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The oxidation of petrogenic organic carbon (OCpetro) is a source of carbon dioxide to the atmosphere over geological timescales. The rates of OCpetro oxidation in locations that experience low rates of denudation remain poorly constrained, despite these landscapes dominating Earth's continental surface area. Here, we track OCpetro oxidation using radiocarbon and the trace element rhenium (Re) in the deep weathering profiles, soils and stream waters of the Susquehanna Shale Hills Critical Zone Observatory (PA, USA). In a ridge‐top borehole, radiocarbon measurements reveal the presence of a broad OCpetro weathering front, with a first‐order assessment of ~40% loss occurring over ~6 m. However, the low OCpetro concentration (< 0.05 wt%) and inputs of radiocarbon throughout the deepest parts of the profile complicate the assessment of OCpetro loss. The OCpetro weathering front coincides with a zone of Re depletion (~90% loss), and we estimate that > 80% of Re in the rock is associated with OCpetro, based on Re/Na and Re/S ratios. Using estimates of long‐term denudation rates, the observed OCpetro loss and the Re proxy are equivalent to a low OCpetro oxidation yield of < 1.7 × 10−2 tC km−2 yr−1. This is consistent with the low OCpetro concentrations and low denudation rates at this location. In addition, we find the surface cycle of Re is decoupled from that of deep weathering, with an enrichment of Re in surface soils and elevated Re concentrations in stream water, precipitation, and shallow groundwater. A mass balance model shows that this can be explained by a historical anthropogenic contribution of Re through atmospheric deposition. We estimate that the topsoil Re pool could take decades to centuries to deplete and call for a renewed focus on anthropogenic perturbation of the surface Re cycle in low denudation rate settings. [ABSTRACT FROM AUTHOR]

The balance between the burial of biospheric organic carbon (OC bio) in the ocean and the oxidation of rock-derived organic carbon across landscapes (OC petro) helps to regulate atmospheric CO 2 and O 2 over geological time. However, we lack reconstructions of these processes over the timescales necessary to properly understand the drivers and feedbacks operating. Here we use a sediment core from the Zhuoshui River delta in Taiwan, which receives sediments from a rapidly uplifting and eroding catchment, to reconstruct the variations in OC content and radiocarbon composition since the Last Glacial Maximum (LGM). We find that the export of OC bio and the oxidation of OC petro are both modulated by climate-driven changes in physical erosion and temperature. During cold and dry periods, such as the LGM and the Younger Dryas (YD), shallow erosion and low temperature enhanced the preservation of OC bio in the biosphere in catchment, while deep erosion and high temperature during warm and wet periods, such as the Holocene, favored the dilution and degradation of OC bio. The weathering intensity of OC petro (ω) was inversely related to physical erosion, suggesting a lower intensity of oxidation during the Holocene period while the overall oxidation flux was enhanced. This suggests that the degree of weathering was primarily controlled by physical erosion. We propose a proxy to estimate the ratio of fluxes of OC bio export and OC petro oxidation, and show that the net balance between these two processes shifted from a carbon sink during the late deglacial period to a carbon source during the mid-late Holocene. Our study reveals that with CO 2 rise, a warmer and wetter climate would promote the exposure and oxidation of OC petro by erosion in this mountain range, leading the organic carbon balance towards a CO 2 source to the atmosphere. • Erosion and temperature control carbon dynamic in erosive setting. • Cold, dry periods boost carbon preservation. • Warm, wet climate shifts mountains to carbon sources. [ABSTRACT FROM AUTHOR]

