1. Sulphate incorporation in monazite lattice and dating the cycle of sulphur in metamorphic belts.
- Author
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Laurent, Antonin, Seydoux-Guillaume, Anne-Magali, Duchene, Stéphanie, Bingen, Bernard, Bosse, Valérie, and Datas, Lucien
- Subjects
GRANITE ,SULFATE minerals ,MONAZITE ,METAMORPHIC rocks ,TRANSMISSION electron microscopes - Abstract
Microgeochemical data and transmission electron microscope (TEM) imaging of S-rich monazite crystals demonstrate that S has been incorporated in the lattice of monazite as a clino-anhydrite component via the following exchange Ca + S = REE + P, and that it is now partly exsolved in nanoclusters (5-10 nm) of CaSO. The sample, an osumilite-bearing ultra-high-temperature granulite from Rogaland, Norway, is characterized by complexly patchy zoned monazite crystals. Three chemical domains are distinguished as (1) a sulphate-rich core (0.45-0.72 wt% SO, Th incorporated as cheralite component), (2) secondary sulphate-bearing domains (SO >0.05 wt%, partly clouded with solid inclusions), and (3) late S-free, Y-rich domains (0.8-2.5 wt% YO, Th accommodated as the huttonite component). These three domains yield distinct isotopic U-Pb ages of 1034 ± 6, 1005 ± 7, and 935 ± 7 Ma, respectively. Uranium-Th-Pb EPMA dating independently confirms these ages. This study illustrates that it is possible to discriminate different generations of monazite based on their S contents. From the petrological context, we propose that sulphate-rich monazite reflects high-temperature Fe-sulphide breakdown under oxidizing conditions, coeval with biotite dehydration melting. Monazite may therefore reveal the presence of S in anatectic melts from high-grade terrains at a specific point in time and date S mobilization from a reduced to an oxidized state. This property can be used to investigate the mineralization potential of a given geological event within a larger orogenic framework. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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