Identification of groundwater recharge sources and processes in a heterogeneous alluvial aquifer: results from multi‐level monitoring of hydrochemistry and environmental isotopes in a riverside agricultural area in Korea

We evaluated sources and pathways of groundwater recharge for a heterogeneous alluvial aquifer beneath an agricultural field, based on multi‐level monitoring of hydrochemistry and environmental isotopes of a riverside groundwater system at Buyeo, Korea. Two distinct groundwater zones were identified with depth: (1) a shallow oxic groundwater zone, characterized by elevated concentrations of NO₃^? and (2) a deeper (>10–14 m from the ground surface) sub‐oxic groundwater zone with high concentrations of dissolved Fe, silica, and HCO₃^?, but little nitrate. The change of redox zones occurred at a depth where the aquifer sediments change from an upper sandy stratum to a silty stratum with mud caps. The δ¹⁸O and δ²H values of groundwater were also different between the two zones. Hydrochemical and δ¹⁸O? δ²H data of oxic groundwater are similar to those of soil water. This illustrates that recharge of oxic groundwater mainly occurs through direct infiltration of rain and irrigation water in the sandy soil area where vegetable cropping with abundant fertilizer use is predominant. Oxic groundwater is therefore severely contaminated by agrochemical pollutants such as nitrate. In contrast, deeper sub‐oxic groundwater contains only small amounts of dissolved oxygen (DO) and NO₃^?. The ³H contents and elevated silica concentrations in sub‐oxic groundwater indicate a somewhat longer mean residence time of groundwater within this part of the aquifer. Sub‐oxic groundwater was also characterized by higher δ¹⁸O and δ²H values and lower d‐excess values, indicating significant evaporation during recharge. We suggest that recharge of sub‐oxic groundwater occurs in the areas of paddy rice fields where standing irrigation and rain water are affected by strong evaporation, and that reducing conditions develop during subsequent sub‐surface infiltration. This study illustrates the existence of two groundwater bodies with different recharge processes within an alluvial aquifer. Copyright © 2009 John Wiley & Sons, Ltd.     

A Geochemical Approach to Determine Sources and Movement of Saline Groundwater in a Coastal Aquifer

Geochemical evaluation of the sources and movement of saline groundwater in coastal aquifers can aid in the initial mapping of the subsurface when geological information is unavailable. Chloride concentrations of groundwater in a coastal aquifer near San Diego, California, range from about 57 to 39,400 mg/L. On the basis of relative proportions of major‐ions, the chemical composition is classified as Na‐Ca‐Cl‐SO₄, Na‐Cl, or Na‐Ca‐Cl type water. δ²H and δ¹⁸O values range from ?47.7‰ to ?12.8‰ and from ?7.0‰ to ?1.2‰, respectively. The isotopically depleted groundwater occurs in the deeper part of the coastal aquifer, and the isotopically enriched groundwater occurs in zones of sea water intrusion. ⁸⁷Sr/⁸⁶Sr ratios range from about 0.7050 to 0.7090, and differ between shallower and deeper flow paths in the coastal aquifer. ³H and ¹⁴C analyses indicate that most of the groundwater was recharged many thousands of years ago. The analysis of multiple chemical and isotopic tracers indicates that the sources and movement of saline groundwater in the San Diego coastal aquifer are dominated by: (1) recharge of local precipitation in relatively shallow parts of the flow system; (2) regional flow of recharge of higher‐elevation precipitation along deep flow paths that freshen a previously saline aquifer; and (3) intrusion of sea water that entered the aquifer primarily during premodern times. Two northwest‐to‐southeast trending sections show the spatial distribution of the different geochemical groups and suggest the subsurface in the coastal aquifer can be separated into two predominant hydrostratigraphic layers.     

Estimating groundwater residence time and recharge patterns in a saline coastal aquifer

