Description: High biological activity causes a distinct seasonality of surface water pH in the North Sea, which is a strong sink for atmospheric CO2 via an effective shelf pump. The intimate connection between the North Sea and the North Atlantic Ocean suggests that the variability of the CO2 system of the North Atlantic Ocean may, in part, be responsible for the observed variability of pH and CO2 in the North Sea. In this work, we demonstrate the role of the North Atlantic Oscillation (NAO), the dominant climate mode for the North Atlantic, in governing this variability. Based on three extensive observational records covering the relevant levels of the NAO index, we provide evidence that the North Sea pH and CO2 system strongly responds to external and internal expressions of the NAO. Under positive NAO, the higher rates of inflow of water from the North Atlantic Ocean and the Baltic outflow lead to a strengthened north-south biogeochemical divide. The limited mixing between the north and south leads to a steeper gradient in pH and partial pressure of CO2 (pCO2) between the two regions in the productive period. This is exacerbated further when coinciding with higher sea surface temperature, which concentrates the net community production in the north through shallower stratification. These effects can be obscured by changing properties of the constituent North Sea water masses, which are also influenced by NAO. Our results highlight the importance of examining interannual trends in the North Sea CO2 system with consideration of the NAO state.

Description: The 3-d coupled physical–biogeochemical model ECOHAM (version 3) was applied to the Northwest-European Shelf (47°41′–63°53′N, 15°5′W–13°55′E) for the years 1993–1996. Carbon fluxes were calculated for the years 1995 and 1996 for the inner shelf region, the North Sea (511,725 km2). This period was chosen because it corresponds to a shift from a very high winter-time North Atlantic Oscillation Index (NAOI) in 1994/1995, to an extremely low one in 1995/1996, with consequences for the North Sea physics and biogeochemistry. During the first half of 1996, the observed mean SST was about 1 °C lower than in 1995; in the southern part of the North Sea the difference was even larger (up to 3 °C). Due to a different wind regime, the normally prevailing anti-clockwise circulation, as found in winter 1995, was replaced by more complicated circulation patterns in winter 1996. Decreased precipitation over the drainage area of the continental rivers led to a reduction in the total (inorganic and organic) riverine carbon load to the North Sea from 476 Gmol C yr−1 in 1995 to 340 Gmol C yr−1 in 1996. In addition, the North Sea took up 503 Gmol C yr−1 of CO2 from the atmosphere. According to our calculations, the North Sea was a sink for atmospheric CO2, at a rate of 0.98 mol C m−2 yr−1, for both years. The North Sea is divided into two sub-systems: the shallow southern North Sea (SNS; 190,765 km2) and the deeper northern North Sea (NNS; 320,960 km2). According to our findings the SNS is a net-autotrophic system (net ecosystem production NEP〉0) but released CO2 to the atmosphere: 159 Gmol C yr−1 in 1995 and 59 Gmol C yr−1 in 1996. There, the temperature-driven release of CO2 outcompetes the biological CO2 drawdown. In the NNS, where respiratory processes prevail (NEP〈0), 662 and 562 Gmol C yr−1 were taken up from the atmosphere in 1995 and 1996, respectively. Stratification separates the productive, upper layer from the deeper layers of the water column where respiration/remineralization takes place. Duration and stability of the stratification are determined by the meteorological conditions, in relation to the NAO. Our results suggest that this mechanism controlling the nutrient supply to the upper layer in the northern and central North Sea has a larger impact on the carbon fluxes than changes in lateral transport due to NAOI variations. The North Sea as a whole imports organic carbon and exports inorganic carbon across the outer boundaries, and was found to be net-heterotrophic, more markedly in 1996 than in 1995.

Description: The Surface Ocean CO2 Atlas (SOCAT), an activity of the international marine carbon research community, provides access to synthesis and gridded fCO2 (fugacity of carbon dioxide) products for the surface oceans. Version 2 of SOCAT is an update of the previous release (version 1) with more data (increased from 6.3 million to 10.1 million surface water fCO2 values) and extended data coverage (from 1968-2007 to 1968-2011). The quality control criteria, while identical in both versions, have been applied more strictly in version 2 than in version 1. The SOCAT website (http://www.socat.info/) has links to quality control comments, metadata, individual data set files, and synthesis and gridded data products. Interactive online tools allow visitors to explore the richness of the data. Applications of SOCAT include process studies, quantification of the ocean carbon sink and its spatial, seasonal, year-to-year and longerterm variation, as well as initialisation or validation of ocean carbon models and coupled climate-carbon models.

