Air-sea CO2 Flux Research Articles

The influence of tides on the marine carbonate chemistry of a coastal polynya in the south-eastern Weddell Sea

Abstract. Tides significantly affect polar coastlines by modulating ice shelf melt and modifying shelf water properties through transport and mixing. However, the effect of tides on the marine carbonate chemistry in such regions, especially around Antarctica, remains largely unexplored. We address this topic with two case studies in a coastal polynya in the south-eastern Weddell Sea, neighbouring the Ekström Ice Shelf. The case studies were conducted in January 2015 (PS89) and January 2019 (PS117), capturing semi-diurnal oscillations in the water column. These are pronounced in both physical and biogeochemical variables for PS89. During rising tide, advection of sea ice meltwater from the north-east created a fresher, warmer, and more deeply mixed water column with lower dissolved inorganic carbon (DIC) and total alkalinity (TA) content. During ebbing tide, water from underneath the ice shelf decreased the polynya's temperature, increased the DIC and TA content, and created a more stratified water column. The variability during the PS117 case study was much smaller, as it had less sea ice meltwater input during rising tide and was better mixed with sub-ice shelf water. The contrasts in the variability between the two case studies could be wind and sea ice driven, and they underline the complexity and highly dynamic nature of the system. The variability in the polynya induced by the tides results in an air–sea CO2 flux that can range between a strong sink (−24 mmol m−2 d−1) and a small source (3 mmol m−2 d−1) on a semi-diurnal timescale. If the variability induced by tides is not taken into account, there is a potential risk of overestimating the polynya's CO2 uptake by 67 % or underestimating it by 73 %, compared to the average flux determined over several days. Depending on the timing of limited sampling, the polynya may appear to be a source or a sink of CO2. Given the disproportionate influence of polynyas on heat and carbon exchange in polar oceans, we recommend future studies around the Antarctic and Arctic coastlines to consider the timing of tidal currents in their sampling strategies and analyses. This will help constrain variability in oceanographic measurements and avoid potential biases in our understanding of these highly complex systems.

Identifying the biological control of the annual and multi-year variations in South Atlantic air–sea CO2 flux

Abstract. The accumulation of anthropogenic CO2 emissions in the atmosphere has been buffered by the absorption of CO2 by the global ocean, which acts as a net CO2 sink. The CO2 flux between the atmosphere and the ocean, which collectively results in the oceanic carbon sink, is spatially and temporally variable, and fully understanding the driving mechanisms behind this flux is key to assessing how the sink may change in the future. In this study a time series decomposition analysis was applied to satellite observations to determine the drivers that control the sea–air difference of CO2 partial pressure (ΔpCO2) and the CO2 flux on seasonal and inter-annual timescales in the South Atlantic Ocean. Linear trends in ΔpCO2 and the CO2 flux were calculated to identify key areas of change. Seasonally, changes in both the ΔpCO2 and CO2 flux were dominated by sea surface temperature (SST) in the subtropics (north of 40∘ S) and were correlated with biological processes in the subpolar regions (south of 40∘ S). In the equatorial Atlantic, analysis of the data indicated that biological processes are likely a key driver as a response to upwelling and riverine inputs. These results highlighted that seasonally ΔpCO2 can act as an indicator to identify drivers of the CO2 flux. Inter-annually, the SST and biological contributions to the CO2 flux in the subtropics were correlated with the multivariate El Niño–Southern Oscillation (ENSO) index (MEI), which leads to a weaker (stronger) CO2 sink in El Niño (La Niña) years. The 16-year time series identified significant trends in ΔpCO2 and CO2 flux; however, these trends were not always consistent in spatial extent. Therefore, predicting the oceanic response to climate change requires the examination of CO2 flux rather than ΔpCO2. Positive CO2 flux trends (weakening sink for atmospheric CO2) were identified within the Benguela upwelling system, consistent with increased upwelling and wind speeds. Negative trends in the CO2 flux (intensifying sink for atmospheric CO2) offshore into the South Atlantic gyre were consistent with an increase in the export of nutrients from mesoscale features, which drives the biological drawdown of CO2. These multi-year trends in the CO2 flux indicate that the biological contribution to changes in the air–sea CO2 flux cannot be overlooked when scaling up to estimates of the global ocean carbon sink.

