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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 organic carbon to the deep sea is comparatively overlooked. Among systems that connect coastal to deep-sea environments, the submarine Congo Canyon is of particular interest since the canyon head starts 30 km into the Congo River estuary, which delivers ∼7 % of the dissolved and particulate organic carbon from the world's rivers. However, sediment and particulate organic carbon 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 submarine Congo 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 ms-1) through the water column, keeping muds in suspension, with a net upslope transport direction. Second, fast-moving (up to 8 ms-1) turbidity currents occur for 35 % of the time during monitoring periods and transport particulate organic carbon with mud and sand at an estimated transit flux that is more than 3 to 6 times the flux induced by tides. 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 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. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

Soils of the northern high latitudes store carbon over millennial timescales (thousands of years) and contain approximately double the carbon stock of the atmosphere (1-3). Warming and associated permafrost thaw can expose soil organic carbon and result in mineralization and carbon dioxide (C[O.sub.2]) release (4-6). However, some of this soil organic carbon may be eroded and transferred to rivers (7-9). If it escapes degradation during river transport and is buried in marine sediments, then it can contribute to a longer-term (more than ten thousand years), geological C[O.sub.2] sink (8-10). Despite this recognition, the erosional flux and fate of particulate organic carbon (POC) in large rivers at high latitudes remains poorly constrained. Here, we quantify the source of POC in the Mackenzie River, the main sediment supplier to the Arctic Ocean (11, 12), and assess its flux and fate. We combine measurements of radiocarbon, stable carbon isotopes and element ratios to correct for rock-derived POC (10, 13, 14). Our samples reveal that the eroded biospheric POC has resided in the basin for millennia, with a mean radiocarbon age of 5,800 ± 800 years, much older than the POC in large tropical rivers (13, 14). From the measured biospheric POC content and variability in annual sediment yield (15), we calculate a biospheric POC flux of [2.2.sup.+1.3.sub.-0.9] teragrams of carbon per year from the Mackenzie River, which is three times the C[O.sub.2] draw down by silicate weathering in this basin (16). Offshore, we find evidence for efficient terrestrial organic carbon burial over the Holocene period, suggesting that erosion of organic carbon-rich, high-latitude soils may result in an important geological C[O.sub.2] sink., Photosynthesis and the production of organic carbon by the terrestrial biosphere (O[C.sub.biosphere]) is a major pathway of atmospheric C[O.sub.2] drawdown. Over millennial timescales, some O[C.sub.biosphere] escapes oxidation and contributes to [...]

The Yellow River is one of the largest suppliers of sediments and organic carbon (OC) to the ocean. Previous studies have revealed that OC transported by the Yellow River largely derives from the erosion of the Chinese Loess Plateau, which is dominated by pre-aged soil carbon and could be efficiently preserved in marine sediments. Here, we used ramped oxidation radiocarbon analysis (RPO-14C) to characterize the age and reactivity distribution of OC in two Yellow River suspended sediment samples and six Bohai Sea and Yellow Sea (BS–YS) surface sediments from a transect along the sediment transport pathway. RPO-14C independently characterizes the full spectrum of OC thermal stability and isotope compositions to reveal the source, age and reactivity structure of OC transported by the Yellow River and preserved in Chinese marginal sea sediments. We calculated the activation energy (E) distribution—a proxy for bonding environment and by extension reactivity—which, combined with 14C and stable carbon isotope (δ 13C) compositions, reveals OC origin and stability. Our data suggest that 96% of OC in Yellow River suspended sediments is biospheric and weathered petrogenic, while unweathered petrogenic OC only accounts for 4% which is almost an order of magnitude lower than the fossil OC estimates (32%) based on compound specific 14C analysis. RPO data reveal the prevalence of aged biospheric loess OC in the Yellow River. We use δ 13C, 14C and RPO-derived activation energy data to quantify the contribution of terrestrial OC to surface sediments in the BS–YS. The resulting estimates of terrestrial OC proto-burial efficiencies yield an average value of 89 ± 30%, revealing overall very high terrestrial OC preservation in the BS–YS. Additionally, and somewhat counter intuitively, we find that the preservation of terrestrial OC decreases with increasing E. This pattern may arise from an enhanced preservation of a pre-aged C 4 plants derived fraction of the loess-derived OC associated with secondary clays characterized by smaller grain size and higher surface area. Alternatively, the high E component of the Yellow River OC might comprise partially weathered petrogenic carbon, undergoing further mineralization during transport from rivers to marginal sea sediments via marine organic matter priming. • RPO-14C characterizes the age and reactivity distribution of Yellow River particulate OC (POC). • Yellow River POC is dominated by millennial aged OC bio with mid to high thermal-stability. • The proto-burial efficiency of Yellow River POC in marine sediments is 89 ± 30%. [ABSTRACT FROM AUTHOR]