Description: Author Posting. © American Geophysical Union, 2005. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 110 (2005): C09S16, doi:10.1029/2004JC002601.

Description: Comparison of eight iron experiments shows that maximum Chl a, the maximum DIC removal, and the overall DIC/Fe efficiency all scale inversely with depth of the wind mixed layer (WML) defining the light environment. Moreover, lateral patch dilution, sea surface irradiance, temperature, and grazing play additional roles. The Southern Ocean experiments were most influenced by very deep WMLs. In contrast, light conditions were most favorable during SEEDS and SERIES as well as during IronEx-2. The two extreme experiments, EisenEx and SEEDS, can be linked via EisenEx bottle incubations with shallower simulated WML depth. Large diatoms always benefit the most from Fe addition, where a remarkably small group of thriving diatom species is dominated by universal response of Pseudo-nitzschia spp. Significant response of these moderate (10–30 μm), medium (30–60 μm), and large (〉60 μm) diatoms is consistent with growth physiology determined for single species in natural seawater. The minimum level of “dissolved” Fe (filtrate 〈 0.2 μm) maintained during an experiment determines the dominant diatom size class. However, this is further complicated by continuous transfer of original truly dissolved reduced Fe(II) into the colloidal pool, which may constitute some 75% of the “dissolved” pool. Depth integration of carbon inventory changes partly compensates the adverse effects of a deep WML due to its greater integration depths, decreasing the differences in responses between the eight experiments. About half of depth-integrated overall primary productivity is reflected in a decrease of DIC. The overall C/Fe efficiency of DIC uptake is DIC/Fe ∼ 5600 for all eight experiments. The increase of particulate organic carbon is about a quarter of the primary production, suggesting food web losses for the other three quarters. Replenishment of DIC by air/sea exchange tends to be a minor few percent of primary CO2 fixation but will continue well after observations have stopped. Export of carbon into deeper waters is difficult to assess and is until now firmly proven and quite modest in only two experiments.

Description: This research was supported by the European Union through programs CARUSO (1998– 2001), IRONAGES (1999 –2003), and COMET (2000–2003); the Netherlands- Bremen Oceanography program NEBROC-1; and the Netherlands Organization for Research NWO through the Netherlands Antarctic Program project FePath. Both the U.S. National Science Foundation and the U.S. Department of Energy provided significant support for the SOFeX program. M.R.L. acknowledges the U.S. National Science Foundation for support of IronEx and SOFeX projects and related studies (OCE-9912230, -9911765, and -0322074).

Description: Author Posting. © American Geophysical Union, 2007. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Global Biogeochemical Cycles 21 (2007): GB4001, doi:10.1029/2006GB002825.

Description: New observations from the North Sea, a NW European shelf sea, show that between 2001 and 2005 the CO2 partial pressure (pCO2) in surface waters rose by 22 μatm, thus faster than atmospheric pCO2, which in the same period rose approximately 11 μatm. The surprisingly rapid decline in air-sea partial pressure difference (ΔpCO2) is primarily a response to an elevated water column inventory of dissolved inorganic carbon (DIC), which, in turn, reflects mostly anthropogenic CO2 input rather than natural interannual variability. The resulting decline in the buffering capacity of the inorganic carbonate system (increasing Revelle factor) sets up a theoretically predicted feedback loop whereby the invasion of anthropogenic CO2 reduces the ocean's ability to uptake additional CO2. Model simulations for the North Atlantic Ocean and thermodynamic principles reveal that this feedback should be stronger, at present, in colder midlatitude and subpolar waters because of the lower present-day buffer capacity and elevated DIC levels driven either by northward advected surface water and/or excess local air-sea CO2 uptake. This buffer capacity feedback mechanism helps to explain at least part of the observed trend of decreasing air-sea ΔpCO2 over time as reported in several other recent North Atlantic studies.

Description: S. Doney and I. Lima were supported by NSF/ONR NOPP (N000140210370) and NASA (NNG05GG30G).