Air-sea CO2 Research Articles

Sea-air CO2 exchanges, pCO2 drivers and phytoplankton communities in the southwestern South Atlantic Ocean during spring

Hydrographic properties and carbon dioxide partial pressure (pCO2) were measured through underway survey of surface waters during spring 2014, mainly along the Surface Haline Front in the continental shelf-break domain in the southwestern South Atlantic Ocean margin. Additionally, discrete seawater surface samples were collected along the ship track to identify the phytoplankton community and measure seawater chemical properties. This study aims to identify the drivers of the marine CO2‑carbonate chemistry and the role played by the phytoplankton composition on changes in the surface marine carbonate properties and the sea-air CO2 exchanges in two biogeochemical provinces (i.e., South Brazil Bight – SBB, and Southern Brazilian Shelf – SBS) governed by the dynamics of the Brazil Current system in the South Atlantic Ocean. The water masses identified on the surface of the region were Tropical Water (mostly present at offshore regions), Subtropical Shelf Water (mostly present over the continental shelf and slope), and Plata Plume Water (present in the south coastal domain of the SBS). On average, the study area behaved as a weak net CO2 outgassing zone of 1.2 ± 2.3 mmol m−2 d−1 during the spring, despite some subregions behaving as CO2 ingassing zones. The CO2 uptake verified in the SBB was related with mesoscale activity bringing cold waters in the region while CO2 uptake in the continental shelf domain of SBS was associated with the presence of cooler and fresher Plata Plume Water. Changes in total alkalinity and dissolved inorganic carbon at surface were mainly governed by CaCO3 production in SBB and seawater dilution in SBS, although other processes may also have influenced on their spatial variability. The dominant phytoplankton groups were haptophytes (31 %), Trichodesmium (21 %), and picocyanobateria (28 %), corresponding to Synechococcus (17 %) and Prochlorococcus (11 %). The dominance of the diatom group was associated with a decrease in sea surface pCO2 (mainly at coastal zones at southern areas), although the sea-air CO2 exchanges were regulated by cooling process due the presence of Plata Plume Water in that region. Changes in surface pH were related to high concentration of Trichodesmium slicks at offshore zones with the highest microalgae concentration, leading to pH drops of up to 0.4. Trichodesmium slicks likely allowed the development of haptophytes in offshore oligotrophic waters due to its role on N2 fixation. An increase of ∼20 % in the dominance of haptophytes contribution was verified in that situation, which was likely in a post-bloom development stage, since an increased dissolved inorganic carbon content was observed, associated with a prevalence of net respiration processes.

Interannual and seasonal variability of the air–sea CO2 exchange at Utö in the coastal region of the Baltic Sea

Abstract. Oceans alleviate the accumulation of atmospheric CO2 by absorbing approximately a quarter of all anthropogenic emissions. In the deep oceans, carbon uptake is dominated by aquatic phase chemistry, whereas in biologically active coastal seas the marine ecosystem and biogeochemistry play an important role in the carbon uptake. Coastal seas are hotspots of organic and inorganic matter transport between the land and the oceans, and thus they are important for the marine carbon cycling. In this study, we investigate the net air–sea CO2 exchange at the Utö Atmospheric and Marine Research Station, located at the southern edge of the Archipelago Sea within the Baltic Sea, using the data collected during 2017–2021. The air–sea fluxes of CO2 were measured using the eddy covariance technique, supported by the flux parameterization based on the pCO2 and wind speed measurements. During the spring–summer months (April–August), the sea was gaining carbon dioxide from the atmosphere, with the highest monthly sink fluxes typically occurring in May, being −0.26 µmol m−2 s−1 on average. The sea was releasing the CO2 to the atmosphere in September–March, and the highest source fluxes were typically observed in September, being 0.42 µmol m−2 s−1 on average. On an annual basis, the study region was found to be a net source of atmospheric CO2, and on average, the annual net exchange was 27.1 gC m−1 yr−1, which is comparable to the exchange observed in the Gulf of Bothnia, the Baltic Sea. The annual net air–sea CO2 exchanges varied between 18.2 (2018) and 39.1 gC m−1 yr−1 (2017). During the coldest year, 2017, the spring–summer sink fluxes remained low compared to the other years, as a result of relatively high seawater pCO2 in summer, which never fell below 220 µatm during that year. The spring–summer phytoplankton blooms of 2017 were weak, possibly due to the cloudy summer and deeply mixed surface layer, which restrained the photosynthetic fixation of dissolved inorganic carbon in the surface waters. The algal blooms in spring–summer 2018 and the consequent pCO2 drawdown were strong, fueled by high pre-spring nutrient concentrations. The systematic positive annual CO2 balances suggest that our coastal study site is affected by carbon flows originating from elsewhere, possibly as organic carbon, which is remineralized and released to the atmosphere as CO2. This coastal source of CO2 fueled by the organic matter originating probably from land ecosystems stresses the importance of understanding the carbon cycling in the land–sea continuum.

