Temporal variations in carbon dioxide and methane concentrations under urban conditions

Temporal variations in the surface concentrations of two greenhouse gases (carbon dioxide and methane) in the atmosphere over a large city are studied on the basis of the data obtained during the 2003–2005 observations at a Moscow station for environmental monitoring. This station is based on the TROICA mobile observatory and located at the meteorological station of the Faculty of Geography, Moscow State University, on Vorob’evy gory. The methods of isolating the background concentrations of greenhouse gases under urban conditions are proposed, and the excess concentrations of CO₂ and CH₄ over their background values are estimated for different seasons and times of day. The CO₂ and CH₄ concentrations are shown to have more pronounced diurnal cycles in summer than in winter. The main causes of temporal variations in the surface concentrations of CO₂ and CH₄ under urban conditions and the differences between the mean concentrations of these greenhouse gases in Moscow and other areas of Russia are analyzed. It is shown that variations in the surface concentrations of carbon dioxide and methane on different time scales are caused by different atmospheric processes (global circulation, mesoscale gravity waves, surface temperature inversions, etc.)     

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).     

<Superscript>222</Superscript>Rn concentrations in the atmospheric surface layer over continental Russia from observations in TROICA experiments

Both space and time variations in the ²²²Rn concentration in the atmospheric surface layer over continental Russia were analyzed on the basis of data obtained in the Transcontinental Observations into the Chemistry of the Atmosphere (TROICA) experiments. The measurements were taken from a mobile laboratory which was part of a passenger train moving along the Trans-Siberian Railway from Moscow to Vladivostok. The factors that affect the spatial distribution of both daily and seasonal variations in the concentrations of ²²²Rn in the surface air were determined: atmospheric vertical stability, geological features of the area under study, and atmospheric precipitation. The influence of temperature inversions on the accumulation of ²²²Rn in the atmospheric surface layer was analyzed. The fluxes of ²²²Rn from the soil into the atmosphere were estimated for different regions of Russia.     

Atmosphere-ocean general circulation model with the carbon cycle

Results from numerical experiments with an atmosphere-ocean general circulation model coupled to the carbon evolution cycle are analyzed. The model is used to carry out an experiment on the simulation of the climate and carbon cycle change in 1861–2100 under a specified scenario of the carbon dioxide emission from fossil fuel and land use. The spatial distribution of vegetation, soil, and oceanic carbon in the 20th century is generally close to available estimates from observational data. The model adequately reproduces the observed growth of atmospheric CO₂ in the 20th century and the uptake of excess carbon by land ecosystems and by the ocean in the 1980s and 1990s. By 2100, the atmospheric CO₂ concentration is calculated to reach 742 ppmv under emission and land-use scenario A1B. The feedback between climate change and the carbon cycle in the model is positive, with a coefficient close to the mean of all the current models. The ocean and land uptakes of the CO₂ emission by 2100 in the model are 25 and 19%, which are also close to the mean over all models.     

Structure of time variations in carbon dioxide in the atmospheric thickness over central Eurasia (Issyk Kul Monitoring Station)

The results are presented of statistical analysis of the data obtained from the 1980–2006 systematic measurements of the volume concentration of carbon dioxide in the atmospheric thickness over central Eurasia. The trends of both monthly and yearly means of CO₂ concentration are determined. During these 26 years, the yearly mean concentration increased by ～42 ppm at a mean rate of (1.56 ± 0.18) ppm per year and reached ～382.7 ppm. General statistical characteristics are found. The distribution function of the monthly mean concentrations of CO₂ is characterized by the presence of a second maximum and a bias of the principal mode toward large values, and the mean (over the measurement time) monthly concentration and the median almost coincide. The distribution function of the yearly mean concentrations of CO₂ is close to a normal distribution, and the mean (over the measurement time) yearly concentration, the median, and the mode also coincide. The trends of short-and long-period variations in the carbon dioxide concentration and their possible relation to a number of geophysical phenomena are revealed. Spectral analysis of the measuring data on CO₂ revealed oscillations with periods of 4, 6, 12, 15, 21, 29, 40, 53, 84, and 183 months. A statistical model with the parameters of these oscillations describes the experimental monthly mean concentrations of carbon dioxide with an rms deviation of 2.3 ppm (±0.6% of the mean over the entire period 361.9 ppm) and the yearly mean concentrations with an rms deviation of 0.9 ppm (～±0.3%).     

