Groundwater components in the alluvial aquifer of the alpine Rhone River valley, Bois de Finges area, Wallis Canton, Switzerland

Source, type, and quantity of various components of groundwater, as well as their spatial and temporal variations were determined by different hydrochemical methods in the alluvial aquifer of the upper Rhone River valley, Bois de Finges, Wallis Canton, Switzerland. The methods used are hydrochemical modeling, stable-isotope analysis, and chemical analysis of surface water and groundwater. Sampling during high- and low-water periods determined the spatial distribution of the water chemistry, whereas monthly sampling over three years provided a basis for understanding seasonal variability. The physico-chemical parameters of the groundwater have spatial and seasonal variations. The groundwater chemical composition of the Rhone alluvial aquifer indicates a mixing of weakly mineralized Rhone River water and SO₄-rich water entering from the south side of the valley. Temporal changes in groundwater chemistry and in groundwater levels reflect the seasonal variations of the different contributors to groundwater recharge. The Rhone River recharges the alluvial aquifer only during the summer high-water period. Electronic Publication     

Groundwater flow modeling of Quaternary aquifer Ras Sudr,Egypt

Recently, Ras Sudr (the delta of Wadi Sudr) area received a great amount of attention due to different development expansion activities directed towards this area. Although Quaternary aquifer is the most prospective aquifer in Ras Sudr area, it has not yet completely evaluated. The present work deals with the simulation of the Quaternary groundwater system using a three-dimensional groundwater flow model. MODFLOW code was applied for designing the model of the Ras Sudr area. This is to recognize the groundwater potential as well as exploitation plan of the most prospective aquifer in the area. The objectives were to determine the hydraulic parameters of the Quaternary aquifer, to estimate the recharge amount to the aquifer, and to determine the hydrochemistry of groundwater in the aquifer. During this work, available data has been collected and some field investigation has been carried out. Groundwater flow model has been simulated using pilot points’ method. SEAWAT has been also applied to simulate the variable-density flow and sea water intrusion from the west. It can be concluded that: (1) the direction of groundwater flow is from the east to the west, (2) the aquifer system attains a small range of log-transformed hydraulic conductivity. It ranges between 3.05 and 3.35 m/day, (3) groundwater would be exploited by about 6.4 × 10⁶ m³/year, (4) the estimated recharge accounts for 3 × 10⁶ m³/year, (5) an estimated subsurface flow from the east accounts for 2.7 × 10⁶ m³/year, (6) the increase of total dissolved solids (TDS) most likely due to dilution of salts along the movement way of groundwater from recharge area to discharge area in addition to a contribution of sea water intrusion from the west. Moreover, it is worth to note that a part of TDS increase might be through up coning from underlying more saline Miocene sediments. It is recommended that: (1) any plan for increasing groundwater abstraction is unaffordable, (2) reliable estimates of groundwater abstraction should be done and (3) automatic well control system should be made.     

Hydrogeology and hydrochemistry of the Parmelia aquifer,northern Perth Basin,Western Australia

This study aims to characterise the hydrogeology and hydrochemistry of the Parmelia aquifer and to understand controls on recent water-level changes as these are needed to underpin a quantitative analysis of recharge. The Parmelia aquifer, a layered sequence of sand, silt and discontinuous lenses of clay, receives diffuse rainfall recharge on its outcrop and groundwater recharge occurs across the Dandaragan Plateau at different rates. Water levels have risen steadily over the last three decades between 10 and 55 cm/y in response to the replacement of native vegetation with pasture and annual crops. The mean aquifer properties from sediment analyses indicate a very wide range of porosity (8.9 – 49.5 %) with an arithmetic mean of 26% and consequently a very broad range of specific yield (0.0004 – 0.4) with an arithmetic mean of 0.14. Groundwater in the Parmelia aquifer has an underlying meteoric origin with compositional changes due to reactions with silicate minerals and leaching of chloride that has concentrated in the soil by evapotranspiration. The hydrochemistry sampled at different depths and locations in the aquifer indicates that the groundwater is not well mixed, and variations arise due to relatively recent recharge that has undergone evaporation in some areas.     

