Association of hydrogeological factors in temporal variations of fluoride concentration in a crystalline aquifer in India

The major part of groundwater in India is found in granitic aquifers. Fluoride in groundwater from a crystalline aquifer in a semi-arid region of granitic rocks in India, known as Maheshwaram watershed, was analyzed for spatial and temporal variability during 1999–2002 to assess the effect of hydrogeological factors on fluoride concentration. Samples were collected from 32 representative wells in the area for the pre- and post-monsoon seasons and analyzed for F content. The CHESS computer program was used to calculate ionic activities of aqueous species and the mineral saturation index (SI) for calcite and fluorite. The GARDENIA computer program was used to calculate the recharge values in the study area. The influences of dissolution kinetics of fluoride minerals and recharge from rainfall on fluoride concentration were of interest and results clearly indicate that fluoride content in groundwater depends on the interaction period of groundwater with host rock. Results could also be utilized for designing remedial measures particularly with dilution method in an optimal way.     

Modeling of water–rock interactions in an aquitard of sandy clay in the coastal area near Beihai,China

Unconsolidated sand, gravel and clay deposits near Beihai and in the Leizhou Peninsula in southern China form an unconfined aquifer, aquitard and a confined aquifer. Water and soil samples were collected from the two aquifers in the coastal Beihai area for the determination of chemical compositions, minerals and soluble ions. Hydrogeochemical modeling of three flow paths through the aquitard are carried out using PHREEQC to determine water–rock interactions along the flow paths. The results indicate that the dissolution of anorthite, fluorite, halite, rhodochrosite and CO₂, and precipitation of potash feldspar and kaolinite may be occurring when groundwater leaks through the aquitard from the unconfined aquifer to the confined aquifer. Cation exchanges between Na and Ca can also happen along the flow paths.     

Geochemical evolution of groundwater in the Maneadero coastal aquifer during a dry year in Baja California, Mexico

Water pumped from 25 shallow wells (<31 m) in the Maneadero unconfined coastal aquifer was studied geochemically in order to determine the short-term compositional variability of the aquifer due to seawater intrusion during a drier than normal year (Fall 2001 to Fall 2002). The groundwater was commonly found to be mixed with seawater, with TDS concentrations in November 2002 ranging from 0.99 to 9.46 g l^–1, having an intermediate Na⁺Cl^– to Ca²⁺Cl^– water-type. Rapid recharge events of short duration, after low and short rainfall events during the study period, are suggested from short-term fluctuations in water quality. Seawater intrusion is progressing faster in the central and southern coastal sections of the aquifer and has recently affected the quality of the sites pumping water to the nearby city of Ensenada. Only one of the wells used for the Ensenada water supply had a TDS concentration lower than the 1.0 g l^–1 official limit. Low flow rates and high residence times of water are inferred to be the cause for high alkalinity in the east-central section of the aquifer. High NO₃ in the east-central aquifer indicates that any NO₃ infiltration due to fertilizer use was only slightly dispersed. After a short rainfall season during winter 2001, a significant decrease was seen for the previously most enriched site. However, concentrations above the 10 mg l^–1 official limit persisted in 2002, affecting one well for urban supply (15.9 mg l^–1). The water from this well is nevertheless mixed with better-quality water from other wells before being distributed through the citys piping system.