Mesoscale eddy effects on sea-air CO2 fluxes in the northern Philippine Sea

To determine the effects of mesoscale eddies on sea-air CO2 flux, we investigated the surface fugacity of CO2 (surface fCO2) distribution in the northern Philippine Sea, where mesoscale eddies are common. Surface fCO2 showed large spatial variations, such that values were high in the non-eddy and cyclonic eddy regions, while they were low within the anticyclonic eddy. The maximum fCO2 was observed in the non-eddy region; higher fCO2 values were observed in the area surrounding the cyclonic eddy than at the center of the cyclonic eddy. Within the cyclonic eddy, the contribution of dissolved inorganic carbon (DIC) enrichment because of upwelling was considerably offset by cooling. In the non-eddy region, the contribution of DIC enrichment from upwelling was rarely offset by cooling; thus, the maximum fCO2 was observed in the non-eddy region. Surface fCO2 showed a robust correlation with sea surface temperature (SST) within the cyclonic and anticyclonic eddies, but it did not display any correlation in the non-eddy region. Temperature was a major factor that controlled surface fCO2 in the anticyclonic eddy, but this effect was absent in the cyclonic eddy. Temperature-normalized fCO2 exhibited a clear negative relationship with SST in the cyclonic eddy and the non-eddy region, indicating that surface fCO2 was considerably affected by the upwelling of high-fCO2 deep water in both regions. Sea-air CO2 fluxes ranged from 0.011 to 9.92 mmol m-2 day-1 and all values were positive, indicating that the entire study area acted as a CO2 source during the research period. The estimated mean sea-air CO2 fluxes in the cyclonic eddy, anticyclonic eddy, and non-eddy region were 1.10 ± 0.75, 0.64 ± 0.66, and 1.42 ± 1.12 mmol m-2 day-1, respectively. The sea-air CO2 fluxes considerably varied according to eddy type; they were almost twofold higher in the cyclonic eddy than in the anticyclonic eddy. In the cyclonic eddy and non-eddy regions, upwelling caused surface fCO2 to increase, thereby increasing sea-air CO2 flux.

FOCI-MOPS v1 – integration of marine biogeochemistry within the Flexible Ocean and Climate Infrastructure version 1 (FOCI 1) Earth system model

Abstract. The consideration of marine biogeochemistry is essential for simulating the carbon cycle in an Earth system model. Here we present the implementation and evaluation of a marine biogeochemical model, the Model of Oceanic Pelagic Stoichiometry (MOPS) in the Flexible Ocean and Climate Infrastructure (FOCI) climate model. FOCI-MOPS enables the simulation of marine biological processes, i.e. the marine carbon, nitrogen, and oxygen cycles with prescribed or prognostic atmospheric CO2 concentration. A series of experiments covering the historical period (1850–2014) were performed following the DECK (Diagnostic, Evaluation and Characterization of Klima) and CMIP6 (Coupled Model Intercomparison Project 6) protocols. Overall, modelled biogeochemical tracer distributions and fluxes, transient evolution in surface air temperature, air–sea CO2 fluxes, and changes in ocean carbon and heat contents are in good agreement with observations. Modelled inorganic and organic tracer distributions are quantitatively evaluated by statistically derived metrics. Results of the FOCI-MOPS model, including sea surface temperature, surface pH, oxygen (100–600 m), nitrate (0–100 m), and primary production, are within the range of other CMIP6 model results. Overall, the evaluation of FOCI-MOPS indicates its suitability for Earth climate system simulations.

Seasonal Water Mass Evolution and Non-Redfield Dynamics Enhance CO2 Uptake in the Chukchi Sea.

