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Collapse of permafrost coasts delivers large quantities of particulate organic carbon (POC) to Arctic coastal areas. With rapidly changing environmental conditions, sediment and organic carbon (OC) mobilization and transport pathways are also changing. Here, we assess the sources and sinks of POC in the highly dynamic nearshore zone of Herschel Island‐Qikiqtaruk (Yukon, Canada). Our results show that POC concentrations sharply decrease, from 15.9 to 0.3 mg L−1, within the first 100–300 m offshore. Simultaneously, radiocarbon ages of POC drop from 16,400 to 3,600 14C years, indicating rapid settling of old permafrost POC to underlying sediments. This suggests that permafrost OC is, apart from a very narrow resuspension zone (, Key Points Suspended particulate organic carbon (POC) sharply decreases in age and concentration within the nearshore zoneBeyond a narrow resuspension zone, permafrost‐derived OC dominates surface sediments, whereas much younger OC is found in the water columnPermafrost‐derived POC is rapidly removed from the water column, showing the critical role of nearshore dynamics for OC transport

Arctic rivers will be increasingly affected by the hydrological and biogeochemical consequences of thawing permafrost. During transport, permafrost-derived organic carbon (OC) can either accumulate in floodplain and shelf sediments or be degraded into greenhouse gases prior to final burial. Thus, the net impact of permafrost OC on climate will ultimately depend on the interplay of complex processes that occur along the source-to-sink system. Here, we focus on the Kolyma River, the largest watershed completely underlain by continuous permafrost, and marine sediments of the East Siberian Sea, as a transect to investigate the fate of permafrost OC along the land-ocean continuum. Three pools of riverine OC were investigated for the Kolyma main stem and five of its tributaries: dissolved OC (DOC), suspended particulate OC (POC), and riverbed sediment OC (SOC). They were compared with earlier findings in marine sediments. Carbon isotopes (δ13C, Δ14C), lignin phenol, and lipid biomarker proxies show a contrasting composition and degradation state of these different carbon pools. Dual C isotope source apportionment calculations imply that old permafrost-OC is mostly associated with sediments (SOC; contribution of 68±10%), and less dominant in POC (38±8%), whereas autochthonous primary production contributes around 44±10% to POC in the main stem and up to 79±11 % in tributaries. Biomarker degradation indices suggest that Kolyma DOC might be relatively degraded, regardless of its generally young age shown by previous studies. In contrast, SOC shows the lowest Δ14C value (oldest OC), yet relatively fresh compositional signatures. Furthermore, decreasing mineral surface area-normalised OC- and biomarker loadings suggest that SOC might be reactive along the land-ocean continuum and almost all parameters were subjected to rapid change when moving from freshwater to the marine environment. This suggests that sedimentary dynamics play a crucial role when targeting permafrost-derived OC in aquatic systems and support earlier studies highlighting the fact that the land-ocean transition zone is an efficient reactor and a dynamic environment. The prevailing inconsistencies between freshwater and marine research (i.e. targeting predominantly DOC and SOC respectively) need to be better aligned in order to determine to what degree thawed permafrost OC may be destined for long-term burial, thereby attenuating further global warming., Biogeosciences, 20 (1), ISSN:1726-4170

Soil temperatures in permafrost (i.e. perennially frozen ground) are rising globally. The increasing temperatures accelerate permafrost thaw and release of organic carbon, that has been locked in permafrost soils since the last glacial period, to the contemporary carbon cycle. The potential remineralisation of organic carbon to greenhouse gases can contribute to further climate warming. Particulate organic carbon (POC) in the Kolyma River is older than dissolved organic carbon (DOC) thus serves as a good tracer for abrupt permafrost thaw (i.e. river bank erosion and thermokarst) that dominantly releases old POC. While dissolved organic carbon (DOC) mobilised from the old Yedoma outcrops on the banks of the Kolyma River is shown to be highly labile, vulnerability of POC to biodegradation is not yet known. In this study we aim to constrain degradation rates for POC in the Kolyma River. To capture seasonal variability of the POC pool and its degradation rate the incubation was conducted both during the spring freshet and in late summer (2019 and 2018, respectively). We incubated whole-water samples over 9 to 15 days and quantified POC (and DOC) loss over time, as well as dissolved inorganic carbon (DIC). The incubation was carried out in the dark. We also tracked changes in POC composition and age with carbon isotopes (d13C-OC, d13C-DIC, ∆14C). Preliminary results from 2018 suggest a decrease in POC concentrations of up to 30 % while those of DOC decrease by up to 11 %. The rate of POC degradation is nearly three times faster than DOC though the absolute amounts of DOC are in turn higher than those of POC (< 1 mg L-1 for POC and ~3 mg L-1 for DOC). Furthermore, the changes in d13C of POC, DOC and DIC suggest ongoing microbial degradation and conversion of organic carbon into inorganic carbon. These first estimates show that POC degrades fairly rapidly while transported in the Kolyma River. A better understanding of POC degradation along lateral flow paths is critical for improving our knowledge of permafrost thaw and its possible climate impacts in the future., EGUsphere