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Resumen Se estudió la geoquímica de aguas bombeadas por medio de 25 pozos no muy profundos (<31 m) en el acuifero costero no confinado de Maneadero con el objetivo de determinar la variación de la composición en el corto plazo en el acuifero por la intrusión de agua de mar durante un año más seco de lo normal (otoño 2001 a otoño 2002). Se observó que comúnmente las aguas subterráneas estaban mezcladas con agua de mar, con concentraciones de sólidos totales disveltos (STD) de entre 0.99--9.46 g l^–1 y un tipo de agua intermedia Na⁺Cl^– to Ca²⁺Cl^–. A partir de las fluctuaciones en la calidad del agua en el corto plazo se puede inferir que se dan eventos de recarga rápida de poca duración después de eventos de poca lluvia de poca duración y poco volumen durante el periodo de estudio. La intrusión de agua de mar está progresando más rápido en el centro y sur del acuifero costero y ha afectado recientemente la calidad de los sitios de bombeo de agua para la ciudad de Ensenada. Solamente uno de los pozos usados para el abastamiento de Ensenada tiene un STD por debajo del límite oficial de 1.0 g l^–1. Se presume que las razones lentas de flujo y los tiempos de residencia largos del agua son la causa de la alta alcalinidad en el centro-este del acuifero. Una concentración alta de NO₃ en el este-centro del acuifero indica que cualquier infiltración de NO₃ por aplicación de fertilizantes ha sido poco dispersad. Después de poca lluvia en el invierno de 2001, se observó una disminución importante en la zona previamente más enriquecida. Sin embargo, concentraciones sobre el límite oficial de 10 mg l^–1 continuaron en 2002, afectando a un pozo para suministro de agua urbana (15.9 mg l^–1). El agua extraída de este pozo es mezclada con agua de mejor calidad y se distribuye por el sistema urbano de suministro de agua.

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Résumé Leau de pompage de 25 puits peu profonds (<31 m) situés dans laquifère côtier non-confiné de Maneadero a été étudiée dans le but de déterminer la variation géochimique à court terme qui résulte de lintrusion deau de mer lors dune année plus sèche quà lhabitude (automne 2001 à automne 2002). Leau souterraine est souvent retrouvée mélangée avec de leau de mer, avec des concentrations en résidus solides dissous (RSD) qui sétalent entre 0.99 et 9.46 g l^–1 pour novembre 2002, avec un type intermédiaire en Na⁺Cl^– jusquà Ca²⁺Cl^–. Les processus suggérés pour les fluctuations rapides de la qualité de leau sont des événements de recharge de courte duré suite à de faibles et brèves périodes de précipitations. Lintrusion deau de mer progresse plus rapidement dans les parties centrales et sud de laquifère côtier où la qualité de leau pompée vers la ville de Ensenada a récemment été affectée. Un seul des puits utilisés par la ville de Ensenada pour lapprovisionnement en eau potable a une concentration en RSD sous la limite officielle permise de 1.0 g l^–1. Le temps de résidence élevé et le faible taux découlement de leau souterraine sont présumés être la cause de lalcalinité élevée dans la partie centrale-est de laquifère. La concentration élevée en NO₃ dans cette partie de laquifère indique que la totalité de linfiltration de NO₃ dû à lutilisation de fertilisants ne sest que très peu dispersée. Suite à une courte saison des pluies à lhiver 2001, une diminution substantielle a été notée au site qui était le plus enrichi avant la saison des pluies. Malgré tout, des concentrations dépassant la limite officielle permise de 10 mg l^–1 ont persisté, affectant un puits utilisé pour lapprovisionnement urbain (15.9 mg l^–1). Leau provenant de ce puits est toutefois mélangée avec de leau de meilleure qualité provenant dautres puits avant dêtre distribuée par laqueduc municipal.

     

Geochemical characteristics of shallow groundwater in Datong basin, northwestern China

Located in semi-arid regions of northwestern China, Datong basin is a Quaternary sedimentary basin, where groundwater is the most important source for water supply. It is very important to study groundwater characteristics and hydrogeochemical processes for better management of the groundwater resource. We have identified five geochemical zones of shallow groundwater (between 5 and 80 m) at Datong: A. Leaching Zone (Zone I); B. Converging Zone (Zone II); C. Enriching Zone (Zone III); D. Reducing Zone (Zone IV); E. Oxidizing Zone (Zone V). In Zones I, II, and V and some parts of Zones III and IV, hydrolysis of albite/K-feldspar/chalcedony system and/or albite/K-feldspar/quartz system enhanced concentrations of Na⁺, K⁺, HCO₃⁻ and silicate. In Zone I, dissolution of carbonate and hydrolysis of feldspar generally controlled the groundwater chemistry. Infiltration of meteoric water promoted the formation of HCO₃⁻ in the water. In Zone II, the main geochemical processes influencing the groundwater chemistry were dissolutions of calcite and dolomite, ion exchange and evaporation. In Zones III and IV, in addition to ion exchange, evaporation and precipitation of calcite and dolomite, leaching of NaHCO₃ in saline–alkaline soils dominated the water quality. Zone IV was under anoxic condition, and reduction reactions led to the decrease of SO₄²⁻, NO₃⁻ and occurrence of H₂S, with the highest arsenic content (mean value of 366 μg/L), far exceeding Maximum Contaminant Level (MCL). Abnormal arsenic in the groundwater resulted in endemic disease of waterborne arsenic poisoning among local people. Zone V overlapped Zone I was intensively affected by coal mining activities. Sulfide minerals, such as pyrite, would have been oxidized when exposed to air due to coal mining, which directly added sulfate to groundwater and thus increased SO₄²⁻ concentration. Oxidization of sulfide minerals also decreased pH and promoted dissolutions of calcite and dolomite.     

