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2.
  • Barker, Abigail, et al. (author)
  • A 5 million year record of compositional variations in mantle sources to magmatism on Santiago, southern Cape Verde archipelago
  • 2010
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 160:1, s. 133-154
  • Journal article (peer-reviewed)abstract
    • High-precision Pb isotope data and Sr–Nd–Hf isotope data are presented together with major and trace element data for samples spanning the 4.6 Ma history of volcanism at Santiago, in the southern Cape Verde islands. Pb isotope data confirm the positive Δ8/4 signature of the southern islands indicating that the north–south compositional heterogeneity in the Cape Verde archipelago has persisted for at least 4.6 Ma. The Santiago volcanics show distinct compositional differences between the old, intermediate and young volcanics, and suggest greater involvement of an enriched mantle (EM1)-like source over time. Isotopic variations in the Santiago volcanics indicate convergence towards a homogeneous EM1-like end-member and distinct temporal variations in the FOZO-like end-member. Santiago and Santo Antão (a northern island, Holm et al. 2006), show a simultaneous decrease in 208Pb/204Pb of the high 206Pb/204Pb FOZO-like source with time. Such systematic archipelago-wide variations in the FOZO-like component suggest that this component is more likely to be present as a coherent package of recycled ocean crust rather than as multiple small heterogeneities dispersed in the upwelling mantle. The temporal variations in 208Pb/204Pb reflect minor lateral variations in Th/U of this recycled ocean crust package entering the melting zone beneath the islands. The location of the EM1-like component is more equivocal. A shallow lithospheric location is possible, but this would require a coincidence between spatial compositional variations in the lithosphere (EM1 is spatially restricted to the southern islands) and flow lines in the upwelling mantle revealed by seismic anisotropy. Therefore, we favour a deeper asthenospheric mantle source for the EM1-like source.
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3.
  • Barker, Abigail K., et al. (author)
  • Magmatic evolution of the Cadamosto Seamount, Cape Verde : Beyond the spatial extent of EM1
  • 2012
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 163:6, s. 949-965
  • Journal article (peer-reviewed)abstract
    • The Cadamosto Seamount is an unusual volcanic centre from Cape Verde, characterised by dominantly evolved volcanics, in contrast to the typically mafic volcanic centres at Cape Verde that exhibit only minor volumes of evolved volcanics. The magmatic evolution of Cadamosto Seamount is investigated to quantify the role of magma-crust interaction and thus provide a perspective on evolved end-member volcanism of Cape Verde. The preservation of mantle source signatures by Nd-Pb isotopes despite extensive magmatic differentiation provides new insights into the spatial distribution of mantle heterogeneity in the Cape Verde archipelago. Magmatic differentiation from nephelinite to phonolite involves fractional crystallisation of clinopyroxene, titanite, apatite, biotite and feldspathoids, with extensive feldspathoid accumulation being recorded in some evolved samples. Clinopyroxene crystallisation pressures of 0.38-0.17 GPa for the nephelinites constrain this extensive fractional crystallisation to the oceanic lithosphere, where no crustal assimilants or rafts of subcontinental lithospheric mantle are available. In turn, magma-crust interaction has influenced the Sr, O and S isotopes of the groundmass and late crystallising feldspathoids, which formed at shallow crustal depths reflecting the availability of oceanic sediments and anhydrite precipitated in the ocean crust. The Nd-Pb isotopes have not been affected by these processes of magma-crust interaction and hence preserve the mantle source signature. The Cadamosto Seamount samples have high Pb-206/Pb-204 (> 19.5), high epsilon Nd (+6 to +7) and negative Delta 8/4Pb, showing affinity with the northern Cape Verde islands as opposed to the adjacent southern islands. Hence, the Cadamosto Seamount in the west is located spatially beyond the EM1-like component found further east. This heterogeneity is not encountered in the oceanic lithosphere beneath the Cadamosto Seamount despite greater extents of fractional crystallisation at oceanic lithospheric depths than the islands of Fogo and Santiago. Our data provide new evidence for the complex geometry of the chemically zoned Cape Verde mantle source.
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4.
  • Barker, Abigail, et al. (author)
  • The magma plumbing system for the 1971 Teneguía eruption on La Palma, Canary Islands
  • 2015
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 170:5-6
  • Journal article (peer-reviewed)abstract
    • The 1971 Teneguía eruption is the most recent volcanic event of the Cumbre Vieja rift zone on La Palma. The eruption produced basanite lavas that host xenoliths, which we investigate to provide insight into the processes of differentiation, assimilation and magma storage beneath La Palma. We compare our results to the older volcanomagmatic systems of the island with the aim to reconstruct the temporal development of the magma plumbing system beneath La Palma.The 1971 lavas are clinopyroxene-olivine-phyric basanites that contain augite, sodic-augite and Aluminium augite. Kaersutite cumulate xenoliths host olivine, clinopyroxene including sodic-diopside, and calcic-amphibole, whereas an analysed leucogabbro xenolith hosts plagioclase, sodic-augite-diopside, calcic-amphibole and hauyne. Mineral and mineral-melt thermobarometry indicate that clinopyroxene and plagioclase in the 1971 Teneguía lavas crystallised at 20 to 45 km depth, coinciding with clinopyroxene and calcic-amphibole crystallisation in the kaersutite cumulate xenoliths at 25 to 45 km and clinopyroxene, calcic-amphibole and plagioclase crystallisation in the leucogabbro xenolith at 30 to 50 km.Combined mineral chemistry and thermobarometry suggest that the magmas had already crystallised, differentiated and formed multiple crystal populations in the oceanic lithospheric mantle. Notably, the magmas that supplied the 1949 and 1971 events appear to have crystallised deeper than the earlier Cumbre Vieja magmas, which suggests progressive underplating beneath the Cumbre Vieja rift zone. In addition, the lavas and xenoliths of the 1971 event crystallised at a common depth, indicating a reused plumbing system and progressive recycling of Ocean Island plutonic complexes during subsequent magmatic activity. 
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5.
  • Barker, Abigail, et al. (author)
  • The role of eclogite in the mantle heterogeneity at Cape Verde
  • 2014
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 168:3, s. 1052-
  • Journal article (peer-reviewed)abstract
    • The Cape Verde hotspot, like many other Ocean Island Basalt provinces, demonstrates isotopic heterogeneity on a 100–200 km scale. The heterogeneity is represented by the appearance of an EM1-like component at several of the southern islands and with a HIMU-like component present throughout the archipelago. Where the EM1-like component is absent, a local DMM-like component replaces the EM1-like component. Various source lithologies, including peridotite, pyroxenite and eclogite have been suggested to contribute to generation of these heterogeneities; however, attempts to quantify such contributions have been limited. We apply the minor elements in olivine approach (Sobolev et al. in Nature 434:590–597, 2005; Science, doi:10.1126/science.1138113,2007), to determine and quantify the contributions of peridotite, pyroxenite and eclogite melts to the mantle heterogeneity observed at Cape Verde. Cores of olivine phenocrysts of the Cape Verde volcanics have low Mn/FeO and low Ni*FeO/MgO that deviate from the negative trend of the global array. The global array is defined by mixing between peridotite and pyroxenite, whereas the Cape Verde volcanics indicate contribution of an additional eclogite source. Eclogite melts escape reaction with peridotite either by efficient extraction in an area of poor mantle flow or by reaction of eclogite melts with peridotite, whereby an abundance of eclogite can seal off the melt from further reaction. Temporal trends of decreasing Mn/FeO indicate that the supply of eclogite melts is increasing. Modelling suggests the local DMM-like end-member is formed from a relatively peridotite-rich melt, while the EM1-like end-member has a closer affinity to a mixed peridotite–pyroxenite–eclogite melt. Notably the HIMU-like component ranges from pyroxenite–peridotite-rich melt to one with up to 77 % eclogite melt as a function of time, implying that sealing of melt pathways is becoming more effective.
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6.
  • Barnes, Christopher, et al. (author)
  • High-spatial resolution dating of monazite and zircon reveals the timing of subduction–exhumation of the Vaimok Lens in the SeveNappe Complex (Scandinavian Caledonides)
  • 2019
  • In: Contributions to Mineralogy and Petrology. - : Springer Berlin/Heidelberg. - 0010-7999 .- 1432-0967. ; 174:1
  • Journal article (peer-reviewed)abstract
    • In-situ monazite Th–U–total Pb dating and zircon LA–ICP–MS depth-profiling was applied to metasedimentary rocks from the Vaimok Lens in the Seve Nappe Complex (SNC), Scandinavian Caledonides. Results of monazite Th–U–total Pb dating, coupled with major and trace element mapping of monazite, revealed 603 ± 16 Ma Neoproterozoic cores surrounded byrims that formed at 498 ± 10 Ma. Monazite rim formation was facilitated via dissolution–reprecipitation of Neoproterozoic monazite. The monazite rims record garnet growth as they are depleted in Y2O3 with respect to the Neoproterozoic cores. Rims are also characterized by relatively high SrO with respect to the cores. Results of the zircon depth-profiling revealed igneous zircon cores with crystallization ages typical for SNC metasediments. Multiple zircon grains also exhibit rims formedby dissolution–reprecipitation that are defined by enrichment of light rare earth elements, U, Th, P, ± Y, and ± Sr. Rims also have subdued Eu anomalies (Eu/Eu* ≈ 0.6–1.2) with respect to the cores. The age of zircon rim formation was calculated from three metasedimentary rocks: 480 ± 22 Ma; 475 ± 26 Ma; and 479 ± 38 Ma. These results show that both monazite and zircon experienced dissolution–reprecipitation under high-pressure conditions. Caledonian monazite formed coeval with garnet growth during subduction of the Vaimok Lens, whereas zircon rim formation coincided with monazite breakdown to apatite, allanite and clinozoisite during initial exhumation.
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7.
