Development and use of in situ laser sulfur isotope analyses for pyrite-anhydrite geothermometry: An example from the pyrite deposits of the Cameros Basin, NE Spain

Citation
J. Alonso-azcarate et al., Development and use of in situ laser sulfur isotope analyses for pyrite-anhydrite geothermometry: An example from the pyrite deposits of the Cameros Basin, NE Spain, GEOCH COS A, 63(3-4), 1999, pp. 509-513
Citations number
9
Categorie Soggetti
Earth Sciences
Journal title
GEOCHIMICA ET COSMOCHIMICA ACTA
ISSN journal
00167037 → ACNP
Volume
63
Issue
3-4
Year of publication
1999
Pages
509 - 513
Database
ISI
SICI code
0016-7037(199902)63:3-4<509:DAUOIS>2.0.ZU;2-N
Abstract
We describe a system for the in situ sulfur isotope analysis of small (>100 mu m) anhydrite crystals and investigate its application to anhydrite-pyri te geothermometry. Anhydrite inclusions (<1 mm) have been analyzed in spect acular, museum quality pyrite crystals from the Mesozoic Cameros Basin in N E Spain. Some of the data yield isotopic equilibrium temperatures (367 +/- 6 degrees C) consistent with other geothermometric estimates of metamorphic temperature. This suggests that isotopic equilibrium was established betwe en the host pyrite and anhydrite inclusions and was not affected by re-equi libration, However, other data points yield anhydrite compositions consiste ntly too S-34-depleted, resulting in a geologically unrealistic temperature (610 +/- 20 degrees C). Experiments show that where pyrite becomes overhea ted by the laser during anhydrite decomposition, solid phase reaction can i ncorporate pyrite-sulfur into the sampled gas in a stoichiometric fashion, therefore, the consistency of the erroneous temperature estimates from this group. Successful analyses are only obtained when overheating of the pyrit e is avoided during laser decomposition of anhydrite inclusions. The laser system allows isotopic measurement of anhydrite inclusions too small to be analyzed conventionally. Copyright (C) 1999 Elsevier Science Ltd.