Assessment of groundwater chemistry in a coastal region (Kunsan, Korea) having complex contaminant sources: a stoichiometric approach

Groundwater chemistry in a coastal region (Kunsan, Korea) having complex contaminant sources was investigated. Water analysis data for 197 groundwater samples collected from the uniformly distributed sixty-six wells were used. Chemical analysis results indicate that groundwaters show wide concentration ranges in major inorganic ions, reflecting complex hydrochemical processes. Due to the complexity of groundwater chemistry, the samples were classified into four groups based on Cl and NO₃ concentrations and the processes controlling water chemistry were evaluated based on the reaction stoichiometry. The results explained the importance of mineral weathering, anthropogenic activities (nitrification and oxidation of organic matters), and Cl-salt inputs (seawater, deicer, NaCl, etc.) on groundwater chemistry. It was revealed that mineral dissolution is the major process controlling the water chemistry of the low Cl and NO₃ group (Group 1). Groundwaters high in NO₃ (Groups 2 and 4) are acidic in nature, and their chemistry is largely influenced by nitrification, oxidation of organic matters and mineral dissolution. In the case of chloride rich waters (Group 3), groundwater chemistry is highly influenced by mineral weathering and seawater intrusion associated with cation-exchange reactions.     

Environmental impact of an urban landfill on a coastal aquifer (El Jadida, Morocco)

The El Jadida landfill is one among many uncontrolled dumping sites in Morocco with no bottom liner. About 150 tons/day of solid wastes from mixed urban and industrial origins are placed directly on the ground. At the site of this landfill, the groundwaters circulate deeply (10–15 m) in the Cenomanian rock (calcareous–marl), which is characterised by an important permeability from cracks. The soil is sand–clay characterized by a weak coefficient of retention.The phreatic water ascends to the bottom of three quarries, which are located within the landfill. These circumstances, along with the lack of a leachate collection system, worsen the risks for a potential deterioration of the aquifer.To evaluate groundwater pollution due to this urban landfill, piezometric level and geochemical analyses have been monitored since 1999 on 60 wells. The landfill leachate has been collected from the three quarries that are located within the landfill. The average results of geochemical analyses show an important polluant charge vehiculed by landfill leachate (chloride = 5680 mg l⁻¹, chemical oxygen demand = 1000 mg l⁻¹, iron = 23 000 μg l⁻¹). They show also an important qualitative degradation of the groundwater, especially in the parts situated in the down gradient area and in direct proximity to the landfill. In these polluted zones, we have observed the following values: higher than 4.5 mS cm⁻¹ in electric conductivity, 1620 and 1000 mg l⁻¹ respectively in chlorides and sulfate (), 15–25 μg l⁻¹ in cadmium, and 60–100 μg l⁻¹ in chromium. These concentrations widely exceed the standard values for potable water.Several determining factors in the evolution of groundwater contamination have been highlighted, such as (1) depth of the water table, (2) permeability of soil and unsaturated zone, (3) effective infiltration, (4) humidity and (5) absence of a system for leachate drainage. So, to reduce the pollution risks of the groundwater, it is necessary to set a system of collection, drainage and treatment of landfill leachates and to emplace an impermeable surface at the site of landfill, in order to limit the infiltration of leachate.     

