Geochemistry of thermal springs,Alhama de Granada (southern Spain)

The waters of the thermal springs at Alhama de Granada vary in temperature between 27 and 45°C. Temporal changes in the composition of the principal spring (Baños Viejos) indicate that a small degree of mixing may occur between deep thermal waters and shallow groundwater. Slight compositional variations also occur between the various thermal springs in the study area. These spatial variations are due to the different local hydrodynamic conditions in the springs. Towards the north in less hydraulically transmissive rocks, cooling of the rising water is more noticeable, as are ion exchange and processes of SO₄ reduction. The chemical composition of the water is related to the dissolution of evaporites (SO₄ and Cl salts), carbonates and silicates, and to the possible existence of sources of S within the rock. Estimates of the mean residence times have been obtained based on ¹⁴C_DIC and T. The state of thermodynamic equilibrium at the spring discharge was calculated using the SOLMINEQ.88 program. The results indicate that all the samples are supersaturated with respect to quartz, chalcedony, cristobalite, calcite, aragonite and dolomite, and undersaturated with respect to gypsum, anhydrite and halite. The use of different geothermometers and modelling of saturation indices for quartz, albite and anhydrite indicate temperatures of about 110°C.     

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.     

Mineral equilibria and geothermometry of the Dalaman–Köyceğiz thermal springs,southern Turkey

The Dalaman and Köyceğiz thermal springs are from karstic limestones belonging to Upper Cretaceous to Burdigalian Beydağları autochthon and Carboniferous to Lutetian Lycian nappes. They have measured temperatures of 24– 41 °C, specific electrical conductivities of 14,310–45,600 μS/cm, and are dominated by Na (1550–8500 mg/kg) and Cl (2725–15,320 mg/kg). The heat source of the geothermal systems of the area is tectonic related and the occurrence of the thermal springs is related to the young normal faults. Meteoric waters and seawaters recharge the reservoir rocks, are heated at depth with increasing geothermal gradient, and move up to the surface through the fractures and faults by convection trend and emerge as thermal springs. While thermal waters move up to the surface, they mix with different proportions of seawater and cold fresh waters. The seawater contribution to the thermal waters varies from 24% to 78%. Lake waters in the area are connected with thermal waters. Consequently, their chemical composition is influenced by the chemistry of thermal waters. Chemical equilibrium modelling based on measured outlet temperatures and measured pH shows that all the waters are oversaturated with respect to quartz and K-mica and undersaturated with respect to Al(OH)₃, anorthite, gypsum, siderite and SiO₂(a). Albite, alunite, aragonite, Ca-montmorillonite, calcite, chalcedony, chlorite, dolomite, Fe(OH)₃(a), fluorite, gypsum, illite, K-feldspar, kaolinite and sepiolite minerals are mostly oversaturated or undersaturated. Mineral saturation studies of the thermal springs indicate that dolomite, chalcedony and quartz are most likely to cause scaling at outlet conditions. Assessments from various chemical geothermometers, and Na–K–Mg ternary and mineral equilibrium diagrams suggest that the reservoir temperature is around 65–90 °C. The temperatures obtained from quartz, quartz-steam loss, Mg/Li geothermometers and mineral equilibrium diagrams give the most reasonable results.     

Hydrogeochemical characteristics and sources of salinity of the springs near Wenquanzhen in the eastern Sichuan Basin,China

Natural springs have the potential to provide important information on hydrogeochemical processes within aquifers. This study used traditional and classic technical methods and procedures to determine the characteristics and evolution of springs to gain further knowledge on the differences between hot saline springs and cold fresh springs. In a short river segment near Wenquanzhen in the eastern Sichuan Basin, southwest China, several natural springs coexist with total dissolved solids (TDS) ranging from less than 1 to 15 g/L and temperatures from 15 to 40 °C. The springs emanate from the outcropping Lower and Middle Triassic carbonates in the river valley cutting the core of an anticline. The cold springs are of Cl·HCO₃-Na·Ca and Cl·SO₄-Na types, and the hot saline springs are mainly of Cl-Na type. The chemistry of the springs has undergone some changes with time. The stable hydrogen and oxygen isotopes indicate that the spring waters are of a meteoric origin. The salinity of the springs originates from dissolution of minerals, including halite, gypsum, calcite and dolomite. The evolution of the springs involves the following mechanisms: the groundwater receives recharge from infiltration of precipitation, then undergoes deep circulation in the core of the anticline (incongruent dissolution of the salt-bearing strata occurs), and emerges in the river valley in the form of hot springs with high TDS. Groundwater also undergoes shallow circulation in the northern and southern flanks of the anticline and appears in the river valley in the form of cold springs with low TDS.

