63 research outputs found

    Melting of Amphibole-bearing Wehrlites: an Experimental Study on the Origin of Ultra-calcic Nepheline-normative Melts

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    Olivine + clinopyroxene ± amphibole cumulates have been widely documented in island arc settings and may constitute a significant portion of the lowermost arc crust. Because of the low melting temperature of amphibole (∼1100°C), such cumulates could melt during intrusion of primary mantle magmas. We have experimentally (piston-cylinder, 0·5-1·0 GPa, 1200-1350°C, Pt-graphite capsules) investigated the melting behaviour of a model amphibole-olivine-clinopyroxene rock, to assess the possible role of such cumulates in island arc magma genesis. Initial melts are controlled by pargasitic amphibole breakdown, are strongly nepheline-normative and are Al2O3-rich. With increasing melt fraction (T > 1190°C at 1·0 GPa), the melts become ultra-calcic while remaining strongly nepheline-normative, and are saturated with olivine and clinopyroxene. The experimental melts have strong compositional similarities to natural nepheline-normative ultra-calcic melt inclusions and lavas exclusively found in arc settings. The experimentally derived phase relations show that such natural melt compositions originate by melting according to the reaction amphibole + clinopyroxene = melt + olivine in the arc crust. Pargasitic amphibole is the key phase in this process, as it lowers melting temperatures and imposes the nepheline-normative signature. Ultra-calcic nepheline-normative melt inclusions are tracers of magma-rock interaction (assimilative recycling) in the arc crus

    Understanding the History of Rocks by the Use of Microbeam Analysis Techniques

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    Ultrafast syn-eruptive degassing and ascent trigger high-energy basic eruptions

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    Lithium gradients in plagioclase are capable of recording extremely short-lived processes associated with gas loss from magmas prior to extrusion at the surface. We present SIMS profiles of the 7Li/30Si ion ratio in plagioclase crystals from products of the paroxysmal sequence that occurred in the period 2011-2013 at Mt. Etna (Italy) in an attempt to constrain the final ascent and degassing processes leading to these powerful eruptions involving basic magma. The observed Li concentrations reflect cycles of Li addition to the melt through gas flushing, and a syn-eruptive stage of magma degassing driven by decompression that finally produce significant Li depletion from the melt. Modeling the decreases in Li concentration in plagioclase by diffusion allowed determination of magma ascent timescales that are on the order of minutes or less. Knowledge of the storage depth beneath the volcano has led to the quantification of a mean magma ascent velocity of ~43 m/s for paroxysmal eruptions at Etna. The importance of these results relies on the application of methods, recently used exclusively for closed-system volcanoes producing violent eruptions, to open-conduit systems that have generally quiet eruptive periods of activity sometimes interrupted by sudden re-awakening and the production of anomalously energetic eruptions.Publishedid 1475V. Processi eruttivi e post-eruttiviJCR Journa

    The crystal structure of piergorite-(Ce), Ca8Ce2(Al0.5 Fe3+0.5) Σ 1(□,Li,Be)2Si6B8O36(OH,F)2: A new borosilicate from Vetralla, Italy, with a modified hellandite-type chain

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    Piergorite-(Ce) is a new mineral found at Tre Croci, Vetralla, Italy with simplified formula Ca8Ce2 (Al0.5Fe0.53+)∑1(□,Li,Be)2Si6B8O36(OH,F)2. It occurs as strong intergrowths of small crystals, colorless to pale yellow, associated with sanidine, mica, magnetite, rutile, titanite, and other Th-U-REE bearing minerals, in miarolitic cavities of a syenitic ejectum. Piergorite-(Ce) is biaxial negative, nα = 1.717 (1), nβ = 1.728 (1), and nγ = 1.735 (1), 2Vmeas = 68(2)°, X = b, and Z ^ c = 7(1)°. Crystals show tabular habit and a very good {010} cleavage; twinning along the (30-1) plane produces “L” forms. The three strongest lines in the simulated powder diffraction pattern (dobs, I, hkl) are: 2.65 Å, 100.0, (213, -413); 1.91 Å, 48.3, (223, -423, 821); 2.90 Å, 44.9, (-603, -612). The structure was solved by Patterson synthesis from X-ray diffraction data [monoclinic, space group P2/a, a = 28.097(3) Å, b = 4.777(1) Å, c = 10.236(2) Å, β = 96.81(1)°, V = 1364.2(7) Å3, Z = 2] and was refined to a final Robs = 0.059 for 6480 Fo with Io > 3σ (Io). The structure shows similarities with the hellandite group because Si and B tetrahedra form chains along c. Hellandite structure is characterized by a single chain of five-membered rings, whereas piergorite-(Ce) shows a double chain of five-membered rings interconnected by a single octahedral site to form a three-dimensional framework containing five independent eightfold-coordinated M sites and a partly occupied T-cavity
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