Environmental isotopic study on the recharge and residence time of groundwater in the Heihe River Basin, northwestern China

The recharge and origin of groundwater and its residence time were studied using environmental isotopic measurements in samples from the Heihe River Basin, China. δ¹⁸O and δD values of both river water and groundwater were within the same ranges as those found in the alluvial fan zone, and lay slightly above the local meteoric water line (δD=6.87δ¹⁸O+3.54). This finding indicated that mountain rivers substantially and rapidly contribute to the water resources in the southern and northern sub-basins. δ¹⁸O and δD values of groundwater in the unconfined aquifers of these sub-basins were close to each other. There was evidence of enrichment of heavy isotopes in groundwater due to evaporation. The most pronounced increase in the δ¹⁸O value occurred in agricultural areas, reflecting the admixture of irrigation return flow. Tritium results in groundwater samples from the unconfined aquifers gave evidence for ongoing recharge, with mean residence times of: less than 36 years in the alluvial fan zone; about 12–16 years in agricultural areas; and about 26 years in the Ejina oasis. In contrast, groundwater in the confined aquifers had ¹⁴C ages between 0 and 10 ka BP.     

Étude du fonctionnement du système aquifére karstique Cénomano-Turonien de l'oued Igrounzar, bassin d'Essaouira, Maroc

In the Meskala-Kourimat area, the Bouabout Syncline aquifer system, intersected by the Igrounzar Wadi, feeds most of the karstic sources of the region. This aquifer is contained within Cenomanian and Turonian limestones and dolomitic limestones. The base of the system corresponds to the lower Cenomanian grey clays, and the top to the Senonian white marls. Hydrodynamic studies of various springs shows that each water source is different from the other, indicating a heterogeneous underground reservoir belonging to a complex karst system. The springs waters show a large chemical variability in space and time. These waters are a mixture of chloride, sulphate, Na and Mg. High Mg contents of some springs result from dissolution of evaporite, confirmed by low Ca/Mg ratios. The total dissolved solids (TDS) in spring water increases from upstream to downstream, probably as a response to residency time, but also due to interaction with Cenomanian evaporites. However, the springs are good for drinking water, as well as for irrigation. The monthly survey of selected springs indicated a large chemical variability but with little or no correlation between discharge and TDS.Stable isotope data (¹⁸O) suggests that the altitude of the recharge area, for this aquifer system, is 1200 m. The ¹⁸O gradient versus altitude, established on springs whose recharge areas are well known is, −0.25% versus SMOW/100 m. When compared with the ‘Meteoric Water Line’ established on worldwide spring water whose recharge areas are well known, the Essaouira Basin shows rain recharge without any significant evaporation.     

Isotopic,hydrologic and geomorphologic approach for the rejuvenation of few drying springs in mountainous region of Dhouli Rao and Kandela,Himachal Pradesh,India

Springs are the only available source of water for domestic and agricultural use in mountainous regions of Dhouli Rao and Kandela in the Sirmaur district of Himachal Pradesh, India. These springs are mainly gravity, contact or fracture and solution tubular (Karst) type. Drying of springs during summer causes much hardship to the inhabitants of this region. Hence, environmental isotopes (²H, ¹⁸O, ³H) were employed along with hydrogeochemistry and geomorphology to identify the recharge zones of the drying springs. From the stable isotope data of rainwater, the altitude effect was estimated (?0.3?‰ for δ¹⁸O per 100 m elevation) and used to determine the recharge zones of the drying springs (+1,000 to +1,430 m amsl). The geo-morphological setting of the valley indicated that either check dam, contour bunding or levees structures with gabion method of rainwater conservation can be implemented to augment the recharge of the springs.     

