Origin and geochemical reaction paths of sabkha brines: Sabkha Jayb Uwayyid, eastern Saudi Arabia

Sabkhas are ubiquitous geomorphic features in eastern Saudi Arabia. Seven brine samples were taken from Sabkha Jayb Uwayyid in eastern Saudi Arabia. Brine chemistry, saturation state with respect to carbonate and evaporate minerals, and evaporation-driven geochemical reaction paths were investigated to delineate the origin of brines and the evolution of both brine chemistry and sabkha mineralogy. The average total dissolved solids in the sabkha brines is 243 g/l. The order of cation dominance is Na⁺   >>  Mg²⁺ >>  Ca²⁺>K⁺, while anion dominance is Cl⁻ >> SO₄ ²⁻ >> HCO₃ ⁻. Based on the chemical divide principle and observed ion ratios, it was concluded that sabkha brines have evolved from deep groundwater rather than from direct rainfall, runoff from the surroundings, or inflow of shallow groundwater. Aqueous speciation simulations show that: (1) all seven brines are supersaturated with respect to calcite, dolomite, and magnesite and undersaturated with respect to halite; (2) three brines are undersaturated with respect to both gypsum and anhydrite, while three brines are supersaturated with respect to both minerals; (3) anhydrite is a more stable solid phase than gypsum in four brines. Evaporation factors required to bring the brines to the halite phase boundary ranged from 1.016 to 4.53. All reaction paths to the halite phase boundary follow the neutral path as CO₂ is degassed and dolomite precipitates from the brines. On average, a sabkha brine containing 1 kg of H₂O precipitates 7.6 g of minerals along the reaction path to the halite phase boundary, of which 52% is anhydrite, 35.3% is gypsum, and 12.7% is dolomite. Bicarbonate is the limiting factor of dolomite precipitation, and sulfate is the limiting factor of gypsum and anhydrite precipitation from sabkha brines.     

Monitoring of playa evaporites as seen with optical remote sensing sensors: case of Chott El Jerid,Tunisia, from 2003 to present

Chott El Jerid in the Zone of Chotts of Tunisia is one of the largest endorheic basins in the world. During the dry period, from May to August, it is generally covered by continental evaporites which result from the desiccation of the lake formed after a flooding event. This lake comprises runoff water from the surrounding relief and also water resurgence. In order to map and monitor these evaporitic surfaces (mineral composition and evolution in space and time), optical multisource, multispectral, and multidate satellite data have been used. Landsat 4–5 TM, Landsat 8 OLI, SPOT 6, and Landsat Surface Reflectance (LSR) constitute the main data set. The central part of the Chott, north and south of the road crossing the Chott over 70 km from Tozeur to Kebili, has been particularly studied, because it corresponds to the major evaporite accumulation zone. These evaporites precipitated as concentric layers (a relatively rare pattern), mainly north of the road, after several recent flooding events during the last 15 years. Winds can play a significant role in the development of the evaporite layers. Image interpretation associated with field data shows that after the final desiccation of the playa lake, the mineralogy of the salt crust comprised an assemblage dominated by halite south of the road and by gypsum north of the road. Halite and gypsum are the only minerals to be identified using satellite remote sensing data. Sulfates such as gypsum can be identified thanks to a drop in reflectance in the short-wave infrared (SWIR) range caused by vibrations of the SO₄ group. Gypsum crusts are more widely distributed than halite crusts. LSR data are particularly suitable for multitemporal comparison because they are calibrated and atmospherically corrected. The classical bull’s eye pattern characterizing evaporitic deposits (from carbonates along the rims to halite, gypsum, and finally potassium-magnesium minerals in the center of the basin) is deeply disturbed by the road crossing Chott El Jerid.     

Hydrogeochemical and isotopic characteristics of the Ilica geothermal system (Erzurum,Turkey)