     

Isotope–geochemical characterization and geothermometrical modeling of Uttarakhand geothermal field,India

Uttarakhand geothermal area, located in the central belt of the Himalayan geothermal province, is one of the important high temperature geothermal fields in India. In this study, the chemical characteristics of the thermal waters are investigated to identify the main geochemical processes affecting the composition of thermal waters during its ascent toward the surface as well as to determine the subsurface temperature of the feeding reservoir. The thermal waters are mainly Ca–Mg–HCO₃ type with moderate silica and TDS concentrations. Mineral saturation states calculated from PHREEQC geochemical code indicate that thermal waters are supersaturated with respect to calcite, dolomite, aragonite, chalcedony, quartz (SI > 0), and undersaturated with respect to gypsum, anhydrite, and amorphous silica (SI < 0). XRD study of the spring deposit samples fairly corroborates the predicted mineral saturation state of the thermal waters. Stable isotopes (δ¹⁸O, δ²H) data confirm the meteoric origin of the thermal waters with no oxygen-18 shift. The mixing phenomenon between thermal water with shallow ground water is substantiated using tritium (³H) and chemical data. The extent of dilution is quantified using tritium content of thermal springs and non-thermal waters. Classical geothermometers, mixing model, and multicomponent fluid geothermometry modeling (GeoT) have been applied to estimate the subsurface reservoir temperature. Among different classical geothermometers, only quartz geothermometer provide somewhat reliable estimation (96–140 °C) of the reservoir temperature. GeoT modeling results suggest that thermal waters have attained simultaneous equilibrium with respect to minerals like calcite, quartz, chalcedony, brucite, tridymite, cristobalite, talc, at the temperature 130 ± 5 °C which is in good agreement with the result obtained from the mixing model.     

Dolomite Versus Calcite Weathering in Hydrogeochemically Diverse Watersheds Established on Bedded Carbonates (Sava and So?a Rivers, Slovenia)

The relative contributions of dolomite to calcite weathering related to riverine fluxes are investigated on a highly resolved spatial scale in the diverse watersheds of Slovenia, which previous work has shown have some of the highest carbonate-weathering intensities in the world and suggests that dolomite weathering is favored over limestone weathering in mixed carbonate watersheds. The forested Sava and So?a River watersheds of Slovenia with their headwaters in the Julian Alps drain alpine regions with thin soils (<30 cm) and dinaric karst regions with thicker soils (0 to greater than 70 cm) all developed over bedded Mesozoic carbonates (limestone and dolomite), and siliclastic sediments is the ideal location for examining temperate zone carbonate weathering. This study extends previous work, presenting geochemical data on source springs and documenting downstream geochemical fluctuations within tributaries of the Sava and So?a Rivers. More refined sampling strategies of springs and discrete drainages permit directly linking the stream Mg²⁺/Ca²⁺ ratios to the local bedrock lithology and the HCO₃ ^? concentrations to the relative soil depths of the tributary drainages. Due to differences in carbonate source lithologies of springs and tributary streams, calcite and dolomite weathering end members can be identified. The Mg²⁺/Ca²⁺ ratio of the main channel of the Sava River indicates that the HCO₃ ^? concentration can be attributed to nearly equal proportions by mass of dolomite relative to calcite mineral weathering (e.g., Mg²⁺/Ca²⁺ mole ratio of 0.33). The HCO₃ ^? concentration and pCO₂ values increase as soil thickness and alluvium increase for discrete spring samples, which are near equilibrium with respect to calcite. Typically, this results in approximately 1.5 meq/l increase in HCO₃ ^? from the alpine to the dinaric karst regions. Streams in general do not change in HCO₃ ^?, Mg²⁺/Ca²⁺, or Mg²⁺/HCO₃ ^? concentrations down course, but warming and degassing of CO₂ produce high degrees of supersaturation with respect to calcite. Carbonate-weathering intensity (mmol/km²-s) is highest within the alpine regions where stream discharge values range widely to extreme values during spring snowmelt. Overall, the elemental fluxes of HCO₃ ^?, Ca²⁺, and Mg²⁺ from the tributary watersheds are proportional to the total water flux because carbonates dissolve rapidly to near equilibrium. Importantly, dolomite weathers preferentially over calcite except for pure limestone catchments.     