A detailed study using environmental tracers such as chloride (Cl^?) and tritium (³H), deuterium (²H) and oxygen (¹⁸O) isotopes was performed in an alluvial coastal aquifer in two contrasting environments (urban and agricultural). These environmental tracers combined with a high‐resolution multi‐level sampling approach were used to estimate groundwater residence time and recharge patterns and to validate the hydrogeochemical conceptual model already proposed in previous studies. δ¹⁸O and δ²H combined with Cl^? data proved that the hypersaline groundwater present in the deepest part of the aquifer was sourced from the underlying hypersaline aquitard via an upward flux. Both chemical and isotopic data were employed to calibrate a density‐dependent numerical model based on SEAWAT 4.0, where ³H and Cl^? were helped quantifying solutes transport within the modelled aquifer. Model results highlighted the differences on estimated recharge in the two contrasting environments, with the urban one exhibiting concentrated recharge because of preferential infiltration associated to the storm water drains network, while scarce local recharge characterized the agriculture setting. In the urban field site, is still possible to recognize at 9 m b.g.l. the input of the atmospheric anthropogenic ³H generated by testing of thermonuclear weapons, while in the agricultural field site, the ³H peak has been washed out at 6 m b.g.l. because the groundwater circulation is restricted only to the upper fresh part of the aquifer, drained by the reclamation system. The presented approach that combined high‐resolution field monitoring, environmental tracers and numerical modelling, resulted effective in validating the conceptual model of the aquifer salinization. Copyright © 2016 John Wiley & Sons, Ltd.     

Groundwater–surface water interactions in a large semi‐arid floodplain: implications for salinity management

Flow regulation and water diversion for irrigation have considerably impacted the exchange of surface water between the Murray River and its floodplains. However, the way in which river regulation has impacted groundwater–surface water interactions is not completely understood, especially in regards to the salinization and accompanying vegetation dieback currently occurring in many of the floodplains. Groundwater–surface water interactions were studied over a 2 year period in the riparian area of a large floodplain (Hattah–Kulkyne, Victoria) using a combination of piezometric surface monitoring and environmental tracers (Cl⁻, δ²H, and δ¹⁸O). Despite being located in a local and regional groundwater discharge zone, the Murray River is a losing stream under low flow conditions at Hattah–Kulkyne. The discharge zone for local groundwater, regional groundwater and bank recharge is in the floodplain within ∼1 km of the river and is probably driven by high rates of transpiration by the riparian Eucalyptus camaldulensis woodland. Environmental tracers data suggest that the origin of groundwater is principally bank recharge in the riparian zone and a combination of diffuse rainfall recharge and localized floodwater recharge elsewhere in the floodplain. Although the Murray River was losing under low flows, bank discharge occurred during some flood recession periods. The way in which the water table responded to changes in river level was a function of the type of stream bank present, with point bars providing a better connection to the alluvial aquifer than the more common clay‐lined banks. Understanding the spatial variability in the hydraulic connection with the river channel and in vertical recharge following inundations will be critical to design effective salinity remediation strategies for large semi‐arid floodplains. Copyright © 2005 John Wiley & Sons, Ltd.     

Groundwater evolution and mean water age inferred from hydrochemical and isotopic tracers in a tropical confined aquifer

The coastal confined aquifer in the Gulf of Urabá (Colombia) is an important water source for the banana agro‐industry as well as for urban and rural communities. However, the main processes controlling recharge and mixing in the aquifer are still poorly understood. Hydrochemical analyses and stable isotope monitoring were conducted to (a) determine groundwater recharge origin, mean groundwater age, and the main processes governing groundwater chemistry and the potential mixing of marine water and the influence of diffusive processes from the two surrounding aquitard layers. Hydrochemical data indicate that the main processes affecting the dissolved chemical composition include cation exchange, dissolution of carbonated and CO₂, and silicate weathering. δ¹⁸O and δ²H compositions combined with ¹⁴C data highlight the differences in climatic conditions between the recharge zone and the confined section of the aquifer, which is close to the Atlantic Ocean. Groundwater samples with ¹⁴C ages from recent to 28,300 years BP show a depleted isotopic trend ranging from ?6.43‰ to ?9.14‰ in δ¹⁸O and from ?43.2‰ to ?65.7‰ in δ²H. The most depleted δ¹⁸O and δ²H compositions suggest a cooler recharge climate than the current conditions (corresponding to the last glacial period of the late Pleistocene). Depleted δ¹³C values in the total dissolved inorganic carbon indicate the existence of organic material oxidation processes within the geologic formation. These results can be used or transferred to enhance groundwater modelling efforts in other confined coastal aquifers of South America where scarcity of long‐term monitoring data limits water resources planification under a changing climate.     

