the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Ocean acidification trends and carbonate system dynamics across the North Atlantic subpolar gyre water masses during 2009–2019
David Curbelo-Hernández
Fiz F. Pérez
Melchor González-Dávila
Sergey V. Gladyshev
Aridane G. González
David González-Santana
Antón Velo
Alexey Sokov
J. Magdalena Santana-Casiano
The CO2–carbonate system dynamics in the North Atlantic subpolar gyre (NASPG) were evaluated between 2009 and 2019. Data were collected aboard eight summer cruises through the Climate and Ocean: Variability, Predictability and Change (CLIVAR) 59.5° N section. The ocean acidification (OA) patterns and the reduction in the saturation state of calcite (ΩCa) and aragonite (ΩArag) in response to the increasing anthropogenic CO2 (Cant) were assessed within the Irminger, Iceland, and Rockall basins during a poorly assessed decade in which the physical patterns reversed in comparison with previous well-known periods. The observed cooling, freshening, and enhanced ventilation increased the interannual rate of accumulation of Cant in the interior ocean by 50 %–86 % and the OA rates by close to 10 %. The OA trends were 0.0013–0.0032 units yr−1 in the Irminger and Iceland basins and 0.0006–0.0024 units yr−1 in the Rockall Trough, causing a decline in ΩCa and ΩArag of 0.004–0.021 and 0.003–0.0013 units yr−1, respectively. The Cant-driven rise in total inorganic carbon (CT) was the main driver of the OA (contributed by 53 %–68 % in upper layers and > 82 % toward the interior ocean) and the reduction in ΩCa and ΩArag (> 64 %). The transient decrease in temperature, salinity, and AT collectively counteracts the CT-driven acidification by 45 %–85 % in the upper layers and in the shallow Rockall Trough and by < 10 % in the interior ocean. The present investigation reports the acceleration of the OA within the NASPG and expands knowledge about the future state of the ocean.
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During the 2010s, the subpolar North Atlantic experienced a 50 %–86 % increase in anthropogenic CO2, accelerating by 7 %–10 % the acidification.
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Anthropogenic CO2 contributed to acidification by 53 %–68 % in upper layers and > 82 % in the interior ocean.
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The acidification trends (0.0006 and 0.0032 units yr−1) declined the ΩCa and ΩArag by 0.004–0.021 and 0.003–0.0013 units yr−1, respectively.
The ocean uptake of approximately one-third of the CO2 released into the atmosphere (Friedlingstein et al., 2023; Gruber et al., 2019) has an important role in climate regulation, causing changes in marine carbonate chemistry. The exponential increase in the global ocean CO2 sink in phase with that of anthropogenic emissions (Friedlingstein et al., 2023) has resulted in a long-term decrease in the concentration of carbonate ions ([CO]) and pH. This process has been collectively referred to as ocean acidification (OA; Caldeira and Wickett, 2003, 2005; Doney et al., 2009; Orr et al., 2005; Raven et al., 2005; Feely et al., 2009) and favours the dissolution of calcium carbonate (CaCO3). It affects not only calcifying marine organisms and ecosystems which use the biogenic CaCO3 forms of calcite and aragonite (e.g. Gattuso et al., 2015; Langdon et al., 2000; Pörtner et al., 2004, 2019; Riebesell et al., 2000) but also the global biogeochemical cycles (Gehlen et al., 2011; Matear and Lenton, 2014).
The absorption of anthropogenic CO2 has reduced the pH of the global surface ocean by 0.1 units since preindustrial times, representing an approximately 30 % increase in acidity (Caldeira and Wickett, 2003). According to the IPCC's Representative Concentration Pathway (RCP) scenarios (Van Vuuren et al., 2011; Moss et al., 2010), which project various future trajectories of greenhouse gas concentrations, the model projections estimate a potential pH decrease of 0.3–0.4 units by the end of the century under the RCP8.5 scenario, which assumes continued high CO2 emissions. In contrast, the most conservative RCP2.6 scenario, which includes significant emission reductions, anticipates a pH drop of 0.2–0.3 units (IPCC, 2013, 2021). However, as the absorption and storing of anthropogenic carbon (Cant), defined as the fraction of inorganic carbon resulting from human emissions (Sarmiento et al., 1992), is not uniform within the ocean (Sabine et al., 2004), OA rates may show a significant spatial variability and should be studied regionally. The temporal evolution of the carbonate system variables in surface waters are monitored and assessed in several time series stations located across different ocean regions (Bates et al., 2014). The largest OA rates are expected to occur across high northern and southern latitudes (Bellerby et al., 2005; Orr et al., 2005), where deep convective overturning and subduction occur, favouring the entrance of Cant in the interior ocean (Maier-Reimer and Hasselmann, 1987; Lazier et al., 2002; Sarmiento et al., 1992).
The North Atlantic is one of the strongest CO2 sinks and stores over 25 % of the Cant accumulated in the global ocean (e.g. Gruber et al., 2019; Khatiwala et al., 2013; Pérez et al., 2008, 2010, 2024; Sabine et al., 2004; Takahashi et al., 2009). The Atlantic Meridional Overturning Circulation (AMOC) plays a significant role by conveying acidified Cant-loaded waters polewards and exporting them to the ocean interior across deep-water formation areas (Lazier et al., 2002; Pérez et al., 2008, 2013; Steinfeldt et al., 2009). It contributes to homogenizing the Cant and pH in the whole water column in such regions and exports these properties southwards to the global deep ocean (Pérez et al., 2018). Thus, the North Atlantic behaves as a crucial region for understanding the impacts of anthropogenic forcing on the global ocean.
OA has been widely studied in the North Atlantic through the monitoring of the ocean physicochemical properties at time series stations (summarized by Bates et al., 2014) placed in subtropical and subpolar latitudes: the European Station for Time-Series in the Ocean of the Canary Islands (ESTOC; 29.04° N, 15.50° W; González-Dávila et al., 2010; González-Dávila and Santana-Casiano, 2023; Santana-Casiano et al., 2007), the Bermuda Atlantic Time-series Study (BATS; 32.0° N, 64.0° W; Bates et al., 2012), the Irminger Sea time series (IRM-TS; 64.3° N, 28.0° W; Olafsson et al., 2010), and the Iceland Sea time series (IS-TS; 68.0° N, 12.66° W; Olafsson et al., 2009, 2010). OA rates have also been evaluated along transects through repeated hydrographic cruises (i.e. Guallart et al., 2015; García-Ibáñez et al., 2016; Vázquez-Rodríguez et al., 2012b) or even covered by volunteer observing ships (Fröb et al., 2019). These investigations have revealed a rate of decrease in pH of ∼ 0.001–0.002 units yr−1. Moreover, González-Dávila and Santana-Casiano (2023) recently indicated that these rates have been increasing since 1995.
The assessment of OA is of special interest across the North Atlantic subpolar gyre (NASPG; 50–60° N), where the atmospheric CO2 sink is particularly strong and the deep-water formation processes favour the storage of Cant through the whole water column (Gruber et al., 2019; Sabine et al., 2004; Watson et al., 2009; Pérez et al. 2008). Likewise, the deep-water formation processes create the largest and deepest ocean environments supersaturated for aragonite (at more than 2000 m depth; Feely et al., 2004; Jiang et al., 2015), which is the main CaCO3 mineral for cold-water corals (CWCs; Roberts et al., 2009) and some pteropods (Bathmann et al., 1991; Urban-Rich et al., 2001). These deep biomes are predicted to be among the first in the global ocean affected by OA, mainly due to the shoaling of the aragonite saturation horizon and its progressive exposition to undersaturated conditions for aragonite at intermediate and deep waters (Gehlen et al., 2014; Guinotte et al., 2006; Raven et al., 2005; Roberts et al., 2009; Turley et al., 2007).
The physical processes along the NASPG, which are subject to significant spatiotemporal variability introduced by the atmospheric forcing and climatology on an interannual scale, directly influenced the biogeochemistry (Corbière et al., 2007; Fröb et al., 2019). The changes in the North Atlantic Current (NAC) modify the poleward heat transport from subtropical latitudes and air–sea interactions, influencing temperature patterns (Josey et al., 2018; Mercier et al., 2015). Recent studies noticed the surface cooling and freshening of the NASPG in the 2010s (Holliday et al., 2020; Josey et al., 2018; Robson et al., 2016; Tesdal et al., 2018) contrasting with the period of warming and salinification in the 1990s extended until 2005 (Häkkinen and Rhines, 2004; Hátún et al., 2005; Robson et al., 2014). Anomalous heat loss and winter deep convection were found to be of high intensity since 2008, contributing to the extreme cold anomaly along the NASPG (e.g. de Jong et al., 2012; de Jong and de Steur, 2016; Fröb et al., 2019, 2016; Gladyshev et al., 2016a, b; Piron et al., 2017; Våge et al., 2009). These fluctuations in the vertical mixing and ocean circulation patterns introduce changes in the distribution of the carbonate system variables.
The estimated OA trend over 1991–2011 for surface waters across the North Atlantic subpolar biome was −0.0020 ± 0.0001 units yr−1 (Lauvset et al., 2015). Chau et al. (2024) recently reported that the surface waters in the Irminger and Iceland basins acidified over 1985–2021 at rates of −0.0016 ± 0.0001 and −0.0014 ± 0.0001 units yr−1. Several observation-based investigations have evaluated the drivers, trends, and impacts of OA through the entire water column in the Irminger and Iceland basins (e.g. Fontela et al., 2020; García-Ibáñez et al., 2016, 2021; Perez et al., 2018; Pérez et al., 2021; Ríos et al., 2015), while few studies have addressed it in the Rockall Trough (e.g. McGrath et al., 2013, 2012a, b; Humphreys et al., 2016) due to the lack of repeated hydrographic sections or time series stations and the subsequent limitation of continuous surface-to-bottom data. The high longitudinal variability in the NASPG caused by the influence of different circulation patterns and water masses (García-Ibáñez et al., 2015, 2018) introduced several physicochemical heterogeneities between the Irminger and Iceland basins and the Rockall basin (Ellett et al., 1986; McGrath et al., 2013, 2012b; Holliday et al., 2000). These differences in the distributions of marine carbonate system (MCS) variables should be considered to improve our understanding of OA in the entire North Atlantic.
