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- Peters, Stefan T. M., et al.
(författare)
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Amphibole megacrysts as a probe into the deep plumbing system of Merapi volcano, Central Java, Indonesia
- 2017
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Ingår i: Contributions to Mineralogy and Petrology. - : SPRINGER. - 0010-7999 .- 1432-0967. ; 172:4
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Tidskriftsartikel (refereegranskat)abstract
- Amphibole has been discussed to potentially represent an important phase during early chemical evolution of arc magmas, but is not commonly observed in eruptive arc rocks. Here, we present an in-depth study of metastable calcic amphibole megacrysts in basaltic andesites of Merapi volcano, Indonesia. Radiogenic Sr and Nd isotope compositions of the amphibole megacrysts overlap with the host rock range, indicating that they represent antecrysts to the host magmas rather than xenocrysts. Amphibolebased barometry suggests that the megacrysts crystallised at pressures of >500 MPa, i.e., in the mid-to lower crust beneath Merapi. Rare-earth element concentrations, in turn, require the absence of magmatic garnet in the Merapi feeding system and, therefore, place an uppermost limit for the pressure of amphibole crystallisation at ca. 800 MPa. The host magmas of the megacrysts seem to have fractionated significant amounts of amphibole and/or clinopyroxene, because of their low Dy/Yb ratios relative to the estimated compositions of the parent magmas to the megacrysts. The megacrysts' parent magmas at depth may thus have evolved by amphibole fractionation, in line with apparently coupled variations of trace element ratios in the megacrysts, such as e.g., decreasing Zr/Hf with Dy/Yb. Moreover, the Th/U ratios of the amphibole megacrysts decrease with increasing Dy/Yb and are lower than Th/U ratios in the basaltic andesite host rocks. Uranium in the megacrysts' parent magmas, therefore, may have occurred predominantly in the tetravalent state, suggesting that magmatic fO(2) in the Merapi plumbing system increased from below the FMQ buffer in the mid-to-lower crust to 0.6-2.2 log units above it in the near surface environment. In addition, some of the amphibole megacrysts experienced dehydrogenation (H-2 loss) and/or dehydration (H2O loss), as recorded by their variable H2O contents and D/H and Fe3+/Fe2+ ratios, and the release of these volatile species into the shallow plumbing system may facilitate Merapi's often erratic eruptive behaviour.
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- Troll, Valentin R., et al.
(författare)
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Global Fe–O isotope correlation reveals magmatic origin of Kiruna-type apatite-iron-oxide ores
- 2019
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Ingår i: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 10:1
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Tidskriftsartikel (refereegranskat)abstract
- Kiruna-type apatite-iron-oxide ores are key iron sources for modern industry, yet their origin remains controversial. Diverse ore-forming processes have been discussed, comprising low-temperature hydrothermal processes versus a high-temperature origin from magma or magmatic fluids. We present an extensive set of new and combined iron and oxygen isotope data from magnetite of Kiruna-type ores from Sweden, Chile and Iran, and compare them with new global reference data from layered intrusions, active volcanic provinces, and established low-temperature and hydrothermal iron ores. We show that approximately 80% of the magnetite from the investigated Kiruna-type ores exhibit δ56Fe and δ18O ratios that overlap with the volcanic and plutonic reference materials (> 800 °C), whereas ~20%, mainly vein-hosted and disseminated magnetite, match the low-temperature reference samples (≤400 °C). Thus, Kiruna-type ores are dominantly magmatic in origin, but may contain late-stage hydrothermal magnetite populations that can locally overprint primary high-temperature magmatic signatures.
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- Weis, Franz A., et al.
(författare)
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Experimental hydration of natural volcanic clinopyroxene phenocrysts under hydrothermal pressures (0.5-3 kbar)
- 2016
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Ingår i: American Mineralogist. - 0003-004X .- 1945-3027. ; 101, s. 2233-2247
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Tidskriftsartikel (refereegranskat)abstract
- Water is a key parameter in mantle rheology, magma genesis, magma evolution, and resulting eruption styles, because it controls the density and the viscosity, as well as the melting and crystallization behavior of a melt. The water content in nominally anhydrous minerals (NAMs) such as clinopyroxene recently has been used as a proxy for magmatic water contents. NAMs, however, may dehydrate during magma degassing and eruption. We performed rehydration experiments on potentially degassed clinopyroxene phenocrysts from various volcanic settings. The experiments were conducted in hydrogen gas at 1 atm or hydrothermal pressures ranging from 0.5 to 3 kbar to test the incorporation of water into natural clinopyroxene under water fugacities similar to those in a volcanic system. Our results show a dependence of the water content in the clinopyroxene crystals with pressure as the phenocrysts begin to dehydrate upon lower water fugacities in the experiments. Water loss or gain in a crystal occurs according to the relatively fast redox-reaction OH- + Fe2+ ↔ O2– + Fe3+ + ½ H2, which was confirmed by Mössbauer spectroscopy. The kinetics of this redox-process are independent of pressure and thus water fugacity. Water contents in rehydrated clinopyroxene crystals can be related to magmatic water contents at various levels in a volcanic system. Our results thus show that the water content in erupted clinopyroxene phenocrysts cannot be taken for granted to be representative of magmatic water contents prior to magma degassing. The conducted experiments indicate the simultaneous dehydration of clinopyroxene along with magma ascent and degassing. Rehydration experiments under hydrothermal pressures, however, may be able to reconstruct clinopyroxene water contents at crystallization prior to dehydration.
