Hydrochemical investigation of water from the Pleistocene wells and springs, Jericho area, Palestine

Rising salinity levels is one of the significant signs of water-quality degradation in groundwater. The alluvial Pleistocene wells in the Jericho area, Palestine show high salinity and a high susceptibility to contamination. Future exploitation and management of the water resources under these conditions will require an in-depth understanding of the sources and mechanisms of contamination. The Jericho area is located in the basin of the Jordan Valley. The basin is underlain by alluvial deposits of soil, sand and gravel of Quaternary units Q1 and Q2, and marl clay and evaporites of the upper part of unit Q2. This paper deals with the source of salinity in the wells penetrating these units, using hydrochemical tracers. The study reveals three main zones of different salinity by using different diagnostic hydrochemical fingerprinting as tracers for elucidating the sources of salinity. It was concluded that the most probable sources of salinity are (1) the geological formations of the region, which form inter-fingering layers of both the Samara and Lisan formations of Pleistocene age, where the eastern Arab Project aquifers show the highest amount of sulphate. The location and geological formation of these wells within the Lisan suggested that the source of high sulphate content is the dissociation of gypsum. (2) The NaCl water within the same area may also be upwelling from a deep brine aquifer or from a fresh-water aquifer which contains salt-bearing rocks with particles becoming finer from west to east. This noticeable high TDS to the east should be affected by the rate of pumping from the upper shallow aquifer, especially in the wells of the Arab Project which are in continuous pumping during the year. (3) The third possible source of salinity is from anthropogenic influences. This can be easily shown by the increment of nitrate, bromide and sulphate, depending on whether the location of the well is coincident with urban or agricultural areas. This reflects the addition of agricultural chemical effluents or sewer pollution from adjacent septic tanks which are mainly constructed in top gravel in the Samara layer. Further studies are required, using different geochemical and isotopic techniques, to confirm these suggested salinity sources.The revised version was published online in March 2005 with corrections to the order of the authors.     

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.     

Investigation of hydrochemical characteristics of groundwater from the Cretaceous-Eocene limestone aquifer in southern Ghana and southern Togo using hierarchical cluster analysis

The most relevant controls on the water quality within the Cretaceous-Eocene limestone aquifer of the Keta Basin, Ghana, and the coastal sedimentary basin of Togo were assessed using Q-mode hierarchical cluster analysis (HCA) and mass-balance modelling. The pattern recognition technique of HCA was employed for partitioning hydrochemical data from a total of 65 surface and borehole samples from the study area into water groups. A spatial plot of the water groups consisting of samples from the limestone aquifer shows that the vast majority of samples belonging to the same group are located in close proximity to one another, suggesting the same processes and/or flow paths in the limestone aquifer system. Geochemical reaction models of selected water groups were constructed using PHREEQC-2. The hydrochemical compositions of the water groups and the mass-balance calculations indicate that the dominant processes and reactions responsible for the hydrochemical evolution in the system are: (1) carbonate equilibria, (2) silicate weathering reactions, (3) limited mixing with saline water, and (4) ion exchange. The combined use of HCA and mass-balance modelling has shown to be a useful approach in interpreting groundwater hydrochemistry in an area where large uncertainties exist in the understanding of the groundwater flow system.     

Springs in a headwater basin in the Deccan Trap country of the Western Ghats, India

Available literature reveals that little work has been done on the origin of springs in a basaltic terrain. Close examination of such springs in about 2,000 km² of the upper Koyna River basin in the Deccan Trap country of the Western Ghats (hills), India, reveals that their origins are dependent on the lithologic character of different basaltic flow units and the existing physiography. Although rainfall, its seasonality and areas of recharge, play vital roles in the recharge of these springs, their yields are also controlled by lithological variations and hydraulic characteristics of their source-aquifers. Chemical concentrations of these springs are heavily dependent on the lithological compositions of the source-aquifers and the residence time of groundwater in these aquifers. Currently, basaltic springs are classified with those issuing from other terrains. However, because the emergence of groundwater in the form of springs is largely controlled by the lithology and the resulting water-bearing properties of the formations, a new classification scheme is proposed that classifies the springs on the basis of their source-aquifers. While tapping springs for drinking/irrigation purposes, it must be remembered that they also sustain thousands of other life forms vital to a balanced ecosystem. Changes in the uses of these springs may also affect other human communities downstream. Therefore, before developing spring flow, a trade-off must be made considering local needs and downstream users. Emphasizing only local human needs may lead to severe intercommunity conflict and negative environmental consequences. Electronic Publication     