This study evaluated the OA in the NASPG across the Irminger, Iceland, and Rockall basins during the 2010s. High-quality direct measurements of CO2 system variables from eight hydrographic cruises occupying 59.5° N between 2009 and 2019 were used to evaluate the drivers and trends of pH and the potential effects of OA on calcifying organisms of changes in calcite (ΩCa) and aragonite (ΩAr) saturation states. This study advances our understanding of the complexities associated with OA in the NASPG and supports ongoing efforts to model and predict future acidification scenarios in the North Atlantic and global ocean.
2.1 Data collection
Data were collected from eight summer cruises conducted along the transverse hydrographic section at 59.5° N between 2009 and 2019 (Daniault et al., 2016; Gladyshev et al., 2016b, 2017, 2018; Sarafanov et al., 2018). This section is part of the World Climate Research Programme (WCRP) within the framework of the Climate and Ocean: Variability, Predictability and Change (CLIVAR) project and covers the length of the subpolar North Atlantic between Scotland and Greenland (4.5–43.0° W), crossing the Irminger and Iceland basins and the Rockall Trough (Fig. 1). Generally, the sampling stations were equidistantly spaced every 20 nmi (∼ ° longitude), and this was repeated in all the cruises except for the cruise of 2016, when the station spacing was decreased to 10 nmi over the Reykjanes Ridge western and eastern slopes. The distance between stations over the eastern Greenland slope and shelf always decreased from 10 nmi to about 2 nmi. The surface-to-bottom sampling and in situ measurements were performed by using an SBE 911plus CTD with an SBE32 Carousel containing 24 Niskin bottles (10 L) with additional sensors for pressure (P), dual temperature (T), salinity (S), and dissolved oxygen (DO). The eight cruises included in the new dataset are the result of an international collaboration between researchers from the P. P. Shirshov Institute of Oceanology at the Russian Academy of Science and the Marine Chemistry research group from the Oceanography and Global Change Institute (QUIMA-IOCAG) at the University of Las Palmas de Gran Canaria (ULPGC). A detailed overview of the cruises is given in Table 1.
2.1.1 CO2 system variable measurements
The analysis of the MCS variables followed the same analytical methodology and provided high-quality CO2 measurements on all the hydrographic cruises. This includes the sampling and data collection techniques and the quality control and calculation procedures published in the updated version of the DOE method manual for CO2 analysis in seawater given by Dickson et al. (2007). The seawater samples were analysed on board for total alkalinity (AT) and total inorganic carbon (CT) determination by using a VINDTA 3C and following Mintrop et al. (2000). The AT was analysed by potentiometric titration with HCl to the carbonic acid endpoint and determined through the development of the full titration curve (Millero et al., 1993; Dickson and Goyet, 1994). The CT was determined through coulometric titration (Johnson et al., 1993). The VINDTA 3C was calibrated through the titration of certified reference materials (CRMs; provided by Andrew Dickson at the Scripps Institution of Oceanography), giving values with an accuracy of ± 1.5 µmol kg−1 for AT and ± 1.0 µmol kg−1 for CT.
Spectrophotometric pH measurements (Clayton and Byrne, 1993) in total scale at a constant temperature of 15 °C (pHT,15) were performed for the cruises between 2009 and 2016. A spectrophotometric pH sensor (SP101-SM) developed by the QUIMA-IOCAG group at the ULPGC in collaboration with SensorLab (González-Dávila et al., 2014, 2016) was used. The method uses four wavelength analyses for pH indicator dyes (m-cresol purple), includes auto-cleaning steps, and performs a blank for pH calculation immediately after the dye injection. The spectrophotometric sensor was in situ tested by using a Tris seawater buffer (Ramette et al., 1977) and provided pHT,15 values with an accuracy of ± 0.002 units. To account for the systematic uncertainty reported by DelValls and Dickson (1998) related to the pK* values of m-cresol purple, and in line with their recommendations, a correction of +0.0047 units was applied to the measured pHT,15. This adjustment ensures that the calculated pH values are consistent with the more accurate pK* determinations.
2.1.2 Dissolved oxygen (DO) measurements
The Winkler method introduced by Winkler (1888) and optimized by Carpenter (1965) and Carrit and Carpenter (1966) was used to analytically determine the dissolved oxygen (DO) of the seawater samples in all the cruises from 2009–2016. The seawater samples for DO determination were collected from the bottle samples in pre-calibrated wide-neck glass bottles, avoiding bubble formation. The temperature of the water was recorded during the sampling. All the reagents and solutions used for dissolved oxygen determination were prepared following the procedures described by Dickson (1995), and their possible impurities were controlled by determining a blank every 2 d.
As DO could not be analytically measured during the cruise of 2019 (due to limitations related to the oceanographic cruise plan), it was computed for this year by comparing the performance of the DO sensor during the cruise of 2019 versus (1) DO data estimated by a neural network for the cruises of 2016 and 2019 and (2) Winkler-measured DO data during the cruise of 2016. The neural network ESPER_NN (Empirical Seawater Property Estimation Routine) introduced by Carter et al. (2021) was used for DO estimations. The computational procedure is detailed in Appendix A.
2.2 Data processing
2.2.1 Evaluation of the internal consistency of the data using CANYON-B
The measured and determined data were compared with estimations given by the Bayesian neural network “CANYON-B” (Bittig et al., 2018), a re-developed and more robust neural network based on CANYON (CArbonate system and Nutrients concentration from hYdrological properties and Oxygen using a Neural-network; Sauzède et al., 2017). CANYON-B estimates the four MCS variables (AT, CT, pH, and pCO2) and macronutrient concentrations (PO, NO, and Si(OH)4, hereinafter PO4, NO3, and Si(OH)4) as a function of a simple set of input variables which include P, T, S, DO, latitude, longitude, and date. This neural network is trained on and validated against bottle data from GLODAPv2 and recent GO-SHIP profiles and compared with sensor data from Argo floats. The standard errors of estimation reported for CANYON-B by Bittig et al. (2018) are 6.3 µmol kg−1 for AT, 7.1 µmol kg−1 for CT, 0.013 units for pH, 20 µatm for pCO2, 0.051 µmol kg−1 for PO4, 0.68 µmol kg−1 for NO3, and 2.3 µmol kg−1 for Si(OH)4. The crossover analysis between measured and estimated data did not show systematic differences but showed individual outliers. The measured data that were higher/lower than the CANYON-B estimate by plus/minus twice the predicted variable uncertainty of the neural network were regarded as outliers and removed from the dataset.
The total number of measured data was 8974 for AT, 7495 for CT, 8706 for pHT,15, 9656 for DO, 9114 for PO4, and 9192 for Si(OH)4. The difference between the measured and CANYON-B-estimated variables (referred to hereinafter as canyon-estimated variables) was performed for each sample in which CANYON-B could be applied (samples with availability of T, S, and DO measurements). The number of data, mean values, and standard deviation of the measured variables for each cruise are summarized in Table S1. The average differences with the 95 % confidence interval for each cruise are shown in Table S2. The average differences for the entire period (2009–2019) were lower than 2.1 µmol kg−1 for AT, 2 µmol kg−1 for CT, 0.0002 for pH, 0.02 µmol kg−1 for PO4, and 0.25 µmol kg−1 for Si(OH)4. The minimal difference between the measured and the canyon-estimated pH instils confidence in the correction applied to the measured pH following DelValls and Dickson (1998).
2.2.2 Computational methods
The computational procedures to calculate MCS variables applied in this investigation used the CO2,SYS programme developed by Lewis and Wallace (1998) and were run with the MATLAB software (van Heuven et al., 2011; Orr et al., 2018; Sharp et al., 2023). The set of constants used for computations includes the carbonic acid dissociation constants of Lueker et al. (2000), the HSO dissociation constant of Dickson (1990), the HF dissociation constant of Pérez and Fraga (1987), and the value of [B]T determined by Lee et al. (2010). The pH in total scale at in situ temperature (pHT) was computed from the measured AT and pHT,15 (the computed CT was given as an output). The pHT for the cruise of 2019, in which direct pH measurements were not performed, was computed from the measured AT and CT.
The saturation states of calcite (ΩCa) and aragonite (ΩArag), determined from the product of the ion concentrations of calcium ([Ca2+]) and carbonate ([CO]) divided by the stoichiometry solubility products (Ksp) for calcite (KCa) and aragonite (KArag) given by Mucci (1983), were generated as outputs of the CO2,SYS computational routine. The decrease in ΩCa and ΩArag reports the adverse impacts of OA on marine calcification processes (e.g. Gattuso et al., 2015; Langdon et al., 2000; Pörtner et al., 2004, 2019; Riebesell et al., 2000).
An internal consistency test was conducted on the three measured MCS variables. The measured variables were compared with canyon-estimated and CO2,SYS-computed variables. The average differences and standard deviations were summarized in Table S2 and ensure the consistency of the observations. In addition, due to gaps in data, an intercomparison between measured and computed CT and pHT,15 was performed. It considers the availability of measurements for each latitude, longitude, and time and the differences between the measured and computed pH with the canyon-estimated pHT. The use of measured or computed CT followed these conditions: (1) if there was measured CT but not measured pH, measured CT was used; (2) if there was measured pH but not measured CT, computed CT was used; (3) and if there was measured CT and pH, measured CT was used when the differences between measured and canyon pHT were lower than the differences between computed and canyon-estimated pHT, while computed CT was used when the opposite happened. In total, 6375 measured and 2872 computed CT data were used in this study (69 % and 31 %, respectively). The average differences on each cruise between the combined (measured and computed, also referred to as “CT (new)”) and canyon-estimated CT variable are provided in Table S2. The amount and percentage of measured and computed CT data per cruise are given in Table S3. As the measured CT was on average 1.9 µmol kg−1 higher than the canyon-estimated and the computed CT was on average 1.7 µmol kg−1 lower, the new compilation based on these previous conditions allowed us to reduce the difference to 1.5 µmol kg−1.
