dc.creatorBarra, Fernando
dc.creatorDeditius, Artur P.
dc.creatorReich Morales, Martín
dc.creatorKilburn, Matt R.
dc.creatorGuagliardo, Paul
dc.creatorRoberts, Malcolm P.
dc.date.accessioned2019-05-29T13:39:09Z
dc.date.available2019-05-29T13:39:09Z
dc.date.created2019-05-29T13:39:09Z
dc.date.issued2017
dc.identifierScientific Reports, Volumen 7, Issue 1, 2017
dc.identifier20452322
dc.identifier10.1038/s41598-017-16380-8
dc.identifierhttps://repositorio.uchile.cl/handle/2250/169024
dc.description.abstractRhenium and osmium isotopes have been used for decades to date the formation of molybdenite (MoS2), a common mineral in ore deposits and the world's main source of molybdenum and rhenium. Understanding the distribution of parent Re-187 and radiogenic daughter Os-187 isotopes in molybdenite is critical in interpreting isotopic measurements because it can compromise the accurate determination and interpretation of mineralization ages. In order to resolve the controls on the distribution of these elements, chemical and isotope mapping of MoS2 grains from representative porphyry copper-molybdenum deposits were performed using electron microprobe and nano-scale secondary ion mass spectrometry. Our results show a heterogeneous distribution of 185,Re-187 and Os-192 isotopes in MoS2, and that both Re-187 and Os-187 isotopes are not decoupled as previously thought. We conclude that Re and Os are structurally bound or present as nanoparticles in or next to molybdenite grains, recording a complex formation history and hindering the use of microbeam techniques for Re-Os molybdenite dating. Our study opens new avenues to explore the effects of isotope nuggeting in geochronometers.
dc.languageen
dc.publisherNature
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceScientific Reports
dc.subjectMultidisciplinary
dc.titleDissecting the Re-Os molybdenite geochronometer
dc.typeArtículo de revista


Este ítem pertenece a la siguiente institución