Abstract
Diamond formation in the Earth has been extensively discussed in recent years on the basis of geochemical analysis of natural materials, high-pressure experimental studies, or theoretical aspects. Here, we demonstrate experimentally for the first time, the spontaneous crystallization of diamond from CH4-rich fluids at pressure, temperature and redox conditions approximating those of the deeper parts of the cratonic lithospheric mantle (5–7 GPa) without using diamond seed crystals or carbides. In these experiments the fluid phase is nearly pure methane, even though the oxygen fugacity was significantly above metal saturation. We propose several previously unidentified mechanisms that may promote diamond formation under such conditions and which may also have implications for the origin of sublithospheric diamonds. These include the hydroxylation of silicate minerals like olivine and pyroxene, H2 incorporation into these phases and the “etching” of graphite by H2 and CH4 and reprecipitation as diamond. This study also serves as a demonstration of our new high-pressure experimental technique for obtaining reduced fluids, which is not only relevant for diamond synthesis, but also for investigating the metasomatic origins of diamond in the upper mantle, which has further implications for the deep carbon cycle.
Highlights
Diamond formation in the Earth has been extensively discussed in recent years on the basis of geochemical analysis of natural materials, high-pressure experimental studies, or theoretical aspects
Diamond formation in the Earth has been extensively discussed in recent years based upon analysis of natural materials, high-pressure experimental studies, or theoretical considerations
Many studies support a metasomatic origin, crystallizing from C-bearing fluids or melts migrating through the lithospheric mantle[6,8,9]
Summary
Diamond formation in the Earth has been extensively discussed in recent years on the basis of geochemical analysis of natural materials, high-pressure experimental studies, or theoretical aspects. Metasomatic crystallization of diamond from C-bearing fluids or melts is generally considered the most common mechanism for diamond formation[8,9] and two essentially mutually exclusive mechanisms can be considered, both of which involve redox reactions: i) the reduction of oxidized carbon in the form of CO2 or carbonate, or ii) the oxidation of reduced carbon from methane or other higher hydrocarbons.
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