Using Generic and Pesticide DRASTIC GIS-based models for vulnerability assessment of the Quaternary aquifer at Sohag, Egypt

Groundwater resources in the Sohag area, Egypt are currently threatened by contamination from municipal and industrial activities, and agricultural pesticides. To cope with the growing population, there has been development in the desert zone on both sides of the Nile Valley including agricultural investment areas, wastewater disposal sites, new urban areas, and industry. Use of agrochemicals in the old cultivated and newly reclaimed lands and wastewater disposal sites in the study area represent the most hazardous contamination sources. Prevention of contamination and management of the Quaternary aquifer is urgently needed. To address vulnerability assessment of the Quaternary aquifer, the Generic and Pesticide DRASTIC GIS-based models have been used. The Generic DRASTIC index ranged between 94 and 189, and the Pesticide DRASTIC index ranged between 94 and 226. The results showed that 83% of the Quaternary aquifer is characterized by the high and very high vulnerability classes to municipal, industrial and agricultural pesticides contamination. It was found that nearly all the development projects are located in the very high vulnerability class areas. Management alternatives for the Quaternary aquifer may be improved by application of these models, allowing sensitive groundwater sources to be protected for continuing use in the future.     

Determining shallow aquifer vulnerability by the DRASTIC model and hydrochemistry in granitic terrain,southern India

Shallow aquifer vulnerability has been assessed using GIS-based DRASTIC model by incorporating the major geological and hydrogeological factors that affect and control the groundwater contamination in a granitic terrain. It provides a relative indication of aquifer vulnerability to the contamination. Further, it has been cross-verified with hydrochemical signatures such as total dissolved solids (TDS), \(\hbox {Cl}^{-},\, \hbox {HCO}_{3}^{-},\, \hbox {SO}_{4}^{2-}\) and \(\hbox {Cl}^{-}/\hbox {HCO}_{3}^{-}\) molar ratios. The results show four zones of aquifer vulnerability (i.e., negligible, low, moderate and high) based on the variation of DRASTIC Vulnerability Index (DVI) between 39 and 132. About 57% area in the central part is found moderately and highly contaminated due to the 80 functional tannery disposals and is more prone to groundwater aquifer vulnerability. The high range values of TDS (2304–39,100 mg/l); \(\hbox {Na}^{+}\)(239– 6,046 mg/l) and \(\hbox {Cl}^{-}\) (532–13,652 mg/l) are well correlated with the observed high vulnerable zones. The values of \(\hbox {Cl}^{-}/\hbox {HCO}_{3}^{-}\) (molar ratios: 1.4–106.8) in the high vulnerable zone obviously indicate deterioration of the aquifer due to contamination. Further cumulative probability distributions of these parameters indicate several threshold values which are able to demarcate the diverse vulnerability zones in granitic terrain.     

氮氧同位素和水化学解析昭通盆地地下水硝酸盐来源及对环境的影响

[研究目的]由于人类活动的影响,地下水硝酸盐(NO3-)污染越来越严重.[研究方法]利用水化学和硝酸盐氮氧同位素(δ15NNO3与δ18ONO3)研究云南昭通盆地地下水NO3-来源与转化过程,用SIAR模型定量计算泉水和民井中不同NO3?来源的比例.[研究结果]结果表明:(1)研究区钻孔水水质良好,但19％的泉水NO3...     

Scenario-based earthquake loss estimation for the city of Cairo,Egypt

This paper describes a multi-tiered loss assessment methodology to estimate seismic monetary implications resulting from structural damage to the building population in Greater Cairo. After outlining a ground-shaking model, data on geological structures and surface soil conditions are collated using a considerable number of boreholes to produce a classification of different soil deposits. An inventory database for the existing building stock is also prepared. The seismic vulnerability of representative reinforced concrete building models, designed according to prevalent codes and construction practices, is evaluated. Capacity spectrum methods are utilised for assessing the structural performance through a multi-level damage scale. A simplified methodology for deriving fragility curves for non-ductile reinforced concrete building classes that typically constitute the building population of the city is adopted. In addition, suitable fragility functions for unreinforced masonry constructions are selected and used for completing the loss model for the study area. The results are finally used to build an event-based loss model caused by possible earthquakes in the region.     