  • Barnes, Christopher J., et al. (author)
  • Zircon and monazite reveal late Cambrian/early Ordovician partial melting of the Central Seve Nappe Complex, Scandinavian Caledonides
  • 2022
  • In: Contributions to Mineralogy and Petrology. - : Springer. - 0010-7999 .- 1432-0967. ; 177:9
  • Journal article (peer-reviewed)abstract
    • The Seve Nappe Complex (SNC) comprises continental rocks of Baltica that were subducted and exhumed during the Caledonian orogeny prior to collision with Laurentia. The tectonic history of the central SNC is investigated by applying in-situ zircon and monazite (Th-)U-Pb geochronology and trace element analysis to (ultra-)high pressure (UHP) paragneisses in the Avardo and Marsfjallet gneisses. Zircons in the Avardo Gneiss exposed at Sippmikk creek exhibit xenocrystic cores with metamorphic rims. Cores show typical igneous REE profiles and were affected by partial Pb-loss. The rims have flat HREE profiles and are interpreted to have crystallized at 482.5 +/- 3.7 Ma during biotite-dehydration melting and peritectic garnet growth. Monazites in the paragneiss are chemically homogeneous and record metamorphism at 420.6 +/- 2.0 Ma. In the Marsfjallet Gneiss exposed near Kittelfjall, monazites exhibit complex zoning with cores enveloped by mantles and rims. The cores are interpreted to have crystallized at 481.6 +/- 2.1 Ma, possibly during garnet resorption. The mantles and rims provide a dispersion of dates and are interpreted to have formed by melt-driven dissolution-reprecipitation of pre-existing monazites until 463.1 +/- 1.8 Ma. Depletion of Y, HREE, and U in the mantles and rims compared to the cores record peritectic garnet and zircon growth. Altogether, the Avardo and Marsfjallet gneisses show evidence of late Cambrian/early Ordovician partial melting (possibly in (U)HP conditions), Middle Ordovician (U)HP metamorphism, and late Silurian tectonism. These results indicate that the SNC underwent south-to-north oblique subduction in late Cambrian time, followed by progressive north-to-south exhumation to crustal levels prior to late Silurian continental collision.
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8.
  • Blythe, Lara, et al. (author)
  • CO2 bubble generation and migration during magma–carbonate interaction
  • 2015
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 169:4
  • Journal article (peer-reviewed)abstract
    • We conducted quantitative textural analysis of vesicles in high temperature and pressure carbonate assimilation experiments (1200 °C, 0.5 GPa) to investigate CO2 generation and subsequent bubble migration from carbonate into magma. We employed Mt. Merapi (Indonesia) and Mt. Vesuvius (Italy) compositions as magmatic starting materials and present three experimental series using (1) a dry basaltic-andesite, (2) a hydrous basaltic-andesite (2 wt% H2O), and (3) a hydrous shoshonite (2 wt% H2O). The duration of the experiments was varied from 0 to 300 s, and carbonate assimilation produced a CO2-rich fluid and CaO-enriched melts in all cases. The rate of carbonate assimilation, however, changed as a function of melt viscosity, which affected the 2D vesicle number, vesicle volume, and vesicle size distribution within each experiment. Relatively low-viscosity melts (i.e. Vesuvius experiments) facilitated efficient removal of bubbles from the reaction site. This allowed carbonate assimilation to continue unhindered and large volumes of CO2 to be liberated, a scenario thought to fuel sustained CO2-driven eruptions at the surface. Conversely, at higher viscosity (i.e. Merapi experiments), bubble migration became progressively inhibited and bubble concentration at the reaction site caused localised volatile over-pressure that can eventually trigger short-lived explosive outbursts. Melt viscosity therefore exerts a fundamental control on carbonate assimilation rates and, by consequence, the style of CO2-fuelled eruptions.
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10.
  • Bosi, Ferdinando, et al. (author)
  • Thermally induced cation redistribution in Fe‑bearing oxy‑dravite and potential geothermometric implications
  • 2016
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 171:5, s. 1-14
  • Journal article (peer-reviewed)abstract
    • Iron-bearing oxy-dravite was thermally treated in air and hydrogen atmosphere at 800 °C to study potential changes in Fe, Mg and Al ordering over the octahedrally coordinated Y and Z sites and to explore possible applications to intersite geothermometry based on tourmaline. Overall, the experimental data (structural refinement, Mössbauer, infrared and optical absorption spectroscopy) show that heating Fe-bearing tourmalines results in disordering of Fe over Y and Z balanced by ordering of Mg at Y, whereas Al does not change appreciably. The Fe disorder depends on temperature, but less on redox conditions. The degree of Fe3+–Fe2+ reduction is limited despite strongly reducing conditions, indicating that the fO2 conditions do not exclusively control the Fe oxidation state at the present experimental conditions. Untreated and treated samples have similar short- and long-range crystal structures, which are explained by stable Al-extended clusters around the O1 and O3 sites. In contrast to the stable Al clusters that preclude any temperature-dependent Mg–Al order– disorder, there occurs Mg diffusion linked to temperaturedependent exchange with Fe. Ferric iron mainly resides around O2− at O1 rather than (OH)−, but its intersite disorder induced by thermal treatment indicates that Fe redistribution is the driving force for Mg–Fe exchange and that its diffusion rates are significant at these temperatures. With increasing temperature, Fe progressively disorders over Y and Z, whereas Mg orders at Y according to the order–disorder reaction: YFe + ZMg → ZFe + YMg. The presented findings are important for interpretation of the post-crystallization history of both tourmaline and tourmaline host rocks and imply that successful tourmaline geothermometers may be developed by thermal calibration of the Mg– Fe order–disorder reaction, whereas any thermometers based on Mg–Al disorder will be insensitive and involve large uncertainties.
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11.
  • Brander, Linus, 1978, et al. (author)
  • Brittle-plastic deformation in initially dry rocks at fluid-present conditions : transient behaviour of feldspar at mid-crustal levels
  • 2012
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 163:3, s. 403-425
  • Journal article (peer-reviewed)abstract
    • We present detailed microstructural and chemical analyses from an initially dry anorthositic rock deformed during wet amphibolite facies conditions. Three different domains representing the microstructural variation of the deformed samples are investigated in detail in terms of fracture morphology and mode, grain characteristics and chemistry of present phases. Results show transient deformational behaviour where a close interaction between brittle, plastic and fluid-assisted deformation mechanisms can be observed. Our analysis allows us to describe the succession, interrelationships and effects of active mechanisms with progressively increasing strain in three so-called stages. In Stage 1, initial fracturing along cleavage planes promoted fluid influx that caused fragmentation and chemical reactions, producing fine-grained mineral assemblages in the fractures. Deformation twins and dislocations developed in clast pieces due to stress relaxation. Passive rotation of conjugate fracture sets and interconnection of intracrystalline fractures formed micro-shear-zones, constituting Stage 2. Microstructures and grain relationships indicate the activity and fluctuation between fracturing, dissolution-precipitation creep, grain boundary sliding and locally dislocation creep, reflecting the transient behaviour of brittle and plastic deformation mechanisms. Further rotation and widening of fractures into overall foliation parallel shear-bands (Stage 3) promoted strain partitioning into these areas through increased fluid influx, influence of fluid-assisted grain boundary sliding, phase mixing and presence of weak phases such as white mica. We suggest that local differences in fluid availability, volume fraction of weak phases produced by fluid present metamorphic reactions coupled with volume increase and local variations in stress concentration induced transient brittle-plastic behaviour. The studied shear-zone represents an example of the transformation of a rigid dry rock to a soft wet rock during deformation through syntectonic fracturing.
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12.
  • Callegaro, S., et al. (author)
  • Geochemistry of deep Tunguska Basin sills, Siberian Traps : correlations and potential implications for the end-Permian environmental crisis
  • 2021
  • In: Contributions to Mineralogy and Petrology. - : Springer Nature. - 0010-7999 .- 1432-0967. ; 176:7
  • Journal article (peer-reviewed)abstract
    • A vast portion of the plumbing system of the Siberian Traps Large Igneous Province (STLIP) is emplaced in the Tunguska Basin, where borehole data reveal ubiquitous and abundant sills with great lateral extension. These intrusions intersect Cambrian-Ordovician evaporite, carbonate and siliciclastic series, and locally coal-bearing Permian host rocks, with a high potential for thermogenic gas generation. Here we present new geochemical data from 71 magmatic and 4 sedimentary rock samples from the Tunguska Basin center and periphery, recovered from 15 deep sills intercepted by boreholes. The studied samples are all low-Ti basalt and basaltic andesites, confirming absence of high-Ti and alkaline STLIP magmatism in the Tunguska Basin. The sills derive from picritic parental melts produced by extensive melting of a mantle source with recycled crustal components below a thinned lithosphere (50-60 km), within the spinel stability field. The mantle source was dominantly peridotitic, with enriched pyroxenitic domains formed by recycled lower crust, in agreement with previous models for the main tholeiitic STLIP phase. Limited amounts (up to 5%) of highly radiogenic granitoids or moderately radiogenic metapelites were assimilated in upper crustal magma reservoirs. After emplacement, sills intruded in Cambrian evaporites assimilated marlstones and interacted with the evaporitic host rocks, probably via fluids and brines. This is the first time that such process is described in subvolcanic rocks from all across the volcanic basin. The sills are correlated geochemically with the established chemostratigraphy for the on-craton STLIP lava piles and intrusions (Norilsk region). Sills correlated with the Morongovsky-Mokulaevsky Fm. and the Norilsk-type intrusions are the most voluminous, present all across the central Tunguska Basin, and bear the strongest evidence of interaction with evaporites. Massive discharge of thermogenic volatiles is suggested by explosive pipes and hydrothermal vent structures throughout the Tunguska Basin. We propose that this voluminous pulse of magmatism is a good candidate for the hitherto unidentified early intrusive phase of the STLIP, and may link the deep Tunguska basin sills to the end-Permian environmental crisis.
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13.