In this paper, the hydrochemical isotopic characteristics of samples collected from geothermal springs in the Ilica geothermal field, Eastern Anatolia of Turkey, are examined and described. Low-temperature geothermal system of Ilica (Erzurum, Turkey) located along the Eastern Anatolian fault zone was investigated for hydrogeochemical and isotopic characteristics. The study of ionic and isotopic contents shows that the thermal water of Ilica is mainly, locally fed by groundwater, which changes chemically and isotopically during its circulation within the major fault zone reaching depths. The thermal spring has a temperature of 29–39 °C, with electrical conductivity ranging from 4,000 to 7,510 µS/cm and the thermal water is of Na–HCO₃–Cl water type. The chemical geothermometers applied in the Ilica geothermal waters yielded a maximum reservoir temperature of 142 °C according to the silica geothermometers. The thermal waters are undersaturated with respect to gypsum, anhydrite and halite, and oversaturated with respect to dolomite. The dolomite mineral possibly caused scaling when obtaining the thermal waters in the study area. According to the enthalpy chloride-mixing model, cold water to the thermal water-mixing ratio is changing between 69.8 and 75 %. The δ¹⁸O–δ²H compositions obviously indicate meteoric origin of the waters. Thermal water springs derived from continental precipitation falling on to higher elevations in the study area. The δ¹³C ratio for dissolved inorganic carbonate in the waters lies between 4.63 and 6.48 ‰. In low-temperature waters carbon is considered as originating from volcanic (mantle) CO₂.     

Assessment of groundwater quality for irrigation purposes and identification of hydrogeochemical evolution mechanisms in Pengyang County, China

Groundwater is an important water source for agricultural irrigation in Penyang County. Some traditional methods such as irrigation coefficient, sodium adsorption ratio, total alkalinity, total salinity and total dissolved solids were employed to assess groundwater quality in this area. In addition, an improved technique for order preference by similarity to ideal solution model was applied for comprehensive assessment. The origin of major ions and groundwater hydrogeochemical evolution was also discussed. Groundwater in Penyang County contains relative concentrations of dominant constituents in the following order: Na⁺ > Ca²⁺ > Mg²⁺ > K⁺ for cations and HCO₃ ^? > SO₄ ^2? > Cl^? > CO₃ ^2? for anions. Groundwater quality is largely excellent and/or good, suggesting general suitability for agricultural use. Calcite and dolomite are found saturated in groundwater and thus tend to precipitate out, while halite, fluorite and gypsum are unsaturated and will dissolve into groundwater during flow. Groundwater in the study area is weathering-dominated, and mineral weathering (carbonate and silicate minerals) and ion exchange are the most important factors controlling groundwater chemistry.     

Identifying key hydrochemical processes in a confined aquifer of an arid basin using multivariate statistical analysis and inverse modeling

Tertiary fractured permeable confined aquifer, which covered about 70 % of the studying area, played an important role in alleviating drinking water shortages. However, about 58 and 79 % of the groundwater samples exceeded the desirable limits for fluoride (1.5 mg/L) and TDS (1,000 mg/L). Two multivariate statistical methods, hierarchical cluster analysis (HCA) and principal components analysis (PCA), were applied to a subgroup of the dataset in terms of their usefulness for groundwater classification, as well as to identify the key processes controlling groundwater geochemistry. In the PCA, two principal factors have been extracted, which could explain 73 % of the total data variability. Among them, factor 1 revealed the source of groundwater salinity and factor 2 explained the elevated fluoride. Two major groups were classified by HCA and Group 1 was near the groundwater recharge zone and Group 2 was mainly distributed over the groundwater discharge zone. Inverse modeling (NETPATH) results indicated that the hydrochemical evolution was primarily controlled by (1) the dissolution of mirabilite, gypsum and halite for the source of groundwater salinity; (2) the release of the adsorbed fluoride through desorption or through competition with HCO₃ ^? under alkalinity condition for the elevated fluoride in the groundwater.     

Specific features of the formation of elementary sedimentary rhythms of rock salt in facies zones of the Permian halogenic basin of the Caspian region

Based on the composition of brine inclusions in halite, the formation conditions of elementary sedimentation rhythms of rock salt were determined in facies zones of the Permian halogenic basin of the Caspian region. The distribution of structural types of halite was analyzed and the rate of brine condensation was estimated by calculating the K⁺ concentration coefficients during the precipitation of 1 m rock salt (K₁ g/l/m) and one elementary rhythm (K₂ g/l/rhythm). It was established that the rock salt of the Karpensk and Lugovsk rhythmic beds (hereafter, rhythmites) at the base and middle part of the halogenic sequence of the Baskunchak structure precipitated in a relatively deep-water lithofacies zone at a constant influx of NaCl-saturated brine and its slow condensation. This is reflected in insignificant variations of the thickness of elementary rhythms. In troughs at the northwestern framing of the depression, rocks salts of the Privolzhsk and partially, Lugovsk rhythmites were precipitated without the condensation of brine owing to the partial dissolution of halite in the coastal zones of the basin. The anomalously thick elementary rhythms (up to 30–40 cm) were composed of coarse-crystalline and water-transparent feather halite deposited at the bottom. A rapid condensation of brine was also noted during the precipitation of rock salt underlying the K-Mg saliferous rocks in the troughs. In this area, the brine experienced density stratification, with the influx of both condensed brine from the central part of the basin and less dense brine from the inlet.     

