A new feature is the data set quality control (QC) flag of E for data from alternative sensors and platforms. The accuracy of surface water f CO 2 has been defined for all data set QC flags. Automated range checking has been carried out for all data sets during their upload into SOCAT. The upgrade of the interactive Data Set Viewer (previously known as the Cruise Data Viewer) allows better interrogation of the SOCAT data collection and rapid creation of high-quality figures for scientific presentations. Automated data upload has been launched for version 4 and will enable more frequent SOCAT releases in the future. Highprofile scientific applications of SOCAT include quantification of the ocean sink for atmospheric carbon dioxide and its long-term variation, detection of ocean acidification, as well as evaluation of coupled-climate and ocean-only biogeochemical models. Users of SOCAT data products are urged to acknowledge the contribution of data providers, as stated in the SOCAT Fair Data Use Statement. This ESSD (Earth System Science Data) "living data" publication documents the methods and data sets used for the assembly of this new version of the SOCAT data collection and compares these with those used for earlier versions of the data collection Sabine et al., 2013;Bakker et al., 2014). Individual data set files, included in the synthesis product, can be downloaded here: doi:10.1594/PANGAEA.849770. The gridded products are available here:

The Arctic icescape is rapidly transforming from a thicker multiyear ice cover to a thinner and largely seasonal first-year ice cover with significant consequences for Arctic primary production. One critical challenge is to understand how productivity will change within the next decades. Recent studies have reported extensive phytoplankton blooms beneath ponded sea ice during summer, indicating that satellite-based Arctic annual primary production estimates may be significantly underestimated. Here we present a unique time-series of a phytoplankton spring bloom observed beneath snow-covered Arctic pack ice. The bloom, dominated by the haptophyte algae Phaeocystis pouchetii, caused near depletion of the surface nitrate inventory and a decline in dissolved inorganic carbon by 16 ± 6 g C m−2. Ocean circulation characteristics in the area indicated that the bloom developed in situ despite the snow-covered sea ice. Leads in the dynamic ice cover provided added sunlight necessary to initiate and sustain the bloom. Phytoplankton blooms beneath snow-covered ice might become more common and widespread in the future Arctic Ocean with frequent lead formation due to thinner and more dynamic sea ice despite projected increases in high-Arctic snowfall. This could alter productivity, marine food webs and carbon sequestration in the Arctic Ocean.

Borealization of the Arctic Ocean future suggests that Arctic borealization will continue under scenarios of global warming. Results from this synthesis further our understanding of the Arctic Ocean's complex and sometimes non-intuitive Arctic response to climate forcing by identifying new feedbacks in the atmosphere-ice-ocean system in which borealization plays a key role.

During a year-round occupation of Amundsen Gulf in the Canadian Arctic Archipelago dissolved inorganic and organic carbon (DIC, DOC), total alkalinity (TA), partial pressure of CO 2 (pCO 2 ) and related parameters were measured over a full annual cycle. A two-box model was used to identify and assess physical, biological, and chemical processes responsible for the seasonal variability of DIC, DOC, TA, and pCO 2 . Surface waters were undersaturated with respect to atmospheric CO 2 throughout the year and constituted a net sink of 1.2 mol C m 22 yr 21 , with ice coverage and ice formation limiting the CO 2 uptake during winter. CO 2 uptake was largely driven by under ice and open-water biological activity, with high subsequent export of organic matter to the deeper water column. Annual net community production (NCP) was 2.1 mol C m 22 yr 21 . Approximately one-half of the overall NCP during the productive season (4.1 mol C m 22 from Apr through Aug) was generated by under-ice algae and amounted to 1.9 mol C m 22 over this period. The surface layer was autotrophic, while the overall heterotrophy of the system was fueled by either sedimentary or lateral inputs of organic matter.

Abstract. The Surface Ocean CO 2 Atlas (SOCAT), an activity of the international marine carbon research community, provides access to synthesis and gridded f CO 2 (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 f CO 2 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.

