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  • 1
    Publication Date: 2020-12-07
    Description: The Vicano–Cimino Volcanic District (VCVD) is related to the post-orogenic magmatic activity of the peri- Tyrrhenian sector of Central Italy. The chemical and isotopic compositions of 333 water discharges and 25 gas emissions indicate the occurrence of two main sources: 1) cold Ca-HCO3 to Ca(Na, K)-HCO3 type waters from relatively shallow aquifers hosted in volcanic and sedimentary formations; and 2) thermal Ca-SO4(HCO3) type waters located in a deep CO2-pressurized reservoir, hosted in carbonate–evaporite rocks and separated from the shallow aquifers by thick sequences of low-permeability formations. Carbon dioxide is mainly produced by thermal metamorphic decarbonation within the deepest and hottest parts of the carbonate–evaporite reservoir (δ13C–CO2 from−3.1 to+2.2‰vs. VPDB), likely affected by a mantle-rooted CO2. ReleaseofCO2-rich gases from the deep aquifer into the overlying shallow aquifers produces high-CO2 springs and bubbling pools. The spatial distribution of thermal waters and CO2-rich cold discharges is strongly controlled by fractures and faults located in correspondencewith buried structural highs. Stable isotopes (δD and δ18O) suggest thatmeteoric water feeds both the shallowand deep reservoirs. The relatively lowR/Ra values (0.27–1.19) indicate that He ismainly deriving from a crustal source, with minor component from the mantle affected by crustal contamination related to the subduction of the Adriatic plate. Consistently, relatively high N2/Ar and N2/3He ratios and positive δ15N–N2 values (from0.91 to 5.7‰vs. air) characterize the VCVD gas discharges, suggesting the occurrence of a significant “excess” nitrogen. Isotopic compositions of CH4 (δ13C–CH4 and δD–CH4 values from−28.9 to−22.1‰vs. VPDB and from −176 to −138‰ vs. VSMOW, respectively), and composition of light alkanes are indicative of prevalent thermogenic CH4, although the occurrence of abiogenic CH4 production cannot be excluded. The δ34S–H2S values (from+9.3 to+11.4‰vs. VCDT) are consistentwith the hypothesis of H2S production fromthermogenic reduction of Triassic anhydrites. Gas geothermometry in the H2O–H2–Ar–H2S system suggests that the VCVD gases equilibrated in a liquid phase at redox conditions controlled by interactions of fluids with the local mineral assemblage at temperatures lower (b200 °C) than that andmeasured in deep (N2000 m) geothermalwells. This confirms that secondary processes, i.e. steam condensation, gas dissolution in shallow aquifers, re-equilibration at lower temperature, and microbial activity, significantly affect the chemistry of the uprising fluids. Thermal water chemistry supports the occurrence in this area of an anomalous heat flowthat, coupledwith the recent demographic growth, makes this site suitable for direct and indirect exploitation of the geothermal resource, in agreement with the preliminary surveys carried out in the 1970's–1990's for geothermal exploration purposes.