Interstitial water and hydrochemistry of a mangrove forest and adjoining water system, south west coast of India

 Eh, pH, salinity, total alkalinity, dissolved O₂, NO₂ ^–, PO₄ ^–3, SiO₂ and NH₄ ⁺ of waters from a mangrove forest, an estuary and a creek connecting the mangrove forest and the estuary have been measured. Further, the chemistry of interstitial waters of surficial and core sediments from the mangrove forest have been analyzed for the above parameters, except dissolved oxygen. To understand the flux of nutrients from the mangrove forest to the adjoining estuary, creek waters were monitored during tidal phases. PO₄ ^–3, SiO₂ and NH₄ ⁺ were found to be at elevated levels in mangrove waters whereas NO₂ ^– shows no variation compared to the estuary. Dissolved O₂ is low in mangrove waters. PO₄ ^–3, NH₄ ⁺ and SiO₂ are several times higher in interstitial waters than in overlying waters. Several fold enrichment of PO₄ ^–3, NH₄ ⁺ and, to some extent, SiO₂ were measured in creek waters during ebbing relative to flooding, indicating that mangroves act as a perennial source for the above nutrients. Received: 26 May 1998 · Accepted: 21 July 1998     

Geochemical survey of Slovenian bottled waters

The geochemistry of the major components and trace elements in Slovenian bottled water available on the market in 2004 and 2008 was studied. The waters were predominantly from the Radenska and Rogaška Slatina mineral water source region. In this paper, a comparison of two data sets from two time periods was performed based on the Kolmogorov–Smirnov independent two-sample test. The bottled waters in the data sets were in agreement with drinking water and mineral water standards. Discrepancies were only present for B and Ni in highly mineralised waters. Analyses of the labels on the bottle packaging showed that the analytical results were in general agreement with the values reported on the labels. At the same time, the values reported on the labels by the producers showed that the chemical compositions of products available on the market for longer time periods vary. Slovenian bottled waters are predominantly controlled by a CaCO₃–CO₂–H₂O system where Na, Cl⁻ and SO₄²⁻ are present as the major components, in different combinations.     

Identifying trends in groundwater quality using residence time indicators: an example from the Permian aquifer of Dumfries, Scotland

The Permian sandstone and breccia aquifer of Dumfries has an important role in supplying water to the principal town in southwest Scotland. The area comprises mainly pastoral farmland with some industry and fish farming. Ongoing development of the aquifer has revealed the existence of complex groundwater flow through fractures and increasing nitrate concentrations. To further investigate these issues, the age and quality of groundwater throughout the aquifer has now been assessed using standard hydrogeochemical techniques together with CFCs and SF₆ as residence time indicators. The aquifer consists of sandstone- and breccia-dominated units: the Locharbriggs Sandstone in the east and the Doweel Breccia in the west. Groundwater throughout the aquifer is of Ca–Mg–HCO₃ type and moderately mineralised; pH is near neutral. The observed groundwater chemistry is the product of maritime rainfall modified by the dissolution of carbonate material in the breccia, sandstone and surficial deposits. CFC and SF₆ concentrations are interpreted on the basis of mixing between older (>50 years) and recent (1990s) components. Although there is generally a higher proportion of older water within the Locharbriggs Sandstone compared to the Doweel Breccia, stable isotope evidence suggests that the older water component in the interbedded sandstones of the breccia is of much greater antiquity, possibly containing an element of palaeowater. Concentrations of nitrate across the aquifer can be directly related to the amount of recent recharge. Modern groundwater contains approximately 9 mg l^–1 NO₃-N and pre-1950s groundwater has approximately 2 mg l^–1 NO₃-N. Nitrate concentrations measured at individual boreholes are explained by the relative proportions of modern and pre-1950s groundwater. If current practices continue, the concentrations of nitrate measured across the Dumfries Basin will rise as the proportion of pre-1950s groundwater diminishes.