A preliminary study of carbon system in the East China Sea

In the central part of the East China Sea, the activity of CO₂ in the surface water and total carbonate, pH and alkalinity in the water column were determined in winter and autumn of 1993. The activity of CO₂ in the continental shelf water was about 50 ppm lower than that of surface air. This decrease corresponds to the absorption of about 40 gC/m²/yr of atmospheric CO₂ in the coastal zone or 1 GtC/yr in the global continental shelf, if this rate is applicable to entire coastal seas. The normalized total carbonate contents were higher in the water near the coast and near the bottom. This increase toward the bottom may be due to the organic matter deposited on the bottom. This conclusion is supported by the distribution of pH. The normalized alkalinity distribution also showed higher values in the near-coast water, but in the surface water, indicating the supply of bicarbonate from river water. The residence time of the East China Sea water, including the Yellow Sea water, has been calculated to be about 0.8 yr from the excess alkalinity and the alkalinity input. Using this residence time and the excess carbonate, we can estimate that the amount of dissolved carbonate transported from the coastal zone to the oceanic basin is about 70 gC/m²/yr or 2 GtC/yr/area-of-global-continental-shelf. This also means that the rivers transport carbon to the oceans at a rate of 30 gC/m²/yr of the coastal sea or 0.8 GtC/yr/ area-of-global shelf, the carbon consisting of dissolved inorganic carbonate and terrestrial organic carbon decomposed on the continental shelf.     

Organic tracers from biomass burning in atmospheric particulate matter over the ocean

Particulate matter from the atmosphere over the Atlantic Ocean along the South American and African Continents has been analyzed for organic tracers from natural and biomass burning emissions. The major biomarker compounds characterized are natural products from continental vegetation consisting primarily of epicuticular wax components. For example, n-alkanes ranged from C₂₅ to C₃₅, with an odd carbon number predominance and carbon maxima (C_max) at 29 or 31. Concentrations of n-alkanes varied from 0.3 to 680 ng/m³. Nevertheless, n-alkanols are the dominant terrestrial tracers in almost all samples (concentrations from 0.1 to 780 ng/m³) and ranged from C₂₂ to C₃₄ with an even carbon number predominance. Despite the major presence of the natural tracers, organic components from biomass burning emissions are also present in the particulate matter. The major tracers from this source are thermal degradation products from the biopolymer cellulose, namely the dianhydromonosaccharide derivatives levoglucosan, galactosan, and mannosan. In general, the concentrations of levoglucosan, the major derivative from this source in all samples, varied from 0.0008 to 0.15 ng/m³ in atmospheric samples collected over the ocean and from 0.04 to 4860 ng/m³ in terrestrial particulate matter, used as reference in this study. Dehydroabietic acid, another marker compound emitted from burning of Gymnosperm fuel, is also detectable in most oceanic samples at concentrations ranging from 0.0001 to 0.4 ng/m³, whereas in terrestrial aerosol particulate matter, this component is present at much higher concentrations (0.23–440 ng/m³). The presence of these tracers in atmospheric particulate matter over the ocean confirms the long-range transport of smoke from biomass burning off the continents.     

The inorganic carbon system in the coastal upwelling region west of Vancouver Island,Canada

We present inorganic carbon data from the coastal upwelling region west of Vancouver Island, Canada $\text{(∼48.5°}\text{N}\text{,}\text{126°}\text{W}\text{)}$ directly after an upwelling event and during summer downwelling in July 1998. The inner-shelf buoyancy current, the outer-shelf and the slope regions are contrasted for both wind regimes (up- and downwelling). Results show strong biological drawdown of the partial pressure of carbon dioxide (pCO₂) in response to upwelling over the outer-shelf. In contrast, measured pCO₂ is exceptionally high $\text{(p}\text{CO}{}_2\text{>1000}\text{ppm}\text{)}$ in the inner-shelf current, where biological uptake of carbon is consistently large. The biological C:N uptake ratio appears to increase when nitrogen becomes limiting (during downwelling), while the POC:PON ratio is relatively constant (slightly lower than the Redfield ratio) suggesting that excess carbon uptake does not go into the POC pool. As expected, large cells dominate where measured primary productivity is greatest. Sub-surface inorganic carbon (and pCO₂) is high over the shelf. We suggest that carbon concentrations may be higher in coastal waters because of remineralization associated with high productivity that is confined to a smaller volume of water by bathymetry. At the coast these sub-surface concentrations are more efficiently mixed into the surface (especially during winter) relative to deeper offshore regions. Thus, despite high primary production, coastal waters may not aid in sequestration of atmospheric carbon.     

