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  • 1
    Publication Date: 2019-11-04
    Description: A compendium of diffusion measurements and their Arrhenius equations for water, carbon dioxide, sulfur, fluorine, and chlorine in silicate melts similar in composition to natural igneous rocks is presented. Water diffusion in silicic melts is well studied and understood, however little data exists for melts of intermediate to basic compositions. The data demonstrate that both the water concentration and the anhydrous melt composition affect the diffusion coefficient of water. Carbon dioxide diffusion appears only weakly dependent, at most, on the volatilefree melt composition and no effect of carbon dioxide concentration has been observed, although few experiments have been performed. Based upon one study, the addition of water to rhyolitic melts increases carbon dioxide diffusion by orders of magnitude to values similar to that of 6 wt% water. Sulfur diffusion in intermediate to silicic melts depends upon the anhydrous melt composition and the water concentration. In water-bearing silicic melts sulfur diffuses 2 to 3 orders of magnitude slower than water. Chlorine diffusion is affected by both water concentration and anhydrous melt composition; its values are typically between those of water and sulfur. Information on fluorine diffusion is rare, but the volatile-free melt composition exerts a strong control on its diffusion. At the present time the diffusion of water, carbon dioxide, sulfur and chlorine can be estimated in silicic melts at magmatic temperatures. The diffusion of water and carbon dioxide in basic to intermediate melts is only known at a limited set of temperatures and compositions. The diffusion data for rhyolitic melts at 800°C together with a standard model for the enrichment of incompatible elements in front of growing crystals demonstrate that rapid crystal growth, greater than 10-10 ms-1, can significantly increase the volatile concentrations at the crystal-melt interface and that any of that melt trapped by the formation of melt inclusions may not be representative of the bulk melt. However, basaltic melt inclusions trapped at 1300°C are more likely to contain bulk melt concentrations of water and carbon dioxide.
    Description: Published
    Description: JCR Journal
    Description: open
    Keywords: diffusion ; silicate melts ; volatiles ; water ; carbon dioxide ; sulfur ; fluorine ; igneous processes ; chlorine ; melt inclusion ; 04. Solid Earth::04.08. Volcanology::04.08.01. Gases ; 04. Solid Earth::04.08. Volcanology::04.08.03. Magmas
    Repository Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Type: article
    Format: 1827621 bytes
    Format: application/pdf
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  • 2
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Noble-gas geochemistry is an important tool for understanding planetary processes from accretion to mantle dynamics and atmospheric formation. Central to much of the modelling of such processes is the crystal–melt partitioning of noble gases during mantle melting, magma ascent and ...
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 346 (1990), S. 459-462 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The photographs in Fig. 1 show selected areas of vertical sections through five different charges that have been rapidly quenched from 1,225 °C and 15 kbar. The majority of the experiments are in the system SiO2-Al2O3-CaO-Na2O-CO2 although minor constituents have been added in some runs. The ...
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  • 4
    Publication Date: 2015-06-13
    Description: We report the results of experiments on two natural marine sediments with different carbonate contents (calcareous clay: CO 2 = 6·1 wt %; marl: CO 2 = 16·2 wt %) at subduction-zone conditions (3 GPa, 750–1200°C). Water (7–15 wt %) was added to the starting materials to simulate the effects of external water addition from within the subducting slab. The onset of melting is at 760°C in water-rich experiments; melt becomes abundant by 800°C. In contrast, the onset of melting in published, water-poor experiments occurs at variable temperatures with the production of significant melt fractions being restricted to more than 900°C (phengite-out). The different solidus temperatures ( T solidus ) can be ascribed to variable fluid X H2O [H 2 O/(CO 2 + H 2 O)], which, in turn, depends on bulk K 2 O, H 2 O and CO 2 . Partial melts in equilibrium with residual garnet, carbonate, quartz/coesite, epidote, rutile, kyanite, phengite, and clinopyroxene are granitic in composition, with substantial dissolved volatiles. Supersolidus runs always contain both silicate melt and solute-rich fluid, indicating that experimental conditions lie below the second critical endpoint in the granite–H 2 O–CO 2 system. Carbonatite melt coexists with silicate melt and solute-rich fluid above 1100°C in the marl. The persistence of carbonate to high temperature, in equilibrium with CO 2 -rich hydrous melts, provides a mechanism to both supply CO 2 to arc magmas and recycle carbon into the deep Earth. The trace element compositions of the experimental glasses constrain the potential contribution of calcareous sediment to arc magmas. The presence of residual epidote and carbonate confers different trace element characteristics when compared with the trace element signal of Ca-poor marine sediments (e.g. pelagic clays). Notably, epidote retains Th and light rare earth elements, such that some melts derived from calcareous sediments have elevated Ba/Th and U/Th, and low La/Sm PUM , thereby resembling fluids conventionally ascribed to altered oceanic crust. Our results emphasize the importance of residual mineralogy, rather than source lithology, in controlling the trace element characteristics of slab-derived fluids.