The Chukchi Sea is an increasing CO2 sink driven by rapid climate changes. Understanding the seasonal variation of air-sea CO2 exchange and the underlying mechanisms of biogeochemical dynamics is important for predicting impacts of climate change on and feedbacks by the ocean. Here, we present a unique data set of underway sea surface partial pressure of CO2 (pCO2) and discrete samples of biogeochemical properties collected in five consecutive cruises in 2014 and examine the seasonal variations in air-sea CO2 flux and net community production (NCP). We found that thermal and non-thermal effects have different impacts on sea surface pCO2 and thus the air-sea CO2 flux in different water masses. The Bering summer water combined with meltwater has a significantly greater atmospheric CO2 uptake potential than that of the Alaskan Coastal Water in the southern Chukchi Sea in summer, due to stronger biological CO2 removal and a weaker thermal effect. By analyzing the seasonal drawdown of dissolved inorganic carbon (DIC) and nutrients, we found that DIC-based NCP was higher than nitrate-based NCP by 66%-84% and attributable to partially decoupled C and N uptake because of a variable phytoplankton stoichiometry. A box model with a non-Redfield C:N uptake ratio can adequately reproduce observed pCO2 and DIC, which reveals that, during the intensive growing season (late spring to early summer), 30%-46% CO2 uptake in the Chukchi Sea was supported by a flexible stoichiometry of phytoplankton. These findings have important ramification for forecasting the responses of CO2 uptake of the Chukchi ecosystem to climate change.

Decrease in air-sea CO2 fluxes caused by persistent marine heatwaves

Regional processes play a key role in the global carbon budget. Major ocean CO2 uptake at mid-latitudes counteracts CO2 release in the tropics, which is modulated by episodes of marine heatwaves. Yet, we lack essential knowledge on persistent marine heatwaves, and their effect on the CO2 sensitive areas. Here we show, using a 1985–2017 joint analysis of reconstructions, ocean reanalysis and in situ and satellite data, that persistent marine heatwaves occur in major CO2 uptake and release areas. Average air-sea CO2 flux density changes from persistent marine heatwaves are strongest in the Pacific Ocean with a 40 ± 9% reduction in CO2 release in the tropics linked to ENSO, and a reduction in CO2 uptake of 29 ± 11% in the North Pacific over the study period. These results provide new insights into the interplay of extreme variability and a critical regulating ocean ecosystem service, and pave the way for future investigations on its evolution under climate change.

Effects of the glacial meltwater supply on carbonate chemistry in Bowdoin Fjord, Northwestern Greenland

To understand the effects of the glacial meltwater supply on carbonate chemistry and the air–sea CO2 flux within the fjord, water samples were collected in Bowdoin Fjord in northwestern Greenland for dissolved inorganic carbon (DIC) concentration, total alkalinity (TA), oxygen isotopic ratio (δ18O), and chlorophyll a concentration analyses in the summers of 2016 and 2017. The partial pressure of CO2 (pCO2) in surface water, calculated from DIC and TA, was less than 200 µatm, and was significantly lower than that in the atmosphere (399 ± 3 µatm). Therefore, surface water of the fjord acts as sink for CO2 in the atmosphere (–4.9 ± 0.7 mmol m–2 d–1). To evaluate the effects of freshwater and land-derived substances by glacial meltwater on pCO2 in the fjord, we calculated the changes of pCO2 in salinity and carbonate chemistry that would result from the inflow of glacial meltwater into the fjord. The calculated pCO2 was high near the calving front, where the contribution of glacier meltwater was significant. Examination of the relationship between salinity-normalized DIC and TA, which was considered DIC and TA input from the land, suggested that the land-derived high pCO2 freshwater affected mainly by the remineralization of the organic matter by bacterial activity was supplied to the Bowdoin Fjord.

