Increase in anthropogenic CO2 in the Atlantic Ocean in the last two decades

Data from the first systematic survey of inorganic carbon parameters on a global scale, the GEOSECS program, are compared with those collected during WOCE/JGOFS to study the changes in carbon and other geochemical properties, and anthropogenic CO₂ increase in the Atlantic Ocean from the 1970s to the early 1990s. This first data-based estimate of CO₂ increase over this period was accomplished by adjusting the GEOSECS data set to be consistent with recent high-quality carbon data. Multiple Linear Regression (MLR) and extended Multiple Linear Regression (eMLR) analyses to these carbon data are applied by regressing DIC with potential temperature, salinity, AOU, silica, and PO₄ in three latitudinal regions for the western and eastern basins in the Atlantic Ocean. The results from MLR (and eMLR provided in parentheses) indicate that the mean anthropogenic CO₂ uptake rate in the western basin is 0.70 (0.53) mol m^?2 yr^?1 for the region north of 15°N; 0.53 (0.36) mol m^?2 yr^?1 for the equatorial region between 15°N and 15°S; and 0.83 (0.35) mol m^?2 yr^?1 in the South Atlantic south of 15°S. For the eastern basin an estimate of 0.57 (0.45) mol m^?2 yr^?1 is obtained for the equatorial region, and 0.28 (0.34) mol m^?2 yr^?1 for the South Atlantic south of 15°S. The results of using eMLR are systematically lower than those from MLR method in the western basin. The anthropogenic CO₂ increase is also estimated in the upper thermocline from salinity normalized DIC after correction for AOU along the isopycnal surfaces. For these depths the results are consistent with the CO₂ uptake rates derived from both MLR and eMLR methods.     

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.     

fCO2 variability at the CARIACO tropical coastal upwelling time series station

Monthly seawater pH and alkalinity measurements were collected between January 1996 and December 2000 at 10°30′N, 64°40′W as part of the CARIACO (CArbon Retention In A Colored Ocean) oceanographic time series. One key objective of CARIACO is to study temporal variability in Total CO₂ (TCO₂) concentrations and CO₂ fugacity (fCO₂) at this tropical coastal wind-driven upwelling site. Between 1996 and 2000, the difference between atmospheric and surface ocean CO₂ concentrations ranged from about − 64.3 to + 62.3 μatm. Physical and biochemical factors, specifically upwelling, temperature, primary production, and TCO₂ concentrations interacted to control temporal variations in fCO₂. Air–sea CO₂ fluxes were typically depressed (0 to + 10 mmol C m^{− 2} day^{− 1}) in the first few months of the year during upwelling. Fluxes were higher during June–November (+ 10 to 20 mmol C m^{− 2} day^{− 1}). Fluxes were generally independent of the slight changes in salinity normally seen at the station, but low positive flux values were seen in the second half of 1999 during a period of anomalously heavy rains and land-derived runoff. During the 5 years of monthly data examined, only two episodes of negative air–sea CO₂ flux were observed. These occurred during short but intense upwelling events in March 1997 (−10 mmol C m^{− 2} day^{− 1}) and March 1998 (− 50 mmol C m^{− 2} day^{− 1}). Therefore, the Cariaco Basin generally acted as a source of CO₂ to the atmosphere in spite of primary productivity in excess of between 300 and 600 g C m^{− 2} year^{− 1}.     

Nitrogen cycling in deep-sea sediments of the Porcupine Abyssal Plain, NE Atlantic