Sea-air CO2 Flux in the South Yellow Sea Based on Seasonal Underway Observations

Sea-air CO2 Flux in the South Yellow Sea Based on Seasonal Underway Observations

Assessment of carbon flux gradients and dominant processes in a subtropical highly urbanized coastal ecosystem

Highly urbanized coastal ecosystems are vital in the global carbon budget. However, there are limited researches on carbon flux gradients in these nearshore areas, considering both natural and anthropogenic influences. Through on-site measurements and field samplings during wet-to-dry season in 2023, this study investigated spatial variations and factors affecting carbon fluxes, focusing on the impacts of salinity and eutrophic status in five geographically connected coastal waters of the Guangdong-Hong Kong-Macau Greater Bay Area (GBA). By estimating carbon exchange at land-sea-air interface, dominant processes in carbon dynamics were identified as well. Results showed that partial pressure of CO2 (pCO2) varied from 391 to 2290 μatm, and sea-air CO2 exchange fluxes (FCO2) ranged from -3.07 to 70.07 mmol m–2 d–1, indicating significant geographical distinctions among five coastal waters of the GBA. The total carbon transport from rivers to these nearshore waters was approximated at 6.44 Tg C yr-1, with the Pearl River (PR) contributing 99.7%, primarily in dissolved forms. Atmospheric CO2 release was calculated at 0.29 Tg C yr-1 for studied five coastal waters, primarily as carbon sources, except for Dapeng Bay (DPB) as a sink. CO2 emissions inversely correlated with salinity, yet positively with eutrophication status, particularly in river-dominated estuaries. Moreover, CO2 flux decreased 23 times as eco-status shift from eutrophic to non-eutrophic. River plumes, terrestrial pollutant inputs, and economic structure were underlying drivers, influencing carbon species concentrations and fluxes. Elevated CO2 concentrations in eutrophic coastal waters were mainly attributed to terrestrial carbon and nutrients inputs, supporting active biological respiration and microbial decomposition. Conversely, carbon dynamics potentially depend on the balance of respiration and photosynthesis in non-eutrophic coastal waters. This study offers high geographic precision and specificity of carbon species, and provides land-sea integration insight to understand carbon dynamic mechanisms, promoting advancements in water quality management and climate mitigation.

Implementation and assessment of a model including mixotrophs and the carbonate cycle (Eco3M_MIX-CarbOx v1.0) in a highly dynamic Mediterranean coastal environment (Bay of Marseille, France) – Part 2: Towards a better representation of total alkalinity when modeling the carbonate system and air–sea CO2 fluxes

Abstract. The Bay of Marseille (BoM), located in the northwestern Mediterranean Sea, is affected by various hydrodynamic processes (e.g., Rhône River intrusion and upwelling events) that result in a highly complex local carbonate system. In any complex environment, the use of models is advantageous since it allows us to identify the different environmental forcings, thereby facilitating a better understanding. By combining approaches from two biogeochemical ocean models and improving the formulation of total alkalinity, we develop a more realistic representation of the carbonate system variables at high temporal resolution, which enables us to study air–sea CO2 fluxes and seawater pCO2 variations more reliably. We apply this new formulation to two particular scenarios that are typical for the BoM: (i) summer upwelling and (ii) Rhône River intrusion events. In both scenarios, our model was able to correctly reproduce the observed patterns of pCO2 variability. Summer upwelling events are typically associated with a pCO2 decrease that mainly results from decreasing near-surface temperatures. Furthermore, Rhône River intrusion events are typically associated with a pCO2 decrease, although, in this case, the pCO2 decrease results from a decrease in salinity and an overall increase in total alkalinity. While we were able to correctly represent the daily range of air–sea CO2 fluxes, the present configuration of Eco3M_MIX-CarbOx does not allow us to correctly reproduce the annual cycle of air–sea CO2 fluxes observed in the area. This pattern directly impacts our estimates of the overall yearly air–sea CO2 flux as, even if the model clearly identifies the bay as a CO2 sink, its magnitude was underestimated, which may be an indication of the limitations inherent in dimensionless models for representing air–sea CO2 fluxes.

