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1.
The major ionic and dissolved inorganic carbon (DIC) concentrations and the stable carbon isotope composition of DIC (δ13CDIC) were measured in a freshwater aquifer contaminated by produced water brine with petroleum hydrocarbons. Our aim was to determine the effects of produced water brine contamination on the carbonate evolution of groundwater. The groundwater was characterized by three distinct anion facies: HCO3−-rich, SO42−-rich and Cl−-rich. The HCO3−-rich groundwater is undergoing closed system carbonate evolution from soil CO2(g) and weathering of aquifer carbonates. The SO42−-rich groundwater evolves from gypsum induced dedolomitization and pyrite oxidation. The Cl−-rich groundwater is contaminated by produced water brine and undergoes common ion induced carbonate precipitation. The δ13CDIC of the HCO3−-rich groundwater was controlled by nearly equal contribution of carbon from soil CO2(g) and the aquifer carbonates, such that the δ13C of carbon added to the groundwater was −11.6‰. In the SO42−-rich groundwater, gypsum induced dedolomitization increased the 13C such that the δ13C of carbon added to the groundwater was −9.4‰. In the produced water brine contaminated Cl−-rich groundwater, common ion induced precipitation of calcite depleted the 13C such that the δ13C of carbon added to the groundwater was −12.7‰. The results of this study demonstrate that produced water brine contamination of fresh groundwater in carbonate aquifers alters the carbonate and carbon isotopic evolution.  相似文献   

2.
Highly mineralized waters of different chemical types and origin occur in the flysch formations and their bedrocks in the western part of the Polish Carpathians. The marine sedimentation water of the flysch formations is not preserved, as the most mineralized and the heaviest isotopic values of flysch waters are characterized by δ18O and δ2H values in the ranges of 5–7‰ and −(20–30)‰, respectively. Their origin is related to the dehydration of clay minerals during burial diagenesis, with molecules of marine water completely removed by molecules of released bound water. They are relatively enriched in Na+ in respect to the marine water, supposedly due to the release of Na+ during the illitization of smectites and preferable incorporation of other cations from the primary brine into newly formed minerals. In some parts of younger formations, i.e. in the Badenian sediments, brines occur with isotopic composition close to SMOW and Cl− contents greatly exceeding the typical marine value of about 19.6 g/L, supposedly due to ultrafiltration. Most probably, the marine water of the flysch formations was similarly enriched chemically in its initial burial stages. Final Cl− contents in diagenetic waters depend on different Cl− contents in the primary brines and on relationships between diagenetic and further ultrafiltration processes. In some areas, diagenetic waters migrate to the surface along fault zones and mix with young local meteoric waters becoming diluted, with the isotope composition scattering along typical mixing lines. In areas with independent CO2 flow from great depths, they form chloride CO2-rich waters. Common CO2-rich waters are formed in areas without near-surface occurrences of diagenetic waters. They change from the HCO3–Ca type for modern waters to HCO3–Mg–Ca, HCO3–Na–Ca and other types with elevated TDS, Mg2+ and/or Na− contents for old waters reaching even those of glacial age. Bedrocks of the flysch are represented by Mesozoic and Paleozoic mudstones, sandstones and carbonates, and in some areas by Badenian sediments. Brines of the Mesozoic and Paleozoic bedrocks are usually significantly enriched in Ca2+ and Mg2+ in comparison with the Badenian brines. By analogy to the deepest brines in the adjacent Upper Silesian Coal Basin, they are supposed to originate from paleometeoric waters of a hot climate.  相似文献   

3.
MIS 11 is often considered to be the best climatic analogue for the Holocene. Many studies have suggested, however, that it is a period of extreme climate warmth comparable in temperatures to the Middle and Late Pliocene. In Britain deposits of the Hoxnian interglacial are correlated to MIS 11 and multi-proxy techniques can be used to reconstruct the climate of this interglacial. Soil, groundwater and freshwater carbonates are common in Hoxnian deposits and the stable isotopic composition of these precipitates can be used to increase our understanding of MIS 11 environments in Britain. Carbonates from Marks Tey, Clacton, Swanscombe, Elveden and West Stow are studied, the stratigraphic context of which indicates that their formation is broadly synchronous (in the mid-Hoxnian, pollen zones Ho II to Ho III). The carbon isotopic composition of groundwater and pedogenic carbonates is typically depleted with respect to δ13C (ca −9 to −8‰ VPDB) reflecting uptake of plant respired CO2 during water migration/recharge. The carbon isotopic composition of lacustrine carbonate is more enriched with respect to δ13C (ca 0-1‰VPDB) reflecting the equilibration of lake waters with atmospheric CO2. The δ18O of groundwater and pedogenic carbonates is slightly more enriched than modern soil carbonates but not as enriched as soil carbonates formed under interglacials that were warmer than the Holocene (i.e. the Cromerian). The stable isotopic composition of Hoxnian carbonates does not, therefore, indicate that this interglacial was characterised by uniquely warm climates in the context of other Middle Pleistocene interglacials and the Holocene. This is contrary to many marine and littoral records from around the world but consistent with environmental records from Britain and Europe.  相似文献   