基于水化学和氢氧同位素的峡口隧道涌水来源识别

峡口隧道是一条位于岩溶山区的深埋特长型隧道,遭遇了历时近两年来源不明的复杂涌水过程。为查明隧道的涌水来源和充水途径,通过解读隧道区的水文地质条件,分析对比不同涌水点的水化学及氢氧同位素组成差异,查明了隧道右洞北侧涌水主要来源于二叠—三叠系岩溶含水层,其他均来自于侏罗系裂隙含水层,二叠系灰岩与泥盆系石英砂岩接触部位发育的岩溶裂隙带为主要的充水途径。     

Temporal variations in the depth-specific hydrochemistry and sewage-related microbiology of an urban sandstone aquifer,Nottingham, United Kingdom

The temporal and spatial characteristics of groundwater recharge in urban environments remain poorly understood. Depth-specific monitoring of groundwater quality in the Triassic Sandstone underlying the city of Nottingham, UK, indicates that contamination results primarily from sewage and atmospheric sources. The temporal and depth-specific characteristics of microbial and inorganic (e.g. nitrate, chloride, sulphate) contamination over the investigation period differ significantly and reflect the contrasting transport characteristics of surface-loaded solutes and particulate microbial species (bacteria and viruses) in the Triassic Sandstone. Differences result from a variety of factors, which include microbial die-off, dilution, and the contaminant-source characteristics. Observations in this study show that low levels of microbial contamination should be expected at depth in fissured sandstone due to aquifer heterogeneities such as fissuring and the occurrence of mudstone bands, though the magnitude of this contamination will vary over time. Furthermore, urban groundwater-protection measures based on solute-transport estimates may not be applicable to microbial contamination. Electronic Publication     

Occurrence of cyclic palustrine and calcrete deposits within the lower Pliocene Hagul formation, East Cairo district, Egypt

A depositional model of the lower Pliocene Hagul formation, which is exposed in the East Cairo district (Egypt), is proposed with more than 10 depositional cycles recognized. Field occurrence, detailed petrographic investigation and geochemical analysis revealed that the sediments within each cycle are the result of three sequential sedimentological processes: (1) alluvial sedimentation, (2) calcretization, and (3) precipitation of palustrine carbonate. It was concluded that Hagul formation has been deposited within the distal part of an alluvial plain during three successive climatic conditions: a humid climate during which alluvial sediments were deposited, a semi-arid climate with episodic precipitation which was favorable for pedogenic calcrete development, and a sub-humid climate during which groundwater level was gradually elevated and groundwater calcrete accumulated. Rising groundwater level continued until shallow wetlands covered the area and palustrine limestone was precipitated. Variations in the thickness and the nature of the host sediment, calcrete and palustrine limestone cycle suggest that each of the sedimentation processes varied from cycle to cycle.     

Controls on the chemical composition of groundwater from alluvial aquifers in the Wanaka and Wakatipu basins, Central Otago, New Zealand

 Groundwater in alluvial aquifers of the Wakatipu and Wanaka basins, Central Otago, New Zealand, has a composition expressed in equivalent units of Ca²⁺≫Mg²⁺≅Na⁺>K⁺ for cations, and HCO₃ ^–≫SO₄ ^2->NO₃ ^–≅Cl^– for anions. Ca²⁺ and HCO₃ ^– occur on a 1 : 1 equivalent basis and account for >80% of the ions in solution. However, some groundwater has increased proportions of Na⁺ and SO₄ ^2-, reflecting a different source for this water. The rock material of the alluvial aquifers of both basins is derived from the erosion and weathering of metamorphic Otago Schist (grey and green schists). Calcite is an accessory mineral in both the grey and green schists at <5% of the rock. Geological mapping of both basins indicates that dissolution of calcite from the schist is the only likely mechanism for producing groundwater with such a constant composition dominated by Ca²⁺ and HCO₃ ^– on a 1 : 1 equivalent basis. Groundwater with higher proportions of Na⁺ and SO₄ ^2- occurs near areas where the schist crops out at the surface, and this groundwater represents deeper and possibly older water derived from basement fluids. Anomalously high K⁺ in the Wakatipu basin and high NO₃ ^– concentrations in the Wanaka basin cannot be accounted for by interaction with basement lithologies, and these concentrations probably represent the influence of anthropogenic sources on groundwater composition. Received, June 1996 Revised, March 1997, July 1997 Accepted, July 1997     

