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  • 1
    Publication Date: 2020-08-12
    Description: The recent discovery in high-pressure experiments of compounds stable to 24–26 GPa with Fe4O5, Fe5O6, Fe7O9, and Fe9O11stoichiometry has raised questions about their existence within the Earth’s mantle. Incorporating both ferric and ferrous iron in their structures, these oxides if present within the Earth could also provide insight into diamond-forming processes at depth in the planet. Here we report the discovery of metallic particles, dominantly of FeNi (Fe0.71Ni0.24Cu0.05), in close spatial relation with nearly pure magnetite grains from a so-called superdeep diamond from the Earth’s mantle. The microstructural relation of magnetite within a ferropericlase (Mg0.60Fe0.40)O matrix suggests exsolution of the former. Taking into account the bulk chemistry reconstructed from the FeNi(Cu) alloy, we propose that it formed by decomposition of a complex metalMoxide (M4O5) with a stoichiometry of (Fe3+2.15Fe2+1.59Ni2+0.17Cu+0.04)Σ=3.95O5. We further suggest a possible link between this phase and variably oxidized ferropericlase that is commonly trapped in superdeep diamond. The observation of FeNi(Cu) metal in relation to magnetite exsolved from ferropericlase is interpreted as arising from a multistage process that starts from diamond encapsulation of ferropericlase followed by decompression and cooling under oxidized conditions, leading to the formation of complex oxides such as Fe4O5that subsequently decompose at shallowerP-Tconditions.
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 2
    Publication Date: 2011-05-01
    Print ISSN: 0034-6748
    Electronic ISSN: 1089-7623
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
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  • 3
    Publication Date: 2013-09-24
    Description: [1]  Lithosphere necking evolution determines the 3D architecture of crustal and upper mantle thinning and related basins, and the heat flow distribution in rifted regions. Despite a large number of studies, lithosphere necking evolution is still a matter of debate. We present result from lithospheric-scale analogue models designed for investigating the necking shape during extension and the vertical distribution of finite deformation in the mechanical lithosphere. In our experiments, lithosphere necking is asymmetric and, in particular, the 3D distribution of thinning is cylindrical in the crust and very heterogeneous in the mantle. Overall, the evolution of rifting and necking progresses from delocalized to localized deformation.
    Print ISSN: 0094-8276
    Electronic ISSN: 1944-8007
    Topics: Geosciences , Physics
    Published by Wiley on behalf of American Geophysical Union (AGU).
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  • 4
    Publication Date: 2011-07-01
    Description: Powder X-ray diffraction patterns between 90 and 935 K have been collected for nine plagioclase samples, with different compositions and degree of Al-Si order. The refined volumes have been modeled using the Wallace and Suzuki formulations based on the Mie-Gruneisen EOS. No significant difference has been found between the Suzuki and Wallace formulations, and between the Einstein and Debye approximations of lattice energy. A Wallace model with the first derivative of the bulk modulus constrained to the experimentally determined values leads to refined Gruneisen parameters between 0.49 and 0.41, without any definite trend between albite and anorthite; the Einstein temperature in intermediate plagioclase is {theta}E ~650 K, but it is lower in albite [{theta}E = 453(5) K]. A good fit with experimental heat capacity data for the An60Ab40 composition has been found using two Einstein-like oscillators with {theta}E1 = 230(3) K and {theta}E2 = 952(7) K, X{theta}E1 = 0.391(5). The change with temperature in An60Ab40 of the Gruneisen parameter is small at T 〉 150 K, with a slight decrease with temperature. Similar results could be obtained by independent refinement of an Einstein model with two oscillators to the volume data for the same composition [{theta}E1 = 205(30) K, {theta}E2 = 873(52) K, and X = 0.36(4)]. The components of the thermal strain tensor with temperature have been calculated and confirm that the greatest deformation is along the a* axis, i.e., along the extension direction of the crankshaft chains of the feldspar structure. Anomalous behavior of the strain tensor components in the a-c plane has been observed in albite and An27Ab73, and is related to an increase in the c unit-cell parameter with decreasing temperature.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 5