A thirty-year artificial recharge experiment in a coastal aquifer in an arid zone: The Teboulba aquifer system (Tunisian Sahel)

With the increased demand for groundwater resulting from fast demographic growth, accelerated urbanization, economic and agricultural activity diversification, and the increase of per capita consumption, ground water resources, in particular in coastal regions, remain relatively low, compared to demand. The groundwater quality and piezometric variations result mainly from intensive exploitation, agricultural activities and the intrusion of seawater. This phenomenon is observed mostly in semi-arid areas, such as the oriental Sahel of Tunisia, where an apparent reduction in rainfall in recent years can be seen. Groundwater becomes overexploited especially as its natural recharge by rainwater does not succeed in maintaining the hydrologic balance. The imbalance between water demand and resources induces the degradation of the water quality. In such a case, the artificial recharge of water-table aquifers by water from dams is a credible alternative to improve the hydrodynamic and physicochemical conditions of the groundwater. Like most coastal aquifers, the Teboulba water-table aquifer is threatened by overexploitation for at least three decades. This threat appears by a considerable piezometric level drop and by water salinisation, due to seawater intrusion. Given this alarming situation, since 1971, artificial recharge through wells with surface water from a dam was tested in order to restore the water levels and to improve water quality. The piezometric and chemical surveys of the Teboulba aquifer permitted one to describe the temporal and spatial piezometric and geochemical conditions of the aquifer and to show the effect of the artificial recharge. Indeed, the artificial recharge undertaken since 1971 made the geochemical and piezometric conditions of the Teboulba aquifer improve. This example is a rare, well-documented case-study of the benefits of artificial recharge in a coastal aquifer, over the long term.     

Olocenic alluvial aquifer of the River Cornia coastal plain (southern Tuscany, Italy): database design for groundwater management

 Hydrogeological research is in progress, utilizing GIS methods, with the principal aim of modelling the Olocenic alluvial aquifer of the River Cornia coastal plain (southern Tuscany, Italy), which has been exploited for drinking water, irrigation, and industrial uses. A consequence of exploitation has been the appearance of wide seawater intrusion. The alluvial aquifer has recently been subjected to new well fields for the supply of drinking water, with an increase of total average discharge of about 4×10⁶ m³/year. This paper presents results obtained from updating and integrating basic knowledge and structuring the database. The hydrogeological study allowed the recognition of the extension of areas that are characterized by a hydraulic head under the sea level, the progressive salinization of the aquifer, and the increase of water deficit in the aquifer which is produced by a progressive extraction of water superior to the natural recharge. In addition, benefits and disadvantages resulting from the location of new well fields in a hydrogeologically favourable zone, and the boundary conditions for much of the area studied have been defined. The GIS was used as support for making and updating the tabular and spatial database with the aim of integrating the local and regional hydrogeological knowledge. This study will permit the realization of a numerical simulation of the groundwater flow of the aquifer aimed at correcting the management of water resources, by means of the GIS-modelling integration. Received: 23 June 1998 · Accepted: 16 November 1998     

Hydrogeochemical stratification of the unconfined Samobor aquifer (Zagreb,Croatia)

In the western part of the city of Zagreb, Croatia, hydrogeochemical and isotopic investigations of the Samobor aquifer were carried out with the aim of determining the differences in hydrogeochemical characteristics at increasing aquifer depths. The aquifer comprises 40-m thick gravelly–sandy deposits, with lenses and interlayers of silt and clay. The analyses have proven that with increasing aquifer depth, there are decreases in groundwater temperature and the values of electrical conductivity and increases in the sodium, iron and manganese concentrations. The δ¹³C distribution shows an evident increase in biogenic carbon concentrations with increasing aquifer depth. The measured specific ¹⁴C activities showed that the deeper part of the aquifer is characterized by slow water exchange, while the shallower part is influenced by current recharge, although the pumping wells located on the well-field downstream penetrate the aquifer fully. A direct exchange of water from the Sava River and groundwater occurs in the near vicinity of the river. This exchange weakens further away, while the difference in hydrogeochemical characteristics between the Sava River water and groundwater increases.     