Assessment of the impact of industrial effluents on water quality in Patancheru and environs, Medak district, Andhra Pradesh, India

The effects of multiple industrial-pollutant sources on the groundwater system were evaluated in the Industrial Development Areas (IDAs) of Medak district, Andhra Pradesh (AP), India. The quality of groundwater in the region has been affected negatively due to the discharge of effluents on open land and into ponds, tanks, and streams. Water samples from surface-water bodies, dug wells,and bore wells were analyzed for their major ion concentrations. The high values of electrical conductivity (EC) and concentrations of Na⁺, Ca²⁺, Cl^–, and HCO₃ ^– indicate the impact of industrial effluents. Based on the hydrochemistry, the groundwater is classified into various types, such as sodium-chloride, sodium-bicarbonate, calcium-chloride, and magnesium-chloride, and its suitability for drinking and irrigation has been assessed. The present studies made it possible to demarcate areas of contaminated groundwater and those prone to contamination in the near future. Water in the area has deteriorated all along Nakka Vagu up to a maximum distance of 500–700 m from the eastern bank. The groundwater quality in and around Patancheru (to a depth of 30 m) has become hazardous. Some possible remedial measures are suggested. Electronic Publication     

Depth of the base of the Jackson aquifer, based on geophysical exploration, southern Jackson Hole, Wyoming, USA

 A geophysical survey was conducted to determine the depth of the base of the water-table aquifer in the southern part of Jackson Hole, Wyoming, USA. Audio-magnetotellurics (AMT) measurements at 77 sites in the study area yielded electrical-resistivity logs of the subsurface, and these were used to infer lithologic changes with depth. A 100–600 ohm-m geoelectric layer, designated the Jackson aquifer, was used to represent surficial saturated, unconsolidated deposits of Quaternary age. The median depth of the base of the Jackson aquifer is estimated to be 200 ft (61 m), based on 62 sites that had sufficient resistivity data. AMT-measured values were kriged to predict the depth to the base of the aquifer throughout the southern part of Jackson Hole. Contour maps of the kriging predictions indicate that the depth of the base of the Jackson aquifer is shallow in the central part of the study area near the East and West Gros Ventre Buttes, deeper in the west near the Teton fault system, and shallow at the southern edge of Jackson Hole. Predicted, contoured depths range from 100 ft (30 m) in the south, near the confluences of Spring Creek and Flat Creek with the Snake River, to 700 ft (210 m) in the west, near the town of Wilson, Wyoming. Received, May 1997 · Revised, February 1998 · Accepted, April 1998     

Chemical and isotopic (B, Sr) composition of alluvial sediments as archive of a past hydrothermal outflow

The geochemical and isotopic signature of Quaternary alluvial sediments filling a post-orogenic basin along the Tyrrhenian coasts of Italy (Cornia Plain, Tuscany) was investigated to unravel possible interactions with geothermal fluids from the Larderello geothermal field. Two cores located in the upper (UCP) and lower (LCP) sector of the plain were sampled to depths of up to 80 m. A third core in a neighbouring area not affected by geothermal activity was also sampled (Arno plain at Pisa), and its sediment composition was used as reference. The Cornia sediments (fraction < 65 μm) show high B, Cs and Sb concentrations related to a peculiar chemical enrichment of the clay fraction. They also show remarkable enrichments in As (up to 1000 μg g^− 1) reflecting a contribution from local ore deposits.⁸⁷Sr/⁸⁶Sr ratios, ranging from 0.71022 to 0.71698, reveal the nature of the weathered mother rocks of the alluvial sediments, whereas the boron isotopic composition, varying from − 20‰ to − 10‰, suggests an interaction between the clay fraction and boron-rich fluids at temperatures greater than 50 °C. This implies that hydrothermal fluids widely circulated within the Cornia basin in the past, ultimately leading to the geochemical anomalies currently recorded in local sediments.Although natural (geogenic) in origin, these anomalies cause severe problems to the regional water management (groundwater exploitation) through leaching of trace elements into circulating groundwater, a phenomenon which has to be carefully studied and monitored.     

