Twenty-two cold and thermal waters from shallow wells sampled in June 1995 in the Vulcano Porto area, Vulcano Island, were analyzed for major and minor chemical constituents, oxygen and hydrogen isotopes and tritium contents, and sulfur isotopes in the dissolved sulfate. The sulfur isotopic composition of the dissolved sulfate ranges between +0.6 and +6.5% (mean +3.7 +- 1.7%), and is interpreted as deriving mainly from fumarolic SO2 undergoing oxidation in deep and shallow aquifers, with possible minor contributions from oxidation of H2S. Dissolution of secondary anhydrite may have been a minor source of the isotopically heavy aqueous sulfate in the cold groundwaters. The chemical and isotopic features of the waters support previous interpretative hydrologic models of Vulcano Porto, which comprise a number of aquifers fed basically by two major end-members, i.e. meteoric water and crater-type fumarolic inputs, the latter in the form of absorbed emissions or condensate. These data, along with the sulfur isotopes of aqueous sulfate, exclude involvement of seawater in the recharge of the groundwater system of the island.
Chemical and isotopic compositions of water and dissolved sulfate from shallow wells on Vulcano Island, Aeolian Archipelago, Italy / Cortecci, G.; Dinelli, E.; Bolognesi, L.; Boschetti, Tiziano; Ferrara, G.. - In: GEOTHERMICS. - ISSN 0375-6505. - 30:(2001), pp. 60-91. [10.1016/S0375-6505(00)00037-7]
Chemical and isotopic compositions of water and dissolved sulfate from shallow wells on Vulcano Island, Aeolian Archipelago, Italy
BOSCHETTI, Tiziano;
2001-01-01
Abstract
Twenty-two cold and thermal waters from shallow wells sampled in June 1995 in the Vulcano Porto area, Vulcano Island, were analyzed for major and minor chemical constituents, oxygen and hydrogen isotopes and tritium contents, and sulfur isotopes in the dissolved sulfate. The sulfur isotopic composition of the dissolved sulfate ranges between +0.6 and +6.5% (mean +3.7 +- 1.7%), and is interpreted as deriving mainly from fumarolic SO2 undergoing oxidation in deep and shallow aquifers, with possible minor contributions from oxidation of H2S. Dissolution of secondary anhydrite may have been a minor source of the isotopically heavy aqueous sulfate in the cold groundwaters. The chemical and isotopic features of the waters support previous interpretative hydrologic models of Vulcano Porto, which comprise a number of aquifers fed basically by two major end-members, i.e. meteoric water and crater-type fumarolic inputs, the latter in the form of absorbed emissions or condensate. These data, along with the sulfur isotopes of aqueous sulfate, exclude involvement of seawater in the recharge of the groundwater system of the island.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.