How it started

Oceanic sediments constitute a substantial carbon source within subduction zones, encompassing both inorganic and organic carbon components that are transported into the subduction factory. Understanding the fate of these carbon inputs in subduction zones is crucial for gaining insights into the global carbon cycling throughout Earth's history. While the significance of carbonate in the subduction-zone carbon cycle has been extensively investigated in recent decades, the importance of organic carbon within subduction-zone lithologies and deep fluids has been relatively overlooked. The deep subduction of reduced organic carbon has impacts on various geological events, including the Great Oxygenation Event, the Lomagundi event, arc carbon isotopic signature and the formation of deep diamonds with light carbon isotopic features.

The problem

Diamond, a high-pressure polyphase of graphite, is estimated to be formed in the lithospheric mantle at depths exceeding 140 km or under pressures greater than 4.5 GPa. An intriguing debate related to crustal recycling into the deep mantle regards the involvement of subduction-derived C in the genesis of diamond. According to the literatures, some diamonds exhibit lighter carbon isotope characteristics (i.e., lower than mantle range), particularly ophiolitic diamonds, which show δ¹³C ranging from −29‰ to −18‰ with a peak value of −25‰. Various theories have been posited to explain the light δ¹³C compositions of these diamonds, including the primordial carbon reservoir, intra-mantle isotopic fractionation, or the incorporation of subducted biogenic/organic carbon³². However, mantle Sr, Nd, and O isotopic geochemistry data rule out the preservation of primordial carbon isotope heterogeneity in Earth’s mantle. Moreover, the narrow range of δ¹³C values from individual diamonds does not support isotope fractionation from a normal mantle carbon source with δ¹³C of –5 ± 2‰. Therefore, the feature of light carbon recorded by ophiolitic diamonds possibly reflects the composition of subducted organic carbon. However, the lack of robust petrological evidence makes this hypothesis arguable.

The solution and results

We conducted fieldwork in the Tianshan UHP area where coesite has been reported from the pelitic schists and collected graphite-bearing pelitic schists. By preliminary microscopic observation, we found many radial cracks developed in the garnet of the graphite-bearing pelitic schists, with quartz crystals at the center of the cracks. This structure, which we termed the ‘coesite pseudomorph’, was caused by the conversion of formerly present coesite to quartz during decompression. We then searched for transparent inclusions in the graphite-bearing garnet crystals and finally identified the coesite inclusions within garnet (Figure 1) by Raman spectroscopy.

Next, we performed organic carbon isotope analysis on graphite-bearing pelitic schists. For each sample, we prepared three types of powders: (i) whole-rock powder, (ii) picked graphite-bearing garnet powder, and (iii) picked graphite-bearing white mica powder. These pelitic schists (bulk-rock powder) have homogeneous δ¹³C_TOC values of −24.7 to −22.5‰ (Figure 2), which fall in the range of typical marine organic matter. The δ¹³C_TOC of picked graphite-bearing garnet crystals and picked graphite-bearing whitemica (phengite and paragonite) are in agreement with that of the bulk rock (Figure 2). This consistency suggests that graphite serves as the primary organic carbon phase in these samples. Our study thus provides petrologic evidence that organic carbon in surface oceanic crustal sediments can be subducted to subarc depths.

Future directions and implications

With the increasing subduction depth, surface-derived disordered organic carbon is transformed to crystalized graphite at subarc depth (around 90 km) and subsequently to diamonds at lithospheric mantle depth (140 km), as illustrated in Figure 3. Further studies are needed to fully elucidate the mechanisms and processes involved in the transition from surface organic carbon to graphite and then to diamonds.