Using hydrochemistry and environmental isotopes in the assessment of groundwater quality in the Euphrates alluvial aquifer,Syria

Hydrochemical and environmental isotope methods were used to characterize the groundwater quality in ten wells belonging to the Euphrates alluvial aquifer in Syria, with the aim to assess the origin and dynamic of groundwater salinization in this system. The Euphrates River (ER) water along its entire course in Syria is rather fresh (TDS < 0.5 g/L), and thus, it is suitable for drinking and irrigation purposes. Groundwater salinity progressively increases from north to south, changing from almost freshwater (TDS < 0.6 g/L), with a Ca–Mg and HCO₃ type near the Syrian–Turkish border to brackish water (1 < TDS < 3 g/L), with a Ca–Mg or Na–Ca–Mg and SO₄–HCO₃ type in the vicinity of Al-Raqqa, and hence it can safely be used for irrigation. Downstream Deir-Ezzor the groundwater quality becomes fairly saline to very saline (3 < TDS < 29 g/L), with a Na–Cl type, and therefore it has an absolute hazard (SAR > 5) for irrigation uses. This pattern of chemical evolution, which is also clearly reflected in the variations of groundwater ionic ratios, completely agrees with the thermodynamic simulation results obtained by an experimental evaporation essay of a water sample taken from the ER near Deir-Ezzor. Stable isotopes permit the distinction between three main evaporation processes: under high, intermediate and low humidity conditions. Radioisotopes (³H and ¹⁴C) indicate the recent age and renewability of groundwater in this aquifer and confirm that its origin is entirely belonged to the ER water, either by direct bilateral interconnection or by vertical infiltration of the irrigation water totally taken from the ER. Relationships between major ions and δ¹⁸O values of the groundwater allow to differentiate between two main enrichment processes: either evaporation only or evaporation plus dissolution, that can explain altogether the development of groundwater salinity in such a dry area.     

Holocene environment and subsistence patterns near the Tree Shelter, Red Sea Mountains, Egypt

The Tree Shelter site dates to the Early to Mid-Holocene (8000 to 4900 ¹⁴C yr BP). Present conditions around the site are hyperarid, but charcoal remains indicate less severe aridity at the time of its occupation. The environment around the site then supported a rich wadi vegetation, which allowed hunting during the Epipaleolithic and herding during the Neolithic occupation. Although more favorable than today, the environmental conditions also displayed a desert character and seem to have limited the range of domestic herbivores introduced in the area.     