Geochemistry and mineralogy of a recent sabkha along the coast of Sinai, Gulf of Suez

Most efforts in the study of sea-marginal sabkhas have concentrated on the Persian Gulf, but little is known about the sediments and mineralogy of sabkhas marginal to other seas. The purpose of this paper was to present some geochemical and mineralogical observations in a recent sabkha on the coast of Sinai along the Gulf of Suez. The sabkha is composed of coarse clastic sediments with marine-derived groundwater at depth of about 1 m. The general morphology, climate and water salinity of the Gulf of Suez resemble those of the Persian Gulf, despite the fact that the content of authigenic evaporites in this sabkha is more sparse. The evaporite minerals accumulated only in the upper 30–40 cm of the sabkha, below that and down to the groundwater table, there is no accumulation of evaporites. Laterally, the salinity of the groundwater in the sabkha and the concentration of evaporites in the sediments above it increase constantly with distance from the shore. In contrast to the Persian Gulf where anhydrite is a major evaporite mineral, in Belayim gypsum is the only calcium sulphate mineral in the recent sabkha. Anhydrite is found only in an old elevated sabkha where it recrystallized from gypsum. The gypsum occurs as interstitial crystal concentrations or lithified horizons almost exclusively at the depth of 20–40 cm below the sabkha surface. Above that, in the uppermost horizons, there is in situ accumulation of interstitial halite crystals. The total concentrations of gypsum and halite are almost equal in this sabkha. The sea water recharge in El Belayim is almost exclusively by seepage through the sabkha sediments and not by flooding. The groundwater under this sabkha is only slightly more saline than the Gulf water, thus, not heavy enough for extensive downward refluxing. The major hydrodynamic process must be upward migration of the brines from the groundwater, precipitating on the way gypsum and later halite with some magnesite. Since the sediments of the sabkha are too coarse to support extensive capillary movement, the brines must, therefore, migrate upwards due to ‘evaporative pumping’.     

An explanation for the varves of the Castile evaporites (Upper Permian), Texas and New Mexico, USA

Abstract Extraordinary sequences of conspicuous, pervasive and laterally persistent varves characterize the Castile evaporites. They occur as singlets (calcite laminae), couplets (calcite laminae interstratified with anhydrite laminae), thick couplets (calcite laminae interstratified with thin anhydrite beds) and triplets (calcite and anhydrite laminae interstratified with thin halite beds). The varves accumulated in a deep (initially ≈ 550 m), persistently stratified, saline lake surrounded by an extinct reef. The lake had formed when the reef grew across a channel between an embayment and the ocean. Although located virtually on the palaeo-equator, the lake experienced negligible meteoric influx and extreme seasonality. During the season of high relative humidity, more marine groundwater entered the lake through the permeable reef barrier than exited as reflux and, secondarily, as evaporation. Consequently, the lake level rose by up to several metres to sea level. The ‘refreshening’ decreased salinity and replenished dissolved CO₂– the critical nutrient limiting growth of indigenous phytoplankton. Algae proliferated, pH increased and CaCO₃ precipitated. It mixed with organic matter to form a thin, dark lamina. During the season of low relative humidity, tens of cubic kilometres of water evaporated from and, secondarily, leaked out through the surrounding reef. More water exited than entered, brine level fell below sea level, and salinity of the upper brine layer increased. Gypsum usually precipitated and rained onto the basin floor forming a couplet; infrequently, halite also precipitated forming a triplet. Every few thousand years, for <50 to several hundred years, the lake became unstratified during the dry season, and wind-induced overturn allowed a layer of gypsum crystals up to ≈ 2 cm high to precipitate on the basin floor. Each layer, now thin beds of anhydrite nodules and anhydrite pseudomorphs after gypsum, and an underlying lamina of CaCO₃ and admixed organic matter formed a thick couplet. The different varve types recur with a period of 1800–3000 years reflecting climatic changes on a millennial time scale.     

