Description: Here we provide CO2-system properties that were continuously measured in a southeast-northwest transect in the South Atlantic Ocean in which six Agulhas eddies were sampled. The Following Ocean Rings in the South Atlantic (FORSA) cruise occurred between 27th June and 15th July 2015, from Cape Town – South Africa to Arraial do Cabo – Brazil, on board the first research cruise of the Brazilian Navy RV Vital de Oliveira, as part of an effort of the Brazilian High Latitude Oceanography Group (GOAL). Finally, it contributed to the activities developed by the following Brazilian networks: GOAL, Brazilian Ocean Acidification Network (BrOA), Brazilian Research Network on Global Climate Change (Rede CLIMA). The focus of the first study using this dataset (Orselli et al. 2019a) was on investigate the role played by the Agulhas eddies on the sea-air CO2 net flux along their trajectories through the South Atlantic Ocean and model the seawater CO2–related properties as function of environmental parameters. This data has been used to contribute to the scientific discussion about the Agulhas eddies impact on the changes of the marine carbonate system, which is an expanding oceanographic subject (Carvalho et al. 2019; Orselli et al. 2019b; Ford et al. 2023). Seawater and atmospheric CO2 molar fraction (xCO2sw and xCO2atm, respectively) were continuously measured during the cruise track, as well as the sea surface temperature (T) and salinity (S). The following sampling methodology is fully described in Orselli et al. (2019a). The underway xCO2 sampling was taken using an autonomous system GO–8050, General Oceanic®, equipped with a non-dispersive infrared gas analyzer (LI–7000, LI–COR®). The underway T and S were sampled using a Sea-Bird® Thermosalinograph SBE21. Seawater intake to feed the continuous systems of the GO-8050 and the SBE21 was set at ~5 m below the sea surface. The xCO2 system was calibrated with four standard gases (CO2 concentrations of 0, 202.10, 403.20, and 595.50 uatm) within a 12 h interval along the entire cruise. Every 3 h the system underwent a standard reading, to check the derivation and allow the xCO2 corrections. The xCO2 measurements were taken within 90 seconds interval. After a hundred of xCO2sw readings, the system was changed to atmosphere and five xCO2atm readings were taken (Pierrot et al., 2009). xCO2 (umol mol–1) inputs were corrected by the CO2 standards (Pierrot et al., 2009). Thermosalinograph data were corrected using the CTD surface data. Then, together with the pressure data, these data were used to calculate the pCO2 of the equilibrator and atmosphere (pCO2eq and pCO2atm, respectively, uatm), following Weiss & Price (1980). Using the pCO2eq, which is calculated at the equilibrator temperature, it is possible to calculate the pCO2 at the in situ temperature (pCO2sw, uatm), according to Takahashi et al. (2009). Another common calculation regarding pCO2sw data, is the temperature-normalized pCO2sw (NpCO2sw, uatm). This means that the temperature effect is removed when one calculates the NpCO2sw for the mean cruise temperature. The procedure followed the Takahashi et al. (2009) and considered the mean cruise temperature of 20.39°C. The results obtained allow one to investigate the exchanges of CO2 at the ocean-atmosphere interface by calculating the pCO2 difference between these two reservoirs (DeltapCO2, DpCO2=pCO2sw–pCO2atm, uatm). Negative (positive) DpCO2 results indicate that the ocean acts as a CO2 sink (source) for the atmosphere. To determine the FCO2, the monthly mean wind speed data of July 2015 (at 10 m height) were extracted from the ERA-Interim atmospheric reanalysis product of the European Centre for Medium Range Weather Forecast (http://apps.ecmwf.int/datasets/data/interim-full-moda/levtype=sfc/) since the use of long-term mean is usual (e.g., Takahashi et al., 2009). The average wind speed for the period and whole area was 6.8 ± 0.6 m s−1, ranging from 5.6 to 8.3 m s−1. The CO2 transfer coefficients proposed by Takahashi et al. (2009) and Wanninkhof (2014) were used. With all these data together, the FCO2 was determined according to Broecker & Peng (1982), where FCO2 is the sea-air CO2 net flux (mmol m–2 d–1; FT09 and FW14 are the Sea-air CO2 flux calculated using the coefficients described in Takahashi et al. (2009) and Wanninkhof (2014), respectively).

