Geun-Ha Park

An updated anthropogenic CO2 inventory in the Atlantic Ocean

[1] This paper presents a comprehensive analysis of the basin-wide inventory of anthropogenic CO2 in the Atlantic Ocean based on high-quality inorganic carbon, alkalinity, chlorofluorocarbon, and nutrient data collected during the World Ocean Circulation Experiment (WOCE) Hydrographic Program, the Joint Global Ocean Flux Study (JGOFS), and the Ocean-Atmosphere Carbon Exchange Study (OACES) surveys of the Atlantic Ocean between 1990 and 1998. Anthropogenic CO2 was separated from the large pool of dissolved inorganic carbon using an extended version of the DC* method originally developed by Gruber et al. [1996]. The extension of the method includes the use of an optimum multiparameter analysis to determine the relative contributions from various source water types to the sample on an isopycnal surface. Total inventories of anthropogenic CO2 in the Atlantic Ocean are highest in the subtropical regions at 20� –40� , whereas anthropogenic CO2 penetrates the deepest in high-latitude regions (>40� N). The deeper penetration at high northern latitudes is largely due to the formation of deep water that feeds the Deep Western Boundary Current, which transports anthropogenic CO2 into the interior. In contrast, waters south of 50� S in the Southern Ocean contain little anthropogenic CO2. Analysis of the data collected during the 1990– 1998 period yielded a total anthropogenic CO2 inventory of 28.4 ± 4.7 Pg C in the North Atlantic (equator-70� N) and of 18.5 ± 3.9 Pg C in the South Atlantic (equator-70� S). These estimated basin-wide inventories of anthropogenic CO2 are in good agreement with previous estimates obtained by Gruber [1998], after accounting for the difference in observational periods. Our calculation of the anthropogenic CO2 inventory in the Atlantic Ocean, in conjunction with the inventories calculated previously for the Indian Ocean [Sabine et al., 1999] and for the Pacific Ocean [Sabine et al., 2002], yields a global anthropogenic CO2 inventory of 112 ± 17 Pg C that has accumulated in the world oceans during the industrial era. This global oceanic uptake accounts for approximately 29% of the total CO2 emissions from the burning of fossil fuels, land-use changes, and cement production during the past 250 years. INDEX TERMS: 1615 Global Change: Biogeochemical processes (4805); 1635 Global Change: Oceans (4203); 4805 Oceanography: Biological and Chemical: Biogeochemical cycles (1615); 4806 Oceanography: Biological and Chemical: Carbon cycling; KEYWORDS: anthropogenic CO2, Atlantic Ocean, air-sea disequilibrium

Variability of global net sea–air CO2 fluxes over the last three decades using empirical relationships

The interannual variability of net sea–air CO2 flux for the period 1982–2007 is obtained from a diagnostic model using empirical subannual relationships between climatological CO2 partial pressure in surface seawater (pCO2SW) and sea surface temperature (SST), along with interannual changes in SST and wind speed. These optimum subannual relationships show significantly better correlation between pCO2SW and SST than the previous relationships using fixed monthly boundaries.Our diagnostic model yields an interannual variability of±0.14 PgC yr−1 (1σ)with a 26-year mean of −1.48 PgC yr−1. The greatest interannual variability is found in the Equatorial Pacific, and significant variability is also found at northern and southern high-latitudes, depending in part, on which wind product is used. We provide an assessment of our approach by applying it to pCO2SW and SST output from a prognostic global biogeochemical ocean model. Our diagnostic approach applied to this model output shows reasonable agreement with the prognostic model net sea–air CO2 fluxes in terms of magnitude and phase of variability, suggesting that our diagnostic approach can capture much of the observed variability on regional to global scale. A notable exception is that our approach shows significantly less variability than the prognostic model in the Southern Ocean.

