On the Nature of Aerosol Particles in the Atmosphere of Irkutsk

Monitoring data on the ion composition of precipitation and the water-soluble fraction of aerosol have been used to identify two types of aerosol particles in the surface atmosphere of Irkutsk (“metal” and “ammonia” groups). The aerosol acidity is basically governed by the acidity of ammonia particles, and the ion composition depends on air relative humidity (RH). Preliminary estimates are given for the distribution of major cations and anions by aerosol groups.     

Temporal Change of Dissolved Inorganic Carbon in the Subsurface Water at Station KNOT (44°N, 155°E) in the Western North Pacific Subpolar Region

The dissolved inorganic carbon (DIC) and related chemical species have been measured from 1992 to 2001 at Station KNOT (44°N, 155°E) in the western North Pacific subpolar region. DIC (1.3∼2.3 µ mol/kg/yr) and apparent oxygen utilization (AOU, 0.7∼1.8 µmol/kg/yr) have increased while total alkalinity remained constant in the intermediate water (26.9∼27.3σ_θ). The increases of DIC in the upper intermediate water (26.9∼27.1σ_θ) were higher than those in the lower one (27.2∼ 27.3σ_θ). The temporal change of DIC would be controlled by the increase of anthropogenic CO₂, the decomposition of organic matter and the non-anthropogenic CO₂ absorbed at the region of intermediate water formation. We estimated the increase of anthropogenic CO₂ to be only 0.5∼0.7 µmol/kg/yr under equilibrium with the atmospheric CO₂ content. The effect of decomposition was estimated to be 0.8 ± 0.7 µmol/kg/yr from AOU increase. The remainder of non-anthropogenic CO₂ had increased by 0.6 ± 1.1 µmol/kg/yr. We suggest that the non-anthropogenic CO₂ increase is controlled by the accumulation of CO₂ liberated back to atmosphere at the region of intermediate water formation due to the decrease of difference between DIC in the winter mixed layer and DIC under equilibrium with the atmospheric CO₂ content, and the reduction of diapycnal vertical water exchange between mixed layer and pycnocline waters. In future, more accurate and longer time series data will be required to confirm our results.     

Annual cycle of fCO2 under sea-ice and in open water in Prydz Bay, East Antarctica

The annual cycle of dissolved nutrients and the fugacity of CO₂ (fCO₂), calculated from the concentration of dissolved inorganic carbon (DIC) and pH, was studied over a 14-month long period (December 1993 to February 1995) at a site in Prydz Bay near Davis Station, Vestfold Hills, East Antarctica. Significant spring decreases in fCO₂ began under the sea-ice in mid-October, when both water column and sea-ice algal activity resulted in the removal of nutrients and DIC and increased pH. Minimum fCO₂ (<100 μatm) and lowest nutrient and DIC concentrations occurred in December and January. The low summer fCO₂ values were clearly the result of biological activity. The seasonal depletion of dissolved nitrate reached 85% in mid-summer when chlorophyll-a concentrations exceeded 15 mg m⁻³. Oceanic uptake of carbon dioxide from the atmosphere, calculated from the fugacity difference and daily wind speeds, averaged more than 30 mmol m⁻² day⁻¹ during the summer ice-free period. This exchange replaced approximately half of the DIC consumed by biological activity. Apparent nutrient utilisation ratios (C/N/P) were close to Redfield values. In autumn fCO₂ began to rise, continuing slowly well into winter, and reaching a maximum close to modern atmospheric values between July and September. This increase can be attributed to a combination of local remineralisation of organic carbon in the water column and the steady increase in the mixing depth of the water column. At first glance, this suggests that air–sea equilibration occurred in winter despite the sea-ice cover, perhaps by horizontal circulation from regions outside the pack ice, or through openings in the ice. However, the persistent 15 to 20% undersaturation of dissolved oxygen throughout the winter suggests an alternate explanation. The late winter fCO₂ level may represent a characteristic established by global circulation, so that as a result of increasing atmospheric CO₂ concentrations, these Antarctic waters are in transition from being a winter-time source of CO₂ to the atmosphere to becoming a sink. Our fCO₂ observations emphasize the need to address seasonal variations in assessing Antarctic contributions to the oceanic control of atmospheric CO₂.     