The Southern Ocean carbon sink has been overestimated in the past three decades

Employing machine learning methods for mapping surface ocean pCO2 has reduced the uncertainty in estimating sea-air CO2 flux. However, a general discrepancy exists between the Southern Ocean carbon sinks derived from pCO2 products and those from biogeochemistry models. Here, by performing a boosting ensemble learning feed-forward neural networks method, we have identified an underestimation of the surface Southern Ocean pCO2 due to notably uneven density of pCO2 measurements between summer and winter, which resulted in about 16% overestimating of Southern Ocean carbon sink over the past three decades. In particular, the Southern Ocean carbon sink since 2010 was notably overestimated by approximately 29%. This overestimation can be mitigated by a winter correction in algorithms, with the average Southern Ocean carbon sink during 1992-2021 corrected to −0.87 PgC yr−1 from the original −1.01 PgC yr−1. Furthermore, the most notable underestimation of surface ocean pCO2 mainly occurred in regions south of 60°S and was hiding under ice cover. As the surface ocean pCO2 under sea ice coverage in the winter is much higher than the atmosphere, if sea ice melts completely, there could be a further reduction of about 0.14 PgC yr−1 in the Southern Ocean carbon sink.

Anthropogenic CO2, air–sea CO2 fluxes, and acidification in the Southern Ocean: results from a time-series analysis at station OISO-KERFIX (51° S–68° E)

Abstract. The temporal variation of the carbonate system, air–sea CO2 fluxes, and pH is analyzed in the southern Indian Ocean, south of the polar front, based on in situ data obtained from 1985 to 2021 at a fixed station (50°40′ S–68°25′ E) and results from a neural network model that reconstructs the fugacity of CO2 (fCO2) and fluxes at monthly scale. Anthropogenic CO2 (Cant) is estimated in the water column and is detected down to the bottom (1600 m) in 1985, resulting in an aragonite saturation horizon at 600 m that migrated up to 400 m in 2021 due to the accumulation of Cant. At the subsurface, the trend of Cant is estimated at +0.53±0.01 µmol kg−1 yr−1 with a detectable increase in the trend in recent years. At the surface during austral winter the oceanic fCO2 increased at a rate close to or slightly lower than in the atmosphere. To the contrary, in summer, we observed contrasting fCO2 and dissolved inorganic carbon (CT) trends depending on the decade and emphasizing the role of biological drivers on air–sea CO2 fluxes and pH inter-annual variability. The regional air–sea CO2 fluxes evolved from an annual source to the atmosphere of 0.8 molC m−2 yr−1 in 1985 to a sink of −0.5 molC m−2 yr−1 in 2020. Over 1985–2020, the annual pH trend in surface waters of -0.0165±0.0040 per decade was mainly controlled by the accumulation of anthropogenic CO2, but the summer pH trends were modulated by natural processes that reduced the acidification rate in the last decade. Using historical data from November 1962, we estimated the long-term trend for fCO2, CT, and pH, confirming that the progressive acidification was driven by the atmospheric CO2 increase. In 59 years this led to a diminution of 11 % for both aragonite and calcite saturation state. As atmospheric CO2 is expected to increase in the future, the pH and carbonate saturation state will decrease at a faster rate than observed in recent years. A projection of future CT concentrations for a high emission scenario (SSP5-8.5) indicates that the surface pH in 2100 would decrease to 7.32 in winter. This is up to −0.86 lower than pre-industrial pH and −0.71 lower than pH observed in 2020. The aragonite undersaturation in surface waters would be reached as soon as 2050 (scenario SSP5-8.5) and 20 years later for a stabilization scenario (SSP2-4.5) with potential impacts on phytoplankton species and higher trophic levels in the rich ecosystems of the Kerguelen Islands area.