    Print ISSN: 0022-3530
    Electronic ISSN: 1460-2415
    Topics: Geosciences
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  • 5
    Publication Date: 2013-10-02
    Description: This study investigates the potential use of confocal micro-Raman spectroscopy for the quantification of CO 2 in geologically relevant glass compositions. A calibration is developed using a wide range of both natural and synthetic glasses that have CO 2 dissolved as carbonate (CO 3 2– ) in the concentration range from 0.2 to 16 wt%. Spectra were acquired in the 200 and 1350 cm –1 frequency region that includes the 1 Raman active vibration for carbonate at 1062–1092 cm –1 and the intensity of this peak is compared to various other peaks representing the aluminosilicate glass structure. The most precise and accurate calibration is found when carbonate peaks are compared to aluminosilicate spectral features in the high-frequency region (HF: 700–1200 cm –1 ), which can be simulated with several Gaussian peaks, directly related to different structural species in the glass. In some samples the "dissolved" CO 3 2– appears to have two different Raman bands, one sharper than the other. This may be consistent with previous suggestions that CO 3 2– has several structural environments in the glass, and is not related to any precipitation of crystalline carbonate from the melt during quenching. The calibration derived using the HF peaks appears linear for both the full range of glass composition considered and the range of CO 2 concentrations, even when multiple carbonate peaks are involved. We propose the following, compositionally independent linear equation to quantify the CO 2 content in glass with micro-Raman spectroscopy \[ \hbox{ wt }\%\hspace{0.17em}{\hbox{ CO }}_{2}=15.17\times {\hbox{ CO }}_{3}/\hbox{ HF } \] where CO 3 /HF is the area ratio of the fitted 1 carbonate peak(s) at 1062–1092 cm –1 to the remaining area of the fitted aluminosilicate envelope from 700–1200 cm –1 . This is similar to the Raman calibration developed for water, but is complicated by the overlapping of these two fitted components. Using error propagation, we propose the calibration accuracy is better than ±0.4 wt% CO 2 for our data set. The 1 Raman peak position for carbonate is not constant and appears to be correlated with the density of the melt (or glass) in some way rather than the chemical composition.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 6
    Publication Date: 2016-06-03
    Description: We present major and trace element data on coexisting garnet and clinopyroxene from experiments carried out between 1.3 and 10 GPa and 970 and 1400 °C. We demonstrate that the lattice strain model, which was developed for applications to mineral-melt partitioning, can be adapted to garnet-clinopyroxene partitioning. Using new and published experimental data we develop a geothermometer for coexisting garnet and clinopyroxene using the concentration of rare earth elements (REE). The thermometer, which is based on an extension of the lattice strain model, exploits the tendency of minerals at elevated temperatures to be less discriminating against cations that are too large or too small for lattice sites. The extent of discrimination against misfit cations is also related to the apparent elasticity of the lattice site on which substitution occurs, in this case the greater stiffness of the dodecahedral X-site in garnet compared with the eightfold M2-site in clinopyroxene. We demonstrate that the ratio of REE in clinopyroxene to that in coexisting garnet is particularly sensitive to temperature. We present a method whereby knowledge of the major and REE chemistry of garnet and clinopyroxene can be used to solve for the equilibrium temperature. The method is applicable to any scenario in which the two minerals are in equilibrium, both above and below the solidus, and where the mole fraction of grossular in garnet is less than 0.4. Our method, which can be widely applied to both peridotitic and eclogitic paragenesis with particular potential for diamond exploration studies, has the advantage over commonly used Fe-Mg exchange thermometers in having a higher closure temperature because of slow interdiffusion of REE. The uncertainty in the calculated temperatures, based on the experimental data set, is less than ±80 °C.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
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  • 7
    Publication Date: 2015-05-20
    Description: Arc magmas erupted at the Earth’s surface are commonly more oxidized than those produced at mid-ocean ridges. Possible explanations for this high oxidation state are that the transfer of fluids during the subduction process results in direct oxidation of the sub-arc mantle wedge, or that oxidation is caused by the effect of later crustal processes, including protracted fractionation and degassing of volatile-rich magmas. This study sets out to investigate the effect of disequilibrium crustal processes that may involve coupled changes in H 2 O content and Fe oxidation state, by examining the degassing and hydration of sulphur-free rhyolites. We show that experimentally hydrated melts record strong increases in Fe 3+ /Fe with increasing H 2 O concentration as a result of changes in water activity. This is relevant for the passage of H 2 O-undersaturated melts from the deep crust towards shallow crustal storage regions, and raises the possibility that vertical variations in f O 2 might develop within arc crust. Conversely, degassing experiments produce an increase in Fe 3+ /Fe with decreasing H 2 O concentration. In this case the oxidation is explained by loss of H 2 as well as H 2 O into bubbles during decompression, consistent with thermodynamic modelling, and is relevant for magmas undergoing shallow degassing en route to the surface. We discuss these results in the context of the possible controls on f O 2 during the generation, storage and ascent of magmas in arc settings, in particular considering the timescales of equilibration relative to observation as this affects the quality of the petrological record of magmatic f O 2 .