Hydrogeochemistry of thermal and mineralized waters in the Diyadin (Ağri) area,Eastern Turkey

The Diyadin Geothermal area, located in the eastern part of Anatolia (Turkey) where there has been recent volcanic activity, is favorable for the formation of geothermal systems. Indeed, the Diyadin geothermal system is located in an active geodynamic zone, where strike-slip faults and tensional cracks have developed due to N–S regional compression. The area is characterized by closely spaced thermal and mineralized springs, with temperatures in the range 30–64 °C, and flowrates 0.5–10 L/s. Thermal spring waters are mainly of Ca(Na)-HCO₃ and Ca(Mg)-SO₄ types, with high salinity, while cold groundwater is mostly of Ca(Na, Mg)-HCO₃ type, with lower salinity. High contents of some minor elements in thermal waters, such as F, B, Li, Rb, Sr and Cs probably derive from enhanced water–rock interaction.Thermal water samples collected from Diyadin are far from chemical equilibrium as the waters flow upward from reservoirs towards spring vents and possibly mix with cooler waters. The temperatures of the deep geothermal reservoirs are estimated to be between 92 and 156 °C in Diyadin field, based on quartz geothermometry, while slightly lower estimates are obtained using chalcedony geothermometers. The isotopic composition of thermal water (δ¹⁸O, δ²H, δ³H) indicates their deep-circulating meteoric origin. The waters are likely to have originated from the percolation of rainwater along fractures and faults to the deep hot reservoir. Subsequent heating by conduction due to the presence of an intrusive cupola associated with the Tendurek volcano, is followed by the ascent of deep waters to the surface along faults and fractures that act as hydrothermal conduits.Modeling of the geothermal fluids indicates that the fluid is oversaturated with calcite, aragonite and dolomite, which matches travertine precipitation in the discharge area. Likewise, the fluid is oversaturated with respect to quartz, and chalcedony indicating the possibility of siliceous precipitation near the discharge areas. A conceptual hydro-geochemical model of the Diyadin thermal waters based on the isotope and chemical analytical results, has been constructed.     

The dolomitization of CaCO3: an experimental study at 252–295°C

The results of experiments on the hydrothermal dolomitization of calcite (between 252 and 295°C) and aragonite (at 252°C) by a 2 M CaCl₂-MgCl₂ aqueous solution are reported and discussed. Dolomitization of calcite proceeds via an intermediate high (ca. 35 mole %) magnesian calcite, whereas that of aragonite is carried out through the conversion of the reactant into a low (5.6 mole %) magnesian calcite which in turn transforms into a high (39.6 mole %) magnesian calcite. Both the intermediate phases and dolomite crystallize through a dissolution-precipitation reaction. The intermediate phases form under local equilibrium within a reaction zone surrounding the dissolving reactant grains. The volume of the reaction zone solution can be estimated from Sr²⁺ and Mg²⁺ partitioning equations. In the case of low magnesian calcite growing at the expense of aragonite at 252°C, the total volume of these zones is in the range of 2 × 10^?5 to 2 × 10^?4 1., out of 5 × 10^?3 1., the volume of the bulk solution.The apparent activation energies for the initial crystallization of high magnesian calcite and dolomite are 48 and 49 kcal/mole, respectively.Calcite transforms completely into dolomite within 100 hr at 252°C. The overall reaction time is reduced to approximately 4 hr at 295°C. The transformation of aragonite to dolomite at 252°C occurs within 24 hr. The nature of the reactant dictates the relative rates of crystallization of the intermediate phases and dolomite. With calcite as reactant, dolomite growth is faster than that of magnesian calcite; this situation is reversed when aragonite is dolomitized.Coprecipitation of Sr²⁺ with dolomite is independent of temperature (within analytical error) between 252 and 295°C. Its partitioning, with respect to calcium, between dolomite and solution results in distribution coefficients in the range of 2.31 × 10^?2 to 2.78 × 10^?2.     