    Description: Published
    Description: 96-114
    Description: 5A. Energia e georisorse
    Description: JCR Journal
    Description: restricted
    Keywords: geothermal resources ; 03. Hydrosphere::03.04. Chemical and biological::03.04.03. Chemistry of waters ; 03. Hydrosphere::03.04. Chemical and biological::03.04.05. Gases ; 03. Hydrosphere::03.04. Chemical and biological::03.04.06. Hydrothermal systems
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 2
    Publication Date: 2020-12-07
    Description: The Principal Cordillera of Central Chile is characterized by two belts of different ages and lithologies: (i) an eastern Mesozoic belt, consisting of limestone- and gypsum-rich sedimentary rocks at the border between Central Chile and Argentina, where the active volcanic arc occurs; and (ii) a western belt of Cenozoic age containing basaltic to andesitic volcanic and volcanoclastic sequences. This distinctive geological setting controls water chemistry of cold and thermal springs in the region, which are fed by meteoric water that circulates through deep regional structures. In the western sector of Principal Cordillera, water–rock interaction processes produce lowTDS, slightly alkaline HCO3 − dominatedwaters, although dissolution of underlyingMesozoic evaporitic rocks occasionally causes SO4 2− and Cl− enrichments. In this area, few Na+–HCO3 − and Na+–SO4 2− waters occurred, being likely produced by a Ca2+–Na+ exchange during water–rock interactions. Differently, the chemical features of Ca2+–Cl−waterswas likely related to an albitization–chloritization process affecting basaltic to andesitic rocks outcropping in this area. Addition of Na+–Cl− brines uprising from the eastern sector through the westverging thrust faults cannot be excluded, as suggested by the occurrence of mantle He (~19%) in dissolved gases. In contrast, in the eastern sector of the study region, mainly characterized by the occurrence of evaporitic sequences and relatively high heat flow,mature Na+–Cl− waters were recognized, the latter being likely related to promising geothermal reservoirs, as supported by the chemical composition of the associated bubbling and fumarolic gases. Their relatively low3He/4He ratios (up to 3.9 Ra)measured in the fumaroles on this area evidenced a significant crustal contamination by radiogenic 4He. The latter was likely due to (i) degassing from 4He-rich magma batches residing in the crust, and/or (ii) addition of fluids interacting with sedimentary rocks. This interpretation is consistent with the measured δ13C-CO2 values (from−13.2 to−5.72‰vs. V-PDB) and the CO2/3He ratios (up to 14.6 × 1010), which suggest that CO2 mostly originates from the limestone-rich basement and recycling of subducted sediments,with an important addition of sedimentary (organic-derived) carbon,whereas mantle degassing contributes at a minor extent. According to geothermometric estimations based on the Na+, K+, Mg2+ and Ca2+ contents, the mature Na+–Cl− rich waters approached a chemical equilibrium with calcite, dolomite, anhydrite, fluorite, albite, K-feldspar and Ca- andMg-saponites at a broad range of temperatures (up to ~300 °C) In the associated gas phase, equilibria of chemical reactions characterized by slowkinetics (e.g. sabatier reaction) suggested significant contributions from hot and oxidizing magmatic gases. This hypothesis is consistent with the δ13C-CO2, Rc/Ra, CO2/3He values of the fumarolic gases. Accordingly, the isotopic signatures of the fumarolic steam is similar to that of fluids discharged from the summit craters of the two active volcanoes in the study area (Tupungatito and Planchón–Peteroa). These results encourage the development of further geochemical and geophysical surveys aimed to provide an exhaustive evaluation of the geothermal potential of these volcanic–hydrothermal systems.