Sulfur Hexafluoride and Potassium Bromide as Groundwater Tracers for Managed Aquifer Recharge

Sulfur hexafluoride (SF₆) is an established tracer for use in managed aquifer recharge projects. SF₆ exsolves from groundwater when it encounters trapped air according to Henry's law. This results in its retardation relative to groundwater flow, which can help determine porous media saturation and flow dynamics. SF₆ and the conservative, nonpartitioning tracer, bromide (Br⁻ added as KBr), were introduced to recharge water infiltrated into stacked glacial aquifers in Thurston County, Washington, providing the opportunity to observe SF₆ partitioning. Br⁻, which is assumed to travel at the same velocity as the groundwater, precedes SF₆ at most monitoring wells (MWs). Average groundwater velocity in the unconfined aquifer in the study area ranges from 3.9 to 40 m/d, except in the southwestern corner where it is slower. SF₆ in the shallow aquifer exhibits an average retardation factor of 2.5 ± 3.8, suggesting an air-to-water ratio on the order of 10⁻³ to 10⁻² in the pore space. Notable differences in tracer arrival times at adjacent wells indicate very heterogeneous conductivity. One MW exhibits double peaks in concentrations of both tracers with different degrees of retardation for the first and second peaks. This suggests multiple flowpaths to the well with variable saturation. The confining layer between the upper two aquifers appears to allow intermittent connection between aquifers but serves as an aquitard in most areas. This study demonstrates the utility of SF₆ partitioning for evaluating hydrologic conditions at prospective recharge sites.     

Chemical and isotopic methods for management of artificial recharge in Mazraha Station (Damascus Basin,Syria)

Artificially enhancing recharge rate into groundwater aquifer at specially designed facilities is an attractive option for increasing the storage capacity of potable water in arid and semi‐arid region such as Damascus basin (Syria). Two dug wells (I and II) for water injection and 24 wells for water extraction are available in Mazraha station for artificial recharge experiment. Chemical and stable isotopes (δ²H and δ¹⁸O) were used to evaluate artificial recharge efficiency. 400 to 500*10³ m³ of spring water were injected annually into the ambient shallow groundwater in Mazraha station, which is used later for drinking purpose. Ambient groundwater and injected spring water are calcium bicarbonate type with EC about 880 ± 60 μS/cm and 300 ± 50 μS/cm, respectively. The injected water is under saturated versus calcite and the ambient groundwater is over saturated, while the recovered water is near equilibrium. It was observed that the injection process formed a chemical dilution plume that improves the groundwater quality. Results demonstrate that the hydraulic conductivity of the aquifer is estimated around 6.8*10^?4 m/s. The effective diameter of artificial recharge is limited to about 250 m from the injection wells. Mixing rate of 30% is required in order to reduce nitrate concentration below 50 mg/l which is considered the maximum concentration limit for potable water. Deuterium and oxygen‐18 relationship demonstrates that mixing line between injected water and ambient groundwater has a slope of 6.1. Oxygen‐18 and Cl^? plot indicates that groundwater salinity origin is from mixing process, and no dissolution and evaporation were observed. These results demonstrate the efficiency of the artificial recharge experiments to restore groundwater storage capacity and to improve the water quality. Copyright © 2011 John Wiley & Sons, Ltd.     

Using hydrochemical,stable isotope,and river water recharge data to identify groundwater flow paths in a deeply buried karst system

The deeply buried river‐connected Xishan karst aquifer (XKA) in western Beijing, China, has been suffering from diminishing recharge for several decades, which in turn leads to the disappearing of spring water outflows and continuously lowering of groundwater level in the area. Thus, it is important to correctly recognize the groundwater recharge and flow paths for the sustainable development of the XKA. To investigate these issues, the hydrochemical and isotopic compositions are analysed for both surface water and groundwater samples collected over an area of about 280 km². Results show that (a) the river water is characterized by high Na contents; (b) the δ²H and δ¹⁸O values in the river water are distinctively higher than those of groundwater samples, after experiencing the long‐time evaporative enrichment in the upstream reservoir; (c) the Sr concentrations and ⁸⁷Sr/⁸⁶Sr ratios of groundwater clearly indicated the interaction between water and carbonate minerals but excluded the water–silicate interaction; and (d) the groundwater samples in the direct recharge area of the XKA have the lowest Na concentrations and the δ²H and δ¹⁸O values. Based on the large differences in the Na contents and ¹⁸O values of groundwater and surface water, a simple two‐component mixing model is developed for the study area and the fractions of the river water are estimated for groundwater samples. We find that the distribution pattern of the river water fractions in the XKA clearly shows a change of directions in the preferential flow path of the groundwater from its source zone to the discharge area. Overall, our results suggest that the recharged surface water can be a useful evidence for delineating the groundwater flow path in river‐connected karst aquifer. This study improves our understanding of the heterogeneity in karst groundwater systems.     