Hydrogeochemistry and quality of groundwater of coastal unconfined aquifer in Amol–Ghaemshahr plain,Mazandaran Province,Northern Iran

Groundwater of the unconfined aquifer (1,100 sq. km) of a two-tier coastal aquifer located in the Amol–Ghaemshahr plain, Mazandaran Province, Northern Iran, is classified into fresh and brackish water types. Fresh groundwater (FGW) samples (n = 36) are characterized by Ca²⁺ > Na⁺ > Mg²⁺ > K⁺ and HCO₃ ^? > Cl^? > SO₄ ^2? > NO₃ ^?. Spearman’s rank correlation coefficient matrices, factor analysis data, values of the C-ratio (av. = 0.89) and CAI and values of the molar ratios of Ca²⁺/HCO₃ ^?, Ca²⁺/SO₄ ^2?, Mg²⁺/HCO₃ ^? and Mg²⁺/SO₄ ^2? indicate that the ionic load in the FGW is derived essentially from carbonic acid-aided weathering of carbonates and aluminosilicates, saline/sea water trapped in the aquifer sediments (now admixed with the groundwater) and ion exchange reactions. Values of the CAI and Na⁺/Cl^? molar ratio suggest that the part of the Ca²⁺ (±Mg²⁺) content in 23 FGW samples is derived from clay minerals of the aquifer matrix, and part of the Na⁺ content in 20, 12, and 3 FGW samples is derived, respectively, from alkali feldspar weathering, clay minerals of the aquifer matrix and rain water and/or halite. Brackish groundwater (BGW) samples (n = 4) contain Cl^? as the dominant anion and their average total ionic concentration (38.65 meq/L) is 1.79 times higher than that of the FGW samples (21.50 meq/L). BGW pockets were generated by non-conservative mixing of FGW with the upconed saline water from the underlying saline groundwater zone of the semi-confined aquifer along bore wells involved in excessive extraction of groundwater from the unconfined aquifer. Groundwater belongs essentially to “high salinity, low sodium” irrigation water class.     

Meganodular anhydritization: a new mechanism of gypsum to anhydrite conversion (Palaeogene–Neogene,Ebro Basin,North‐east Spain)

A number of Palaeogene to Early Neogene gypsum units are located along the southern margins of the Ebro Basin (North‐east Spain). These marginal units, of Eocene to Lower Miocene age, formed and accumulated deposits of Ca sulphates (gypsum and anhydrite) in small, shallow saline lakes of low ionic concentration. The lakes were fed mainly by ground water from deep regional aquifers whose recharge areas were located in the mountain chains bounding the basin, and these aquifers recycled and delivered Ca sulphate and Na chloride from Mesozoic evaporites (Triassic and Lower Jurassic). In outcrop, the marginal sulphate units are largely secondary gypsum after anhydrite and exhibit meganodules (from 0·5 to >5 m across) and large irregular masses. In the sub‐surface these meganodules and masses are mostly made of anhydrite, which replaced the original primary gypsum. The isotopic composition (11·1 to 17·4‰ for δ¹⁸O_VSMOW; 10·7 to 15·3‰ for δ³⁴S_VCDT) of secondary gypsum in this meganodular facies indicates that the precursor anhydrite derived from in situ replacement of an initial primary gypsum. As a result of ascending circulation of deep regional fluid flows through the gypsum units near the basin margins, the gypsum was partly altered to anhydrite within burial conditions from shallow to moderate depths (from some metres to a few hundred metres?). At such depths, the temperatures and solute contents of these regional flows exceeded those of the ground water today. These palaeoflows became anhydritizing solutions and partly altered the subsiding gypsum units before they became totally transformed by deep burial anhydritization. The characteristics of the meganodular anhydritization (for example, size and geometry of the meganodules and irregular masses, spatial arrangement, relations with the associated lithologies and the depositional cycles, presence of an enterolithic vein complex and palaeogeographic distribution) are compared with those of the anhydritization generated both in a sabkha setting or under deep burial conditions, and a number of fundamental differences are highlighted.     

Hydrogeochemical characterization and evolution of a regional karst aquifer in the Cuatrociénegas area,Mexico