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Resumen El acuífero de areniscas y brechas Pérmicas de Dumfries desempeña un papel importante en el abastecimiento a la ciudad principal del Sudoeste de Escocia. El área comprende sobretodo tierras de pastoreo y granjas, junto con algunas industrias y piscifactorías. El desarrollo iniciado en el acuífero ha revelado la existencia de un complicado flujo subterráneo a través de las fracturas y de un aumento progresivo en la concentración de nitrato. Con el fin de profundizar en el conocimiento de estos temas, se ha determinado la edad y calidad de las aguas subterráneas en todo el acuífero por medio de técnicas hidrogeoquímicas estándar y de indicadores del tiempo de residencia como los clorofluorcarbonados (CFCs) y el fluoruro de azufre (SF₆). El acuífero está formado por las areniscas de Locharbriggs, al Este, y las brechas de Doweel, hacia el Oeste. Las aguas subterráneas son de tipo bicarbonatadas cálcico-magnésicas y presentan una mineralización moderada, mientras que el pH es prácticamente neutro. La química de las aguas subterráneas es el resultado del aerosol marino modificado por la disolución de materiales carbonatados en las brechas, areniscas y depósitos superficiales. Las concentraciones de CFCs y SF₆ se interpretan a partir de una mezcla de aguas entre una componente antigua (más de 50 años) y una reciente (de la década de 1990). Aunque en general se da una mayor proporción de aguas antiguas en las areniscas de Locharbriggs que en las Brechas de Doweel, los isótopos estables sugieren que la componente de aguas antiguas en las intercalaciones de areniscas que aparecen en la formación de brechas es mucho más antigua, y que, posiblemente, se trate de paleoaguas. Las concentraciones de nitrato en el acuífero pueden ser relacionadas directamente con la aportación de recarga reciente. Las aguas subterráneas modernas contienen aproximadamente 9 mg l^–1 de nitrato, mientras que las aguas subterráneas anteriores a 1950 tienen unos 2 mg l^–1. Se puede explicar las concentraciones de nitrato en pozos individuales por las proporciones relativas de aguas subterráneas modernas y anteriores a 1950. Si las prácticas actuales continúan, se producirá un aumento de las concentraciones de nitrato en la cuenca de Dumfries debido a la disminución de la proporción de aguas antiguas.

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Résumé L'aquifère des grès et brèches du Permien de Dumfries joue un rôle important dans l'alimentation en eau de la principale ville du sud-ouest de l'Écosse. La région est principalement soumise à de l'élevage pastoral avec quelques industries et des piscicultures. La progression de l'exploitation de cet aquifère a révélé l'existence d'un écoulement souterrain complexe en fractures et des concentrations en nitrate croissantes. Dans le but d'étudier ces deux points plus en détail, l'âge et la qualité de l'eau souterraine dans tout l'aquifère ont été évalués en utilisant des techniques hydrogéochimiques conventionnelles avec les CFC et SF₆ comme marqueurs du temps de séjour. L'aquifère est constitué par des unités dominées par des brèches et des grès: les grès de Locharbriggs à l'est et les brèches de Doweel à l'ouest. L'eau souterraine dans tout l'aquifère a un faciès bicarbonaté calcique et magnésien et est moyennement minéralisée; le pH est proche de la neutralité. Le chimisme observé de l'eau souterraine résulte des apports marins par la pluie modifiés par la dissolution du matériau carbonaté des brèches, des grès et des formations superficielles. Les concentrations en CFC et SF₆ sont interprétées sur la base d'un mélange entre des composantes ancienne (>50 ans) et récente (années 1990). Bien qu'il y ait en général une plus forte proportion d'eau ancienne dans les grès de Locharbriggs que dans la brèche de Doweel, les isotopes stables suggèrent que la composante d'eau ancienne dans les grès interstratifiés des brèches est beaucoup plus ancienne, contenant probablement un élément d'eau fossile. Les concentrations en nitrate dans l'aquifère peuvent être directement reliées au taux de recharge récente. L'eau souterraine moderne contient approximativement 9 mg l^–1 en NO₃-N et l'eau souterraine d'avant 1950 environ 2 mg l^–1 en NO₃-N. Les concentrations en nitrate mesurées dans des forages individuels sont expliquées par des proportions relatives d'eaux souterraines moderne et antérieure à 1950. Si les pratiques actuelles continuent, les concentrations en nitrate mesurées dans le bassin de Dumfries augmenteront alors que la part de l'eau souterraine d'avant 1950 diminuera.

