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2019
Carter, BR, Feely RA, Wanninkhof R, Kouketsu S, Sonnerup RE, Pardo PC, Sabine CL, Johnson GC, Sloyan BM, Murata A, Mecking S, Tilbrook B, Speer K, Talley LD, Millero FJ, Wijffels SE, Macdonald AM, Gruber N, Bullister JL.  2019.  Pacific anthropogenic carbon between 1991 and 2017. Global Biogeochemical Cycles. 33:597-617.   10.1029/2018gb006154   AbstractWebsite

We estimate anthropogenic carbon (C-anth) accumulation rates in the Pacific Ocean between 1991 and 2017 from 14 hydrographic sections that have been occupied two to four times over the past few decades, with most sections having been recently measured as part of the Global Ocean Ship-based Hydrographic Investigations Program. The rate of change of C-anth is estimated using a new method that combines the extended multiple linear regression method with improvements to address the challenges of analyzing multiple occupations of sections spaced irregularly in time. The C-anth accumulation rate over the top 1,500 m of the Pacific increased from 8.8 (+/- 1.1, 1 sigma) Pg of carbon per decade between 1995 and 2005 to 11.7 (+/- 1.1) PgC per decade between 2005 and 2015. For the entire Pacific, about half of this decadal increase in the accumulation rate is attributable to the increase in atmospheric CO2, while in the South Pacific subtropical gyre this fraction is closer to one fifth. This suggests a substantial enhancement of the accumulation of C-anth in the South Pacific by circulation variability and implies that a meaningful portion of the reinvigoration of the global CO2 sink that occurred between similar to 2000 and similar to 2010 could be driven by enhanced ocean C-anth uptake and advection into this gyre. Our assessment suggests that the accuracy of C-anth accumulation rate reconstructions along survey lines is limited by the accuracy of the full suite of hydrographic data and that a continuation of repeated surveys is a critical component of future carbon cycle monitoring.

2017
Johnson, KS, Plant JN, Dunne JP, Talley LD, Sarmiento JL.  2017.  Annual nitrate drawdown observed by SOCCOM profiling floats and the relationship to annual net community production. Journal of Geophysical Research-Oceans. 122:6668-6683.   10.1002/2017jc012839   AbstractWebsite

Annual nitrate cycles have been measured throughout the pelagic waters of the Southern Ocean, including regions with seasonal ice cover and southern hemisphere subtropical zones. Vertically resolved nitrate measurements were made using in situ ultraviolet spectrophotometer (ISUS) and submersible ultraviolet nitrate analyzer (SUNA) optical nitrate sensors deployed on profiling floats. Thirty-one floats returned 40 complete annual cycles. The mean nitrate profile from the month with the highest winter nitrate minus the mean profile from the month with the lowest nitrate yields the annual nitrate drawdown. This quantity was integrated to 200 m depth and converted to carbon using the Redfield ratio to estimate annual net community production (ANCP) throughout the Southern Ocean south of 30 degrees S. A well-defined, zonal mean distribution is found with highest values (3-4 mol C m(-2) yr(-1)) from 40 to 50 degrees S. Lowest values are found in the subtropics and in the seasonal ice zone. The area weighted mean was 2.9 mol C m(-2) yr(-1) for all regions south of 40 degrees S. Cumulative ANCP south of 50 degrees S is 1.3 Pg C yr(-1). This represents about 13% of global ANCP in about 14% of the global ocean area. Plain Language Summary This manuscript reports on 40 annual cycles of nitrate observed by chemical sensors on SOCCOM profiling floats. The annual drawdown in nitrate concentration by phytoplankton is used to assess the spatial variability of annual net community production in the Southern Ocean. This ANCP is a key component of the global carbon cycle and it exerts an important control on atmospheric carbon dioxide. We show that the results are consistent with our prior understanding of Southern Ocean ANCP, which has required decades of observations to accumulate. The profiling floats now enable annual resolution of this key process. The results also highlight spatial variability in ANCP in the Southern Ocean.

Johnson, KS, Plant JN, Coletti LJ, Jannasch HW, Sakamoto CM, Riser SC, Swift DD, Williams NL, Boss E, Haentjens N, Talley LD, Sarmiento JL.  2017.  Biogeochemical sensor performance in the SOCCOM profiling float array. Journal of Geophysical Research-Oceans. 122:6416-6436.   10.1002/2017jc012838   AbstractWebsite

The Southern Ocean Carbon and Climate Observations and Modeling (SOCCOM) program has begun deploying a large array of biogeochemical sensors on profiling floats in the Southern Ocean. As of February 2016, 86 floats have been deployed. Here the focus is on 56 floats with quality-controlled and adjusted data that have been in the water at least 6 months. The floats carry oxygen, nitrate, pH, chlorophyll fluorescence, and optical backscatter sensors. The raw data generated by these sensors can suffer from inaccurate initial calibrations and from sensor drift over time. Procedures to correct the data are defined. The initial accuracy of the adjusted concentrations is assessed by comparing the corrected data to laboratory measurements made on samples collected by a hydrographic cast with a rosette sampler at the float deployment station. The long-term accuracy of the corrected data is compared to the GLODAPv2 data set whenever a float made a profile within 20 km of a GLODAPv2 station. Based on these assessments, the fleet average oxygen data are accurate to 1 +/- 1%, nitrate to within 0.5 +/- 0.5 mu mol kg(-1), and pH to 0.005 +/- 0.007, where the error limit is 1 standard deviation of the fleet data. The bio-optical measurements of chlorophyll fluorescence and optical backscatter are used to estimate chlorophyll a and particulate organic carbon concentration. The particulate organic carbon concentrations inferred from optical backscatter appear accurate to with 35 mg C m(-3) or 20%, whichever is larger. Factors affecting the accuracy of the estimated chlorophyll a concentrations are evaluated.

2015
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.