Reaction induced nucleation and growth v. grain coarsening in contact metamorphic, impure carbonates

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Reaction induced nucleation and growth v. grain coarsening in contact metamorphic, impure carbonates. / Berger, Alfons; Brodhag, Sabine; Herwegh, Marco.

I: Journal of Metamorphic Geology, Bind 28, Nr. 8, 2010, s. 809-824.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Berger, A, Brodhag, S & Herwegh, M 2010, 'Reaction induced nucleation and growth v. grain coarsening in contact metamorphic, impure carbonates', Journal of Metamorphic Geology, bind 28, nr. 8, s. 809-824. https://doi.org/10.1111/j.1525-1314.2010.00894.x

APA

Berger, A., Brodhag, S., & Herwegh, M. (2010). Reaction induced nucleation and growth v. grain coarsening in contact metamorphic, impure carbonates. Journal of Metamorphic Geology, 28(8), 809-824. https://doi.org/10.1111/j.1525-1314.2010.00894.x

Vancouver

Berger A, Brodhag S, Herwegh M. Reaction induced nucleation and growth v. grain coarsening in contact metamorphic, impure carbonates. Journal of Metamorphic Geology. 2010;28(8):809-824. https://doi.org/10.1111/j.1525-1314.2010.00894.x

Author

Berger, Alfons ; Brodhag, Sabine ; Herwegh, Marco. / Reaction induced nucleation and growth v. grain coarsening in contact metamorphic, impure carbonates. I: Journal of Metamorphic Geology. 2010 ; Bind 28, Nr. 8. s. 809-824.

Bibtex

@article{15c8956025cb11df8ed1000ea68e967b,
title = "Reaction induced nucleation and growth v. grain coarsening in contact metamorphic, impure carbonates",
abstract = "The understanding of the evolution of microstructures in a metamorphic rock requires insights into the nucleation and growth history of individual grains, as well as the coarsening processes of the entire aggregate. These two processes are compared in impure carbonates from the contact metamorphic aureole of the Adamello pluton (N-Italy). As a function of increasing distance from the pluton contact, the investigated samples have peak metamorphic temperatures ranging from the stability field of diopside/tremolite down to diagenetic conditions. All samples consist of calcite as the dominant matrix phase, but additionally contain variable amounts of other minerals, the so-called second phases. These second phases are mostly silicate minerals and can be described in a KCMASHC system (K2O, CaO, MgO, Al2O3, SiO2, H2O, CO2), but with variable K/Mg ratios. The modelled and observed metamorphic evolution of these samples are combined with the quantification of the microstructures, i.e. mean grain sizes and crystal size distributions. Growth of the matrix phase and second phases strongly depends on each other owing to coupled grain coarsening. The matrix phase is controlled by the interparticle distances between the second phases, while the second phases need the matrix grain boundary network for mass transfer processes during both grain coarsening and mineral reactions. Interestingly, similar final mean grain sizes of primary second phase and second phases newly formed by nucleation are observed, although the latter formed later but at higher temperatures. Moreover, different kinetic processes, attributed to different driving forces for growth of the newly nucleated grains in comparison with coarsening processes of the pre-existing phases, must have been involved. Chemically induced driving forces of grain growth during reactions are orders of magnitudes larger compared to surface energy, allowing new reaction products subjected to fast growth rates to attain similar grain sizes as phases which underwent long-term grain coarsening. In contrast, observed variations in grain size of the same mineral in samples with a similar T–t history indicate that transport properties depend not only on the growth and coarsening kinetics of the second phases but also on the microstructure of the dominant matrix phase during coupled grain coarsening. Resulting microstructural phenomena such as overgrowth and therefore preservation of former stable minerals by the matrix phase may provide new constraints on the temporal variation of microstructures and provide a unique source for the interpretation of the evolution of metamorphic microstructures. ",
author = "Alfons Berger and Sabine Brodhag and Marco Herwegh",
year = "2010",
doi = "10.1111/j.1525-1314.2010.00894.x",
language = "English",
volume = "28",
pages = "809--824",
journal = "Journal of Metamorphic Geology",
issn = "0263-4929",
publisher = "Wiley-Blackwell",
number = "8",

}

RIS

TY - JOUR

T1 - Reaction induced nucleation and growth v. grain coarsening in contact metamorphic, impure carbonates