The Cuatrociénegas area is useful for the investigation of the effect of groundwater extraction in the Chihuahuan freshwater xeric ecoregion. It has been investigated at this time using a selection of geochemical indicators (major, minor and trace elements) and δ³⁴S data, to characterize the origin of groundwater, the main geochemical processes and the mineral/groundwater interactions controlling the baseline geochemistry. The area is composed of limestones of Mesozoic age, with a composite thickness of about 500 m, overlaid by basin fill (poorly consolidated young sediments). Substantial water extraction and modification of natural discharges from the area along the last century have produced a detrimental impact on ecosystem structure and function. Water–rock interactions, mixing and evaporative processes dominate the baseline groundwater quality. Natural recharge is HCO₃–Ca type in equilibrium with calcite, low salinity (TDS?<?500 mg/L), Cl^? lower than 11 mg/L and average Li⁺ concentration of 0.005 mg/L. Along the groundwater flow systems, δ³⁴S evidence and mass transfer calculations indicate that Cretaceous gypsum dissolution and dedolomitization reactions adjust water composition to the SO₄–Ca type. The increase of water–rock interaction is reflected by Cl^? values increase (average 68 mg/L), TDS up to about 1500 mg/L and an average Li⁺ concentration of 0.063 mg/L. Calculations with chemical geothermometers indicate that temperature at depth could be at maximum of 15–20 °C higher than field-measured temperature for pozas. After groundwater is discharged to the surface, chemical evolution continues; water evaporation, CO₂ degassing and precipitation of minerals such as gypsum, calcite and kaolinite represent the final processes and reactions controlling water chemical composition.     

The geochemical and isotopic record of evaporite recycling in spas and salterns of the Basque Cantabrian basin, Spain

Evaporite outcrops are rare in the Basque Cantabrian basin due to a rainy climate, but saline springs with total dissolved solids ranging from 0.8 to 260 g/L are common and have long been used to supply spas and salterns. New and existing hydrochemistry of saline springs are used to provide additional insight on the origin and underground extent of their poorly known source evaporites. Saline water hydrochemistry is related to dissolution of halite and gypsum from two evaporitic successions (Triassic “Keuper” and Lower Cretaceous “Wealden”), as supported by rock samples from outcrops and oil exploration drill cuttings. The δ³⁴S value of gypsum in the Keuper evaporites and sulfate in the springs is δ³⁴S_SO4 = 14.06 ± 1.07‰ and δ¹⁸O_SO4 = 13.41 ± 1.44‰, and the relationship between Cl/Br ratio of halite and water shows that waters have dissolved halite with Br content between 124 and 288 ppm. The δ³⁴S value of gypsum in the Wealden evaporites and sulfate in the springs is δ³⁴S_SO4 = 19.66 ± 1.76‰, δ¹⁸O_SO4 = 14.93 ± 2.35‰, and the relationship between Cl/Br ratio of halite and water shows that waters have dissolved halite with Br content between 15 and 160 ppm. Wealden evaporites formed in a continental setting after the dissolution of Keuper salt. Gypsum δ³⁴S_SO4 and δ¹⁸O_SO4 modification from Keuper to Wealden evaporites was due mainly to bacterial SO₄ reduction in an anoxic, organic matter-rich environment. Saline springs with Wealden δ³⁴S_SO4 values are present in a 70 × 20 km wide area. Saline water temperatures, their δ²H_H2O and δ¹⁸O_H2O values, and the geological structure defines a hydrogeological model, where meteoric water recharges at heights up to 620 m above spring levels and circulates down to 720 m below them, thereby constraining the height range of evaporite dissolution. Groundwater flow towards saline springs is driven by gravity and buoyancy forces constrained by a thrust and fault network.     

Flux of nutrients and heavy metals from the Melai River sub-catchment into Lake Chini, Pekan, Pahang, Malaysia

This study was carried out to determine the flux of nutrients and heavy metals from the Melai sub-catchment into Lake Chini through the process of erosion. Melai River is one of the seven feeder rivers that contributed to the present water level of Lake Chini. Three properties of soils, such as particle size, organic matter content, and soil hydraulic conductivity and three chemical soil properties, such as available nutrients, dissolved nutrients, and heavy metals, were analyzed and interpreted. Potential soil loss was estimated using the revised universal soil loss equation model. The results show that the soil textures in the study area consist of clay, silty clay, clay loam, and sandy silt loam. The organic matter content ranges from 3.40 to 9.92 %, while the hydraulic conductivity ranges from 5.2 to 25.3 cm/h. Mean values of available P, K, and Mg amount was 8.5 ± 3.7 μg/g, 24.5 ± 3.4 μg/g, and 20.7 ± 18.6 μg/g, respectively. The highest concentration of soluble nutrients was SO ₄ ^?2 (815.8 ± 624.1 μg/g), followed by NO₃ ^?-N (295.5 ± 372.7 μg/g), NH₄ ⁺-N (24.5 ± 22.1 μg/g) and PO₄ ^3? (2.0 ± 0.8 μg/g). The rainfall erosivity value was 1658.7 MJ mm/ha/h/year. The soil erodibility and slope factor ranges from 0.06 to 0.26 ton h/MJ/mm and 7.63 to 18.33, respectively. The rate of soil loss from the Melai sub-catchment in the present condition is very low (0.0028 ton/ha/year) to low (18.93 ton/ha/year), and low level flow of nutrients and heavy metals, indicating that the Melai River was not the contaminant source of sediments, nutrients, and heavy metals to the lake.     