  • Chadwick, J.P., et al. (author)
  • Petrology and geochemistry of igneous inclusions in recent Merapi deposits : a window into the sub-volcanic plumbing system
  • 2013
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 165:2, s. 259-282
  • Journal article (peer-reviewed)abstract
    • Recent basaltic-andesite lavas from Merapi volcano contain abundant and varied igneous inclusions suggesting a complex sub-volcanic magmatic system for Merapi volcano. In order to better understand the processes occurring beneath Merapi, we have studied this suite of inclusions by petrography, geochemistry and geobarometric calculations. The inclusions may be classified into four main suites: (1) highly crystalline basaltic-andesite inclusions, (2) co-magmatic enclaves, (3) plutonic crystalline inclusions and (4) amphibole megacrysts. Highly crystalline basaltic-andesite inclusions and co-magmatic enclaves typically display liquid–liquid relationships with their host rocks, indicating mixing and mingling of distinct magmas. Co-magmatic enclaves are basaltic in composition and occasionally display chilled margins, whereas highly crystalline basaltic-andesite inclusions usually lack chilling. Plutonic inclusions have variable grain sizes and occasionally possess crystal layering with a spectrum of compositions spanning from gabbro to diorite. Plagioclase, pyroxene and amphibole are the dominant phases present in both the inclusions and the host lavas. Mineral compositions of the inclusions largely overlap with compositions of minerals in recent and historic basaltic-andesites and the enclaves they contain, indicating a cognate or ‘antelithic’ nature for most of the plutonic inclusions. Many of the plutonic inclusions plot together with the host basaltic-andesites along fractional crystallisation trends from parental basalt to andesite compositions. Results for mineral geobarometry on the inclusions suggest a crystallisation history for the plutonic inclusions and the recent and historic Merapi magmas that spans the full depth of the crust, indicating a multi-chamber magma system with high amounts of semi-molten crystalline mush. There, crystallisation, crystal accumulation, magma mixing and mafic recharge take place. Comparison of the barometric results with whole rock Sr, Nd, and Pb isotope data for the inclusions suggests input of crustal material as magma ascends from depth, with a significant late addition of sedimentary material from the uppermost crust. The type of multi-chamber plumbing system envisaged contains large portions of crystal mush and provides ample opportunity to recycle the magmatic crystalline roots as well as interact with the surrounding host lithologies.
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14.
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15.
  • Cruz-Uribe, A. M., et al. (author)
  • Trace element and isotopic zoning of garnetite veins in amphibolitized eclogite, Franciscan Complex, California, USA
  • 2021
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 176:5
  • Journal article (peer-reviewed)abstract
    • Here we present major element, trace element, and oxygen isotope data for garnet from an amphibolitized eclogite block from Ring Mountain, Franciscan Complex, California, USA. Garnetite veins 1-5 cm thick are laterally continuous up to 10 m within an Mg-rich blackwall zone of the eclogite block. Complex major and trace element zoning patterns reveal multiple stages of garnet growth in both the matrix and garnetite veins. Similarities in major and trace element zoning between matrix and vein garnet suggest that crystallization of the garnetite veins began toward the end of matrix garnet core growth, and continued throughout the garnet growth history of the rock. Oscillatory zoning in rare-earth elements suggests garnet growth in pulses, with matrix-diffusion-limited growth in between pulses. Oxygen isotope analyses of matrix and vein garnet have a range in delta O-18 values of 5.3-11.1 parts per thousand. Differences in delta O-18 values of up to similar to 4 parts per thousand between garnet core and rim are observed in both the matrix and vein; garnet cores range from 9.8 to 11.1 parts per thousand (median 10.4 parts per thousand), garnet mantles range from 8.3 to 10.0 parts per thousand (median 9.7 parts per thousand), and garnet rims range from 5.8 to 7.8 parts per thousand (median 6.7 parts per thousand). Late-stage vein crystallization appears as a garnet "cement" that fills in a network of small (typically 5-50 mu m) garnet cores, and likely crystallized from an amorphous phase. The low delta O-18 values of this latest stage of garnet growth are consistent with interaction with serpentinites, and likely represent the physical incorporation of the eclogite block into the serpentinite matrix melange.
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16.
  • Dahrén, Börje, et al. (author)
  • Magma plumbing beneath Anak Krakatau volcano, Indonesia : evidence for multiple magma storage regions
  • 2012
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 163:4, s. 631-651
  • Journal article (peer-reviewed)abstract
    • Understanding magma plumbing is essential for predicting the behaviour of explosive volcanoes. We investigate magma plumbing at the highly active Anak Krakatau volcano (Indonesia), situated on the rim of the 1883 Krakatau caldera by employing a suite of thermobarometric models. These include clinopyroxene-melt thermobarometry, plagioclase-melt thermobarometry, clinopyroxene composition barometry and olivine-melt thermometry. Petrological studies have previously identified shallow magma storage in the region of 2–8 km beneath Krakatau, while existing seismic evidence points towards mid- to deep-crustal storage zone(s), at 9 and 22 km, respectively. Our results show that clinopyroxene in Anak Krakatau lavas crystallized at a depth of 7–12 km, while plagioclase records both shallow crustal (3–7 km) and sub-Moho (23–28 km) levels of crystallization. These magma storage regions coincide with well-constrained major lithological boundaries in the crust, implying that magma ascent and storage at Anak Krakatau is strongly controlled by crustal properties. A tandem seismic tomography survey independently identified a separate upper crustal (<7 km) and a lower to mid-crustal magma storage region (>7 km). Both petrological and seismic methods are sensitive in detecting magma bodies in the crust, but suffer from various limitations. Combined geophysical and petrological surveys, in turn, offer increased potential for a comprehensive characterization of magma plumbing at active volcanic complexes.
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17.
  • Day, James M. D., et al. (author)
  • Early Eocene Arctic volcanism from carbonate-metasomatized mantle
  • 2023
  • In: Contributions to Mineralogy and Petrology. - : Springer Nature. - 0010-7999 .- 1432-0967. ; 178:12
  • Journal article (peer-reviewed)abstract
    • Melilitite, nephelinite, basanite, and alkali basalt, along with phonolite differentiates, form the Freemans Cove Complex (FCC) in the south-eastern extremity of Bathurst Island (Nunavut, Canada). New Ar-40/Ar-39 chronology indicates their emplacement between similar to 56 and similar to 54 million years ago within a localized extensional structure. Melilitites and nephelinites, along with phonolite differentiates, likely relate to the beginning and end phases of extension, whereas alkali basalts were emplaced during a main extensional episode at similar to 55 Ma. The melilitites, nephelinites, and alkali basalts show no strong evidence for significant assimilation of crust, in contrast to some phonolites. Partial melting occurred within both the garnet- and spinel-facies mantle and sampled sources with He, O, Nd, Hf, and Os isotope characteristics indicative of peridotite with two distinct components. The first, expressed in higher degree partial melts, represents a relatively depleted component ("A"; He-3/He-4 similar to 8 R-A, epsilon(i)(Nd) similar to + 3 epsilon(Hf)i similar to + 7, gamma(Os)i similar to 0). The second was an enriched component ("B" He-3/He-4 < 3 R-A, epsilon(Nd)i < - 1 epsilon(Hf)i < + 3, gamma(Os)i > + 70) sampled by the lowest degree partial melts and represents carbonate-metasomatized peridotite. Magmatism in the FCC shows that rifting extended from the Labrador Sea to Bathurst Island and reached a zenith at similar to 55 Ma, during the Eurekan orogeny. The incompatible trace-element abundances and isotopic signatures of FCC rocks indicate melt generation occurred at the base of relatively thin lithosphere at the margin of a thick craton, with no mantle plume influence. FCC melt compositions are distinct from other continental rift magmatic provinces worldwide, and their metasomatized mantle source was plausibly formed synchronously with emplacement of Cretaceous kimberlites. The FCC illustrates that the range of isotopic compositions preserved in continental rift magmas are likely to be dominated by temporal changes in the extent of partial melting, as well as by the timing and degree of metasomatism recorded in the underlying continental lithosphere.
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18.
  • de Hoog, Cees-Jan, 1969, et al. (author)
  • Oxidized sulfur-rich mafic magma at Mount Pinatubo, Philippines
  • 2004
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 146:6, s. 750-761
  • Journal article (peer-reviewed)abstract
    • Basaltic fragments enclosed in andesitic dome lavas and pyroclastic flows erupted during the early stages of the 1991 eruption of Mount Pinatubo, Philippines, contain amphiboles that crystallized during the injection of mafic magma into a dacitic magma body. The amphiboles contain abundant melt inclusions, which recorded the mixing of andesitic melt in the mafic magma and rhyolitic melt in the dacitic magma. The least evolved melt inclusions have high sulfur contents (up to 1,700 ppm) mostly as SO4 2?, which suggests an oxidized state of the magma (NNO+1.4). The intrinsically oxidized nature of the mafic magma is confirmed by spinel?olivine oxygen barometry. The value is comparable to that of the dacitic magma (NNO+1.6). Hence, models invoking mixing as a means of releasing sulfur from the melt are not applicable to Pinatubo. Instead, the oxidized state of the dacitic magma likely reflects that of parental mafic magma and the source region in the sub-arc mantle. Our results fit a model in which long-lived SO2 discharge from underplated mafic magma accumulated in the overlying dacitic magma and immiscible aqueous fluids. The fluids were the most likely source of sulfur that was released into the atmosphere during the cataclysmic eruption. The concurrence of highly oxidized basaltic magma and disproportionate sulfur output during the 1991 Mt. Pinatubo eruption suggests that oxidized mafic melt is an efficient medium for transferring sulfur from the mantle to shallow crustal levels and the atmosphere. As it can carry large amounts of sulfur, effectively scavenge sulfides from the source mantle and discharge SO2 during ascent, oxidized mafic magma forms arc volcanoes with high sulfur fluxes, and potentially contributes to the formation of metallic sulfide deposits.
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19.
  • Fassmer, K., et al. (author)
  • Middle Ordovician subduction of continental crust in the Scandinavian Caledonides - an example from Tjeliken, Seve Nappe Complex, Sweden.