Stable isotopic and geochemical identification of groundwater evolution and recharge sources in the arid Shule River Basin of Northwestern China

Stable isotopic (δD_VSMOW and δ¹⁸O_VSMOW) and geochemical signatures were employed to constrain the geochemical evolution and sources of groundwater recharge in the arid Shule River Basin, Northwestern China, where extensive groundwater extraction occurs for agricultural and domestic supply. Springs in the mountain front of the Qilian Mountains, the Yumen‐Tashi groundwater (YTG), and the Guazhou groundwater (GZG) were Ca‐HCO₃, Ca‐Mg‐HCO₃‐SO₄ and Na‐Mg‐SO₄‐Cl type waters, respectively. Total dissolved solids (TDS) and major ion (Mg²⁺, Na⁺, Ca²⁺, K⁺, SO₄^2?, Cl^? and NO₃^?) concentrations of groundwater gradually increase from the mountain front to the lower reaches of the Guazhou Basin. Geochemical evolution in groundwater was possibly due to a combination of mineral dissolution, mixing processes and evapotranspiration along groundwater flow paths. The isotopic and geochemical variations in melt water, springs, river water, YTG and GZG, together with the end‐member mixing analysis (EMMA) indicate that the springs in the mountain front mainly originate from precipitation, the infiltration of melt water and river in the upper reaches; the lateral groundwater from the mountain front and river water in the middle reaches are probably effective recharge sources for the YTG, while contribution of precipitation to YTG is extremely limited; the GZG is mainly recharged by lateral groundwater flow from the Yumen‐Tashi Basin and irrigation return flow. The general characteristics of groundwater in the Shule River Basin have been initially identified, and the results should facilitate integrated management of groundwater and surface water resources in the study area. Copyright © 2015 John Wiley & Sons, Ltd.     

Complementary use of dating and hydrochemical tools to assess mixing processes involving centenarian groundwater in a geologically complex alpine karst aquifer

Environmental dating tracers (³H, ³He, ⁴He, CFC-12, CFC-11, and SF₆) and the natural spring response (hydrochemistry, water temperature, and hydrodynamics) were jointly used to assess mixing processes and to characterize groundwater flow in a relatively small carbonate aquifer with complex geology in southern Spain. Results evidence a marked karst behaviour of some temporary outlets, with sharp and rapid responses to precipitation events, while some perennial springs show buffer and delayed variations with respect to recharge periods. The general geochemical evolution shows a pattern, from higher to lower altitudes, in which mineralization and the Mg/Ca ratio rise, evidencing longer water–rock interaction. The large SF₆ concentrations in groundwater suggest terrigenic production, whereas CFC-11 values are affected by sorption or degradation. The groundwater age in the perennial springs—as deduced from CFC-12 and ³H/³He—points to mean residence times of several decades, although the large amount of radiogenic ⁴He in samples indicate a contribution of old groundwater (free of ³H and CFC-12). Lumped parameter models and shape-free models were created based on ³H, tritiogenic ³He, CFC-12, and radiogenic ⁴He data in order to interpret the age distribution of the samples. Results evidence the existence of two mixing components, with an old fraction ranging between 160 and 220 years in age. The correlation of physicochemical parameters with some dating parameters, derived from the mixing models, serves to explain the hydrogeochemical processes occurring within the system. Altogether, long residence times are shown to be possible in small alpine systems with a clearly karst behaviour if the geological setting features highly tectonized media including units with diverse hydrogeological characteristics. These findings highlight the importance of applying different approaches, including groundwater dating techniques, when studying such groundwater flow regimes.     

Insights into groundwater salinization from hydrogeochemical and isotopic evidence in an arid inland basin