Stable isotope composition of modern bryozoan skeletal carbonate from the Otago Shelf,New Zealand

The oxygen (δ¹⁸O) and carbon (δ¹³C) isotope ratios of 10 species of living Bryozoa collected from the Otago Shelf, New Zealand were analysed to assess the extent to which isotopic equilibrium (relative to inorganic equilibrium isotope fractionation) is attained during the precipitation of skeletal calcium carbonate. The data reveal that whereas eight species of Bryozoa synthesise skeletal carbonate in apparent oxygen isotope equilibrium with respect to environmental conditions, two species (Celleporina grandis and Hippomonavella flexuosa) yield δ¹⁸O_calcite values which indicate significant disequilibrium oxygen isotope fractionation during calcification. Sufficient data are available from one species (C. grandis) to demonstrate that disequilibrium is probably related to kinetic factors associated with diffusion‐controlled transport of HCO₃‐ to the site of calcite precipitation. Carbon isotope signatures indicate significant departures from inorganic isotope equilibrium in all but one bryozoan species (Hippomenella vellicata). Although greater uncertainties are associated with estimates of the isotopic composition of total dissolved inorganic carbon (δ¹³C_SDIC), the data suggest that two factors—kinetic fractionation and incorporation of respiratory CO₂—are important in controlling carbon isotope disequilibrium. Where bryozoan species exhibit evidence for disequilibrium in both oxygen and carbon isotope systems (C. grandis, H. flexuosa), it is likely that kinetic factors are primarily responsible for observed departures from carbon isotope equilibrium. In contrast, the probable explanation for those species which display evidence for carbon isotope disequilibrium only, is that skeletal carbonate is precipitated from a DIC pool modified by the incorporation of respiratory CO₂. Differences between the carbon isotope composition of skeletal elements from the same species and co‐existing species living in the same community suggests that significant variations may occur in the extent to which marine DIC and respiratory CO₂ are utilised during calcification. Additional studies of carbon pathways associated with calcification are required to assess the relative effects of kinetic, metabolic, and environmental factors on the carbon isotopic composition of bryozoan skeletal carbonate.     

Biogeochemical ocean-atmosphere transfers in the Arabian Sea

Transfers of some important biogenic atmospheric constituents, carbon dioxide (CO₂), methane (CH₄), molecular nitrogen (N₂), nitrous oxide (N₂O), nitrate , ammonia (NH₃), methylamines (MAs) and dimethylsulphide (DMS), across the air–sea interface are investigated using published data generated mostly during the Arabian Sea Process Study (1992–1997) of the Joint Global Ocean Flux Study (JGOFS). The most important contribution of the region to biogeochemical fluxes is through the production of N₂ and N₂O facilitated by an acute, mid-water deficiency of dissolved oxygen (O₂); emissions of these gases to the atmosphere from the Arabian Sea are globally significant. For the other constituents, especially CO₂, even though the surface concentrations and atmospheric fluxes exhibit extremely large variations both in space and time, arising from the unique physical forcing and associated biogeochemical environment, the overall significance in terms of their global fluxes is not much because of the relatively small area of the Arabian Sea. Distribution and air–sea exchanges of some of these constituents are likely to be greatly influenced by alterations of the subsurface O₂ field forced by human-induced eutrophication and/or modifications to the regional hydrography.     