2.2.3 Anthropogenic CO2 (Cant) calculation
The anthropogenic CO2 (Cant) was estimated by using the biogeochemical back-calculation ϕCT° method, which has an overall estimated uncertainty of ± 5.2 µmol kg−1 (Pérez et al., 2008; Vázquez-Rodríguez et al., 2009). The method considers the change in CT between the preindustrial era (1750) and the time of the observations, along with the processes involved in the uptake and distribution of Cant (biogeochemistry, mixing processes, and air–sea fluxes). The Cant was calculated (Eq. 1) as the difference between the CT at the time of observation, the CT that the seawater would have in equilibrium with a preindustrial atmosphere (preformed CT, ), the offsets of such equilibrium values (air–sea CO2 disequilibrium, ), and the changes in CT due to the organic and carbonate pumps (). The CT and AT at the time of observations and the preformed AT () are needed as input parameters, and the computational procedure was described by Vázquez-Rodríguez et al. (2012a).
The ϕCT° method is an improved process-based Cant estimation method tested and widely applied in the Atlantic Ocean (Vázquez-Rodríguez et al., 2009), which presents distinctive characteristics relative to existing Cant approaches, such as the classical ΔC* (GSS' 96; Gruber et al., 1996) and the TrOCA (Touratier et al., 2007). The main advantages of the ϕCT° method were described by Pérez et al. (2008).
2.2.4 Hydrographic characterization
The characterization of the basins and water masses was done by considering the 2009–2019 mean combined 59.5° N section constructed with potential vorticity, dissolved oxygen and salinity together with the large-scale circulation in the North Atlantic (e.g. Lherminier et al., 2010; Pérez et al., 2021; Sarafanov et al., 2012; Schmitz and McCartney, 1993; Schott and Brandt, 2007; Sutherland and Pickart, 2008). A schematic diagram with the main surface and deep currents in the NASPG is depicted in Fig. 1a. The basin division considered the NAC pathways and revealed a west-to-east distribution comprising the Irminger and Iceland basins and the Rockall Trough. The Iceland basin was delimited along its eastern boundary by the central NAC branches around the northern part of the Hatton Bank and George Bligh Bank and along its western boundary by the return current over the eastern flank of the Reykjanes Ridge slope. This suggests that the Iceland basin could be longitudinally separated into two subregions: the western Iceland basin (24.0–29.5° W) and the eastern Iceland basin (14.0–24.0° W).
The upper layers were mainly occupied by Subpolar Mode Water (SPMW) and North Atlantic Central Water (NACW). SPMW is formed in the Iceland basin (McCartney and Talley, 1982; Brambilla and Talley, 2008; Tsuchiya et al., 1992; van Aken and Becker, 1996), flows eastward to the Rockall Trough, and recirculates across the Reykjanes Ridge (Brambilla and Talley, 2008). In the Irminger basin, SPMW flows with the Irminger Current to the north over the western Reykjanes Ridge flank and to the south over the eastern Greenland slope (Fig. 1a). Thus, SPMW signal was detected in the western and eastern Irminger basin up to 400–700 m depth and limited to subsurface depths in the central part of the basin. NACW was placed above SPMW east of the Irminger basin and separated into two branches: eastern North Atlantic Central Water (ENACW), formed by winter convection in the inter-gyre region and moved poleward from the Bay of Biscay through the Rockall Trough (Harvey, 1982; Pollard et al., 1996), and western North Atlantic Central Water (WNACW), flowing northward with the NAC along the western Iceland basin. The intermediate layers were mainly occupied by Labrador Sea Water (LSW), formed in the Labrador Sea and transported eastward (e.g. Pickart et al., 2003; Fröb et al., 2016). The LSW path diverges into two cores when it reaches the Reykjanes Ridge (Álvarez et al., 2004; Pickart et al., 2003): a fraction of LSW rapidly moved to the Irminger basin and incorporated into the Deep Western Boundary Current (DWBC) (Bersch et al., 2007), and a second LSW core was transported eastward into the Iceland and Rockall basins. In the Irminger and western Iceland basin, LSW placed above Iceland–Scotland Overflow Water (ISOW), which originated from the overflow of Norwegian Sea waters over the Iceland–Scotland ridges and flowed southward and below 1500 m depth through the western NASPG (van Aken and de Boer, 1995; Dickson et al., 2002; Fogelqvist et al., 2003). The bottom of the western Irminger basin was occupied by Denmark Strait Overflow Water (DSOW), recently formed from deep waters from the Nordic seas flowing southward over the Greenland–Iceland ridge and sinking through the eastern Greenland slope (Read, 2000; Stramma et al., 2004; Yashayaev and Dickson, 2008). LSW core transported eastwards rises in depth through the western Hatton Bank flank and occupies the bottom depths in the eastern Iceland basin and in the Rockall Trough. A low-ventilated thermocline layer is placed between SPMW and LSW in the eastern NASPG (García-Ibáñez et al., 2016), which represents the product of mixing with waters coming from the south (i.e. Mediterranean Waters; MW).
To enhance the comprehension of the spatial distribution and trends of the biogeochemical variables and to facilitate comparisons with previous studies along the NASPG, the hydrographic characterization was simplified based on the following principles: (1) the Iceland basin was not divided into its western and eastern parts, and its longitudinal span was delimited by the Reykjanes Ridge (29.5° W) and the Hatton Bank (17° W); (2) upper Labrador Sea Water (uLSW) was separated from deeper LSW (e.g. Stramma et al., 2004); (3) the weak and spatially limited influence of the return current and WNACW was removed by considering the upper and intermediate layers of both the Irminger basin and the Iceland basin fully occupied by SPMW above uLSW; and (4) only the eastern branch of NACW (ENACW), placed above SPMW, was contemplated for the upper Rockall Trough.
The whole water column was separated into layers delimited by potential density isopycnals at a reference pressure of 0 dbar following Azetsu-Scott et al. (2003), Kieke et al. (2007), Pérez et al. (2008), and Yashayaev et al. (2008). The vertically distributed water masses separated into density layers are represented for the entire section in Fig. 1b. The vertical characterization in density layers allows us to consistently compare the low-variable physical and chemical properties within each water mass, enabling us to assume linearity in the ocean CO2 system. The determination of the isopycnal limits between layers in the Irminger and Iceland basins followed previous biogeochemical studies in the western boundary of the North Atlantic (Fontela et al., 2020; García-Ibáñez et al., 2016; Pérez et al., 2008, 2010; Vázquez-Rodríguez et al., 2012a). The surface-to-bottom distribution of the main water masses in these basins (with their respective σ0 lower limits shown in brackets) was SPMW (27.68 kg m−3), uLSW (27.76 kg m−3), LSW (27.81 kg m−3), and ISOW (27.88 kg m−3). The low-temperature and low-salinity DSOW was considered at the bottom of the westernmost part of the Irminger basin. The hydrography of the Rockall Trough has been characterized in previous studies in the northeastern Atlantic (e.g. Ellett et al., 1986; Harvey, 1982; McGrath et al., 2012a, b; Holliday et al., 2000), with the main water masses surface-to-bottom distributed as ENACW (27.35 kg m−3), SPMW (27.68 kg m−3), and LSW (bottom).
2.2.5 Data adjustment for trend computation
The interannual trends were analysed through the whole water column across the Irminger, Iceland, and Rockall basins by yearly averaging the variables for each layer, following previous studies in the NASPG (e.g. Fontela et al., 2020; Garciìa-IbaìnÞez et al., 2016). Linear regressions were applied to the mean values, in which the value of the slope gives the ratios of interannual changes. The errors of the means were calculated through the relation of the standard deviation and the square root of the number of bottle samples in each layer and cruise (). The standard errors of the slopes were calculated by accounting for the error propagation of the annual mean values. The Pearson correlation test was employed to assess the strength and direction of the linear regressions and to evaluate the significance of the interannual trends. This test provided correlation coefficients (r2) and corresponding p-values to determine statistical significance. The p-values ≤ 0.01 indicated that the trends were statistically significant at the 99 % confidence level, the p-values ≤ 0.05 indicated that the trends were statistically significant at the 95 % confidence level, and the p-values ≤ 0.1 indicated that the trends were statistically significant at the 90 % level. Trends with p-values > 0.1 were regarded as not statistically significant but provided an estimation of the temporal evolution of the variables in their respective layers. These not statistically significant trends were explained by the high variability and changes in the low-limit depth of the layers encountered between consecutive years.
As there was a lack of in situ measurements and sampling along the western half of the Irminger basin (36.5–42.5° W) on the cruise of 2019 (due to permit restrictions on studying the national waters of Denmark), the GO-SHIP A25-OVIDE data for the cruise of 2018 (available at SEANOE, https://www.seanoe.org/, last access: 9 December 2024; Lherminier et al., 2022) were considered to adjust the 2019 data. The average values were calculated with both the available data in the easternmost part of the Irminger basin during the cruise of 2019 and the A25-OVIDE-2018 data available in the same part of the section (29.6–36.5° W). The difference between these average values provides the variation in each variable from 2018 to 2019, which can be extrapolated to the western part of the Irminger basin by assuming linearity in the temporal evolution. Thus, the average values for 2019 were adjusted by applying the product with the calculated change between 2018 and 2019.
2.2.6 Deconvolution of the trends
OA trends arise due to the combined variations in T, S, CT, and AT. The influence of each driver on OA and subsequent impacts on marine calcification processes was analysed by assuming linearity and employing a first-order Taylor series deconvolution (Sarmiento and Gruber, 2006) to evaluate the trends for pHT (Fröb et al., 2019; García-Ibáñez et al., 2016; Pérez et al., 2021; Takahashi et al., 1993; Tjiputra et al., 2014) and Ω (García-Ibáñez et al., 2021). The interannual rates of change in pHT and Ω result from the sum of their partial derivatives versus T, S, CT, and AT, calculated based on the mean properties of each layer. The most recent equation defined by Pérez et al. (2021) was used (Eq. 2), in which X represents pHT, ΩCa, and ΩArag. and salinity-normalized CT and AT (NCT and NAT, normalized to a constant salinity of 35) were used to remove the effect of the freshwater fluxes and evaporation/precipitation effects.
It is important to remark that the changes in NAT and NCT are linked with biogeochemical processes which have different influences: the processes involved in the organic carbon pump contribute to strongly change the NCT weakly affecting the NAT, while those involved in the carbonate pump affect the NAT twice as much as NCT. The complexity and heterogeneity of the processes that govern the pHT change were considered by this equation.