In the Manas River basin (MRB), groundwater salinization has become a major concern, impeding groundwater use considerably. Isotopic and hydrogeochemical characteristics of 73 groundwater and 11 surface water samples from the basin were analysed to determine the salinization process and potential sources of salinity. Groundwater salinity ranged from 0.2 to 11.91 g/L, and high salinities were generally located in the discharge area, arable land irrigated by groundwater, and depression cone area. The quantitative contributions of the evaporation effect were calculated, and the various groundwater contributions of transpiration, mineral dissolution, and agricultural irrigation were identified using hydrogeochemical diagrams and δD and δ¹⁸O compositions of the groundwater and surface water samples. The average evaporation contribution ratios to salinity were 5.87% and 32.7% in groundwater and surface water, respectively. From the piedmont plain to the desert plain, the average groundwater loss by evaporation increased from 7% to 29%. However, the increases in salinity by evaporation were small according to the deuterium excess signals. Mineral dissolution, transpiration, and agricultural irrigation activities were the major causes of groundwater salinization. Isotopic information revealed that river leakage quickly infiltrated into aquifers in the piedmont area with weak evaporation effects. The recharge water interacted with the sediments and dissolved minerals and subsequently increased the salinity along the flow path. In the irrigation land, shallow groundwater salinity and Cl^? concentrations increased but not δ¹⁸O, suggesting that both the leaching of soil salts due to irrigation and transpiration effect dominated in controlling the hydrogeochemistry. Depleted δ¹⁸O and high Cl^? concentrations in the middle and deep groundwater revealed the combined effects of mixing with paleo‐water and mineral dissolution with a long residence time. These results could contribute to the management of groundwater sources and future utilization programs in the MRB and similar areas.     

Multivariate statistical analysis and environmental isotopes of Amman/Wadi Sir (B2/A7) groundwater,Yarmouk River Basin,Jordan

Multivariate statistical techniques, cluster and factor analyses were applied on the Amman/Wadi Sir groundwater chemistry, Yarmouk River basin, north Jordan. The main objective was to investigate the main processes affecting the groundwater chemical quality and its evolution. The k‐means cluster analysis yields three groups with distinct ionic concentrations. Cluster 1 comprises the vast majority of the sampled wells, and the water that belongs to this cluster can be classified as freshwater. Cluster 2 comprises only 2% of the sampled wells; it has the highest ionic concentration. The water of this cluster can be classified as brackish water. Cluster 3 involves 23% of the sampled wells, and it has total ionic concentration intermediate to that of clusters 1 and 2. Factor analysis yields a three‐factor model, which explains 76.77% of the groundwater quality variation. Factor 1 ‘salinity factor’ involves EC, Na⁺, Cl^‐, SO₄^‐2, K⁺ and Mg⁺² and reflects groundwater salinization because of overpumping. Factor 2 ‘hardness factor’ includes Ca⁺², HCO₃^‐ and the pH value and signifies soil–water/rock interaction. Factor 3 ‘nitrate factor’ involves only NO₃^‐ and points to groundwater contamination because of human activities, mainly untreated wastewater, and crops and animal cultivation in the unconfined portion of the aquifer. Factors 1 and 3 can be described as human‐induced factors, whereas factor 2 can be described as geogenic factor. Factors' scores were mapped to deduce the controlling processes on the groundwater chemistry. Stable isotope composition of ¹⁸O and ²H has revealed that the groundwater is a mixture of two water types. The radioactive isotopes tritium and ¹⁴ C were used to evaluate present day recharge to the aquifer and to estimate the groundwater age, respectively. Present day recharge to the groundwater is taking place in the unconfined portion of the aquifer as it is indicated by the measurable tritium content and low groundwater age. Copyright © 2012 John Wiley & Sons, Ltd.     

Modelling the effects of land‐use change on water and salt delivery from a catchment affected by dryland salinity in south‐east Australia

A comprehensive framework for the assessment of water and salt balance for large catchments affected by dryland salinity is applied to the Boorowa River catchment (1550 km²), located in south‐eastern Australia. The framework comprised two models, each focusing on a different aspect and operating on a different scale. A quasi‐physical semi‐distributed model CATSALT was used to estimate runoff and salt fluxes from different source areas within the catchment. The effects of land use, climate, topography, soils and geology are included. A groundwater model FLOWTUBE was used to estimate the long‐term effects of land‐use change on groundwater discharge. Unlike conventional salinity studies that focus on groundwater alone, this study makes use of a new approach to explore surface and groundwater interactions with salt stores and the stream. Land‐use change scenarios based on increased perennial pasture and tree‐cover content of the vegetation, aimed at high leakage and saline discharge areas, are investigated. Likely downstream impacts of the reduction in flow and salt export are estimated. The water balance model was able to simulate both the daily observed stream flow and salt load at the catchment outlet for high and low flow conditions satisfactorily. Mean leakage rate of about 23·2 mm year^?1 under current land use for the Boorowa catchment was estimated. The corresponding mean runoff and salt export from the catchment were 89 382 ML year^?1 and 38 938 t year^?1, respectively. Investigation of various land‐use change scenarios indicates that changing annual pastures and cropping areas to perennial pastures is not likely to result in substantial improvement of water quality in the Boorowa River. A land‐use change of about 20% tree‐cover, specifically targeting high recharge and the saline discharge areas, would be needed to decrease stream salinity by 150 µS cm^?1 from its current level. Stream salinity reductions of about 20 µS cm^?1 in the main Lachlan River downstream of the confluence of the Boorowa River is predicted. The FLOWTUBE modelling within the Boorowa River catchment indicated that discharge areas under increased recharge conditions could re‐equilibrate in around 20 years for the catchment, and around 15 years for individual hillslopes. Copyright © 2004 John Wiley & Sons, Ltd.     