Comments on: “Underwater measurements of carbon dioxide evolution in marine plant communities: A new method” by J. Silva and R. Santos [Estuarine,Coastal and Shelf Science 78(2008) 827–830]

Silva et al. propose a new method for quantifying benthic net community production (NCP) of tidal flats under submerged condition, based on the monitoring of water pCO₂ in a transparent benthic chamber around high tide. I demonstrate here with theoretical considerations that this method is inappropriate for coastal environments, because it allows only the quantification of the change in the dissolved CO₂ which, at classical seawater pH, is only ∼10% of the change of the dissolved inorganic carbon (DIC). Total Alkalinity and/or DIC must be measured at the beginning and end of incubations in order to compute NCP in coastal environments. However, I also demonstrate that when pH is below 7, more than 95% of the DIC change occurs in the CO₂ pool. The method proposed by Silva et al. is thus valuable for freshwater environments with acidic, low alkalinity waters, where monitoring the water pCO₂ in a vial or chamber provides alone a very close approximation of the planktonic or benthic net community production.     

Doubled CO2 impact on subarctic marine carbon cycle: a case study at Ocean Station P

Along with meteorological observations, complementary and systematic oceanographic observations of various physical, biological and chemical parameters have been made at Ocean Station P (OSP) (50°N, 145°W) since the early 1950s. These decadal time scale data have contributed to a better understanding of the physical, biological and chemical processes in the surface layer of the northeastern subarctic region of the Pacific Ocean. These data have demonstrated the importance of the North Pacific in the global carbon cycle and, in particular, the role of biological/chemical processes in the net exchange of CO₂ across the air–sea interface. Although we do not fully comprehend how climatic variations influence marine communities or marine biogeochemistry, previous studies have provided some basic understanding of the mechanisms controlling the seasonal and inter-annual variations of biological and chemical parameters (such as phytoplankton, bacteria, nitrate/ammonium concentration) at OSP, and how they affect the carbon cycling in the subarctic North Pacific. In this study, we investigate how these mechanisms might alter the seasonal variations of these parameters at OSP under a 2XCO₂ condition. We examine these influences using a new biological model calibrated by the climatological data from OSP. For the 2XCO₂ simulation, the biological model is driven off line (i.e., no feedback to the ocean/atmospheric model components) by the climatology plus 2XCO₂−1XCO₂ outputs from a global surface ocean model and the Canadian GCM. Under the 2XCO₂ condition, the upper layer ocean shows an increase in the entrainment rate at the bottom of the mixed layer for OSP during the late autumn and winter seasons, resulting in an increase in the f-ratio. Although there is an overall increase in the primary production (PP) by 3–18%, a decrease in the biomass of small phytoplankton and microzooplankton (due to mesozooplankton grazing) lowers the concentration of dissolved organic matter (DOM) by 4–25%. The model also predicts a significant increase in the concentrations of nitrate and ammonium, and in bacterial production during July and August. Doubling of the atmospheric CO₂ from 330 to 660 ppm forces the marine pCO₂ to increase by about 63%, much of which is driven by an increased flux of CO₂ from the atmosphere to the oceans.     

Effects of CO<Subscript>2</Subscript> Enrichment on Marine Phytoplankton

Rising atmospheric CO₂ and deliberate CO₂ sequestration in the ocean change seawater carbonate chemistry in a similar way, lowering seawater pH, carbonate ion concentration and carbonate saturation state and increasing dissolved CO₂ concentration. These changes affect marine plankton in various ways. On the organismal level, a moderate increase in CO₂ facilitates photosynthetic carbon fixation of some phytoplankton groups. It also enhances the release of dissolved carbohydrates, most notably during the decline of nutrient-limited phytoplankton blooms. A decrease in the carbonate saturation state represses biogenic calcification of the predominant marine calcifying organisms, foraminifera and coccolithophorids. On the ecosystem level these responses influence phytoplankton species composition and succession, favouring algal species which predominantly rely on CO₂ utilization. Increased phytoplankton exudation promotes particle aggregation and marine snow formation, enhancing the vertical flux of biogenic material. A decrease in calcification may affect the competitive advantage of calcifying organisms, with possible impacts on their distribution and abundance. On the biogeochemical level, biological responses to CO₂ enrichment and the related changes in carbonate chemistry can strongly alter the cycling of carbon and other bio-active elements in the ocean. Both decreasing calcification and enhanced carbon overproduction due to release of extracellular carbohydrates have the potential to increase the CO₂ storage capacity of the ocean. Although the significance of such biological responses to CO₂ enrichment becomes increasingly evident, our ability to make reliable predictions of their future developments and to quantify their potential ecological and biogeochemical impacts is still in its infancy. This revised version was published online in July 2006 with corrections to the Cover Date.     