Regional differences in the air–sea CO2 flux between 3 and 14°S in the south-western tropical Atlantic

Context The fugacity of surface-seawater CO2 (fCO2sw) and the sea–air CO2 fluxes in the south-western tropical Atlantic (SWTA) were studied to increase the knowledge about the carbon cycle in this region. Aims This paper aims to describe the distribution of fCO2sw in SWTA. Methods The fCO2sw was measured from 2008 to 2020 by volunteer merchant ships with an onboard system that measures pCO2 while the vessels were underway. Key results Higher values occurred north of 8°S than in the region south of 8°S. The north is a strong source of CO2 for the atmosphere, with an annual mean value of 3.14 ± 0.52 mmol m−2 day−1. The south is a weaker source of CO2, with an annual average of 0.93 ± 0.90 mmol m−2 day−1. In the months of July and August, a weak sink of CO2 was observed, with a mean of −0.55 mmol m−2 day−1. Conclusions and implications The differences between these two regions are explained by the origin of the surface-water masses encountered along the ship track. The central branch of the South Equatorial Current (SEC) transports surface water, with a higher CO2 concentration and lower salinity, north of 8°S, whereas the surface waters between 8 and 14°S come from the southern branch of the SEC. The intertropical convergence zone is another physical process influencing the region north of 8°S.

CO2 sink and source zones delimited by marine fronts in the Drake Passage

Net sea-air CO2 fluxes (FCO2) in the Drake Passage (DP) were studied at a climatological scale (1999–2019) using observations from the Surface Ocean CO2 Atlas (SOCAT) database. Based on the monthly climatological position of the main circumpolar fronts of the DP (the Subantarctic Front (SAF), the Polar Front (PF) and the Southern Antarctic Circumpolar Current Front (SACCF)) and the thermal and nonthermal contributions to FCO2, we present a regional subdivision into different regimes that provide new insights into the processes controlling these fluxes. Our results indicate that the region in the north of SAF (R1) behaves as an annual CO2 sink (-1.3 ± 1.0 mmol m−2 d−1); this sink weakens between SAF-PF (R2) and PF-SACCF (R3) and the region south of SACCF (R4) acts as an annual CO2 source (2.2 ± 3.3 mmol m−2 d−1). The annual mean CO2 uptake in DP is 1.3 ± 15.5 Tg C yr-1. Analysis of thermal (TE) and nonthermal (nonTE) effects on seasonal sea surface CO2 partial pressure (pCO2sw) variability indicates that DP is mainly dominated by nonTE. Results emphasize that carbon fluxes are driven by mesoscale and submesoscale processes north of the PF and by the upwelling of Upper Circumpolar Deep Waters in the Antarctic boundary of the DP, while seasonal patterns are mostly modulated by local factors such as nutrient availability, biological activity and ice cover.

Carbonate system variability in the Mediterranean Sea: a modelling study

A basin-scale Mediterranean carbonate system model has been setup, building on the POSEIDON operational biogeochemical model. The spatial variability of carbonate system variables from a 13-year simulation (2010-2022) was validated against CARIMED in situ data (DIC, TA, pCO2), showing reasonable agreement in reproducing the observed patterns and preserving the dynamics in different areas, except a slight overestimation (~15 µmol/kg) of TA in the Eastern Levantine. The time-variability of model outputs (DIC, TA, pCO2, pH) was validated, against available time-series from Western (DYFAMED, Villefranche-PointB) and Eastern Mediterranean (HCB) sites, showing good agreement with the data, particularly for pCO2, pH and DIC. The model failed to reproduce the observed late summer peak of TA at DYFAMED/PointB sites, which may be partly attributed to the advection of lower alkalinity Atlantic water in the area. The seasonal variability of DIC and pCO2@20°C was found to be mainly controlled by winter mixing and the subsequent increase of primary production and net CO2 biological uptake, which appeared overestimated at HCB. Along with the reference simulation, three sensitivity simulations were performed, de-activating the effect of biology, evaporation and CO2 air-sea fluxes on DIC and TA, in order to gain insight on the processes regulating the simulated carbonate system variability. The effect of biological processes on DIC was found more significant (peak during spring) in the more productive North Western Mediterranean, while evaporation had a stronger impact (peak during late summer) in the Levantine basin. CO2 air-sea flux was higher in the Western Mediterranean, particularly the Gulf of Lions and Alboran Sea, as well as in river influenced areas, such as the N. Adriatic and along the pathway of the Black Sea Water in the Aegean. A weak release of CO2 was found in the Eastern Levantine and Libyan Sea. Its basin average (+2.1 mmol/m2/day) and positive trend (+0.1 mmol/m2/day/year) indicates a gradually increasing net CO2 ocean uptake. The simulated positive trends of DIC (0.77 μmol/kg/year) and TA (0.53 μmol/kg/year) in the North Western Mediterranean were consistent with observational and modelling studies, in constrast with the Levantine basin, where no significant trends were found for TA.

