Phase Equilibria Analysis for Metacarbonate With Applications to Zoned Calc‐Silicate Aureoles

ABSTRACT Carbonate rocks react with infiltrating hydrothermal fluids to produce zoned calcsilicate assemblages in contact aureoles. Petrogenetic grids provide valuable insights into phase relations, metamorphic temperature ( T ) and the fluid composition ( X ) of the metacarbonate systems, as well as semi‐quantification of the prograde decarbonation at convergent boundaries. In this study, we constructed T ‐ X CO2 (composition of H 2 O–CO 2 binary fluid) grids in the system CFMASHc (CaO–FeO–MgO–Al 2 O 3 –SiO 2 –H 2 O–CO 2 ), supplemented with Fe 2 O 3 or TiO 2 , and its subsystems (CMASHc, CMSHc, CFSHc and CASHc). The grids were constructed to encompass upper crustal conditions, with temperatures ranging from 300°C to 1000°C at 2 kbar and 4 kbar, and X CO2 from 0 to 0.8 (0 = pure water). We adopted internally consistent thermodynamic datasets and compatible activity–composition models for solid solutions. The grids illustrate the index minerals and field gradients observed in classical aureoles. Typical calcsilicate assemblages in these contact aureoles appear along a heating trajectory at a relatively low X CO2 , in the sequence of talc, tremolite, diopside (±olivine), garnet and wollastonite. The grids in the CASHc, CMSHc and CMASHc subsystems are sufficient to cover important reactions that lead to the formation and decomposition of these minerals. The grids with an additional TiO 2 component help interpret phase relations involving rutile, titanite and ilmenite. In addition, we note that phase relations calculated with endmember carbonates are practically similar to those calculated for a complete ternary solid‐solution model at low‐to‐mid temperatures (< 600 °C). In this study, we recalculated reactions in subsystem grids from previous studies across various P ‐ T ‐ X CO2 conditions within a consistent framework. These results are contextualized with natural assemblages and applied to constrain the field gradient of a representative contact aureole. By incorporating additional components, the grids accommodate a broader range of assemblages observed in metacarbonate rocks. Together, these expanded grids provide a robust framework for future studies of contact metamorphism in metacarbonate systems. The calculated phase equilibria were specifically applied to a contact aureole in southern Tibet, with temperature estimations derived from the phase equilibria aligning closely with a conduction model based on the timescales from diffusion speedometry.

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Publication Details

Journal
Journal of Metamorphic Geology
Published
2025-03-19
DOI
https://doi.org/10.1111/jmg.12814
Citations
1
Primary Topic
Geological and Geochemical Analysis
Type
article
Field-Weighted Citation Impact
1.87

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article

Phase Equilibria Analysis for Metacarbonate With Applications to Zoned Calc‐Silicate Aureoles

Xu Chu, Zhenhao Zhou
1 citations
Journal of Metamorphic Geology
Geological and Geochemical Analysis
1.87
article

Phase Equilibria Analysis for Metacarbonate With Applications to Zoned Calc‐Silicate Aureoles

Xu Chu, Zhenhao Zhou
article en
1 citations

Abstract

ABSTRACT Carbonate rocks react with infiltrating hydrothermal fluids to produce zoned calcsilicate assemblages in contact aureoles. Petrogenetic grids provide valuable insights into phase relations, metamorphic temperature ( T ) and the fluid composition ( X ) of the metacarbonate systems, as well as semi‐quantification of the prograde decarbonation at convergent boundaries. In this study, we constructed T ‐ X CO2 (composition of H 2 O–CO 2 binary fluid) grids in the system CFMASHc (CaO–FeO–MgO–Al 2 O 3 –SiO 2 –H 2 O–CO 2 ), supplemented with Fe 2 O 3 or TiO 2 , and its subsystems (CMASHc, CMSHc, CFSHc and CASHc). The grids were constructed to encompass upper crustal conditions, with temperatures ranging from 300°C to 1000°C at 2 kbar and 4 kbar, and X CO2 from 0 to 0.8 (0 = pure water). We adopted internally consistent thermodynamic datasets and compatible activity–composition models for solid solutions. The grids illustrate the index minerals and field gradients observed in classical aureoles. Typical calcsilicate assemblages in these contact aureoles appear along a heating trajectory at a relatively low X CO2 , in the sequence of talc, tremolite, diopside (±olivine), garnet and wollastonite. The grids in the CASHc, CMSHc and CMASHc subsystems are sufficient to cover important reactions that lead to the formation and decomposition of these minerals. The grids with an additional TiO 2 component help interpret phase relations involving rutile, titanite and ilmenite. In addition, we note that phase relations calculated with endmember carbonates are practically similar to those calculated for a complete ternary solid‐solution model at low‐to‐mid temperatures (< 600 °C). In this study, we recalculated reactions in subsystem grids from previous studies across various P ‐ T ‐ X CO2 conditions within a consistent framework. These results are contextualized with natural assemblages and applied to constrain the field gradient of a representative contact aureole. By incorporating additional components, the grids accommodate a broader range of assemblages observed in metacarbonate rocks. Together, these expanded grids provide a robust framework for future studies of contact metamorphism in metacarbonate systems. The calculated phase equilibria were specifically applied to a contact aureole in southern Tibet, with temperature estimations derived from the phase equilibria aligning closely with a conduction model based on the timescales from diffusion speedometry.

Journal of Metamorphic GeologyVol. 43(5)
Florida State University (US), University of Toronto (CA)
National Natural Science Foundation of China, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 20%
Geological and Geochemical Analysis
1.87
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