Acidification at the Surface in the East Sea: A Coupled Climate-carbon Cycle Model Study

This modeling study investigates the impacts of increasing atmospheric CO₂ concentration on acidification in the East Sea. A historical simulation for the past three decades (1980 to 2010) was performed using the Hadley Centre Global Environmental Model (version 2), a coupled climate model with atmospheric, terrestrial and ocean cycles. As the atmospheric CO₂ concentration increased, acidification progressed in the surface waters of the marginal sea. The acidification was similar in magnitude to observations and models of acidification in the global ocean. However, in the global ocean, the acidification appears to be due to increased in-situ oceanic CO₂ uptake, whereas local processes had stronger effects in the East Sea. pH was lowered by surface warming and by the influx of water with higher dissolved inorganic carbon (DIC) from the northwestern Pacific. Due to the enhanced advection of DIC, the partial pressure of CO₂ increased faster than in the overlying air; consequently, the in-situ oceanic uptake of CO₂ decreased.     

Uptake mechanism of anthropogenic CO<Subscript>2</Subscript> in the Kuroshio Extension region in an ocean general circulation model

The uptake mechanism of anthropogenic CO₂ in the Kuroshio Extension is examined by a Lagrangian approach using a biogeochemical model embedded in an ocean general circulation model. It is found that the uptake of anthropogenic CO₂ is caused mainly by the increase of pCO₂ dependency of seawater on temperature, which is caused by greater dissolved inorganic carbon concentration in the modern state than in the pre-industrial state. In contrast with the view of previous studies, the effect of the vertical entrainment, which brings waters that last contacted the atmosphere with the past lower CO₂ concentration, is comparatively small. Winter uptake of anthropogenic CO₂ increases with the rise of the atmospheric CO₂ level, while summer uptake is relatively stable, resulting in a larger seasonal cycle of the uptake. This increase is significant, especially in the Kuroshio Extension region. It is newly suggested that this increase in the Kuroshio Extension region is largely caused by the combined effects of the increased pCO₂ dependency of the sea water on the temperature and the seasonal difference in cooling.     

Seasonal and spatial variations in the partial pressure of carbon dioxide in a eutrophic brackish lake,Lake Hamana,Japan

The dissolved inorganic carbon and total alkalinity in the surface brackish waters of Lake Hamana were investigated monthly from October 2017 to September 2019 at 14 stations. The partial pressure of carbon dioxide (pCO₂) in the surface water ranged from 29 to 1476 μatm and was undersaturated for atmospheric CO₂ during the observation periods, although most coastal waters were net source areas because of the large amount of terrestrial organic and inorganic carbon input. Since there was a strong negative correlation between pCO₂ and the dissolved oxygen, seasonal and temporal variations in pCO₂ were mainly derived from phytoplankton activity. The high phytoplankton activity induced by the effluents from sewage treatment plants, which was low in carbon and high in nitrogen. Therefore, in urbanized coastal waters with sewage treatment plants, such as the coastal waters of Japan, there is a possibility of shifting from weaker carbon dioxide source areas to sink areas. However, pCO₂ was oversaturated at the polluted river mouth, especially after high precipitation events due to the large carbon supply.