Much attention has been focused on fine‐grained sediments carried as suspended load in rivers due to their potential to transport, disperse, and preserve organic carbon (OC), while the transfer and fate of OC associated with coarser‐grained sediments in fluvial systems have been less extensively studied. Here, sedimentological, geochemical, and biomolecular characteristics of sediments from river depth profiles reveal distinct hydrodynamic behavior for different pools of OC within the Mackenzie River system. Higher radiocarbon (14C) contents, low N/OC ratios, and elevated plant‐derived biomarker loadings suggest a systematic transport of submerged vascular plant debris above the active riverbed in large channels both upstream of and within the delta. Subzero temperatures hinder OC degradation promoting the accumulation and waterlogging of plant detritus within the watershed. Once entrained into a channel, sustained flow strength and buoyancy prevent plant debris from settling and keep it suspended in the water column above the riverbed. Helical flow motions within meandering river segments concentrate lithogenic and organic debris near the inner river bends forming a sediment‐laden plume. Moving offshore, we observe a lack of discrete, particulate OC in continental shelf sediments, suggesting preferential trapping of coarse debris within deltaic and neritic environments. The delivery of waterlogged plant detritus transport and high sediment loads during the spring flood may reduce oxygen exposure times and microbial decomposition, leading to enhanced sequestration of biospheric OC. Undercurrents enriched in coarse, relatively fresh plant fragments appear to be reoccurring features, highlighting a poorly understood yet significant mechanism operating within the terrestrial carbon cycle. Plain Language Summary: Coarse sediments are generally neglected as pathways and sinks of terrestrial organic carbon (OC) due to their presumed low OC contents and preservation potential. However, sedimentological and geochemical properties of sediments collected from the Mackenzie River reveal the co‐occurrence of coarse‐grained lithogenic particles with substantial quantities of pieces of plant biomass close to the riverbed. We argue that cold conditions in Arctic regions limit organic matter decomposition and favor the accumulation and water saturation of plant debris. These plant fragments will initially sink but are carried along the riverbed due to their shape, which is more elongated and planar than other particles. As rivers meander and navigate bends, water flow can divert coarser particles toward the inner bend, creating sediment‐laden undercurrents. We find that offshore in the Arctic Ocean, discrete plant detritus is apparently less common and we suggest that these particles are trapped within the Mackenzie Delta. The large amount of sediment exported during the spring flood promotes rapid burial of plant debris, likely preventing the decomposition of OC and the release of CO2 to the atmosphere. Our observations reveal a previously hidden mechanism that transports OC‐rich detritus within river systems that needs to be accounted for. [ABSTRACT FROM AUTHOR]

Lithospheric organic carbon ( “ petrogenic ” ; OC petro ) is oxidized during exhumation and subsequent erosion of mountain ranges. This process is a considerable source of carbon dioxide (CO2) to the atmosphere over geologic time scales, but the mechanisms that govern oxidation rates in mountain landscapes are poorly constrained. We demonstrate that, on average, 67 ± 11% of the OC petro initially present in bedrock exhumed from the tropical, rapidly eroding Central Range of Taiwan is oxidized in soils, leading to CO2 emissions of 6.1 to 18.6 metric tons of carbon per square kilometer per year. The molecular and isotopic evolution of bulk OC and lipid biomarkers during soil formation reveals that OC petro remineralization is microbially mediated. Rapid oxidation in mountain soils drives CO2 emission fluxes that increase with erosion rate, thereby counteracting CO2 drawdown by silicate weathering and biospheric OC burial. [ABSTRACT FROM AUTHOR]

Rapid erosion in mountain forests results in high rates of biospheric particulate organic carbon (POC) export by rivers, which can contribute to atmospheric carbon dioxide drawdown. However, coarse POC (CPOC) carried by particles >~1 mm is rarely quantified. In a forested pre-Alpine catchment, we measured CPOC transport rates and found that they increase more rapidly with water discharge than fine POC (<1 mm) and dissolved organic carbon (DOC). As a result, decadal estimates of CPOC yield of 12.3 ± 1.9 t C km^yr"1 are higher than for fine POC and DOC, even when excluding 4 extreme flood events. When including these floods, CPOC dominates organic carbon discharge (~80%). Most CPOC (69%) was water logged and denser than water, suggesting that CPOC has the potential to contribute to long-term sedimentary burial. Global fluxes remain poorly constrained, but if the transport behavior of CPOC shown here is common to other mountain streams and rivers, then neglecting CPOC discharge could lead to a large underestimation of the global transfer of biospheric POC from land to ocean. [ABSTRACT FROM AUTHOR]

