Alkaline sulphate fluids produced in a magmatic hydrothermal system
Alkaline sulphate fluids produced in a magmatic hydrothermal system
Alkaline sulphate fluids produced in a magmatic hydrothermal system
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The Black Pool <strong>in</strong> the crater of El Chichón, Mexico, is a muddy, closed pool, with a<br />
temperature and chemical composition similar to the alkal<strong>in</strong>e <strong>sulphate</strong> spr<strong>in</strong>gs of Savo, but<br />
with a slightly acidic pH. Taran et al. (1998) observe that the spr<strong>in</strong>g is dilute, but compare its<br />
chemistry to steam-heated acid-<strong>sulphate</strong> spr<strong>in</strong>gs with<strong>in</strong> the volcanic crater, imply<strong>in</strong>g a steamheated<br />
orig<strong>in</strong>. Sulphur isotopes can be used to dist<strong>in</strong>guish the steam-heated and alkal<strong>in</strong>e<br />
<strong>sulphate</strong> spr<strong>in</strong>gs at Savo, and dilution of an acid <strong>sulphate</strong> spr<strong>in</strong>g cannot account for the high<br />
SiO 2 and consistent (high) Na/K temperatures of the alkal<strong>in</strong>e spr<strong>in</strong>gs.<br />
Stimac et al. (2004) suggest a steam and gas condensation orig<strong>in</strong> for the (pre-1991 eruption)<br />
Upper Maranout spr<strong>in</strong>gs of P<strong>in</strong>atubo, as do Giggenbach et al. (1990) for Las Nereidas spr<strong>in</strong>gs<br />
of Nevado del Ruiz (Colombia). These spr<strong>in</strong>gs, with elevated bicarbonate concentrations, are<br />
more similar <strong>in</strong> chemistry to the cooler bicarbonate-<strong>sulphate</strong> spr<strong>in</strong>gs of Savo. At P<strong>in</strong>atubo,<br />
Ruiz and Savo, the bicarbonate-enriched spr<strong>in</strong>gs are peripheral to the high temperature <strong>fluids</strong>,<br />
and have relatively low temperatures. At Savo, <strong>sulphate</strong> would appear to be derived from<br />
mix<strong>in</strong>g with alkal<strong>in</strong>e <strong>sulphate</strong> <strong>fluids</strong> rather than from oxidation of H 2 S, based on their stable<br />
isotope compositions (“Other spr<strong>in</strong>gs”; Fig. 3) as compared to the native sulphur, acid and<br />
alkal<strong>in</strong>e spr<strong>in</strong>gs.<br />
Thjórsárdalur spr<strong>in</strong>g (Table 7), is from an area of high gas flux on Iceland. Arnórsson et al.<br />
(1983) suggested its high-<strong>sulphate</strong> chemistry is formed by the dissolution and oxidation of<br />
secondary pyrite. This process is not dissimilar to the process as envisaged at Savo, with the<br />
dissolution of secondary <strong>hydrothermal</strong> alteration assemblages buffer<strong>in</strong>g the fluid composition<br />
dur<strong>in</strong>g dilution. Sulphur isotopes from the alkal<strong>in</strong>e <strong>sulphate</strong> spr<strong>in</strong>gs suggest that anhydrite<br />
and <strong>sulphate</strong> derived from SO 2 disproportionation contributes to the spr<strong>in</strong>gs at Savo, rather<br />
than exclusively the oxidation of pyrite – which would result <strong>in</strong> similar isotopic compositions<br />
between native sulphur, acid <strong>sulphate</strong> and alkal<strong>in</strong>e spr<strong>in</strong>gs.<br />
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