  • 2017
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 172
  • Journal article (peer-reviewed)abstract
    • The Seve Nappe Complex of the Scandinavian Caledonides is thought to be derived from the distal passive margin of Baltica which collided with Laurentia in the Scandian Phase of the Caledonian Orogeny at 430–400 Ma. Parts of the Seve Nappe Complex were affected by pre-Scandian high- and ultrahigh-pressure metamorphism, in a tectonic framework that is still unclear, partly due to uncertainties about the exact timing. Previous age determinations yielded between ~ 505 and ~ 446 Ma, with a general trend of older ages in the North (Norrbotten) than in the South (Jämtland). New age determinations were performed on eclogite and garnet–phengite gneiss at Tjeliken in northern Jämtland. Thermodynamic modelling yielded peak metamorphic conditions of 25–27 kbar/680–760 °C for the garnet–phengite gneiss, similar to published peak metamorphic conditions of the eclogite (25–26 kbar/650–700 °C). Metamorphic rims of zircons from the garnet–phengite gneiss were dated using secondary ion mass spectrometry and yielded a concordia age of 458.9 ± 2.5 Ma. Lu–Hf garnet-whole rock dating yielded 458 ± 1.0 Ma for the eclogite. Garnet in the eclogite shows prograde major-element zoning and concentration of Lu in the cores, indicating that this age is related to garnet growth during pressure increase, i.e. subduction. The identical ages from both rock types, coinciding with published Sm–Nd ages from the eclogite, confirm subduction of the Seve Nappe Complex in Northern Jämtland during the Middle Ordovician in a fast subduction–exhumation cycle.
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20.
  • Halama, R., et al. (author)
  • Boron isotope record of peak metamorphic ultrahigh-pressure and retrograde fluid-rock interaction in white mica (Lago di Cignana, Western Alps)
  • 2020
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 175:3
  • Journal article (peer-reviewed)abstract
    • This study presents boron (B) concentration and isotope data for white mica from (ultra)high-pressure (UHP), subduction-related metamorphic rocks from Lago di Cignana (Western Alps, Italy). These rocks are of specific geological interest, because they comprise the most deeply subducted rocks of oceanic origin worldwide. Boron geochemistry can track fluid-rock interaction during their metamorphic evolution and provide important insights into mass transfer processes in subduction zones. The highest B contents (up to 345 mu g/g B) occur in peak metamorphic phengite from a garnet-phengite quartzite. The B isotopic composition is variable (delta B-11 = - 10.3 to - 3.6%) and correlates positively with B concentrations. Based on similar textures and major element mica composition, neither textural differences, prograde growth zoning, diffusion nor a retrograde overprint can explain this correlation. Modelling shows that B devolatilization during metamorphism can explain the general trend, but fails to account for the wide compositional and isotopic variability in a single, well-equilibrated sample. We, therefore, argue that this trend represents fluid-rock interaction during peak metamorphic conditions. This interpretation is supported by fluid-rock interaction modelling of boron leaching and boron addition that can successfully reproduce the observed spread in delta B-11 and [B]. Taking into account the local availability of serpentinites as potential source rocks of the fluids, the temperatures reached during peak metamorphism that allow for serpentine dehydration, and the high positive delta B-11 values (delta B-11 = 20 +/- 5) modelled for the fluids, an influx of serpentinite-derived fluid appears likely. Paragonite in lawsonite pseudomorphs in an eclogite and phengite from a retrogressed metabasite have B contents between 12 and 68 mu g/g and delta B-11 values that cluster around 0% (delta B-11 = - 5.0 to + 3.5). White mica in both samples is related to distinct stages of retrograde metamorphism during exhumation of the rocks. The variable B geochemistry can be successfully modelled as fluid-rock interaction with low-to-moderate (< 3) fluid/rock ratios, where mica equilibrates with a fluid into which B preferentially partitions, causing leaching of B from the rock. The metamorphic rocks from Lago di Cignana show variable retention of B in white mica during subduction-related metamorphism and exhumation. The variability in the B geochemical signature in white mica is significant and enhances our understanding of metamorphic processes and their role in element transfer in subduction zones.
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21.
  • Halldórsson, Sæmundur A., et al. (author)
  • Petrology and geochemistry of the 2014–2015 Holuhraun eruption, central Iceland : compositional and mineralogical characteristics, temporal variability and magma storage
  • 2018
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 173:8
  • Journal article (peer-reviewed)abstract
    • The 2014–2015 Holuhraun fissure eruption provided a rare opportunity to study in detail the magmatic processes and magma plumbing system dynamics during a 6-month-long, moderate- to large-volume basaltic fissure eruption. In this contribution, we present a comprehensive dataset, including major and trace elements of whole-rock and glassy tephra samples, mineral chemistry, and radiogenic and oxygen isotope analyses from an extensive set of samples (n = 62) that were collected systematically in several field campaigns throughout the entire eruptive period. We also present the first detailed chemical and isotopic characterization of magmatic sulfides from Iceland. In conjunction with a unique set of geophysical data, our approach provides a detailed temporal and spatial resolution of magmatic processes before and during this eruption. The 2014–2015 Holuhraun magma is compositionally indistinguishable from recent basalts erupted from the Bárðarbunga volcanic system, consistent with seismic observations for magma ascent close to the Bárðarbunga central volcano, followed by dyke propagation to the Holuhraun eruption site. Whole-rock elemental and isotopic compositions are remarkably constant throughout the eruption. Moreover, the inferred depth of the magma reservoir tapped during the eruption is consistently 8 ± 5 km, in agreement with geodetic observations and melt inclusion entrapment pressures, but inconsistent with vertically extensive multi-tiered magma storage prior to eruption. The near constancy in the chemical and isotopic composition of the lava is consistent with the efficient homogenization of mantle-derived compositional variability. In contrast, occurrence of different mineral populations, including sulfide globules, which display significant compositional variability, requires a more complex earlier magmatic history. This may include sampling of heterogeneous mantle melts that mixed, crystallized and finally homogenized at mid- to lower-crustal conditions.
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22.
  • Heinonen, Jussi S., et al. (author)
  • Enrichment of 18O in the mantle sources of the Antarctic portion of the Karoo large igneous province
  • 2018
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 173:3
  • Journal article (peer-reviewed)abstract
    • Karoo continental flood basalt (CFB) province is known for its highly variable trace element and isotopic composition, often attributed to the involvement of continental lithospheric sources. Here, we report oxygen isotopic compositions measured with secondary ion mass spectrometry for hand-picked olivine phenocrysts from ~ 190 to 180 Ma CFBs and intrusive rocks from Vestfjella, western Dronning Maud Land, that form an Antarctic extension of the Karoo province. The Vestfjella lavas exhibit heterogeneous trace element and radiogenic isotope compositions (e.g., εNd from − 16 to + 2 at 180 Ma) and the involvement of continental lithospheric mantle and/or crust in their petrogenesis has previously been suggested. Importantly, our sample set also includes rare primitive dikes that have been derived from depleted asthenospheric mantle sources (εNd up to + 8 at 180 Ma). The majority of the oxygen isotopic compositions of the olivines from these dike rocks (δ18O = 4.4–5.2‰; Fo = 78–92 mol%) are also compatible with such sources. The olivine phenocrysts in the lavas, however, are characterized by notably higher δ18O (6.2–7.5‰; Fo = 70–88 mol%); and one of the dike samples gives intermediate compositions (5.2‒6.1‰, Fo = 83–87 mol%) between the other dikes and the CFBs. The oxygen isotopic compositions do not correlate with radiogenic isotope compositions susceptible to crustal assimilation (Sr, Nd, and Pb) or with geochemical indicators of pyroxene-rich mantle sources. Instead, δ18O correlates positively with enrichments in large-ion lithophile elements (especially K) and 187Os. We suggest that the oxygen isotopic compositions of the Vestfjella CFB olivines primarily record large-scale subduction-related metasomatism of the sub-Gondwanan mantle (base of the lithosphere or deeper) prior to Karoo magmatism. The overall influence of such sources to Karoo magmatism is not known, but, in addition to continental lithosphere, they may be responsible for some of the geochemical heterogeneity observed in the CFBs.
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23.
  • Högdahl, Karin, et al. (author)
  • Reactive monazite and robust zircon growth in diatexitesand leucogranites from a hot, slowly cooled orogen : implicationsfor the Palaeoproterozoic tectonic evolution of the central Fennoscandian Shield, Sweden
  • 2012
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 163:1, s. 167-188
  • Journal article (peer-reviewed)abstract
    • Monazite in melt-producing, poly-metamorphic terranes can grow, dissolve or reprecipitate at different stages during orogenic evolution particularly in hot, slowly cooling orogens such as the Svecofennian. Owing to the high heat flow in such orogens, small variations in pressure, temperature or deformation intensity may promote a mineral reaction. Monazite in diatexites and leucogranites from two Svecofennian domains yields older, coeval and younger U–Pb SIMS and EMP ages than zircon from the same rock. As zircon precipitated during the melt-bearing stage, its U–Pb ages reflect the timing of peak metamorphism, which is associated with partial melting and leucogranite formation. In one of the domains, the Granite and Diatexite Belt, zircon ages range between 1.87 and 1.86 Ga, whereas monazite yields two distinct double peaks at 1.87–1.86 and 1.82–1.80 Ga. The younger double peak is related to monazite growth or reprecipitation during subsolidus conditions associated with deformation along late-orogenic shear zones. Magmatic monazite in leucogranite records systematic variations in composition and age during growth that can be directly linked to Th/U ratios and preferential growth sites of zircon, reflecting the transition from melt to melt crystallisation of the magma. In the adjacent Ljusdal Domain, peak metamorphism in amphibolite facies occurred at 1.83–1.82 Ga as given by both zircon and monazite chronology. Pre-partial melting, 1.85 Ga contact metamorphic monazite is preserved, in spite of the high-grade overprint. By combining structural analysis, petrography and monazite and zircon geochronology, a metamorphic terrane boundary has been identified. It is concluded that the boundary formed by crustal shortening accommodated by major thrusting.
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24.
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25.