The vertical distribution of the physical and biogeochemical variables is depicted for the cruises of 2009 and 2016 in Figs. 2, 3, S2, and S3. The subsurface layers were characterized by warmer and saltier waters than intermediate and deep layers among the three basins (Fig. 2a and b). A west-to-east increase in temperature and salinity throughout the water column was observed in all the cruises. The temperature and salinity signals were highest in the Rockall Trough (4.5–11.0 °C and 35.0–35.4, respectively), followed by the Iceland basin (3.0–7.5 °C and 34.9–35.2, respectively) and the Irminger basin (1.5–6.5 °C and 34.8–35.1, respectively). The longitudinal differences in temperature were more remarkable toward the upper layers through the SPMW and uLSW.
The spatial variability in the physical properties introduced heterogeneities in the distribution of the CO2 system variables. The AT shows a well-correlated linear relationship with salinity throughout the region (AT=54.57 (± 0.36) salinity + 396.7 (± 12.7); r2=0.90 and p-value < 0.01; standard error of estimate of 2.9 µmol kg−1), with lower and vertically homogenized average values in the Irminger basin (2302.8–2307.3 µmol kg−1 in subsurface waters and 2298.8–2301.0 µmol kg−1 in bottom waters) and Iceland basin (2308.7–2315.0 µmol kg−1 in subsurface waters and 2305.2–2308.0 µmol kg−1 in bottom waters) compared to the Rockall Trough (2317.9–2329.1 µmol kg−1 in subsurface waters and 2308.5–2310.9 µmol kg−1 in bottom waters).
The upper layers were characterized by low CT values (2153.7–2160.8 µmol kg−1 in the Irminger basin, 2158.1–2168.4 µmol kg−1 in the Iceland basin, and 2120.1–2131.0 µmol kg−1 in the Rockall Trough), while a rapid increment with depth was found below 100–200 m depth (2154.7–2171.2 µmol kg−1 throughout the section). The notable difference in the distribution of AT and CT (Figs. 2c and 3a, respectively) compared to that of NAT and NCT (Fig. S2) elucidated the remarkable significance of freshwater fluxes on the carbon variable fluctuations during the period of study. The entrance of Cant through the atmosphere–seawater interface caused higher Cant values in the upper layers (higher than 50 µmol kg−1 in the first 1000 m depth; Fig. 3b). The natural component of the CT (; Fig. 3c) correlated with CT (r2=0.87), and showed a distribution characterized by low surface (< 2110 µmol kg−1) and high bottom (> 2130 µmol kg−1) concentrations.
The pHT (Fig. 2d) rapidly decreased with depth, showing the effect of biological uptake in the upper layers and remineralization in deeper areas. The subsurface layer up to 100–200 m depth exhibited pHT values higher than 8.025 units, which fell to 7.975 units in the bottom layers. The pHT profiles reported an intrusion of remineralized and poorly oxygenated water between 500 and 1000 m depth with relatively low pHT (< 7.975) compared to adjacent layers in the Iceland basin and in the western part of the Rockall Trough. This thermocline layer was previously observed at ∼ 500 m depth by García-Ibáñez et al. (2016) along a more meridional transect which crossed the Iceland basin northwest–southeast. It introduces differences in the intermediate water masses between the Iceland and Rockall basins and the Irminger basin.
The spatial and interannual fluctuations in the ventilation rates through changes in the water mass formation and respiration processes represent a source of variability in the biogeochemical patterns. The apparent oxygen utilization (AOU), defined as the difference between saturated oxygen (calculated following Benson and Krause, 1984) and measured oxygen, was used to assess the ventilation of the water masses (Fig. 2e). The high AOU values indicate low ventilation, while low AOU values indicate the opposite. The slow renewal of waters with high AOU favours the accumulation of the product of remineralization (de la Paz et al., 2017). Thus, the areas with higher AOU (Fig. 2e) were found to have a high concentration of CT and a low pHT (Figs. 3a and 2d, respectively). The near-surface waters permanently in contact with the atmosphere exhibited the lowest AOU values (< 20 µmol kg−1). The Irminger Basin presents the most significant water column ventilation among the entire section, with maximum AOU ranging from 35 to 50 µmol kg−1 at the LSW and ISOW and the remarkable intrusion of oxygenated DSOW (> 260 µmol kg−1 DO) over the continental slope with AOU ranging from 30 to 40 µmol kg−1. The intermediate and deep layers of the Iceland and Rockall basins were less ventilated, with AOU values higher than 45–50 µmol kg−1. The thermocline layer placed between 500 and 1000 m depth along these two basins presented the highest maximum AOU throughout the period (> 60 µmol kg−1). The stagnation of these waters corresponds with the high CT and low pHT (Figs. 3a and 2d, respectively) encountered at intermediate depths and should be considered in their temporal evolution.
The temporal distribution and trends of the average physicochemical properties (Figs. 4, 5, 6, S4, S5, and S6) revealed remarkable heterogeneities in their interannual evolution within the period 2009–2019 among the different basins and water masses. The interannual trends are presented along with their respective standard error of estimate and correlation factors (r2 and p-value) in Tables 2 and S4. The observed decrease in temperature and salinity, which was more pronounced in subsurface layers, and its implication on the MCS variations are discussed in Sect. 4.
4.1 Reversal of the physical trends during 2009–2019
The present investigation revealed the cooling and freshening of the upper ocean in the NASPG within the period 2009–2019 (Fig. 4; Table 2), as recently reported since the reversal of climatic trend and surface physical properties occurring after 2005 (Holliday et al., 2020; Josey et al., 2018; Robson et al., 2016; Tesdal et al., 2018). The temperature decreased in the upper ocean (with more than 95 % level of confidence in SPMW, while not statistically significant in ENACW) by 0.05–0.08 °C yr−1 (Table 2), which is consistent with the ratio of heat loss per decade among the first 700 m depth equivalent to approximately −0.45 °C decade−1 (−0.045 °C yr−1) encountered over the period 2005-2014 (Robson et al., 2016). The interannual temperature trends in subsurface layers (Table 2) similarly draw the cooling observed in the Irminger basin between 2008 and 2017 (−0.05 and −0.11 °C yr−1 for summer and winter, respectively; Leseurre et al., 2020) and the winter average surface cooling along the entire NASPG between 2004 and 2017 (−0.08 ± 0.02 °C yr−1; Fröb et al., 2019). The decrement in subsurface salinity (with more than 95 % level of confidence in both SPMW and ENACW) of 0.006–0.018 yr−1 (Table 2) agreed with the interannual rates provided by Tesdal et al. (2018) for the Irminger basin (−0.007 ± 0.002 yr−1) and for the central eastern NASPG (−0.020 ± 0.003 yr−1) over the period 2004–2015.
The fluctuations in physical properties were linked to a decrease in oceanic heat transport and storage within the NASPG, which has been attributed to changes in the AMOC over decadal to multidecadal timescales (Balmaseda et al., 2007; Desbruyères et al., 2013; Mercier et al., 2015; Smeed et al., 2018). However, the assessment of the temporal evolution of the AMOC in high latitudes remains uncertain, and there is no evidence of its impact on physical patterns across the NASPG on an interannual scale (Jackson et al., 2022). The changes in the atmospheric forcing also account for the variability in the upper-ocean physical properties and can have a cumulative effect over several years (Balmaseda et al., 2007; Böning et al., 2006; Eden and Willebrand, 2001; Marsh et al., 2005).
The distribution of the water mass properties, the processes of vertical and horizontal mixing, and the circulation patterns in the Irminger and Iceland basins were described by García-Ibáñez et al. (2016, 2018). The poleward path of the ENACW (Pollard et al., 1996) and its mixing with waters moving from the west across the NASPG (Ellett et al., 1986) accounted for the highest subsurface temperature and salinity signals observed in the Iceland basin and even more in the Rockall Trough. The SPMW and LSW in the Rockall Trough exhibited higher temperature and salinity signals in the order of ∼ 1 °C and ∼ 0.05–0.1, respectively, compared to the Irminger and Iceland basins (Fig. 4). The NASPG circulation patterns account for these differences by the eastward transport of these water masses, which subduct below the ENACW in the Rockall Trough and mix with warmer and more saline intermediate waters (i.e. Mediterranean Water) moving from the south (e.g. Ellett et al., 1986; Harvey, 1982; Holliday et al., 2000).
The low temperature and salinity signals in the less stratified Irminger basin (Fig. 2) experienced weaker interannual decreases in subsurface layers and higher rates of cooling and freshening in intermediate and deep waters compared with the Iceland and Rockall basins (Fig. 4; Table 2). These longitudinal thermohaline heterogeneities were related to the enhancement of vertical mixing processes in areas of water mass formation along the western NASPG (Fröb et al., 2016; García-Ibáñez et al., 2015; Pickart et al., 2003; Piron et al., 2017) and to the water mass transformation along the NAC (Brambilla and Talley, 2008). The strongest decrement in subsurface temperature and salinity along the Iceland and Rockall basins (Fig. 4; Table 2) coincided with the significant event of heat loss and freshening observed by Holliday et al. (2020) in the eastern NASPG over the period 2012–2016, the so-called Great Salinity Anomaly. This pattern was not easily discernible in the Irminger basin due to the transport of freshwater through the Fram Strait and due to the redirection of the Labrador Current combined with changing wind stress curl (Holliday et al., 2020).
4.2 Evaluation of the interannual trends in CT in response to changes in Cant and Cnat
The changes in the physical patterns influenced the interannual variability in the MCS. The increase in CT expected in the upper ocean due to the atmospheric CO2 uptake was offset by the cooling and freshening (and de-alkalinization) of the subsurface layers. The observed rates of increase in CT (Table 2) did not show notable differences with respect to the interannual trends determined from previous decades in the Irminger and Iceland basins (0.62–0.82 and 0.38–0.64 µmol kg−1 yr−1, respectively; García-Ibáñez et al., 2016) and at IRM-TS and IS-TS (0.49–0.71 and 0.39-0.94 µmol kg−1 yr−1, respectively; Pérez et al., 2021). The interannual rates of increase in NCT were higher than those of CT in the subsurface layers, while the trends were similar among the intermediate and deep layers (Table 2). A detailed description of the interannual AT trends is provided in Appendix B.
