Boron isotope composition of melt inclusions from porphyry systems of the Central Andes: a reconnaissance study
Author
dc.contributor.author
Wittenbrink, Jens
Author
dc.contributor.author
Lehmann, Bernd
es_CL
Author
dc.contributor.author
Wiedenbeck, Michael
es_CL
Author
dc.contributor.author
Wallianos, Alex
es_CL
Author
dc.contributor.author
Dietrich, Andreas
es_CL
Author
dc.contributor.author
Palacios Monasterio, Carlos
es_CL
Admission date
dc.date.accessioned
2013-12-27T13:21:52Z
Available date
dc.date.available
2013-12-27T13:21:52Z
Publication date
dc.date.issued
2009
Cita de ítem
dc.identifier.citation
Terra Nova, 21, 111–118, 2009
en_US
Identifier
dc.identifier.other
doi: 10.1111/j.1365-3121.2008.00863.x
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/125876
Abstract
dc.description.abstract
Quartz-hosted melt inclusions from latite dykes of the Eocene El
Salvador copper porphyry system in northern Chile display wide
ranges in both boron concentration (15–155 p.p.m. B) and
isotope composition (d11B )7 to +12&; n = 10), likely reflecting
slab-derived fluid input from seawater-altered oceanic crust. In
contrast, the major Miocene tin-silver and tin porphyry systems
in the Bolivian back-arc region (Cerro Rico de Potosi, Chorolque,
Llallagua) have distinctly different melt inclusion compositions
with d11B of )11.4 ± 2.7& (n = 10), and magmatic boron
enrichment up to several hundred p.p.m. B. The ‘seawater’
signature in the El Salvador melt inclusions explains the oxidized
mineral assemblage of the copper porphyry system, as opposed
to the more reduced nature of the Bolivian tin porphyry systems,
which reflect intracrustal melting of pelitic rocks.