4.
178 groundwater and surface waters have been sampled from April to September 1994 in an endoreic basin located in the N of Mexico (Comarca Lagunera). In this area, groundwater has been exploited over the past century mainly for irrigation and cattle supply. Recent intensive pumping has caused the lowering of the water table at a rate of 1 m a−1 Chemical analyses have been performed on all collected samples and 37 of them have been selected for isotopic measurements (18O,2H,13C and14C). Water stable isotope contents (18O,2H) show an increasing evaporation of the groundwater towards the Nazas river. They also indicate that the recharge occurs from the Nazas river and from the mountains surrounding the depression (Sierra Madre Occidental). Water presents a large spatial variability of the chemical facies (SO4Ca, SO4ClNa, HCO3-Ca and HCO3-Na) which is in relation with (i) their interaction with the geological formations of the basin (carbonates, gypsum and various silicates) and (ii) evaporation. This evaporation occurs in the upper part of the unsaturated zone during infiltration especially for the groundwater sampled near the Nazas river. The14C activity varies between 110.4 (± 1.1) and 4.0 (±0.2) pmc. The13C contents of the total dissolved inorganic C (TDIC) range between −11.0 and −3.6‰. The calculated13C contents of the CO2 in equilibrium with the TDIC, varying between −18.4%0 to −10.9% indicate two origins of C in solution: the carbonate matrix (δ13C= +0.9‰) and the soil CO2 (δ13C from −27.7‰ to −21.7‰ for the cultivated areas). Mean residence times have been determined after correction of the initial activities for dead C from the rock matrix. The mean residence times confirm a modern recharge of the groundwater from the Nazas and indicate the presence of palaeowaters in the northern and southern parts of the basin (up to 30 ka BP).  相似文献   

5.
Applications of speleothem calcite geochemistry in climate change studies require the evaluation of the accuracy and sensitivity of speleothem proxies to correctly infer paleoclimatic information. The present study of Harrison’s Cave, Barbados, uses the analysis of the modern climatology and groundwater system to evaluate controls on the C and O isotopic composition of modern speleothems. This new approach directly compares the δ18O and δ13C values of modern speleothems with the values for their corresponding drip waters in order to assess the degree to which isotopic equilibrium is achieved during calcite precipitation. If modern speleothems can be demonstrated to precipitate in isotopic equilibrium, then ancient speleothems, suitable for paleoclimatic studies, from the same cave environment may also have been precipitated in isotopic equilibrium. If modern speleothems are precipitated out of isotopic equilibrium, then the magnitude and direction of the C and O isotopic offsets may allow specific kinetic and/or equilibrium isotopic fractionation mechanisms to be identified.Carbon isotope values for the majority of modern speleothem samples from Harrison’s Cave fall within the range of equilibrium values predicted from the combined use of (1) calcite-water fractionation factors from the literature, (2) measured temperatures, and (3) measured δ13C values of the dissolved inorganic carbon of drip waters. Calcite samples range from ∼0.8‰ higher to ∼1.1‰ lower than predicted values. The 13C depletions are likely caused by kinetically driven departures in the fractionation between HCO3− (aq) and CaCO3 from equilibrium conditions, caused by rapid calcite growth. 13C enrichments can be accounted for by Rayleigh distillation of the HCO3− (aq) reservoir during degassing of 13C-depleted CO2.Modern speleothems from Harrison’s Cave are not in O isotopic equilibrium with their corresponding drip waters and are 0.2‰ to 2.3‰ enriched in 18O relative to equilibrium values. δ18O variations in modern calcite are likely controlled by kinetically driven changes in the fractionation between HCO3− (aq) and CaCO3 from equilibrium conditions to nonequilibrium conditions, consistent with rapid calcite growth. In contrast to δ13C, δ18O values of modern calcite may not be affected by Rayleigh distillation during degassing because CO2 hydration and hydroxylation reactions will buffer the O isotopic composition of the HCO3− (aq) reservoir. If the effects of Rayleigh distillation manifest themselves in the O isotopic system, they will result in 18O enrichment in the HCO3− (aq) reservoir and ultimately in the precipitated CaCO3.  相似文献   

