Origin of secondary sulfate minerals on active andesitic stratovolcanoes

• Published in: Chemical geology Vol. 215; no. 1; pp. 37 - 60
• Main Authors: Zimbelman, D.R., Rye, R.O., Breit, G.N.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 15-02-2005
• Subjects: Acid-sulfate alteration; Alunite; Chemical modeling; Hydroxysulfates; Jarosite; Stable isotopes; Stratovolcanoes; Sulfates; Alunite; Chemical modeling; Hydroxysulfates; Stable isotopes; Jarosite; Stratovolcanoes; Acid-sulfate alteration; Sulfates
• ISSN: 0009-2541; 1872-6836
• DOI: 10.1016/j.chemgeo.2004.06.056

Sulfate minerals in altered rocks on the upper flanks and summits of active andesitic stratovolcanoes result from multiple processes. The origin of these sulfates at five active volcanoes, Citlaltépetl (Mexico), and Mount Adams, Hood, Rainier, and Shasta (Cascade Range, USA), was investigated using field observations, petrography, mineralogy, chemical modeling, and stable-isotope data. The four general groups of sulfate minerals identified are: (1) alunite group, (2) jarosite group, (3) readily soluble Fe- and Al-hydroxysulfates, and (4) simple alkaline-earth sulfates such as anhydrite, gypsum, and barite. Generalized assemblages of spatially associated secondary minerals were recognized: (1) alunite+silica±pyrite±kaolinite±gypsum±sulfur, (2) jarosite+alunite+silica; (3) jarosite+smectite+silica±pyrite, (4) Fe- and Al-hydroxysulfates+silica, and (5) simple sulfates+silica±Al-hydroxysulfates±alunite.
Isotopic data verify that all sulfate and sulfide minerals and their associated alteration assemblages result largely from the introduction of sulfur
-bearing magmatic gases into meteoric water in the upper levels of the volcanoes. The sulfur and oxygen isotopic data for all minerals indicate the general mixing of aqueous sulfate derived from deep (largely disproportionation of SO
2 in magmatic vapor) and shallow (oxidation of pyrite or H
2S) sources. The hydrogen and oxygen isotopic data of alunite indicate the mixing of magmatic and meteoric fluids. Some alunite-group minerals, along with kaolinite, formed from sulfuric acid created by the disproportionation of SO
2 in a condensing magmatic vapor. Such alunite, observed only in those volcanoes whose interiors are exposed by erosion or edifice collapse, may have
δ
34S values that reflect equilibrium (350±50 °C) between aqueous sulfate and H
2S. Alunite with
δ
34S values indicating disequilibrium between parent aqueous sulfate and H
2S may form from aqueous sulfate created in higher level low-temperature environments in which SO
2 is scrubbed out by groundwater or where H
2S is oxidized. Jarosite-group minerals associated with smectite in only slightly altered volcanic rock are formed largely from aqueous sulfate derived from supergene oxidation of hydrothermal pyrite above the water table. Soluble Al- and Fe-hydroxysulfates form in low-pH surface environments, especially around fumaroles, and from the oxidation of hydrothermal pyrite. Anhydrite/gypsum, often associated with native sulfur and occasionally with small amounts of barite, also commonly form around fumaroles. Some occurrences of anhydrite/gypsum may be secondary, derived from the dissolution and reprecipitation of soluble sulfate. Edifice collapse may also reveal deep veins of anhydrite/gypsum±barite that formed from the mixing of saline fluids with magmatic sulfate and dilute meteoric water. Alteration along structures associated with both hydrothermal and supergene sulfates, as well as the position of paleo-water tables, may be important factors in edifice collapse and resulting debris flows at some volcanoes.