Uranium isotopic evidence for the origin of the Bahariya iron deposits, Egypt

The economic iron ore deposits of Egypt are located at Bahariya Oasis in the Lower Middle Eocene limestone. The main iron minerals are goethite, hematite, siderite, pyrite, and jarosite. Manganese minerals are pyrolusite and manganite. Gangue minerals are barite, glauconite, gibbsite, alunite, quartz, halite, kaolinite, illite, smectite, palygorskite, and halloysite. Geochemical comparison between the ore and the Nubia sandstone showed that the ore is depleted in the residual elements (Al, Ti, V, and Ni) and enriched in the mobile elements (Fe, Mn, Zn, Ba, and U) which indicates that the Bahariya iron ore is not a lateritic deposit despite the deep weathering in this area. On the other hand, the Nubia sandstone showed depletion in the mobile elements, which demonstrates the leaching process in the Nubia Aquifer. The presence of such indicator minerals as jarosite, alunite, glauconite, gibbsite, palygorskite, and halloysite indicate that the ore was deposited under strong acidic conditions in fresh water.Isotopic analyses of the uranium in the amorphous and crystalline phases of the ore, in the country rocks, and dissolved in the Nubia Aquifer water, all support the conclusion that U and Fe were precipitated together from warm ascending groundwater. U and Fe display strong co-variation in the ore, and the ²³⁴U/²³⁸U activity ratio of the newly precipitated U in the country rock and the leached component of U in the groundwater are identical. There is only slightly more uranium in the amorphous phase than in the crystalline and only a slightly lower ²³⁴U/²³⁸U activity ratio, suggesting that the iron in the two phases have a similar origin. Comparison of the excess ²³⁴U in the water and in the total ore leads to the conclusion that the precipitation of the U, and by inference the iron, occurred within the last million years. However, that both precipitation and leaching of U have occurred over the last 300,000 years is evidenced by the extreme ²³⁰Th/²³⁴U disequilibria observed in some of the samples. Some of the amorphous depositional events have been very recent, perhaps within the last 10,000 years.     

Groundwater recharge and flow in the Lower Cretaceous Nubian Sandstone aquifer in the Sinai Peninsula, using isotopic techniques and hydrochemistry

The present work was conducted in the Sinai Peninsula (1) to identify the recharge and flow characteristics and to evaluate the continuity of the Lower Cretaceous Nubian Sandstone aquifer; and (2) to provide information for the aquifer's rational appraisal. Isotopic and hydrochemical compositions combined with the geological and hydrogeological settings were used for this purpose. A considerable depletion in isotopic content (oxygen-18 and deuterium) and low d-excess values exist in the studied groundwater, reflecting the contribution of old meteoric water that recharged the aquifer in pluvial times. Modern recharge also occurs from precipitation that falls on the aquifer outcrops. The wide scatter of the data points around the two meteoric lines, the global meteoric water line (GMWL) and Mediterranean meteoric water line (MMWL), in the δ¹⁸O–δD diagram indicates considerable variation in recharge conditions (amount, altitude, temperature, air masses, distances from catchment, overland flow, etc.). The isotopic composition in the El-Bruk area is minimum (¹⁸O=–9.53‰), very close to the average value of the Western Desert Nubian Sandstone (¹⁸O=–10‰), where the local structural and lithologic conditions retard groundwater flow and the main bulk of water becomes noncyclic. The continuity of the aquifer in northern and central Sinai is evidenced by the isotopic similarity between samples taken from above and below the central Sinai Ragabet El-Naam fault, the distribution of potentiometric head, and hydrogeological cross sections. The combination of isotopic composition in terms of ¹⁸O and chemical composition in terms of TDS and salt contents is the basis for separating the studied groundwater into groups that reflect the recharge sources and isotopic and chemical modifications during flow. Electronic Publication     

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.     

Application of major and trace elements as well as boron isotopes for tracing hydrochemical processes: the case of Trifilia coastal karst aquifer,Greece

The Trifilia karst aquifer presents a complex hydrochemical character due to the intricate geochemical processes that take place in the area. Their discernment was achieved by using the chemical analyses of major, trace elements and boron isotopes. Major ion composition indicates mixing between seawater and freshwater is occurring. Five hydrochemical zones corresponding to five respective groundwater types were distinguished, in which the chemical composition of groundwater is influenced mainly due to the different salinization grade of the aquifer. The relatively increased temperature of the aquifer indicates the presence of hydrothermal waters. Boron isotopes and trace elements indicate that the intruding seawater has been hydrothermally altered, as it is shown by the δ¹¹B depleted signature and the increased concentrations of Li and Sr. Trace elements analyses showed that the groundwater is enriched in various metallic elements, which derive from the solid hydrocarbons (bitumens), contained in the carbonate sediments of the Tripolis zone. The concentration of these trace elements depends on the redox environment. Thus, in reductive conditions As, Mn, Co and NH₄ concentrations are high, in oxidized conditions the V, Se, Mo, Tl and U concentration increases while Ni is not redox sensitive and present high concentration in both environments.