Time-series observation of dissolved inorganic carbon and nutrients in the northwestern North Pacific

Time-series measurements of dissolved inorganic carbon (DIC) and nutrient concentrations were conducted in the northwestern North Pacific from October 2002 to August 2004. Assuming that data obtained in different years represented time-series seasonal data for a single year, vertical distributions of DIC and nutrients showed large seasonal variabilities in the surface layer (∼100 m). Seasonal variabilities in normalized DIC (nDIC) and nitrate concentrations at the sea surface were estimated to be 81–113 μmol kg⁻¹ and 12.7–15.7 μmol kg⁻¹, respectively, in the Western Subarctic Gyre. The variability in nutrients between May and July was generally at least double that in other seasons. In the Western Subarctic Gyre, estimations based on statistical analyses revealed that seasonal new production was 39–61 gC m⁻² and tended to be higher in the southwestern regions or coastal regions. The seasonal new productions in the northwestern North Pacific were two or more times higher than in the North Pacific subtropical gyre and the northeastern North Pacific. It is likely that this difference is due to spatial variations in the concentrations of trace metals and the species of phytoplankton present. In addition, from estimations of surface pCO₂ it was verified that the Western Subarctic Gyre is a source of atmospheric CO₂ between February and May and a sink for CO₂ between July and October.     

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.

     

Precise determination of the cerium isotopic compositions of surface seawater in the Northwest Pacific Ocean and Tokyo Bay

We succeeded in determining the Ce isotopic composition (¹³⁸Ce/¹⁴²Ce) in seawater with an error of 2σ_m = 0.3–0.7 of ε unit. In this study, 1000–3000 L of seawater samples were passed through MnO₂ fibers to concentrate Ce and Nd for precise measurement of their isotope ratios. Four surface seawater samples of the northwestern Pacific and a coastal sample in Tokyo Bay were analyzed. Most Ce isotope ratios in the surface water showed positive ε_Ce values (+ 0.8 to + 1.4) in the northwestern Pacific Ocean. These values indicate that Ce in the surface water originates from the continental crust preferentially over mantle-derived materials. We examined binary mixing model between the continental crust and mid-ocean ridge basalt. However the model could not explain both isotopic compositions and concentrations, which implies that the atmospheric input was a possible pathway for Ce into the ocean. A negative ε_Ce value was observed in Tokyo Bay, suggesting mantle-derived sources.     

Dynamics of surface-air pollution during the passage of a cold front

The dynamics of meteorological parameters, of sodar data on the temperature stratification of the atmospheric boundary layer, and of surface contents of pollutants (nitrogen oxides, carbon monoxide, and ozone) during the passage over Moscow of a structurally complex prominent cold front are discussed. It is shown that the cold front passage is accompanied by stepwise increases in the NO, NO₂, and CO surface contents. A probable cause of this phenomenon is a quick entrainment of smoke plumes from high-altitude sources of pollution into the surface turbulent air near the frontal boundary. Intense advection of cold air at the rear of the cyclone can lead to the development of an unstable stratification in the atmospheric boundary layer even in the nighttime. Under these conditions, the minute-scale variability of contents of trace gases increases abruptly as compared to that occurring in the frontal zone of the cyclone prior to the passage of the front. This effect is statistically significant. The dynamics of surface ozone reflects an increase in its background concentrations in arctic air masses.     