Evidence for episodic cementation and diagenetic recording of seismic pumping events,North Coles Levee,California, U.S.A.

Bands of calcite and dolomite cements alternating with zones of nearly carbonate-free sand occur in the Stevens sandston aat North Coles Levee, San Joaquin, Valley, California. Temperatures calculated from O isotopes suggest that the calcite cement bands were emplaced episodically as a result of repeated injections of hot water from deeper in the section. Burial analysis suggests that these cements precipitated from 7 Ma to the present over the temperature range of 45 to ∼95°C.Carbon isotope data suggest that the C in the cements is a mixture derived from two sources, detrital shell material (δ¹³C(PDB)≈) and CO₂ liberated from maturing kerogen (δ¹³C ≈ −24). Plots of δ¹³C vs time and depth of crystallization show that the cementation sequence was: (1) dolomite cements, possibly concretionary, precipitated at depths <1–2 km and at temperatures <45°C; (2) calcite cements with δ¹³C(PDB) values as low as −13, crystallized from depths between 1220 and 1820 m (4000 and 6000 ft) and at temperatures between 45 and 80°C; (3) calcite cements with δ¹³C(PDB) values approaching zero and calculated temperatures of crystallization up to the present reservoir temperature of 95±3°C.A log of δ¹³C vs calculated depth of crystallization correlates with the stratigraphic column at North Coles Levee. If the correlation is valid the light δ¹³ in each cement sample can be tied to its source. A model based on this interpretation suggests that the early, light C was derived from maturing kerogen in the Kreyenhagen Formation (Eocene) as it passed through the oil window between 4 and 5 Ma. The subsequent passage of younger sediments with less organic material produced correspondingly smaller amounts of light CO₂ which was reflected in the relatively heavier C isotopes in the later cements.It is suggested that the epidsodic injections of hot water carried dissolved gases and minerals, principally calcite, upward from rocks as deep as 2–3 km below the Stevens sandstone and reprecipitated the calcite in more permeable zones in the rock. Degassing of CO₂ from rising pore waters likely triggered the precipitation and accounts for the relatively large volumes of cement. The Sibson model for seismic pumping of pore fluids is considered a likely explanation for the observed cementation.     

Hydrogeological investigations of thermal waters in the Sfax Basin (Tunisia)

The Sfax Basin in eastern Tunisia is bounded to the east by the Mediterranean Sea. Thermal waters of the Sfax area have measured temperatures of 23–36°C, and electrical conductivities of 3,200 and 14,980 μS/cm. Most of the thermal waters are characterized as Na–Cl type although there are a few Na–SO₄–Cl waters. They issue from Miocene units which are made up sands and sandstones interbedded with clay. The Quaternary sediments cap the system. The heat source is high geothermal gradient which are determined downhole temperature measurements caused by graben tectonics of the area. The results of mineral equilibrium modeling indicate that the thermal waters of the Sfax Basin are undersaturated with respect to gypsum, anhydrite and fluorite, oversaturated with respect to kaolinite, dolomite, calcite, microcline, quartz, chalcedony, and muscovite. Assessments from various chemical geothermometers, Na–K–Mg ternary and mineral equilibrium diagrams suggest that the reservoir temperature of the Sfax area can reach up to 120°C. According to δ¹⁸O and δ²H values, all thermal and cold groundwater is of meteoric origin.     

