study agree with those noted for other aquifers in the south-central and southwestern USA. Electronic Publication     

Hydrochemical and isotopic behaviour of a Saharan phreatic aquifer suffering severe natural and anthropic constraints (case of Oued-Souf region, Algeria)

An approach combining the use of water dissolved chemical species and isotopic fingerprints has been used to understand the behavior of a phreatic aquifer and to determine the origin of its different water components. This aquifer is located in the large sedimentary basin of the Great Oriental Erg (Algeria) and overlies two deeper aquifers: the Complexe Terminal (CT) and the Continental Intercalaire (CI). Besides the deterioration of its groundwater quality, its water table has risen during the last 20 years. A water budget surplus between 950 and 2500 l s^?1 was estimated. Down-gradient groundwater evolution (south-north) has shown that the mineralisation increases from 1.23 to 5.20 g l^?1 due to evaporite minerals dissolution. Chemical and isotopic data demonstrated that in addition to rainfall there is a contribution from the CT and CI aquifers. The latter are tritium-free and less mineralized than the phreatic aquifer. Their radiocarbon contents are very low (<10 pmC, percent modern Carbon) (Pleistocene recharge) whereas quite the contrary is observed for the superficial aquifer which exhibits fairly high and variable C-14 activities (50–100 pmC), evidence of recent recharge. On the basis of tritium contents, two groundwater groups were identified for the phreatic aquifer.     

Dryland salinity processes within the discharge zone of a local groundwater system,southeastern Australia

Detailed study of a localised saline discharge zone in southeastern Australia shows that the salinisation is mostly due to the shallow water table (<1–2 m from the surface). Direct evaporation, particularly in summer, leads to extremely high soil–water salinities at the surface, even though the underlying groundwater is moderately fresh. Groundwater discharge is localised at a break of slope, where the water table intersects the surface, and where the transition from permeable sands to clay-rich sediments inhibits lateral groundwater flow. Higher salt concentrations build up in the clays because of the long residence times during which soil-waters are exposed to evapotranspiration and the reduced potential for salts to be flushed from the sediments. As a result the saline discharge area does not correspond to the part of the site with the largest salt store. Results of the study demonstrate that for dryland salinisation to occur, the groundwater beneath the discharge zone need not be saline, and the presence of a large salt store does not necessarily lead to problems of dryland salinisation if, as in the clay-rich sediments at the site, the salt lies below the pasture root zone. Furthermore, mobilisation of salt stores within low permeability sediments by rising groundwater may be minor.

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Résumé L’étude détaillée d’une zone localisée d’émergence salée au sud-est de l’Australie montre que la salinisation est surtout due à la nappe phréatique (<1–2 m sous la surface). L’évaporation directe, particulièrement durant l’été, conduit à des salinités de l’eau du sol extrêmement élevées à la surface, même si l’eau souterraine sous-jacente est modérément douce. L’émergence de l’eau souterraine est localisée à la rupture de pente, là où la nappe phréatique rencontre la surface du sol et où la transition entre sables perméables et sédiments riches en argiles inhibe les écoulements d’eau souterraine latéraux. Les plus fortes concentrations en sel s’accumulent dans les argiles du fait de temps de résidence élevés, durant lesquels les eaux du sol sont exposées à l’évapotranspiration et à un lessivage réduit des sédiments. Il en résulte que l’aire d’émergence des eaux salées ne correspond pas à la partie du site rencontrant la réserve de sel la plus importante. Les résultats de l’étude démontrent que pour que la salinisation d’une zone aride devienne effective, l’eau souterraine sous la zone ne doit pas être forcément salée, et la présence d’une zone étendue de réserve de sel ne conduit pas forcément à des problèmes de salinisation de zones arides si, comme dans les sédiments argileux du site, le sel ne repose pas sous la zone de pature. De plus, la mobilisation des réserves de sel dans les sédiments peu perméables par la montée du niveau de l’eau souterraine devrait être mineure.