Coupling isotopic and piezometric data to infer groundwater recharge mechanisms in arid areas: example of Samail Catchment,Oman

Hydrochemistry and well hydrographs are coupled to assess groundwater recharge in the regional catchment of Samail, Oman. The complex geology comprises three aquifers: limestones of the Hajar Supergroup (HSG) at the highlands of North Oman Mountains (NOM); fractured/weathered ophiolites; and Quaternary alluvium. Groundwater flows south–north from the NOM to the coast. Samples from groundwater wells and springs (38) were analyzed for isotopes and major ions. Corrected ¹⁴C dating reveals modern groundwater across the entire catchment, while ⁸⁷Sr/⁸⁶Sr (0.70810–0.70895) shows greater homogeneity. Groundwater in the upper catchment is depleted in ²H and ¹⁸O, indicating a high-altitude recharge source (NOM), and becomes enriched downstream, with a slope indicating an evaporation effect. The hydrographs of nested piezometers located in the upper, middle and lower catchment show different recharge responses between deep and shallower depths. Head difference in response to recharge is observed upstream, suggesting a lateral recharge mechanism, contrary to vertical recharge downstream reflected in identical recharge responses. The homogeneous ⁸⁷Sr/⁸⁶Sr ratio, head changes, downstream enrichment of ²H and ¹⁸O, and the presence of modern groundwater throughout the catchment suggest that groundwater recharge takes place across the entire catchment and that the three aquifers are hydraulically connected. The recharge estimated using the chloride mass balance method is in the range of 0–43% of the mean annual rainfall.     

Milankovitch cyclicity in Purbeck peritidal limestones of the Prebetic (Berriasian, southern Spain)

Peritidal carbonate rocks (Purbeck facies) of the uppermost Portlandian to Berriasian in the type section of the Sierra del Pozo Formation in the Prebetic Zone, southern Spain, are divisible into 141 shallowing upward cycles averaging 2 m in thickness. The subtidal facies in these cycles consist of micritic or marly limestones with dasycladacean algae and lituolids; the intertidal facies are micritic limestones containing birdseyes and miliolids; the supratidal facies comprise laminated algal limestones, the tops of which display desiccation cracks and rhizocretions, or more locally palaeosols, calcretes, or palaeokarst surfaces. A statistical study, using power spectra of the Fast Fourier Transform, demonstrates that the periodicity of these cycles is in the Milankovitch frequency band. Most sedimentary cycles correspond to the obliquity cycles; eccentricity and precession cycles have also been recognized. Using a Fischer plot, third-order tectono-eustatic cycles are recognized, which can be correlated with the eustatic curve of the Exxon chart. The shallowing upward sequences are characterized by a distinctive pattern of geochemical parameters. Carbon and oxygen isotopic (δ¹³C and δ¹⁸O) variations, calcium and magnesium carbonate contents and the abundance of organic matter and trace elements (Mn and Sr) all have predictable patterns of distribution within the sequences. The Sr content of the subtidal facies is relatively high whereas the δ¹³C and δ¹⁸O ratios are quite low; in the intertidal facies the Sr and Mn levels fall concomitantly with a rise in δ¹³C and δ¹⁸O. The highest δ¹³C and δ¹⁸O values occur in the lower part of the supratidal facies, whereas in the upper part of δ values and Sr contents drop sharply. Cyclic variations in evaporation and in meteoric water influence, determined from oxygen isotopic composition, reveal that the cyclicity of the beds containing the most limestones (supratidal) and those with the most marls (subtidal) is related to climatic changes. The coldest periods are those represented by supratidal deposits, when the sea level was at its lowest. During the warmest periods, when the overall sea level was higher, subtidal deposits accumulated in the region. A genetic model is proposed, according to which the asymmetrical sedimentary cycles occur in response to glacio-eustatic changes with a periodicity similar to that of Plio-Pleistocene sea-level variations, but with a much lower range due to the smaller extent of polar ice caps during the Early Cretaceous. The glacio-eustatic changes involved a rapid sea-level rise and a slow sea-level fall.     

