2006 Philadelphia Annual Meeting (22–25 October 2006)

Paper No. 12
Presentation Time: 4:30 PM

SYNCHROTRON STUDIES OF SULFUR SPECIATION IN SILICATE GLASSES: IMPLICATIONS FOR THE SULFUR CONTENT OF MAGMATIC SYSTEMS


JUGO, Pedro J., Earth Sciences, Laurentian University, 935 Ramsey Lake Rd, Sudbury, ON P3E 2C6, Canada and WILKE, Max, Institut für Geowissenschaften, Universität Potsdam, Postfach 601553, Potsdam, D-14415, Germany, pjugo@laurentian.ca

Sulfur is an element of interest in magmatic-hydrothermal systems because its behavior is directly related to a variety of geological processes (e.g. formation of ore deposits, global cooling by S-rich explosive volcanism). Sulfur is sensitive to oxygen fugacity (fO2) variations and can be present in silicate melts as sulfide (S2-), sulfate (S6+), sulfite (S4+) or combinations of these species. Understanding how S speciation changes as a function of fO2 is of interest because S speciation determines the amount of sulfur that magmas can dissolve and that can be transferred to a magmatic volatile phase. We used X-ray Absorption Near Edge Structure (XANES) at the S K-edge to determine S speciation in natural basaltic glasses (from several locations worldwide) and in glasses of basaltic and andesitic composition synthesized in a piston-cylinder apparatus at 1 GPa and between 1100 oC and 1350 oC. In some experiments a strong fO2 gradient was imposed, creating reduction profiles that record the continuous transition from sulfide to sulfate species. The analyses were performed at the European Synchrotron Radiation Facility (ESRF), beamline ID21, using a combination of “broad” and “focused” beams (200 and 0.8µm diameter, respectively). The high spatial resolution of the focused beam, in combination with our experimental approach, provided unique insights into the S speciation transition in silicate melts. Our results show the coexistence of S4+ and S6+ species and S2- and S6+ species. However, we did not observe coexistence of S2- and S4+ species in our samples. The results from “reduction-profile” experiments (showing a continuous variation in the proportion of S2- and S6+) were used to calculate how S solubility in silicate melts changes from sulfide dominated to sulfate dominated system. This is especially relevant for arc magmas because their fO2 overlaps with the range in fO2 for the transition from S2- to S6+ in silicate melts.