Hydrodynamic and isotopic investigations for evaluating the mechanisms and amount of groundwater seepage through a rockslide dam

This study addresses the influence of landslide dams on surface water drainage and groundwater flow. In the study area of Scanno Lake and Sagittario River (Central Italy), a limestone rockslide‐avalanche formed a lake, which has an outlet that is occasionally active, showing infiltration into the rockslide dam. Several springs are present at the lake's base and are partly fed by seepage through the rockslide debris. Piezometric surveys, discharge measurements, pumping tests and chemical analyses are tools used to build a conceptual model of the groundwater flow and to evaluate the flow through the rockslide debris. Seasonal water isotopic signatures validate the assumed model, showing a mixing of infiltration recharge and groundwater seepage throughout the rockslide debris. Various recharge areas have been found for springs, pointing out those directly fed by the rockslide debris aquifer. Hypotheses about seasonal groundwater mixing between the regional carbonate aquifer and the rockslide debris aquifer are supported by isotope results. Seasonal changes in groundwater table level due to recharge and surface losses from seasonal outlet have been correlated with isotopic groundwater composition from the rockslide debris aquifer and the downstream springs; this relationship highlights the role of the rockslide dam body on the hydrodynamics of the studied area. Relationships between surface waters and groundwater in the area have been completely understood on the basis of water isotopic fingerprinting, finally obtaining a complete evaluation of groundwater renewable resources and its regimen. Copyright © 2010 John Wiley & Sons, Ltd.     

Groundwater dating with 3H and SF6 in relation to mixing patterns,transport modelling and hydrochemistry

A comprehensive study of a sandy aquifer of deltaic origin in southern Poland included water chemistry, isotopes, dissolved trace gases and transport modelling. Tritium, sulphur hexafluoride (SF₆) and freons (F‐11, F‐12 and F‐113) showed the presence of modern waters in the recharge areas and shallow confined parts of the aquifer. The presence of older Holocene waters farther from the recharge areas was indicated by lack of ³H, SF₆ contents ≤0·02 fmol l⁻¹ and relatively low ¹⁴C values. The discharge from the system is by upward seepage in the valley of a major river. Pre‐Holocene waters of a cooler climate, identified on the basis of δ¹⁸O, δ²H, ¹⁴C, Ne and Ar data, were found in some distant wells. Concentrations of N₂, Ne and Ar determined by gas chromatography were used for calculating the noble gas temperatures, air excess needed for correction of SF₆, and nitrogen content released by denitrification process. The time series of ³H content available for some wells supplied quantitative information on age distributions and the total mean ages of flow through the unsaturated and saturated zones. The derived ³H age distributions turned out to be very wide, with mean values in the range of about 30 to 160 years. For each well with determined ³H age, the SF₆ data showed either a lower age range or the possibility of a lower age as expected due to shorter travel times of SF₆ through the unsaturated zone, which most probably also resulted in different types of age distributions of these tracers. Freons appeared to be of little use for individual age determinations. A quantitative estimation of two‐component mixing from SF₆ ³H relations is not possible unless the travel time of ³H through the unsaturated zone is comparable to that of SF₆. The ratio of integrals of the response function over the age range with tracer and the whole response function yields the ratio of water with tracer to total flow of water. That ratio is a tracer‐dependent function of time. Transport modelling of SF₆ tracer done with MT3D code yielded initially large discrepancies between calculated and measured tracer concentrations. Some discrepancies remained even after calibration of the transport model with SF₆. Simulation of tritium contents with a calibrated transport model yielded reasonable agreement with measured contents in some wells and indicated a need for further investigations, particularly in the eastern part of the aquifer. The existence of distinct hydrochemical zones is consistent with the tracer data; young waters with measurable ³H and SF₆ contents are aerobic and of HCO₃ Ca or HCO₃ SO₄ Ca types. Slightly elevated Na and Cl contents, as well as the highest concentrations of SO₄ and NO₃ within this zone are due to anthropogenic influences. Anaerobic conditions prevail in the far field, under the confining cover, where pre‐bomb era Holocene waters dominate. In that zone, dissolved oxygen, NO₃ and U contents are reduced, and Fe, Mn and NH₄ contents increase. In the third zone, early Holocene and glacial waters occur. They are of HCO₃ Ca Na or HCO₃ Na types, with TDS values higher than 1 g l⁻¹ and Na content higher than 200 mg l⁻¹, due to either small admixtures of ascending or diffusing older water or freshening of marine sediments, a process that is probably occurring till the present time. Copyright © 2005 John Wiley & Sons, Ltd.     