Environmental isotopic and hydrochemical study of water in the karst aquifer and submarine springs of the Syrian coast

The groundwater of major karst systems and submarine springs in the coastal limestone aquifer of Syria has been investigated using chemical and isotopic techniques. The δ¹⁸O values of groundwater range from ?6.8 to ?5.05‰, while those for submarine springs vary from ?6.34 to +1.08‰ (eastern Mediterranean seawater samples have a mean of +1.7‰). Groundwater originates from the direct infiltration of atmospheric water. Stable isotopes show that the elevation of the recharge zones feeding the Banyas area (400–600 m a.s.l.) is higher than that feeding the Amrit area (100–300 m a.s.l.). The ¹⁸O_extracted (¹⁸O content of the seawater contribution) for the major submarine springs suggests a mean recharge area elevation of 600–700 m a.s.l., and lower than 400 m a.s.l. for the spring close to Amrit. Based on the measured velocity and the percentage of fresh water at the submarine springs outlet, the estimated discharge rate is 350 million m³/year. The tritium concentrations in groundwater (1.6–5.9 TU) are low and very close to the current rainfall values (2.9–5.6 TU). Adopting a model with exponential time distribution, the mean turnover time of groundwater in the Al-sen spring was evaluated to be 60 years. A value of about 3.7 billion m³ was obtained for the maximum groundwater reservoir size.     

A hydrochemical study of the Hammam Righa geothermal waters in north-central Algeria

This study focuses on the hydrochemical characteristics of 47 water samples collected from thermal and cold springs that emerge from the Hammam Righa geothermal field, located in north-central Algeria. The aquifer that feeds these springs is mainly situated in the deeply fractured Jurassic limestone and dolomite of the Zaccar Mount. Measured discharge temperatures of the cold waters range from 16.0 to 26.5 °C and the hot waters from 32.1 to 68.2 °C. All waters exhibited a near-neutral pH of 6.0–7.6. The thermal waters had a high total dissolved solids (TDS) content of up to 2527 mg/l, while the TDS for cold waters was 659.0–852.0 mg/l. Chemical analyses suggest that two main types of water exist: hot waters in the upflow area of the Ca–Na–SO₄ type (Hammam Righa) and cold waters in the recharge zone of the Ca–Na–HCO₃ type (Zaccar Mount). Reservoir temperatures were estimated using silica geothermometers and fluid/mineral equilibria at 78, 92, and 95 °C for HR4, HR2, and HR1, respectively. Stable isotopic analyses of the δ¹⁸O and δD composition of the waters suggest that the thermal waters of Hammam Righa are of meteoric origin. We conclude that meteoric recharge infiltrates through the fractured dolomitic limestones of the Zaccar Mount and is conductively heated at a depth of 2.1–2.2 km. The hot waters then interact at depth with Triassic evaporites located in the hydrothermal conduit (fault), giving rise to the Ca–Na–SO₄ water type. As they ascend to the surface, the thermal waters mix with shallower Mg-rich groundwater, resulting in waters that plot in the immature water field in the Na–K–Mg diagram. The mixing trend between cold groundwaters from the recharge zone area (Zaccar Mount) and hot waters in the upflow area (Hammam Righa) is apparent via a chloride-enthalpy diagram that shows a mixing ratio of 22.6 < R < 29.2 %. We summarize these results with a geothermal conceptual model of the Hammam Righa geothermal field.     

Evaluation of bulk carbonate δ13C data from Triassic hemipelagites and the initial composition of carbonate mud