The entrance of Cant through the air–sea interface and its accumulation dominated the observed increase in CT (Fig. 5 and Table 2). The increase in ventilation over 2009–2019, shown by the negative AOU trends (Fig. S6 and Table S4), favoured the vertical mixing. The upper waters, due to be in contact with the atmosphere and have high biological production rates during the warm months, show high Cant and low Cnat contents. The enhanced transport of upper waters toward the interior ocean explained the rapid growth in Cant at intermediate and deep layers. The Cant trends ranged between 0.85 and 1.77 µmol kg−1 yr−1 (statistically significant at the 99 % level). They were higher than those observed on a decadal to multidecadal scale since the late 20th century in the Irminger and Iceland basins (0.21–0.89 µmol kg−1 yr−1 during 1991–2015; García-Ibáñez et al., 2016; and 0.38–1.15 µmol kg−1 yr−1 during 1983–2013; Pérez et al., 2021), which show the enhancement in the Cant accumulation on interannual scales during periods of high ventilation, as previously reported by Pérez et al. (2008). The Cnat shows an inverse relationship with Cant at intermediate and deep layers (r2 > 0.5; statistically significant at the 95 % level of confidence) and weakly decreased across the western deep-convection NASPG (Fig. 5 and Table 2). The growth in phytoplankton biomass (Ostle et al., 2022), together with the enhanced export toward the interior ocean under increasing ventilation, accounts for the observed decrease in Cnat in upper waters. The Cnat showed a weaker decrease at intermediate and deep layers due to the dominance of remineralization, which was not intense enough at this time of the year to neutralize the downward transport of low-Cnat water from the surface but partially compensated for its effect. The observed variations in Cnat between years, which were strongly linked with fluctuations in the biological processes, explained its non-significant trends at several layers. The changes in the circulation pattern of the NASGP, and thus in the horizontal advection related with the climatological forcing (Balmaseda et al., 2007; Desbruyères et al., 2013; Mercier et al., 2015; Thomas et al., 2008; Xu et al., 2013), could behave as a source of variability for both Cant and Cnat and also implies differences between consecutive years.
The vertical distribution of Cant and Cnat along the transect (Fig. 3b and c) reflects the higher stratification in the Iceland and Rockall basins compared to the well vertically mixed Irminger basin. It represents a source of variability in the interannual changes in Cant among the different layers and basins (Fig. 4; Table 2). In the western NASPG, the surface heat loss and enhanced deep convection processes favour the solubility and subsequent uptake of atmospheric CO2 and inject oxygenated and CO2-rich waters into deeper layers (Messias et al., 2008). It likely accounts for intermediate and deep layers in the Irminger basin exhibiting the highest Cant accumulation rates in the NASPG (Fig. 5; Table 2). The highest ventilation of the interior ocean in the Irminger basin was demonstrated by its minimum AOU values (Figs. 2 and S6). It induced a rapid surface-to-bottom transport of Cant shown by its highest rates of increase in intermediate and deep waters throughout the region (Fig. 5; Table 2). The high Cant values and their rapid increment at DSOW were explained by the improved oxygenation of this layer at shallower depths (interannual AOU trends given in Table S4) and its subduction through the continental slope below ISOW.
In the eastern NASPG, the stratification weakened due to the path of the NAC warming the upper water column eastward and accounted for slowing down the increase in Cant in the Iceland basin. An exception is the Rockall basin, in which the relatively warm and salty ENACW (Figs. 2 and 4) showed the maximum Cant (58–68 µmol kg−1) and minimum CT (2120–2131 µmol kg−1) and Cnat (2058–2070 µmol kg−1) throughout the region (Figs. 3 and 5). The enhanced oxygenation of the ENACW (AOU < 20 µmol kg−1 and reaching the oxygen saturation after 2014) was related, with its high rates of renovation due to its path from the south (Pollard et al., 1996) and its mixing with waters moving eastward (Ellett et al., 1986). This favoured the transport of subsurface waters with relatively high Cant content from lower latitudes into the Rockall Trough and introduced wide differences with respect to adjacent deeper layers moving from the western NASPG, which strengthened the stratification. As the NAC transports nutrient-rich waters northward and eastward into subsurface layers in the Rockall Trough, biological production tends to increase, and it actively reduced the CO2 excess from the ENACW (McGrath et al., 2012b), as proved by the observed low CT and Cnat. The ENACW presented relatively low Cnat and CT (Fig. 5) and high AT and NAT in 2014. These variations indicated that the increase in carbonate and bicarbonate concentrations raising AT and NAT was compensated for by the depletion in dissolved CO2. The relatively high temperature and NAT in 2014 likely indicated an improved spreading of subsurface waters from subtropical latitudes into the Rockall Trough. The enhanced biological production in these waters, together with the reduction in solubility due to warming which favours the CO2 evasion to the atmosphere, accounts for the decreasing Cnat and thus CT.
The strong interannual increase in the ENACW ventilation during this decade increased the Cant and decreased the Cnat (Rodgers et al., 2009), keeping the CT approximately constant (Table 2). The poorly ventilated thermocline (AOU > 60 µmol kg−1), placed between 500–1000 m in the eastern NASPG, induced a Cnat-driven increase in CT among the SPMW and uLSW. However, its intrusion does not present relevant variations with time and thus does not introduce differences in the interannual trends in the biogeochemical properties.
4.3 Acidification trends
The interannual pHT trends (Fig. 6, Table 2) exhibited the acidification of the whole water column in NASPG during the period 2009–2019. Despite the acidification rates observed in most subsurface waters among the three basins not being significant at the 90 % confidence level (Table 2), they were consistent in the interval of 0.001 units yr−1 with the rates observed during longer periods at time series stations located across the North Atlantic: at subtropical latitudes (0.0018 ± 0.0002 units yr−1 during 1995–2014 and 0.0020 ± 0.0001 units yr−1 during 1995-2023 at ESTOC; González-Dávila and Santana-Casiano, 2023; and 0.0017 ± 0.0001 units yr−1 during 1983–2014 at BATS; Bates et al., 2014) and subpolar latitudes (−0.0017± 0.0002 units yr−1 at IRM-TS during 1983–2013 and −0.0026 ± 0.0002 units yr−1 at IS-TS during 1985–2013, summarized by Pérez et al., 2021). In addition, the changes in the surface pHT trends were reported by Leseurre et al. (2020) in the western NASPG within a wide latitudinal area (54–64° N) during the period 2008–2017 in comparison with the periods 1993–1997 and 2001–2007. However, the highly significant cooling observed in SPMW, the year-to-year variations in ventilation (shown by the annual average AOU and its trends in Fig. S6), and thus the variations in Cnat and Cant (Fig. 5) introduced relevant changes in pHT on an interannual scale and explained the low-significance trends. The extremely negative NAO index of 2009–2010 (Jung et al., 2011) weakened the wind forcing, which implies variability in the circulation patterns and physical properties of the surface waters, consequently reducing deep convection. This was observed in the slowdown in ventilation from 2009–2010 (Fig. S6) in the Irminger and Iceland basins which caused a relative increase in Cnat and decrease in Cant (Fig. 5).
The highest acidification rates were found through intermediate and deep waters in the Irminger and Iceland basins, coinciding with the highest rates of increase in Cant (Table 2; trends statistically significant at more than 95 % level of confidence). The exception is the DSOW, which presented an interannual decrease in pHT in phase with that of the uLSW. This singularity was previously observed by García-Ibáñez et al. (2016), who noticed the similar trends between the DSOW and LSW attributed to the recent formation and sink through the continental slope of the DSOW. The acidification rates found among the uLSW, LSW, and ISOW (0.0026–0.0032 units yr−1) experienced, on an interannual scale, an acceleration in comparison with previous reports based on long-term records (e.g. 0.0009–0.0017 units yr−1 estimated for 1981–2008 by Vázquez-Rodríguez et al. (2012b); 0.0013–0.0016 units yr−1 estimated for 1991–2015 by García-Ibáñez et al., 2016; 0.0015–0.0019 units yr−1 estimated for 1983–2013 at the IRM-TS by Pérez et al., 2021; and 0.0019 ± 0.0001 units yr−1 estimated for 1993–2017 by Leseurre et al., 2020). Contrasting the rates of change in pHT during the decade of study with those encountered by these multidecadal evaluations (and considering the total number of years comprising each of the studies and the changes in the ion hydrogen concentration [H]), we estimate an acceleration in the rates of acidification of 0.4 %–5.4 % in the Irminger basin and 1.0 %–9.0 % in the Iceland basin during the 2010s since the late 20th century. This acceleration was mainly attributed to increased deep-water ventilation (shown in the rapid decrease in AOU in Fig. S6) favouring the progressive increase in the accumulation of Cant and Cnat toward intermediate deep layers, in which cooling was not significant in the Irminger basin and not intense enough in both basins to compensate the acidification.
Despite the similarities encountered in the pHT trends among both basins, the average values presented differences which may be closely linked with the transport and transformation of the water masses along the NASPG and mainly modulated by the Reykjanes Ridge (García-Ibáñez et al., 2015, 2016, 2018). The transformation of the SPMW formed in the Iceland basin (McCartney and Talley, 1982; Brambilla and Talley, 2008; Tsuchiya et al., 1992; van Aken and Becker, 1996) and flowing with the NAC across the Reykjanes Ridge (Brambilla and Talley, 2008) accounted for the lower pHT values in the Irminger basin. The differences in pHT found at intermediate and deep layers were related to the divergence of the LSW path into two cores when it reaches the Reykjanes Ridge (Álvarez et al., 2004; Pickart et al., 2003) and the ISOW path flowing southward along the western Iceland basin and recirculating northward into the eastern Irminger basin (Dickson and Brown, 1994; Saunders, 2001). These differences in the spreading of water masses enhanced the ventilation in the Irminger basin favouring the fall in pHT compared with the Iceland basin. The rise in the ISOW following the Reykjanes Ridge slope through its eastern flank favoured a strong vertical mixing over and around the ridge (Ferron et al., 2014) and a reduction in the LSW core in the Iceland basin (García-Ibáñez et al., 2015), contributing to the resemblance of pHT values and trends among the uLSW and LSW in this basin.