Marine Heatwave and Terrestrial Drought Reduced CO2 Uptake in the East China Sea in 2022

Against the background of climate warming, marine heatwaves (MHWs) and terrestrial drought events have become increasingly frequent in recent decades. However, the combined effects of MHWs and terrestrial drought on CO2 uptake in marginal seas are still unclear. The East China Sea (ECS) experienced an intense and long-lasting MHW accompanied by an extreme terrestrial drought in the Changjiang basin in the summer of 2022. In this study, we employed multi-source satellite remote sensing products to reveal the patterns, magnitude, and potential drivers of CO2 flux changes in the ECS resulting from the compounding MHW and terrestrial drought extremes. The CO2 uptake of the ECS reduced by 17.0% (1.06 Tg C) in the latter half of 2022 and the Changjiang River plume region shifted from a CO2 sink to a source (releasing 0.11 Tg C) in July-September. In the majority of the ECS, the positive sea surface temperature (SST) anomaly during the MHW diminished the solubility of CO2 in seawater, thereby reducing CO2 uptake. Moreover, the reduction in nutrient input associated with terrestrial drought, which is unfavorable to phytoplankton growth, further reduced the capacity of CO2 uptake. Meanwhile, the CO2 sink doubled for the offshore waters of the ECS continental shelf in July-September 2022, indicating the complexity and heterogeneity of the impacts of extreme climatic events in marginal seas. This study is of great significance in improving the estimation results of CO2 fluxes in marginal seas and understanding sea–air CO2 exchanges against the background of global climate change.

Remotely sensed retrieval of air-sea carbon flux and acidification risk in Chinese Bohai Sea based on a semi-analytical mechanism model with hour-level GOCI image and ERA5 reanalysis data

Marine carbon sinks act as a buffer against global warming, but raise the risk of acidification, especially in the marginal shelf seas which are rich in terrigenous carbon input. The Chinese Bohai Sea performs generally as a weak carbon source while carbon fluxes (fCO2), pH, and aragonite saturation states (Ωarag) vary in time and space under intensive land-sea interaction. However, there are still 1) insufficient spatiotemporal resolution in existing remotely sensed retrieval of carbon flux, 2) inadequate analytic mechanism for existing empirical models, which are not suitable for case II waters in Bohai Sea, and 3) limited research on remotely sensed retrieval of acidification risk expressed as pH and Ωarag. Thus, we proposed a semi-analytical mechanism algorithm (MeSAA) to gain seawater partial pressure of CO2 (pCO2sw) with hour-level GOCI imagery and seawater carbonate equilibrium equation (CO2SYS). With the assistance of ERA5 reanalysis data, the gained pCO2sw was then used to obtain fCO2 by using the sea-air CO2 partial pressure difference (ΔpCO2) method. Similarly, with the assistance of remotely sensed retrieval, two indices, pH and Ωarag were also gained from CO2SYS to identify the acidification risk. The results showed that Bohai Sea was a weak carbon source with the positive values of fCO2 (0.5–6 mmol C·m−2·day−1) and total emission (0.956 Tg C·yr−1). It suffered from a high acidification risk, especially in three bays with low values of Ωarag (1.15–1.3) from May to September 2011. Although photosynthetic carbon sequestration was intensive near shore, it could not consume the large amount of the rich carbon input, and resulting a monthly increase for pCO2sw and fCO2 and a monthly decrease for pH and Ωarag from May to September. The distribution of pCO2sw was in accord with a former study, but the values were not. The local parameter adjustment of MeSAA in the Bohai Sea was analyzed for this issue, so did the effect of uncertainty analysis of mapping at different time scales (hourly and daily). Moreover, the contrast of absolute deviation and relative deviation on different time scales verified the advantage of hour-level GOCI imagery in improving assessment accuracies. This study gained a more precise change trend of pCO2sw, fCO2, pH, and Ωarag in the Bohai Sea from May to September 2011, which would be beneficial to the study of the carbon cycle in the marginal sea of the shelf under the conditions of climate change.