    Description: Published
    Description: 97-113
    Description: 1V. Storia e struttura dei sistemi vulcanici
    Description: JCR Journal
    Description: restricted
    Keywords: Fluid geochemistry ; Central Chile ; Water–gas–rock interaction ; Hydrothermal reservoir ; Geothermal resource ; Volcanoes ; 03. Hydrosphere::03.02. Hydrology::03.02.03. Groundwater processes ; 03. Hydrosphere::03.04. Chemical and biological::03.04.03. Chemistry of waters ; 03. Hydrosphere::03.04. Chemical and biological::03.04.05. Gases ; 03. Hydrosphere::03.04. Chemical and biological::03.04.06. Hydrothermal systems ; 04. Solid Earth::04.04. Geology::04.04.12. Fluid Geochemistry ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 3
    Publication Date: 2017-04-04
    Description: A geochemical survey of 197 fluid discharges (cold and thermal waters and bubbling pools) and 15 gas emissions from the western sector of the Sabatini Volcanic District and the Tolfa Mountains (Latium, Central Italy) was carried out in 2007–2008. The chemical and isotopic compositions of the fluid discharges indicate the occurrence of two main sources: 1) relatively shallow aquifers with Ca(Na,K)–HCO3 and Ca(Mg)–HCO3 compositions when trapped in volcanic and sedimentary formations, respectively; and 2) a deep reservoir, which is hosted in the Mesozoic carbonate sequence, rich in CO2 and having a Ca–SO4(HCO3) composition. Dissolution of a CO2-rich gas phase into the shallow aquifers produces high-TDS and high-pCO2 cold waters, while oxidation of deep-derived H2S to SO4 2− generates low-pH (b4) sulfate waters. The δ13C–CO2 values for gas emissions (from−2.8 to+2.7‰vs. VPDB) suggest that the origin of CO2 associated with the deep fluids ismainly related to thermo-metamorphic reactions within the carbonate reservoir, although significant mantle contribution may also occur. However, R/Ra values (0.37–0.62) indicate that He is mainly produced by a crustal source, with a minor component from a crust-contaminated mantle. On the basis of the δ13C–CH4 and δD–CH4 values (from −25.7 to −19.5‰ vs. VPDB and from −152 to −93.4‰ vs. VSMOW, respectively) CH4 production is associated with thermogenic processes, possibly related to abiogenic CO2 reduction within the carbonate reservoir. The δ34S–H2S values (from+9.3 to +10.4‰ vs. VCDT) are consistent with the hypothesis of a sedimentary source of sulfur from thermogenic reduction of Triassic sulfates. Geothermometric evaluations based on chemical equilibria CO2–CH4 and, separately, H2S suggest that the reservoir equilibriumtemperature is up to ~300 °C. The δDand δ18O data indicate thatwater recharging both the shallow and deep aquifers has a meteoric origin. Fluid geochemistry, coupled with gravimetric data and tectonic lineaments, supports the idea that significant contributions from a deep-seated geothermal brine are present in the Stigliano thermal fluid discharges. Exploration surveys investigated this area during 70's–90's for geothermal purposes. Nevertheless, presently the area is still under-exploited. The presence of thermal waters and anomalous heat flow together with the demographic growth of the last years,makes this site a suitable location for direct applications of the geothermal resource.
    Description: Published
    Description: 160-181
    Description: 2.4. TTC - Laboratori di geochimica dei fluidi
    Description: JCR Journal
    Description: reserved
    Keywords: Geochemistry Water Gas Stable isotope Geothermometry Central Italy ; 03. Hydrosphere::03.04. Chemical and biological::03.04.03. Chemistry of waters ; 03. Hydrosphere::03.04. Chemical and biological::03.04.05. Gases ; 03. Hydrosphere::03.04. Chemical and biological::03.04.06. Hydrothermal systems
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 4
    Publication Date: 2017-04-04
    Description: A geochemical survey of the main thermal waters discharging in the southwestern part of the Domuyo volcanic complex (Argentina),where the latest volcanic activity dates to 0.11 Ma, has highlighted the extraordinarily high heat loss from this remote site in Patagonia. The thermal water discharges are mostly Na-Cl in composition and have TDS values up to 3.78 g L−1 (El Humazo). A simple hydrogeochemical approach shows that 1,100 to 1,300 kg s−1 of boiling waters, which have been affected by shallow steam separation, flow into the main drainage of the area (Rio Varvarco). A dramatic increase of the most conservative species such as Na, Cl and Li from the Rio Varvarco fromupstreamto downstreamwas observed and related solely to the contribution of hydrothermal fluids. The equilibrium temperatures of the discharging thermal fluids, calculated on the basis of the Na-K-Mg geothermometer, are between 190 °C and 230 °C. If we refer to a liquid originally at 220 °C (enthalpy = 944 J g−1), the thermal energy release can be estimated as high as 1.1±0.2 GW, a value that ismuch higher than the natural release of heat in other important geothermal fields worldwide, e.g., Mutnovsky (Russia), Wairakei (New Zealand) and Lassen Peak (USA). This value is the second highest measured advective heat flux from any hydrothermal system on Earth after Yellowstone.