AU - Berger, Alfons

AU - Brodhag, Sabine

AU - Herwegh, Marco

PY - 2010

Y1 - 2010

N2 - The understanding of the evolution of microstructures in a metamorphic rock requires insights into the nucleation and growth history of individual grains, as well as the coarsening processes of the entire aggregate. These two processes are compared in impure carbonates from the contact metamorphic aureole of the Adamello pluton (N-Italy). As a function of increasing distance from the pluton contact, the investigated samples have peak metamorphic temperatures ranging from the stability field of diopside/tremolite down to diagenetic conditions. All samples consist of calcite as the dominant matrix phase, but additionally contain variable amounts of other minerals, the so-called second phases. These second phases are mostly silicate minerals and can be described in a KCMASHC system (K2O, CaO, MgO, Al2O3, SiO2, H2O, CO2), but with variable K/Mg ratios. The modelled and observed metamorphic evolution of these samples are combined with the quantification of the microstructures, i.e. mean grain sizes and crystal size distributions. Growth of the matrix phase and second phases strongly depends on each other owing to coupled grain coarsening. The matrix phase is controlled by the interparticle distances between the second phases, while the second phases need the matrix grain boundary network for mass transfer processes during both grain coarsening and mineral reactions. Interestingly, similar final mean grain sizes of primary second phase and second phases newly formed by nucleation are observed, although the latter formed later but at higher temperatures. Moreover, different kinetic processes, attributed to different driving forces for growth of the newly nucleated grains in comparison with coarsening processes of the pre-existing phases, must have been involved. Chemically induced driving forces of grain growth during reactions are orders of magnitudes larger compared to surface energy, allowing new reaction products subjected to fast growth rates to attain similar grain sizes as phases which underwent long-term grain coarsening. In contrast, observed variations in grain size of the same mineral in samples with a similar T–t history indicate that transport properties depend not only on the growth and coarsening kinetics of the second phases but also on the microstructure of the dominant matrix phase during coupled grain coarsening. Resulting microstructural phenomena such as overgrowth and therefore preservation of former stable minerals by the matrix phase may provide new constraints on the temporal variation of microstructures and provide a unique source for the interpretation of the evolution of metamorphic microstructures.

AB - The understanding of the evolution of microstructures in a metamorphic rock requires insights into the nucleation and growth history of individual grains, as well as the coarsening processes of the entire aggregate. These two processes are compared in impure carbonates from the contact metamorphic aureole of the Adamello pluton (N-Italy). As a function of increasing distance from the pluton contact, the investigated samples have peak metamorphic temperatures ranging from the stability field of diopside/tremolite down to diagenetic conditions. All samples consist of calcite as the dominant matrix phase, but additionally contain variable amounts of other minerals, the so-called second phases. These second phases are mostly silicate minerals and can be described in a KCMASHC system (K2O, CaO, MgO, Al2O3, SiO2, H2O, CO2), but with variable K/Mg ratios. The modelled and observed metamorphic evolution of these samples are combined with the quantification of the microstructures, i.e. mean grain sizes and crystal size distributions. Growth of the matrix phase and second phases strongly depends on each other owing to coupled grain coarsening. The matrix phase is controlled by the interparticle distances between the second phases, while the second phases need the matrix grain boundary network for mass transfer processes during both grain coarsening and mineral reactions. Interestingly, similar final mean grain sizes of primary second phase and second phases newly formed by nucleation are observed, although the latter formed later but at higher temperatures. Moreover, different kinetic processes, attributed to different driving forces for growth of the newly nucleated grains in comparison with coarsening processes of the pre-existing phases, must have been involved. Chemically induced driving forces of grain growth during reactions are orders of magnitudes larger compared to surface energy, allowing new reaction products subjected to fast growth rates to attain similar grain sizes as phases which underwent long-term grain coarsening. In contrast, observed variations in grain size of the same mineral in samples with a similar T–t history indicate that transport properties depend not only on the growth and coarsening kinetics of the second phases but also on the microstructure of the dominant matrix phase during coupled grain coarsening. Resulting microstructural phenomena such as overgrowth and therefore preservation of former stable minerals by the matrix phase may provide new constraints on the temporal variation of microstructures and provide a unique source for the interpretation of the evolution of metamorphic microstructures.

U2 - 10.1111/j.1525-1314.2010.00894.x

DO - 10.1111/j.1525-1314.2010.00894.x

M3 - Journal article

VL - 28

SP - 809

EP - 824

JO - Journal of Metamorphic Geology

JF - Journal of Metamorphic Geology

SN - 0263-4929

IS - 8

ER -

ID: 18336371