A decade of marine inorganic carbon chemistry observations in the northern Gulf of Alaska – insights into an environment in transition

Abstract. As elsewhere in the global ocean, the Gulf of Alaska is experiencing the rapid onset of ocean acidification (OA) driven by oceanic absorption of anthropogenic emissions of carbon dioxide from the atmosphere. In support of OA research and monitoring, we present here a data product of marine inorganic carbon chemistry parameters measured from seawater samples taken during biannual cruises between 2008 and 2017 in the northern Gulf of Alaska. Samples were collected each May and September over the 10 year period using a conductivity, temperature, depth (CTD) profiler coupled with a Niskin bottle rosette at stations including a long-term hydrographic survey transect known as the Gulf of Alaska (GAK) Line. This dataset includes discrete seawater measurements such as dissolved inorganic carbon and total alkalinity, which allows the calculation of other marine carbon parameters, including carbonate mineral saturation states, carbon dioxide (CO2), and pH. Cumulative daily Bakun upwelling indices illustrate the pattern of downwelling in the northern Gulf of Alaska, with a period of relaxation spanning between the May and September cruises. The observed time and space variability impart challenges for disentangling the OA signal despite this dataset spanning a decade. However, this data product greatly enhances our understanding of seasonal and interannual variability in the marine inorganic carbon system parameters. The product can also aid in the ground truthing of biogeochemical models, refining estimates of sea–air CO2 exchange, and determining appropriate CO2 parameter ranges for experiments targeting potentially vulnerable species. Data are available at https://doi.org/10.25921/x9sg-9b08 (Monacci et al., 2023).

Seagrass Blue Carbon Stock and Air–Sea CO2 Fluxes in the Karimunjawa Islands, Indonesia during Southeast Monsoon Season

Research focusing on seagrass ecosystems as carbon storage has been conducted in various Indonesian waters. However, an essential aspect that remains unexplored is the simultaneous analysis of blue carbon storage in seagrass alongside carbon dioxide (CO2) flux values, particularly within Karimunjawa waters. This study aims to assess the organic carbon stock and sea–air CO2 flux in seagrass ecosystems in Karimunjawa. Our hypothesis posits that although seagrass ecosystems release CO2 into the water, their role as blue carbon ecosystems enables them to absorb and accumulate organic carbon within seagrass biomass and sediments. This investigation took place in Karimunjawa waters, encompassing both vegetated (seagrass meadows) and unvegetated (non-seagrass meadows) areas during August 2019, 2020, and 2022. Over this period, the organic carbon stock in seagrass and sediment displayed an increase, rising from 28.90 to 35.70 gCorg m−2 in 2019 and from 37.80 to 45.25 gCorg m−2 in 2022. Notably, the expanse of seagrass meadows in Karimunjawa dwindled by 328.33 ha from 2019 to 2022, resulting in a total carbon stock reduction of the seagrass meadows of 452.39 tC to 218.78 tC. Sediment emerges as a pivotal element in the storage of blue carbon in seagrass, with sedimentary organic carbon outweighing seagrass biomass in storage capacity. The conditions in Karimunjawa, including a high A:B ratio, low dry bulk density, and elevated water content, foster a favorable environment for sediment carbon absorption and storage, facilitated by the waters’ CO2 emission during the southeast monsoon season. Notably, our findings reveal that CO2 release within vegetated areas is lower compared to unvegetated areas. This outcome underscores how seagrass ecosystems can mitigate CO2 release through their adeptness at storing organic carbon within biomass and sediment. However, the presence of inorganic carbon in the form of calcium carbonate introduces a nuanced dynamic. This external source, stemming from allochthonous origins like mangroves, brown algae like Padina pavonica, and calcareous epiphytes, leads to an increase in sedimentary organic carbon stock of 53.2 ± 6.82 gCorg m−2. Moreover, it triggers the release of CO2 into the atmosphere, quantified at 83.4 ± 18.26 mmol CO2 m−2 d−1.