Evaluation of nitrate levels in groundwater under agricultural fields in two pilot areas in central Chile: A hydrogeological and geochemical approach

The aim of this study is to evaluate the impact of the application of industrial fertilizers and liquid swine manure in groundwater in two pilot agricultural areas, San Pedro and Pichidegua, which have been under long‐term historic use of fertilizers. A comprehensive hydrogeological investigation was carried out to define the geology and the groundwater flow system. Chemical and isotopic tools were used to evaluate the distribution and behavior of the nitrate in the groundwater. The isotopic tools included δ¹⁸O, δ²H, and ³H, which provide information about the origin and residence time of the groundwater; δ¹⁵N‐NO₃^? and δ¹⁸O‐NO₃^?, which provide information about nitrate sources and processes that can affect nitrate along the groundwater flow system. The application rate of liquid manure and other fertilizers all together with land uses was also evaluated. The hydrogeological investigation identified the presence of a confined aquifer underneath a thick low‐permeability aquitard, whose extension covers most of the two study areas. The nitrate concentration data, excepting a few points in zones located near recharge areas in the upper part of the basins and lower areas at the valley outlets (San Pedro), showed nitrate concentration below 10 mgN/L at the regional scale. The isotope data for nitrate showed no influence of the liquid swine manure in the groundwater at the regional scale, except for the high part of the basins and the outlet of the San Pedro valley, which are areas fertilized by manure. This data showed that the regional aquifer on both pilot study areas is protected by the thick low‐permeability aquitard, which is playing an important role on nitrate attenuation. Evidence of denitrification was also found on both shallow and deep groundwater in the Pichidegua site. This study showed that a comprehensive hydrogeological characterization complemented by chemical and isotope data is key for understanding nitrate distribution and concentration in aquifers from areas with intensive agriculture activities.     

Forest fire effects on groundwater in a coastal aquifer (Ravenna,Italy)

We examined the fire‐induced changes in groundwater recharge rate. This aspect is particularly important in the case of large forested areas growing over a coastal aquifer affected by saltwater intrusion. In the Ravenna coastal area (Italy), pine forests grow on coastal dune belts, overlying a sandy unconfined aquifer, which is strongly affected by marine ingression. Three groundwater profiles across the forest and perpendicular to the coastline were monitored for groundwater level, physical, and chemical parameters. The aims were to define groundwater quality, recharge rate, freshwater volume, and highlight change, which occurred after a forest fire with reference to pre‐fire conditions. Analytical solutions based on Darcy Law and the Dupuit Equation were applied to calculate unconfined flow and compare recharge rates among the profiles. The estimated recharge rates increased in the partially and completely burnt areas (219 and 511 mm year^?1, respectively) compared with the pristine pine forest area (73 mm year^?1). Although pre‐fire conditions were similar in all monitored profiles, a post‐fire decrease in salinity was observed across the burnt forest, along with an increase in infiltration and freshwater lens thickness. This was attributed to decrease canopy interception and evapotranspiration caused by vegetation absence after the fire. This research provided an example of positive forest fire feedback on the quantity and quality of fresh groundwater resources in a lowland coastal aquifer affected by saltwater intrusion, with limited availability of freshwater resources. The fire provided an opportunity to evaluate a new forest management approach and consider the restoration and promotion of native dune herbaceous vegetation.     