    Description: Published
    Description: 71–77
    Description: 4V. Vulcani e ambiente
    Description: JCR Journal
    Description: restricted
    Keywords: Domuyo volcano ; Argentine Patagonia ; Geothermal potential ; Water geochemistry ; 03. Hydrosphere::03.04. Chemical and biological::03.04.03. Chemistry of waters ; 03. Hydrosphere::03.04. Chemical and biological::03.04.06. Hydrothermal systems
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 5
    Publication Date: 2023-03-13
    Description: Arsenic concentrations were analysed for 328 water samples collected in the Vicano–Cimino Volcanic District (VCVD), an areawhere severe contamination of groundwater has become a serious problemfollowing the recent application of the EU Directive on the maximum allowable concentration level for As in drinking waters. In addition, uranium and vanadium concentrations were also analysed in light of the enhanced interest on their environmental toxicity. Waters were collected from springs and wells fed by cold and shallow volcanic–sedimentary aquifers, which locally represent the main drinking water source. Thermal springs (≤63 °C) related to an active hydrothermal reservoir and waters associated with a CO2-rich gas phase of deep provenance were also analysed. The collected data showed that the As concentrations in the shallow aquifers varied in a wide range (0.05–300 μg/L) and were primarily controlled by water–rock interaction processes. High As concentrations (up to 300 μg/L) were measured in springs and wells discharging from the volcanic products, and about 66% exceeded the limit of 10 μg/L for drinkingwaters,whereaswaters circulatingwithin the sedimentary formations displayed much lower values (0.05–13 μg/L; ~4% exceeding the threshold limit). Thermal waters showed the highest As concentrations (up to 610 μg/L) as the result of the enhanced solubility of As-rich volcanic rocks during water–rock interaction processes at high temperatures. Where the local structural setting favoured the rise of fluids from the deep hydrothermal reservoir and their interaction with the shallow volcanic aquifer, relatively higher concentrations were found. Moreover, well overexploitation likely caused the lateral inflow of As-rich waters towards not contaminated areas. Uraniumand vanadiumconcentrations ofwaters circulating in the volcanic rocks ranged from0.01 to 85 μg/L and 0.05 to 62 μg/L, respectively. Less than 2% of analysed samples exceeded theWorld Health Organization's provisional guidelines for U (30 μg/L), while none of them was above the Italian limit value of V in drinking water (120 μg/L). Lower U (0.07–22 μg/L and 0.02–13 μg/L, respectively) and V concentrations (0.05–24 μg/L and 0.18–17 μg/L, respectively) were measured in the water samples from the sedimentary aquifer and thermal waters. Local lithology appeared as the main factor affecting the U and V contents in the shallow aquifers, due to the high concentrations of these two elements in the volcanic formations when compared to the sedimentary units. In addition, high U concentrations were found in correspondence with U mineralization occurring within the VCVD, fromwhich U is released in solution mainly through supergene oxidative alteration. Redox conditions seem to play amajor role in controlling the concentrations of U and V inwaters. Oxidizing conditions characterizing the cold waters favour the formation of soluble U- and V-species, whereas thermal waters under anoxic conditions are dominated by relatively insoluble species. Geostatistical techniques were used to draw contour maps by using variogram models and kriging estimation aimed to define the areas of potential health risk characterized by As, U and V-rich waters, thus providing a useful tool for water management in a naturally contaminated area to local Authorities.
    Description: Published
    Description: 123-133
    Description: 6A. Monitoraggio ambientale, sicurezza e territorio
    Description: JCR Journal
    Description: open
    Keywords: Arsenic Uranium Vanadium Central Italy Volcanic–sedimentary aquifers Geostatistical techniques ; 03. Hydrosphere::03.04. Chemical and biological::03.04.03. Chemistry of waters
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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