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Resumen El estudio detallado de una zona local de descarga salina en el sudeste de Australia, muestra que la salinización es principalmente debido a un nivel freático poco profundo (<1–2 m de la superficie). La evaporación Directa, particularmente en verano, conlleva a salinidades de suelo-agua sumamente altas en la superficie, aunque el agua subterránea subyacente es moderadamente dulce. La descarga de Agua subterránea se localiza en una interrupción de la ladera, dónde el nivel freático intercepta la superficie, y donde la transición de las arenas permeables a los sedimentos ricos en arcilla inhibe el flujo lateral del agua subterránea. Las concentraciones de sal más altas se forman en las arcillas debido a los tiempos de residencia largos durante los cuales se exponen el conjunto suelo-agua a la evapotranspiración y también por el potencial reducido para las sales de ser expulsadas de los sedimentos. Como resultado el área de la descarga salina no corresponde a la parte del sitio con el contenido de sal más grande. Los resultados del estudio demuestran que para que ocurra la salinización en terrenos secos, el agua subterránea bajo la de zona de descarga no necesita ser salina, y que la presencia de un almacenamiento de sal grande, no necesariamente lleva a los problemas de salinización en terrenos secos si, como en los sedimentos ricos en arcilla del sitio, la sal yace debajo de la zona de raíz de la pastura. Además, la movilidad de depósitos de sal dentro de los sedimentos de permeabilidad baja pueden ser menores, por causa del agua subterránea ascendente.

     

Use of chloride-mass balance and environmental isotopes for evaluation of groundwater recharge in the alluvial aquifer, Wadi Tharad, western Saudi Arabia

Groundwater recharge estimation has become a priority issue for humid and arid regions, especially in regions like Saudi Arabia, where the precipitation varies over space and time as a result of topography and seasonality. Wadi Tharad is a typical arid area in western Saudi Arabia. Within its drainage area of 400 km², the groundwater system shows a graded hydrochemical zonation from the hydrocarbonate in the upper reach to the chloride zone in the lower reach. The saturation index (SI) varies depending on the concentrations of carbonate minerals; the mean for calcite and dolomite is about in equilibrium (e.g., zero value). As halite and gypsum indices are negative, it is undersaturated. Isotopic compositions of H and O in the groundwater show that the groundwater recharge resources are mainly from meteoric water. The chloride-mass balance method was refined to estimate the amount of recharge, which is probably 11% of the effective annual rainfall. These results can be used to improve the accuracy of future groundwater management and development schemes.     

Groundwater recharge and salinization in the arid coastal plain aquifer of the Wadi Watir delta,Sinai, Egypt

The Quaternary coastal plain aquifer down gradient of the Wadi Watir catchment is the main source of potable groundwater in the arid region of south Sinai, Egypt. The scarcity of rainfall over the last decade, combined with high groundwater pumping rates, have resulted in water-quality degradation in the main well field and in wells along the coast. Understanding the sources of groundwater salinization and amount of average annual recharge is critical for developing sustainable groundwater management strategies for the long-term prevention of groundwater quality deterioration. A combination of geochemistry, conservative ions (Cl and Br), and isotopic tracers (^87/86Sr, δ⁸¹Br, δ³⁷Cl), in conjunction with groundwater modeling, is an effective method to assess and manage groundwater resources in the Wadi Watir delta aquifers. High groundwater salinity, including high Cl and Br concentrations, is recorded inland in the deep drilled wells located in the main well field and in wells along the coast. The range of Cl/Br ratios for shallow and deep groundwaters in the delta (∼50–97) fall between the end member values of the recharge water that comes from the up gradient watershed, and evaporated seawater of marine origin, which is significantly different than the ratio in modern seawater (228). The ^87/86Sr and δ⁸¹Br isotopic values were higher in the recharge water (0.70,723 < ^87/86Sr < 0.70,894, +0.94 < δ⁸¹Br < +1.28‰), and lower in the deep groundwater (0.70,698 < ^87/86Sr < 0.70,705, +0.22‰ < δ⁸¹Br < +0.41‰). The δ³⁷Cl isotopic values were lower in the recharge water (−0.48 < δ³⁷Cl < −0.06‰) and higher in the deep groundwater (−0.01 < δ³⁷Cl < +0.22‰). The isotopic values of strontium, chloride, and bromide in groundwater from the Wadi Watir delta aquifers indicate that the main groundwater recharge source comes from the up gradient catchment along the main stream channel entering the delta. The solute-weighted mass balance mixing models show that groundwater in the main well field contains 4–10% deep saline groundwater, and groundwater in some wells along the coast contain 2–6% seawater and 18–29% deep saline groundwater.A three-dimensional, variable-density, flow-and-transport SEAWAT model was developed using groundwater isotopes (⁸⁷Sr/⁸⁶Sr, δ³⁷Cl and δ⁸¹Br) and calibrated using historical records of groundwater level and salinity. δ¹⁸O was used to normalize the evaporative effect on shallow groundwater salinity for model calibration. The model shows how groundwater salinity and hydrologic data can be used in SEAWAT to understand recharge mechanisms, estimate groundwater recharge rates, and simulate the upwelling of deep saline groundwater and seawater intrusion. The model indicates that most of the groundwater recharge occurs near the outlet of the main channel. Average annual recharge to delta alluvial aquifers for 1982 to 2009 is estimated to be 2.16 × 10⁶ m³/yr. The main factors that control groundwater salinity are overpumping and recharge availability.     