Influence of ignimbrite on the chemistry of river water in Shirasu plateau,Japan

River, rain and spring water samples from a region covered in “Shirasu” ignimbrite were collected on Kyushu Island, Japan. The analytical results were subjected to multivariate statistical analysis and stoichiometric calculation to understand the geographical distribution of chemical components in water and to extract geochemical underlying factors. The multivariate statistical analysis showed that the river-water chemistry is only slightly influenced by hot springs or polluted waters, but is highly controlled by weathering of ignimbrite. On the basis of the stoichiometric calculation based on water–rock interaction, the water chemistry was successfully estimated by a simple equation:\({\left[ {{\text{Si}}} \right]}{\text{ = 2}}{\left[ {{\text{Na}}^{{\text{ + }}} } \right]}{\text{ + }}{\left[ {{\text{Mg}}^{{{\text{2 + }}}} } \right]}\) in the upstream area, complemented by \({\left[ {{\text{Si}}} \right]}{\text{ = }}{\left[ {{\text{Na}}^{{\text{ + }}} } \right]}{\text{ - 3}}{\left[ {{\text{K}}^{{\text{ + }}} } \right]}{\text{ + }}{\left[ {{\text{Mg}}^{{{\text{2 + }}}} } \right]}{\text{ - 2}}{\left[ {{\text{Ca}}^{{{\text{2 + }}}} } \right]}\) in the downstream area.     

Hydrogeochemical study in the Main Ethiopian Rift: new insights to the source and enrichment mechanism of fluoride

The central Main Ethiopian Rift suffers a severe water quality problem, characterized by an anomalously high fluoride (F) content that causes an endemic fluorosis disease. The current study, conducted in the Ziway–Shala lakes basin, indicates that the F content exceeds the permissible limit for drinking prescribed by the World Health Organization (WHO; 1.5 mg/l) in many important wells (up to 20 mg/l), with even more extreme F concentration in hot springs and alkaline lakes (up to 97 and 384 mg/l respectively). The groundwater and surface water from the highlands, typically characterized by low total dissolved solids (TDS) and Ca (Mg)–HCO₃ hydrochemical facies, do not show high F content. The subsequent interaction of these waters with the various rocks of the rift valley induces a general increase of the TDS, and a variation of the chemical signature towards Na–HCO₃ compositions, with a parallel enrichment of F. The interacting matrixes are mainly rhyolites consisting of volcanic glass and only rare F-bearing accessory minerals (such as alkali amphibole). Comparing the abundance and the composition of the glassy groundmass with other mineral phases, it appears that the former stores most of the total F budget. This glassy material is extremely reactive, and its weathering products (i.e. fluvio/volcano-lacustrine sediments) further concentrate the fluoride. The interaction of these “weathered/reworked” volcanic products with water and carbon dioxide at high pH causes the release of fluoride into the interacting water. This mainly occurs by a process of base-exchange softening with the neo-formed clay minerals (i.e. Ca–Mg uptake by the aquifer matrix, with release of Na into the groundwater). This is plausibly the main enrichment mechanism that explains the high F content of the local groundwater, as evidenced by positive correlation between F, pH, and Na, and inverse correlation between F and Ca (Mg). Saturation indices (SI) have been calculated (using PHREEQC-2) for the different water groups, highlighting that the studied waters are undersaturated in fluorite. In these conditions, fluoride cannot precipitate as CaF₂, and so mobilizes freely without forming other complexes. These results have important implications for the development of new exploitation strategies and accurate planning of new drilling sites. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Hydrogeochemical analysis of salinization processes in the coastal aquifer of Oropesa (Castellón, Spain)

 The coastal aquifer of Oropesa is affected by salinization processes undoubtedly associated with intense groundwater exploitation for agriculture supply. The aquifer corresponds geologically to a tectonic depression with Plioquaternary fill. Hydrogeologically, this aquifer is detrital, with intergranular porosity, which receives substantial recharge from adjacent Mesozoic aquifers. Contact with the sea, in addition to the presence of cultivated soil requiring extreme exploitation of groundwater, frequently give rise to processes of seawater intrusion. The present research is an attempt to understand the saltwater intrusion in this aquifer, using hydrochemical analyses of the behavior of certain minor ions that could help in the characterization process. In the case of the Oropesa sector, groundwater salinization does not appear to be attributable solely to the intrusion of seawater, but there are also anomalies related largely to the geology of the sector and its surroundings, the type of recharge, the hydrodynamic conditions in the specific area, etc. Received: 23 January 1995 · Accepted: 12 September 1995     