The effect of meteorology on air pollution in Moscow during the summer episodes of 2010

Relations between short-term variations in the concentrations of aerosol (PM₁₀) and carbon monoxide (CO) and meteorological characteristics are considered for the episodes of severe atmospheric pollution in the region of Moscow in the summer of 2010. The assumption is made and substantiated that the observed (in late June) severe aerosol pollution of the atmosphere over Moscow was caused by air masses arrived from soil-drought regions of southern Russia. In August, during the episodes of advection of forest-fire products, the maximum surface concentrations of pollutants were observed in Moscow mainly at 11:00–12:00 under a convective burst into the atmospheric boundary layer and at night in the presence of local wind-velocity maxima or low-level jet streams within the inversion layer. On the basis of results from an analysis of these air-pollution episodes before and after fires, it is concluded that the shearing instability of wind velocity favors the surface-air purification under ordinary conditions and an increase in the surface concentrations of pollutants during their advection (long-range transport, natural-fire plumes, etc.). It is shown that the pollution of the air basin over the megapolis with biomass-combustion products in 2010 led to an increase in the thermal stability of the atmospheric surface layer and in the duration of radiation inversions, as well as to an attenuation of the processes of purification in the urban heat island.     

Combined effects of photosynthesis and calcification on the partial pressure of carbon dioxide in seawater

The effects of marine photosynthesis and calcification on the partial pressure of carbon dioxide in seawater (P _{CO 2}) are examined in the light of recent studies and using original model calculations. The ratio of organic carbon to inorganic carbon production (R _OI) determines whether an ecosystem is a net sink or source for atmospheric CO₂. TheP _{CO 2} maintains its initial value when the photosynthetic rate is approximately 0.6 times the calcification rate under normal sea surface condition. In case of higherR _OI, theP _{CO 2} decreases and seawater can absorb atmospheric CO₂. The ratio of organic carbon to inorganic carbon production can be used as a potential indicator of sink-source behavior in aquatic photo-calcifying systems.     

Fluxes,source and transport of organic matter in the western Sea of Okhotsk: Stable carbon isotopic ratios of n-alkanes and total organic carbon

Settling particles and surface sediments collected from the western region of the Sea of Okhotsk were analyzed for total organic carbon (TOC), long-chain n-alkanes and their stable carbon isotope ratio (δ¹³C) to investigate sources and transport of total and terrestrial organic matter in the western region of the sea. The δ¹³C measurements of TOC in time-series sediment traps indicate lateral transport of resuspended organic matter from the northwestern continental shelf to the area off Sakhalin via the dense shelf water (DSW) flow at intermediate depth. The n-alkanes in the surface sediments showed strong odd carbon number predominance with relatively lighter δ¹³C values (from −33‰ to −30‰). They fall within the typical values of C3-angiosperms, which is the main vegetation in east Russia, including the Amur River basin. On the other hand, the molecular distributions and δ¹³C values of n-alkanes in the settling particles clearly showed two different sources: terrestrial plant and petroleum in the Sea of Okhotsk. We reconstructed seasonal change in the fluxes of terrestrial n-alkanes in settling particles using the mixing model proposed by Lichtfouse and Eglinton [1995. ¹³C and ¹⁴C evidence of a soil by fossil fuel and reconstruction of the composition of the pollutant. Organic Geochemistry 23, 969–973]. Results of the terrestrial n-alkane fluxes indicate that there are two transport pathways of terrestrial plant n-alkanes to sediments off Sakhalin, the Sea of Okhotsk. One is lateral transport of resuspended particles with lithogenic material from the northwestern continental shelf by the DSW flow. Another is the vertical transport of terrestrial plant n-alkanes, which is independent of transport of lithogenic material. The latter may include dry/wet deposition of aerosol particles derived from terrestrial higher plants possibly associated with forest fires in Siberia.     