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Hydrochemical tracers in the middle Rio Grande Basin,USA: 2. Calibration of a groundwater-flow model

The calibration of a groundwater model with the aid of hydrochemical data has demonstrated that low recharge rates in the Middle Rio Grande Basin may be responsible for a groundwater trough in the center of the basin and for a substantial amount of Rio Grande water in the regional flow system. Earlier models of the basin had difficulty reproducing these features without any hydrochemical data to constrain the rates and distribution of recharge. The objective of this study was to use the large quantity of available hydrochemical data to help calibrate the model parameters, including the recharge rates. The model was constructed using the US Geological Surveys software MODFLOW, MODPATH, and UCODE, and calibrated using ¹⁴C activities and the positions of certain flow zones defined by the hydrochemical data. Parameter estimation was performed using a combination of nonlinear regression techniques and a manual search for the minimum difference between field and simulated observations. The calibrated recharge values were substantially smaller than those used in previous models. Results from a 30,000-year transient simulation suggest that recharge was at a maximum about 20,000 years ago and at a minimum about 10,000 years ago.

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Resumen La calibración de un modelo de aguas subterráneas con el apoyo de datos hidroquímicos ha demostrado que la recarga relativamente baja en la cuenca media del Río Grande es probablemente responsable de una depresión de aguas subterráneas en el centro de la cuenca y de la presencia de una cantidad considerable de agua del Río Grande en el acuífero del Grupo Santa Fe. Los modelos propuestos con anterioridad para la cuenca tenían dificultades para reproducir estas características ya que no tenían datos hidroquímicos que permitieran delimitar los ritmos y distribución de recarga. El objetivo del presente estudio consistió en utilizar una gran cantidad de datos hidroquímicos disponibles para ayudar a calibrar los parámetros del modelo, incluyendo los ritmos de recarga. El modelo se construyó utilizando los modelos MODFLOW, MODPATH, y UCODE del USGS, mientras que la calibración se realizó en base a concentraciones de ¹⁴C y a la posición de ciertas zonas definidas con los datos hidroquímicos. La estimación de parámetros se realizó en base a una combinación de técnicas de regresiones no lineares y a una búsqueda a viva fuerza del error mínimo entre los datos observados y los simulados. Los valores de recarga calibrados fueron significativamente más bajos que los estimados en los modelos anteriores. Los resultados de una simulación transitoria de 30,000 años sugieren que la recarga durante la última glacial máxima (LGM) fue diez veces el ritmo moderno, pero que la recarga que ocurrió inmediatamente después de la LGM fue más baja que el ritmo moderno.

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Résumé Le calibrage dun modèle hydrogéologique avec laide de données hydrochimiques a démontré que la recharge relativement faible dans le Grand Bassin du Middle Rio est vraisemblablement responsable dune dépression des eaux souterraines dans le centre du bassin et de la présence dune quantité substantielle deau du Rio Grande dans laquifère du Groupe de Santa Fe. Les modèles antérieurs avaient des difficultés à reproduire ses conclusions sans laide de données hydrochimiques pour contraindre les taux et la distribution de la recharge. Lobjectif de cette étude était dutiliser une grande quantité de données hydrochimiques permettant de calibrer les paramètres du modèle, et notamment les taux de recharge. Le modèle a été construit avec les logiciels MODFLOW, MODPATH et UCODE, et calibré en utilisant les concentrations en ¹⁴C et la position de certaines zones définies par les données hydrochimiques. Lestimation de certains paramètres a été réalisée en utilisant une combinaison de techniques de régression non linéaire et une méthode de recherche exhaustive (Brute Force Search) de lerreur minimum entre les résultats des observations et les simulations. Les valeurs de la recharge calibrée sont substantiellement plus basses que celles estimées dans les modèles antérieurs. Les résultats dune simulation en régime transitoire sur 30.000 ans suggèrent que la recharge au maximum de la dernière glaciation (last glacial maximum, LGM) était 10 fois supérieure au taux actuel, mais que la recharge qui a suivit la LGM était plus bas que la recharge actuelle.

