Geochemical constraints on the Hadean environment from mineral fingerprints of prokaryotes

The environmental conditions on the Earth before 4 billion years ago are highly uncertain, largely because of the lack of a substantial rock record from this period. During this time interval, known as the Hadean, the young planet transformed from an uninhabited world to the one capable of supporting, and inhabited by the first living cells. These cells formed in a fluid environment they could not at first control, with homeostatic mechanisms developing only later. It is therefore possible that present-day organisms retain some record of the primordial fluid in which the first cells formed. Here we present new data on the elemental compositions and mineral fingerprints of both Bacteria and Archaea, using these data to constrain the environment in which life formed. The cradle solution that produced this elemental signature was saturated in barite, sphene, chalcedony, apatite, and clay minerals. The presence of these minerals, as well as other chemical features, suggests that the cradle environment of life may have been a weathering fluid interacting with dry-land silicate rocks. The specific mineral assemblage provides evidence for a moderate Hadean climate with dry and wet seasons and a lower atmospheric abundance of CO2 than is present today.Fil: Novoselov, Alexey A.. Universidad de Concepción; ChileFil: Silva, Dailto. Universidade Estadual de Campinas; BrasilFil: Schneider, Jerusa. Universidade Estadual de Campinas; BrasilFil: Abrevaya, Ximena Celeste. Consejo Nacional de Investigaciónes Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Astronomía y Física del Espacio. - Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Astronomía y Física del Espacio; ArgentinaFil: Chaffin, Michael S.. State University Of Colorado Boulder; Estados UnidosFil: Serrano, Paloma. Alfred Wegener Institute Helmholtz Centre For Polar And Marine Research,; AlemaniaFil: Navarro, Margareth Sugano. Universidade Estadual de Campinas; BrasilFil: Conti, Maria Josiane. André Tosello Institute; BrasilFil: Souza Filho, Carlos Roberto de. Universidade Estadual de Campinas; Brasi

Application of different geothermometrical techniques to a low enthalpy thermal system

The reservoir temperature of the waters in the low temperature carbonate-evaporitic geothermal system of Arnedillo has been estimated by using two different techniques: 1) chemical geothermometers and 2) geothermometrical modelling. By combining the results of both techniques a reliable range of temperature of 90 ± 20 oC has been proposed for the waters in the reservoir. Despite being a carbonate-evaporitic system, the cationic geothermometers have provided good results, which, together with the geothermometrical modelling, indicate that the waters have reached equilibrium with anhydrite, quartz, calcite, dolomite, albite and K-feldspar in the reservoir

Groundwater mixing and geochemical assessment of low-enthalpy resources in the geothermal field of southwestern Tunisia

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Multicomponent geothermometry applied to a medium-low enthalpy carbonate-evaporite geothermal reservoir

Abstract To improve knowledge of the thermal state of medium to low-enthalpy thermal systems hosted in carbonate-evaporite rocks, a mineral-solution equilibrium model was compared to other theoretical geothermometers. We use the GeoT code, which uses as input the chemical composition of water and saturation indices of minerals to calculate water-rock equilibrium over a temperature range of interest. The calculations were applied to the medium and low enthalpy geothermal systems in the Tyrrhenian-Apennine area (central Italy). The lithology consists of a Paleozoic metamorphic basement, overlain by Mesozoic carbonate–evaporite- and Oligocene–Middle Miocene flysch formations, and Quaternary volcanic complexes associated with crustal extension. A regional aquifer is hosted in the carbonate-evaporite formations, and smaller aquifers are hosted in the volcanic rocks. Reservoir temperatures were calculated based on the chemical composition of springs and wells in Central Italy (sampled previously), and in the Cimino-Vicano hydrothermal system (sampled in 2012). Chalcedony and quartz geothermometers provide realistic temperatures. The sensitivity of the model is tested for CO 2 degassing and input minerals. The results of optimized GeoT simulations show that all the samples are affected by degassing during their rise to the surface and that for computing a realistic reservoir temperature it is necessary to consider the principal minerals of the geothermal reservoir (particularly gypsum, quartz, dolomite, aragonite and calcite). The equilibrium temperatures range from 48-115 °C. The statistical approach of "best clustering minerals" solves the problems related to cation or single component geothermometers. Multicomponent geothermometry coupled with optimization provides a reliable approach to reconstruct fluid composition at depth and estimate reservoir temperatures