Arctic rivers will be increasingly affected by the hydrological and biogeochemical effects of thawing permafrost. During transport, permafrost thaw-derived organic carbon (OC) can be degraded into greenhouse gases and potentially add to further climate warming, or transported to the shelf seas and buried in marine sediments, attenuating this ‘permafrost carbon feedback’. To assess the transport pathways and fate of permafrost-OC, we focus on the river-shelf continuum of the Kolyma River, the largest river on Earth completely underlain by continuous permafrost. Three pools of riverine OC were investigated: dissolved OC (DOC), suspended particulate OC (POC), and river sediment OC (SOC). Preliminary results of bulk carbon isotopes (δ13C, Δ14C) and molecular biomarkers (lignin phenols, leaf wax lipids) show contrasts in composition and degradation state for these carbon pools. Old permafrost-OC seems to be mostly associated with SOC, and less dominant in POC. However, while SOC shows the oldest Δ14C signal, lignin phenol results (e.g., acid to aldehyde ratios) suggest this material is the least degraded. In contrast, DOC shows more degraded signal, even at the outflow of an active permafrost thaw site. Our study serves as a terrestrial extension to earlier investigated marine sediments from the Kolyma paleoriver transect in the East Siberian Sea. It also highlights the value of connecting terrestrial and marine observations to gain insight into the complete pathway of permafrost-OC, from the moment of thaw, via aquatic transport and degradation, towards storage in marine sediments.

Massive amounts of Saharan dust are blown from the coast of northern Africa across the Atlantic Ocean towards the Americas each year. This dust has, depending on its chemistry, direct and indirect effects on global climate which include reflection and absorption of solar radiation as well as transport and deposition of nutrients and metals fertilizing both ocean and land. To determine the temporal and spatial variability of Saharan dust transport and deposition and their marine environmental effects across the equatorial North Atlantic Ocean, we have set up a monitoring experiment using deep-ocean sediment traps as well as land-based dust collectors. The sediment traps were deployed at five ocean sites along a transatlantic transect between north-west Africa and the Caribbean along 12° N, in a downwind extension of the land-based dust collectors placed at 19° N on the Mauritanian coast in Iouîk. In this paper, we lay out the setup of the monitoring experiment and present the particle fluxes from sediment trap sampling over 24 continuous and synchronized intervals from October 2012 through to November 2013. We establish the temporal distribution of the particle fluxes deposited in the Atlantic and compare chemical compositions with the land-based dust collectors propagating to the downwind sediment trap sites, and with satellite observations of Saharan dust outbreaks. First-year results show that the total mass fluxes in the ocean are highest at the sampling sites in the east and west, closest to the African continent and the Caribbean, respectively. Element ratios reveal that the lithogenic particles deposited nearest to Africa are most similar in composition to the Saharan dust collected in Iouîk. Downwind increasing Al, Fe and K contents suggest a downwind change in the mineralogical composition of Saharan dust and indicate an increasing contribution of clay minerals towards the west. In the westernmost Atlantic Ocean, admixture of re-suspended clay-sized sediments advected towards the deep sediment trap cannot be excluded. Seasonality is most prominent near both continents but generally weak, with mass fluxes dominated by calcium carbonate and clear seasonal maxima of biogenic silica towards the west. The monitoring experiment is now extended, with autonomous dust sampling buoys for better quantification of Saharan dust transport and deposition from source to sink and their impact on fertilization and carbon export to the deep ocean.