Hydrochemical classification and multivariate statistical analysis of groundwater from Wadi Sahba area in central Saudi Arabia

The central region of Saudi Arabia is underlain by thick sedimentary formations belonging to the Mesozoic and Cenozoic era. These sedimentary formations form a prolific aquifer supplying groundwater for agricultural and domestic usage in and around Riyadh. The region south of Riyadh City is well known for agricultural activities. Wadi Sahba, which is an eastward extension of Wadi Nisah, has readily available groundwater resources in the Cretaceous Biyadh sandstone aquifer to sustain agricultural activities. The objective of the present study was the hydrochemical assessment of groundwater in the area to understand the main hydrological processes which influence groundwater chemistry. To achieve this objective, 20 groundwater samples were collected from agricultural farms in the Wadi Sahba in central Saudi Arabia, and the major physiochemical constituents were analyzed and interpreted. The average TDS value of the analyzed samples is 1578.05 mg/l, whereas the average EC concentration is 3220.05 μS/cm. Groundwater facies classification inferred from the Piper plot shows that groundwater in the study area belongs to the Ca-SO₄-Cl type and Ca-Na-SO₄-Cl type. The Ca-SO₄-Cl type of groundwater facies is influenced mainly by gypsum dissolution and base ion exchange, whereas the Ca-Na-SO₄-Cl type is influenced by gypsum and halite dissolution. All the groundwater samples are undersaturated with respect to these two principal mineral phases. The Q-mode cluster analysis results in two main groups of groundwater samples, mainly based on the TDS content. Cluster 1 has an average TDS value of 1980 mg/l, whereas cluster 2 has an average TDS of 1176 mg/l. The groundwater facies identified through the Piper plot reflects the major hydrological processes controlling groundwater chemistry in the area and was found to be more useful in this study as compared to cluster analysis.     

The origin of sulphur in gypsum and dissolved sulphate in the Central Namib Desert,Namibia

This study investigates the sulphur source of gypsum sulphate and dissolved groundwater sulphate in the Central Namib Desert, home to one of Africa's most extensive gypsum (CaSO₄·2H₂O) accumulations. It investigates previously suggested sulphate precursors such as bedrock sulphides and decompositional marine biogenic H₂S and studies the importance of other potential sources in order to determine the origin of gypsum and dissolved sulphate in the region. An attempt has been made to sample all possible sulphur sources, pathways and types of gypsum accumulations in the Central Namib Desert. We have subjected those samples to sulphur isotopic analyses and have compiled existing results. In addition, ionic ratios of Cl/SO₄ are used to determine the presence of non-sea-salt (NSS) sulphur in groundwater and to investigate processes affecting groundwater sulphate. In contrast to previous work, this study proposes that the sulphur cycle, and the formation of gypsum, in the Namib Desert appears to be dominated by the deposition of atmospheric sulphates of phytoplanktonic origin, part of the primary marine production of the Benguela upwelling cells. The aerosol sulphates are subjected to terrestrial storage within the gypsum deposits on the hyper-arid gravel plain and are traceable in groundwater including coastal sabkhas. The hypothesis of decompositional marine biogenic H₂S or bedrock sulphide sources, as considered previously for the Namib Desert, cannot account for the widespread accumulation of gypsum in the region. The study area in the Central Namib Desert, between the Kuiseb and Omaruru rivers, features extensive gypsum accumulations in a ca. 50–70 km wide band, parallel to the shore. They consist of surficial or shallow pedogenic gypsum crusts in the desert pavement, hydromorphic playa or sabkha gypsum, as thin isolated pockets on bedrock ridges and as discrete masses of gypsum selenite along some faults. The sulphur isotopic values (δ³⁴S ‰CDT) of these occurrences are between δ³⁴S +13.0 and +18.8‰, with lower values in proximity to sulphuric ore bodies (δ³⁴S +3.1 and +3.4‰). Damaran bedrock sulphides have a wide range from δ³⁴S −4.1 to +13.8‰ but seem to be significant sources on a local scale at the most. Dissolved sulphate at playas, sabkhas, springs, boreholes and ephemeral rivers have an overall range between δ³⁴S +9.8 and +20.8‰. However, they do not show a systematic geographical trend. The Kalahari waters have lower values, between δ³⁴S +5.9 and +12.3‰. Authigenic gypsum from submarine sediments in the upwelling zone of the Benguela Current between Oranjemund and Walvis Bay ranges between δ³⁴S −34.6 to −4.6‰. A single dry atmospheric deposition sample produced a value of δ³⁴S +15.9‰. These sulphur isotopic results, complemented by meteorological, hydrological and geological information, suggest that sulphate in the Namib Desert is mainly derived from NSS sulphur, in particular oxidation products of marine dimethyl sulphide CH₃SCH₃ (DMS). The hyper-arid conditions prevailing along the Namibian coast since Miocene times favour the overall preservation of the sulphate minerals. However, sporadic and relatively wetter periods have promoted gypsum formation: the segregation of sulphates from the more soluble halite, and the gradual seaward redistribution of sulphate. This study suggests that the extreme productivity of the Benguela Current contributes towards the sulphur budget in the adjacent Namib Desert.     