Rates of transformation, recycling and burial of nitrogen and their temporal and spatial variability were investigated in deep-sea sediments of the Porcupine Abyssal Plain (PAP), NE Atlantic during eight cruises from 1996 to 2000. Benthic fluxes of ammonium (NH₄) and nitrate (NO₃) were measured in situ using a benthic lander. Fluxes of dissolved organic nitrogen (DON) and denitrification rates were calculated from pore water profiles of DON and NO₃, respectively. Burial of nitrogen was calculated from down core profiles of nitrogen in the solid phase together with ¹⁴C-based sediment accumulation rates and dry bulk density. Average NH₄ and NO₃-effluxes were 7.4 ± 19 μmol m⁻² d⁻¹ (n = 7) and 52 ± 30 μmol m⁻² d⁻¹ (n = 14), respectively, during the period 1996–2000. During the same period, the DON-flux was 11 ± 5.6 μmol m⁻² d⁻¹ (n = 5) and the denitrification rate was 5.1 ± 3.0 μmol m⁻² d⁻¹ (n = 22). Temporal and spatial variations were only found in the benthic NO₃ fluxes. The average burial rate was 4.6 ± 0.9 μmol m⁻² d⁻¹. On average over the sampling period, the recycling efficiency of the PON input to the sediment was 94% and the burial efficiency hence 6%. The DON flux constituted 14% of the nitrogen recycled, and it was of similar magnitude as the sum of burial and denitrification. By assuming the PAP is representative of all deep-sea areas, rates of denitrification, burial and DON efflux were extrapolated to the total area of the deep-sea floor (>2000 m) and integrated values of denitrification and burial of 8 ± 5 and 7 ± 1 Tg N year⁻¹, respectively, were obtained. This value of total deep-sea sediment denitrification corresponds to 3–12% of the global ocean benthic denitrification. Burial in deep-sea sediments makes up at least 25% of the global ocean nitrogen burial. The integrated DON flux from the deep-sea floor is comparable in magnitude to a reported global riverine input of DON suggesting that deep-sea sediments constitute an important source of DON to the world ocean.     

A seasonal carbon budget for the sub-Antarctic Ocean, South of Australia

Changes from winter (July) to summer (February) in mixed layer carbon tracers and nutrients measured in the sub-Antarctic zone (SAZ), south of Australia, were used to derive a seasonal carbon budget. The region showed a strong winter to summer decrease in dissolved inorganic carbon (DIC;  45 µmol/kg) and fugacity of carbon dioxide (fCO₂;  25 µatm), and an increase in stable carbon isotopic composition of DIC (δ¹³C_DIC;  0.5‰), based on data collected between November 1997 and July 1999.The observed mixed layer changes are due to a combination of ocean mixing, air–sea exchange of CO₂, and biological carbon production and export. After correction for mixing, we find that DIC decreases by up to 42 ± 3 µmol/kg from winter (July) to summer (February), with δ¹³C_DIC enriched by up to 0.45 ± 0.05‰ for the same period. The enrichment of δ¹³C_DIC between winter and summer is due to the preferential uptake of ¹²CO₂ by marine phytoplankton during photosynthesis. Biological processes dominate the seasonal carbon budget (≈ 80%), while air–sea exchange of CO₂ (≈ 10%) and mixing (≈ 10%) have smaller effects. We found the seasonal amplitude of fCO₂ to be about half that of a study undertaken during 1991–1995 [Metzl, N., Tilbrook, B. and Poisson, A., 1999. The annual fCO₂ cycle and the air–sea CO₂ flux in the sub-Antarctic Ocean. Tellus Series B—Chemical and Physical Meteorology, 51(4): 849–861.] for the same region, indicating that SAZ may undergo significant inter-annual variations in surface fCO₂. The seasonal DIC depletion implies a minimum biological carbon export of 3400 mmol C/ m² from July to February. A comparison with nutrient changes indicates that organic carbon export occurs close to Redfield values (ΔP:ΔN:ΔC = 1:16:119). Extrapolating our estimates to the circumpolar sub-Antarctic Ocean implies a minimum organic carbon export of 0.65 GtC from the July to February period, about 5–7% of estimates of global export flux. Our estimate for biological carbon export is an order of magnitude greater than anthropogenic CO₂ uptake in the same region and suggests that changes in biological export in the region may have large implications for future CO₂ uptake by the ocean.     