Bulk carbonate samples of hemipelagic limestone–marl alternations from the Middle and Upper Triassic of Italy are analysed for their isotopic compositions. Middle Triassic samples are representative of the Livinallongo Formation of the Dolomites, while Upper Triassic hemipelagites were sampled in the Pignola 2 section, within the Calcari con Selce Formation of the Southern Apennines in Southern Italy. Triassic hemipelagites occur either as nodular limestones with chert nodules or as plane‐bedded limestone–marl alternations which are locally silicified. In the Middle Triassic Livinallongo Formation, diagenetic alteration primarily affected the stable isotopic composition of sediment surrounding carbonate nodules, whereas the latter show almost pristine compositions. Diagenesis lowered the carbon and oxygen isotope values of bulk carbonate and introduced a strong correlation between δ¹³C and δ¹⁸O values. In the Middle Triassic successions of the Dolomites, bulk carbonate of nodular limestone facies is most commonly unaltered, whereas carbonate of the plane‐bedded facies is uniformly affected by diagenetic alteration. In contrast to carbonate nodules, plane‐bedded facies often show compaction features. Although both types of pelagic carbonate rocks show very similar petrographic characteristics, scanning electron microscopy studies reveal that nodular limestone consists of micrite (< 5 μm in diameter), whereas samples of the plane‐bedded facies are composed of calcite crystals ca 10 μm in size showing pitted, polished surfaces. These observations suggest that nodular and plane‐bedded facies underwent different diagenetic pathways determined by the prevailing mineralogy of the precursor sediment, i.e. probably high‐Mg calcite in the nodular facies and aragonite in the case of the plane‐bedded facies. Similar to Middle Triassic nodular facies, Upper Triassic nodular limestones of the Lagonegro Basin are also characterized by uncorrelated δ¹³C and δ¹⁸O values and exhibit small, less than 5 μm size, crystals. The alternation of calcitic and aragonitic precursors in the Middle Triassic of the Dolomites is thought to mirror rapid changes in the type of carbonate production of adjacent platforms. Bioturbation and dissolution of metastable carbonate grains played a key role during early lithification of nodular limestone beds, whereby early stabilization recorded the carbon isotopic composition of sea water. The bulk carbonate δ¹³C values of Middle and Upper Triassic hemipelagites from Italy agree with those of Tethyan low‐Mg calcite shells of articulate brachiopods, confirming that Triassic hemipelagites retained the primary carbon isotopic composition of the bottom sea water. A trend of increasing δ¹³C from the Late Anisian to the Early Carnian, partly seen in the data set presented here, is also recognized in successions from tropical palaeolatitudes elsewhere. The carbon isotopic composition of Middle and Upper Triassic nodular hemipelagic limestones can thus be used for chemostratigraphic correlation and palaeoenvironmental studies.     

Using multiple chemical indicators to characterize and determine the age of groundwater from selected vents of the Silver Springs Group, central Florida, USA

The Silver Springs Group, Florida (USA), forms the headwaters of the Silver River and supports a diverse ecosystem. The 30 headwater springs divide into five subgroups based on chemistry. Five selected spring vents were sampled in 2007 to better understand the contaminant sources and groundwater flow system. Elevated nitrate-N concentrations (>0.8 mg/L) in the five spring vents likely originate from inorganic (fertilizers) and organic sources, based on nitrogen and oxygen isotope ratios of nitrate. Evidence for denitrification in the Lost River Boil spring includes enriched δ¹⁵N and δ¹⁸O, excess N₂ gas, and low dissolved O₂ concentrations (<0.5 mg/L). Multiple age-tracer data (SF₆, ³H, tritiogenic ³He) for the two uppermost springs (Mammoth East and Mammoth West) indicate a binary mixture dominated by recent recharge water (mean age 6–7 years, and 87–97% young water). Tracer data for the three downstream spring vents (Lost River Boil, Catfish Hotel-1, and Catfish Conventional Hall-1) indicate exponential mixtures with mean ages of 26–35 years. Contamination from non-atmospheric sources of CFCs and SF₅CF₃ precluded their use as age tracers here. Variations in chemistry were consistent with mean groundwater age, as nitrate-N and dissolved O₂ concentrations were higher in younger waters, and the Ca/Mg ratio decreased with increasing mean age.     

Hydrogeological and hydrochemical investigation of groundwater using environmental isotopes (18O, 2H, 3H, 14C) and chemical tracers: a case study of the intermediate aquifer,Sfax, southeastern Tunisia