  • Jaranowski, Maciej, et al. (author)
  • U-Pb and trace element zircon and apatite petrochronology of eclogites from the Scandinavian Caledonides
  • 2023
  • In: Contributions to Mineralogy and Petrology. - : Springer. - 0010-7999 .- 1432-0967. ; 178
  • Journal article (peer-reviewed)abstract
    • The petrochronological records of eclogites in the Scandinavian Caledonides are investigated using EPMA and LA-ICPMS of zircon and apatite for U-Pb geochronology, combined with major and trace element characteristics. Metamorphic zircon from two eclogites from the Lofoten-Vesteralen Complex (Lofoten Archipelago region) collectively yielded a Concordia age 427.8 & PLUSMN; 5.7 Ma and an upper intercept U-Pb age 425 & PLUSMN; 30 Ma. Apatites from the same eclogites provided U-Pb lower intercepts at 322 & PLUSMN; 28 Ma and 354 & PLUSMN; 33 Ma, with the latter also yielding a younger age of 227 & PLUSMN; 24 Ma. Two eclogites from the Lower Seve Nappe (Northern Jamtland) demonstrate different zircon and apatite age records. Metamorphic zircon provided Concordia ages of 467.2 & PLUSMN; 5.9 Ma and 444.5 & PLUSMN; 5.5 Ma, which resolve the age of prograde metamorphism and zircon growth during retrogression, respectively. The lower intercept U-Pb ages of apatites from the same eclogites are 436 & PLUSMN; 18 and 415 & PLUSMN; 25 Ma, respectively. In combination with their geochemical characteristics, they suggest two separate stages of exhumation of eclogite bodies in the Lower Seve Nappe. Zircons from an eclogite from the Blaho Nappe (Nordoyane Archipelago) yielded a continuum of concordant U-Pb dates from ca. 435 to 395 Ma, which suggests several cycles of HT metamorphism within short intervals. Distinctive trace element characteristics of apatites from the Blaho Nappe eclogite suggest formation coeval with zircon and garnet during HT metamorphism, but Pb diffusion behaved as an open system until cooling during exhumation of the nappe at 390 & PLUSMN; 12 Ma (lower intercept U-Pb age of apatite). To summarize, this study presents the high potential of coupled zircon and apatite petrochronology of eclogites in resolving their metamorphic evolution, particularly with respect to using trace element characteristics of apatites to constrain the records of their growth, alterations and the meaning of their U-Pb age record.
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26.
  • Jeffery, Adam J., et al. (author)
  • The pre-eruptive magma plumbing system of the 2007–2008 dome-forming eruption of Kelut volcano, East Java, Indonesia
  • 2013
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 166:1, s. 275-308
  • Journal article (peer-reviewed)abstract
    • Kelut volcano, East Java, is an active volcanic complex hosting a summit crater lake that has been the source of some of Indonesia’s most destructive lahars. In November 2007, an effusive eruption lasting approximately 7 months led to the formation of a 260-m-high and 400-m-wide lava dome that displaced most of the crater lake. The 2007–2008 Kelut dome comprises crystal-rich basaltic andesite with a texturally complex crystal cargo of strongly zoned and in part resorbed plagioclase (An47–94), orthopyroxene (En64–72, Fs24–32, Wo2–4), clinopyroxene (En40–48, Fs14–19, Wo34–46), Ti-magnetite (Usp16–34) and trace amounts of apatite, as well as ubiquitous glomerocrysts of varying magmatic mineral assemblages. In addition, the notable occurrence of magmatic and crustal xenoliths (meta-basalts, amphibole-bearing cumulates, and skarn-type calc-silicates and meta-volcaniclastic rocks) is a distinct feature of the dome. New petrographical, whole rock major and trace element data, mineral chemistry as well as oxygen isotope data for both whole rocks and minerals indicate a complex regime of magma-mixing, decompression-driven resorption, degassing and crystallisation and crustal assimilation within the Kelut plumbing system prior to extrusion of the dome. Detailed investigation of plagioclase textures alongside crystal size distribution analyses provide evidence for magma mixing as a major pre-eruptive process that blends multiple crystal cargoes together. Distinct magma storage zones are postulated, with a deeper zone at lower crustal levels or near the crust-mantle boundary (>15 km depth), a second zone at mid-crustal levels (~10 km depth) and several magma storage zones distributed throughout the uppermost crust (<10 km depth). Plagioclase-melt and amphibole hygrometry indicate magmatic H2O contents ranging from ~8.1 to 8.6 wt.% in the lower crustal system to ~1.5 to 3.3 wt.% in the mid to upper crust. Pyroxene and plagioclase δ18O values range from 5.4 to 6.7 ‰, and 6.5 to 7.6 ‰, respectively. A single whole rock analysis of the 2007–2008 dome lava gave a δ18O value of 7.6 ‰, whereas meta-basaltic and calc-silicate xenoliths are characterised by δ18O values of 6.2 and 10.3 ‰, respectively. Magmatic δ18O values calculated from individual pyroxene and plagioclase analyses range from 5.7 to 7.0 ‰, and 6.2 to 7.4 ‰, respectively. This range in O-isotopic compositions is explained by crystallisation of pyroxenes in the lower to mid-crust, where crustal contamination is either absent or masked by assimilation of material having similar δ18O values to the ascending melts. This population is mixed with isotopically distinct plagioclase and pyroxenes that crystallised from a more contaminated magma in the upper crustal system. Binary bulk mixing models suggest that shallow-level, recycled volcaniclastic sedimentary rocks together with calc-silicates and/or limestones are the most likely contaminants of the 2007–2008 Kelut magma, with the volcaniclastic sediments being dominant.
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27.
  • Jolis, Ester Muñoz, et al. (author)
  • Experimental simulation of magma-carbonate interaction beneath Mt. Vesuvius, Italy
  • 2013
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 166:5, s. 1335-1353
  • Journal article (peer-reviewed)abstract
    • We simulated the process of magma-carbonate interaction beneath Mt. Vesuvius in short duration piston-cylinder experiments under controlled magmatic conditions (from 0 to 300 s at 0.5 GPa and 1,200 A degrees C), using a Vesuvius shoshonite composition and upper crustal limestone and dolostone as starting materials. Backscattered electron images and chemical analysis (major and trace elements and Sr isotopes) of sequential experimental products allow us to identify the textural and chemical evolution of carbonated products during the assimilation process. We demonstrate that melt-carbonate interaction can be extremely fast (minutes), and results in dynamic contamination of the host melt with respect to Ca, Mg and Sr-87/Sr-86, coupled with intense CO2 vesiculation at the melt-carbonate interface. Binary mixing between carbonate and uncontaminated melt cannot explain the geochemical variations of the experimental charges in full and convection and diffusion likely also operated in the charges. Physical mixing and mingling driven by exsolving volatiles seems to be a key process to promote melt homogenisation. Our results reinforce hypotheses that magma-carbonate interaction is a relevant and ongoing process at Mt. Vesuvius and one that may operate not only on a geological, but on a human timescale.
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28.
  • Konrad-Schmolke, Matthias, 1970, et al. (author)
  • Thermodynamic modelling of diffusion-controlled garnet growth
  • 2005
  • In: Contributions to Mineralogy and Petrology. - 0010-7999 .- 1432-0967. ; 16, s. 181-195
  • Journal article (peer-reviewed)abstract
    • Numerical thermodynamic modelling of mineral composition and modes for specified pressure-temperature paths reveals the strong influence of fractional garnet crystallisation, as well as water fractionation, on garnet growth histories in high pressure rocks. Disequilibrium element incorporation in garnet due to the development of chemical inhomogeneities around porphyroblasts leads to pronounced episodic growth and may even cause growth interruptions. Discontinuous growth, together with pressure- and temperature-dependent changes in garnet chemistry, cause zonation patterns that are indicative of different degrees of disequilibrium element incorporation. Chemical inhomogeneities in the matrix surrounding garnet porphyroblasts strongly affect garnet growth and lead to compositional discontinuities and steep compositional gradients in the garnet zonation pattern. Further, intergranular diffusion-controlled calcium incorporation can lead to a characteristic rise in grossular and spessartine contents at lower metamorphic conditions. The observation that garnet zonation patterns diagnostic of large and small fractionation effects coexist within the same sample suggests that garnet growth is often controlled by small-scale variations in the bulk rock chemistry. Therefore, the spatial distribution of garnet grains and their zonation patterns, together with numerical growth models of garnet zonation patterns, yield information about the processes limiting garnet growth. These processes include intercrystalline element transport and dissolution of pre-existing grains. Discontinuities in garnet growth induced by limited element supply can mask traces of the thermobarometric history of the rock. Therefore, thermodynamic modelling that considers fractional disequilibrium crystallisation is required to interpret compositional garnet zonation in terms of a quantitative pressure and temperature path of the host rock
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29.
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30.
  • Kosminska, Karolina, et al. (author)
  • Monazite in the eclogite and blueschist of the Svalbard Caledonides : its origin and forming-reactions
  • 2023
  • In: Contributions to Mineralogy and Petrology. - : Springer. - 0010-7999 .- 1432-0967. ; 178
  • Journal article (peer-reviewed)abstract
    • High-pressure low-temperature rocks from Svalbard are an excellent target for studying metamorphic reactions in Phanerozoic subduction zones. This study reveals the presence of monazite in an eclogite and a blueschist from the Vestgotabreen Complex, southwestern Svalbard. In order to investigate the monazite-forming reaction, we obtained pressure-temperature estimates coupled with U-Pb and Lu-Hf dating. Combined geothermobarometry allows to constrain three evolutionary stages of garnet growth in the eclogite: nucleation (1.6 & PLUSMN; 0.3 GPa at 460 & PLUSMN; 60 & DEG;C), peak-pressure (2.3 & PLUSMN; 0.3 GPa at 507 & PLUSMN; 60 & DEG;C), and peak-temperature (2.1 & PLUSMN; 0.3 GPa at 553 & PLUSMN; 60 & DEG;C). A zircon age of 482 & PLUSMN; 10 Ma is interpreted to belong to the prograde part of the pressure-temperature path. Monazite forms inclusions within garnet rims, or it is surrounded by allanite and apatite, altogether forming pseudomorphs of a tabular shape in the matrix. Textures, geothermobarometry and geochronology support the conclusion the monazite formed under high-pressure conditions at 471 & PLUSMN; 6 Ma. We propose that the monazite crystallization in the eclogite happened due to a decomposition of accessory phases during the decompression after peak-pressure of the metamorphic cycle. Monazite in the blueschist occurs as inclusions in garnet cores and gives an indicative age of 486 & PLUSMN; 6 Ma, which is interpreted to reflect the prograde growth of the garnet. Lu-Hf garnet dating resolves an age of peak-pressure metamorphism in the blueschist at 471.1 & PLUSMN; 4 Ma under conditions of 2.0 & PLUSMN; 0.03 GPa and 500 & PLUSMN; 30 & DEG;C. The Vestgotabreen Complex provides evidence for an early Ordovician modern-style subduction system in the proximity of the Baltica margin. Hence, this study also supports the tectonic models that favour a mixed Baltican and Laurentian provenance of south-western Svalbard.
