The largest negative carbon isotope excursions in Neoproterozoic carbonates caused by recycled carbonatite volcanic ash.

The late Ediacaran Shuram Excursion (SE) records the most prominent negative δ13C excursions (δ13C = -12‰) during Earth's history. It has been hypothesized to have resulted from oxidation of dissolved organic matter, diagenetic or authigenic precipitates. However, the origin of the SE remains enigmatic; current models face challenges regarding the significant amount of atmospheric oxygen needed to balance such extensive oxidation and sustained inputs of light carbon with extremely negative C isotope compositions. Here, we show that the Doushantuo Formation at the Jiulongwan section in South China, a key stratum recording the SE event, contains mineralogical and geochemical signatures related to igneous processes. Both the occurrence of ankerite, feldspar, moissanite and euhedral quartz in the SE samples and the relatively consistent Ce anomalies of carbonate and O isotopes of quartz indicate a contribution from an igneous source. In particular, the SE samples have trace element and C isotope compositions similar to those of recycled carbonatites formed by decarbonation and melting of sedimentary carbonate rocks. These observations suggest that the deep cycle of ancient carbonate rocks, which were subjected to decarbonation during subduction, melting and eruption related to the breakup of the Rodinia supercontinent, contributed to the SE. This igneous model for the SE may provide a connection between the deep and shallow carbon cycles of the Earth.

First direct evidence of sedimentary carbonate recycling in subduction-related xenoliths.

Carbon in rocks and its rate of exchange with the exosphere is the least understood part of the carbon cycle. The amount of carbonate subducted as sediments and ocean crust is poorly known, but essential to mass balance the cycle. We describe carbonatite melt pockets in mantle peridotite xenoliths from Dalihu (northern China), which provide firsthand evidence for the recycling of carbonate sediments within the subduction system. These pockets retain the low trace element contents and δ(18)OSMOW = 21.1 ± 0.3 of argillaceous carbonate sediments, representing wholesale melting of carbonates instead of filtered recycling of carbon by redox freezing and melting. They also contain microscopic diamonds, partly transformed to graphite, indicating that depths >120 km were reached, as well as a bizarre mixture of carbides and metal alloys indicative of extremely reducing conditions. Subducted carbonates form diapirs that move rapidly upwards through the mantle wedge, reacting with peridotite, assimilating silicate minerals and releasing CO2, thus promoting their rapid emplacement. The assimilation process produces very local disequilibrium and divergent redox conditions that result in carbides and metal alloys, which help to interpret other occurrences of rock exhumed from ultra-deep conditions.