利用观测孔中地下水位潮汐效应计算天津滨海新区含水层参数

在沿海地区,尤其是围海造陆工程形成的陆域地区地下水水位受潮汐影响较大,使传统水文地质试验求取含水层参数存在较大误差。因此通过合理概化地下水在潮汐作用下运动规律,建立数学模型,推导解析公式求取沿海含水层参数具有重要意义。分析天津滨海新区两处观测孔地下水位及潮汐波动特征,在滞后时间不明显的情况下,利用观测孔水位变幅数据计算了含水层水头扩散系数,并根据承压含水层储水系数经验值进一步获得含水层渗透系数。通过两个观测孔分别计算,对比计算结果互相验证发现,该方法取得了令人满意的结果。利用地下水潮汐效应计算含水层参数可以广泛应用于沿海地区水文地质工作中。     

鄂尔多斯沙漠高原白垩系地下水水化学演化的多元统计分析

结合稳定同位素( D、18O、13C) ,应用聚类分析和因子分析两种多元统计分析方法,对鄂尔多斯沙漠高原白垩系含水层地下水水化学演化特征进行研究。结果表明: 研究区环河组和洛河组地下水均可分为3 大类,且大致在地下水补给区、径流区和排泄区分别聚类,每一类的水化学特征和同位素特征均存在一定的差异; 研究区地下水均起源于大气降水,发生了岩盐溶滤、碳酸盐矿物溶解、硫酸盐矿物溶解、硅酸盐矿物溶解和阳离子交换等水文地球化学作用。相对洛河组地下水,环河组地下水水化学演化特征还受到了大气降水稀释作用和酸碱演化的影响。     

Hydrogeochemical effects of groundwater mining of the Sierra de Crevillente Aquifer (Alicante,Spain)

The groundwater mining of the Crevillente aquifer (southeastern Spain) has resulted in the progressive deterioration of water quality, with particularly significant increases in chloride, sulfate, and sodium. The possibility of a vertical hydrochemical zoning is deduced that would require examining the importance of the geometry and lithology (evaporitic materials) in the salinization process. The time of water-rock contact (residence time) and dilution by infiltration of rainwater also influences the hydrogeochemistry of the aquifer. The hydrochemical data are useful in defining the conceptual model of the aquifer, completely karstified with relative homogeneity.Project AMB92-0211 (CICYT)     

Evolution of groundwater salinity in the unconfined aquifer of Bou-Areg, Northeastern Mediterranean coast, Morocco

The Bou-Areg plain in the Mediterranean coast at the North-eastern of Morocco is characterized by a semi-arid climate. The aquifer consists of two sedimentary formations of Plio-quaternary age: the upper formation of fine silts and the lower one of coarse silts with sand and gravels. The aquifer is underlain by marly bedrock of Miocene age that dips toward the coastal lagoon of Bou-Areg. The hydrodynamic characteristics vary between 10⁻⁴ and 10⁻³ m/s; and transmissivities range between 10⁻⁴ and 10⁻¹ m²/s. The general direction of flow is SW to NE, toward the lagoon. The aquifer is crossed by the river Selouane, which also ends in the lagoon. The groundwater is characterized by a high salinity that can reach 7.5 g/l. The highest values are observed in the upstream and in the downstream sectors of the aquifer. The temporal evolution of the physico-chemical parameters depends on the climatic conditions and piezometric variations. The analysis of the spatio-temporal distribution of the physico-chemical parameters suggests different sources of groundwater salinization: the seawater intrusion, the influence of marly gypsum-bearing terrains, and the influence of anthropogenic products as the agricultural fertilizers, which cause great nitrate concentrations that vary between 80 and 140 mg/l.     

