Abstract

To explore the mantle source properties and the magmatic evolution process for intraplate basaltic lavas, as well as to investigate the potential of Cr isotopes to trace recycled crustal materials, we present Cr isotope compositions for 72 well-characterized samples of Cenozoic intraplate basaltic lavas from eastern China. These basalts display a resolvable δ53Cr range of −0.24‰ to −0.03‰ (n = 72), comparable to MORB and OIB. With respect to the evolved lavas, their δ53Cr scatter can be interpreted as a result of fractional crystallization of predominant olivine (or/and clinopyroxene) with 1% to 3% spinel from heterogeneous magma sources under different oxygen fugacity conditions. Combined with Sr-Nd-Zn-Fe isotope data, the least evolved basalts with MgO of ∼10% display a large δ53Cr range, indicating the presence of different magma component end-members, including one low-Si and two high-Si components. Two high-Si enriched components have δ53Cr values lower than those of primitive N-MORB and OIB magmas, consistent with their derivations most likely from relatively enriched mantle pyroxenites. Notably, the low-Si nephelinitic component could not be a simple end-member as proposed before. Correlations of δ53Cr with εNd(t)-87Sr/86Sr(i)-Fe/Mn-Ti/Ti*-Hf/Hf*-δ66Zn-δ56Fe [Ti/Ti* = TiN/(NdN-0.055 × SmN0.333 × GdN0.722), Hf/Hf* = HfN/(SmN × NdN)0.5. N represents the primitive mantle-normalized values] for nephelinites from both the North China Block and the South China Block suggest mixing between partial melts of carbonated peridotite and pyroxenite sources. The carbonated peridotite derived melt is characterized by depleted SrNd isotopes, low Fe/Mn, Ti/Ti* and Hf/Hf* ratios, and heavier than BSE's Cr-Fe-Zn isotope compositions. The highly oxidized environment induced by carbonatization effectively reduces Cr isotope fractionation between melts and residues during partial melting of the carbonated peridotite, resulting in the heavy Cr isotope feature of melts being inherited from the carbonated mantle source, consistent with the heavy Cr isotope compositions of carbonated mantle xenoliths obtained previously. Thus, this work highlights that Cr isotopes might act as a potential tracer for subducted sedimentary carbonates.

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