    Print ISSN: 0022-3530
    Electronic ISSN: 1460-2415
    Topics: Geosciences
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  • 8
    Publication Date: 2011-07-24
    Description: We present new experiments, combined with a re-evaluation of published data, to characterize the topology of the silicate–carbonate two-liquid solvus in the five-component system SiO 2 –Na 2 O–Al 2 O 3 –CaO–CO 2 (SNAC + CO 2 ). Conjugate liquid compositions have been determined for a wide range of pressures (0·1–2·5 GPa) and temperatures (1225–1700°C) as well as variable degrees of CO 2 saturation. The expansion of the two-liquid field with increasing pressure and/or decreasing temperature, and the contraction of the two-liquid field for conditions where P CO2 〈 P total is accurately presented for the first time. The shape of the two-liquid solvus suggests that alkali-rich carbonatites can have a range of SiO 2 + Al 2 O 3 contents down to very low values (〈1 wt %), but that low-alkali or alkali-free immiscible carbonatites will always have SiO 2 + Al 2 O 3 contents greater than 10–15 wt %. The most commonly observed carbonatite rock compositions observed at the Earth’s surface all tend towards low contents of alkalis SiO 2 and Al 2 O 3 and would have fractionated silicate phases from the carbonatite parental melts, possibly associated with alkali loss to coexisting fluids. Our results also show that carbonate liquid exsolution can occur from a CO 2 -undersaturated ( P CO2 〈 P tot ) silicate melt. Although the expanded high-pressure miscibility gap appears favourable for producing natural silicate melt compositions, a low-pressure (〈1·0 GPa) magma chamber in the crust or perhaps in the shallow mantle below a rift provides the most likely environment for immiscibility to arise owing to the lower CO 2 demand of the silicate magma. Unusual textures in some experiments, suggestive of a deformable liquid state for the CaCO 3 phase, are conclusively shown to be characteristic of a non-quenchable, high-temperature polymorph of solid calcite. Similar calcite globules with this rounded appearance, which are also observed in some nephelinite lavas and mantle xenoliths, must be solid calcite and not immiscible liquids. This is consistent with the high SiO 2 + Al 2 O 3 requirement of low-alkali or alkali-free immiscible carbonate liquids.
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  • 9
    Publication Date: 2017-04-04
    Description: Many plutons preserve evidence of magma mixing between hydrous mafic magmas and resident felsic crystal-rich mushes. To investigate water transfer processes in such systems following thermal equilibration, we conducted 24 h experiments to establish the petrological evolution of a water-undersaturated (4 wt% H 2 O in the interstitial melt) quartz-bearing dacite crystal mush (0.5–0.8 in crystal fraction) intruded by a water-saturated (≥6 wt% H 2 O), initially crystal-free, andesite magma at 950 °C and 4 kbar (12 km depth). Our results show isothermal undercooling resulting from a change in liquidus temperatures of the interacting magmas due to their changing water content. Specifically, mafic samples dramatically crystallize during water escape into the felsic end-members and consequent increase in liquidus temperature. Conversely, the addition of water to the felsic mush reduces the liquidus temperature, leading to an increase in melt fraction. The experiments provide insights into how volatiles contribute to crystal mush rejuvenation (i.e., increase of melt fraction). However, H 2 O diffusion alone is not sufficient to promote melt extraction from short- and long-lived mushes in the Earth’s crust.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
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  • 10
    Publication Date: 1960-03-01
    Print ISSN: 0010-4620
    Electronic ISSN: 1460-2067
    Topics: Computer Science
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