The upper waters of the Rockall Trough presented the maximum pHT throughout the transect (8.02–8.08 units). The observed strong pHT fluctuations between years related to interannual changes in the NAC do not allow us to discern trends with an interval of confidence equal to or greater than 90 %. The interannual decrease in pHT in the ENACW (∼ 0.001 units yr−1) was half that observed along southernmost transects in the Rockall Trough between 1991 and 2010 (∼ 0.002 units yr−1; McGrath et al., 2012a). The temporal distribution of the average pHT (Fig. 6), highly influenced by the high ventilation (seen in minimum AOU values that are highly variable between years and which tend to decrease with 99 % statistical confidence; Fig. S6 and Table S4), allows us to discern two periods: the approximately constant ventilation rates keep a steady state in terms of pHT during 2009–2011, while the progressive renewal and oxygenation of subsurface waters after 2012 (and peaking in this year) increase the pHT. The renewal of waters in the shallow Rockall Trough, in contrast with the westernmost NASPG, was primarily driven by lateral rather than vertical advection. The modifications of the ENACW through air–sea exchange and mixing with adjacent waters modulated its properties at different timescales (Holliday et al., 2000) and caused the observed variations in the MCS. The variations in pHT between consecutive years after 2012 may be attributed to the fluctuations in the spreading into the Rockall Trough of several water masses occupying different depths coming from the south and east (Ellett et al., 1986; Pollard et al., 1996). Holliday et al. (2020) reported the reduction in the spreading of saline subsurface waters from subtropical latitudes and the diversion of Arctic freshwater from the western boundary into the eastern NASPG during 2012–2016. The subsequent freshening of the ENACW compensated for the increase in AT expected without the effect of salinity (seen in the decreasing AT against the increasing NAT; Fig. S4 and Table S4) and weakened the increase in CT expected due to poleward advection (see in the slowdown in the rise of CT in comparison to that of NCT; Figs. 5 and S5 and Tables 2 and S4). The CT remains approximately constant (Fig. 5 and Table 2) due to the increase in Cant (0.85 ± 0.11 µmol kg−1 yr−1; p-value < 0.01) being neutralized by the decrease in Cnat (−0.84 ± 0.50 µmol kg−1 yr−1; p-value < 0.1). These findings suggest that the atmospheric CO2 invasion was offset by the growing phytoplankton biomass favouring its biological uptake (Ostle et al., 2022) and by the weakening transport of remineralized and saline water from the south (Holliday et al., 2020), thus compensating for the acidification of the ENACW.
The SPMW among the Iceland and Rockall basins showed similar pHT trends (Table 2) due to the emplacement of the poorly oxygenated thermocline at these depths (García-Ibáñez et al., 2016). The approximately constant AOU at SPMW in the eastern NASPG (Fig. S6) proved its steady ventilation, which can introduce differences in the acidification rates among the layers comprising the Rockall Trough. The influence of the cooling and freshening of deeper areas due to the spreading and horizontal mixing was notable in the LSW, which presented slightly higher pHT values in the Rockall Trough with respect to the adjacent Iceland basin.
4.4 Interannual changes in ΩCa and ΩArag
The analysis of the changes in ΩCa and ΩArag hold significance in elucidating the potential effects of OA over the CaCO3 species calcite and aragonite, thereby offering insights into their potential implications for marine calcifying organisms and ecosystems. The vertical distribution of ΩCa and ΩArag is presented in Fig. S3. The upper and intermediate layers up to 2100–2400 m depth of the Irminger and Iceland basins and the whole Rockall basin were supersaturated for aragonite (ΩArag > 1), while the DSOW was undersaturated (ΩArag < 1). The ISOW, with ΩArag ranging between 1.0 and 1.1 at the beginning of the decade, crossed to undersaturated conditions at the end of the decade due to the progressive rise of the aragonite saturation horizon (depth at which ΩArag=1). The whole water column throughout the section was supersaturated for calcite (ΩCa > 1) due to its lower solubility (Mucci, 1983). The ΩCa and ΩArag in the SPMW (2.2–2.7 and 1.4–1.7 units, respectively) were lower than those encountered equatorward in the subsurface Atlantic (> 4.0 and > 2.5 units, respectively; González-Dávila et al., 2010; González-Dávila and Santana-Casiano, 2023). The poleward pathway of low-latitude upper waters through the Rockall Trough explained the higher ΩCa and ΩArag found in the ENACW (3.0–3.6 and 1.8–2.3 units, respectively). The reduction in ΩCa and ΩArag towards higher latitudes in the upper and intermediate layers smooths the vertical gradients in the NASPG compared to the subtropical latitudes (González-Dávila et al., 2010; González-Dávila and Santana-Casiano, 2023).
The correlation of Ω with pHT (r2=0.90) with a level of significance higher than 99 % explains that the individual components driving OA accompanied the decline in Ω. The interannual trends in ΩCa and ΩArag (Fig. 7, Table 2) exhibited the decrement through the whole water column along the NASPG with a level of statistical confidence generally higher than 90 %. The rates of decline for ΩCa and ΩArag in the SPMW (0.011–0.021 and 0.007–0.013 units yr−1, respectively) were consistent with the trends observed up to 100 m depth at ESTOC between 1995 and 2023 (0.019 ± 0.001 and 0.012 ± 0.001 units yr−1, respectively; González-Dávila and Santana-Casiano, 2023) and in surface waters at the IS-TS between 1985 and 2008 (0.0117 ± 0.0011 and 0.0072 ± 0.0007 units yr−1, respectively; Olafsson et al., 2009). The ΩArag trend estimated for SPMW in the Irminger basin (−0.007 ± 0.003 units yr−1) is consistent with that reported for surface waters by Bates et al. (2014) over 1983–2014 (−0.008 ± 0.004 units yr−1) and falls within the range of those estimated during summer by Leseurre et al. (2020) over 2008–2017 (−0.005 ± 0.001 units yr−1). Chau et al. (2014) recently deduced from reconstructed products a slower decrease (−0.004 ± 0.001 units yr−1), highlighting the large uncertainty in the estimations of interannual trends for pH and ΩArag across the NASPG due to the low data-sampling frequency at their monitoring sites. The decline in ΩArag in the SPMW accelerated by ∼ 26 % and ∼ 51 % in the Irminger and Iceland basins, respectively, in comparison with the trends given for the period 1991–2018 (0.0052 ± 0.0006 and 0.0049 ± 0.0015 units yr−1, respectively; García-Ibáñez et al., 2021). The observed decrease in ΩArag in the SPMW was ∼ 23 % faster in the Rockall Trough than in the adjacent Iceland basin. The interannual decline in ΩCa and ΩArag in the ENACW (0.012 and 0.008 units yr−1, respectively) agreed with these previous observations but were not statistically significant, likely due to the high variability modifying the changes in pHT in this layer (see Sect. 4.2). Despite the acceleration of the acidification rates toward intermediate and deep layers, the declining rates weakened for ΩCa and even more for ΩArag (Table 2). Moreover, the vertical profiles were approximately constant throughout the section in contrast with the heterogeneous vertical distribution of pHT between basins. This behaviour was previously observed in the Irminger and Iceland basins by García-Ibáñez et al. (2021) and explained by pressure- and temperature-induced changes in the speciation of the CO2–carbonate chemistry species (Jiang et al., 2015) and in the solubility of calcite and aragonite (Mucci, 1983). Their combined action counterbalanced the alterations resulting from acidification, particularly in colder deep waters, where the solubility of calcite and aragonite was reduced (García-Ibáñez et al., 2021). However, the decrease in ΩCa and ΩArag along the uLSW, LSW, and ISOW accelerated by 40 %–75 % in relation to the trends reported by García-Ibáñez et al. (2021) for the Irminger and Iceland basins. The LSW and ISOW presented faster-declining rates for ΩCa and ΩArag in the Irminger basin (Table 2), which may be caused by the enhanced ventilation of the interior ocean which accelerated the acidification (see Sect. 4.2). The westward rise in the depth of these layers along the Greenland continental slope, accompanied by a subsequent elevation in the horizons of solubility, resulted in reduced buffering capacity against acidification effects in the Irminger basin when compared to the Iceland basin. In contrast, the rise in the depth of LSW in the Rockall Trough favours the increment of ∼ 0.2 units in ΩCa and Arag with respect to the Iceland basin but had no influence on the interannual trends, which coincided. The ΩCa and ΩArag in the DSOW, despite showing a trend accelerated by ∼ 30 % compared to that observed by García-Ibáñez et al. (2021), presented the weakest interannual decreases throughout the section (0.004 ± 0.003 and 0.002 ± 0.001 units yr−1, respectively) due to the high pressure and low temperatures compensating for the rapid acidification (Fig. 6, Table 2).
The decrease in Ω could have severe consequences on organisms reliant on aragonite, which is less resistant to dissolution than calcite (Mucci, 1983; Broecker and Peng, 1983) and is thus expected to experience relatively higher susceptibility to the effects of OA over shorter timescales (Raven et al., 2005). The progressive reduction in ΩArag has driven a long-term decrease in the depth of the aragonite saturation horizon (ΩArag=1) by 80–400 m since the preindustrial era (Álvarez et al., 2003; Feely et al., 2004; Pérez et al., 2013, 2018; Tanhua et al., 2007; Wallace, 2001) and is projected to shoal by more than 2000 m by the end of the century under the IS92a scenario (Orr et al., 2005). The vertical section of ΩArag in Fig. S3 shows the shallower aragonite saturation horizon during 2009 and 2016 compared to preindustrial times. Likewise, Orr et al. (2005) suggested that high-latitude surface waters could become undersaturated if the atmospheric CO2 concentration doubles the preindustrial concentration within the next 50 years. This would reduce the calcification rates in some shallow calcifying organisms by more than 50 % (Feely et al., 2004).