Major element concentrations and stable (δ¹⁸O and δ²H) and radiogenic (³H and ¹⁴C) isotopes in groundwater have proved useful tracers for understanding the geochemical processes that control groundwater mineralization and for identifying recharge sources in the semi-arid region of Sfax (southeastern Tunisia). Major-ion chemical data indicate that the origins of the salinity in the groundwater are the water–rock interactions, mainly the dissolution of evaporitic minerals, as well as the cation exchange with clay minerals. The δ¹⁸O and δ²H relationships suggest variations in groundwater recharge mechanisms. Strong evaporation during recharge with limited rapid water infiltration is evident in the groundwater of the intermediate aquifer. The mixing with old groundwater in some areas explains the low stable isotope values of some groundwater samples. Groundwaters from the intermediate aquifer are classified into two main water types: Ca-Na-SO₄ and Ca-Na-Cl-SO₄. The high nitrate concentrations suggest an anthropogenic source of nitrogen contamination caused by intensive agricultural activities in the area. The stable isotopic signatures reveal three water groups: non-evaporated waters that indicate recharge by recent infiltrated water; evaporated waters that are characterized by relatively enriched δ¹⁸O and δ²H contents; and mixed groundwater (old/recent) or ancient groundwater, characterized by their depleted isotopic composition. Tritium data support the existence of recent limited recharge; however, other low tritium values are indicative of pre-nuclear recharge and/or mixing between pre-nuclear and contemporaneous recharge. The carbon-14 activities indicate that the groundwaters were mostly recharged under different climatic conditions during the cooler periods of the late Pleistocene and Holocene.

     

Stable isotopes (2H, 18O and 13C) in groundwaters from the northwestern portion of the Guarani Aquifer System (Brazil)

The groundwater flow pattern of the western part of the Guarani Aquifer System (GAS), Brazil, is characterized by three regional recharge areas in the north, and a potentiometric divide in the south, which trends north–south approximately. Groundwater flow is radial from these regional recharge areas toward the center of Paraná Sedimentary Basin and toward the western outcrop areas at the border of the Pantanal Matogrossense, because of the potentiometric divide. The isotopic composition of GAS groundwater leads to understanding the paleoclimatic conditions in the regional recharge areas. The δ¹⁸O and δ²H isotopic ratios of GAS groundwaters vary, respectively, from –9.1 to –4.8‰ V-SMOW and –58.4 to –21.7‰ V-SMOW. In the recharge zones, enriched δ¹⁸O values are observed, while in the confined zone lighter δ¹⁸O values are observed. These suggest that climatic conditions were 10°C cooler than the present during the recharge of these waters. The δ¹³C ratios in groundwater of GAS, in the study area, vary from –19.5 to –6.5‰ VPDB, increasing along the regional flow lines toward the confined zone. This variation is related to dissolution of carbonate cement in the sandstones.     

Identifying groundwater recharge connections in the Moscow (USA) sub-basin using isotopic tracers and a soil moisture routing model

Globally, aquifers are suffering from large abstractions resulting in groundwater level declines. These declines can be caused by excessive abstraction for drinking water, irrigation purposes or industrial use. Basaltic aquifers also face these conflicts. A large flood basalt area (1.1?×?10⁵ km²) can be found in the Northwest of the USA. This Columbia River Basalt Group (CRBG) consists of a thick series of basalt flows of Miocene age. The two major hydrogeological units (Wanapum and Grand Ronde formations) are widely used for water abstraction. The mean decline over recent decades has been 0.6 m year^?1. At present day, abstraction wells are drying up, and base flow of rivers is reduced. At the eastern part of CRBG, the Moscow sub-basin on the Idaho/Washington State border can be found. Although a thick poorly permeable clay layer exists on top of the basalt aquifer, groundwater level dynamics suggest that groundwater recharge occurs at certain locations. A set of wells and springs has been monitored bi-weekly for 9 months for δ¹⁸O and δ²H. Large isotopic fluctuations and d-excess values close to the meteoric water line in some wells are indicating that recharge occurs at the granite/basalt interface through lateral flow paths in and below the clay. A soil moisture routing (SMR) model showed that most recharge occurs on the granitic mountains. The basaltic aquifer receives recharge from these sedimentary zones around the granite/basalt interface. The identification of these types of areas is of major importance for future managed-aquifer recharge solutions to solve problems of groundwater depletion.     

