The depth of sub-lithospheric diamond formation and the redistribution of carbon in the deep mantle

Most diamonds form in the Earth's lithosphere but a small proportion contain Si-rich majoritic garnet inclusions that indicate formation in the deeper mantle. The compositions of syngenetic garnet inclusions can potential yield information on both the depth and mantle lithology in which the diamonds formed. Pressure dependent changes in garnet compositions have been calibrated using the results of experiments conducted in a multi-anvil apparatus at pressures between 6 and 16 GPa and temperatures of 1000 to 1400 degrees C. Using the results of these experiments a barometer was formulated based on an empirical parameterisation of the two major majoritic substitutions, referred to as majorite (Maj; Al3+ = Mg2+ + Si4+), and Na-majorite (Na-Maj; Mg2+ + Al3+ = Na+ + Si4+). Moreover, previously published experimental garnet compositions from basaltic, kimberlite, komatiite and peridotite bulk compositions were included in the calibration, which consequently covers pressures from 6 to 20 GPa and temperatures from 900 to 2100 degrees C. Experimental pressures are reproduced over these conditions with a standard deviation of 0.86 GPa. The barometer is used to determine equilibration pressures of approximately 500 reported garnet inclusions in diamonds from a range of localities. As the majority of these inclusions are proposed to be syngenetic this allows a detailed picture of diamond formation depths and associated source rocks to be established using inclusion chemistry. Geographic differences in diamond source rocks are mapped within the sub-lithospheric mantle to over 500 km depth. Continuous diamond formation occurs over this depth range within lithologies with eclogitic affinities but also in lithologies that appear transitional between eclogitic and peridotitic bulk compositions, with an affinity to pyroxenites. The geographic differences between eclogitic and pyroxenitic diamond source rocks are rationalised in terms of diamond formation within downwelling and upwelling regimes respectively. Macroscopic diamond formation in rocks with pyroxenite compositions are likely facilitated in the deep mantle by higher average oxidation states and low mineral H2O solubility compared to the surrounding mantle, which aid the mobility of C-O-H volatile species. The apparent lack of inclusions with a peridotite affinity may result from generally low oxygen fugacities in such lithologies, which reduces carbon mobility, and the lack of a suitable oxidising agent to allow diamonds to form from CH4. This glimpse of deep carbon cycle processes implies that heterogeneities in the carbon content, redox state and chemical composition of the mantle may be strongly coupled. (C) 2016 Elsevier B.V. All rights reserved.