Polychlorinated biphenyls residues in surface sediments of the eutrophic Chaohu Lake (China): characteristics, risk, and correlation with trophic status

Twenty-eight polychlorinated biphenyls (PCB) congeners were measured in surface sediments from Chaohu Lake to assess their characteristics, potential risk, and the correlation with lake trophic status. PCB levels ranged from 11.074 to 42.712 ng g^?1 dry weight (d.w.) in the western lake and 2.017 to 20.189 ng g^?1 d.w. in the eastern lake. The highest concentrations were found at the sites near the inlets of western lake tributary rivers where big cities and industrial centers are located. Congeners concentrations showed decreasing order of tetra-CB > tri-CB > deca-CB (PCB-209 detected) > penta-CB > hexa-CB > di-CB > hepta-CB > Octa-CB. It indicated that light and heavy Aroclor mixtures were simultaneously used surrounding the lake basin. PCB levels in the western lake are potentially dangerous to humans and the local fauna. There was a significant positive relationship between tetra-CB (one abundant PCB congener) concentration distribution and sediment grain size in the 16–64 μm fraction, whereas a negative correlation was found in the 4–8 μm fraction. Furthermore, PCB distributions were positively correlated with the total organic carbon of sediments and lake trophic status, especially in the more seriously polluted western lake zone. However, the correlation completely disappeared in eastern lake zone. It suggested that PCB contamination might be attributed to industrial wastewaters and domestic sewages from western lake basin, reaching the lake through rivers, rains and floods.     

Diagenesis of a mixed siliciclastic/evaporitic sequence of the Middle Muschelkalk (Middle Triassic), the Catalan Coastal Range, NE Spain

The Middle Muschelkalk (Middle Triassic) of the Catalan Coastal Range (north-east Spain) comprises sandstone, mudstone, anhydrite and minor carbonate layers. Interbedded sandstones and mudstones which are dominant in the north-eastern parts of the basin are terminal alluvial fan deposits. South-westward in the basin, the rocks become dominated by interbedded evaporites and mudstones deposited in sabkha/mudflat environments. The diagenetic and pore water evolution patterns of the Middle Muschelkalk suggest a strong facies control. During eodiagenesis, formation of microdolomite, anhydrite, baryte, magnesite, K-feldspar and mixed-layer chlorite/smectite was favoured within and adjacent to the sabkha/mudflat facies, whereas calcite, haematite, mixed-layer illite/smectite and quartz formed mainly in the alluvial facies. Low δ¹⁸O_SMOW values for microdolomite (+23.7 to +28.4%) and K-feldspar overgrowths (+17.3 to +17.7%) suggest either low-temperature, isotopic disequilibrium or precipitation from low-¹⁸O porewaters. Low-¹⁸O waters might have developed, at least in part, during low-temperature alteration of volcanic rock fragments. During mesodiagenesis, precipitation of quartz overgrowths and coarse dolomite occurred in the alluvial sandstones, whereas recrystallization of microdolomite was dominant in the sabkha/mudflat facies. The isotopic compositions of these mesogenetic phases reflect increasing temperature during burial. Upon uplift and erosion, telogenetic calcite and trace haematite precipitated in fractures and replaced dolomite. The isotopic composition of the calcite (δ¹⁸O_SMOW=+21.5 to +25.6%o; δ¹³C= 7.7 to - 5.6%o) and presence of haematite indicate infiltration of meteoric waters.     