Monsoon- and ENSO-driven surface-water pCO2 variation in the tropical West Pacific since the Last Glacial Maximum

The East Asian monsoon (EAM) and El Niño-Southern Oscillation (ENSO) are large-scale oceanic-atmospheric fluctuations that dominate climate variability in the tropical Pacific Ocean. Although the effects of EAM and ENSO on physical and biological processes are increasingly understood, little is known about their influence on seawater carbonate chemistry in the tropical Pacific, especially in the geological past. Here, we present reconstructed variations in surface-water pCO2 (pCO2(sw)) and their deviation from atmospheric pCO2 (ΔpCO2(sw-atm)) in the western Philippine Sea (WPS) since 27 ka. Our record displays covariation between ΔpCO2(sw-atm) and the intensity of the East Asian summer monsoon (EASM) since the Last Glacial Maximum (LGM), suggesting that EASM-driven upwelling controls long-term changes in surface-water carbonate chemistry and air-sea CO2 fluxes. Rapid changes in ΔpCO2(sw-atm) were linked to the ENSO-like state and, to a lesser extent, the East Asian winter monsoon (EAWM) during the Last Deglaciation, with low values corresponding to La Niña-like phases and strong EAWM during Heinrich Event 1, the Allerød and the Younger Dryas, and high values corresponding to El Niño-like phases and weak EAWM during the Bølling and Pre-Boreal. This interpretation is supported by the relationship of EAM and ENSO to modern surface-water carbonate chemistry in the WPS. Our new record, combined with previously published data, suggests that the tropical Pacific played a minimal role in sequestering CO2(atm) during the LGM. Tropical Pacific surface waters overall became a pronounced CO2 source to the atmosphere during the Last Deglaciation, possibly making a substantial contribution to the deglacial pCO2(atm) rise. We infer that this flux was mainly due to ENSO-related patterns of vertical stratification or lateral advection, perhaps in addition to equatorial upwelling of southern-sourced waters already enriched in dissolved inorganic carbon. Our findings indicate that tropical conditions (i.e., EAM and ENSO-like state) played a crucial role in glacial-interglacial pCO2(atm) changes, suggesting that this is an important area for future research into the causes of glacial pCO2(atm) cycles.

Seasonal Variability in Chlorophyll and Air-Sea CO2 Flux in the Sri Lanka Dome: Hydrodynamic Implications

Multiple upwelling systems develop in the Indian Ocean during the summer monsoon. The Sri Lanka dome (SLD), which occurs in the open ocean off the east coast of Sri Lanka from June to September, is distinct from those near the coast. The SLD is characterized by uplifted thermocline and increased chlorophyll concentration. Mechanisms of the upwelling and its biogeochemical response are not well understood. Here, we explored the dynamics of the chlorophyll and sea-to-air CO2 flux in the SLD using ocean color and altimetry remote sensing data, together with other reanalysis products. We found that the occurrence of high chlorophyll concentration and sea-to-air CO2 flux happens along the pathway of the southwest monsoon current (SMC). The annual cycle of chlorophyll in the SLD has a one-month lag relative to that in the southern coast of Sri Lanka. The positive wind stress curl that forms in the SLD during the summer does not fully explain the seasonal chlorophyll maximum. Transport of the SMC, eddy activity, and associated frontal processes also play an important role in regulating the variability in chlorophyll. In the SLD, upwelled subsurface water has excess dissolved inorganic carbon (DIC) relative to the conventional Redfield ratio between DIC and nutrients; thus, upwelling and sub-mesoscale processes determine this region to be a net carbon source to the atmosphere.