6.
New isotopic and chemical data on the sodium bicarbonate water and associated gases from the Razdolnoe Spa located in the coastal zone of Primorsky Kray of the Russian Far East, together with previous stable isotope data (δ18O, δD, δ13C), allow elucidation of the origin and evolution of the groundwater and gases from the spa. The water is characterized by low temperature (12 °C), TDS – 2.5–6.0 g/L, high contents of B (∼5 mg/L) and F (4.5 mg/L) and low contents of Cl and SO4. Water isotopic composition indicates its essentially meteoric origin which may comply with an older groundwater that was recharged under different (colder) climatic conditions. Major components of bubbling gases are CH4 (68 vol%), N2 (28%) and CO2 (4%). The obtained values δ13C and δD for CO2 and CH4 definitely indicate the marine microbial origin of methane. Thus the high methane content in the waters relates to the biochemical processes and presence of a dispersed organic matter in the host rocks. Based on the regional hydrogeology and the geological structure of the Razdolnoe Spa, Mesozoic fractured rocks containing Na–HCO3 mineral water and gases are reservoir rocks, a chemical composition of water and gases originates in different environmental conditions.  相似文献   

7.
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.  相似文献   

8.
Many waters sampled in Yellowstone National Park, both high-temperature (30–94 °C) and low-temperature (0–30 °C), are acid–sulfate type with pH values of 1–5. Sulfuric acid is the dominant component, especially as pH values decrease below 3, and it forms from the oxidation of elemental S whose origin is H2S in hot gases derived from boiling of hydrothermal waters at depth. Four determinations of pH were obtained: (1) field pH at field temperature, (2) laboratory pH at laboratory temperature, (3) pH based on acidity titration, and (4) pH based on charge imbalance (at both laboratory and field temperatures). Laboratory pH, charge imbalance pH (at laboratory temperature), and acidity pH were in close agreement for pH < 2.7. Field pH measurements were predominantly used because the charge imbalance was <±10%. When the charge imbalance was generally >±10%, a selection process was used to compare acidity, laboratory, and charge balance pH to arrive at the best estimate. Differences between laboratory and field pH can be explained based on Fe oxidation, H2S or S2O3 oxidation, CO2 degassing, and the temperature-dependence of pK2 for H2SO4. Charge imbalances are shown to be dependent on a speciation model for pH values <3. The highest SO4 concentrations, in the thousands of mg/L, result from evaporative concentration at elevated temperatures as shown by the consistently high δ18O values (−10‰ to −3‰) and a δD vs. δ18O slope of 3, reflecting kinetic fractionation. Low SO4 concentrations (<100 mg/L) for thermal waters (>350 mg/L Cl) decrease as the Cl− concentration increases from boiling which appears inconsistent with the hypothesis of H2S oxidation as a source of hydrothermal SO4. This trend is consistent with the alternate hypothesis of anhydrite solubility equilibrium. Acid–sulfate water analyses are occasionally high in As, Hg, and NH3 concentrations but in contrast to acid mine waters they are low to below detection in Cu, Zn, Cd, and Pb concentrations. Even concentrations of SO4, Fe, and Al are much lower in thermal waters than acid mine waters of the same pH. This difference in water chemistry may explain why certain species of fly larvae live comfortably in Yellowstone’s acid waters but have not been observed in acid rock drainage of the same pH.  相似文献   