Hydrogeochemical and isotopic evidence of groundwater evolution and recharge in aquifers in Beijing Plain, China

An investigation was conducted in Beijing to identify the groundwater evolution and recharge in the quaternary aquifers. Water samples were collected from precipitation, rivers, wells, and springs for hydrochemical and isotopic measurements. The recharge and the origin of groundwater and its residence time were further studied. The groundwater in the upper aquifer is characterized by Ca-Mg-HCO₃ type in the upstream area and Na-HCO₃ type in the downstream area of the groundwater flow field. The groundwater in the lower aquifer is mainly characterized by Ca-Mg-HCO₃ type in the upstream area and Ca-Na-Mg-HCO₃ and Na-Ca-Mg-HCO₃ type in the downstream area. The δD and δ¹⁸O in precipitation are linearly correlated, which is similar to WMWL. The δD and δ¹⁸O values of river, well and spring water are within the same ranges as those found in the alluvial fan zone, and lay slightly above or below LMWL. The δD and δ¹⁸O values have a decreasing trend generally following the precipitation → surface water → shallow groundwater → spring water → deep groundwater direction. There is evidence of enrichment of heavy isotopes in groundwater due to evaporation. Tritium values of unconfined groundwater give evidence for ongoing recharge in modern times with mean residence times <50 a. It shows a clear renewal evolution along the groundwater flow paths and represents modern recharge locally from precipitation and surface water to the shallow aquifers (<150 m). In contrast, according to ¹⁴C ages in the confined aquifers and residence time of groundwater flow lines, the deep groundwater is approximately or older than 10 ka, and was recharged during a period when the climate was wetter and colder mainly from the piedmont surrounding the plain. The groundwater exploitation is considered to be “mined unsustainably” because more water is withdrawn than it is replenished.     

Early Callovian ingression in southwestern Gondwana. Palaeoenvironmental evolution of the carbonate ramp (Calabozo Formation) in southwestern Mendoza,Neuquen basin,Argentina

The carbonatic sequence of the Calabozo Formation (Lower Callovian) developed in southwestern Gondwana, within the northern area of the Neuquén basin, and is widespread in thin isolated outcrops in southwestern Mendoza province, Argentina. This paper describes the facies, microfacies and geochemical-isotopic analysis carried out in five studied localities, which allowed to define the paleoenvironmental conditions of a homoclinal shallow ramp model, highly influenced by sea level fluctuations, where outer, mid and inner ramp subenvironments were identified. The outer ramp subenvironment was only recognized in the south of the depocenter and is characterized by proximal outer ramp facies with shale levels and interbedded mudstone and packstone layers. The mid ramp subenvironment is formed by low energy facies (wackestone) affected by storms (packstones, grainstones and floatstones). The inner ramp subenvironment is the most predominant and is characterized by tidal flat facies (wackestones, packstones and grainstones) over which a complex of shoals (grainstones and packstones) dissected by tidal channels (packstone, grainstones and floatstones) developed. In the north area, protected environment facies were recorded (bioturbated wackestones and packstones). The vertical distribution of facies indicates that the paleoenvironmental evolution of the Calabozo Formation results from a highstand stage in the depocenter, culminating in a supratidal environment, with stromatolitic levels interbedded with anhydrite originated under restricted water circulation conditions due to a progressive isolation of the basin. δ¹³C and δ¹⁸O values of the carbonates of the Calabozo Formation suggest an isotopic signature influenced by local palaeoenvironmental parameters and diagenetic overprints. The δ¹³C and δ¹⁸O oscillations between the carbonates of the different studied sections are related with lateral facies variations within the carbonate ramp accompanied with dissimilar reactivities in relation to diagenetic fluids. The δ¹⁸O values of all sections exhibit a rather broad scatter which may be attributed to diagenesis and recrystallisation while the carbon isotopic composition has been less affected by those processes. Carbon isotope system has best retained the primary isotopic signal and δ¹³C values (0–3.9‰) are within the Callovian isotope range. The ⁸⁷Sr/⁸⁶Sr ratios of the bulk carbonates of El Plomo creek, La Vaina creek and Potimalal River sections are in agreement with the Callovian seawater Sr-isotope curve.     