The planktonic aragonite-producing pteropods (e.g. Limacina helicina and Clio pyramidata), which have high population densities in subpolar regions up 300 m depth (Bathmann et al., 1991; Urban-Rich et al., 2001) and play a key role in the export flux of both carbonate and organic carbon (Accornero et al., 2003; Collier et al., 2000), are expected to be highly vulnerable to OA if the aragonite saturation horizon continues to shoal (Orr et al., 2005). The undersaturation toward the intermediate and upper layers negatively influences the aragonite-based CWCs (e.g. Lophelia pertusa and Madrepora oculata), which show their highest diversity and population along the NASPG between 200 and 1000 m depth in the global ocean (Roberts et al., 2009). In fact, several studies reported that CWC ecosystems are anticipated to be among the first deep-sea ecosystems to experience acidification threats (Gehlen et al 2014; Guinotte et al., 2006; Maier et al., 2009; Raven et al., 2005; Roberts et al., 2009; Turley et al., 2007), particularly in the North Atlantic (Pérez et al., 2018). The findings presented here contribute to a deeper understanding of the biological impacts of OA along the NASPG.
4.5 Processes controlling OA and Ω trends
Due to the variety of processes involved in OA, a decomposition of the pHT and trends into the individual components that govern their spatiotemporal variability took place (see Sect. 2.2.6). The interannual variations in pHT () and Ω () explained by fluctuations in temperature ( and ), salinity ( and ), AT ( and ), and CT ( and ) were calculated for each layer and basin (Eq. 2) and are summarized in Tables 3 and 4. The positive contributions of each of the drivers indicate increments, while negative contributions indicate the opposite. The cumulative changes resulting from the distinct drivers (referred to with the subscript “calculated” in Tables 3 and 4) were consistent with the observed pHT trends (referred to with the subscript “obs” in Tables 3 and 4), thereby instilling confidence in the methodology. An exception was found at the DSOW, in which the strong NAT decrease had a crucial influence on the declining Ω.
The minimal differences between observed and calculated rates of change have added coherence to the non-significant trends identified for pHT and Ω trends and/or their drivers in some basins and layers (Tables 2, 3, and S4). In the entire section at SPMW, the (calculated), explained by the cumulative impact of its drivers (all of them statistically significant at the 95 % level of confidence), aligns within a range of < 0.0002 units yr−1 with (obs) (which was not significant). In the Irminger and Iceland basins at intermediate and deep layers, the (obs) (statistically significant at least at the 95 % level of confidence) was consistent within the range of < 0.001 units yr−1 with (calculated) (T, S, and NAT show non-significant trends at some of the intermediate and deep layers). The interannual variations were non-significant for pHT for its drivers in the Rockall Trough at LSW and ENACW. The high temporal dispersion of average data in these layers was mainly related to the rise in depth of LSW along the eastern continental slope and its mixing with shallower waters coming from subtropical latitudes (Ellett et al., 1986; Harvey, 1982; Holliday et al., 2000). The substantial variability in the Rockall Trough made it difficult to discern OA patterns and its drivers on an interannual scale. Therefore, long-term monitoring and the development of multidecadal-scale studies are required in this area to derive significant conclusions.
The cooling and freshening modified the physically driven pHT changes compared with those encountered by García-Ibáñez et al. (2016) during previous decades in the western NASPG. The cooling contributed to an increase in the pHT and compensated for the observed acidification rate. The increase in pHT due to temperature fluctuations was at its maximum at SPMW (∼ 0.001 units yr−1) and negligible in deeper layers (< 0.0003 units yr−1 at uLSW and below). The increase in pHT due to salinity fluctuations was minimal (< 0.0001 units yr−1) through the whole water column in the three basins, reflecting that the observed freshening caused insignificant changes in pHT. The temperature and salinity contributed by 19.1 %–26.5 % and 1.2 %–3.3 %, respectively, to the total pHT change in the upper layers, while presented an influence 3 times lower toward the interior ocean (1.3 %–7.6 % and < 0.6 %, respectively). The enhanced convective processes in the Irminger basin (e.g. Fröb et al., 2016; García-Ibáñez et al., 2015; Gladyshev et al., 2016a, b; Piron et al., 2017), together with the rapid transport of LSW from the Labrador Sea to the Irminger basin (Yashayaev et al., 2007), introduced differences to the thermally driven pHT in the Iceland basin, as previously reported by García-Ibáñez et al. (2016). The advection of LSW through the Greenland continental slope also affected the DSOW (Read, 2000; Yashayaev and Dickson, 2008), which shows thermally driven pHT changes consistent with those encountered through the LSW in the Irminger basin.
Despite the negligible direct contribution of the salinity fluctuations over the pHT changes, the freshwater fluxes influence the distribution of AT and CT, indirectly affecting pHT trends. After removing salinity effects, NAT shows positive trends in subsurface layers and negative trends toward the interior ocean (Fig. S4 and Table S4; detailed in Appendix B). The changes in NAT described the 7.8 %–10.1 % of the total pHT change at SPMW. The NAT-driven pHT changes weakened with depth (Table 3) due to the insignificantly interannual changes in NAT through LSW and ISOW (Table S4). The weak contribution of NAT in these layers (1.3 %–5.1 %) could be related to the difficulty in reversing the large alkalinization until the 2000s, resulting from the slowdown in the formation of LSW since the mid-1990s (Lazier et al., 2002; Yashayaev, 2007), which was transmitted towards deeper overflow waters (Sarafanov et al., 2010). The substantial interannual changes and the abrupt change between periods of increase and decrease in the seawater properties at DSOW (Yashayaev et al., 2003; Stramma et al., 2004) linked with changes in the LSW formation (Dickson et al., 2002) explain the rapid decrease in NAT (Table S4), which explains the 14.6 % decline in the pHT.
The increase in NCT driven by the rise in Cant was found to govern the acidification, with a contribution higher than the 67 % across the entire water column. The NCT-driven pHT decline was close to twice the observed and calculated acidification rates through the SPMW (Table 3). However, the contribution of NCT at SPMW (67 %–69 %) was lower than that encountered toward the interior ocean (82 %–96 %) due to the relevance of temperature and AT over pHT trends in the upper layers. The cooling and increase in NAT counteracted the acidification expected by the increasing CT at SPMW by 28 %–34 % and 11 %–15 %, respectively. In the intermediate and deep layers, the thermal neutralization of the CT-driven acidification was weaker (1.5 %–9.3 %) and the decreasing NAT contributed to decreasing the pHT by < 15 %. Freshening played a minor role in countering acidification (< 6 % in upper layers and < 2 % in the interior ocean).
In line with the declining pHT, 79 %–83 % of the decrease in Ω in subsurface layers was attributed to the Cant-driven rise in NCT, with this influence reaching up to 97 % in deeper waters. The increase in NAT in the SPMW accounted for 10.4 %–13.0 % in the trends and counteracted its NCT-driven decrease by 12.6 %–16.2 %. The contribution of the NAT fall and reversal toward deeper waters explained < 6 % of the decline in the uLSW, LSW, and ISOW in the Irminger basin and < 11 % in the Iceland basin. The pronounced impact of the rapid decrease in NAT on the acidification of the DSOW (see Sect. 4.3) depicted the greater contribution of NAT encountered in the Irminger basin (16 %) and compensated for the NCT-driven decrease in Ω by 36.4 %. In the Rockall Trough, the contribution of NCT changes was reduced in the LSW (78.2 %–79.0 %) compared to the Irminger basin (94.5 %), while the effect of NAT fluctuations tripled until reaching 12.6 %–12.7 %.
Despite the crucial role of cooling in mitigating acidification, temperature fluctuations have the opposite effect on Ω due to the thermodynamic relationship inherent in the acid–base equilibrium of the CO2–carbonate system (Dickson and Millero, 1987). In the Irminger and Iceland basins, the observed decrease in temperature contributed negligibly to the decline in Ω (3.6 % in the SPMW and less than 2 % in intermediate and deep waters). The influence of salinity, as with the pHT trends, was minimal: the observed freshening slightly elevated the trends, offsetting the decline by 4.6 %–4.7 % in the SPMW, 1.1 %–2.1 % in the uLSW and LSW, and 0.5 %–1.2 % in the ISOW and DSOW. Even with the slightly faster cooling and freshening observed in the Rockall Trough, the contributions of temperature and salinity to Ω did not exceed 7 % in any of its layers.
This research has evaluated the interannual changes in the basin-wide MCS dynamics along the NASPG during 2009–2019. Despite the observational period being relatively short for quantifying long-term trends and formulating significant future projections, the findings have allowed us to evaluate the ocean response, in terms of MCS dynamics and on an interannual scale, to changes in deep-water convection and to isolate events affecting the physical patterns. The assessment of OA within the Irminger and Iceland basins was enhanced by supplying novel data and trends spanning 1 decade in which the physical patterns reversed. Additionally, the study provides an unprecedented analysis of the physicochemical variations in the Rockall Trough, which is crucial for the assessment of the entire longitudinal span of the NASPG. It facilitates a more accurate understanding of the mechanisms dictating basin-scale acidification processes and advances our understanding of OA in the North Atlantic and the global ocean.
Overall, the entrance and accumulation of Cant and interannual acidification trends were strongly affected by the cooling, freshening, and enhancement in the oxygenation during this decade. The longitudinal span of the NASPG and the differences in circulation patterns, water masses, and bathymetry behaved as a source of spatiotemporal variability. The interannual acidification trends of the main water masses across the NASPG ranged between 0.0006–0.0032 units yr−1 and caused a decline in the ΩCa and ΩArag of 0.004–0.021 and 0.003–0.013 units yr−1, respectively. The convective processes increased the accumulation rates of Cant in the interior ocean by 50 %–86 % and accelerated the acidification rates by around 10 % compared to previous decades in the Irminger and Iceland basins. The shallower hydrography of the Rockall Trough and the poleward circulation patterns accounted for differences in the acidification rates with respect to the surrounding waters.
The Cant-driven increase in NCT was found to govern the acidification of the NASPG, with contributions exceeding 60 %. The combined effect of the decreasing temperature, salinity, and NAT neutralized close to one-half of the acidification along the entire longitudinal span of the SPMW. The enhanced deep-water ventilation in the western NASPG slowed down the cooling and freshening toward the interior ocean, weakening the physical counterbalance of acidification.