Description: The role of Antarctic Bottom Water (AABW) in changing the ocean circulation and controlling climate variability is widely known. However, a comprehensive understanding of the relative contribution and variability of Antarctic regional deep water mass varieties that form AABW is still lacking. Using a high-quality dataset comprising three decades of observational shipboard surveys in the Weddell Sea (1984–2014), we updated the structure, composition and hydrographic properties variability of the Weddell Sea deep-layer, and quantified the contribution of the source waters composing Weddell Sea Bottom Water (WSBW) in its main formation zone. Shifts in WSBW hydrographic properties towards less dense varieties likely equate to less WSBW being produced over time. WSBW is primarily composed of 71 ± 4% of modified-Warm Deep Water (mWDW) and 29 ± 4% of Dense Shelf Waters, with the latter composed by ~ two-thirds (19 ± 2%) of High Salinity Shelf Water and ~ one-third (10 ± 6%) of Ice Shelf Water. Further, we show evidence that WSBW variability in the eastern Weddell Sea is driven by changes in the inflow of Dense Shelf Waters and bottom water from the Indian Sector of the Southern Ocean. This was observed through the rise of the WSBW contribution to the total mixture after 2005, following a twenty-year period (1984–2004) of decreasing contribution.

Description: Highlights • Shifts in WSBW properties to less dense varieties likely equate to less formation of WSBW. • The decline of WSBW volume ceased around 2005 and likely recovering after that. • Dense Shelf Waters drive and modulate the recent WSBW variability. • WSBW is composed by 71% of mWDW and 29% of Dense Shelf Waters. Abstract The role of Antarctic Bottom Water (AABW) in changing the ocean circulation and controlling climate variability is widely known. However, a comprehensive understanding of the relative contribution and variability of Antarctic regional deep water mass varieties that form AABW is still lacking. Using a high-quality dataset comprising three decades of observational shipboard surveys in the Weddell Sea (1984–2014), we updated the structure, composition and hydrographic properties variability of the Weddell Sea deep-layer, and quantified the contribution of the source waters composing Weddell Sea Bottom Water (WSBW) in its main formation zone. Shifts in WSBW hydrographic properties towards less dense varieties likely equate to less WSBW being produced over time. WSBW is primarily composed of 71 ± 4% of modified-Warm Deep Water (mWDW) and 29 ± 4% of Dense Shelf Waters, with the latter composed by ~ two-thirds (19 ± 2%) of High Salinity Shelf Water and ~ one-third (10 ± 6%) of Ice Shelf Water. Further, we show evidence that WSBW variability in the eastern Weddell Sea is driven by changes in the inflow of Dense Shelf Waters and bottom water from the Indian Sector of the Southern Ocean. This was observed through the rise of the WSBW contribution to the total mixture after 2005, following a twenty-year period (1984–2004) of decreasing contribution.

Description: We investigate the spatiotemporal variability of the source water masses (i.e., varieties of Subtropical Mode Water – STMW) that contribute to the South Atlantic Central Water (SACW) in the South Atlantic Ocean. Thus, the composition of the SACW layer is updated. For this investigation, we applied an optimum multiparameter (OMP) analysis and used the conservative and semi-conservative parameters available from the World Ocean Database and Argo floats for the South Atlantic Ocean. The STMW18 (at upper levels) sourced in the central and eastern regions of the South Atlantic and the STMW12 (at lower levels) sourced at the boundaries of the South Atlantic Subtropical Front are the main contributors to the SACW. Although also important, the contribution of STMW14 (sourced in the Brazil-Malvinas Confluence zone) is regionally confined by the Brazil Current recirculation gyre. The contributions from Subtropical Indian Mode Water (SIMW) increased westward along the Agulhas Corridor, while the contribution from STMW12 decreased. The relatively low contribution from SIMW matches the results of previous studies regarding the influence of these waters in the climatology of the South Atlantic Ocean. However, it cannot be ignored, since the results bring new light to further investigations of the mixing processes in the ocean interior of the South Atlantic Ocean.

Description: The Southern Ocean is a key region for analyzing environmental drivers that regulate sea-air CO2 exchanges. These CO2 fluxes are influenced by several mesoscale structures, such as meanders, eddies and other mechanisms responsible for energy dissipation. Aiming to better understand sea-air CO2 dynamics in the northern Antarctica Peninsula, we investigated an anticyclonic stationary eddy located south of Clarence Island, in the eastern basin of Bransfield Strait – named the Antarctica Slope Front bifurcation (ASFb) eddy. Physical, chemical and biological data were sampled, and remote sensing measurements taken, in the region during late summer conditions in February 2020. The eddy’s core consisted of cold (0.31 °C), salty (34.38) and carbon-rich (2247 μmol kg−1) waters with dissolved oxygen depletion (337 μmol kg−1). The core retains a mixture of local surface waters with waters derived from Circumpolar Deep Water (i.e., Warm Deep Water from the Weddell Sea and modified Circumpolar Deep Water from the Bransfield Strait) and Dense Shelf Water. The ASFb eddy acts as a CO2 outgassing structure that reaches a CO2 emission to the atmosphere of ∼1.5 mmol m−2 d–1 in the eddy’s core, mostly due to enhanced dissolved inorganic carbon (DIC). The results suggest that surface variation in DIC in the eddy’s core is modulated by (i) the entrainment of CO2-rich intermediate waters at ∼500 m, (ii) low primary productivity, associated with small phytoplankton cells such as cryptophytes and green flagellates, and (iii) respiration processes caused by heterotrophic organisms (i.e., zooplankton community). By providing a comprehensive view of these physical and biogeochemical properties of this stationary eddy, our results are key to adding new insights to a better understanding of the behavior of mesoscale features influencing sea-air CO2 exchanges in polar environments.