中国南海、东海及黄海海域海气二氧化碳通量与生产力的物理生物地球化学模拟研究

Marginal seas play important roles in regulating the global carbon budget, but there are great uncertainties in estimating carbon sources and sinks in the continental margins. A Pacific basin-wide physical-biogeochemical model is used to estimate primary productivity and air-sea CO_2 flux in the South China Sea(SCS), the East China Sea(ECS), and the Yellow Sea(YS). The model is forced with daily air-sea fluxes which are derived from the NCEP2 reanalysis from 1982 to 2005. During the period of time, the modeled monthly-mean air-sea CO_2 fluxes in these three marginal seas altered from an atmospheric carbon sink in winter to a source in summer. On annualmean basis, the SCS acts as a source of carbon to the atmosphere(16 Tg/a, calculated by carbon, released to the atmosphere), and the ECS and the YS are sinks for atmospheric carbon(–6.73 Tg/a and –5.23 Tg/a, respectively,absorbed by the ocean). The model results suggest that the sea surface temperature(SST) controls the spatial and temporal variations of the oceanic pCO_2 in the SCS and ECS, and biological removal of carbon plays a compensating role in modulating the variability of the oceanic pCO_2 and determining its strength in each sea,especially in the ECS and the SCS. However, the biological activity is the dominating factor for controlling the oceanic pCO_2 in the YS. The modeled depth-integrated primary production(IPP) over the euphotic zone shows seasonal variation features with annual-mean values of 293, 297, and 315 mg/(m~2·d) in the SCS, the ECS, and the YS, respectively. The model-integrated annual-mean new production(uptake of nitrate) values, as in carbon units, are 103, 109, and 139 mg/(m~2·d), which yield the f-ratios of 0.35, 0.37, and 0.45 for the SCS, the ECS, and the YS, respectively. Compared to the productivity in the ECS and the YS, the seasonal variation of biological productivity in the SCS is rather weak. The atmospheric pCO_2 increases from 1982 to 2005, which is consistent with the anthropogenic CO_2 input to the atmosphere. The oceanic pCO_2 increases in responses to the atmospheric pCO_2 that drives air-sea CO_2 flux in the model. The modeled increase rate of oceanic pCO_2 is0.91 μatm/a in the YS, 1.04 μatm/a in the ECS, and 1.66 μatm/a in the SCS, respectively.     

Variations in the total column amounts of carbon monoxide and methane in the Antarctic atmosphere

The results of measuring the total contents of carbon monoxide and methane via the method of solar-absorption spectroscopy are presented. The measurements were performed at the Molodezhnaya Station in 1977–1978, at the Mirny Observatory from 1982 to 1992, and at the Novolazarevskaya Station from 2003 to 2006. The character of seasonal variations in the contents of these gases in the Antarctic atmosphere is described and compared to the intra-annual variation of their surface concentrations measured at the Syowa Station (Japan). Synchronous intra-annual variations in the contents of carbon monoxide in the atmospheric column and in its surface concentrations are observed, while the spring maximum content of methane is observed three months after the maximum of its surface concentration. Synchronous seasonal variations in the total content of methane and ozone are observed, which makes it possible to suggest that the Antarctic circumpolar vortex has a significant influence on the characteristics of the vertical distribution of methane during Antarctic spring. Quantitative estimates of the parameters of multiyear variations in the contents of CO and CH₄ are given. The content of methane was increasing (although with different rates) during the entire observation period 1977–2006. The content of CO was observed to increase until 1992 and to decrease during 2003–2006.     

Air pollution over European Russia and Ukraine under the hot summer conditions of 2010

Variations in the concentrations of both primary (PM₁₀, CO, and NO_x) and secondary (ozone) pollutants in the atmosphere over the Moscow and Kirov regions, Kiev, and Crimea under the conditions of the anomalously hot summer of 2011 are given and analyzed. The concentrations of ozone, PM₁₀, CO, and NO_x in the atmosphere over the Moscow region exceeded their maximum permissible levels almost continuously from late July to late August 2010. The highest level of atmospheric pollution was observed on August 4–9, when the Moscow region was within a severe plume of forest and peatbog fires. The maximum single concentrations of ozone, which exceeded its maximum permissible level two-three times, were accompanied by high concentrations of combustion products: the concentrations of PM₁₀ and CO were also three-seven times higher than their maximum permissible concentrations. The maximum levels of air pollution were observed under the meteorological conditions that were unfavorable for pollution scattering, first of all, at a small vertical temperature gradient in the lower atmospheric boundary layer. The number of additional cases of mortality due to the exceeded maximum permissible concentrations of PM₁₀ and ozone in the atmosphere over Moscow was estimated. Under the weather conditions that were close to those for the Moscow region, the air quality remained mainly satisfactory in the Kirov region, Kiev, and Crimea, which were almost not affected by fires.     

