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Geochemical and isotopic data suggest that the source regions of oceanic basalts may contain pyroxenite in addition to peridotite. In order to incorporate the wide range of compositions and melting behaviors of pyroxenites into mantle melting models, we have developed a new parameterization, Melt‐PX, which predicts near‐solidus temperatures and extents of melting as a function of temperature and pressure for mantle pyroxenites. We used 183 high‐pressure experiments (25 compositions; 0.9–5 GPa; 1150–1675°C) to constrain a model of melt fraction versus temperature from 5% melting up to the disappearance of clinopyroxene for pyroxenites as a function of pressure, temperature, and bulk composition. When applied to the global set of experimental data, our model reproduces the experimental F values with a standard error of estimate of 13% absolute; temperatures at which the pyroxenite is 5% molten are reproduced with a standard error of estimate of 30°C over a temperature range of ~500°C and a pressure range of ~4 GPa. In conjunction with parameterizations of peridotite melting, Melt‐PX can be used to model the partial melting of multilithologic mantle sources—including the effects of varying the composition and the modal proportion of pyroxenite in such source regions. Examples of such applications include calculations of isentropic decompression melting of a mixed peridotite + pyroxenite mantle; these show that although the potential temperature of the upwelling mantle plays an important role in defining the extent of magma production, the composition and mass fraction of the pyroxenite also exert strong controls.

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Using Melt-PX to model the decompression melting of a heterogeneous mantle, I investigated the role of major-element composition of the lithologies present in the source on magmatic productivity, and trace element and isotopic melt compositions, independently of the bulk mantle composition. My calculations demonstrate that the volume of magma produced is not significantly affected by the nature of the lithological heterogeneity, but depends on the bulk mantle composition. However, an isochemical bulk mantle can produce contrasting trace element and isotopic melt compositions depending on the major-element compositions of the lithologies present in the source. Results show that the observed crust thickness of the Icelandic rift zones is consistent with about 10 % of recycled crust in the source, but also demonstrate there is no need to involve the contribution of melts derived from a recycled basalt component to explain the compositional variability of the Icelandic basalts in rift zones, and rather advance the contribution of olivine-bearing hybrid lithologies formed by solid-state reactions between the recycled crust and the peridotite.

The Earth's mantle is heterogeneous as a result of early planetary differentiation and subsequent crustal recycling during plate tectonics. Radiogenic isotope signatures of midocean ridge basalts have been used for decades to map mantle composition, defining the depleted mantle end member. These lavas, however, homogenize via magma mixing and may not capture the full chemical variability of their mantle source. Here we show that the depleted mantle is significantly more heterogeneous than previously inferred from the compositions of lavas at the surface, extending to highly enriched compositions. We perform high spatial resolution isotopic analyses on clinopyroxene and plagioclase from lower crustal gabbros drilled on a depleted ridge segment of the northern Mid-Atlantic Ridge. These primitive cumulate minerals record nearly the full heterogeneity observed along the northern Mid-Atlantic Ridge, including hotspots. Our results demonstrate that substantial mantle heterogeneity is concealed in the lower oceanic crust and that melts derived from distinct mantle components can be delivered to the lower crust on a centimetre scale. These findings provide a starting point for re-evaluation of models of plate recycling, mantle convection, and melt transport in the mantle and the crust. The mantle, Earth's largest geochemical reservoir and main source of volcanism, records the timeintegrated history of recycling of oceanic lithosphere and its overlying sediments during the plate tectonic cycle 1,2. The compositional heterogeneity thus generated within the mantle reflects this