    Publication Date: 2011-07-01
    Description: In situ, high-pressure single-crystal X-ray diffraction experiments were performed on a feldspar with composition SrAl2Si2O8 (space group I2/c). The measurements were performed at 19 different pressures up to 7.9 GPa. The unit-cell parameters and the unit-cell volume show a strong discontinuity at 6.6 GPa indicating a first-order phase transition. The systematic absences clearly show that the transition occurs from I2/c to P21/c space group symmetry, as for the transition recently reported for a feldspar with composition Sr0.8Ca0.2Al2Si2O8. Our results suggest that the P21/c phase is softer than the I2/c one. Moreover, within the I2/c symmetry two pressure-volume trends are evident due to a volume softening above 4.2 GPa. The softening did not allow fitting the data to a single equation of state, and only the data up to 3.67 were fitted with a third-order Birch-Murnaghan equation of state. Based on our and previous experimental results we propose a possible composition-pressure stability field for the Sr-rich side along the CaAl2Si2O8-SrAl2Si2O8 join.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 6
    Publication Date: 2012-02-01
    Description: In order to evaluate the effects of Te-for-S substitution in the minerals of the argyrodite group, the crystal structure and chemical composition of a crystal of Te-rich canfieldite from the Lengenbach quarry, Binntal, Switzerland, was investigated. The unit-cell parameters are a 11.0003(6) Å and V 1331.1(1) Å3. The structure was solved and refined in the space group F4̅3m to R1 = 0.0308 for 194 independent reflections and 21 parameters. Quantitative analysis led to the chemical formula Ag8.05(Sn1.03Ge0.01)∑1.04(S3.95Te1.95Se0.01)∑5.91, ideally Ag8Sn(S,Te)6. The crystal structure of Te-rich canfieldite was found to be topologically identical to that of putzite, (Cu4.7Ag3.3)GeS6. Neglecting the short Ag-Ag contacts (due to disorder), the two Ag atoms in the structure can be considered as three-fold (Ag1) and four-fold (Ag2) coordinated. Tin adopts a regular tetrahedral coordination. The refinement of the site-occupancy factor indicates Te to be disordered over the three anion positions (i.e., X1, X2, and X3), with a preference for the X1 site.
    Print ISSN: 0008-4476
    Topics: Geosciences
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  • 7
    Publication Date: 2012-04-01
    Description: A single crystal of natural berthierite, FeSb2S4, was investigated at high pressure by means of X-ray diffraction using a diamond-anvil cell equipped with diamond backing plates. No phase transitions were indicated up to 8 GPa. The third-order Birch–Murnaghan equation of state, calculated using high-accuracy volume–pressure data up to 8.05 GPa, gave the following coefficients: V0 = 608.78(7) Å3, KT0 = 37.2(2) GPa and K′ = 7.0(1). The evolution of the structure as a function of pressure has been determined at seven different pressures up to 7.41 GPa. As in other structures with stereochemically active lone-electron pairs (LEP), the Sb3+ LEP, influencing long Sb–S bonds in berthierite, accommodate most of the compression. The Fe octahedron, which is the stiffest coordination polyhedron in berthierite, increases its distortion until approximately 5 GPa, but shows pronounced stiffening at higher pressures. This deformation at high pressures can be related to an increase in the Jahn–Teller effect on the Fe2+ coordination. The influence of Fe on compressional behavior makes a distinct difference between the compression of berthierite and that of stibnite, Sb2S3. The bridging Fe coordination between the structural rods in berthierite makes it stiffer. This, together with the direct structural relation to the analogous PbBi2S4, galenobismutite, makes the compressional characteristics of berthierite more akin to those of galenobismutite, despite quantitative differences in the stereochemical expression of the LEP of Sb3+ and Bi3+.
