Search

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO(2)) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 +/- 4.7 Tg C yr(-1) over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermally-driven, air-sea fCO(2) gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 +/- 3.1 Tg C yr(-1), while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 +/- 6.0 Tg C yr(-1)).

Shelf seas play an important role in the global carbon cycle, absorbing atmospheric carbon dioxide (CO2) and exporting carbon (C) to the open ocean and sediments. The magnitude of these processes is poorly constrained, because observations are typically interpolated over multiple years. Here, we used 298500 observations of CO2 fugacity (fCO2) from a single year (2015), to estimate the net influx of atmospheric CO2 as 26.2 ± 4.7 Tg C yr−1 over the open NW European shelf. CO2 influx from the atmosphere was dominated by influx during winter as a consequence of high winds, despite a smaller, thermally-driven, air-sea fCO2 gradient compared to the larger, biologically-driven summer gradient. In order to understand this climate regulation service, we constructed a carbon-budget supplemented by data from the literature, where the NW European shelf is treated as a box with carbon entering and leaving the box. This budget showed that net C-burial was a small sink of 1.3 ± 3.1 Tg C yr−1, while CO2 efflux from estuaries to the atmosphere, removed the majority of river C-inputs. In contrast, the input from the Baltic Sea likely contributes to net export via the continental shelf pump and advection (34.4 ± 6.0 Tg C yr−1).

Biogeochemical variations of surface water in the Northeast Atlantic (Bay of Biscay) were examined using high-frequency underway measurements combined with monthly sampling of carbon-related variables. The mechanisms controlling seasonal CO2 variability were investigated by distinguishing the contributions of biological and physical processes to the monthly changes in dissolved inorganic carbon (DIC) and partial pressure of CO2 (pCO2). The seasonality of DIC (47–81 µmol kg−1) had a single peak with a winter maximum primarily driven by vertical mixing and a summer minimum driven by spring biological removal. Non-Redfield C:N uptake was observed in the nutrient-depleted summer but not during the spring bloom. In the North Atlantic, pCO2 seasonality shows a latitudinal transition: from the temperature-dominated oligotrophic subtropical gyre to the subpolar region where pCO2 is dominated by changing concentrations of DIC. In the midlatitude Bay of Biscay, the annual cycle of pCO2 (61–75 µatm) showed a double-peak distribution. The summer pCO2 peak was mainly driven by temperature increase, while the winter peak resulted from the dominant effect of entrainment of subsurface water. Interannual variations of DIC were more pronounced in winter and were driven by the changes in the strength of winter mixing. Higher wintertime concentrations and seasonal amplitudes of DIC were observed in cold years when the mixed-layer depths were deeper, which appears to be associated with negative phases of the North Atlantic Oscillation. The Bay of Biscay shows a decrease of CO2 uptake in 2008–2010 (−0.97 and −0.75 mol m−2 yr−1) compared to 2002–2004 (−1.47 and −1.68 mol m−2 yr−1).