Geochemistry and Provenance of Springs in a Baja California Sur Mountain Catchment

Fractured rock aquifers cover much of Earth's surface and are important mountain sites for groundwater recharge but are poorly understood. To investigate groundwater systematics of a fractured-dominated aquifer in Baja California Sur, Mexico, we examined the spatial patterns of aquifer recharge and connectivity using the geochemistry of springs. We evaluate a range of geochemical data within the context of two endmember hypotheses describing spatial recharge patterns and fracture connectivity. Hypothesis 1 is that the aquifer system is segmented, and springs are fed by local recharge. Hypothesis 2 is that the aquifer system is well connected, with dominant recharge occurring in the higher elevations. The study site is a small <15 km² catchment. Thirty-four distinct springs and two wells were identified in the study area, and 24 of these sites were sampled for geochemical analyses along an elevation gradient and canyon transect. These analyses included major ion composition, trace element and strontium isotopes, δ¹⁸O and δ²H isotopes, radiocarbon, and tritium. δ¹⁸O and δ²H isotopes suggest that the precipitation feeding the groundwater system has at least two distinct sources. Carbon isotopes showed a change along the canyon transect, suggesting that shorter flowpaths feed springs in the top of the transect, and longer flowpaths discharge near the bottom. Geochemical interpretations support a combination of the two proposed hypotheses. Understanding of the connectivity and provenance of these springs is significant as they are the primary source of water for the communities that inhabit this region and may be impacted by changes in recharge and use.     

Groundwater flow modelling of Kwa Ibo River watershed,southeastern Nigeria

Groundwater flow modelling of the Kwa Ibo River watershed in Abia State of Nigeria is presented in this paper with the aim of assessing the degree of interaction between the Kwa Ibo River and the groundwater regime of the thick sandy aquifer. The local geology of the area comprises the Quaternary to recent Benin Formation. Potential aquifer zones that were delineated earlier using geoelectrical resistivity soundings and borehole data for the area formed the basis for groundwater flow modelling. The watershed has been modelled with a grid of 65 rows by 43 columns and with two layers. Lateral inflow from the north has been simulated with constant heads at the Government College, Umuahia, and outflow at Usaka Elegu in the south. The Kwa Ibo River traverses the middle of the watershed from north to south. The river‐stage data at Umudike, Amawom, Ntalakwu and Usaka Elegu have been used for assigning surface water levels and riverbed elevations in the model. Permeability distribution was found to vary from 3 to 14·5 m day^?1. Natural recharge due to rainfall formed the main input to the aquifer system, and abstraction from wells was the main output. A steady‐state groundwater flow simulation was carried out and calibrated against the May 1980 water levels using 26 observation wells. The model computations have converged after 123 iterations. Under the transient‐state calibration, the highest rainfall (and hence groundwater recharge) over the 10‐year study period was recorded in 1996, whereas the lowest was recorded in 1991. The computed groundwater balance of 55 274 m³ day^?1 was comparable to that estimated from field investigations. Results from the modelling show that abstraction is much less than groundwater recharge. Hence there is the possibility for additional groundwater exploitation in the watershed through drilling of boreholes. Copyright © 2008 John Wiley & Sons, Ltd.     

Recharge and mineralization of groundwater of the Upper Cretaceous aquifer in Orontes basin,Syria

Abstract

Chemical and isotopic data of groundwater of the Upper Cretaceous aquifer in the Orontes basin, Syria, have been used to assess the groundwater geochemistry, the origin of groundwater recharge and groundwater residence time. The chemical data indicate that dissolution of evaporite minerals is the main process controlling groundwater mineralization. The composition of stable isotopes δ¹⁸O and δ²H, together with ¹⁴C activity, reflect the existence of three different groups: (a) groundwater in the Coastal Mountains with δ¹⁸O of –6.65‰, quite similar to modern-day precipitation, and high ¹⁴C (>50 pmC); (b) groundwater in the unconfined aquifer of the Hama Uplift, which has δ¹⁸O of –5.52‰ and ¹⁴C near 20 pmC, and is recharged locally; and (c) groundwater from the confined aquifer of the Homs Depression, which is characterized by more depleted δ¹⁸O,, –8.01‰, and low ¹⁴C (<7 pmC), and might be recharged in the northern piedmont of the Anti-Lebanon Mountains. The distinctive isotope signatures of the latter two groups indicate different recharge elevations and palaeoclimatic effects. The low recharge rate of the groundwater in the Hama Uplift aquifer, and the even slower recharge rate in the Homs Depression aquifer, are reflected by groundwater ¹⁴C residence times of 5 and over 22 Ka BP, respectively.

Editor D. Koutsoyiannis

Citation Al-Charideh, A., 2013. Recharge and mineralization of groundwater of the Upper Cretaceous aquifer in Orontes basin (Syria). Hydrological Sciences Journal, 58 (2), 452–467.