Dynamics of the Seawater Carbonate System in the East Siberian Sea: The Diversity of Driving Forces

The East Siberian Sea (ESS) is a large and the shallowest part of the Arctic Ocean. It is characterized by high biogeochemical activity, but the seawater carbonate system remains understudied, especially during the late autumn season. Data from the research vessel (RV) “Professor Multanovsky” cruise were used to assess the dynamics of the seawater carbonate system, air–sea CO2 fluxes, and the calcium carbonate corrosive waters in the two biogeochemical provinces of the ESS shortly before freeze-up. The ESS waters were mainly a sink for atmospheric CO2 due to the limited dispersion of river waters, autumn water cooling, and phytoplankton blooms in its eastern autotrophic province. The mean value of the CO2 air–sea flux was 11.2 mmol m−2 day−1. The rate of CO2 uptake in the eastern ESS was an order of magnitude larger than that in the western ESS. The specific waters and ice cover dynamics determined intensive photosynthesis processes identified on the eastern shelf and in the northern deep oligotrophic waters. A part of the surface and most of the bottom ESS waters were corrosive with respect to calcium carbonate, with the lowest saturation state of aragonite (0.22) in the bottom layer of the eastern ESS. The eastern ESS was the main source of these waters into the deep basin. The observed export of corrosive shelf waters to the deep sea can have a potential impact on the ocean water ecosystem in the case of mixing with layers inhabited by calcifying organisms.

Disentangling the impact of Atlantic Niño on sea-air CO2 flux

Atlantic Niño is a major tropical interannual climate variability mode of the sea surface temperature (SST) that occurs during boreal summer and shares many similarities with the tropical Pacific El Niño. Although the tropical Atlantic is an important source of CO2 to the atmosphere, the impact of Atlantic Niño on the sea-air CO2 exchange is not well understood. Here we show that the Atlantic Niño enhances (weakens) CO2 outgassing in the central (western) tropical Atlantic. In the western basin, freshwater-induced changes in surface salinity, which considerably modulate the surface ocean CO2 partial pressure (pCO2), are the primary driver for the observed CO2 flux variations. In contrast, pCO2 anomalies in the central basin are dominated by the SST-driven solubility change. This multi-variable mechanism for pCO2 anomaly differs remarkably from the Pacific where the response is predominantly controlled by upwelling-induced dissolved inorganic carbon anomalies. The contrasting behavior is characterized by the high CO2 buffering capacity in the Atlantic, where the subsurface water mass contains higher alkalinity than in the Pacific.

Regulation of CO2 by the sea in areas around Latin America in a context of climate change.

Anthropogenic activities are increasing the atmospheric carbon dioxide (CO2); around a third of the CO2 emitted by these activities has been taken up by the ocean. Nevertheless, this marine ecosystem service of regulation remains largely invisible to society, and not enough is known about regional differences and trends in sea-air CO2 fluxes (FCO2), especially in the Southern Hemisphere. The objectives of this work were as follows: first to put values of FCO2 integrated over the exclusive economic zones (EEZ) of five Latin-American countries (Argentina, Brazil, Mexico, Peru, and Venezuela) into perspective regarding total country-level greenhouse gases (GHG) emissions. Second, to assess the variability of two main biological factors affecting FCO2 at marine ecological time series (METS) in these areas. FCO2 over the EEZs were estimated using the NEMO model, and GHG emissions were taken from reports to the UN Framework Convention on Climate Change. For each METS, the variability in phytoplankton biomass (indexed by chlorophyll-a concentration, Chla) and abundance of different cell sizes (phy-size) were analyzed at two time periods (2000-2015 and 2007-2015). Estimates of FCO2 at the analyzed EEZs showed high variability among each other and non-negligible values in the context of greenhouse gas emissions. The trends observed at the METS indicated, in some cases, an increase in Chla (e.g., EPEA-Argentina) and a decrease in others (e.g., IMARPE-Peru). Evidence of increasing populations of small size-phytoplankton was observed (e.g., EPEA-Argentina, Ensenada-Mexico), which would affect the carbon export to the deep ocean. These results highlight the relevance of ocean health and its ecosystem service of regulation when discussing carbon net emissions and budgets.

Antarctica Slope Front bifurcation eddy: A stationary feature influencing CO2 dynamics in the northern Antarctic Peninsula

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

Construction of a High Spatiotemporal Resolution Dataset of Satellite-DerivedpCO2and Air–Sea CO2Flux in the South China Sea (2003–2019)

Construction of a High Spatiotemporal Resolution Dataset of Satellite-Derived<i>p</i>CO₂and Air–Sea CO₂Flux in the South China Sea (2003–2019)

Sea-air CO 2 fluxes along the Brazilian continental margin

Sea-air CO 2 fluxes along the Brazilian continental margin