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Abstract 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 to 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. 

Abstract We present phase‐equilibria experiments of a K‐bearing, depleted peridotite (Mg# 92) fluxed with a mixed CO₂‐H₂O fluid (0.5 wt.% CO₂and 0.94 wt.% H₂O in the bulk) to gain insight into the stability of volatile‐bearing partial melts versus volatile‐bearing mineral phases in a depleted peridotite system. Experiments were performed at 850–1150 °C and 2–4 GPa using a piston‐cylinder and a multianvil apparatus. Olivine, orthopyroxene, clinopyroxene, and spinel/garnet are present at all experimental conditions. Textural confirmation of partial melt is made at temperatures as low as 1000 °C at 2 GPa, 950 °C at 3 GPa, and 1000 °C at 4 GPa marking the onset of melting at 900–1000 °C at 2 GPa, 850–950 °C at 3 GPa, and 950–1000 °C at 3 GPa. Phlogopite and magnesite breakdown at 900–1000 °C at 2 GPa, 950–1000 °C at 3 GPa, and 1000–1050 °C at 4 GPa. Comparison with previously published experiments in depleted peridotite system with identical CO₂‐H₂O content introduced via a silicic melt show that introduction of CO₂‐H₂O as fluid lowers the temperature of phlogopite breakdown by 150–200 °C at 2–4 GPa and stabilizes partial melts at lower temperatures. Our study thus, shows that the volatile‐bearing phase present in the cratonic mantle is controlled by bulk composition and is affected by the process of volatile addition during craton formation in a subduction zone. In addition, volatile introduction via melt versus aqueous fluid, leads to different proportion of anhydrous phases such as olivine and orthopyroxene. Considering the agent of metasomatism is thus critical to evaluate how the bulk composition of depleted peridotite is modified, leading to potential stability of volatile‐bearing phases as the cause of anomalously low shear wave velocity in mantle domains such as mid lithospheric discontinuities beneath continents.