Recent increase of DIC in the western North Pacific

The temporal variation of the total dissolved inorganic carbon (DIC) content in the western North Pacific is investigated by comparing the DIC distribution obtained from the data sets of three different periods, the GEOSECS data observed in 1973, the CO₂ dynamics Cruise data observed in 1982, and recent Japanese data sets observed during the early 1990s. The overall feature of the signal of temporal DIC change during 1973 and early 1990s agreed with that of former studies, and did not significantly change with the calculation scheme (the grid-selection method vs. the multiple regression method). The observed increase in DIC among the different time scales showed a good inner consistency, which also indicates the stability of the method used in the DIC change calculation. The apparent rate of increase of the DIC inventory in the upper 1000 m water column, however, differed significantly by the data set used for the calculation: It was 5.6±2.4 g C/m²/year, based on the data comparison between 1982 and the early 1990s, while it became 7.6±2.4 g C/m²/year when based on the data between 1973 and the early 1990s. This result provides us an information about the data-dependency on the former estimation of temporal DIC change.     

Total amount of oceanic excess CO2 taken from the North Pacific subpolar region

Concentrations of total carbonate, alkalinity and dissolved oxygen were obtained near the 1973 GEOSECS stations in the North Pacific subpolar region north of 40°N along 175°E between 1993 and 1994. A difference of excess CO₂ content between the GEOSECS and our expeditions was estimated. The maximum difference in water column inventory of excess CO₂ has increased by about 280 gC m^–2 above 2000 m depth which apparently means an uptake of excess CO₂ taken from air to sea during the last two decades. An averaged value of the annual flux of excess CO₂ at 75–1000 m depth was 8.63±2.01 gC m^–2yr^–1 in the North Pacific subpolar region. By introducing the annual flux of excess CO₂ into a two-box model for the North Pacific subpolar region, a penetration factor of excess CO₂ from air to sea was obtained to be 1.08×10^–2 gC m^–3ppm^–1 in the North Pacific subpolar region. Based on this factor, the surface concentration of excess CO₂ in the North Pacific subpolar region was estimated to be 68 mole I^–1, suggesting that the North Pacific subpolar region absorbed atmospheric excess CO₂ more than the saturated concentration of excess CO₂. Total amount of excess CO₂ taken from the North Pacific subpolar region by 1993 was estimated to be 36.2×10¹⁵ gC, which was equal to about one tenth of that released by human activities after the preindustrial era.     

Inorganic carbon in the central California upwelling system during the 1997–1999 El Niño–La Niña event

Sea surface pCO₂ was monitored during 49 cruises from February 1997 to December 1999 along a section perpendicular to the central California Coast. Continuous measurements of the ocean–atmosphere difference of pCO₂ were made on a mooring in the same region from July 1997 to December 1999. The El Niño/La Niña cycle of 1997–1999 had a significant influence on local ocean–atmosphere CO₂ transfer. During the warm anomaly associated with El Niño, upwelling was suppressed and average sea surface pCO₂ was below atmospheric level. High rainfall and river runoff in the late winter and early spring of 1998 produced areas where pCO₂ was depressed by as much as 100 μatm. A flux ranging from 0.3 to 0.7 mol C m⁻² y⁻¹ from the atmosphere into the ocean was estimated for the El Niño period from wind and ΔpCO₂ data. Temperatures and upwelling returned to near normal in the summer of 1998, but a cold anomaly developed during autumn of that year. Temperature and pCO₂ data indicate that upwelling continued throughout much of the 1998–1999 winter and intensified significantly in the spring of 1999. During strong upwelling events, the estimate of ocean to atmosphere flux approached rates of 50 mol C m⁻² y⁻¹. The estimate for the average CO₂ flux from July 1998 to July 1999 was 1.5–2.2 mol C m⁻² y⁻¹ from the ocean to the atmosphere. While the flux estimate for the El Niño time period may be applicable to a larger area, the high ocean to atmosphere fluxes during La Niña might be the result of sampling near a zone of intense upwelling.     

Was a carbon balance measured in the equatorial Pacific during JGOFS?