Abstract. Freshwater discharge from glaciers is increasing across the Arctic in response to anthropogenic climate change, which raises questions about the potential downstream effects in the marine environment. Whilst a combination of long-term monitoring programmes and intensive Arctic field campaigns have improved our knowledge of glacier–ocean interactions in recent years, especially with respect to fjord/ocean circulation, there are extensive knowledge gaps concerning how glaciers affect marine biogeochemistry and productivity. Following two cross-cutting disciplinary International Arctic Science Committee (IASC) workshops addressing the importance of glaciers for the marine ecosystem, here we review the state of the art concerning how freshwater discharge affects the marine environment with a specific focus on marine biogeochemistry and biological productivity. Using a series of Arctic case studies (Nuup Kangerlua/Godthåbsfjord, Kongsfjorden, Kangerluarsuup Sermia/Bowdoin Fjord, Young Sound and Sermilik Fjord), the interconnected effects of freshwater discharge on fjord–shelf exchange, nutrient availability, the carbonate system, the carbon cycle and the microbial food web are investigated. Key findings are that whether the effect of glacier discharge on marine primary production is positive or negative is highly dependent on a combination of factors. These include glacier type (marine- or land-terminating), fjord–glacier geometry and the limiting resource(s) for phytoplankton growth in a specific spatio-temporal region (light, macronutrients or micronutrients). Arctic glacier fjords therefore often exhibit distinct discharge–productivity relationships, and multiple case-studies must be considered in order to understand the net effects of glacier discharge on Arctic marine ecosystems.

In order to investigate the effect of glacial water on the CO 2 system in the fjord, we studied the variability of the total alkalinity (A T ), total dissolved inorganic carbon (C T ), dissolved inorganic nutrients, oxygen isotopic ratio (d 18 O), and freshwater fractions from the glacier front to the outer Tempelfjorden on Spitsbergen in winter 2012 (January, March, and April) and 2013 (April) and summer/fall 2013 (September).The two contrasting years clearly showed that the influence of freshwater, mixing, and haline convection affected the chemical and physical characteristics of the fjord. The seasonal variability showed the lowest calcium carbonate saturation state (X) and pH values in March 2012 coinciding with the highest freshwater fractions. The highest X and pH were found in September 2013, mostly due to CO 2 uptake during primary production. Overall, we found that increased freshwater supply decreased X, pH, and A T . On the other hand, we observed higher A T relative to salinity in the freshwater end-member in the mild and rainy winter of 2012 (1142 lmol kg 21 ) compared to A T in 2013 (526 lmol kg 21 ). Observations of calcite and dolomite crystals in the glacial ice suggested supply of carbonate-rich glacial drainage water to the fjord. This implies that winters with a large amount of glacial drainage water partly provide a lessening of further ocean acidification, which will also affect the air-sea CO 2 exchange.

[1] From sea-ice formation in November 2007 to onset of ice melt in May 2008, we studied the carbonate system in first-year Arctic sea ice, focusing on the impact of calcium-carbonate (CaCO 3 ) saturation states of aragonite (XAr) and calcite (XCa) at the ice-water interface (UIW). Based on total inorganic carbon (C T ) and total alkalinity (A T ), and derived pH, CO 2 , carbonate ion ( [CO 3 22 ]) concentrations and X, we investigated the major drivers such as brine rejection, CaCO 3 precipitation, bacterial respiration, primary production and CO 2 -gas flux in sea ice, brine, frost flowers and UIW. We estimated large variability in sea-ice C T at the top, mid, and bottom ice. Changes due to CaCO 3 and CO 2 -gas flux had large impact on C T in the whole ice core from March to May, bacterial respiration was important at the bottom ice during all months, and primary production in May. It was evident that the sea-ice processes had large impact on UIW, resulting in a five times larger seasonal amplitude of the carbonate system, relative to the upper 20 m. During ice formation, [CO 2 ] increased by 30 mmol kg 21 , [CO 3 22 ] decreased by 50 mmol kg 21, and the XAr decreased by 0.8 in the UIW due to CO 2 -enriched brine from solid CaCO 3 . Conversely, during ice melt, [CO 3 22 ] increased by 90 mmol kg 21 in the UIW, and X increased by 1.4 between March and May, likely due to CaCO 3 dissolution and primary production. We estimated that increased ice melt would lead to enhanced oceanic uptake of inorganic carbon to the surface layer.