Ancient refractory asthenosphere revealed by mantle re-melting at the Arctic Mid Atlantic Ridge

The upper mantle is a heterogeneous mixture of refractory and recycled crustal domains. The recycled portions, more fertile and thus preferentially melted, dominate the composition of the basalts erupted on the surface, whereas the imprint of melting of the refractory counterparts is more difficult to discern from the basalt chemistry. Contrasting radiogenic isotopic signatures of mid-ocean ridge basalts and oceanic mantle, however, show that Hf isotope ratios may provide hints for melting of refractory source materials despite ubiquitous magma mixing during ascent and stalling in the crust. This property may allow identifying contributions from depleted mantle materials unseen in other isotope systematics in basalts. Here, we show that basalts from Mohns and Knipovich ridges, two >500-km long oblique super-segments in the Arctic Atlantic, have distinctly high Hf isotope ratios, not mirrored by comparatively high Nd and low Sr and Pb isotope ratios. These compositions can be explained if a highly depleted asthenospheric mantle melts beneath this section of the Arctic Mid Atlantic Ridge. We argue that this depleted source consists of high proportions of ancient (>1 Ga), ultra-depleted mantle, previously drained of enriched components before being re-melted in its current location following a recent ridge-jump, allowing the identification of ultra-depleted mantle components in the arctic subridge mantle

Genesis of oceanic oxide gabbros and gabbronorites during reactive melt migration at transform walls (Doldrums Megatransform System; 7-8°N Mid-Atlantic Ridge)

The Doldrums Megatransform System (~7-8°N, Mid-Atlantic Ridge) shows a complex architecture including four intra-transform ridge segments bounded by five active transform faults. Lower crustal rocks are exposed along the Doldrums and Vernadsky transform walls that bound the northernmost intra-transform ridge segment. The recovered gabbros are characterized by variably evolved chemical compositions, ranging from olivine gabbros to gabbronorites and oxide gabbros, and lack the most primitive gabbroic endmembers (troctolites, dunites). Notably, the numerous recovered gabbronorites show up to 20 vol% of coarse-grained orthopyroxene. Although covariations in mineral and bulk-rock chemical compositions of the olivine and oxide gabbros define trends of crystallization from a common parental melt, the gabbronorites show elevated light over heavy rare earth elements (LREE/HREE) ratios in both bulk-rock and mineral compositions. These features are not consistent with a petrological evolution driven solely by fractional crystallization, which cannot produce the preferential enrichments in highly incompatible elements documented in the orthopyroxene-bearing lithologies. We suggest that gabbronorites crystallized from evolved melts percolating and partly assimilating a pre-existing olivine gabbro matrix. Saturation in orthopyroxene and selective enrichments in LREE relative to M-HREE are both triggered by an increase in assimilated crystal mass, which ranges from negligible in the oxide-gabbros to abundant in the gabbronorites. This melt-rock reaction process has been related to lateral melt migration beneath ridge-transform intersections, where variably evolved melts injected from the peripheral parts of the melting region towards the transform zone may interact with a gabbroic crystal mush to form abundant oxide-bearing gabbronoritic associations