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Orogenic peridotites in the crystalline basement of the northwestern Bohemian Massif contain multiphase solid inclusions (MSI), which are interpreted to be crystallisation products of trapped former carbonate–silicate melts metasomatizing their host rocks. We applied conventional thermobarometry and forward thermodynamic modelling to constrain the P–T evolution ranging from the peak metamorphic conditions of the investigated harzburgite and lherzolite, through entrapment of the melts in the outer parts of garnets, to the (re)-equilibration of the MSI assemblages. The peak conditions of c. 1100 °C/4.5–5.5 GPa are recorded by garnet cores and large pyroxene porphyroclasts. The melt entrapment, during which garnet outer parts grew, was associated with influx of the metasomatizing liquids and probably took place during the early stage of the exhumation. Thermodynamic model of amphibole-free MSI assemblage comprising kinoshitalite/Ba-rich phlogopite (approximated by phlogopite in the model), dolomite, magnesite, clinopyroxene, orthopyroxene, garnet and chromite provided robust estimate of P and T of its (re)-equilibration, c. 900–1000 °C, 1.8–2.2 GPa. Furthermore, the lack of olivine reflects co-existence of COH fluid with high X(CO2) = CO2/(CO2 + H2O) ≥ 0.6. Models employing identical P–T–X(CO2) parameters successfully reproduced the other two amphibole-bearing assemblages observed. The modelled stability fields show perfect alignment with a characteristic isobaric segment of the solidus curve of carbonated peridotite. This co-incidence implies that the (re)-equilibration corresponds to the termination of the melt crystallisation once the near-isothermal exhumation path intersected the solidus. Decreased solubility of silicates at the carbonated peridotite “solidus ledge”, inferred from the published experimental data, as well as concentric textures of some MSI indicates sequential crystallisation from the early silicates to late dolomite. The carbonated “solidus ledge” is a relatively narrow boundary in the lithospheric mantle capable of an abrupt immobilisation of fluxing or transported carbonated melts. The investigated rocks are estimated to store approximately 0.02 kg C/m3 (or 6 ppm C) occurring as carbonates in the MSI.
Orogenic peridotites in the crystalline basement of the northwestern Bohemian Massif contain multiphase solid inclusions (MSI), which are interpreted to be crystallisation products of trapped former carbonate–silicate melts metasomatizing their host rocks. We applied conventional thermobarometry and forward thermodynamic modelling to constrain the P–T evolution ranging from the peak metamorphic conditions of the investigated harzburgite and lherzolite, through entrapment of the melts in the outer parts of garnets, to the (re)-equilibration of the MSI assemblages. The peak conditions of c. 1100 °C/4.5–5.5 GPa are recorded by garnet cores and large pyroxene porphyroclasts. The melt entrapment, during which garnet outer parts grew, was associated with influx of the metasomatizing liquids and probably took place during the early stage of the exhumation. Thermodynamic model of amphibole-free MSI assemblage comprising kinoshitalite/Ba-rich phlogopite (approximated by phlogopite in the model), dolomite, magnesite, clinopyroxene, orthopyroxene, garnet and chromite provided robust estimate of P and T of its (re)-equilibration, c. 900–1000 °C, 1.8–2.2 GPa. Furthermore, the lack of olivine reflects co-existence of COH fluid with high X(CO2) = CO2/(CO2 + H2O) ≥ 0.6. Models employing identical P–T–X(CO2) parameters successfully reproduced the other two amphibole-bearing assemblages observed. The modelled stability fields show perfect alignment with a characteristic isobaric segment of the solidus curve of carbonated peridotite. This co-incidence implies that the (re)-equilibration corresponds to the termination of the melt crystallisation once the near-isothermal exhumation path intersected the solidus. Decreased solubility of silicates at the carbonated peridotite “solidus ledge”, inferred from the published experimental data, as well as concentric textures of some MSI indicates sequential crystallisation from the early silicates to late dolomite. The carbonated “solidus ledge” is a relatively narrow boundary in the lithospheric mantle capable of an abrupt immobilisation of fluxing or transported carbonated melts. The investigated rocks are estimated to store approximately 0.02 kg C/m3 (or 6 ppm C) occurring as carbonates in the MSI.
Many lines of evidence from high P-T experiments, thermodynamic models, and natural observations suggest that slab-derived aqueous fluids, which flux mantle wedges contain variable amounts of dissolved carbon. However, constraints on the effects of H2O-CO2 fluids on mantle melting, particularly at mantle wedge P-T conditions, are limited. Here we present new piston cylinder experiments on fertile and depleted peridotite compositions with 3.5 wt.% H2O and XCO2 [= molar CO2 / (CO2 + H2O)] of 0.04-0.17. Experiments were performed at 2-3 GPa and 1350 °C to assess how temperature, peridotite fertility, and XCO2 of slab-derived fluid affects partial melting in mantle wedges. All experiments produce olivine + orthopyroxene + 7 to 41 wt.% partial melt. Our new data, along with previous lower temperature data, show that as mantle wedge temperature increases, primary melts become richer in SiO2, FeO* and MgO and poorer CaO, Al2O3 and alkalis when influenced by H2O-CO2 fluids. At constant P-T and bulk H2O content, the extent of melting in the mantle wedge is largely controlled by peridotite fertility and XCO2 of slab-fluid. High XCO2 depleted compositions generate ~ 7 wt.% melt whereas, at identical P-T, low XCO2 fertile compositions generate ~ 30-40 wt.% melt. Additionally, peridotite fertility and XCO2 have significant effects on peridotite partial melt compositions. At a constant P-T-XCO2, fertile peridotites generate melts richer in CaO and Al2O3 and poorer in SiO2, MgO+FeO, and alkalis. Similar to previous experimental studies, at a constant P-T-fertility condition, as XCO2 increases, SiO2 and CaO of melts systematically decrease and increase, respectively. Such distinctive effects of oxidized form of dissolved carbon on peridotite partial melt compositions are not observed if the carbon-bearing fluid is reduced, such as CH4-bearing. Considering the large effect of XCO2 on melt SiO2 and CaO concentrations and the relatively oxidized nature of arc magmas, we compare the SiO2/CaO of our experimental melts and melts from previous peridotite + H2O ± CO2 studies to the SiO2/CaO systematics of primitive arc basalts and ultra-calcic, silica-undersaturated arc melt inclusions. From this comparison, we demonstrate that across most P-T-fertility conditions predicted for mantle wedges, partial melts from bulk compositions with XCO2 ≥ 0.11 have lower SiO2/CaO than all primitive arc melts found globally, even when correcting for olivine fractionation, whereas partial melts from bulk compositions with XCO2 = 0.04 overlap the lower end of the SiO2/CaO field defined by natural data. These results suggest that the upper XCO2 limit of slab-fluids influencing primary arc magma formation is 0.04 < XCO2 < 0.11, and this upper limit is likely to apply globally. Lastly, we show that the anomalous SiO2/CaO and CaO/Al2O3 signatures observed in ultra-calcic arc melt inclusions can be reproduced by partial melting of either CO2-bearing hydrous fertile and depleted peridotites with 0 < XCO2 < 0.11 at 2-3 GPa, or from nominally CO2-free hydrous fertile peridotites at P > 3 GPa.
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