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

被引:14
作者
Alonso-Azcárate, J [1 ]
Boyce, AJ
Bottrell, SH
Macaulay, CI
Rodas, M
Fallick, AE
Mas, JR
机构
[1] Univ Castilla La Mancha, Fa CC Medio Ambiente, Dept Geol, Fabr Armas, Toledo 21004, Spain
[2] Scottish Univ Res & Reactor Ctr, Glasgow G75 0QF, Lanark, Scotland
[3] Univ Leeds, Dept Earth Sci, Leeds LS2 9JT, W Yorkshire, England
[4] Univ Complutense Madrid, Fac Ciencias Geol, Dept Cristalog & Mineral, E-28040 Madrid, Spain
[5] Univ Complutense Madrid, Fac Ciencias Geol, Dept Estratig, E-28040 Madrid, Spain
[6] CSIC, Inst Geol Econ, E-28040 Madrid, Spain
基金
英国自然环境研究理事会;
关键词
D O I
10.1016/S0016-7037(99)00022-8
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
We describe a system for the in situ sulfur isotope analysis of small (>100 mu m) anhydrite crystals and investigate its application to anhydrite-pyrite geothermometry. Anhydrite inclusions (<1 mm) have been analyzed in spectacular, museum quality pyrite crystals from the Mesozoic Cameros Basin in NE 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 between the host pyrite and anhydrite inclusions and was not affected by re-equilibration, However, other data points yield anhydrite compositions consistently too S-34-depleted, resulting in a geologically unrealistic temperature (610 +/- 20 degrees C). Experiments show that where pyrite becomes overheated by the laser during anhydrite decomposition, solid phase reaction can incorporate 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 pyrite 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.
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页码:509 / 513
页数:5
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