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31.
  • Kusebauch, C., et al. (author)
  • Apatite as probe for the halogen composition of metamorphic fluids (Bamble Sector, SE Norway)
  • 2015
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 170, s. 1-20
  • Journal article (peer-reviewed)abstract
    • Halogen composition of replaced apatite formed during a regional metasomatic event (Bamble Sector, SE Norway) reveals information about the composition and evolution of the hydrothermal fluid. Infiltration and pervasive fluid flow of highly saline fluids into gabbroic bodies lead to scapolitization and amphibolitization, where magmatic Cl-rich apatite reacts with the hydrothermal fluid to form OH- and/or F-rich apatite. Apatite from highly altered samples adjacent to the shear zone has highest F (up to 15,000 µg/g) and lowest Br (4–25 µg/g) concentrations, whereas apatite from least altered samples has very low F (30–200 µg/g) and high Br (30–85 µg/g). In addition, individual replaced apatite grains show a zonation in F with high concentrations along rims and cracks and low F in core regions. Iodine concentrations remain rather constant as low values of 0.18–0.70 µg/g. We interpret all observed compositional features of replaced apatite to be the result of a continuous evolution of the fluid during fluid–rock interaction. Due to its high compatibility, F from the infiltrating fluid is incorporated early into recrystallized apatite (close to shear zone and rims of individual apatite grains). In contrast, Br as an incompatible halogen becomes enriched in the fluid and is highest in the most evolved fluid. Using experimental partition data between replaced apatite and fluid, we calculated F concentrations of the evolving fluid to decrease from 60 to <1 µg/g and Br to increase from ~1200 to ~5000 µg/g; I concentrations of the fluid are constant in the order of 370 µg/g. Although Cl is expected to show a similar behavior as Br, replaced apatite has constant Cl concentrations throughout the alteration sequence (~1 wt.%), which is likely the result of a rather constant Cl activity in the fluid. Chlorine stable isotope values of individual apatite grains are heterogeneous and range from −1.2 to +3.7 ‰. High δ 37Cl values are generally correlated with OH-rich zones of replaced apatite, whereas low δ 37Cl values are measured in F-rich zones of replaced apatite and in Cl-apatite of probably magmatic origin. Though apatite δ 37Cl values follow the general bulk trend, the individual δ 37Cl signature seems to reflect the highly localized composition of interfacial fluid at the reaction front. Our observations suggest that apatite can be used as a fluid probe for F, Br, and I to detect a compositional evolution of the fluid, which can be quantified by using experimentally derived partition coefficients. Partitioning of Cl and Cl stable isotopes between highly saline fluids and apatite is complex and likely controlled by more unknown factors than just the Cl concentration.
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32.
  • Laurent, Antonin T., et al. (author)
  • Decoding a protracted zircon geochronological record in ultrahigh temperature granulite, and persistence of partial melting in the crust, Rogaland, Norway
  • 2018
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 173:4
  • Journal article (peer-reviewed)abstract
    • This contribution evaluates the relation between protracted zircon geochronological signal and protracted crustal melting in the course of polyphase high to ultrahigh temperature (UHT; T > 900 °C) granulite facies metamorphism. New U–Pb, oxygen isotope, trace element, ion imaging and cathodoluminescence (CL) imaging data in zircon are reported from five samples from Rogaland, South Norway. The data reveal that the spread of apparent age captured by zircon, between 1040 and 930 Ma, results both from open-system growth and closed-system post-crystallization disturbance. Post-crystallization disturbance is evidenced by inverse age zoning induced by solid-state recrystallization of metamict cores that received an alpha dose above 35 × 1017 α  g−1. Zircon neocrystallization is documented by CL-dark domains displaying O isotope open-system behaviour. In UHT samples, O isotopic ratios are homogenous (δ18O = 8.91 ± 0.08‰), pointing to high-temperature diffusion. Scanning ion imaging of these CL-dark domains did not reveal unsupported radiogenic Pb. The continuous geochronological signal retrieved from the CL-dark zircon in UHT samples is similar to that of monazite for the two recognized metamorphic phases (M1: 1040–990 Ma; M2: 940–930 Ma). A specific zircon-forming event is identified in the orthopyroxene and UHT zone with a probability peak at ca. 975 Ma, lasting until ca. 955 Ma. Coupling U–Pb geochronology and Ti-in-zircon thermometry provides firm evidence of protracted melting lasting up to 110 My (1040–930 Ma) in the UHT zone, 85 My (ca. 1040–955 Ma) in the orthopyroxene zone and some 40 My (ca. 1040–1000 Ma) in the regional basement. These results demonstrate the persistence of melt over long timescales in the crust, punctuated by two UHT incursions.
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33.
  • Lewerentz, Alexander, et al. (author)
  • Baddeleyite formation in zircon by Ca-bearing fluids in silica-saturated systems in nature and experiment : resetting of the U-Pb geochronometer
  • 2019
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 174:8
  • Journal article (peer-reviewed)abstract
    • Intergrowths of baddeleyite have been found in zircon grain interiors from amphibolite- and granulite-facies felsic rocks from southwest Greenland. The zircon grains are either close to or in direct contact with quartz. A series of experiments has been conducted using natural, unaltered zircon grains +/- SiO2 in H2O-CaCl2, and H2O-Ca(OH)(2) solutions with varying molar proportions of Ca to Si at 900 degrees C; 1000MPa and 600 degrees C; 400MPa for 4-50days. Experimental results indicate that baddeleyite formed in the reacted zircon if the molar amount of Ca was close to or greater than Si in the system. The baddeleyite primarily takes the form of bead-like trails along the reaction front between the altered and unaltered zircon. Uranium, Th, and Y+REE were detected in both the newly formed baddeleyite and in the altered zircon, while Pb was effectively absent in both phases. Formation of baddeleyite from zircon in the silica-saturated rocks only appears to be possible when Ca saturates the system, such that the Si is tied up as CaSiO3 lowering the silica activity to <1. This highly localized (mu m to nm scale) effect in natural quartz-bearing rocks, where baddeleyite forms in the interiors of zircon grains in contact with quartz, implies that metastability in natural rock-forming systems can occur on a very small scale. Non-incorporation of Pb in the newly formed baddeleyite, or in areas of the zircon altered by fluids, implies that either could be used to date the metasomatic event responsible for their formation.
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34.
  • Manzotti, Paola, et al. (author)
  • A journey towards the forbidden zone : a new, cold, UHP unit in the Dora-Maira Massif (Western Alps)
  • 2022
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 177:6
  • Journal article (peer-reviewed)abstract
    • The distribution of ultrahigh-pressure metamorphism (UHP) at the scale of a mountain belt is of prime importance for deciphering its past subduction history. In the Western Alps, coesite has been recognized in the southern Dora-Maira Massif, in the lens-shaped Brossasco-Isasca Unit, but has not been found up to now in the other parts of the massif. We report the discovery of a new UHP unit in the northern Dora-Maira Massif (Western Alps), named Chasteiran Unit. It is only a few tens of metres thick and consists of graphite-rich, garnet–chloritoid micaschists, whose protoliths may be black shales of Silurian age. Garnet inclusions (chloritoid, rutile) and its growth zoning allow to precisely model the P–T evolution. Coesite crystals, which are pristine or partially transformed to palisade quartz occur as inclusions in the garnet outer cores. According to thermodynamic modelling, garnet displays a continuous record of growth during the prograde increase in P and T (25–27 kbar 470–500 °C) (stage 1), up to the coesite stability field (27–28 kbar 510–530 °C) (stage 2), as well as sub-isothermal decompression of about 10 kbar (down to 15 kbar 500–515 °C) (stage 3). The main regional, composite, foliation, marked by chloritoid and rutile, began to develop during this stage, and was then overprinted by chlorite–ilmenite (stage 4). The Chasteiran Unit is discontinuously exposed in the immediate hangingwall of the Pinerolo Unit, and it is located far away from, and without physical links to the classic UHP Brossasco-Isasca Unit. Moreover, it records a different, much colder, P–T evolution, showing that different slices were detached from the downgoing subduction slab. The Chasteiran Unit is the fourth and the coldest Alpine UHP unit known so far in the entire Alpine belt. Its P–T conditions are comparable to the ones of the Tian Shan coesite–chloritoid-bearing rocks. 
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35.