The likelihood that the carbon fluxes measured as part of the US-JGOFS field program in the equatorial Pacific ocean (EgPac) during 1992 yielded a balanced carbon budget for the surface ocean was determined. The major carbon fluxes incorporated into a surface carbon budget were: new production, particulate organic carbon (POC) and dissolved organic carbon (DOC) export, CaC0₃ export, C0₂ gas evasion, dissolved inorganic carbon (DIC) supply, and the time rate of charge. The ratio of the measured concentration gradients of DOC and DIC provided a constraint on the ratio of POC/DOC export. Uncertainties of ±30–50% for individual carbon flux measurements reduce the likelihood that a carbon balance can be measured during a JGOFS process-type study. As a benchmark, carbon fluxes were prescribed to yield a hypothetical surface carbon budget that was, on average, balanced. Given the typical errors in the individual carbon fluxes, however, there was only about a 30% chance that this hypothetical budget could be measured to be balanced to ±50%. Using this benchmark, it was determined that there was a 95 % chance that the carbon flux measurements yielded a surface DIC budget balanced (to ±50%) during El Nino conditions in boreal spring 1992, when the total organic carbon export rate was - 5 mmol C m-2 day- 1 and the POC export was 3 mmol C m⁻² day⁻¹. In boreal fall 1992, during cold period conditions, there was a 70% chance that the surface carbon DIC budget was balanced when the total organic carbon export rate was 20 mmol C m⁻² day⁻¹ and export was -13 mmol C m-2 day-'. The DOC to DIC concentration gradient ratio of - -0.15, measured in depth profiles down to 100m and in surface waters, was used as an important constraint that most (> 70%) of the organic carbon exported from the euphotic zone was POC rather than DOC. If a balanced surface DIC budget was used to test the compatibility of individual carbon fluxes measured during EgPac, then a three- to four-fold increase in total and particulate organic carbon export between spring and fall is indicated. This increase was not reflected in the POC loss rates measured by drifting sediment trap collections or estimated by²³⁴Th deficiencies coupled with the C/Th measured on suspended particles.     

Seasonal and interannual variability of the air–sea CO2 flux in the Atlantic sector of the Barents Sea

The seasonal and interannual variability of the air–sea CO₂ flux (F) in the Atlantic sector of the Barents Sea have been investigated. Data for seawater fugacity of CO₂ (fCO₂^sw) acquired during five cruises in the region were used to identify and validate an empirical procedure to compute fCO₂^sw from phosphate (PO₄), seawater temperature (T), and salinity (S). This procedure was then applied to time series data of T, S, and PO₄ collected in the Barents Sea Opening during the period 1990–1999, and the resulting fCO₂^sw estimates were combined with data for the atmospheric mole fraction of CO₂, sea level pressure, and wind speed to evaluate F.The results show that the Atlantic sector of the Barents Sea is an annual sink of atmospheric CO₂. The monthly mean uptake increases nearly monotonically from 0.101 mol C m^− 2 in midwinter to 0.656 mol C m^− 2 in midfall before it gradually decreases to the winter value. Interannual variability in the monthly mean flux was evaluated for the winter, summer, and fall seasons and was found to be ± 0.071 mol C m^− 2 month^− 1. The variability is controlled mainly through combined variation of fCO₂^sw and wind speed. The annual mean uptake of atmospheric CO₂ in the region was estimated to 4.27 ± 0.68 mol C m^− 2.     

The carbonic system distribution and fluxes in the NE Atlantic during Spring 1991

The potential of the North Atlantic as a sink for atmospheric CO₂ was investigated by studying the carbonic system using data obtained during the spring of 1991. The air-sea flux of CO₂ was related to chlorophyll and other environmental variables, and the regeneration of carbon in the mid-ocean studied by examining vertical sections representative of the study area.Poor correlations were found between pCO₂ and chlorophyll throughout much of the study area, although a good correlation was found along 16°W. The highest air-sea fluxes of CO₂ were calculated for areas where chlorophyll was highest (45°13′N, 16°04′W), and where the greatest wind speeds occurred (47°51′N, 28°18′W). The mean CO₂ flux from the atmosphere to the ocean during the study period (May) was calculated as 0.65mmol m⁻²d⁻¹, which compares well with other studies. Regression equations were developed to predict total inorganic carbon from nutrients; errors were typically less than 1 μmol kg⁻¹. Regeneration of carbon in the mid-ocean occurred in two principal stages: 0–1000m and>2300m. Regeneration in the upper zone was dominated by soft tissue carbon (86%), with skeletal carbon (calcite) contributing only 14%. The fraction of regenerated carbon of skeletal origin increased to 51% in the>2300m zone.     