     

Characteristics of groundwater in Northeast Qinghai-Tibet Plateau and its response to climate change and human activities: A case study of Delingha,Qaidam Basin

Delingha is located in the northeast margin of Qaidam Basin. Bayin River alluvial proluvial fan is the main aquifer of Delingha, in which groundwater generally flows from north to south. The hydrochemistry results showed that two different hydrochemical evolution paths formed along southeast and southwest directions, respectively. Cl-Na type groundwater was formed in front of Gahai Lake, and SO₄·HCO₃-Na·Ca type groundwater was formed in front of Keluke Lake. The results of deuterium (D) and ¹⁸O revealed that the groundwater mainly originated from the continuous accumulation of precipitation during geological history under cold and humid climate conditions. In addition, results of ¹⁴C indicated that the groundwater age was more than 1140 years, implying relatively poor renewal capability of regional groundwater. Moreover, our numerical modeling results showed that the regional groundwater level will continue to rise under the warm and humid climate conditions.© 2021 China Geology Editorial Office.     

Storm pulse chemographs of saturation index and carbon dioxide pressure: implications for shifting recharge sources during storm events in the karst aquifer at Fort Campbell,Kentucky/Tennessee,USA

Continuous records of discharge, specific conductance, and temperature were collected through a series of storm pulses on two limestone springs at Fort Campbell, western Kentucky/Tennessee, USA. Water samples, collected at short time intervals across the same storm pulses, were analyzed for calcium, magnesium, bicarbonate, total organic carbon, and pH. Chemographs of calcium, calcite saturation index, and carbon dioxide partial pressure were superimposed on the storm hydrographs. Calcium concentration and specific conductance track together and dip to a minimum either coincident with the peak of the hydrograph or lag slightly behind it. The CO₂ pressure continues to rise on the recession limb of the hydrograph and, as a result, the saturation index decreases on the recession limb of the hydrograph. These results are interpreted as being due to dispersed infiltration through CO₂-rich soils lagging the arrival of quickflow from sinkhole recharge in the transport of storm flow to the springs. Karst spring hydrographs reflect not only the changing mix of base flow and storm flow but also a shift in source of recharge water over the course of the storm.

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Resumen Se ha registrado en continuo la descarga, conductancia específica y temperatura de una serie de episodios de tormenta en dos manantiales en calizas ubicados en Fort Campbell, en el oeste de Kentucky/Tennessee (Estados Unidos de América). Se ha analizado muestras de agua recogidas en breves intervalos de tiempo durante los episodios de tormenta, determinando el calcio, magnesio, bicarbonato, carbono orgánico total y pH. Se ha superpuesto quimiogramas de calcio, índice de saturación en calcita y presión parcial de dióxido de carbono en los hidrogramas de las tormentas. La concentración de calcio y la conductancia específica se comportan de forma similar y presentan un mínimo que coincide también con un pico del hidrograma o que se retrasa ligeramente con respecto a él. La presión de dióxido de carbono sigue aumentando en la rama de recesión del hidrograma y, como consecuencia, disminuye el índice de saturación de la rama de recesión del hidrograma. Se interpreta que estos resultados son debidos a la infiltración dispersa a través de suelos enriquecidos en dióxido de carbono que retrasan el flujo rápido desde la recarga en los sumideros hasta su afloramiento en los manantiales. Los hidrogramas en manantiales kársticos reflejan no sólo la mezcla cambiante del flujo de base y el de tormenta, sino también el cambio en el origen del agua de recarga durante el curso de la tormenta.

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Résumé Lenregistrement en continu du débit, de la conductivité et de la température de leau a été réalisé au cours dune série de crues à deux sources émergeant de calcaires, à Fort Campbell (Kentucky occidental, Tennessee, États-Unis). Des échantillons deau, prélevés à de courts pas de temps lors de ces crues, ont été analysés pour le calcium, le magnésium, les bicarbonates, le carbone organique total et le pH. Les chimiogrammes de calcium, dindice de saturation de la calcite et de la pression partielle en CO₂ ont été superposés aux hydrogrammes de crue. La concentration en calcium et la conductivité de leau se suivent bien et passent par un minimum correspondant au pic de lhydrogramme ou légèrement retardé. La pression partielle en CO₂ continue de croître au cours de la récession de lhydrogramme de même que lindice de saturation de la calcite décroît. Ces résultats sont interprétés comme étant dus à linfiltration dispersée au travers de sols riches en CO₂, décalée par rapport à larrivée de lécoulement rapide provenant de la recharge, à partir dune perte, de lécoulement de crue vers les sources. Les hydrogrammes de sources karstiques ne reflètent pas seulement le mélange variable de lécoulement de base et de lécoulement de crue, mais également un changement dorigine de leau de la recharge au cours de lépisode de crue.