  • Manzotti, Paola, et al. (author)
  • Missing lawsonite and aragonite found : P-T and fluid composition in meta-marls from the Combin Zone (Western Alps)
  • 2021
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 176:8
  • Journal article (peer-reviewed)abstract
    • We report the first findings of several occurrences of lawsonite and metamorphic aragonite in the meta-sediments from the Combin Zone (Piemonte-Liguria ocean, Western Alps), where the early blueschist-facies episode is poorly documented. New field and metamorphic data (thermodynamic modelling and Raman spectroscopy on carbonaceous material) are used to elucidate the P-T evolution and fluid composition of the Combin Zone and investigate the lawsonite growth and breakdown reactions. Two tectonometamorphic units have been identified within the Combin Zone with distinct geometry, lithological content and P-T conditions. In the higher grade unit, metamorphic aragonite occurs as inclusions in titanite. Lawsonite and garnet were stable at peak P-T conditions (similar to 16-17 kbar and 460-480 degrees C) at very low X(CO2) values. Lawsonite is systematically pseudomorphed, but preserves hourglass zoning or internal fabric associated with the prograde ductile deformation. The lower grade unit (similar to 8 +1 kbar similar to 370-400 degrees C) is discontinuously exposed along the western base of the continental Dent Blanche nappe and records P-T conditions similar to those recorded by the Dent Blanche nappe. A metamorphic discontinuity is, therefore, documented between the largest part of the Combin Zone on the one hand, and the Dent Blanche nappe on the other hand. The discovery of lawsonite and metamorphic aragonite allows a better understanding of the large-scale metamorphic structure of the Western Alps.
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36.
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37.
  • Menegon, Luca, et al. (author)
  • The effect of Dauphin, twinning on plastic strain in quartz
  • 2011
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 161:4, s. 635-652
  • Journal article (peer-reviewed)abstract
    • We present an electron backscatter diffraction analysis of five quartz porphyroclasts in a greenschist facies (T = 300-400A degrees C) granitoid protomylonite from the Arolla unit of the NW Alps. Mechanical Dauphin, twinning developed pervasively during the incipient stage of deformation within two porphyroclasts oriented with a negative rhomb plane {z} almost orthogonal to the compression direction (z-twin orientation). Twinning was driven by the anisotropy in the elastic compliance of quartz and resulted in the alignment of the poles of the planes of the more compliant positive rhomb {r} nearly parallel to the compression direction (r-twin orientation). In contrast, we report the lack of twinning in two porphyroclasts already oriented with one of the {r} planes orthogonal to the compression direction. One twinned porphyroclast has been investigated with more detail. It shows the localization of much of the plastic strain into discrete r-twins as a consequence of the higher amount of elastic strain energy stored by r-twins in comparison to z-twins. The presence of Dauphin, twins induced a switch in the dominant active slip systems during plastic deformation, from basal < a > (regions without twinning) to {pi} and {pi'} < a > (pervasively twinned regions). Dynamic recrystallization is localized along an r-twin and occurred dominantly by progressive subgrain rotation, with a local component of bulging recrystallization. Part of the recrystallized grains underwent rigid-body rotation, approximately about the bulk vorticity axis, which accounts for the development of large misorientation angles. The recrystallized grain size piezometer for quartz yields differential stress of 100 MPa. The comparison of this palaeostress estimate with literature data suggests that mechanical Dauphin, twinning could have a potential use as palaeopiezometer in quartz-bearing rocks.
  •  
38.
  • Menneken, M., et al. (author)
  • CO2 fluid inclusions in Jack Hills zircons.
  • 2017
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 172
  • Journal article (peer-reviewed)abstract
    • The discovery of Hadean to Paleoarchean zircons in a metaconglomerate from Jack Hills, Western Australia, has catalyzed intensive study of these zircons and their mineral inclusions, as they represent unique geochemical archives that can be used to unravel the geological evolution of early Earth. Here, we report the occurrence and physical properties of previously undetected CO2 inclusions that were identified in 3.36–3.47 Ga and 3.80–4.13 Ga zircon grains by confocal micro-Raman spectroscopy. Minimum P–T conditions of zircon formation were determined from the highest density of the inclusions, determined from the density-dependence of the Fermi diad splitting in the Raman spectrum and Ti-in-zircon thermometry. For both age periods, the CO2 densities and Ti-in-zircon temperatures correspond to high-grade metamorphic conditions (≥5 to ≥7 kbar/~670 to 770 °C) that are typical of mid-crustal regional metamorphism throughout Earth’s history. In addition, fully enclosed, highly disordered graphitic carbon inclusions were identified in two zircon grains from the older population that also contained CO2 inclusions. Transmission electron microscopy on one of these inclusions revealed that carbon forms a thin amorphous film on the inclusion wall, whereas the rest of the volume was probably occupied by CO2 prior to analysis. This indicates a close relationship between CO2 and the reduced carbon inclusions and, in particular that the carbon precipitated from a CO2-rich fluid, which is inconsistent with the recently proposed biogenic origin of carbon inclusions found in Hadean zircons from Jack Hills.
  •  
39.
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40.
  • Muir, Duncan D., et al. (author)
  • Petrological imaging of an active pluton beneath Cerro Uturuncu, Bolivia
  • 2014
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 167:3, s. 980-
  • Journal article (peer-reviewed)abstract
    • Uturuncu is a dormant volcano in the Altiplano of SW Bolivia. A present day similar to 70 km diameter interferometric synthetic aperture radar (InSAR) anomaly roughly centred on Uturuncu's edifice is believed to be a result of magma intrusion into an active crustal pluton. Past activity at the volcano, spanning 0.89 to 0.27 Ma, is exclusively effusive and almost all lavas and domes are dacitic with phenocrysts of plagioclase, orthopyroxene, biotite, ilmenite and Ti-magnetite plus or minus quartz, and microlites of plagioclase and orthopyroxene set in rhyolitic groundmass glass. Plagioclasehosted melt inclusions (MI) are rhyolitic with major element compositions that are similar to groundmass glasses. H2O concentrations plotted versus incompatible elements for individual samples describe a trend typical of near-isobaric, volatile-saturated crystallisation. At 870 degrees C, the average magma temperature calculated from Fe-Ti oxides, the average H2O of 3.2 +/- 0.7 wt% and CO2 typically <160 ppm equate to MI trapping pressures of 50-120 MPa, approximately 2-4.5 km below surface. Such shallow storage precludes the role of dacite magma emplacement into preeruptive storage regions as being the cause of the observed InSAR anomaly. Storage pressures, whole-rock (WR) chemistry and phase assemblage are remarkably consistent across the eruptive history of the volcano, although magmatic temperatures calculated from Fe-Ti oxide geothermometry, zircon saturation thermometry using MI and orthopyroxenemelt thermometry range from 760 to 925 degrees C at NNO +/- 1 log. This large temperature range is similar to that of saturation temperatures of observed phases in experimental data on Uturuncu dacites. The variation in calculated temperatures is attributed to piecemeal construction of the active pluton by successive inputs of new magma into a growing volume of plutonic mush. Fluctuating temperatures within the mush can account for sieve-textured cores and complex zoning in plagioclase phenocrysts, resorption of quartz and biotite phenocrysts and apatite microlites. That Fe-Ti oxide temperatures vary by similar to 50-100 degrees C in a single thin section indicates that magmas were not homogenised effectively prior to eruption. Phenocryst contents do not correlate with calculated magmatic temperatures, consistent with crystal entrainment from the mush during magma ascent and eruption. Microlites grew during ascent from the magma storage region. Variability in the proportion of microlites is attributed to differing ascent and effusion rates with faster rates in general for lavas >0.5 Ma compared to those <0.5 Ma. High microlite contents of domes indicate that effusion rates were probably slowest in dome-forming eruptions. Linear trends in WR major and trace element chemistries, highly variable, bimodal mineral compositions, and the presence of mafic enclaves in lavas demonstrate that intrusion of more mafic magmas into the evolving, shallow plutonic mush also occurred further amplifying local temperature fluctuations. Crystallisation and resorption of accessory phases, particularly ilmenite and apatite, can be detected in MI and groundmass glass trace element covariation trends, which are oblique to WRs. Marked variability of Ba, Sr and La in MI can be attributed to temperature-controlled, localised crystallisation of plagioclase, orthopyroxene and biotite within the evolving mush.
  •  
41.
  • Myhill, Robert, et al. (author)
  • On the P-T fO(2) stability of Fe4O5, Fe5O6 and Fe4O5-rich solid solutions
  • 2016
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 171:5
  • Journal article (peer-reviewed)abstract
    • The high-pressure phases Fe4O5 and Fe506 have recently been added to the list of known iron oxides. As mixed -valence phases, it has been suggested that they could form in the Earth's mantle once the dominant minerals become saturated in ferric iron. The possibility that Fe4O5 could exist in the mantle is also supported by the fact that it forms extensive solid solutions with both Mg2+ and Cr3+. In this study, we present the results of high-pressure and high-temperature multi -anvil experiments performed between 5 and 24 GPa at 1000-1400 degrees C aimed at constraining the stability field of the Fe4O5 phase. We combine these results with published phase equilibria, equation of state and Fe Mg partitioning data to estimate the thermodynamic properties of Fe4O5, Fe5O6 and the (Mg,Fe)(2)Fe2O5 solid solution. Using our thermodynamic model, the oxygen fugacity at which the high-pressure iron oxides become stable is calculated and the redox stability of (Mg,Fe)(2)Fe2O5 in an assemblage of olivine and pyroxene is calculated as a function of the bulk Fe/(Fe + Mg) ratio. Fe4O5 and (Mg,Fe)(2)Fe2O5 are stable at oxygen fugacities higher than the diamond stability field and are, therefore, unlikely to be found as inclusions in diamonds. The stability field of Fe5O6, on the other hand, extends to oxygen fugacities compatible with diamond formation. Using the Mg Fe solid solution model, we show that Fe4O5-structured phases would be restricted to aluminium -poor environments in the mantle such as dunites or silica iron oxide rich sediments transported into the mantle via subduction.
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42.
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43.
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44.
  • Peters, Stefan T. M., et al. (author)
  • Amphibole megacrysts as a probe into the deep plumbing system of Merapi volcano, Central Java, Indonesia
  • 2017
  • In: Contributions to Mineralogy and Petrology. - : SPRINGER. - 0010-7999 .- 1432-0967. ; 172:4
  • Journal article (peer-reviewed)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.
  •  
45.