9.
Stable isotopes (H, O, C) were determined for ground and surface waters collected from two relatively undisturbed massive sulfide deposits (Halfmile Lake and Restigouche) in the Bathurst Mining Camp (BMC), New Brunswick, Canada. Additional waters from active and inactive mines in the BMC were also collected. Oxygen and hydrogen isotopes of surface and shallow groundwaters from both the Halfmile Lake and Restigouche deposits are remarkably uniform (− 13 to − 14‰ and − 85 to − 95‰ for δ18OVSMOW and δ2HVSMOW, respectively). These values are lighter than predicted for northern New Brunswick and, combined with elevated deuterium excess values, suggest that recharge waters are dominated by winter precipitation, recharged during spring melting. Deeper groundwaters from the Restigouche deposit, and from active and inactive mines have heavier δ18OVSMOW ratios (up to − 10.8‰) than shallow groundwaters suggesting recharge under warmer climate or mixing with Shield-type brines. Some of the co-variation in Cl concentrations and δ18OVSMOW ratios can be explained by mixing between saline and shallow recharge water end-members. Carbon isotopic compositions of dissolved inorganic carbon (DIC) are variable, ranging from − 15 to − 5‰ δ13CVPDB for most ground and surface waters. Much of the variation in the carbon isotopes is consistent with closed system groundwater evolution involving soil zone CO2 and fracture zone carbonate minerals (calcite, dolomite and siderite; average = − 6.5‰ δ13CVPDB). The DIC of saline Restigouche deposit groundwater is isotopically heavy (∼+ 12‰ δ13CVPDB), indicating carbon isotopic fractionation from methanogenesis via CO2 reduction, consistent with the lack of dissolved sulfate in these waters and the observation of CH4-degassing during sampling.  相似文献   

10.
In this study, the geochemistry and origin of natural gas and formation waters in Devonian age organic-rich shales and reservoir sandstones across the northern Appalachian Basin margin (western New York, eastern Ohio, northwestern Pennsylvania, and eastern Kentucky) were investigated. Additional samples were collected from Mississippian Berea Sandstone, Silurian Medina Sandstone and Ordovician Trenton/Black River Group oil and gas wells for comparison. Dissolved gases in shallow groundwaters in Devonian organic-rich shales along Lake Erie contain detectable CH4 (0.01–50.55 mol%) with low δ13C–CH4 values (−74.68 to −57.86‰) and no higher chain hydrocarbons, characteristics typical of microbial gas. Nevertheless, these groundwaters have only moderate alkalinity (1.14–8.72 meq/kg) and relatively low δ13C values of dissolved inorganic C (DIC) (−24.8 to −0.6‰), suggesting that microbial methanogenesis is limited. The majority of natural gases in Devonian organic-rich shales and sandstones at depth (>168 m) in the northern Appalachian Basin have a low CH4 to ethane and propane ratios (3–35 mol%; C1/C2 + C3) and high δ13C and δD values of CH4 (−53.35 to −40.24‰, and −315.0 to −174.6‰, respectively), which increase in depth, reservoir age and thermal maturity; the molecular and isotopic signature of these gases show that CH4 was generated via thermogenic processes. Despite this, the geochemistry of co-produced brines shows evidence for microbial activity. High δ13C values of DIC (>+10‰), slightly elevated alkalinity (up to 12.01 meq/kg) and low SO4 values (<1 mmole/L) in select Devonian organic-rich shale and sandstone formation water samples suggest the presence of methanogenesis, while low δ13C–DIC values (<−22‰) and relatively high SO4 concentrations (up to 12.31 mmole/L) in many brine samples point to SO4 reduction, which likely limits microbial CH4 generation in the Appalachian Basin. Together the formation water and gas results suggest that the vast majority of CH4 in the Devonian organic-rich shales and sandstones across the northern Appalachian Basin margin is thermogenic in origin. Small accumulations of microbial CH4 are present at shallow depths along Lake Erie and in western NY.  相似文献   

11.
The δ13C values of dissolved HCO3? in 75 water samples from 15 oil and gas fields (San Joaquin Valley, Calif., and the Houston-Galveston and Corpus Christi areas of Texas) were determined to study the sources of CO2 of the dissolved species and carbonate cements that modify the porosity and permeability of many petroleum reservoir rocks. The reservoir rocks are sandstones which range in age from Eocene through Miocene. The δ13C values of total HCO3? indicate that the carbon in the dissolved carbonate species and carbonate cements is mainly of organic origin.The range of δ13C values for the HCO3? of these waters is ?20–28 per mil relative to PDB. This wide range of δ13C values is explained by three mechanisms. Microbiological degradation of organic matter appears to be the dominant process controlling the extremely low and high δ13C values of HCO3? in the shallow production zones where the subsurface temperatures are less than 80°C. The extremely low δ13C values (< ?10 per mil) are obtained in waters where concentrations of SO42? are more than 25 mg/l and probably result from the degradation of organic acid anions by sulfate-reducing bacteria (SO42? + CH3COO? → 2HCO3? + HS?). The high δ13C values probably result from the degradation of these anions by methanogenic bacteria (CH3COO? + H2OaiHCO3? + CH4).Thermal decarboxylation of short-chain aliphatic acid anions (principally acetate) to produce CO2 and CH4 is probably the major source of CO2 for production zones with subsurface temperatures greater than 80°C. The δ13C values of HCO3? for waters from zones with temperatures greater than 100°C result from isotopic equilibration between CO2 and CH4. At these high temperatures, δ13C values of HCO3? decrease with increasing temperatures and decreasing concentrations of these acid anions.  相似文献   