Influence of the Nocturnal Effect on the Estimated Global CO2 Flux

We found that significant errors occurred when diurnal data instead of diurnal–nocturnal data were used to calculate the daily sea-air CO2 flux (F). As the errors were mainly associated with the partial pressure of CO2 in seawater (pCO2w) and the sea surface temperature (SST) in the control experiment, pCO2w and SST equations were established, which are called the nocturnal effect of the CO2 flux. The root-mean-square error between the real daily CO2 flux (Freal) and the daily CO2 flux corrected for the nocturnal effect (Fcom) was 11.93 mmol m−2 d−1, which was significantly lower than that between the Freal value and the diurnal CO2 flux (Fday) (46.32 mmol m−2 d−1). Thus, the errors associated with using diurnal data to calculate the CO2 flux can be reduced by accounting for the nocturnal effect. The mean global daily CO2 flux estimated based on the nocturnal effect and the sub-regional pCO2w algorithm (cor_Fcom) was −6.86 mol m−2 y−1 (September 2020–August 2021), which was greater by 0.75 mol m−2 y−1 than that based solely on the sub-regional pCO2w algorithm (day_Fcom = −7.61 mol m−2 y−1). That is, compared with cor_Fcom, the global day_Fcom value overestimated the CO2 sink of the global ocean by 10.89%.

Persistent Continental Shelf Carbon Sink at the Ieodo Ocean Research Station in the Northern East China Sea

Hourly (2017–2021) to seasonal (2015–2021) inorganic C data were collected at the Ieodo Ocean Research Station (32.07°N and 125.10°E) in the northern East China Sea (ECS), located under the influence of the nutrient-rich Changjiang Diluted Water (CDW). An increase in phytoplankton biomass from April to mid-August (the warming period) equalized much of the temperature-driven increase in the surface pCO2 and thus, made the northern ECS a moderate sink of atmospheric CO2. From November to March (the cooling period), a large pCO2 reduction, driven by a temperature reduction, and a high air–sea CO2 exchange rate, because of high windspeeds, transformed the basin into a substantial CO2 sink, yielding an annual net C uptake of 61.7 g C m–2 yr–1. The effects of biological production and temperature change on seawater pCO2 (and thus, the net air–sea CO2 flux) were decoupled each season and acted in concert to increase the net annual CO2 sink by the region. The present study provided the observational and mechanistic lines of evidence for confirming “continental shelf C pump”—a mechanism in the shallow waters of the continental shelves that accumulate a significant amount of C (via reinforced cooling and promoted biological C uptake) that is transported from the basin surface waters to the interior of the adjacent deep ocean. In the future, an increasing input of anthropogenic nutrients into the northern ECS is likely to make the region a stronger CO2 sink.

Wintertime process study of the North Brazil Current rings reveals the region as a larger sink for CO<sub>2</sub> than expected

Abstract. The key processes driving the air–sea CO2 fluxes in the western tropical Atlantic (WTA) in winter are poorly known. WTA is a highly dynamic oceanic region, expected to have a dominant role in the variability in CO2 air–sea fluxes. In early 2020 (February), this region was the site of a large in situ survey and studied in wider context through satellite measurements. The North Brazil Current (NBC) flows northward along the coast of South America, retroflects close to 8∘ N and pinches off the world's largest eddies, the NBC rings. The rings are formed to the north of the Amazon River mouth when freshwater discharge is still significant in winter (a time period of relatively low run-off). We show that in February 2020, the region (5–16∘ N, 50–59∘ W) is a CO2 sink from the atmosphere to the ocean (−1.7 Tg C per month), a factor of 10 greater than previously estimated. The spatial distribution of CO2 fugacity is strongly influenced by eddies south of 12∘ N. During the campaign, a nutrient-rich freshwater plume from the Amazon River is entrained by a ring from the shelf up to 12∘ N leading to high phytoplankton concentration and significant carbon drawdown (∼20 % of the total sink). In trapping equatorial waters, NBC rings are a small source of CO2. The less variable North Atlantic subtropical water extends from 12∘ N northward and represents ∼60 % of the total sink due to the lower temperature associated with winter cooling and strong winds. Our results, in identifying the key processes influencing the air–sea CO2 flux in the WTA, highlight the role of eddy interactions with the Amazon River plume. It sheds light on how a lack of data impeded a correct assessment of the flux in the past, as well as on the necessity of taking into account features at meso- and small scales.

