Abstract.A well-documented, publicly available, global data set of surface ocean carbon dioxide (CO 2 ) parameters has been called for by international groups for nearly two decades. The Surface Ocean CO 2 Atlas (SOCAT) project was initiated by the international marine carbon science community in 2007 with the aim of providing a comprehensive, publicly available, regularly updated, global data set of marine surface CO 2 , which had been subject to quality control (QC). Many additional CO 2 data, not yet made public via the Carbon Dioxide Information Analysis Center (CDIAC), were retrieved from data originators, public websites and other data centres. All data were put in a uniform format following a strict protocol. Quality control was carried out according to clearly defined criteria. Regional specialists performed the quality control, using state-of-the-art web-based tools, specially developed for accomplishing this global team effort. SOCAT version 1.5 was made public in September 2011 and holds 6.3 million quality controlled surface CO 2 data points from the global oceans and coastal seas, spanning four decades . Three types of data products are available: individual cruise files, a merged complete data set and gridded products. With the rapid expansion of marine CO 2 data collection and the importance of quantifying net global oceanic CO 2 uptake and its changes, sustained data synthesis and data access are priorities. Data coverage MotivationThe net absorption of CO 2 by the oceans, caused by rising atmospheric CO 2 concentrations since the industrial revolution, has been responsible for removing CO 2 equivalent to approximately 50 % of the fossil fuel and cement manufacturing emissions or about 30 % of the total anthropogenic emissions, including land use change (Sabine et al., 2004). Because of the availability of the carbonate ion, an important species of the dissolved inorganic carbon pool, and carbonate sediments, the oceans have a tremendous CO 2 uptake capacity and will, on timescales of ten to hundred thousand years, absorb all but a small fraction of the fossil CO 2 that has been and will be emitted (Archer et al., 1997). Meanwhile the changes in ocean CO 2 uptake, relying on factors such as ocean circulation and biology, will be among the decisive factors for the evolution of future atmospheric CO 2 concentrations and climate development (e.g., Friedlingstein et al., 2006;Riebesell et al., 2009). Presently there are two types of globally coordinated efforts that seek to resolve the dynamics of ocean CO 2 uptake through observations: repeat hydrography and surface ocean CO 2 observations (Gruber et al., 2010;Sabine et al., 2010). While repeat hydrography aims to assess variations in the ocean inventory of CO 2 on decadal timescales, surface ocean observations may resolve variations on seasonal to interannual timescales due to the higher sampling frequency. This high sampling frequency has been made possible by the advent of autonomous instruments and sensors for the nearcontinuous determination o...

Seven years of near-continuous observations from the Ocean Station Papa (OSP) surface mooring were used to evaluate drivers of marine carbon cycling in the eastern subarctic Pacific. Processes contributing to mixed layer carbon inventory changes throughout each deployment year were quantitatively assessed using a time-dependent mass balance approach in which total alkalinity and dissolved inorganic carbon were used as tracers. By using two mixed layer carbon tracers, it was possible to isolate the influences of net community production (NCP) and calcification. Our results indicate that the annual NCP at OSP is 2 ± 1 mol C m À2 yr À1 and the annual calcification is 0.3 ± 0.3 mol C m À2 yr À1. Piecing together evidence for potentially significant dissolved organic carbon cycling in this region, we estimate a particulate inorganic carbon to particulate organic carbon ratio between 0.15 and 0.25. This is at least double the global average, adding to the growing evidence that calcifying organisms play an important role in carbon export at this location. These results, coupled with significant seasonality in the NCP, suggest that carbon cycling near OSP may be more complex than previously thought and highlight the importance of continuous observations for robust assessments of biogeochemical cycling.

No abstract

Syntheses of carbonate chemistry spatial patterns are important for predicting ocean acidification impacts, but are lacking in coastal oceans. Here, we show that along the North American Atlantic and Gulf coasts the meridional distributions of dissolved inorganic carbon (DIC) and carbonate mineral saturation state (Ω) are controlled by partial equilibrium with the atmosphere resulting in relatively low DIC and high Ω in warm southern waters and the opposite in cold northern waters. However, pH and the partial pressure of CO2 (pCO2) do not exhibit a simple spatial pattern and are controlled by local physical and net biological processes which impede equilibrium with the atmosphere. Along the Pacific coast, upwelling brings subsurface waters with low Ω and pH to the surface where net biological production works to raise their values. Different temperature sensitivities of carbonate properties and different timescales of influencing processes lead to contrasting property distributions within and among margins.