Carbonate chemistry of groundwater from chalk,Givendale, East Yorkshire

Precipitation, soil and spring waters from an outlier of Chalk were analysed over a one year period for field pH, and contents of Ca⁺², Mg⁺², HCO₃^? and other dissolved solids. Measured soil log PCO₂ (atm) varied between a minimum of ?2.60 and maximum of ?1.46, and could be predicted from measurements of soil temperature. Soil waters evolved under open system conditions with respect to soil CO₂, and were undersaturated with calcite during the winter recharge period.The chemistry of the springs is related to their topographic position. Group 1 springs, located below a feather edge of chalk, had both their minimum and maximum PCO₂s predicted by the soil CO₂ data, suggesting open system CO₂ evolution. Group 2 springs, located along the scarp slope had minimum PCO₂s predicted by the soil data, but maximum PCO₂s which could only be explained by a closed system evolution from the maximum soil CO₂ observed. Group 1 springs were close to calcite saturation, whereas Group 2 springs were significantly undersaturated with calcite. The two groups could be identified by linear discriminant analysis of measured Ca²⁺, pH and HCO₃^? concentrations.     

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.     

Fluorapatite and fluorite solubility controls on geothermal waters in Yellowstone National Park

Potential solubility controls on phosphorus in Yellowstone National Park geothermal waters were investigated using the analytical phosphate estimates of Stauffer and Thompson (1978), the computer program, WATEQF, and adopting the equilibrium constant: $\text{log}\text{K}{}_{\mathrm{25°}}\text{= ?61.4}$ for fluorapatite (FAP = Ca₅(PO₄)₃F) dissolution. The near-boiling high-Cl geyser and spring effluents are at or near saturation with respect to (with) FAP. The sixteen representative springs in this category had FAP saturation indices ($\text{S.I. =}\text{log}\text{IAP/K}{}_{\mathrm{r}}$) ranging from ? 3.2 to +4.9 and averaging +0.9. The strongly positive indices were all associated with the highly alkaline conditions resulting from adiabatic cooling in the near surface environment. Hot spring waters indicating extensive dilution (reduced Cl) by meteoric water have lower pH's, and despite PO₄ and Ca concentrations an order of magnitude higher than the geysers, are still frequently undersaturated with FAP. The travertine-depositing “Mixed-water” springs are invariably supersaturated with FAP at ground surface and at or near saturation with hydroxylapatite. Supersaturation may result from kinetic inhibition of apatite crystallization by the elevated Mg²⁺, HCO₃^?, and lower temperatures in these springs. The phosphates may be residuals of the meteoric dilution water.Separately, if Strübel's temperature-dependent estimates of fluorite (CaF₂) solubility are adopted, the high-Cl geysers and springs on “Geyser Hill” and at Norris are consistently undersaturated with CaF₂ at the 90–100° orifice temperatures. The apparent disequilibrium may reflect fluorite equilibration at the much higher temperatures (> 200°C) in the deeper enthalpy reservoirs.     

Geothermometry and circulation depth of groundwater in Semnan thermal springs,Northern Iran

Semnan thermal springs with high TDS and moderate temperature are located northwest of Semnan, the northern part of Iran. The spatial and temporal variations of physicochemical characteristics of the thermal and cold springs were investigated for the recognition of origin and dominant hydrogeochemical processes. Results show that the thermal springs have the same origin, but due to different ascending flow paths and different conductive cooling mechanism, their temperatures vary. The chemical composition of thermal waters is controlled by dolomite, halite and sulfate minerals dissolution and calcite precipitation and bacterial sulfate reduction. The concentration of major and trace elements in the thermal springs does not change in wet and dry seasons notably because they are derived from old groundwater with deep circulation and high temperature. Seasonal change in the concentration of some trace elements is due to the seasonal variation of pH, Eh, temperature and dilution by shallow waters. Decreasing SO₄ and carbonate saturation index and increasing Na/Cl ratios and Ca content in the dry season show dilution effect caused by the previous heavy rainfall events. The temperature of the heating reservoir based on K–Mg, chalcedony, quartz and chemical equilibrium approach was approximately estimated in the range of 60–80 °C. Hydrogeologically, a conceptual model was suggested for the thermal springs. The general groundwater flow direction is probably from the dolomite Lar Formation in Chenaran anticline toward the adjacent syncline in a confined condition, and then a thrust fault acts as a conduit and redirects the thermal water to the emerging springs at the surface.     