     

The contribution of atmospheric acid deposition to ocean acidification in the subtropical North Atlantic Ocean

The absorption of anthropogenic CO₂ and atmospheric deposition of acidity can both contribute to the acidification of the global ocean. Rainfall pH measurements and chemical compositions monitored on the island of Bermuda since 1980, and a long-term seawater CO₂ time-series (1983–2005) in the subtropical North Atlantic Ocean near Bermuda were used to evaluate the influence of acidic deposition on the acidification of oligotrophic waters of the North Atlantic Ocean and coastal waters of the coral reef ecosystem of Bermuda. Since the early 1980's, the average annual wet deposition of acidity at Bermuda was 15 ± 14 mmol m^− 2 year^− 1, while surface seawater pH decreased by 0.0017 ± 0.0001 pH units each year. The gradual acidification of subtropical gyre waters was primarily due to uptake of anthropogenic CO₂. We estimate that direct atmospheric acid deposition contributed 2% to the acidification of surface waters in the subtropical North Atlantic Ocean, although this value likely represents an upper limit. Acidifying deposition had negligible influence on seawater CO₂ chemistry of the Bermuda coral reef, with no evident impact on hard coral calcification.     

CO2 cycling in the coastal ocean. I – A numerical analysis of the southeastern Bering Sea with applications to the Chukchi Sea and the northern Gulf of Mexico

A quasi-two dimensional model of the carbon and nitrogen cycling above the 70m isobath of the southeastern Bering Sea at 57°N replicates the observed seasonal cycles of nitrate, ammonium, ΣCO₂, pCO₂, light penetration, chlorophyll, phytoplankton growth rate, and primary production, as constrained by changes in wind, incident radiation, temperature, ice cover, vertical and lateral mixing, grazing stress, benthic processing of phytodetritus and zooplankton fecal pellets, and the pelagic microbial loop of DOC, bacteria, and their predators. About half of the seasonal resupply of nitrate stocks to their initial winter conditions is derived from in situ nitrification, with the rest obtained from deep-sea influxes. Under the present conditions of atmospheric forcing, shelf-break exchange, and food web structure, this shelf ecosystem serves as a sink for atmospheric CO₂, with storage in the forms of exported DOC, DIC, and unutilized POC (phytoplankton, bacteria, and fecal pellets).As a consequence of just the rising levels of atmospheric pCO₂ since the the Industrial Revolution, however, the biophysical CO₂ status of the Southeastern Bering Sea shelf may have switched over the last 250 years, from a prior source to the present sink, since this relatively pristine ecosystem has unergone little eutrophication. Such fluctuations of CO₂ status may thus be reversed by the physical processes of : (1) reduction of atmospheric pCO₂, (2) increased on welling of deep-sea ΣCO₂, and (3) warming of shelf waters. Based on our application of this model to the Chukchi Sea and the Gulf of Mexico, about 1.0–1.2 gigatons C y^-1 of atmospheric CO₂ may now be sequestered by temperate and polar shelf ecosystems. When tropical systems are included, however, a positive net sink of only 0.6–0.8. × 10¹⁵g C y⁻¹ may prevail over all shelves.     

Time series of carbonate system variables off Otaru coast in Hokkaido, Japan

We report several biogeochemical parameters (dissolved inorganic carbon (DIC), total alkalinity (TA), dissolved oxygen (DO), phosphate (PO₄), nitrate + nitrite (NO₃ + NO₂), silicate (Si(OH)₄)) in a region off Otaru coast in Hokkaido, Japan on a “weekly” basis during the period of April 2002–May 2003. To better understand the long-term temporal variations of the main factors affecting CO₂ flux in this coastal region and its role as a sink/source of atmospheric CO₂, we constructed an algorithm of DIC and TA using other hydrographic properties. We estimated the CO₂ flux across the air–sea interface by using the classical bulk method. During 1998–2003 in our study region, the estimated fCO_2sea ranged about 185–335 μatm. The maximum of fCO_2sea in the summer was primarily due to the change of water temperature. The minimum of fCO_2sea in the early spring can be explained not only by the change of water temperature but also the change of nutrients and chlorophyll-a. To clarify the factors affecting fCO_2sea (water temperature, salinity, and biological activity), we carried out a sensitivity analysis of these effects on the variation of fCO_2sea. In spring, the biological effect had the largest effect for the minimum of fCO_2sea (40%). In summer, the water temperature effect had the largest effect for the maximum of fCO_2sea (25%). In fall, the water temperature effect had the largest effect for the minimum of fCO_2sea (53%). In winter, the biological effect had the largest effect for the minimum of fCO_2sea (35%).We found that our study region was a sink region of CO₂ throughout a year (−0.78 mol/m²/yr). Furthermore, we estimated that the increase of fCO_2sea was about 0.56 μatm/yr under equilibrium with the atmospheric CO₂ content for the period 1998–2003, with the temporal changes in the variables (T, S, PO₄) on fCO_2sea, thus as the maximum trend of each variable on fCO_2sea was 0.22 μatm/yr, and the trend of residual fCO₂ including gas exchange was 0.34 μatm/yr. This result suggests that interaction among variables would affect gas exchange between air and sea effects on fCO_2sea. We conclude that this study region as a representative coastal region of marginal seas of the North Pacific is special because it was measured, but there is no particular significance in comparison to any other area.     

