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  5. Hydrothermal processes governing the geochemistry of the crater fumaroles at Mount Etna volcano (Italy)
 
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Hydrothermal processes governing the geochemistry of the crater fumaroles at Mount Etna volcano (Italy)

Author(s)
Liotta, M.  
Istituto Nazionale di Geofisica e Vulcanologia, Sezione Palermo, Palermo, Italia  
Paonita, A.  
Istituto Nazionale di Geofisica e Vulcanologia, Sezione Palermo, Palermo, Italia  
Caracausi, A.  
Istituto Nazionale di Geofisica e Vulcanologia, Sezione Palermo, Palermo, Italia  
Martelli, M.  
Istituto Nazionale di Geofisica e Vulcanologia, Sezione Palermo, Palermo, Italia  
Rizzo, A.  
Istituto Nazionale di Geofisica e Vulcanologia, Sezione Palermo, Palermo, Italia  
Favara, R.  
Istituto Nazionale di Geofisica e Vulcanologia, Sezione Palermo, Palermo, Italia  
Language
English
Obiettivo Specifico
1.5. TTC - Sorveglianza dell'attività eruttiva dei vulcani
Status
Published
JCR Journal
JCR Journal
Journal
Chemical Geology  
Issue/vol(year)
/278(2010)
Pages (printed)
92-104
Date Issued
November 2, 2010
DOI
10.1016/j.chemgeo.2010.09.004
URI
https://www.earth-prints.org/handle/2122/6344
Subjects
04. Solid Earth::04.04. Geology::04.04.12. Fluid Geochemistry  
Subjects

Fumaroles Volcanic ga...

Abstract
We investigated the geochemistry of the fumaroles at the summit area of Mt. Etna, including sulfur speciation
and the content of acidic gases. The carbon-isotope composition of the Etnean plume was also measured in
order to compare it to that of fumaroles. Two types of fumaroles were identified: (i) low-temperature
fumaroles, which are dominated by CO2 with minor amounts of SO2 and H2S, and negligible chlorine contents,
and (ii) high-temperature fumaroles, which are strongly air-contaminated and characterized by appreciable
amounts of volcanogenic carbon, sulfur, and chlorine. As recognized by Martelli et al. (2008), both groups of
fumaroles are fed by the degassing of an underlying magma; nevertheless, compositional data clearly show
that secondary processes affect the composition of the fluids once they leave the magma body. Here a model
of cooling and condensation of fluids is proposed to explore such postmagmatic processes. The model, which
uses Etnean plume geochemistry as starting composition of fluids exsolved from magma, shows that SO2 and
H2S control the redox conditions of the gas mixture during the cooling, until the reactions involving CO/CO2
and H2/H2O ratios are fully quenched at temperatures around 350–450 °C. The dissolution of gases in water,
subsequent to condensation, must occur at thermobaric conditions over 50 bar and 260 °C, which allows (a)
total removal of HCl, (b) partial removal of sulfur species while preserving the SO2/H2S ratio, and (c) the C/S
ratio to increase by almost 10-fold relative to that in the plume. The observed CH4/CO2 ratios are higher than
those calculated for the Etnean magmatic gas, and hence they provide evidence of modest contributions from
peripheral hydrothermal fluids during the migration of magmatic gases toward the surface in both low- and
high-temperature fumaroles. Due to the peculiar thermodynamic conditions, the model predicts that carbon
isotopes do not experience any postmagmatic fractionation, and hence the isotopic composition of the
fumaroles is representative of magmatic carbon. Measurements of the carbon-isotope composition of the
plume corroborate these findings.
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