Geochemical characterization of surface water and spring water in SE Kashmir Valley,western Himalaya: Implications to water–rock interaction

Water samples from precipitation, glacier melt, snow melt, glacial lake, streams and karst springs were collected across SE of Kashmir Valley, to understand the hydrogeochemical processes governing the evolution of the water in a natural and non-industrial area of western Himalayas. The time series data on solute chemistry suggest that the hydrochemical processes controlling the chemistry of spring waters is more complex than the surface water. This is attributed to more time available for infiltrating water to interact with the diverse host lithology. Total dissolved solids (TDS), in general, increases with decrease in altitude. However, high TDS of some streams at higher altitudes and low TDS of some springs at lower altitudes indicated contribution of high TDS waters from glacial lakes and low TDS waters from streams, respectively. The results show that some karst springs are recharged by surface water; Achabalnag by the Bringi stream and Andernag and Martandnag by the Liddar stream. Calcite dissolution, dedolomitization and silicate weathering were found to be the main processes controlling the chemistry of the spring waters and calcite dissolution as the dominant process in controlling the chemistry of the surface waters. The spring waters were undersaturated with respect to calcite and dolomite in most of the seasons except in November, which is attributed to the replenishment of the CO₂ by recharging waters during most of the seasons.     

Geochemical characterization and origins of the thermal springs in southern Gaoligong Mountains,China

Hydrogeochemistry and environmental isotope data were utilized to understand origins and characteristics of the thermal springs in southern Gaoligong Mountains, China. The groundwater at the thermal springs has low values of total dissolved solids, and its main water types are Na-HCO₃. The thermal springs are mainly recharged from meteoric precipitations. The recharge areas are located near the springs at an approximate elevation of 1,800 m. The groundwater of the thermal springs is immature and partially equilibrated with a strong mixture of the shallow cold waters during the flow process. The shallow cold water accounts for more than 90 %. The temperatures of thermal reservoir that feed the springs are between 146 and 260 °C, and the calculated groundwater circulation depths range from 2,000 to 5,700 m below ground surface.     

Origin and migration of palaeofluids in the Upper Visean of the Campine Basin, northern Belgium

Upper Visean limestones in the Campine Basin of northern Belgium are intensively fractured. The largest and most common fractures are cemented by non-ferroan, dull brown-orange luminescent blocky calcite. First melting temperatures of fluid inclusions in these calcites are around -57°C, suggesting that precipitation of the cements occurred from NaCl-CaCl₂-MgCl₂ fluids. The final melting temperatures (T_m^ice) are between -5 and -33°C. The broad range in the T_m^ice data can be explained by the mixing of high salinity fluids with meteoric waters, but other hypotheses may also be valid. Homogenization temperatures from blocky calcite cements in the shelf limestones are interpreted to have formed between 45 and 75°C. In carbonates which were deposited close to and at the shelf margin, precipitation temperatures were possibly in the range 70-85°C and 72-93°C, respectively. On the shelf, the calcites have a δ¹⁸O around -9.3‰ PDB and they are interpreted to have grown in a fluid with a δ¹⁸O between −3.5 and +1.0‰ SMOW. At the shelf margin, blocky calcites (δ¹⁸O∼ - 13.5‰ PDB) could have precipitated from a fluid with a δ¹⁸O betweenn -4.0 and -1.1‰ SMOW. The highest oxygen isotopic compositions are comparable to those of Late Carboniferous marine fluids (δ¹⁸O= - 1‰ SMOW). The lowest values are more positive than a previously reported composition for Carboniferous meteoric waters (δ¹⁸O= -7‰ SMOW). Precipitation is likely to have occurred in marine-derived fluids, which mixed with meteoric waters sourced from near the Brabant Massif. Fluids with a similar negative oxygen isotopic composition and high salinity are actually present in Palaeozoic formations. The higher temperature range in the limestones near the shelf margin is explained by the upward migration of fluids from the ‘basinal’ area along fractures and faults into the shelf.     

