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Williams, NL, Juranek LW, Feely RA, Johnson KS, Sarmiento JL, Talley LD, Dickson AG, Gray AR, Wanninkhof R, Russell JL, Riser SC, Takeshita Y.  2017.  Calculating surface ocean pCO(2) from biogeochemical Argo floats equipped with pH: An uncertainty analysis. Global Biogeochemical Cycles. 31:591-604.   10.1002/2016gb005541   AbstractWebsite

More than 74 biogeochemical profiling floats that measure water column pH, oxygen, nitrate, fluorescence, and backscattering at 10 day intervals have been deployed throughout the Southern Ocean. Calculating the surface ocean partial pressure of carbon dioxide (pCO(2sw)) from float pH has uncertainty contributions from the pH sensor, the alkalinity estimate, and carbonate system equilibrium constants, resulting in a relative standard uncertainty in pCO(2sw) of 2.7% (or 11 mu atm at pCO(2sw) of 400 mu atm). The calculated pCO(2sw) from several floats spanning a range of oceanographic regimes are compared to existing climatologies. In some locations, such as the subantarctic zone, the float data closely match the climatologies, but in the polar Antarctic zone significantly higher pCO(2sw) are calculated in the wintertime implying a greater air-sea CO2 efflux estimate. Our results based on four representative floats suggest that despite their uncertainty relative to direct measurements, the float data can be used to improve estimates for air-sea carbon flux, as well as to increase knowledge of spatial, seasonal, and interannual variability in this flux. Plain Language Summary The Southern Ocean is a key player in the global flow of carbon, yet it is hard to reach, and there are relatively few measurements there, especially in winter. Measuring the amount of carbon dioxide gas in seawater is key to advancing our understanding of the Southern Ocean. More than 74 robotic floats that use sensors to measure seawater properties have been deployed throughout the Southern Ocean, and each has a lifetime of around 5 years. It is currently not possible to directly measure carbon dioxide gas from these floats; however, it is possible to estimate carbon dioxide from things that the float can measure, like pH, a measure of ocean acidity. Here surface ocean carbon dioxide is estimated from several floats and compared to two ship-based estimates. In some locations, the floats closely match the existing estimates, but in other locations the floats see significantly higher surface ocean carbon dioxide in the wintertime, reinforcing the idea that the Southern Ocean's role in the global carbon cycle needs a closer look. Our results show that despite not measuring carbon dioxide directly, these floats will help scientists learn a lot about the Southern Ocean's part in the global flow of carbon.

Williams, NL, Feely RA, Sabine CL, Dickson AG, Swift JH, Talley LD, Russell JL.  2015.  Quantifying anthropogenic carbon inventory changes in the Pacific sector of the Southern Ocean. Marine Chemistry. 174:147-160.   10.1016/j.marchem.2015.06.015   AbstractWebsite

The Southern Ocean plays a major role in mediating the uptake, transport, and long-term storage of anthropogenic carbon dioxide (CO2) into the deep ocean. Examining the magnitude and spatial distribution of this oceanic carbon uptake is critical to understanding how the earth's carbon system will react to continued increases in this greenhouse gas. Here, we use the extended multiple linear regression technique to quantify the total and anthropogenic change in dissolved inorganic carbon (DIC) along the S04P and P16S CLIVAR/U.S. Global Ocean Carbon and Repeat Hydrography Program lines south of 67 degrees S in the Pacific sector of the Southern Ocean between 1992 and 2011 using discrete bottle measurements from repeat occupations. Along the S04P section, which is located in the seasonal sea ice zone south of the Antarctic Circumpolar Current in the Pacific, the anthropogenic component of the DIC increase from 1992 to 2011 is mostly found in the Antarctic Surface Water (AASW, upper 100 m), while the increase in DIC below the mixed layer in the Circumpolar Deep Water can be primarily attributed to either a slowdown in circulation or decreased ventilation of deeper, high CO2 waters. In the AASW we calculate an anthropogenic increase in DIC of 12-18 mu mol kg(-1) and an average storage rate of anthropogenic CO2 of 0.10 +/- 0.02 mol m(-2) yr(-1) for this region compared to a global average of 0.5 +/- 0.2 mol m(-2) yr(-1). In surface waters this anthropogenic CO2 uptake results in an average pH decrease of 0.0022 +/- 0.0004 pH units yr(-1), a 0.47 +/- 0.10% yr(-1) decrease in the saturation state of aragonite (Omega(Aragonite)) and a 2.0 +/- 0.7 m yr(-1) shoaling of the aragonite saturation horizons (calculated for the Omega(Aragonite) = 1.3 contour). (C) 2015 Published by Elsevier B.V.