Monthly and seasonal variations in the surface carbonate system and air–sea CO2 flux of the Yellow Sea

Surface carbonate chemistry in the Yellow Sea was investigated based on discrete seawater samples collected from 2017 to 2020 at the Socheongcho Ocean Research Station (S-ORS; 37.423°N, 124.738°E). Records of carbon parameters, including seawater CO2 partial pressure (pCO2), revealed considerable seasonal variations, with amplitudes comparable to those observed across the western part of the Yellow Sea. The study site acted as a modest sink (−0.13 mol C m−2 yr−1) for atmospheric CO2. Biological processes (primary production and respiration) and physical conditions (temperature and degree of stratification) determined seawater pCO2, which fluctuated on an intraseasonal timescale between oversaturated and undersaturated with respect to atmospheric pCO2. Variation in pCO2 was significant in summer, depending on the biological carbon drawdown and tidal mixing-induced upwelling (increased pCO2 up to ~1000 μatm). The intraseasonal variability in seawater pCO2 may bias estimated air–sea CO2 fluxes, if measurements with a coarser (seasonal) time resolution are used.

Data-based estimates of interannual sea–air CO<sub>2</sub> flux variations 1957–2020 and their relation to environmental drivers

Abstract. This study considers year-to-year and decadal variations in as well as secular trends of the sea–air CO2 flux over the 1957–2020 period, as constrained by the pCO2 measurements from the SOCATv2021 database. In a first step, we relate interannual anomalies in ocean-internal carbon sources and sinks to local interannual anomalies in sea surface temperature (SST), the temporal changes in SST (dSST/dt), and squared wind speed (u2), employing a multi-linear regression. In the tropical Pacific, we find interannual variability to be dominated by dSST/dt, as arising from variations in the upwelling of colder and more carbon-rich waters into the mixed layer. In the eastern upwelling zones as well as in circumpolar bands in the high latitudes of both hemispheres, we find sensitivity to wind speed, compatible with the entrainment of carbon-rich water during wind-driven deepening of the mixed layer and wind-driven upwelling. In the Southern Ocean, the secular increase in wind speed leads to a secular increase in the carbon source into the mixed layer, with an estimated reduction in the sink trend in the range of 17 % to 42 %. In a second step, we combined the result of the multi-linear regression and an explicitly interannual pCO2-based additive correction into a “hybrid” estimate of the sea–air CO2 flux over the period 1957–2020. As a pCO2 mapping method, it combines (a) the ability of a regression to bridge data gaps and extrapolate into the early decades almost void of pCO2 data based on process-related observables and (b) the ability of an auto-regressive interpolation to follow signals even if not represented in the chosen set of explanatory variables. The “hybrid” estimate can be applied as an ocean flux prior for atmospheric CO2 inversions covering the whole period of atmospheric CO2 data since 1957.

Effects of Shellfish and Macro-Algae IMTA in North China on the Environment, Inorganic Carbon System, Organic Carbon System, and Sea–Air CO2 Fluxes

Shellfish and macro-algae integrated multi-trophic aquaculture (IMTA) contribute greatly to the sustainability of aquaculture. However, the effects of large-scale shellfish and macro-algae aquaculture on the functions of the ocean carbon sink are not clear. To clarify these effects, we studied the spatial and temporal changes of inorganic and organic carbon systems in seawater under different aquaculture modes (monoculture or polyculture of shellfish and macro-algae) in Sanggou Bay, together with the variation of other environmental factors. The results show that the summertime dissolved oxygen (DO) concentration in the shellfish culture zone was significantly lower than other zones (p < 0.05), with a minimum value of 7.07 ± 0.25 mg/L. The variation of pH and total alkalinity (TA) were large across different culture modes, and the seawater in the shellfish culture zone had the lowest pH and TA than the other zones. Seasonal environment and aquaculture modes significantly affected the variation of dissolved inorganic carbon (DIC), CO2 partial pressure (pCO2), dissolved organic carbon (DOC), and particulate organic carbon (POC) concentrations. The highest values of DIC, pCO2, and POC appeared in summer, and the lowest appeared in winter. For DOC concentration, the lowest value appeared in autumn. Spatially, DIC and pCO2 were highest in the shellfish culture zone and lowest in the macro-algae culture zone, DOC was highest in the macro-algae culture zone and lowest in the shellfish culture zone, and POC was lower in the shellfish culture zone and macro-algae culture zone and higher in the remaining zones. The results of sea–air CO2 fluxes showed that except for the shellfish culture zone during summertime, which released CO2 to the atmosphere, all culture zones were the sinks of atmospheric CO2 during the culture period, with the whole bay being a strong CO2 sink during autumn and winter. In summary, large-scale shellfish–macro-algae IMTA plays an important role in the local carbon cycle and contributes to mitigating ocean acidification and hypoxia.

