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  • 1
    Publication Date: 2020-08-26
    Description: Nickel is a strongly compatible element in olivine, and thus fractional crystallization of olivine typically results in a concave-up trend on a Fo-Ni diagram. "Ni-enriched" olivine compositions are considered those that fall above such a crystallization trend. To explain Ni-enriched olivine crystals, we develop a set of theoretical and computational models to describe how primitive olivine phenocrysts from a parent (high-Mg, high-Ni) basalt re-equilibrate with an evolved (low-Mg, low-Ni) melt through diffusion. These models describe the progressive loss of Fo and Ni in olivine cores during protracted diffusion for various crystal shapes and different relative diffusivities for Ni and Fe-Mg. In the case when the diffusivity of Ni is lower than that for Fe-Mg interdiffusion, then olivine phenocrysts affected by protracted diffusion form a concave-down trend that contrasts with the concave-up crystallization trend. Models for different simple geometries show that the concavity of the diffusion trend does not depend on the size of the crystals and only weakly depends on their shape. We also find that the effect of diffusion anisotropy on trend concavity is in the same magnitude as the effect of crystal shape. Thus, both diffusion anisotropy and crystal shape do not significantly change the concave-down diffusion trend. Three-dimensional numerical diffusion models using a range of more complex, realistic olivine morphologies with anisotropy corroborate this conclusion. Thus, the curvature of the concave-down diffusion trend is mainly determined by the ratio of Ni and Fe-Mg diffusion coefficients. The initial and final points of the diffusion trend are in turn determined by the compositional contrast between mafic and more evolved melts that have mixed to cause disequilibrium between olivine cores and surrounding melt. We present several examples of measurements on olivine from arc basalts from Kamchatka, and several published olivine datasets from mafic magmas from non-subduction settings (lamproites and kimberlites) that are consistent with diffusion-controlled Fo-Ni behaviour. In each case the ratio of Ni and Fe-Mg diffusion coefficients is indicated to be 
    Print ISSN: 0022-3530
    Electronic ISSN: 1460-2415
    Topics: Geosciences
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  • 2
    Publication Date: 2020-06-17
    Description: Petrological and geochemical (major element, trace element, Sr–Nd isotope) data for recent (〈5 kyr old) basalts that sporadically erupt on the western flank of Piton de la Fournaise (PdF), one of the most active volcanoes on Earth, allow the tracking of magma transfer and evolution from mantle to crustal depths. In the western peripheral area of PdF we document the broadly synchronous eruptions of (1) primitive olivine and olivine–clinopyroxene transitional basalts with tholeiitic affinity 30 that are closely associated in space with (2) transitional olivine basalts with alkaline affinity, and (3) hybrid lavas, intermediate between the ‘alkaline’ and the ‘tholeiitic’ end-members. The composition of the latter overlaps with that of the lavas frequently erupted from the conduit system feeding the main summit cone. AlphaMELTS modelling, and fluid inclusion and clinopyroxene barometry, constrain the conditions of magma storage at 10–30 km, and the ascent of magma from the upper 35 mantle to the shallow crustal plumbing system. Variable degrees of mantle melting, together with minor source heterogeneity and contamination with cumulate-derived partial melts, contribute to the diversity of PdF magmas. However, all these processes do not represent the dominant factors that produce the large variability we found in major element composition. Indeed, the composition of basalts erupted from PdF peripheral centers is strongly controlled by polybaric olivine–clinopyr- 40 oxene fractionation at pressures higher than 3 kbar. Crystal textures and geochemical modelling suggest that fast magma ascent is critical to prevent clinopyroxene dissolution. Conversely, longlasting magma stagnation promotes pyroxene resorption and magma differentiation. ‘Central’ eruptions occurring close to the PdF summit cone emit variably more evolved melts, which result from olivine–clinopyroxene–plagioclase differentiation at intermediate–shallow pressure (〈3 kbar and in most cases 〈1 kbar). Deep and extensive magma mixing before injection into the crustal magma conduit system, located below the summit region, results in the apparent homogeneity of basalts erupted from the central area. As regards ‘peripheral’ eruptions, deep-seated stagnation of basaltic melts and differentiation at the mantle–crust transition zone (c. 4 kbar) produces a range of 5 magma compositions. We demonstrate that rapid magma ascent from deep-seated reservoirs can bypass the central plumbing system. The eruptions of these magmas both in the central area and on the densely populated flanks have major consequences in terms of volcanic hazard at PdF.
    Description: Published
    Description: 1717–1752
    Description: 2V. Struttura e sistema di alimentazione dei vulcani
    Description: JCR Journal
    Keywords: transitional basalts ; clinopyroxene crystallization and resorption ; mantle–crust underplating
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
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  • 3
    Publication Date: 2021-07-27
    Description: Three synthetic reference glasses were prepared by directly fusing and stirring 3.8 kg of high-purity oxide powders to provide reference materials for microanalytical work. These glasses have andesitic major compositions and are doped with fifty-four trace elements in nearly identical abundance (500, 50, 5 µg g−1) using oxide powders or element solutions, and are named ARM-1, 2 and 3, respectively. We further document that sector-field (SF) ICP-MS (Element 2 or Element XR) is capable of sweeping seventy-seven isotopes (from 7Li to 238U, a total of sixty-eight elements) in 1 s and, thus, is able to quantify up to sixty-eight elements by laser sampling. Micro- and bulk analyses indicate that the glasses are homogeneous with respect to major and trace elements. This paper provides preliminary data for the ARM glasses using a variety of analytical techniques (EPMA, XRF, ICP-OES, ICP-MS, LA-Q-ICP-MS and LA-SF-ICP-MS) performed in ten laboratories. Discrepancies in the data of V, Cr, Ni and Tl exist, mainly caused by analytical limitations. Preliminary reference and information values for fifty-six elements were calculated with uncertainties [2 relative standard error (RSE)] estimated in the range of 1–20%.
    Keywords: 551.9 ; glass reference materials ; microanalysis ; sector-field ICP-MS ; LA-ICP-MS ; multiple-element quantification
    Language: English
    Type: article
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