12.
Aqueous alteration of primitive meteorites was among the earliest geological processes during the evolution of our solar system. ‘Clumped-isotope’ thermometry of carbonates in the CM chondrites, Cold Bokkeveld, Murray, and Murchison, demonstrates that they underwent aqueous alteration at 20-71 °C from a fluid with δ18OVSMOW of 2.0‰ to 8.1‰ and δ17OVSMOW of −0.1‰ to 3.0‰. The δ13CVPDB values of these carbonates exhibit a negative correlation with the δ18OVSMOW of their formation waters, consistent with formation and escape of 13C-depleted CH4 during aqueous alteration. Methane generation under these conditions implies that the alteration fluid was characterized by an Eh ? −0.67 and pH ? 12.5 (or lower at the highest alteration temperatures). Our findings suggest that methane generation may have been a widespread consequence of planetesimal and planetary aqueous alteration, perhaps explaining the occurrence of methane on Titan, Triton, Pluto, and other Kuiper-belt objects.  相似文献   

13.
Thermal water samples and related young and fossil mineralization from a geothermal system at the northern margin of the Upper Rhine Graben have been investigated by combining hydrochemistry with stable and Sr isotope geochemistry. Actively discharging thermal springs and mineralization are present in a structural zone that extends over at least 60 km along strike, with two of the main centers of hydrothermal activity being Wiesbaden and Bad Nauheim. This setting provides the rare opportunity to link the chemistry and isotopic signatures of modern thermal waters directly with fossil mineralization dating back to at least 500–800 ka. The fossil thermal spring mineralization can be classified into two major types: barite-(pyrite) fracture filling associated with laterally-extensive silicification; and barite, goethite and silica impregnation mineralization in Tertiary sediments. Additionally, carbonatic sinters occur around active springs. Strontium isotope and trace element data suggest that mixing of a hot (>100 °C), deep-sourced thermal water with cooler groundwater from shallow aquifers is responsible for present-day thermal spring discharge and fossil mineralization. The correlation between both Sr and S isotope ratios and the elevation of the barite mineralization relative to the present-day water table in Wiesbaden is explained by mixing of deep-sourced thermal water having high 87Sr/86Sr and low δ34S with shallow groundwater of lower 87Sr/86Sr and higher δ34S. The Sr isotope data demonstrate that the hot thermal waters originate from an aquifer in the Variscan crystalline basement at depths of 3–5 km. The S isotope data show that impregnation-type mineralization is strongly influenced by mixing with SO4 that has high δ34S values. The fracture style mineralization formed by cooling of the thermal waters, whereas impregnation-type mineralization precipitated by mixing with SO4-rich groundwater percolating through the sediments.  相似文献   

14.
Continental carbonates of Quaternary age in southern Italy commonly exhibit the facies of calcareous tufa, often reported as related to shallow aquifers fed by meteoric waters and to organic processes. A close spatial relationship exists between the mappable tufa deposits and major Quaternary extensional faults. With respect to the Ca‐Mg‐HCO3 composition of limestone aquifers’ springs, tufa‐depositing springs exhibit higher salinity and alkalinity, are slightly warmer, have lower pH and are enriched in SO4 and CO2. Their δ13C values are systematically positive and compatible with a deep‐seated carbon source. A clear input of soil‐derived organic carbon is indicated only for small, non‐mappable tufas deposited by perched springs. The dataset indicates that the large tufa deposits owe their origin to a supplementary source of CO2 advected by degassing through active faults, as a necessary prerequisite for inducing a rise of total dissolved salts and alkalinity. Meteoric waters that have come from a shallow aquifer are able to precipitate only limited amount of carbonates.  相似文献   