Decadal Variability of Satellite-Derived Air–Sea CO2 Flux in Southwestern Part of the Bay of Bengal

Decadal Variability of Satellite-Derived Air–Sea CO2 Flux in Southwestern Part of the Bay of Bengal

Comprehending the role of different mechanisms and drivers affecting the sea-surface pCO2 and the air-sea CO2 fluxes in the Bay of Bengal: A modeling study

We apply a coupled physical and biogeochemical (ROMS+PISCES) to understand the influence of distinct drivers and mechanisms on the sea-surface pCO2 and the air-sea CO2 flux of the Bay of Bengal (BoB). The model evaluation suggests that the model simulated sea-surface pCO2 is in accord with the observations. The north of BoB is found to be a sink for the atmospheric CO2, whereas the rest of the region acts as a source. The effect of dissolved inorganic carbon (DIC) and the total alkalinity (TALK) is found to be predominant but is contrasting in nature. Mixing-induced changes in DIC and TALK results in high pCO2 (+570μatm) and, consequently, the positive CO2 flux. The biological activity does draw down the surface pCO2 (−120μatm) but is insufficient in completely opposing the effect of mixing. The uptake of CO2 in the north is due to the CO2 solubility, which is a function of salinity and temperature. The northern rivers, having a high discharge rate, reduce the salinity and temperatures in the north, which possibly aids in this region to be a sink. In the northeast monsoon season, the impact of temperature and DIC is high and opposing. The TALK reduces the pCO2 in the northeast monsoon, but the magnitude is low. The pCO2 in the southwest monsoon is influenced primarily by temperature, whereas in the postmonsoon monsoon, the freshwater dominates. The pre-monsoon season experiences the TALK, temperature, and freshwater increase the pCO2 anomalies, and only the DIC reduces pCO2 anomalies.

Tidal mixing of estuarine and coastal waters in the western English Channel is a control on spatial and temporal variability in seawater CO<sub>2</sub>

Abstract. Surface ocean carbon dioxide (CO2) measurements are used to compute the oceanic air–sea CO2 flux. The CO2 flux component from rivers and estuaries is uncertain due to the high spatial and seasonal heterogeneity of CO2 in coastal waters. Existing high-quality CO2 instrumentation predominantly utilises showerhead and percolating style equilibrators optimised for open-ocean observations. The intervals between measurements made with such instrumentation make it difficult to resolve the fine-scale spatial variability of surface water CO2 at timescales relevant to the high frequency variability in estuarine and coastal environments. Here we present a novel dataset with unprecedented frequency and spatial resolution transects made at the Western Channel Observatory in the south-west of the UK from June to September 2016, using a fast-response seawater CO2 system. Novel observations were made along the estuarine–coastal continuum at different stages of the tide and reveal distinct spatial patterns in the surface water CO2 fugacity (fCO2) at different stages of the tidal cycle. Changes in salinity and fCO2 were closely correlated at all stages of the tidal cycle and suggest that the mixing of oceanic and riverine endmembers partially determines the variations in fCO2. The correlation between salinity and fCO2 was different in Cawsand Bay, which could be due to enhanced gas exchange or to enhanced biological activity in the region. The observations demonstrate the complex dynamics determining spatial and temporal patterns of salinity and fCO2 in the region. Spatial variations in observed surface salinity were used to validate the output of a regional high-resolution hydrodynamic model. The model enables a novel estimate of the air–sea CO2 flux in the estuarine–coastal zone. Air–sea CO2 flux variability in the estuarine–coastal boundary region is influenced by the state of the tide because of strong CO2 outgassing from the river plume. The observations and model output demonstrate that undersampling the complex tidal and mixing processes characteristic of estuarine and coastal environment biases quantification of air–sea CO2 fluxes in coastal waters. The results provide a mechanism to support critical national and regional policy implementation by reducing uncertainty in carbon budgets.