Description: Flow of dense shelf water provide an efficient mechanism for pumping CO 2 to the deep ocean along the continental shelf slope, particularly around the Antarctic bottom water (AABW) formation areas where much of the global bottom water is formed. However, the contribution of the formation of AABW to sequestering anthropogenic carbon ( C ant ) and its consequences remain unclear. Here, we show prominent transport of C ant (25.0 ± 4.7 Tg C yr −1 ) into the deep ocean (〉2,000 m) in four AABW formation regions around Antarctica based on an integrated observational data set (1974–2018). This maintains a lower C ant in the upper waters than that of other open oceans to sustain a stronger CO 2 uptake capacity (16.9 ± 3.8 Tg C yr −1 ). Nevertheless, the accumulation of C ant can further trigger acidification of AABW at a rate of −0.0006 ± 0.0001 pH unit yr −1 . Our findings elucidate the prominent role of AABW in controlling the Southern Ocean carbon uptake and storage to mitigate climate change, whereas its side effects (e.g., acidification) could also spread to other ocean basins via the global ocean conveyor belt. Plain Language Summary The Southern Ocean is thought to uptake and store a large amount of anthropogenic CO 2 ( C ant ), but little attention has been paid to the Antarctic coastal regions in the south of 60°S, mainly due to the lack of observations. Based on an integrated data set, we discovered the deep penetration of C ant and a visible pattern of relatively high concentration of C ant along the AABW formation pathway, and the concentration of C ant along the shelf‐slope is higher than that of other marginal seas at low‐mid latitudes, implying a highly effective C ant transport in AABW formation areas. We also found strong upper‐layer CO 2 uptake and a significant acidification rate in the deep waters of the Southern Ocean due to the AABW‐driven CO 2 transport, which is 3 times faster than those in other deep oceans. It is therefore crucial to understand how the Antarctic shelf regions affect the global carbon cycle through the uptake and transport of anthropogenic CO 2 , which also drives acidification in the other ocean basins. Key Points We show evidence for the accumulation of C ant along the Antarctic shelf‐slope into the deep ocean The process of AABW formation drives C ant downward transport at 25.0 ± 4.7 Tg C yr −1 , sustaining the CO 2 uptake in the surface ocean This further triggers acidification of AABW at a rate of −0.0006 ± 0.0001 pH unit yr −1 , which is faster than in other deep oceans

Description: The wind-driven part of the South Atlantic Ocean is primarily ventilated through central and intermediate water formation. Through the water mass formation processes, anthropogenic carbon (C-ant) is introduced into the ocean's interior which in turn makes the South Atlantic region vulnerable to ocean acidification. C-ant and the accompanying acidification effects have been estimated for individual sections in the region since the 1980s but a comprehensive synthesis for the entire basin is still lacking. Here, we quantified the C-ant accumulation rates and examined the changes in the carbonate system properties for the South Atlantic using a modified extended multiple linear regression method applied to five hydrographic sections and data from the GLODAPv2.2021 product. From 1989 to 2019, a mean C-ant column inventory change of 0.94 +/- 0.39 mol C m(-2) yr(-1) was found. C-ant accumulation rates of 0.89 +/- 0.33 mu mol kg(-1) yr(-1) and 0.30 +/- 0.29 mu mol kg(-1) yr(-1) were observed in central and intermediate waters, accompanied by acidification rates of -0.0020 +/- 0.0007 pH units yr(-1) and -0.0009 +/- 0.0009 pH units yr(-1), respectively. Furthermore, increased remineralization was observed in intermediate waters, amplifying the acidification of this water mass, especially at the African coast along 25 degrees S. This increase in remineralization is likely related to circulation changes and increased biological activity nearshore. Assuming no changes in the observed trends, South Atlantic intermediate waters will become unsaturated with respect to aragonite in similar to 30 years, while the central water of the eastern margins will become unsaturated in similar to 10 years.