Experimental Constraints on CO2 Solubility in Rhyolitic Slab Melts – Implications for Carbon Flux in Subduction Zone
Abstract:
Our previous experiments have constrained CO2 content in silicic slab melts as a function of P (1.5-3.0 GPa) and melt H2O content (0.5-3.0 wt.%) [3]. Here we extend our experiments to constrain the effect of temperature (1100-1400 °C) and fO2 (CO2 vapor-saturated [3] and graphite-saturated) on CO2 solubility and speciation in natural rhyolitic melts. From our data, we constructed empirical and thermodynamic models to calculate CO2 content in slab melts at P and T appropriate for the sub-arc region of the subducting slab at variable fO2 [4]. These experiments and models show that CO2 solubility increases with increasing P, fO2, and melt H2O contents to ~3.5 wt.%, while there is a only slight increase in CO2 solubility with increasing T though the effect is much smaller.
Our study constrains the extent of C-cycling to the deep interior and to the arc source for graphite-saturated domains of the downgoing crust. Further, there is a general correspondence between CO2 solubility in slab-derived, rhyolitic melts at sub-arc depth with measured CO2 outflux at arcs [5]. For hotter slabs (T>800 °C) the calculated CO2 contents using our thermodynamic model, for example, are 1.5-3.4 wt.% for a low-H2O melt generated near the FMQ buffer and correspond to arc fluxes of 50-500 × 109 mol/yr. For colder slabs (T<800 °C) the calculated CO2 contents are 0.9-1.6 wt.% for a low-H2O melt generated near the FMQ buffer and correspond to arc fluxes of 0.1-15 ×1 09 mol/yr. This correspondence suggests that slab-derived silicic melt may be the chief agent of C-transport from slab to mantle wedge.
[1] Plank and Langmuir (1993) Nature, 362, 739-743; [2] Prouteau et al. (2001) Nature, 410, 197-200; [3] Duncan and Dasgupta. (2014) GCA, 124, 328-347; [4] Syracuse et al. (2010) PEPI, 183, 73-90; [5] Fischer et al. (2008) Geochem. J., 42, 21-38.