Carbon dioxide content in the atmospheric thickness over central Eurasia (Issyk Kul Monitoring Station)

The refined data obtained from the spectroscopic measurements of carbon dioxide in the column of the continental atmosphere over the Issyk Kul Monitoring Station during the period 1980–2006 and the results of their comparison with the data obtained from the measurements of carbon dioxide in air samples and with the mean zonal empirical model of the Climate Monitoring and Diagnostics Laboratory (CMDL) are given. Seasonal variations and a long-term trend of carbon dioxide concentration in the atmospheric thickness over a 25-year period of measurements are analyzed. The monthly mean concentration of CO₂ is increased by ～40.5 ppm, and the linear-trend index is 1.62 ppm per year. The results of the aircraft measurements of CO₂ concentration in air samples are, on the average, in agreement with the data obtained from the spectroscopic measurements of carbon dioxide concentration in the atmospheric column. The CO₂ concentration in the surface air varies from day to day, and only its minimum values coincide with the CO₂ concentration in the atmospheric thickness. The results of measurements of CO₂ concentration in the atmospheric thickness and in the atmospheric surface layer over the KZD and KZM stations nearest to each other are, on the whole, in disagreement; moreover, the KZD and KZM data are inconsistent. The CO₂ concentration in the atmospheric thickness is, on the average, 1–2% higher than that obtained with the CMDL model for 42.6° N latitude. The coefficient of correlation between the measurement results and model data is high (r= 0.95).     

Summer and winter air–sea CO2 fluxes in the Southern Ocean

The seasonal variability of the carbon dioxide (CO₂) system in the Southern Ocean, south of 50°S, is analysed from observations obtained in January and August 2000 during OISO cruises conducted in the Indian Antarctic sector. In the seasonal ice zone, SIZ (south of 58°S), surface ocean CO₂ concentrations are well below equilibrium during austral summer. During this season, when sea-ice is not obstructing gas exchange at the air–sea interface, the oceanic CO₂ sink ranges from −2 to −4 mmol/m²/d in the SIZ. In the permanent open ocean zone, POOZ (50–58°S), surface oceanic fugacity fCO₂ increases from summer to winter. The seasonal fCO₂ variations (from 10 to 30 μatm) are relatively low compared to seasonal amplitudes observed in the subtropics or the subantarctic zones. However, these variations in the POOZ are large enough to cross the atmospheric level from summer to winter. Therefore, this region is neither a permanent CO₂ sink nor a permanent CO₂ source. In the POOZ, air–sea CO₂ fluxes calculated from observations are about −1.1 mmol/m²/d in January (a small sink) and 2.5 mmol/m²/d in August (a source). These estimates obtained for only two periods of the year need to be extrapolated on a monthly scale in order to calculate an integrated air–sea CO₂ flux on an annual basis. For doing this, we use a biogeochemical model that creates annual cycles for nitrate, inorganic carbon, total alkalinity and fCO₂. The changing pattern of ocean CO₂ summer sink and winter source is well reproduced by the model. It is controlled mainly by the balance between summer primary production and winter deep vertical mixing. In the POOZ, the annual air–sea CO₂ flux is about −0.5 mol/m²/yr, which is small compared to previous estimates based on oceanic observations but comparable to the small CO₂ sink deduced from atmospheric inverse methods. For reducing the uncertainties attached to the global ocean CO₂ sink south of the Polar Front the regional results presented here should be synthetized with historical and new observations, especially during winter, in other sectors of the Southern Ocean.     