Moderate CO2 sink due to phytoplankton bloom following a typhoon passage over the East China Sea

In September 2017, following passage of Typhoon Talim, daily satellite imagery captured a large area (∼300-km long and ∼160-km wide) of high concentration of chlorophyll a (Chl a) that persisted for at least 8 days on the East China Sea (ECS) shelf. Ship-based measurements were conducted 5–6 days after the passage of Talim. Results showed that surface seawater within the area of high Chl a concentration had features of high salinity, low temperature, and low partial pressure of CO2 (pCO2) in comparison with surrounding seawater. The high Chl a concentration reflected a phytoplankton bloom triggered by upwelling nutrient-rich deeper water attributable to the passage of Typhoon Talim. The change in surface pCO2 in the area of high Chl a concentration was explained by the combined effects of upwelling deeper water and subsequent biological production. The air–sea CO2 flux in the area of high Chl a concentration was −2.8 ± 0.4 mmol m−2 d−1 in the post-typhoon stage, which turned the study area from near equilibrium (0.3 ± 0.3 mmol m−2 d−1 in the surrounding water) to a moderate CO2 sink. This phytoplankton bloom absorbed 0.013 Tg C during the 8 days following the passage of Talim, effectively canceling out 28% of the typhoon-induced CO2 efflux during typhoon passage across the ECS. Therefore, the effect of typhoons on air–sea CO2 flux in the post-typhoon stage cannot be ignored.

Attribution of Space-Time Variability in Global-Ocean Dissolved Inorganic Carbon.

The inventory and variability of oceanic dissolved inorganic carbon (DIC) is driven by the interplay of physical, chemical, and biological processes. Quantifying the spatiotemporal variability of these drivers is crucial for a mechanistic understanding of the ocean carbon sink and its future trajectory. Here, we use the Estimating the Circulation and Climate of the Ocean‐Darwin ocean biogeochemistry state estimate to generate a global‐ocean, data‐constrained DIC budget and investigate how spatial and seasonal‐to‐interannual variability in three‐dimensional circulation, air‐sea CO2 flux, and biological processes have modulated the ocean sink for 1995–2018. Our results demonstrate substantial compensation between budget terms, resulting in distinct upper‐ocean carbon regimes. For example, boundary current regions have strong contributions from vertical diffusion while equatorial regions exhibit compensation between upwelling and biological processes. When integrated across the full ocean depth, the 24‐year DIC mass increase of 64 Pg C (2.7 Pg C year−1) primarily tracks the anthropogenic CO2 growth rate, with biological processes providing a small contribution of 2% (1.4 Pg C). In the upper 100 m, which stores roughly 13% (8.1 Pg C) of the global increase, we find that circulation provides the largest DIC gain (6.3 Pg C year−1) and biological processes are the largest loss (8.6 Pg C year−1). Interannual variability is dominated by vertical advection in equatorial regions, with the 1997–1998 El Niño‐Southern Oscillation causing the largest year‐to‐year change in upper‐ocean DIC (2.1 Pg C). Our results provide a novel, data‐constrained framework for an improved mechanistic understanding of natural and anthropogenic perturbations to the ocean sink.