How can we trace mantle oxidation state in the Archaean?

Plate tectonics exerts a first-order control on the interaction between Earth’s reservoirs. Atmospherically-altered surface materials are recycled to the mantle via subduction, while volatiles from the mantle are liberated to the atmosphere via volcanism. This cycle regulates much of Earth’s climate, ocean levels and metallogenetic processes within the continental crust. However, the interplay between Earth’s atmospheric changes and the geochemical evolution of mantle-derived magmas has remained obscure in deep geological time. This has led to multiple conflicting models for crustal evolution in the early Earth.

A time-integrated evolution of mantle-crust-atmosphere-hydrosphere interaction is yet to be fully established. For instance, secular change of the ocean and atmosphere system is evident from several proxies but the feedback of these changes to magmatic and geochemical processes in the lithosphere remains unclear. Moreover, no clear consensus has been reached on the timing of modern-style plate tectonic initiation and the evolution of net growth of the continental crust.

To explain overt and cryptic global trends in the geochemistry of magmatic rocks, a better understanding of mineral reactions and how these control trace element evolution in magmas at the lithosphere-scale is paramount. For example, the elemental and isotopic composition of apatite inclusions hosted by zircon offers a way to better understand the evolution of magmas and, to some extent, the nature of magma sources. These proxies rely on the robust data acquisition of isotope ratios from multiple isotope systems with different geochemical behaviour, such as U-Pb, O and Lu-Hf in the host zircon crystal. 

A combination of methods and proxies including the elemental composition of apatite via EPMA and oxygen fugacity based on sulphur speciation via μ-XANES of apatite inclusions has been applied to ancient sub-arc magmas formed in regions akin to modern subduction zones. These magmas share a common mantle source but crystallised more than 200 million years apart (at 2.35 and 2.13 billion years ago). Importantly, they bracket the Great Oxidation Event, when atmospheric oxygen levels increased by five orders of magnitude, causing a permanent and dramatic change in Earth’s surface chemistry. As such, these sub-arc magmas were investigated as potential tracers of the interaction between Earth’s atmosphere and the mantle.

The information from several inclusions from co-magmatic rocks have then been interpreted in the light of U-Pb, Lu-Hf, trace elements and oxygen isotope analyses of the host zircon grains. Altogether, the results show a shift in oxygen fugacity of sub-arc magmas across the Great Oxidation Event. The change in oxygen fugacity is thought to be caused by recycling into the mantle of sediments that had been geochemically altered at the surface by the increase in atmospheric oxygen levels. This study opens a wide window of opportunities for the time-integrated investigation of the interaction between atmosphere and oceans with the evolving terrestrial mantle. In particular, we have a tool to investigate the Archaean mantle and assess the degree to which oxidation may have occurred prior to the Great Oxygenation Event, as has been implied from some previous studies.