Composition and origin of thermal waters in the Gulf of Suez area,Egypt

Thermal waters with discharge temperatures ranging from 32 to 70°C are being discharged along the Gulf of Suez (Egypt) from springs and shallow artesian wells. A comprehensive chemical and isotopic study of these waters supports previous suggestions that the waters are paleometeoric waters from the Nubian sandstone aquifer. The chemical and isotopic compositions of solutes indicate possible contributions from Tertiary sedimentary aquifer rocks and windblown deposits (marine aerosols and/or evaporite dust) in the recharge area. There is no chemical or isotopic evidence for mixing with Red Sea water. Gas effervescence from the Hammam Faraoun thermal water contains about 4% CH₄ (δ¹³C = −32.6‰) and 0.03% He having an isotopic ratio consistent with a mixture of crustal and magmatic He (³He/⁴He = 0.26 Re). Geothermometers for the thermal waters indicate maximum equilibration temperatures near 100°C. The waters could have been heated by percolation to a depth of several km along the regional geothermal gradient.     

Hydrogeochemical factors effecting the scaling problem in Balçova geothermal field,İzmir, Turkey

Reservoir fluid compositions have been assessed from analytical data on water samples collected from thermal and cold waters in Balçova geothermal field. The results of mineral equilibrium modelling indicate that the waters, with some exceptions, are systematically supersaturated with respect to calcite, aragonite, dolomite, chalcedony and quartz, but undersaturated with respect to amorphous silica, celestite, anhydrite and gypsum and undersaturated or supersaturated with respect to barite, low-albite, K-feldspar, gibbsite and Fe(OH)₃(a). Calculation of mineral saturation states and geochemical analyses of scale and field observations show that carbonate minerals (calcite, aragonite and dolomite) are most likely to be precipitated as a scale type. Besides carbonates, scale formation risk of amorphous silica, Fe(OH)₃(a), anhydrite, barite and celestite minerals should be taken into account in some wells and surface equipment. Most of the waters, with some exceptions, have carbonate scaling risk at all temperatures, whereas the other scaling risks only exist over a limited temperature range. While silica, Fe(OH)₃(a) and barite show a scaling tendency at low temperatures, anhydrite and celestite scaling occurs at higher temperatures.     

Evidence for high temperature and 18O‐enriched fluids in the Arab‐D of the Ghawar Field,Saudi Arabia

Using the clumped isotope method, the temperature of dolomite and calcite formation and the oxygen isotopic composition (δ¹⁸O_w) of the diagenetic fluids have been determined in a core taken from the Arab‐D of the Ghawar field, the largest oil reservoir in the world. These analyses show that while the dolomites and limestones throughout the major zones of the reservoir recrystallized at temperatures between ca 80°C and 100°C, the carbonates near the top of the reservoir formed at significantly lower temperatures (20 to 30°C). Although the δ¹⁸O values of the diagenetic fluids show large variations ranging from ca <0‰ to ca +8‰, the variations exhibit consistent downhole changes, with the highest values being associated with the portion of the reservoir with the highest permeability and porosity. Within the limestones, dolomites and dolomites associated with the zone of high permeability, there are statistically significant different trends between the δ¹⁸O_w values and recrystallization temperature. These relationships have different intercepts suggesting that fluids with varying δ¹⁸O_w values were involved in the formation of dolomite and limestone compared to the formation of dolomite associated with the zone of high permeability. These new data obtained using the clumped isotope technique show how dolomitization and recrystallization by deep‐seated brines with elevated δ¹⁸O_w values influence the δ¹⁸O values of carbonates, possibly leading to erroneous interpretations unless temperatures can be adequately constrained.