Migration of recharge waters downgradient from the Santa Catalina Mountains into the Tucson basin aquifer, Arizona, USA

 Aquifers in the arid alluvial basins of the southwestern U.S. are recharged predominantly by infiltration from streams and playas within the basins and by water entering along the margins of the basins. The Tucson basin of southeastern Arizona is such a basin. The Santa Catalina Mountains form the northern boundary of this basin and receive more than twice as much precipitation (ca. 700 mm/year) as does the basin itself (ca. 300 mm/year). In this study environmental isotopes were employed to investigate the migration of precipitation basinward through shallow joints and fractures. Water samples were obtained from springs and runoff in the Santa Catalina Mountains and from wells in the foothills of the Santa Catalina Mountains. Stable isotopes (δD and δ¹⁸O) and thermonuclear-bomb-produced tritium enabled qualitative characterization of flow paths and flow velocities. Stable-isotope measurements show no direct altitude effect. Tritium values indicate that although a few springs and wells discharge pre-bomb water, most springs discharge waters from the 1960s or later. Received, February 1997 · Revised, September 1997 · Accepted, September 1997     

Environmental tracers as indicators of karst conduits in groundwater in South Dakota,USA

Environmental tracers sampled from the carbonate Madison aquifer on the eastern flank of the Black Hills, South Dakota, USA indicated the approximate locations of four major karst conduits. Contamination issues are a major concern because these conduits are characterized by direct connections to sinking streams, high groundwater velocities, and proximity to public water supplies. Objectives of the study were to estimate approximate conduit locations and assess possible anthropogenic influences associated with conduits. Anomalies of young groundwater based on chlorofluorocarbons (CFCs), tritium, and electrical conductivity (EC) indicated fast moving, focused flow and thus the likely presence of conduits. δ¹⁸O was useful for determining sources of recharge for each conduit, and nitrate was a useful tracer for assessing flow paths for anthropogenic influences. Two of the four conduits terminate at or near a large spring complex. CFC apparent ages ranged from 15 years near conduits to >50 years in other areas. Nitrate-N concentrations >0.4 mg/L in groundwater were associated with each of the four conduits compared with concentrations ranging from <0.1 to 0.4 mg/L in other areas. These higher nitrate-N concentrations probably do not result from sinking streams but rather from other areas of infiltration.     

Recharge areas and geochemical evolution of groundwater in an alluvial aquifer system in the Sultanate of Oman

A regional hydrogeochemical model was developed to evaluate the geochemical evolution of different groundwaters in an alluvial aquifer system in the Interior of Oman. In combination with environmental isotopes the model is able to extract qualitative and quantitative information about recharge, groundwater flow paths and hydraulic connections between different aquifers. The main source of water to the alluvial aquifer along the flow paths of Wadi Abyadh and Wadi Muaydin in the piedmont is groundwater from the high-altitude areas of the Jabal Akhdar and local infiltration along the wadi channels. In contrast, the piedmont alluvial aquifer along Wadi Halfayn is primarily replenished by lateral recharge from the ophiolite foothills to the east besides smaller contributions from the Jabal Akhdar and local infiltration. Further down gradient in the Southern Alluvial Plain aquifer a significant source of recharge is direct infiltration of rain and surface runoff, originating from a moisture source that approaches Oman from the south. The model shows that the main geochemical evolution of the alluvial groundwaters occurs along the flow path from the piedmont to the Southern Alluvial Plain, where dedolomitization is responsible for the observed changes in the chemical and carbon isotope composition in these waters.