Oxidation of rock-derived, petrogenic, organic carbon (OC petro ) during weathering of sedimentary rocks is a major source of carbon dioxide (CO 2 ) to the atmosphere. This geological respiration is thought to be enhanced by physical erosion, suggesting that mountain belts could release large amounts of CO 2 to counter the CO 2 sequestration achieved by the erosion, riverine transfer and oceanic burial of organic carbon from the terrestrial biosphere. However, OC petro oxidation rates in mountain belts have not been quantified. Here we use rhenium (Re) as a proxy to track OC petro oxidation in mountain river catchments of Taiwan, where existing measurements of physical erosion rate allow the controls on OC petro oxidation to be assessed. Re has been shown to be closely associated with OC petro in rocks and following oxidation during chemical weathering forms a soluble oxyanion ( ReO 4 − ) which contributes to the dissolved load of rivers. Soils on meta-sedimentary rocks in Taiwan show that Re loss is coupled to OC petro loss during weathering, confirming previous observations from soil profiles on sedimentary rocks elsewhere. In Taiwan rivers, dissolved Re flux increases with the catchment-average sediment yield, suggesting that physical erosion rate is a major control on OC petro oxidation. Based on our current understanding of Re mobility during weathering, the dissolved Re flux can be used to quantify an upper bound on the OC petro oxidation rate and the associated CO 2 transfer. The estimated CO 2 release from this mountain belt by OC petro oxidation does not negate estimates of CO 2 sequestration by burial of biospheric OC offshore. The findings are compared to OC transfers estimated for the Himalaya, where OC petro oxidation in the mountain belt remains unconstrained. Together, these cases suggest that mountain building in the tropics can result in a net sink of OC which sequesters atmospheric CO 2 . [ABSTRACT FROM AUTHOR]

We investigate the routing and transfer of particulate organic carbon (POC) from the western Southern Alps, New Zealand, using organic carbon (Corg) and nitrogen (Norg) concentrations and stable carbon isotopes (δ13Corg). In this active mountain belt, sediment discharge is dominated by landslide-derived material. Landsliding acts to homogenize the geochemically diverse hillslope POC, mixing POC from the standing biomass and soil with the fossil POC from bedrock. As a result, the POC in river sediment at the mountain front is a binary mixture of fossil and nonfossil carbon sourced from many landslide deposits. We calculate that nonfossil biogenic POC makes up 63 ± 7% of the total POC in the suspended load of rivers draining the western Southern Alps. The erosional flux of biogenic POC from these catchments represents a transfer of 39 tC km-2 a-1 of atmospheric CO2 averaged over the west flank of the mountain belt. If more than 10% of this POC is preserved in sediments on geological timescales, then this process is the most significant way in which the Southern Alps and similar, tectonically active mountain belts with restricted alluvial aprons consume atmospheric CO2. [ABSTRACT FROM AUTHOR]

Abstract: Rapidly eroding, coastal mountain belts, where steep rivers and submarine channels connect upland sources to nearby marine sinks are hotspots of organic carbon transfer from life biomass, soil and exhumed bedrock into geological storage. Using observations from the Southern Alps of New Zealand, and Taiwan, we have mapped this organic pathway to geological carbon sequestration, and can evaluate the magnitude and efficiency of transfers between sources and sinks. We demonstrate that POC is harvested by landsliding, but importantly also by common and widespread surface runoff on steep hillslopes. Although terrestrially sourced POC is found in many sedimentary environments associated with mountain belts and frontier basins, it appears to be most abundantly trapped and preserved in marine turbidites. The loss of all forms of POC in onward transport through short, steep routing systems to this repository is limited. This is in marked contrast to larger routing systems, in which only the most resilient forms of POC survive into long-term deposition. [Copyright &y& Elsevier]