Climate change is expected to have a strong effect on the Eastern Siberian Arctic Shelf (ESAS) region, which includes 40% of the Arctic shelves and comprises the Laptev and East Siberian seas. The largest organic carbon pool, the dissolved organic carbon (DOC), may change significantly due to changes in both riverine inputs and transformation rates; however, the present DOC inventories and transformation patterns are poorly understood. Using samples from the International Siberian Shelf Study 2008, this study examines for the first time DOC removal in Arctic shelf waters with residence times that range from months to years. Removals of up to 10%–20% were found in the Lena River estuary, consistent with earlier studies in this area, where surface waters were shown to have a residence time of approximately 2 months. In contrast, the DOC concentrations showed a strong nonconservative pattern in areas with freshwater residence times of several years. The average losses of DOC were estimated to be 30%–50% during mixing along the shelf, corresponding to a first‐order removal rate constant of 0.3 yr−1. These data provide the first observational evidence for losses of DOC in the Arctic shelf seas, and the calculated DOC deficit reflects DOC losses that are higher than recent model estimates for the region. Overall, a large proportion of riverine DOC is removed from the surface waters across the Arctic shelves. Such significant losses must be included in models of the carbon cycle for the Arctic Ocean, especially since the breakdown of terrestrial DOC to CO2 in Arctic shelf seas may constitute a positive feedback mechanism for Arctic climate warming. These data also provide a baseline for considering the effects of future changes in carbon fluxes, as the vast northern carbon‐rich permafrost areas draining into the Arctic are affected by global warming.
The Lena River integrates biogeochemical signals from its vast drainage basin, and the integrated signal reaches far out over the Arctic Ocean. Transformation of riverine organic carbon (OC) into mineral carbon, and mineral carbon into the organic form in the Lena River watershed, can be considered to be quasi-steady-state processes. An increase in Lena discharge exerts opposite effects on total organic (TOC) and total inorganic (TCO2) carbon: TOC concentration increases, while TCO2 concentration decreases. Significant inter-annual variability in mean values of TCO2, TOC, and their sum (total carbon, TC) has been found. This variability is determined by changes in land hydrology which cause differences in the Lena River discharge. There is a negative correlation in the Lena River between TC in September and its mean discharge in August; a time shift of about one month is required for water to travel from Yakutsk to the Laptev Sea. Total carbon entering the sea with the Lena discharge is estimated to be almost 10 Tg C yr−1. The annual Lena River discharge of particulate organic carbon (POC) can be as high as 0.38 Tg (moderate to high estimate). If we instead accept Lisytsin's (1994) statement that 85–95 % of total particulate matter (PM) (and POC) precipitates on the marginal "filter", then only about 0.03–0.04 Tg of Lena River POC reaches the Laptev Sea. The Lena's POC export would then be two orders of magnitude less than the annual input of eroded terrestrial carbon onto the shelf of the Laptev and East Siberian seas, which is estimated to be about 4 Tg. Observations support the hypothesis of a dominant role for coastal erosion (Semiletov, 1999a, b) in East Siberian Arctic Shelf (ESAS) sedimentation and the dynamics of the carbon/carbonate system. The Lena River is characterized by relatively high concentrations of the primary greenhouse gases, dissolved carbon dioxide (CO2) and methane (CH4). During all seasons the river is supersaturated in CO2 compared to the atmosphere, by up to 1.5–2 fold in summer, and 4–5 fold in winter. This results in a significant CO2 supersaturation in the adjacent coastal sea. Localized areas of dissolved CH4 along the Lena River and in the Lena delta channels may reach 100 nM, but the CH4 concentration decreases to 5–20 nM towards the sea, which suggests that riverborne export of CH4 plays but a minor role in determining the ESAS CH4 budget in coastal waters. Instead, the seabed appears to be the source that provides most of the CH4 to the Arctic Ocean.