The Arctic Ocean receives an estimated amount of 40 × 1012 g organic carbon (OC) through inflow of rivers every year (Holmes et al., 2012; McClelland et al., 2016). A large part of the Arctic Ocean watershed is underlain by permafrost that experiences widescale warming exposing more OC to thaw and degradation (Biskaborn et al., 2019). Arctic Rivers will be increasingly affected by the hydrological and biogeochemical effects of thawing permafrost. During transport, permafrost-OC can be degraded into greenhouse gasses and potentially add to further climate warming (Schuur et al., 2015). However, a significant amount of this OC is transported all the way to the shelf and is buried in marine sediments, attenuating greenhouse gas emissions (Vonk & Gustafsson, 2013). The East Siberian Arctic Shelf is the largest and shallowest shelf in the Arctic Ocean (Stein & MacDonald, 2004). It receives significant amounts of terrestrial OC, delivered through coastal erosion and fluvial input (Gustafsson et al., 2011; Sánchez-García et al., 2011; Vonk et al., 2012). This region is also warming rapidly, and is strongly affected by the loss of sea ice, increasing the open water extent and wave, storm and tidal impact on the coast (Biskaborn et al., 2019; IPCC, 2014). In this study, we focus on the biogeochemical cycling of OC along the river-shelf continuum of the Kolyma river, the largest river completely underlain by continuous permafrost. To quantify the flux of OC and to link its source to its potential sink in the East Siberian Sea, we have sampled dissolved OC, particulate OC and sediment OC along a transect from an active permafrost thaw site near Cherskiy towards the outer Kolyma delta near Ambarchik. On all of these samples isotopic (δ13C, Δ14C) and molecular (lipid biomarkers, lignin phenols) analyses will be used to characterise the OC and assess its degradation status. This, in combination with published data from the East Siberian Shelf close to the Kolyma delta and earlier studies on the Kolyma river, will give us insight in the complete pathway of permafrost-OC from the moment of thaw to degradation during transport and ultimate storage in marine sediments.

Massive amounts of Saharan dust are blown from the African coast across the Atlantic Ocean towards the Americas each year. This dust has, depending on its chemistry, direct and indirect effects on global climate including reflection and absorption of solar radiation as well as transport and deposition of nutrients and metals fertilizing both ocean and land. To determine the temporal and spatial variability of Saharan dust transport and deposition and their marine environmental effects across the equatorial North Atlantic Ocean, we have set up a monitoring experiment using deep-ocean sediment traps as well as land-based dust collectors. The sediment traps were deployed at five ocean sites along a transatlantic transect between northwest Africa and the Caribbean along 12⁰ N, in a down-wind extension of the land-based dust collectors placed at 19⁰ N on the Mauritanian coast in Iwik. In this paper, we lay out the setup of the monitoring experiment and present the particle fluxes from sediment trap sampling over 24 continuous and synchronised intervals from October 2012 through to November 2013. We establish the temporal distribution of the particle fluxes deposited in the Atlantic and compare chemical compositions with the land-based dust collectors propagating to the down-wind sediment trap sites, and with satellite observations of Saharan dust outbreaks. First-year results show that the total mass fluxes in the ocean are highest at the sampling sites in the east and west, closest to the African continent and the Caribbean, respectively. Element ratios reveal that the lithogenic particles deposited nearest to Africa are most similar in composition to the Saharan dust collected in Iwik. Down-wind increasing Al, Fe and K contents suggest a downwind change in the mineralogical composition of Saharan dust and indicate an increasing contribution of clay minerals towards the west. In the westernmost Atlantic, admixture of re-suspended clay-sized sediments advected towards the deep sediment trap cannot be excluded. Seasonality is most prominent near both continents but generally weak, with mass fluxes dominated by calcium carbonate and clear seasonal maxima of biogenic silica towards the west. The monitoring experiment is now extended with autonomous dust sampling buoys for better quantification Saharan dust transport and deposition from source to sink and its impact on fertilization and carbon export to the deep ocean.