Large accumulation of anthropogenic CO2 in the East (Japan) Sea and its significant impact on carbonate chemistry

Received 19 December 2005; revised 10 July 2006; accepted 26 July 2006; published 22 November 2006. [1] This paper reports on a basin-wide inventory of anthropogenic CO2 in the East (Japan) Sea determined from high-quality alkalinity, chlorofluorocarbon, and nutrient data collected during a summertime survey in 1999 and total dissolved inorganic carbon data calculated from pH and alkalinity measurements. The data set comprises measurements from 203 hydrographic stations and covers most of the East Sea with the exception of the northwestern boundary region. Anthropogenic CO2 concentrations are estimated by separating this value from total dissolved inorganic carbon using a tracerbased (chlorofluorocarbon) separation technique. Wintertime surface CFC-12 data collected in regions of deep water formation off Vladivostok, Russia, improve the accuracy of estimates of anthropogenic CO2 concentrations by providing improved airsea CO2 disequilibrium values for intermediate and deep waters. Our calculation yields a total anthropogenic CO2 inventory in the East Sea of 0.40 ± 0.06 petagrams of carbon as of 1999. Anthropogenic CO2 has already reached the bottom of the East Sea, largely owing to the effective transport of anthropogenic CO2 from the surface to the ocean interior via deep water formation in the waters off Vladivostok. The highest specific column inventory (vertically integrated inventory per square meter) of anthropogenic CO2 of 80 mol C m � 2 is found in the Japan Basin (40N� 44N). Comparison of this inventory with those for other major basins of the same latitude band reveal that the East Sea values are much higher than the inventory for the Pacific Ocean (20� 30 mol C m � 2 ) and are similar to the inventory for the North Atlantic (66� 72 mol C m � 2 ). The substantial accumulation of anthropogenic CO2 in the East Sea during the industrial era has caused the aragonite and calcite saturation horizons to move upward by 80� 220 m and 500� 700 m, respectively. These upward movements are approximately 5 times greater than those found in the North Pacific. Both the large accumulation of anthropogenic CO2 and its significant impact on carbonate chemistry in the East Sea suggest that this sea is an important site for monitoring the future impact of the oceanic invasion of anthropogenic CO2.

Physical and biological control of aragonite saturation in the coastal waters of southern South Korea under the influence of freshwater

We investigated the aragonite saturation state (Ωarag) during all four seasons in a coastal region of southern Korea that receives considerable freshwater input. The surface Ωarag values were higher during productive seasons with enhanced freshwater influences, likely due to an increased net removal of dissolved inorganic carbon (DIC) from the water column (i.e., biological control). In addition, during the productive seasons, enhancement of Ωarag was observed with decreasing salinity within a linear mixing zone present between river-influenced surface and saltier bottom waters. DIC appeared to be effectively sequestered from the warmer, less salty surface water by downward flux of organic matter, but not significantly affected by the relatively DIC-rich, cooler and saltier bottom waters under strong stratification conditions during these seasons (i.e., physical control). Low phytoplankton productivity and seasonal breakdown of the stratification caused reduced saturation in other seasons and made the study area a weak sink for atmospheric CO2.

Recent increase in surface fCO2 in the western subtropical North Pacific

We observed unusually high levels (> 440 μatm) of carbon dioxide fugacity (fCO2) in surface seawater in the western subtropical North Pacific, the area where Subtropical Mode Water is formed, during summer 2015. The NOAA Kuroshio Extension Observatory moored buoy located in this region also measured high CO2 values, up to 500 μatm during this period. These high sea surface fCO2 (fCO2SW) values are explained by much higher normalized total dissolved inorganic carbon and slightly higher normalized total alkalinity concentrations in this region compared to the equatorial Pacific. Moreover, these values are much higher than the climatological CO2 values, even considering increasing atmospheric CO2, indicating a recent large increase in sea surface CO2 concentrations. A large seasonal change in sea surface temperature contributed to higher surface fCO2SW in the summer of 2015.