Modelling hydrostratigraphy and groundwater flow of a fractured and karst aquifer in a Mediterranean basin (Salento peninsula, southeastern Italy)

The control exerted by the hydrostratigraphic structure on aquifer recharge, groundwater flow and discharge along the coastal areas of a Mediterranean basin (Salento peninsula, about 5,000?km² wide, southern Italy) is assessed through the development and application of a groundwater flow model based on the reconstruction of the hydrostratigraphic architecture at the regional scale. The hydrostratigraphic model, obtained by processing surface and subsurface data, is applied to map the top of the main aquifer, which is hosted in the deep hydrostratigraphic unit corresponding to Cretaceous and Oligocene limestones with complex geometrical relationships with the sea. It is also used to estimate the aquifer recharge, which occurs by percolation through overlying younger sediments with low permeability. These data are completed with information about the soil use to estimate water abstraction for irrigation and with literature data to estimate the water abstraction for drinking and industrial purposes. The above-sketched conceptual model is the basis for a finite difference groundwater 2D pseudo-stationary flow model, which assumes the following fundamental approximations: the fractured and karst limestone hydrostratigraphic unit can be approximated, at the model scale, as a continuous medium for which the discrete Darcy??s law is valid; the transition zone between salt and fresh water is so small with respect to the grid spacing that the Ghyben?CHerzberg??s approximation for a sharp interface can be applied. Along the coastline different boundary conditions are assigned if the top of the limestone hydrostratigraphic unit lies either above the sea level (the aquifer has a free surface and fresh water is drained), or below the sea level (the aquifer is under pressure and the contact with sea occurs off-shore). The groundwater flow model correctly predicts the areas where the aquifer is fully saturated with salt water.     

海潮引起初始水位倾斜的滨海承压含水层地下水位 变化的数值模拟

海潮波动可以引起海岸带地下水位发生波动。建立了基于有限差分法的滨海地区一维承压含水层地下水运动数值模型。将潮汐波动概化为正弦波,模拟了滨海地区地下水位随潮汐波动的变化。通过与初始水位水平的承压含水层水位变化的比较表明,受海潮影响的滨海承压含水层地下水位与海潮有相似的波动特征,但变幅减小,受海潮的影响程度与离海岸的距离有关,随着离海岸距离的增加,地下水位的变幅及潮汐效率呈负指数函数衰减,但比前者变化程度稍缓,地下水位对海潮的滞后时间随距离呈线性增加。     

Evolution of the groundwater environment under a long-term exploitation in the coastal area near Zhanjiang, China

Aquifers consisting of unconsolidated sediments in the coastal area near Zhanjiang in southern China are grouped into the shallow, middle-deep and deep aquifer systems. Groundwater exploitation began in the 1950s in this district and has increased from year to year since 1980. Measurements of groundwater levels and monitoring data of groundwater chemistry at some 60 wells since 1981 are examined to analyze the evolution of hydrodynamics and hydrochemistry in the coastal aquifers. The results indicate that groundwater levels in the middle-deep and deep aquifer systems have fallen continuously and the extents of the depression cones in water levels have increased in the past two decades, even though the water levels recovered to some degree during the period of 1997–2001. In 2004, the lowest water levels in the middle-deep and deep aquifer systems were 23.58 and 21.84 m below sea level, respectively. The groundwater has TDS ranging from 40 to 550 mg/L, and is of low pH, commonly varies between 4 and 7. Concentrations of total iron and manganese exceed the concentration limits of the drinking water standards. The hardness is in the range of 10–250 mg/L. Chloride contents of the groundwater range from 10 to 60 mg/L. The chloride and TDS do not show systematically increasing trends. Although the water levels in the exploitation center near the coast are significantly lower than the sea level and the depression cones of water levels in the middle-deep and deep aquifer systems have expanded to the sea, sea water intrusion has not been observed until recently. This phenomenon is quite unique in the coastal area near Zhanjiang.     

Hydrochemical evolution and water quality along the groundwater flow path in the Sandıklı plain, Afyon, Turkey

 An unconfined aquifer system suggests an open system in the study area. Hydrochemical evolution is related to the flow path of groundwater. The groundwaters are divided into two hydrochemical facies in the study area, 1) Ca–Mg–HCO₃ and 2) Ca–Mg–SO₄HCO₃. Facies 1 has shallow (young) waters which dominate in recharge areas during rapid flow conditions, whereas facies 2 may show shallow and mixed waters which dominate intermediate or discharge areas during low flow conditions. Ionic concentrations, TDS, EC and water quality are related to groundwater residence time and groundwater types. The groundwaters in the plain are chemically potable and suitable for both domestic and agricultural purposes. Received: 20 May 1996 · Accepted: 30 July 1996