Biogeochemical study of a coccolithophore bloom in the northern Bay of Biscay (NE Atlantic Ocean) in June 2004

The present paper synthesizes data obtained during a multidisciplinary cruise carried out in June 2004 at the continental margin of the northern Bay of Biscay. The data-set allows to describe the different stages of a coccolithophore bloom dominated by Emiliania huxleyi. The cruise was carried out after the main spring phytoplankton bloom that started in mid-April and peaked in mid-May. Consequently, low phosphate (PO₄ < 0.2 μM) and silicate (DSi < 2.0 μM) concentrations, low partial pressure of carbon dioxide (pCO₂) and high calcite saturation degree in surface waters combined with thermal stratification, probably favoured the blooming of coccolithophores. During the period of the year our cruise was carried out, internal tides induce enhanced vertical mixing at the continental shelf break leading to the injection of inorganic nutrients to surface waters that probably trigger the bloom. The bloom developed as the water-column stratified and as the water mass was advected over the continental shelf, following the general residual circulation in the area. The most developed phase of the bloom was sampled in a remote sensed high reflectance (HR) patch over the continental shelf that was characterized by low chlorophyll-a (Chl-a) concentration in surface waters (<1.0 μg L^?1), high particulate inorganic carbon (PIC) concentration (～8 μmol L^?1) and coccolithophore abundance up to 57 × 10⁶ cells L^?1. Transparent exopolymer particles (TEP) concentrations ranged between 15 and 75 μg C L^?1 and carbon content of TEP represented up to 26% of the particulate organic carbon (POC; maximum concentration of 15.5 μmol L^?1 in the upper 40 m). Integrated primary production (PP) ranged between 210 and 680 mg C m^?2 d^?1 and integrated calcification (CAL) ranged between 14 and 140 mg C m^?2 d^?1, within the range of PP and CAL values previously reported during coccolithophore blooms in open and shelf waters of the North Atlantic Ocean. Bacterial protein production (BPP) measurements in surface waters (0.3–0.7 μg C L^?1 h^?1) were much higher than those reported during early phases of coccolithophore blooms in natural conditions, but similar to those during peak and declining coocolithophorid blooms reported in mesocosms. Total alkalinity anomalies with respect to conservative mixing (ΔTA) down to ?49 μmol kg^?1 are consistent with the occurrence of biogenic precipitation of calcite, while pCO₂ remained 15–107 μatm lower than atmospheric equilibrium (372 μatm). The correlation between ΔTA and pCO₂ suggested that pCO₂ increased in part due to calcification, but this increase was insufficient to overcome the background under-saturation of CO₂. This is related to the biogeochemical history of the water masses due to net carbon fixation by the successive phytoplankton blooms in the area prior to the cruise, hence, the investigated area remained a sink for atmospheric CO₂ despite calcification.     

A 1998–1992 comparison of inorganic carbon and its transport across 24.5°N in the Atlantic

In January and February 1998, when an unprecedented fourth repetition of the zonal hydrographic transect at 24.5°N in the Atlantic was undertaken, carbon measurements were obtained for the second time in less than a decade. The field of total carbon along this section is compared to that provided by 1992 cruise which followed a similar path (albeit in a different season). Consistent with the increase in atmospheric carbon levels, an increase in anthropogenic carbon concentrations of 8±3 μmolkg⁻¹ was found in the surface layers. Using an inverse analysis to determine estimates of absolute velocity, the flux of inorganic carbon across 24.5° is estimated to be −0.74±0.91 and −1.31±0.99 PgCyr⁻¹ southward in 1998 and 1992, respectively. Estimates of total inorganic carbon flux depend strongly upon the estimated mass transport, particularly of the Deep Western Boundary Current. The 1998 estimate reduces the large regional divergence in the meridional carbon transport suggested by previous studies and brings into question the idea that the tropical Atlantic constantly outgasses carbon, while the subpolar Atlantic sequesters it. Uncertainty in the carbon transports themselves, dominated by the uncertainty in the total mass transport estimates, are a hindrance to determining the “true” picture.The flux of anthropogenic carbon (C_ANTH) across the two transects is estimated as northward at 0.20±0.08 and 0.17±0.06 PgCyr⁻¹ for the 1998 and 1992 sections, respectively. The net transport of C_ANTH across 24.5°N is strongly affected by the difference in concentrations between the northward flowing shallow Florida Current and the mass balancing, interior return flow. The net northward transport of C_ANTH is opposite the net flow of total carbon and suggests, as has been found by others, that the pre-industrial southward transport of carbon within the Atlantic was stronger than it is today. Combining these flux results with estimates of atmospheric and riverine inorganic carbon input, it is determined that today's oceanic carbon system differs from the pre-industrial system in that today there is an uptake of anthropogenic carbon to the south that is advected northward and stored within the North Atlantic basin.