Fe–O stable isotope pairs elucidate a high-temperature origin of Chilean iron oxide-apatite deposits
Author
dc.contributor.author
Bilenker, Laura
Author
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Simon, Aadam
Author
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Reich Morales, Martín
Author
dc.contributor.author
Lundstrom, Craig
Author
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Gajos, Norbert
Author
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Bindeman, Ilya
Author
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Barra Pantoja, Fernando
Author
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Munizaga, Rodrigo
Admission date
dc.date.accessioned
2016-06-28T21:24:03Z
Available date
dc.date.available
2016-06-28T21:24:03Z
Publication date
dc.date.issued
2016
Cita de ítem
dc.identifier.citation
Geochimica et Cosmochimica Acta 177 (2016) 94–104
en_US
Identifier
dc.identifier.issn
0016-7037
Identifier
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DOI: 10.1016/j.gca.2016.01.009
Identifier
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https://repositorio.uchile.cl/handle/2250/139202
General note
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Artículo de publicación ISI
en_US
Abstract
dc.description.abstract
Iron oxide–apatite (IOA) ore deposits occur globally and can host millions to billions of tons of Fe in addition to economic
reserves of other metals such as rare earth elements, which are critical for the expected growth of technology and renewable
energy resources. In this study, we pair the stable Fe and O isotope compositions of magnetite samples from several IOA
deposits to constrain the source reservoir of these elements in IOAs. Since magnetite constitutes up to 90 modal% of many
IOAs, identifying the source of Fe and O within the magnetite may elucidate high-temperature and/or lower-temperature processes
responsible for their formation. Here, we focus on the world-class Los Colorados IOA in the Chilean iron belt (CIB),
and present data for magnetite from other Fe oxide deposits in the CIB (El Laco, Mariela). We also report Fe and O isotopic
values for other IOA deposits, including Mineville, New York (USA) and the type locale, Kiruna (Sweden). The ranges of Fe
isotopic composition (d56Fe, 56Fe/54Fe relative to IRMM-14) of magnetite from the Chilean deposits are: Los Colorados,
d56Fe (±2r) = 0.08 ± 0.03‰ to 0.24 ± 0.08‰; El Laco, d56Fe = 0.20 ± 0.03‰ to 0.53 ± 0.03‰; Mariela, d56Fe = 0.13
± 0.03‰. The O isotopic composition (d18O, 18O/16O relative to VSMOW) of the same Chilean magnetite samples are:
Los Colorados, d18O (±2r) = 1.92 ± 0.08‰ to 3.17 ± 0.03‰; El Laco, d18O = 4.00 ± 0.10‰ to 4.34 ± 0.10‰; Mariela,
d18O = (1.48 ± 0.04‰). The d18O and d56Fe values for Kiruna magnetite yield an average of 1.76 ± 0.25‰ and 0.16
± 0.07‰, respectively. The Fe and O isotope data from the Chilean IOAs fit unequivocally within the range of magnetite
formed by high-temperature magmatic or magmatic–hydrothermal processes (i.e., d56Fe 0.06–0.49‰ and d18O = 1.0–
4.5‰), consistent with a high-temperature origin for Chilean IOA deposits. Additionally, minimum formation temperatures
calculated by using the measured D18O values of coexisting Los Colorados magnetite and actinolite separates (630 C) as well
as Fe numbers of actinolite grains (610–820 C) are consistent with this interpretation. We also present Fe isotope data from
magmatic magnetite of the Bushveld Complex, South Africa, where d56Fe ranges from 0.28 ± 0.04‰ to 0.86 ± 0.07‰. Based
on these data and comparison to published Fe and O stable isotope values of igneous magnetite, we propose extending the
magmatic/high-temperature d56Fe range to 0.86‰. Considering that the Chilean IOAs and Kiruna deposit are representative
of IOA deposits worldwide, the Fe and O stable isotope data indicate that IOAs are formed by high-temperature (magmatic)
processes.
en_US
Patrocinador
dc.description.sponsorship
Society of Economic Geologists
UM Department of Earth & Environmental Sciences
NSF
EAR 1264537
EAR 1264560
EAR 1250239
Fondecyt
1140780
Millennium Science Initiative grant "Nucleaus for Metal Tracing Along Subduction"
NC130065
FONDAP
15090013