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     

Stable-isotopes of groundwaters from the Albuquerque, New Mexico, basin: one decade later

In the spring of 1995, 24 samples were collected from a widely distributed system of municipal water wells in Albuquerque, N.M., and analyzed for hydrogen (δD) and oxygen (δ¹⁸O) isotopic compositions. δD values for 15 of these samples are largely similar to those reported by Yapp in 1985, but have locally become more negative by as much as 5 per mil (ö). δD–δ¹⁸O data define two endmembers that are well aligned along the familiar meteoric water line (MWL): (1) the eastern domain (mountain precipitation runoff), having δD>–86ö (similar to the criteria of Yapp) and δ¹⁸O>–12.1ö (this work); and (2) a central basin domain, which may be in part derived from water seepage from the Rio Grande, having δD<–95ö and δ¹⁸O<–13.2ö. Only a few wells across the basin have δD values near the "baseline" value of the Rio Grande, defined by Yapp as –92ö. The proximity of these wells to the Rio Grande is consistent with recharge by seepage from the river bed under baseline conditions. Extensive pumping in the eastern domain and West Mesa areas may be partly responsible for an apparent expansion of the central-basin regime of water more depleted in δD, much as a plume migrating in response to transient perturbations in original hydraulic gradients. Vertically stacked groundwater occurrences having limited interconnection are inferred from the significant differences in isotopic compositions of samples from two wells screened at multiple depths. The central and western parts of the basin are little influenced by contributions from the eastern domain. Some groundwaters from the western part of the basin plot below the MWL and clearly cannot be mixtures solely of the eastern domain and central basin endmembers. The origins of these western groundwaters and the most depleted central basin groundwaters are as yet unknown, but we speculate they may have received recharge under climatic conditions different from the present.     

Tracing ionic sources and geochemical evolution of groundwater in the Intermountain Una basin in outer NW Himalaya,Himachal Pradesh,India

The present research aims to identify sources of ions and factors controlling the geochemical evolution of groundwater in an intermountain basin, comprising hill and valley fill region, of Outer Himalaya in Himachal Pradesh, India. The groundwater samples collected from 81 tubewells and handpumps are analyzed for major ions, trace metals and stable isotopes (δ¹⁸O and δD). Geochemically the dominant hydrochemical facies in the Una basin are Ca–HCO₃, Ca–Mg–HCO₃ and Na–Cl types at few locations. A relatively lower ionic concentration in the valley fills indicates dilution and low residence time of water to interact with the aquifer mass due to high porosity and permeability. The ionic ratios of 0.9, 0.8 and 3.8 to 5.7, respectively, for (Ca?+?Mg): HCO₃, (Ca?+?Mg): (HCO₃?+?SO₄) and Na: Cl, suggests that ionic composition of groundwater is mainly controlled by rock weathering of, particularly by dissolution/precipitation of calcrete and calcite hosted in rock veins and Ca–Na feldspar hosted in conglomerate deposits derived from the Higher and Lesser Himalaya during the formation of Siwalik rocks. Although Na, K, NO₃ and SO₄ are introduced in the groundwater through agricultural practices, Na has also been introduced through ion exchange processes that have occurred during water–rock interaction, as indicated by negative CAI values. Factor analysis further suggests three major factors affecting the water chemistry of the area. The first two factors are associated with rock weathering while the third is anthropogenic processes associated with high nitrate and iron concentration. High concentrations of Fe and Mn ions that are exceeded that of WHO and BIS standards are also present at few locations. The recharge of groundwater in the Outer Himalaya is entirely through Indian Southwest Monsoon (ISM) and depleted ratios of δ¹⁸O/δD in valley region indicate infiltration from irrigation in recharging the groundwater and fractionation of isotopes of precipitation due to evaporation before infiltration. High d-excess values and inverse relation with δ¹⁸O are indicative of secondary evaporation of precipitation during recharge of groundwater.     