  • Ranta, E., et al. (author)
  • Fluid-rock reactions in the 1.3Ga siderite carbonatite of the GrOnnedal-ika alkaline complex, Southwest Greenland
  • 2018
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 173:10
  • Journal article (peer-reviewed)abstract
    • Petrogenetic studies of carbonatites are challenging, because carbonatite mineral assemblages and mineral chemistry typically reflect both variable pressure-temperature conditions during crystallization and fluid-rock interaction caused by magmatic-hydrothermal fluids. However, this complexity results in recognizable alteration textures and trace-element signatures in the mineral archive that can be used to reconstruct the magmatic evolution and fluid-rock interaction history of carbonatites. We present new LA-ICP-MS trace-element data for magnetite, calcite, siderite, and ankerite-dolomite-kutnohorite from the iron-rich carbonatites of the 1.3Ga GrOnnedal-ika alkaline complex, Southwest Greenland. We use these data, in combination with detailed cathodoluminescence imaging, to identify magmatic and secondary geochemical fingerprints preserved in these minerals. The chemical and textural gradients show that a 55m-thick basaltic dike that crosscuts the carbonatite intrusion has acted as the pathway for hydrothermal fluids enriched in F and CO2, which have caused mobilization of the LREEs, Nb, Ta, Ba, Sr, Mn, and P. These fluids reacted with and altered the composition of the surrounding carbonatites up to a distance of 40m from the dike contact and caused formation of magnetite through oxidation of siderite. Our results can be used for discrimination between primary magmatic minerals and later alteration-related assemblages in carbonatites in general, which can lead to a better understanding of how these rare rocks are formed. Our data provide evidence that siderite-bearing ferrocarbonatites can form during late stages of calciocarbonatitic magma evolution.
  •  
46.
  • Rimsa, Andrius, et al. (author)
  • Constraints on incipient charnockite formation from zircon geochronology and rare earth element characteristics
  • 2007
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 154:3, s. 357-369
  • Journal article (peer-reviewed)abstract
    • We present high spatial resolution ion-microprobe U-Th-Pb geochronology and rare earth element (REE) data combined with cathodoluminescence (CL) and back-scattered electron (BSE) imaging for complex zircons in incipient charnockites from Sondrum, SW Sweden. Examination of closely paired samples across the dehydration zone demonstrates that incipient charnockite formation at Sondrum is a zircon-forming process. We determined the age of the dehydration event (i.e. charnockitisation) to 1,397 +/- 4 Ma (2 sigma, MSWD = 1.7). This is the first successful attempt to date incipient charnockite formation using U-Pb systematics of zircon. Internal structure, chemical and isotopic characteristics of zircon indicate that the granitic pegmatite in the core of the incipient charnockite is a melting zone. Commonly observed bulk rock HREE depletion in incipient charnockites is not caused by zircon dissolution but by involvement of garnet as a reactant in the dehydration reactions. Moreover, REE patterns of the newly formed zircon are HREE-enriched, indicating non-concurrent growth and suggesting that the degree of charnockite depletion in HREE might be controlled by the volume of newly formed zircon.
  •  
47.
  • Romer, Rolf L., et al. (author)
  • Alpine and pre-Alpine magmatism in the root-zone of the western Central Alps
  • 1996
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 123, s. 138-158
  • Journal article (peer-reviewed)abstract
    • The highest grade of metamorphism and associated structural elements in orogenic belts may be inherited from earlier orogenic events. We illustrate this point using magmatic and metamorphic rocks from the southern steep belt of the Lepontine Gneiss Dome (Central Alps). The U-Pb zircon ages from an anatectic granite at Verampio and migmatites at Corcapolo and Lavertezzo yield 280-290 Ma, i.e., Hercynian ages. These ages indicate that the highest grade of metamorphism in several crystalline nappes of the Lepontine Gneiss Dome is pre-Alpine. Alpine metamorphism reached sufficiently high grade to reset the Rb-Sr and K-Ar systematics of mica and amphibole, but generally did not result in crustal melting, except in the steep belt to the north of the Insubric Line, where numerous 29 to 26 Ma old pegmatites and aplites had intruded syn- and post-kinematically into gneisses of the ductile Simplon Shear Zone. The emplacement age of these pegmatites gives a minimum estimate for the age of the Alpine metamorphic peak in the Monte Rosa nappe. The U-Pb titanite ages of 33 to 31 Ma from felsic porphyritic veins represent a minimum-age estimate for Alpine metamorphism in the Sesia Zone. A porphyric vein emplaced at 448±5 Ma (U-Pb monazite) demonstrates that there existed a consolidated Caledonian basement in the Sesia Zone.
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48.
  • Scherstén, Anders, et al. (author)
  • Dating mafic–ultramafic intrusions by ion-microprobing contact-melt zircon: examples from SW Sweden
  • 2000
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 39:1, s. 115-125
  • Journal article (peer-reviewed)abstract
    • Zircons from anatectic melts of the country rocks of three Proterozoic mafic–ultramafic intrusions from the Sveconorwegian Province in SW Sweden were microanalyzed for U–Th–Pb and rare earth elements. Melting and interaction of the wall rocks with the intrusions gave rise to new magmas that crystallized zircon as new grains and overgrowths on xenocrysts. The ages of the intrusions can be determined by dating this newly crystallized zircon. The method is applied to three intrusions that present different degrees of complexity, related to age differences between intrusion and country rocks, and the effects of post-intrusive metamorphism. By careful study of cathodoluminescent images and selection of ion probe spots in zircon grains, we show that this approach is a powerful tool for obtaining accurate and precise ages. In the contact melts around the 916 ± 11 Ma Hakefjorden Complex, Pb-loss occurred in some U-rich parts of xenocrystic zircon due to the heat from the intrusion. In back-veins of the 1624 ± 6 Ma Olstorp intrusion we succeeded in geochemically distinguishing new magmatic from xenocrystic zircon despite small age differences. At Borås the mafic intrusion mixed with country rock granite to form a tonalite in which new zircon grew at 1674 ± 8 Ma. Reworking of zircon occurred during 930+33/–34 Ma upper amphibolite facies Sveconorwegian metamorphism. Pb-loss was the result of re-equilibration with metamorphic fluids. REE-profiles show consistent differences between xenocrystic, magmatic, and metamorphic zircon in all cases. They typically differ in Lu/LaN, Ce/Ce*, and Eu/Eu*, and igneous zircon with marked positive Ce/Ce* and negative Eu/Eu* lost its anomalies during metamorphism.
  •  
49.
  • Skelton, Alasdair, et al. (author)
  • Fluid–rock interaction at a carbonatite-gneiss contact, Alnö, Sweden
  • 2007
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 154, s. 75-90
  • Journal article (peer-reviewed)abstract
    • We evaluate balanced metasomatic reactionsand model coupled reactive and isotopic transportat a carbonatite-gneiss contact at Alno, Sweden.We interpret structurally channelled fluid flow alongthe carbonatite-gneiss contact at ~640C. This caused(1) metasomatism of the gneiss, by the reaction:biotite + quartz + oligoclase + K2O + Na2O +/- CaO +/-MgO +/- FeO = albite + K-feldspar + arfvedsonite +aegirene-augite + H2O + SiO2, (2) metasomatism ofcarbonatite by the reaction: calcite + SiO2 = wollastonite+ CO2, and (3) isotopic homogenization of themetasomatised region. We suggest that reactiveweakening caused the metasomatised region to widenand that the metasomatic reactions are chemically(and possibly mechanically) coupled. Spatial separationof reaction and isotope fronts in the carbonatiteconforms to a chromatographic model which assumeslocal calcite–fluid equilibrium, yields a timescale of10^2–10^4 years for fluid–rock interaction and confirmsthat chemical transport towards the carbonatiteinterior was mainly by diffusion. We conclude thatmost silicate phases present in the studied carbonatitewere acquired by corrosion and assimilation of ijolite, as a reactive by-product of this process and bymetasomatism. The carbonatite was thus a relativelypure calcite–H2O–CO2–salt melt or fluid.Keywords Carbonatite, Fluid flow, Metasomatism, Alno
  •  
50.
  • Svahnberg, Henrik, et al. (author)
  • Interaction of chemical and physical processes during deformation at fluid-present conditions : a case study from an anorthosite leucogabbro deformed at amphibolite facies conditions
  • 2013
  • In: Contributions to Mineralogy and Petrology. - : Springer Science and Business Media LLC. - 0010-7999 .- 1432-0967. ; 165:3, s. 543-562
  • Journal article (peer-reviewed)abstract
    • We present microstructural and chemical analyses of chemically zoned and recrystallized plagioclase grains in variably strained samples of a naturally deformed anorthosite-leucogabbro, southern West Greenland. The recorded microstructures formed in the presence of fluids at mid-crustal conditions (620-640 A degrees C, 7.4-8.6 kbar). Recrystallized plagioclase grains (average grain size 342 mu m) with a random crystallographic orientation are volumetrically dominant in high-strain areas. They are characterized by asymmetric chemical zoning (An(80) cores and An(64) rims) that are directly associated with areas exhibiting high amphibole content and phase mixing. Analyses of zoning indicate anisotropic behaviour of bytownite plagioclase with a preferred replacement in the direction and along the (001) plane. In areas of high finite strain, recrystallization of plagioclase dominantly occurred by bulging recrystallization and is intimately linked to the chemical zoning. The lack of CPO as well as the developed asymmetric zoning can be explained by the activity of grain boundary sliding accommodated by dissolution and precipitation creep (DPC). In low-strain domains, grain size is on average larger and the rim distribution is not related to the inferred stress axes indicating chemically induced grain replacement instead of stress-related DPC. We suggest that during deformation, in high-strain areas, pre-existing phase mixture and stress induced DPC-caused grain rotations that allowed a deformation-enhanced heterogeneous fluid influx. This resulted in local plagioclase replacement through interface-coupled dissolution and precipitation and chemically induced grain boundary migration, accompanied by bulging recrystallization, along with neocrystallization of other phases. This study illustrates a strong interaction and feedback between physical and chemical processes where the amount of stress and fluids dictates the dominant active process. The interaction is a cause of deformation and external fluid infiltration with a result of strain localization and chemical re-equilibration at amphibolite facies conditions.
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