    Print ISSN: 0008-4476
    Topics: Geosciences
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  • 8
    Publication Date: 2011-11-01
    Description: Experimental data demonstrates that the resorption morphology of diamond greatly depends on the composition of the reacting fluid and can be used to constrain the composition of mantle fluids in diamond source areas and magmatic fluid in kimberlite magma. This requires a model that describes how different fluids interact with the diamond surface. This study uses atomic force microscopy (AFM) to quantitatively characterize the crystallographic orientation of micro-faces that form individual etch pits on diamond surfaces produced naturally in a kimberlite magma and experimentally in H2O-rich and CO2-rich fluids at 1150, 1250, and 1350 {degrees}C and 1 GPa. Dissolution features were examined on {111} diamond faces with the AFM scan areas ranging from 30 x 30 to 1 x 1 m. The study shows that the extremely different resorption features developed on diamond surface during dissolution in H2O- and CO2-rich fluids, are formed by the same set of micro-faces with angles ~7, 11, 16, and 22{degrees}, corresponding to the {433}, {322}, {221}, and {321} faces, respectively. This suggests that diamond has similar dissolution rates in the same directions of the diamond lattice in both H2O- and CO2-rich fluid but that the mechanism of material removal is different. Reaction with H2O-rich fluid develops regular features due to layer-by-layer carbon removal. In CO2-rich fluid, deep etch pits with irregular walls form when dissolution is focused around the outcropping dislocations. The size and shape of the etch pits and their association with the outcropping dislocations depend on temperature and could be used to constrain the crystallization conditions of kimberlite magma. Natural kimberlite-induced resorption features indicate high H2O:CO2 ratios in kimberlitic fluid.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 9
    Publication Date: 2011-02-01
    Description: The volume and unit-cell parameters of analbite (i.e., NaAlSi3O8 with complete Al,Si disorder) have been determined by single-crystal X-ray diffraction to a maximum pressure of ~8.71 GPa. The volume variation with pressure is described by a fourth-order Birch-Murnaghan equation of state with K0T = 50.3(5) GPa, K0' = 8.9(5), and K0'' = -2.4(3) GPa-1. The value of the room-pressure bulk modulus is ~4% lower than that of low albite, and the onset of volume softening in analbite is at ~6.7 GPa, some 1.7 GPa higher than the onset in albite. The anisotropy of compression of analbite is less than that in albite. Single-crystal structure determinations of analbite to ~9.4 GPa show that there is no significant detectable compression of the T-O bonds within the structure, and the compression of the framework of tetrahedra is therefore accommodated by changes in the T-O-T angles, which result in significant compression of the "crankshaft chains" within the framework. No significant shear of the tetrahedral rings of analbite was detected, in contrast to the structural compression of albite. Overall, the structural changes that occur in analbite from 0.0001 to 9.4 GPa resemble those seen in ordered albite over the pressure range 0.0001-4 GPa. Therefore analbite shows a significantly greater structural rigidity than low albite up to pressures of 9.4 GPa.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 10
    Publication Date: 2011-03-01
    Description: The Bader's topological analysis of the electron density obtained via ab initio quantum mechanical simulation at Hartree-Fock and DFT level has been performed for experimentally in situ heated structures of enstatite-protoenstatite MgSiO3. The measurements have been performed in the temperature range 1200-1400 K. The work was aimed at characterizing both the evolution of the electron arrangement in the crystal and that of the crystal-structure at the enstatite-protoenstatite phase transition in terms of topology of the electron density, with particular care about the Mg-O and the O-O bonds. The observed breaking of some chemical bonds with increasing temperature and/or due to the phase transformation have been explained, for the first time, in the light of a topological mechanism based on the Catastrophe Theory applied to the framework of the Bader's theory.
    Print ISSN: 0935-1221
    Electronic ISSN: 1617-4011
    Topics: Geosciences
    Published by Schweizerbart
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