15.
《Applied Geochemistry》2001,16(6):633-649
Water inflows in the Gotthard Highway Tunnel and in the Gotthard Exploration Tunnel are meteoric waters infiltrating at different elevations, on both sides of an important orographic divide. Limited interaction of meteoric waters with gneissic rocks produces Ca–HCO3 and Na–Ca–HCO3 waters, whereas prolonged interaction of meteoric waters with the same rocks generates Na–HCO3 to Na–SO4 waters. Waters circulating in Triassic carbonate-evaporite rocks have a Ca–SO4 composition. Calcium-Na–SO4 waters are also present. They can be produced through interaction of either Na–HCO3 waters with anhydrite or Ca–SO4 waters with a local gneissic rock, as suggested by reaction path modeling. An analogous simulation indicates that Na–HCO3 waters are generated through interaction of Ca–HCO3 waters with a local gneissic rock. The two main SO4-sources present in the Alps are leaching of upper Triassic sulfate minerals and oxidative dissolution of sulfide minerals of crystalline rocks. Values of δ34SSO4 < ∼+9‰ are due to oxidative dissolution of sulfide minerals, whereas δ34SSO4 >∼+9‰ are controlled either by bacterial SO4 reduction or leaching of upper Triassic sulfate minerals. Most waters have temperatures similar to the expected values for a geothermal gradient of 22°C/km and are close to thermal equilibrium with rocks. However relatively large, descending flows of cold waters and ascending flows of warm waters are present in both tunnels and determine substantial cooling and heating, respectively, of the interacting rocks. The most import upflow zone of warm, Na-rich waters is below Guspisbach, in the Gotthard Highway Tunnel, at 6.2–9.0 km from the southern portal. These warm waters have equilibrium temperatures of 65–75°C and therefore constitute an important low-enthalpy geothermal resource.  相似文献   

16.
Thirty-nine samples of both cold and thermal karst groundwater from Taiyuan, northern China were collected and analyzed with the aim of developing a better understanding of the geochemical processes that control the groundwater quality evolution in the region’s carbonate aquifers. The region’s karst groundwater system was divided into three geologically distinct sub-systems, namely, the Xishan Mountain karst groundwater subsystem (XMK), the Dongshan Mountain karst groundwater subsystem (DMK) and the Beishan Mountain karst groundwater subsystem (BMK). Hydrochemical properties of the karst groundwaters evolve from the recharge zones towards the cold water discharge zones and further towards the thermal water discharge zones. In the XMK and the DMK, the hydrochemical type of the groundwater evolves from HCO3-Ca·Mg in the recharge - flow-through zone, to HCO3·SO4-Ca·Mg/SO4·HCO3-Ca·Mg in the cold water discharge zone, and further to SO4-Ca·Mg in the thermal water discharge zone. By contrast, the water type changes from HCO3-Ca·Mg to HCO3·SO4-Ca·Mg in the BMK, with almost invariable TDS and temperatures all along from the recharge to the discharge zone. The concentrations of Sr, Si, Fe, F− and of some trace elements (Al, B, Li, Mn, Mo, Co, Ni) increase as groundwater temperature increases. Different hydrogeochemical processes occur in the three karst groundwater sub-systems. In the XMK and the DMK, the geochemical evolution of the groundwater is jointly controlled by carbonate dissolution/precipitation, gypsum dissolution and dedolomitization, while only calcite and dolomite dissolution/precipitation occurs in the BMK without dedolomitization. The hydrogeochemical data of the karst groundwaters were used to construct individual geochemical reaction models for each of the three different karst groundwater sub-systems. The modeling results confirm that dedolomization is the major process controlling hydrochemical changes in the XMK and the DMK. In the thermal groundwaters, the dissolution rates of fluorite, siderite and strontianite were found to exceed those of the cold karst groundwater systems, which can explain the higher concentrations of F−, Fe and Sr2+ that are found in these waters.  相似文献   

