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  • Mineralogical Society of America  (13)
  • Blackwell Publishing Ltd  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of metamorphic geology 8 (1990), S. 0 
    ISSN: 1525-1314
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences
    Notes: Olivine-plagioclase coronas in metagabbros from the Adirondack Mountains, New York (USA) are spatially well-organized reaction textures consisting most commonly of sequential layers of orthopyroxene, clinopyroxene, plagioclase, and garnet; the textures are characteristic of diffusion-controlled reaction kinetics. Although similar coronas have been interpreted by previous workers in terms of an isochemical steady-state diffusion model, petrographical relations and material-balance calculations establish that coronas in the Adirondack metagabbros cannot be treated as isochemical and do not form in a single-stage steady-state process; instead they evolve through time in a complex open-system reaction.In this study, the isochemical diffusion model is modified to account for elemental fluxes across the outer boundaries of the coronal reaction band, thereby approximating the open-system behaviour of the coronas. The sequence and relative proportions of product minerals calculated by the open-system steady-state model correspond closely to those observed in coronas of the Adirondacks, over a wide range of values for the relative diffusivities of chemical components involved in the reaction, regardless of the particular method used to determine material balance in the reaction texture.Despite this correspondence, petrographical evidence for successive replacement of coronal product layers reveals that the Adirondack coronas evolved through one or more transient states, rather than forming in a single-stage steady-state process. There is no evidence that the successive replacement of coronal product layers resulted from changes in pressure or temperature, but there is petrographical evidence that these changes resulted from modification of the composition of reactant plagioclase as the corona-forming reaction proceeded. This is confirmed by the fact that the evolution of the coronas over time can be replicated with the open-system diffusion model by simulating the effect of the gradual exhaustion of plagioclase as a source of the Ca and Si components required for reaction. These simulations suggest that successive stages in the evolution of the coronas are characterized by these product sequences: (i) orthopyroxene-clinopyroxene-plagioclase-garnet; (ii) orthopyroxene-clinopyroxene-garnet; and (iii) orthopyroxene-garnet. All of these stages, and the transitions between them, are observed petrographically. Coronas in Adirondack metagabbros appear, therefore, to have originated in a complex, open-system, diffusion-controlled reaction in which the product assemblages changed as the reaction progressed.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2015-08-15
    Description: The equilibrium model of prograde metamorphism, in which rocks are regarded as departing only negligibly from equilibrium states as they recrystallize, has generated a wealth of petrologic insights. But mounting evidence from diverse approaches and observations over a range of scales has revealed that kinetic impediments to reaction may prevent metamorphic rocks from attaining rock-wide chemical equilibrium along their prograde crystallization paths. To illustrate the resulting potential for inaccurate interpretation if kinetic factors are disregarded, we briefly review several case studies, including: out-of-sequence, metastable, and displaced isograds in contact aureoles; paragenetic sequences documenting overstepped, disequilibrium reaction paths; patterns of compositional zoning in garnet demonstrating partial chemical equilibrium; petrologic incongruities between observation and thermodynamic prediction; and inhibited reaction progress revealed by petrologically constrained numerical simulations of garnet crystallization. While the equilibrium model provides an indispensable framework for the study of metamorphic systems, these examples emphasize that all reactions require departures from rock-wide equilibrium, so all rocks must traverse kinetically sensitive reaction paths during recrystallization. Mindfulness of the potential significance of kinetic influences opens new avenues for petrologic investigation, thereby enhancing both analysis and interpretation.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 3
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    Unknown
    Mineralogical Society of America
    Publication Date: 2012-10-01
    Description: Numerical simulation of the evolution of stranded diffusion profiles in partially resorbed garnet crystals from the aureole of the Makhavinekh Lake Pluton, Labrador, yields quantitative determinations of rates of diffusion of Y, rare earth elements (REEs), and Cr at ~700–900 °C, 0.53 GPa. Diffusion coefficients for these trivalent cations are 0.5–1.5 log 10 units smaller than those for major divalent cations measured in the same crystals, but diffusivities for trivalent cations are all equal to one another to within ±0.25 log 10 unit. Integration of these new data with previously published results resolves some prior inconsistencies, and defines the dependence of diffusivities for Y, the REEs, and Cr on temperature, pressure, and oxygen fugacity, while accounting for minor effects of ionic radius and host-crystal composition. Nd, Sm, and Eu—elements that are strongly depleted in rims of relict garnet crystals due to preferential partitioning out of garnet during resorption—evolve small but distinct maxima from initially nearly flat profiles; this "uphill diffusion" results from cross-coupling with Y and the other REEs, which are strongly concentrated in relict garnet rims by resorption. The weak dependence of diffusivity on ionic radius and host-crystal composition, the near-equivalence of diffusivities of Y+REEs with that of Cr, and the strong positive cross-coupling among Y+REEs are all explained by a diffusion mechanism that links the mobility of VIII Y+REEs with that of VI Al; this is likely a consequence of the dominance of the menzerite-(Y) component as a means of incorporating Y+REEs in the garnet structure. However, the variety of possible substitution mechanisms that may enable Y+REE incorporation into garnet, and the degree to which each may be favored in different regimes of temperature, pressure, and oxygen fugacity, imply a potential for great complexity, as the net diffusional flux may result from the superposed effect of multiple diffusion mechanisms, each with different kinetics.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 4