Weathering and anthropogenic influences on the water and sediment chemistry of Wular Lake,Kashmir Himalaya

This paper presents a study on the Wular Lake which is the largest fresh water tectonic lake of Kashmir Valley, India. One hundred and ninety-six (196) water samples and hundred (100) sediment samples (n = 296) have been collected to assess the weathering and Anthropogenic impact on water and sediment chemistry of the lake. The results showed a significant seasonal variability in average concentration of major ions being highest in summer and spring and lower in winter and autumn seasons. The study revealed that lake water is alkaline in nature characterised by medium total dissolved solids and electrical conductivity. The concentration of the major ion towards the lake central showed a decreasing trend from the shore line. The order of major cations and anions was Ca²⁺ > Mg²⁺ > Na⁺ > K⁺ and HCO₃ ^? > SO₄ ^2? > Cl^?, respectively. The geochemical processes suggested that the chemical composition lake water is mostly influenced by the lithology of the basin (carbonates, silicates and sulphates) which had played a significant role in modifying the hydrogeochemical facies in the form of Ca–HCO₃, Mg–HCO₃ and hybrid type. Chemical index of alteration values of Wular Lake sediments reflect moderate weathering of the catchment area. Compared to upper continental crust and the post-Archean Shale, the sediments have higher Si, Ti, Mg and Ca contents and lower Al, Fe, Na, K, P, Zn, Pb, Ni, Cu content. Geoaccumulation index (Igeo) and US Environmental Protection Agency sediment quality standards indicated that there is no pollution effect of heavy metals (Zn, Mn, Pb, Ni and Co).The study also suggested that Wular Lake is characterised by both natural and anthropogenic influences.     

Characteristics of groundwater in karstic region in northeastern Vietnam

The groundwater in the karst region of northeastern Vietnam is found in various structural zones such as the Ha Lang, Song Hien, Hon Gai, Song Lo, Song Gam, and Hoang Lien Son Zones, etc. Results from this study show that groundwater in this region is at different depths: ~120 m deep at Quang Ninh, ~100 m at Lang Son, ~80 m at Cao Bang (The most water-abundant depth observed at Cao Bang varies from 40 to 45 m) while it varies from 18–25 to 80 m deep at Quan Ba (Ha Giang), especially at Meo Vac (Ha Giang), where groundwater is observed at 700–800 m deep (equivalent to local base level of the Nho Que River). Overall, groundwater in the region is fresh with total minerals varying from 250 to 400 mg/l; except for the coastal area of Quang Ninh, where groundwater is characterized by much higher total minerals (M = 3–18 g/l) due to the mixing with the saline sea water. The chemistry of water in the region demonstrates that the water is mainly bicarbonate with a [HCO₃ ^?] concentration varying from 150 to 265 mg/l, pH is of 6.5–8.1, and its hardness is of 3.7–6.0 meq/l.     

Playa sediments of the Didwana Lake,Rajasthan: A new environment for surficial-type uranium mineralisation in India

The Didwana playa, the second largest playa in the eastern part of the Thar desert, is 5.6 km long and 2.4 km wide and supports commercial salt production. The thickness of lake sediment package is reported to be 20 m and comprises fine grained clays and silts, with abundant calcite, gypsum, and halite, associated with hypersaline water. Isolated hills of graphitic phyllite and quartzite are seen on the western side of the lake. During the course of investigations for uranium in surficial environment of semi-arid terrain of Rajasthan, ground water sampling defined a NE-SW trending uranium halo encompassing the Didwana playa. Subsequent sampling of unlined dug wells, up to water table in central part of the playa, indicated uranium values up to 190 ppm and 2072 ppb in lake sediments and brine respectively. These values are of the order of 21 ppm and 192 ppb towards the southwestern periphery of the lake. The average uranium content, as inferred from 12 samples in the central part of the lake, is around 60 ppm over a thickness of 5 m. It appears that the uranium is loosely bonded to the sediments in amorphous form and is, hence, easily leachable. Samples of brine (n=10), from both the central and southwestern portions of the lake, analysed high (1,67,500–3,00,000 mg/l) TDS, HCO₃⁻ (1128–8395 mg/l), and SO₄ (30,536–88,000 mg/l). These are of alkaline (pH: 7.2–9.3) and reducing (Eh: −200 to −340 mV) nature. Under these Eh-pH conditions below the groundwater table, and for such uranium bearing groundwater, precipitation of primary uranium is expected. It is, therefore, modelled that uranium in lake sediment package above water table is concentrated by evaporation process and by chemical reduction below the water table.