17.
The geothermal field at Hofsstadir northern Snæfellsnes peninsula, Iceland produces low-temperature geothermal water with about 5.4‰ salinity. The fluid temperature is 87 °C, near the reservoir temperature of 90 °C as assessed from mineral solution/equilibrium conditions. The stable isotopic ratios δ2H and δ18O show that the water is significantly lighter than present day precipitation anywhere on the Snæfellsnes peninsula. It is offset from the meteoric water line towards isotopically depleted 18O values, most likely due to CO2(g) – H2O exchange at earlier times during evolution of the system. Such a concentration of stable isotopes is unique for Icelandic groundwaters and has not been encountered anywhere else in Iceland. The water may either have its origin far north of the Bay of Breidafjörður in the highland of the western fjordlands or dating back to a Pre-Holocene age when local precipitation was considerably lighter due to the cold climate at that time. The water is highly concentrated in Ca in comparison with seawater and also compared to that of geothermal saline water elsewhere, which indicates intensive and prolonged water–rock interaction. The 14C concentration is low, about 7.4 pMC (percent modern C), compared to the cold local groundwater of about 74.6 pMC. δ13C for the thermal and cold waters is −4.9‰ and −2.3‰, respectively. The geothermal water is used for heating the small town of Stykkishólmur through a central heat exchanger plant due to the high salinity of the water. The outbuilding of a health resort has been planned and the water has been used successfully for the treatment of psoriasis and is claimed to have beneficial effects in bathing therapy for rheumatism as well as for drinking cures.  相似文献   

18.
The Imphal valley is an intramontane basin confined within an anticlinorium of several anticlines and synclines in the Disang Group of rocks of Tertiary age. This valley of more than 2 million people is occupied by fluvio-lacustrine deposits of Quaternary age and is located in the central part of the Indo-Myanmar range of Northeast India. The hydrogeochemical parameters of temperature, pH, ORP, TDS, Na, Cl, Br, Ba, B, Sr, Li, δ18O, HCO3, K, Mg, Ca, NO3, PO4, SO4 in 173 samples using ion-chromatograph, ICP (AES), ICP (OES), ICP (MS) and 37 dugwells were studied to understand the occurrence and origin of salinization process for the first time. The order of abundance of ions is identified as HCO3 > Na > Cl > Ca > Mg > K > NO3 > PO4 > Sr > Br > B>Ba > Li > SO4. Five hydrochemical facies (Na–Cl, Ca–Mg–HCO3, Na–HCO3, Ca–Mg–HCO3–Cl and Ca–Mg–Cl) represent the types of waters. The saline-dominated water types (Na–Cl and Na–HCO3) represent piedmont and the rest of the facies represent alluvial plain and flood plain groundwaters. Durov’s diagram reveales initial and intermediate stages of groundwater evolution. Isotope δ18O, Gibbs diagram and ions scatter plots suggest evaporation and crystallization processes leading to halite encrustation in the Disang shales. Negative Eh, low NO3 and the absence of SO4 indicates reduced condition coupled with rich dissolve organic matters leading to elevation of salts in soils around piedmont where the rock type is exclusively of the Disang shales. Trilinear plot, correlation matrix and water table flow analysis suggest salinization of groundwater originates in piedmont groundwater and disseminates towards alluvial plain and flood plain along the flow path.  相似文献   

19.
《Applied Geochemistry》2005,20(1):41-54
The Pisa plain contains a multilayered confined aquifer made up of Pleistocene sands and gravels. The groundwater from the wells tapping these horizons are generally of poor quality: they exhibit significant TDS, relatively high Cl content and considerable hardness. During geothermal prospecting of the Pisa plain, about 80 wells ranging in depth from 20 to 250 m were sampled, and both chemical (major ions) and isotope analyses were conducted. The data collected show that TDS is strongly influenced by HCO3 and Cl, and that a 3-component mixing process affects the groundwater’s chemical composition. The end members of this mixing process have been identified as: (a) diluted HCO3 meteoric water, which enters the plain mainly from the eastern and northern sides of the study area; (b) Cl-rich water, which largely characterizes the shallow sandy horizons of the multilayered aquifer system and has been attributed to the presence of seawater, as also suggested by δ18O data; and (c) SO4-rich groundwater, which is linked to the hot groundwater circulation within Mesozoic carbonate formations and, at first sight, seemed to affect only the gravelly aquifer. A SO4-rich water also contributes to the sandy aquifer; it probably enters the plain both laterally, from the margins of the Pisan Mountains and from depth, but promptly undergoes substantial SO4 reduction processes by bacteria. That such processes are at work is suggested both by the low SO4 and high HCO3 concentrations found in the well waters and by their C and S isotope compositions. The collected data have allowed zones with higher quality waters to be identified, which may someday be used for the local water supply.  相似文献   

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