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Resumen Un modelo hidrogeoquímico regional fue desarrollado, para evaluar la evolución geoquímica de diferentes aguas subterráneas en un sistema acuífero aluvial ubicado en el interior de Omán. El modelo, en combinación con isótopos ambientales, es capaz de obtener información cualitativa y cuantitativa sobre recarga, direcciones de flujo de agua subterránea y sobre las conexiones hidráulicas entre diferentes acuíferos. La fuente principal de agua para el acuífero aluvial en el piedemonte son las aguas subterráneas, a lo largo de las direcciones de flujo del Wadi Abyadh y del Wadi Muaydin, desde las áreas de gran altura de Jabal Akhdar y como infiltración local a lo largo de los canales del wadi. En contraste, el acuífero aluvial del piedemonte a lo largo del Wadi Halfayn, esta alimentado principalmente por recarga lateral desde las partes bajas de las montañas de ofiolitas hacia el Este, además por pequeñas contribuciones desde el Jabal Akhdar e infiltración local. Siguiendo gradiente abajo en el acuífero de la Llanura Aluvial del Sur, allí tanto la infiltración directa de lluvia, como la escorrentía superficial constituyen fuentes significativas de recarga, las cuales se originan en una fuente de humedad que llega a Omán proveniente del Sur. El modelo muestra, que la evolución geoquímica principal de las aguas subterráneas en el aluvión, sucede a lo largo de la dirección de flujo, que va desde el piedemonte hacia la Llanura Aluvial Sur, en donde el proceso de des-dolomitización es el responsable de los cambios observados en la composición química y también del contenido de isótopos de carbono en estas aguas.

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Résumé On a développé un modèle régional hydrogéochimique pour évaluer lévolution géochimique des différentes eaux souterraines dans le système aquifère de lintérieur dOman. Avec la contribution des isotopes denvironnement, le modèle est capable de fournir des informations qualitatives et quantitatives sur la recharge, les directions découlement et sur les connections hydrauliques entre les différents aquifères du système. La source principale pour laquifère situé au long de la direction découlement des oueds de Abdyah et de Muaydin dans le piémont est leau souterraine provenant des zones de haute altitude de Jabal Akhbar ainsi que linfiltration locale au long des canaux de loued. Par contre, à part dune petite contribution provenant des infiltrations locaux et de Jabal Akhbar, l aquifère alluvial de Wadi Halfayan est en principal alimenté par la recharge latérale provenant des ophiolites situées dans la partie est. Les plus importantes sources de recharge dans laval de laquifère de la Plaine Alluviale sont linfiltration directe et le ruissellement provenant dune source dhumidité qui sapproche dOman par le sud. Le modèle montre que la principale évolution géochimique se produise au long de la direction découlement qui part de piémont de la Plaine Alluviale du Sud, où le procès de dédolomisation est responsable pour les changements observés dans la composition géochimique et en carbone des eaux.

     

Deep reaching fluid flow in the North East German Basin: origin and processes of groundwater salinisation

Major element chemistry, rare-earth element distribution, and H and O isotopes are conjointly used to study the sources of salinisation and interaquifer flow of saline groundwater in the North East German Basin. Chemical analyses from hydrocarbon exploration campaigns showed evidence of the existence of two different groups of brines: halite and halite Ca–Cl brines. Residual brines and leachates are identified by Br^?/Cl^? ratios. Most of the brines are dissolution brines of Permian evaporites. New analyses show that the pattern of rare-earth elements and yttrium (REY) are closely linked to H and O isotope distribution. Thermal brines from deep wells and artesian wells indicate isotopically evaporated brines, which chemically interacted with their aquifer environment. Isotopes and rare-earth element patterns prove that cross flow exists, especially in the post-Rupelian aquifer. However, even at depths exceeding 2,000 m, interaquifer flow takes place. The rare-earth element pattern and H and O isotopes identify locally ascending brines. A large-scale lateral groundwater flow has to be assumed because all pre-Rupelian aquifer systems to a depth of at least 500 m are isotopically characterised by Recent or Pleistocene recharge conditions.