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- Weis, Franz A., 1988-
(författare)
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Hydrogen in nominally anhydrous silicate minerals : Quantification methods, incorporation mechanisms and geological applications
- 2016
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The aim of this thesis is to increase our knowledge and understanding of trace water concentrations in nominally anhydrous minerals (NAMs). Special focus is put on the de- and rehydration mechanisms of clinopyroxene crystals in volcanic systems, how these minerals can be used to investigate the volatile content of mantle rocks and melts on both Earth and other planetary bodies (e.g., Mars). Various analytical techniques for water concentration analysis were evaluated.The first part of the thesis focusses on rehydration experiments in hydrogen gas at 1 atm and under hydrothermal pressures from 0.5 to 3 kbar on volcanic clinopyroxene crystals in order to test hydrogen incorporation and loss from crystals and how their initial water content at crystallization prior to dehydration may be restored. The results show that extensive dehydration may occur during magma ascent and degassing but may be hindered by fast ascent rates with limited volatile loss. De- and rehydration processes are governed by the redox-reaction OH- + Fe2+ ↔ O2- + Fe3+ + ½ H2. Performing rehydration experiments at different pressures can restore the water contents of clinopyroxene at various levels in the volcanic systems. Subsequently water contents of magmas and mantle sources can be deduced based on crystal/melt partition coefficients. This thesis provides examples from the Canary Islands, Merapi volcano in Indonesia and the famous Nakhla meteorite. Using NAMs as a proxy for magmatic and mantle water contents may provide a very good method especially for planetary science where sample material is limited.The thesis’ second part focusses on analytical methods to measure the concentration of water in NAMs. Specifically the application of Raman spectroscopy and proton-proton scattering are tested. The hydrated mineral zoisite is thoroughly analyzed in order to be used as an external standard material. Polarized single crystal spectra helped to determine the orientation of the OH-dipole in zoisite. Further, Transmission Raman spectroscopy and a new method for the preparation of very thin samples for proton-proton scattering were developed and tested. The results provide new possibilities for the concentration analysis of water in NAMs such as three dimensional distribution and high spatial resolution.
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- Weis, Franz A., et al.
(författare)
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Magmatic water contents determined through clinopyroxene : Examples from the Western Canary Islands, Spain
- 2015
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Ingår i: Geochemistry Geophysics Geosystems. - 1525-2027. ; 16:7, s. 2127-2146
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Tidskriftsartikel (refereegranskat)abstract
- Water is a key parameter in magma genesis, magma evolution, and resulting eruption styles, because it controls the density, the viscosity, as well as the melting and crystallization behavior of a melt. The parental water content of a magma is usually measured through melt inclusions in minerals such as olivine, a method which may be hampered, however, by the lack of melt inclusions suitable for analysis, or postentrapment changes in their water content. An alternative way to reconstruct the water content of a magma is to use nominally anhydrous minerals (NAMs), such as pyroxene, which take up low concentrations of hydrogen as a function of the magma's water content. During magma degassing and eruption, however, NAMs may dehydrate. We therefore tested a method to reconstruct the water contents of dehydrated clinopyroxene phenocrysts from the Western Canary islands (n=28) through rehydration experiments followed by infrared and Mossbauer spectroscopy. Employing currently available crystal/melt partitioning data, the results of the experiments were used to calculate parental water contents of 0.710.07 to 1.490.15 wt % H2O for Western Canary magmas during clinopyroxene crystallization at upper mantle conditions. This H2O range is in agreement with calculated water contents using plagioclase-liquid-hygrometry, and with previously published data for mafic lavas from the Canary Islands and comparable ocean island systems elsewhere. Utilizing NAMs in combination with hydrogen treatment can therefore serve as a proxy for pre-eruptive H2O contents, which we anticipate becoming a useful method applicable to mafic rocks where pyroxene is the main phenocryst phase.
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| 9. |
- Weis, Franz A., et al.
(författare)
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Polarized IR and Raman spectra of zoisite : insights into OH-dipole orientation and the luminescence
- 2016
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Ingår i: European journal of mineralogy. - : Schweizerbart. - 0935-1221 .- 1617-4011. ; 38:3, s. 537-543
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Tidskriftsartikel (refereegranskat)abstract
- The OH-dipole in the mineral zoisite has been a topic of discussion regarding its general orientation and vibrational modes. We present new polarized single-crystal Raman and infrared spectra and verify the orientation of the OH-dipole along the crystallographic c axis with a slight deviation towards the crystallographic a axis. Polarized Raman and FTIR spectra confirm that the OH band at 3150 cm(-1) corresponds to the O(10)-H center dot center dot center dot O(4) hydrogen bridge and exclude a previously suggested second hydrogen bridge O(10)-H center dot center dot center dot O(2). Further, Raman spectra provide insights on the luminescence of zoisite and the interference of luminescence peaks in the OH-region.
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