    Publication Date: 2014-10-02
    Description: The ubiquity of quartz in continental crust, and the involvement of SiO 2 in multiple metamorphic processes such as reactions, fluid flux, and solution-transfer processes, makes quartz an obvious choice for reconstructing prograde metamorphic conditions in various rock types. Recent studies have shown the usefulness of analyzing Ti distribution in quartz to constrain pressure-temperature-(relative) time-deformation ( P-T-t-D ) in metamorphosed tectonites. New high-precision single-crystal X-ray diffraction volume constraints on Ti-doped and chemically pure quartz provide further evidence for substitution of Ti 4+ for Si 4+ in the tetrahedral site in quartz, with resultant lattice strain on the structure. Recent applications of the Ti-in-quartz thermobarometer to dynamically recrystallized quartz have identified recrystallized subgrains that contain lower Ti concentrations ([Ti]) than their host porphyroclasts. In addition, [Ti] are lower than expected for the temperatures of recrystallization. Atomistic simulations that estimate energetic perturbations resulting from Ti incorporation into the quartz lattice indicate that significant increases in strain energy occur only at very high [Ti]; the strain-energy increase is negligible for [Ti] typical of quartz grown under mid-crustal conditions. This suggests that lattice strain rarely provides an appreciable driving force for Ti loss from quartz; instead, it appears that subgrain boundaries and dislocation arrays migrating through recrystallizing quartz crystals can promote localized re-equilibration, thermodynamically regulated by the composition of the intergranular medium (typically undersaturated in Ti). It therefore appears that analyses from dynamically recrystallized quartz cannot be meaningfully interpreted until methods are developed that can account quantitatively for the reduction of Ti resulting from crystal plastic flow.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 5
    Publication Date: 2014-08-13
    Description: Numerical simulation of stranded diffusion profiles in partially resorbed garnet crystals from the aureole of the Makhavinekh Lake Pluton (Labrador, Canada) yields quantitative rates of intracrystalline diffusion for Li in garnet. Diffusion coefficients for Li at 700–900 °C and 0.53 GPa are 0.5–1.5 log 10 units lower than those for divalent cations in the same samples, and match those for Y and Yb. This correspondence likely stems from coupled substitution of Li and Y (or REE) ions in the garnet structure: the requirement of local electroneutrality limits Li mobility to be no faster than that of Y+REEs. Because of this coupling, Li zoning in garnet is retained to comparatively high temperatures, making garnet a valuable monitor of the behavior of Li in deep crustal systems.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
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  • 6
    Publication Date: 2014-05-16
    Description: Yttrium and the rare-earth elements (Y+REEs) are incorporated into aluminosilicate garnet as trivalent ions replacing divalent Mg, Fe, Mn, or Ca ("M 2+ ") in dodecahedral sites, which requires some form of coupled substitution to maintain electroneutrality. We compare the energetic costs of competing coupled-substitution schemes, using lattice dynamics calculations to assess defect energies and exchange energies for each scheme. Substitutions with relatively low energetic costs introduce menzerite-like components via the exchange vector [YM –1 ·(Mg,Fe)Al –1 ], or alkali components via the exchange vector [Y(Na,Li)M –2 ]. Substitutions with substantially higher energetic costs introduce a vacancy component via the exchange vector [Y 2 M –3 ], or the yttrogarnet (YAG) component via the exchange vector [YM –1 ·AlSi –1 ], or a component with octahedral Li via the exchange vector [Y 2 M –2 ·LiAl –1 ]. Energetic costs decrease significantly as the host-garnet unit-cell dimension expands, decrease very modestly as temperature rises or pressure falls, and decrease substantially with the contraction in ionic radius across the lanthanide series. These results, combined with critical re-examination of arguments cited in favor of each substitution scheme in natural occurrences, suggest that Y+REE incorporation in natural garnet is dominated by coupled substitutions that introduce menzerite and alkali components, that the YAG substitution plays only a subsidiary role, and that the other schemes are likely to be of very minor importance.
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    Electronic ISSN: 1945-3027
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  • 7
    Publication Date: 2013-12-27
    Description: Garnet bears witness to the importance of kinetics during metamorphism in its microstructural features, compositional zoning, and diffusional response to thermal events. Porphyroblastic textures carry quantitative signals of protracted nucleation and sluggish intergranular diffusion, key impediments to reaction progress that may result in crystallization under conditions well removed from equilibrium. Growth zoning in garnet reveals partial chemical equilibration with matrix minerals: intergranular transport keeps pace with garnet growth for some elements but not for others, leading to variable degrees and length scales of chemical equilibration. Partial relaxation of compositional zoning by intracrystalline diffusion is a sensitive and quantitative indicator of thermal history, constraining rates and timescales of peak metamorphic heating, processes of burial and exhumation, and retrogression on cooling.
    Print ISSN: 1811-5209
    Electronic ISSN: 1811-5217
    Topics: Geosciences
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  • 8
    Publication Date: 2013-12-01
    Print ISSN: 1811-5209
    Electronic ISSN: 1811-5217
    Topics: Geosciences
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  • 9
    Publication Date: 2012-09-24
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 10
    Publication Date: 2014-10-01
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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