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Chemical weathering of sedimentary rocks can release carbon dioxide (CO2) and consume oxygen (O2) via the oxidation of petrogenic organic carbon and sulfide minerals. These pathways govern Earth's surface system and climate over geological timescales, but the present-day weathering fluxes and their environmental controls are only partly constrained due to a lack of in situ measurements. Here, we investigate the gaseous exchange of CO2 and O2 during the oxidative weathering of black shales and marls exposed in the French southern Alps. On six field trips over 1 year, we use drilled headspace chambers to measure the CO2 concentrations in the shallow critical zone and quantify CO2 fluxes in real time. Importantly, we develop a new approach to estimate the volume of rock that contributes CO2 to a chamber, and assess effective diffusive gas exchange, by first quantifying the mass of CO2 that is stored in a chamber and connected rock pores. Both rock types are characterized by similar contributing rock volumes and diffusive movement of CO2. However, CO2 emissions differed between the rock types, with yields over rock outcrop surfaces (inferred from the contributing rock volume and the local weathering depths) ranging on average between 73 and 1108 tCkm-2yr-1 for black shales and between 43 and 873 tCkm-2yr-1 for marls over the study period. Having quantified diffusive processes, chamber-based O2 concentration measurements are used to calculate O2 fluxes. The rate of O2 consumption increased with production of CO2, and with increased temperature, with an average O2:CO2 molar ratio of 10:1. If O2 consumption occurs by both rock organic carbon oxidation and carbonate dissolution coupled to sulfide oxidation, either an additional O2 sink needs to be identified or significant export of dissolved inorganic carbon occurs from the weathering zone. Together, our findings refine the tools we have to probe CO2 and O2 exchange in rocks at Earth's surface and shed new light on CO2 and

Submarine turbidity currents form the largest sediment accumulations on Earth, raising the question of their role in global carbon cycles. It was previously inferred that terrestrial organic carbon was primarily incinerated on shelves and that most turbidity current systems are presently inactive. Turbidity currents were thus not considered in global carbon cycles, and the burial efficiency of global terrestrial organic carbon was considered low to moderate (∼10–44%). However, recent work has shown that burial of terrestrial organic carbon by turbidity currents is highly efficient (>60–100%) in a range of settings and that flows occur more frequently than once thought, although they were far more active at sea-level lowstands. This leads to revised global estimates for mass flux (∼62–90 Mt C/year) and burial efficiency (∼31–45%) of terrestrial organic carbon in marine sediments. Greatly increased burial fluxes during sea-level lowstands are also likely underestimated; thus, organic carbon cycling by turbidity currents could play a role in long-term changes in atmospheric CO2 and climate. Expected final online publication date for the Annual Review of Marine Science, Volume 16 is January 2024. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.

The transfer of carbon from land to the near-coastal ocean is increasingly being recognized in global carbon budgets. However, a more direct transfer of terrestrial carbon to the deep-sea is comparatively overlooked. Among systems that connect coastal to deep-sea environments, the Congo Submarine Canyon is of particular interest since the canyon head starts 30 km into the Congo River estuary, which delivers ~7 % of the total organic carbon from the world’s rivers. However, carbon and sediment transport mechanisms that operate in the Congo Canyon, and submarine canyons more globally, are poorly constrained compared to rivers because monitoring of deep-sea canyons remains challenging. Using a novel array of acoustic instruments, sediment traps and cores, this study seeks to understand the hydrodynamic processes that control delivery of particulate organic carbon via the Congo Submarine Canyon to the deep-sea. We show that particulate organic carbon transport in the canyon-axis is modulated by two processes. First, we observe periods where the canyon dynamics are dominated by tides, which induce a background oscillatory flow (speeds of up to 0.15 m/s) through the water column, keeping muds in suspension, with a net upslope transport direction. Second, fast-moving (up to 8 m/s) turbidity currents occur for 35 % of the time during monitoring periods and transport both muddy and sandy particulate organic carbon at an estimated transit flux that is more than ten times the flux induced by tides. Remarkably, organic carbon transported and deposited in the submarine canyon has a similar isotopic composition to organic carbon in the Congo River, and in the deep-sea fan at 5 km of water depth. Episodic turbidity currents, together with background tidal currents thus promote efficient transfer of river-derived particulate organic carbon in the Congo Submarine Fan, leading to some of the highest terrestrial carbon preservation rates observed in marine sediments globally.