Impact of rock-water interactions and recharge on water resources quality of the Agadir-Essaouira basin,southwestern Morocco

The Agadir-Essaouira area in the occidental High Atlas Mountains of Morocco is characterized by a semi-arid climate. The scarcity and quality of water resources, exacerbated by long drought periods, constitute a major problem for a sustainable development of this region. Groundwater resources of carbonate units within Jurassic and Cretaceous aquifers are requested for drinking and irrigation purposes. In this study, we collected 84 samples from wells, boreholes, springs, and rivers. Hydrochemical and isotopic data were used to examine the mineralization and origin of water, which control groundwater quality. The chemical composition of water seems to be controlled by water-rock interactions, such as dissolution of carbonates (calcite and dolomite), weathering of gypsum, as well as ion exchange processes, which explain the observed variability. Stable isotopes results show that groundwater from the mainly marly Cretaceous aquifer are submitted to an evaporation effect, while samples from the chiefly calcareous Jurassic aquifer indicate a meteoric origin, due to a rapid infiltration of recharge runoff through the karstic outcrops. The low values of δ¹⁸O and δ²H suggest a local recharge from areas with elevations ranging from 400 to 1200 m for the Cretaceous aquifer and from 800 to 1500 m for the Jurassic units.     

Isotopic variations of oxygen and hydrogen in groundwater of carbonate aquifer in an arid environment

The stable isotopic characteristics were used together with the total chloride to assess changes in groundwater from recharge zones into the carbonate aquifer in an arid environment. The aquifer under study represents a major source of groundwater and thermal springs in Al-Ain city, which are located at the northern part of Jabal Hafit in the United Arab Emirates (UAE). The relationship between oxygen and hydrogen isotopic composition of groundwater is established and is described by δD?=?2.2δ¹⁸O???9.96. The lower slope and y-intercept of groundwater samples relative to the local meteoric waterline suggests that the isotopic enrichment is due to the evaporation of shallow groundwater after recharge occurs. The majority of the shallow groundwater samples have a negative deuterium excess (d-excess) which might be ascribed to high a degree of evaporation, while most of the groundwater samples from deep wells, have a positive value of d-excess which may be related to a low degree of evaporation. The δ¹⁸O values of the thermal waters suggest enrichment towards δ¹⁸O of the carbonate rocks because of the exchange with oxygen at higher temperatures. A possible mixing between thermal or hot water and shallow groundwater is evident in some samples as reflected by δD vs. Cl and d-excess vs. δ¹⁸O plots.     

Hydrogeochemical investigation of Küçük Menderes River coastal wetland,Selçuk–Izmir,Turkey

Küçük Menderes River forms a rich coastal wetland inside in the Selçuk plain. Three saline/brackish lakes, one swamp and Küçük Menderes River are these wetlands’ components. Alkaline-slightly alkaline type lakes are recharged from precipitation and karstic springs that discharge from marble-schist and marble-alluvium contacts in the northern and southern parts of the study area. Water types of the wetland are Na–Cl and Na–Ca–Mg–HCO₃–Cl in both rainy and dry seasons. Both seawater intrusion and evaporation, as being the sources of the ions, justify the presence of Na–Cl, Na–SO₄ and Cl–SO₄, in the wetland water. Environmental isotopes were used to identify the relationship between wetland and groundwater in the Selçuk plain. The δ¹⁸O and δD composition of wetland area samples have changed between ?6.42 to ?4.56‰, and ?36.40 to ?23.80‰, respectively. The lakes and rivers are plotted on the mixing line by slope of 5.2 and these data indicate that wetland is affected from seawater intrusion. The recharge area that was sampled in order to compare the wetland has Ca–HCO₃ water type with a neutral-slightly alkaline pH values and the main hydrogeochemical process is weathering the different types of silicates. Iron, manganese and selenium are the dominant minor ions due to the high biological activities and organic matters in the lakes. There are two contamination risks for this wetland: (1) waste disposal site and (2) water treatment plant where the purified waters are released into the river. EC, Al, As, Cd, Cu, Fe and Zn values exceed those of aquatic life standards. In the near future these sites will pose a danger for wetland wild life and surrounding irrigation water suppliers.