The hydrologic response to climate forcing in the Indo-Pacific warm pool region has varied spatially over the past 25,000 years. For example, drier conditions are inferred on Java and Borneo for the period following the end of the Last Glacial Maximum, whereas wetter conditions are reconstructed for northwest Australia. The response of vegetation to these past rainfall variations is poorly constrained. Using a suite of 30 surface marine sediment samples from throughout the Indo-Pacific warm pool, we demonstrate that today the stable isotopic composition of vascular plant fatty acids (δ13Cfa) reflects the regional vegetation composition. This in turn is controlled by the seasonality of rainfall consistent with dry season water stress. Applying this proxy in a sediment core from offshore northeast Borneo, we show broadly similar vegetation cover during the Last Glacial Maximum and the Holocene, suggesting that, despite generally drier glacial conditions, there was no pronounced dry season. In contrast, δ13Cfa and pollen data from a core off the coast of Sumba indicate an expansion of C4 herbs during the most recent glaciation, implying enhanced aridity and water stress during the dry season. Holocene vegetation trends are also consistent with a response to dry season water stress. We therefore conclude that vegetation in tropical monsoon regions is susceptible to increases in water stress arising from an enhanced seasonality of rainfall, as has occurred in past decades. [ABSTRACT FROM AUTHOR]

Abstract: Organic matter carried by rivers and deposited in continental and marine sediments contains valuable information on past environmental conditions and their impact on the terrestrial biosphere. In order to use sedimentary records to reconstruct past environmental conditions on the continents, such as vegetation cover and type, or precipitation intensity, we need to understand the provenance of the organic signatures and how they are transferred, and potentially modified, by fluvial transport to the sedimentary reservoir. In particular, we need to understand how environmental conditions are imprinted in the composition of riverine particulate organic carbon. Here we investigate the stable carbon and hydrogen isotopic signatures of vascular plant leaf wax biomarkers in the modern-day Ganges and Brahmaputra river complex, one of the largest fluvial systems on Earth. The distribution of n-alkanes and n-alkanoic acids in Ganges–Brahmaputra river sediments suggests that vascular plant inputs are consistently a significant component of the organic carbon pool. Molecular δ13C measurements reveal that C3 vegetation inputs delivered by the Himalayan rivers are partly degraded and replaced by mixed C3/C4 vegetation input in the floodplain. The hydrogen isotopic composition of long-chain (C24+) n-alkanoic acids, in combination with their stable C isotopic composition, provides constraints on the isotopic composition of the environmental water used by higher plants within the drainage basin. Calculated compositions compare well with the depleted δD isotopic ratios of the river water during the summer monsoon, suggesting that H-isotopic compositions of long-chain alkanoic acids are a valuable proxy for the composition of summer monsoon moisture in the Ganges–Brahmaputra basin. Detailed studies of the “isotopic anatomy” of modern river systems are critical for informed interpretation of marine sedimentary records in river-influenced continental margins. [Copyright &y& Elsevier]

• Global compilation of compound-specific n -alkyl lipid 14C data. • Intrinsic and extrinsic processes determine the plant wax 14C composition. • Plant wax mean age primarily controlled by temperature and precipitation. Sedimentary high molecular weight (HMW) n -alkyl lipids derived from the waxes of terrestrial plants are common target compounds in biogeochemical and paleoenvironmental research. These plant waxes derive predominantly from the epicuticular cover of vascular plant leaves and their relative and absolute abundances and stable isotopic composition can be used as proxies to decipher, e.g., continental climate and land-ocean carbon transfer processes. In marine sediments, however, compound-specific radiocarbon analysis has revealed that plant waxes are often not syn -depositional, but instead are substantially 14C-depleted ('pre-aged') upon deposition. This 14C-depletion can be caused by various processes that either promote retention of plant waxes during transport from source to sink such as storage in soils or entrainment in deposition-resuspension loops in rivers and on continental shelves or, alternatively, by processes that add HMW n -alkyl lipids from other sources (e.g., petrogenic inputs). Here, we review the intrinsic and extrinsic processes affecting the sedimentary plant wax 14C composition (ranging from chemical processes to continental-scale environmental conditions), how plant wax 14C compositions translate into mean ages, and which processes control plant wax mean ages in marine sediments. Finally, we use a compilation of available and new compound-specific plant wax 14C data to provide a synthesis and evaluate the major controls on plant wax mean ages in marine sediments at the global scale. [ABSTRACT FROM AUTHOR]