Mineral equilibria and thermodynamic uncertainties in the geothermometrical characterisation of carbonate geothermal systems of low temperature. The case of the Alhama-Jaraba system (Spain)

Geothermometrical characterisation of low-temperature, carbonate-evaporitic geothermal systems is usually hampered by the lack of appropriate mineral equilibria to successfully use most of the classical geothermometers and/or by the thermodynamic uncertainties affecting some of the most probable mineral equilibria in low temperature conditions. This situation is further hindered if the thermal waters are additionally affected by secondary processes (e.g., CO2 loss) during their ascent to surface. All these problems cluster together in the low-temperature Alhama-Jaraba thermal system, hosted in carbonate rocks, with spring temperatures about 30 °C and waters of Ca-Mg−HCO3/SO4 type. This system, one of the largest naturally flowing (600 L/s) low temperature thermal systems in Europe, is used in this paper as a suitable frame to assess the problems in the application of chemical geothermometrical techniques (classical geothermometers and geothermometrical modelling) and to provide a methodology that could be used in this type of geothermal system or in potential CO2 storage sites in similar aquifers. The results obtained have shown that the effects of the secondary processes can be avoided by selecting the samples unaffected by such processes and, therefore, representative of the conditions at depth, or by applying existing methodologies to reconstruct the original composition, as is usually done for medium to high temperature systems. The effective mineral equilibria at depth depend on the temperature, the residence time and the specific lithological/mineralogical characteristics of the system studied. In the present case, the mineral equilibria on which classical cation geothermometers are based have not been attained. The low proportion of evaporitic minerals in the hosting aquifer prevents the system from reaching anhydrite equilibrium, otherwise common in carbonate-evaporitic systems and necessary for the specific SO4-F geothermometer or the specially reliable quartz (or chalcedony) – anhydrite equilibrium in the geothermometrical modelling of these geothermal systems. Under these circumstances, the temperature estimation must rely on quartz (or chalcedony), clay minerals and, especially, calcite and dolomite. However, clay minerals and dolomite present important thermodynamic uncertainties related to possible variations in composition or crystallinity degree for clays and order/disorder degree for dolomite. To deal with these problems, a sensitivity analysis to the thermodynamic data for clay minerals has been carried out, comparing the results obtained when considering different solubility data. The uncertainties associated with dolomite have been addressed by reviewing the solubility data available for dolomites with different order degrees and performing specific calculations for the order degree of the dolomite in the aquifer. This approach can be used to find the most adequate dolomite thermodynamic data for the system under consideration, including medium-high temperature geothermal systems. Finally, the temperature estimation of the Alhama-Jaraba waters in the deep reservoir has been obtained from simultaneous equilibria of quartz, calcite, partially disordered dolomite and some aluminosilicate phases. The obtained value of 51 ± 14 °C is within the uncertainty range normally affecting this type of estimations and is coherent with independent estimations from geophysical data

Geochemical evolution of thermal waters in carbonate – evaporitic systems: The triggering effect of halite dissolution in the dedolomitisation and albitisation processes

