scholarly journals Multi-decadal uptake of carbon dioxide into subtropical mode water of the North Atlantic Ocean

2011 ◽  
Vol 8 (6) ◽  
pp. 12451-12476 ◽  
Author(s):  
N. R. Bates

Abstract. Natural climate variability impacts the multi-decadal uptake of anthropogenic carbon dioxide (Cant) into the North Atlantic Ocean subpolar and subtropical gyres. Previous studies have shown that there is significant uptake of CO2 into the subtropical mode water (STMW) that forms south of the Gulf Stream in winter and constitutes the dominant upper-ocean water mass in the subtropical gyre of the North Atlantic Ocean. Observations at the Bermuda Atlantic Time-series Study (BATS) site near Bermuda show an increase in dissolved inorganic carbon (DIC) of +1.51 ± 0.08 μmol kg−1 yr−1 between 1988 and 2011. It is estimated that the sink of CO2 into STMW was 0.985 ± 0.018 Pg C (Pg = 1015 g C) between 1988 and 2011 (~70 % of which is due to uptake of Cant). However, the STMW sink of CO2 was strongly coupled to the North Atlantic Oscillation (NAO) with large uptake of CO2 into STMW during the 1990s (NAO positive phase). In contrast, uptake of CO2 into STMW was much reduced in the 2000s during the NAO neutral/negative phase. Thus, NAO induced variability of the STMW CO2 sink is important when evaluating multi-decadal changes in North Atlantic Ocean CO2 sinks.

2012 ◽  
Vol 9 (7) ◽  
pp. 2649-2659 ◽  
Author(s):  
N. R. Bates

Abstract. Natural climate variability impacts the multi-decadal uptake of anthropogenic carbon dioxide (Cant) into the North Atlantic Ocean subpolar and subtropical gyres. Previous studies have shown that there is significant uptake of CO2 into subtropical mode water (STMW) of the North Atlantic. STMW forms south of the Gulf Stream in winter and constitutes the dominant upper-ocean water mass in the subtropical gyre of the North Atlantic Ocean. Observations at the Bermuda Atlantic Time-series Study (BATS) site near Bermuda show an increase in dissolved inorganic carbon (DIC) of +1.51 ± 0.08 μmol kg−1 yr−1 between 1988 and 2011, but also an increase in ocean acidification indicators such as pH at rates (−0.0022 ± 0.0002 yr−1) higher than the surface ocean (Bates et al., 2012). It is estimated that the sink of CO2 into STMW was 0.985 ± 0.018 Pg C (Pg = 1015 g C) between 1988 and 2011 (70 ± 1.8% of which is due to uptake of Cant). The sink of CO2 into the STMW is 20% of the CO2 uptake in the North Atlantic Ocean between 14°–50° N (Takahashi et al., 2009). However, the STMW sink of CO2 was strongly coupled to the North Atlantic Oscillation (NAO), with large uptake of CO2 into STMW during the 1990s during a predominantly NAO positive phase. In contrast, uptake of CO2 into STMW was much reduced in the 2000s during the NAO neutral/negative phase. Thus, NAO induced variability of the STMW CO2 sink is important when evaluating multi-decadal changes in North Atlantic Ocean CO2 sinks.


Nature ◽  
2002 ◽  
Vol 420 (6915) ◽  
pp. 489-493 ◽  
Author(s):  
Nicholas R. Bates ◽  
A. Christine Pequignet ◽  
Rodney J. Johnson ◽  
Nicolas Gruber

2021 ◽  
Author(s):  
Ilaria Stendardo ◽  
Bruno Buongiorno Nardelli ◽  
Sara Durante

<p>In the subpolar North Atlantic Ocean, Subpolar Mode Waters (SPMWs) are formed during late winter convection following the cyclonic circulation of the subpolar gyre. SPMWs participate in the upper flow of the Atlantic overturning circulation (AMOC) and provide much of the water that is eventually transformed into several components of the North Atlantic deep water (NADW), the cold, deep part of the AMOC. In a warming climate, an increase in upper ocean stratification is expected to lead to a reduced ventilation and a loss of oxygen. Thus, understanding how mode waters are affected by ventilation changes will help us to better understand the variability in the AMOC. In particular, we would like to address how the volume occupied by SPMWs has varied over the last decades due to ventilation changes, and what are the aspects driving the subpolar mode water formation, their interannual variations as well as the impact of the variability in the mixing and subduction and vertical dynamics on ocean deoxygenation. For this purpose, we use two observation-based 3D products from Copernicus Marine Service (CMEMS), the ARMOR3D and the OMEGA3D datasets. The first consists of 3D temperature and salinity fields, from the surface to 1500 m depth, available weekly over a regular grid at 1/4° horizontal resolution from 1993 to present. The second consists of observation-based quasi-geostrophic vertical and horizontal ocean currents with the same temporal and spatial resolution as ARMOR3D.</p>


2012 ◽  
Vol 9 (1) ◽  
pp. 989-1019 ◽  
Author(s):  
N. R. Bates ◽  
M. H. P. Best ◽  
K. Neely ◽  
R. Garley ◽  
A. G. Dickson ◽  
...  

Abstract. Fossil fuel use, cement manufacture and land-use changes are the primary sources of anthropogenic carbon dioxide (CO2) to the atmosphere, with the ocean absorbing 30 %. Ocean uptake and chemical equilibration of anthropogenic CO2with seawater results in a gradual reduction in seawater pH and saturation states (Ω) for calcium carbonate (CaCO3) minerals in a process termed ocean acidification. Assessing the present and future impact of ocean acidification on marine ecosystems requires detection of the multi-decadal rate of change across ocean basins and at ocean time-series sites. Here, we show the longest continuous record of ocean CO2 changes and ocean acidification in the North Atlantic subtropical gyre near Bermuda from 1983–2011. Dissolved inorganic carbon (DIC) and partial pressure of CO2 (pCO2) increased in surface seawater by ~40 μmol kg−1 and ~50 μatm (~20 %), respectively. Increasing Revelle factor (β) values imply that the capacity of North Atlantic surface waters to absorb CO2 has also diminished. As indicators of ocean acidification, seawater pH decreased by ~0.05 (0.0017 yr−1) and Ω values by ~7–8 %. Such data provide critically needed multi-decadal information for assessing the North Atlantic Ocean CO2sink and the pH changes that determine marine ecosystem responses to ocean acidification.


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