Possible reasons for low climate-model sensitivity to increased carbon dioxide concentrations

The sensitivities of two climate-model versions—INMCM4 which participated in the Coupled Model Intercomparison Project, Phase 5 (CMIP5), and a new INMCM5 version with increased vertical and horizontal resolutions in its atmospheric block—to the quadrupled concentration of CO₂ are studied. When the CO₂ concentration is quadrupled, the equilibrium increase in surface temperature amounts to about 4.2 K for INMCM4, which is lower than that for other models that participated in the CMIP5. When the CO₂ concentration increases, the cloud radiative forcing in the model decreases; in this case, one portion of this decrease occurs during the first year after the concentration of CO₂ is quadrupled and the other portion almost linearly depends on the value of global warming. The results of additional numerical experiments with the model show that a rapid decrease in cloud-radiative forcing results from variations in stratification in the atmospheric surface boundary layer and associated increased cloudiness. The portion of a linear decrease in cloud-radiative forcing with increased temperature is associated with an increase in the water content of model clouds at higher temperatures. The elimination of these two mechanisms allows one to increase the model sensitivity to the quadrupled concentration of CO₂ up to 5.2 K.     

Recent increase in surface fCO<Subscript>2</Subscript> in the western subtropical North Pacific

We observed unusually high levels (> 440 μatm) of carbon dioxide fugacity (fCO₂) in surface seawater in the western subtropical North Pacific, the area where Subtropical Mode Water is formed, during summer 2015. The NOAA Kuroshio Extension Observatory moored buoy located in this region also measured high CO₂ values, up to 500 μatm during this period. These high sea surface fCO₂ (fCO_2SW) values are explained by much higher normalized total dissolved inorganic carbon and slightly higher normalized total alkalinity concentrations in this region compared to the equatorial Pacific. Moreover, these values are much higher than the climatological CO₂ values, even considering increasing atmospheric CO₂, indicating a recent large increase in sea surface CO₂ concentrations. A large seasonal change in sea surface temperature contributed to higher surface fCO_2SW in the summer of 2015.     

Simulation of export production and biological pump structure in the South China Sea

The export flux of particulate organic carbon (POC) consumes upwelled dissolved inorganic carbon (DIC), which hinders surplus CO₂ being released to the atmosphere. The export flux of POC is therefore crucial to the carbon and biogeochemical cycles. This study aims to model the long-term (1958–2009) variation of export flux and structure of the biological pump in the South China Sea (SCS) using a three-dimensional physical-biogeochemical coupled (ROMS-CoSiNE) model. The modeled POC export flux in the northeastern and north central SCS is high in winter and low in summer, whereas the flux in the central, southwestern and southern SCS varies following a “W” shape: two maxima in winter and summer, and two minima in spring and autumn. The pattern follows the variation of the East Asian monsoon and is consistent with observations. On the interannual scale, export flux is anti-phased with the El Niño-Southern Oscillation such that El Niño (La Niña) conditions correspond to low (high) export flux. Modeled annual mean POC export flux reaches up to 1.95 mmol m^–2 day^–1, which is underestimated comparing with field observations. The f-ratio is estimated to be ~0.4. The b value of the Martin equation for POC is 1.18±0.03. Remineralization rate of POC is greater than the classical Martin equation but is consistent with its subtropical counterparts. The modeled results indicate that the SCS is a weak source of atmospheric CO₂ with a flux estimated at 1.0 mmol m^–2 day^–1. The modeled results provide an insight of the temporal and spatial variability of the carbon cycle in this monsoon-driven, semi-enclosed basin.