Noelia Fajar

Decadal acidification in the water masses of the Atlantic Ocean

Significance We provide the first (to our knowledge) observation-based acidification trends in the water masses of the Atlantic basin over the past two decades and compare them with climate model results. Observations and model output confirm that pH changes in surface layers are dominated by the anthropogenic component. In mode and intermediate waters, the anthropogenic and natural components are of the same order of magnitude and sign. Large changes in the natural component of newly formed mode and intermediate waters are associated with latitudinal shifts of these water masses caused by the Southern Annular Mode in the South Atlantic and by changes in the rates of water mass formation in the North Atlantic. Global ocean acidification is caused primarily by the ocean’s uptake of CO2 as a consequence of increasing atmospheric CO2 levels. We present observations of the oceanic decrease in pH at the basin scale (50°S–36°N) for the Atlantic Ocean over two decades (1993–2013). Changes in pH associated with the uptake of anthropogenic CO2 (ΔpHCant) and with variations caused by biological activity and ocean circulation (ΔpHNat) are evaluated for different water masses. Output from an Institut Pierre Simon Laplace climate model is used to place the results into a longer-term perspective and to elucidate the mechanisms responsible for pH change. The largest decreases in pH (∆pH) were observed in central, mode, and intermediate waters, with a maximum ΔpH value in South Atlantic Central Waters of −0.042 ± 0.003. The ΔpH trended toward zero in deep and bottom waters. Observations and model results show that pH changes generally are dominated by the anthropogenic component, which accounts for rates between −0.0015 and −0.0020/y in the central waters. The anthropogenic and natural components are of the same order of magnitude and reinforce one another in mode and intermediate waters over the time period. Large negative ΔpHNat values observed in mode and intermediate waters are driven primarily by changes in CO2 content and are consistent with (i) a poleward shift of the formation region during the positive phase of the Southern Annular Mode in the South Atlantic and (ii) an increase in the rate of the water mass formation in the North Atlantic.

Transports and budgets of anthropogenic CO2 in the tropical North Atlantic in 1992–1993 and 2010–2011

The meridional transport of anthropogenic CO2 (Cant) in the tropical North Atlantic (TNA) is investigated using data from transoceanic sections along 7.5°N and 24.5°N, carried out in the early 1990s and 2010s. The net Cant transport across both sections is northward. At 7.5°N, this transport increased from 315 ± 47 kmol s−1 in 1993 to 493 ± 51 kmol s−1 in 2010; similarly, across 24.5°N it grew from 530 ± 46 kmol s−1 in 1992 to 662 ± 49 kmol s−1 in 2011. These changes result from modifications in the intermediate and deep circulation patterns, as well as from Cant increase within the thermocline waters. In deep waters, lateral advection causes a net Cant input of 112 ± 60 kmol s−1 (234 ± 65 kmol s−1) in 1992–1993 (2010–2011); within these deep waters, the storage rate of Cant is not statistically different from the net Cant input, 139 ± 21 kmol s−1 (188 ± 21 kmol s−1) in 1992–1993 (2010–2011). The Cant increase in deep waters is due to the large injection of Cant across the 24.5°N by the Deep Western Boundary Current and the northward recirculation of North Atlantic Deep Water along 7.5°N. In contrast, a large net Cant output in the upper layer is caused by the Florida Current. Despite this net Cant output, the Cant accumulates at a rate of 215 ± 24 kmol s−1 (291 ± 24 kmol s−1) referenced to year 1993 (2010). From the two Cant budgets, we infer a Cant air-sea flux of 0.23 ± 0.02 Pg yr−1in the TNA, much larger than previous estimates.

Ocean acidification along the 24.5°N section in the subtropical North Atlantic

Ocean acidification is directly related to increasing atmospheric CO2 levels due to human activities and the active role of the global ocean in absorbing part of this anthropogenic CO2. Here we present an assessment of the pH changes that have occurred along 24.5°N in the subtropical North Atlantic through comparison of pH observations conducted in 1992 and 2011. It reveals an overall decline in pH values in the first 1000 dbar of the water column. The deconvolution of the temporal pH differences into anthropogenic and nonanthropogenic components reveals that natural variability, mostly owed to a decrease in oxygen levels in particular regions of the section, explains the vertical distribution of the larger pH decreases (up to −0.05 pH units), which are found within the permanent thermocline. The detection of long-term trends in dissolved oxygen in the studied region gains importance for future pH projections, as these changes modulate the anthropogenically derived acidification. The anthropogenic forcing explains significant acidification deeper than 1000 dbar in the western basin, within the Deep Western Boundary Current.

Spectrophotometric measurements of the carbonate ion concentration:aragonite saturation states in the Mediterranean Sea and Atlantic Ocean

Measurements of ocean pH, alkalinity, and carbonate ion concentrations ([CO3(2-)]) during three cruises in the Atlantic Ocean and one in the Mediterranean Sea were used to assess the reliability of the recent spectrophotometric [CO3(2-)] methodology and to determine aragonite saturation states. Measurements of [CO3(2-)] along the Atlantic Ocean showed high consistency with the [CO3(2-)] values calculated from pH and alkalinity, with negligible biases (0.4 ± 3.4 μmol·kg(-1)). In the warm, salty, high alkalinity and high pH Mediterranean waters, the spectrophotometric [CO3(2-)] methodology underestimates the measured [CO3(2-)] (4.0 ± 5.0 μmol·kg(-1)), with anomalies positively correlated to salinity. These waters also exhibited high in situ [CO3(2-)] compared to the expected aragonite saturation. The very high buffering capacity allows the Mediterranean Sea waters to remain over the saturation level of aragonite for long periods of time. Conversely, the relatively thick layer of undersaturated waters between 500 and 1000 m depths in the Tropical Atlantic is expected to progress to even more negative undersaturation values. Moreover, the northern North Atlantic presents [CO3(2-)] slightly above the level of aragonite saturation, and the expected anthropogenic acidification could result in reductions of the aragonite saturation levels during future decades, acting as a stressor for the large population of cold-water-coral communities.

Carbon Data Obtained During the R/V Hesperides Cruise in the Atlantic Ocean on CLIVAR Repeat Hydrography Section A06, (5 April - 16 May, 2010)

The item is made of 2 files, of which 1 is the dataset and the other include detailed information about measures realized.-- Dataset contributed to the Project Carbochange

Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Sarmiento de Gamboa Cruise in the North Atlantic Ocean on CLIVAR Repeat Hydrography Section OVIDE-2012 (June 23 - July 20, 2012)

The item is made of 2 files, of which 1 is the dataset and the other include a small description of the measured variables.-- Aida F. Rios ... et al.-- Dataset contributed to the Project Carbochange

Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Thalassa Cruise in the North Atlantic Ocean on CLIVAR Repeat Hydrography Section OVIDE-2008 (June 6 - July 11, 2008)

The item is made of 2 files, of which 1 is the dataset and the other include a small description of the measured variables.-- Dataset contributed to the Project Carbochange.-- More information in http://hdl.handle.net/10261/115861