The Fitero and Arnedillo geothermal systems are located in the NW part of the Iberian Range (Northern Spain). The geothermal reservoir is hosted in the Lower Jurassic carbonates, in contact with the evaporitic Keuper Facies. Thermal waters are of chloride-sodium type with discharge temperature of about 45 °C and near neutral pH. The Arnedillo waters are more saline with higher Na, Cl and sulphate contents, but lower Ca and Mg than the Fitero waters. All waters have attained mineral equilibrium at depth with calcite, dolomite, anhydrite, quartz, albite, K-feldspar and other aluminosilicates, except for the Fitero waters, which have not reached the equilibrium with the aluminosilicates. The calculated reservoir temperature is 81 ± 11 °C in Fitero and 87 ± 13 °C in Arnedillo. In order to identify the reasons for the differences found between the two systems some inverse and forward geochemical calculations were performed and the main water-rock interaction processes responsible for the chemical evolution of these waters have been evaluated. Halite dissolution has been found to be the triggering factor for the two most important geochemical processes in the system: a) albitisation process, due to the common ion effect (Na); and b) dedolomitisation process, associated with the salinity increase, which enhance the dissolution of anhydrite and, in turn, produces the precipitation of calcite (common ion effect, Ca) and the concomitant dissolution of dolomite. Halite dissolution may be an important driving force in the geochemical evolution of groundwater systems in contact with carbonates and evaporites, where equilibrium with K-feldspar, albite and anhydrite has already been attained. The evolution of the processes at pH, temperature and salinity ranges wider than those in the Fitero-Arnedillo system has been theoretically examined with additional reaction-path simulations, in order to generalise the geochemical behaviour of these processes in other environments

INVESTIGATION OF GEOTHERMAL ENERGY POTENTIAL USING ELECTRICAL RESISTIVITY SURVEY AND CHEMICAL GEOTHERMOMETERS: A STUDY OF THE MANGHOPIR HOT SPRING KARACHI, SINDH PAKISTAN

Electrical resistivity survey and chemical geothermometers methods were used to find the geothermal gradient energy potential of the Manghopir hot spring which is located in Karachi, Sindh. Schlumberger electrode configurations were used to demarcate the two shallow potential subsurface aquifers. At various depths, three lithological units were encountered: alluvium, sandstone, and shale. The first thermal water aquifer lies below at the average depth of 10m and average thickness of 9 m lies in sandstone lithology of Nari Formation of Oligocene age. The second thermal water aquifer encountered at the average depth of 68 m and the average thickness of aquifer was 40.5m in sandstone lithology of Nari Formation. The surface water temperature was calculated with digital thermometer which shows the range in between 48 °C to 50 °C and subsurface temperature was calculated with the help of chemical geothermometers. The Na–K geothermometers indicate the subsurface equilibrium reservoir temperature in the range of 135.52 °C,125.54 °C, 172.964 °C and 184.08°C and the Na-K-Ca chemical geothermometers indicate the subsurface reservoir temperature 148.493°C. The Na-K-Ca geothermometers show a high temperature, but the reservoir temperature appears to be lower due to the mixing of sea water with the chemical composition of hot spring water within the subsurface aquifers

A multicomponent geothermometer for high-temperature basalt settings

For successful geothermal reservoir exploration, accurate temperature estimation is essential. Since reservoir temperature estimation frequently involves high uncertainties when using conventional solute geothermometers, a new statistical approach is proposed. The focus of this study is on the development of a new multicomponent geothermometer tool which requires a significantly reduced data set compared to existing approaches. The method is validated against reservoir temperature measurements in the Krafla and the Reykjanes geothermal systems. A site-specific basaltic mineral set was selected as the basis to compute the equilibrium temperatures. These high-enthalpy geothermal reservoirs are located in the neo-volcanic zone of Iceland where the fluid temperatures are known to reach up to 350 °C at a depth of 2000 m. During ascent, the fluid composition is prone to changes as well as possible phase segregation due to depressurization and boiling. Therefore, to reduce the uncertainty of temperature estimations, reservoir temperature conditions are numerically reconstructed with sensitivity analyses considering pH, aluminium concentration, and steam loss. The evaluation of the geochemical data and the sensitivity analyses were calculated via a numerical in-house tool called MulT_predict. In all cases, the temperature estimations match with the in situ temperatures measured at Krafla and Reykjanes. The development of this method tends to be a promising and precise tool for reservoir temperature estimation. The developed methodology is a fast and easy-to-handle exploration tool that can be applied to standard geochemical data without the need for a sophisticated gas analysis yet obtaining very accurate results