The present investigation emphasizes the progressive increase in the uptake and accumulation of Cant and the subsequent acceleration in OA along the NASPG. Novel data and results provided could be compared with other repeated hydrographic section data at mid- and high latitudes in the North Atlantic, such as the A02, A25, AR07E, and AR28 framed in the GO-SHIP programme, and are used in conjunction to develop future investigations. Additionally, they contribute to the improvement of the projections pertaining to the future state of the oceans run by models and forecasts. Considering the important variability in the mechanism controlling the distribution of the physico-biogeochemical properties and particularly the OA in the North Atlantic, this research aims to highlight the necessity of continuing to monitor and sample the whole water column through repeated hydrographic sections, especially through the highly variable but less assessed easternmost part.
The sensor-measured DO data for the cruise of 2019 were corrected by considering the DO output data given by the neural network ESPER_NN (Carter et al., 2021) for the cruises of 2016 and 2019 (hereinafter ESPER-estimated DO) and the Winkler-measured DO during the cruise of 2016. Among the 16 equations provided by the ESPER_NN, which differently combine seawater properties as predictors, we use Eq. (8), which only needs the T and S an inputs (due to lack of measured macronutrients during the cruise of 2019), along with latitude, longitude, depth, and date (see Table 2 in Carter et al., 2021). The reported root-mean-square error (RMSE) of Eq. (8) for DO estimations in the global ocean is ± 9.7 µmol kg−1, which is reduced for intermediate waters (1000–1500 m) to ± 5.9 µmol kg−1 (see Table 7 in Carter et al., 2021). Additionally, a new set of DO for 2019 based on Winkler data for 2016 was computed, which was referred to in this study as “pseudo-Winkler” data. The difference between Winkler-measured and ESPER-estimated DO during 2016 was interpolated to the longitudes and depths of the samples of 2019 by applying Delaunay triangulation. The pseudo-Winkler data were described as the sum of these interpolated differences and the ESPER-estimated DO data for 2019. The longitudinal distribution of measured and ESPER-estimated DO data for 2016 and 2019 is depicted in Figs. S1a and S1b. The interpolated pseudo-Winkler data for the cruise of 2019 are included in Fig. S1a.
The sensor records of DO in 2019 were on average 4.90 µmol kg−1 lower than the ESPER-estimated and 10.31 µmol kg−1 lower than the pseudo-Winkler. A higher discrepancy was observed in the average sensor-measured DO in the eastern part (237.60 ± 15.00 µmol kg−1) compared with the western part (281.40 ± 14.75 µmol kg−1). The average differences (measured minus ESPER-estimated DO and measured minus pseudo-Winkler DO, ΔDOmeas-ESPER and ΔDOmeas-pseudoWinkler, respectively; Figs. S2c and S1d) show that the sensor records were strongly underestimated in the eastern part (−20.98 ± 10.91 and −28.77 ± 12.60 µmol kg−1, respectively) and weakly overestimated in the western part (8.59 ± 8.53 and 5.18 ± 12.02 µmol kg−1, respectively) during the cruise of 2019. These differences were corrected separately west and east of 21.5° W by using the relationship . The averages of this relationship in the western and eastern parts of the transect (0.016 and −0.12 µmol kg−1, respectively) were used as corrector factors. The corrected DO values were given by the product of the measured DO and .
The interannual trends in AT (Fig. S4 and Table S4) were found to be highly impacted by freshening, with decreasing rates ranging from −0.33 to −0.71 µmol kg−1 yr−1 among the SPMW and ENACW and from −0.01 to −0.18 µmol kg−1 yr−1 within the uLSW, LSW, ISOW, and DSOW. It contrasts with the minimal interannual changes and slight rates of increase in AT encountered among the different layers by García-Ibáñez et al. (2016) from 1991 to 2015 in the Irminger basin (between 0.10 and 0.28 µmol kg−1 yr−1) and in the Iceland basin (between −0.04 and 0.07 µmol kg−1 yr−1) and with the trends reported for the period 1983–2013 by Pérez et al. (2021) at the IRM-TS (between 0.13 and 0.22 µmol kg−1 yr−1) and at the IS-TS (between −0.04 and 0.15 µmol kg−1 yr−1). These heterogeneities in the temporal evolution of the AT were driven by the decadal salinification of the whole water column observed since the late 20th century and interrupted by interannual freshening episodes such as during the 2010s.
The interannual increase in NAT in upper layers could be related to acidification, which favours the dissolution of carbonates, combined with increasing biological production reported for upper layers across the NASPG (Ostle et al, 2022). It contrasts with the constantly weak decrease in NAT in intermediate and deep layers, in which the accelerated acidification was compensated by the dominance of remineralization processes over lower biological uptake. Consequently, the positive NAT trends encountered in the upper layers led to a rise in pHT, while the diminished NAT contributed to decreasing the pHT toward the interior ocean.
The relationship has increased at a rate of 0.5 ± 0.2 µmol kg−1 yr−1 (p-value < 0.05) due to the combined action of the freshening (Fig. 4) and the progressive increase in AT-rich water inflows through upper layers (observed in the positive trends in NAT in SPMW and ENACW; Fig. S4). This was likely associated with the stagnation of AT-rich subtropical waters in the upper layers due to the slowdown of the NASPG since the mid-1990s (e.g. Böning et al., 2006; Häkkinen and Rhines, 2004), along with changes in the spreading of waters from higher latitudes influenced by melting.
The MATLAB and R codes for CANYONB (Bittig et al., 2018) are available at https://github.com/HCBScienceProducts/CANYON-B (last access: 9 December 2024). The MATLAB and R codes for ESPER_NN (Carter et al., 2021) are available at https://github.com/BRCScienceProducts/ESPER (last access: 9 December 2024). The anthropogenic carbon calculation (Pérez et al., 2008; Vázquez-Rodríguez et al., 2009) was run using the MATLAB code developed by the Oceanology group at the IIM-CSIC available at http://oceano.iim.csic.es/co2group (last access: 9 December 2024; Oceanology group, 2016). The CO2SYS programme for MATLAB (van Heuven et al., 2011; Orr et al., 2018; Sharp et al., 2023) is available at https://github.com/jonathansharp/CO2-System-ExtdTS29 (last access: 9 December 2024).
The measured surface-to-bottom CLIVAR data (2009–2019) used in this investigation are published at Zenodo (https://doi.org/10.5281/zenodo.10276221; Santana-Casiano et al., 2023). The GO-SHIP A25-OVIDE data for the cruise of 2018 are available at SEANOE (https://www.seanoe.org/data/00762/87394/, Lherminier et al., 2022).
The supplement related to this article is available online at: https://doi.org/10.5194/bg-21-5561-2024-supplement.
DCH contributed to data analysis and wrote the article. FFP, DCH, AV, DGS, AGG, MGD, and JMSC worked on the design, conceptualization, and data preparation. SG, AS, MGD, JMSC, AGG, and DGS participated in eight, four, seven, seven, two, and two cruises, respectively. SG and AS were the chief scientists on all cruises and were responsible for the operational and maintenance procedures for the CTD and additional sensors and thus for physical and sensor-measured variables. MGD and JMSC acquired funding from the ULPGC to provide resources for the Spanish team. SG and AS acquired the funding for ship time and the provision of resources for all cruise participants. All authors critically reviewed the article.
The contact author has declared that none of the authors has any competing interests.
Publisher’s note: Copernicus Publications remains neutral with regard to jurisdictional claims made in the text, published maps, institutional affiliations, or any other geographical representation in this paper. While Copernicus Publications makes every effort to include appropriate place names, the final responsibility lies with the authors.
The participation on the cruises for the Spanish team from the ULPGC was funded by the Spanish Ministry of Science under the Complementary Actions CTM2008-05255, CTM2010-09514-E, and CTM2011-12984-E (years 2009–2011); by the FP7 European project CARBOCHANGE under grant agreement no. 264879; and by the Spanish Innovation and Science Ministry through projects EACFe (CTM2014-52342-P) and ATOPFe (CTM2017-83476-P). Sergey V. Gladyshev and Alexey Sokov were supported by FMWE-2023-0002. Fiz F. Pérez and Antón Velo were supported by the BOCATS2 (PID2019-104279GB-C21) project funded by MCIN/AEI/10.13039/501100011033 and by the EuroGO-SHIP project (Horizon Europe #101094690). The participation of David Curbelo-Hernández was funded by the PhD grant PIFULPGC-2020-2 ARTHUM-2. We thank the technician and researchers Adrian Castro Álamo (two cruises), Anna Barrera Galderique (three cruises), Rayco Alvarado Medina (two cruises), and Pilar Aparicio Rizzo (one cruise) who helped with in situ analysis. We also thank the technicians at the P. P. Shirshov Institute of Oceanology of the Russian Academy of Science for the in situ analysis of dissolved oxygen and nutrients.
This research has been supported by the Ministerio de Ciencia e Innovación (grant nos. CTM2008-05255, CTM2010-09514-E, CTM2011-12984-E, CTM2014-52342-P, CTM2017-83476-P, and PID2019-104279GB-C21); the HORIZON EUROPE Research Infrastructures (grant no. 101094690); the Universidad de Las Palmas de Gran Canaria (grant no. PIFULPGC-2020-2 ARTHUM-2); and the Shirshov Institute of Oceanology, Russian Academy of Sciences (grant no. FMWE-2023-0002).
This paper was edited by Frédéric Gazeau and reviewed by two anonymous referees.
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- Abstract
- Key points
- Introduction
- Methodology
- Results
- Discussion
- Conclusions
- Appendix A: Correction of dissolved oxygen records for the cruise of 2019
- Appendix B: Interannual trends in AT and NAT
- Code availability
- Data availability
- Author contributions
- Competing interests
- Disclaimer
- Acknowledgements
- Financial support
- Review statement
- References
- Supplement
- Abstract
- Key points
- Introduction
- Methodology
- Results
- Discussion
- Conclusions
- Appendix A: Correction of dissolved oxygen records for the cruise of 2019
- Appendix B: Interannual trends in AT and NAT
- Code availability
- Data availability
- Author contributions
- Competing interests
- Disclaimer
- Acknowledgements
- Financial support
- Review statement
- References
- Supplement