Interannual variations of the Antarctic Ocean CO2 uptake from 1986 to 1994

The interannual variations of CO₂ sources and sinks in the surface waters of the Antarctic Ocean (south of 50°S) were studied between 1986 and 1994. An existing, slightly modified one-dimensional model describing the mixed-layer carbon cycle was used for this study and forced by available satellite-derived and climatological data. Between 1986 and 1994, the mean Antarctic Ocean CO₂ uptake was 0.53 Pg C year⁻¹ with an interannual variability of 0.15 Pg C year⁻¹.Interannual variation of the Antarctic Ocean CO₂ uptake is related to the Antarctic Circumpolar Wave (ACW), which affects sea surface temperature (SST), wind-speed and sea-ice extent. The CO₂ uptake in the Antarctic Ocean has increased from 1986 to 1994 by 0.32 Pg C. It was found that over the 9 years, the surface ocean carbon dioxide fugacity (fCO₂) increase was half that of the atmospheric CO₂ increase inducing an increase of the air–sea fCO₂ gradient. This effect is responsible for 60% of the Antarctic Ocean CO₂ uptake increase between 1986 and 1994, as the ACW effect cancels out over the 9 years investigated.     

Seasonal evolution of hydrographic properties in the Antarctic circumpolar current at 170°W during 1997–1998

This paper discusses the seasonal evolution of the hydrographic and biogeochemical properties in the Antarctic Circumpolar Current (ACC) during the US Joint Global Ocean Flux (JGOFS) Antarctic Environment and Southern Ocean Process Study (AESOPS) in 1997–1998. The location of the study region south of New Zealand along 170°W was selected based on the zonal orientation and meridional separation of the physical and chemical fronts found in that region. Here we endeavor to describe the seasonal changes of the macronutrients, fluorescence chlorophyll_, particulate organic carbon (POC), and carbon dioxide (CO₂) in the upper 400 m of the ACC during the evolution of the seasonal phytoplankton bloom found in this area. While the ACC has extreme variability in the meridional sense (due to fronts, etc.), it appears to be actually quite uniform in the zonal sense. This is reflected by the fact that a good deal of the seasonal zonal changes in nutrients distributions at 170°W follow a pattern that reflects what would be expected if the changes are associated with seasonal biological productivity. Also at 170°W, the productivity of the upper waters does not appear to be limited by availability of phosphate or nitrate. While there is a significant decrease (or uptake) of inorganic nitrogen, phosphate and silicate associated with the seasonal phytoplankton bloom, none of the nutrients, except perhaps silicate (north of the silicate front) are actually depleted within the euphotic zone. At the end of the growing season, nutrient concentrations rapidly approached their pre-bloom levels. Inspection of the ratios of apparent nutrient drawdown near 64°S suggests N/P apparent drawdowns to have a ratio of 10 and N/Si apparent drawdowns to have a ratio of >4. These ratios suggest a bloom that was dominated by Fe limited diatoms. In addition, the surface water in the Polar Front (PF) and the Antarctic Zone (AZ) just to the south of the PF take up atmospheric CO₂ at a rate 2–3 times as fast as the mean global ocean rate during the summer season but nearly zero during the rest of year. This represents an important process for the transport of atmospheric CO₂ into the deep ocean interior. Finally, the net CO₂ utilization or the net community production during the 2.5 growing months between the initiation of phytoplankton blooms and mid-January increase southward from 1.5 mol C m⁻² at 55°S to 2.2 mol C m⁻² to 65°S across the Polar Frontal Zone (PFZ) into the AZ.     

Vertical profiles of nitrous oxide and dissolved oxygen in marine sediments

The whole core squeezing method was used to simultaneously obtain profiles of nitrous oxide (N₂O), nitrogenous nutrients, and dissolved oxygen in sediments of Koaziro Bay, Japan (coastal water), the East China Sea (marginal sea), and the central Pacific Ocean (open ocean). In the spring of Koaziro Bay, subsurface peaks of interstitial N₂O (0.5–3.5 cm depth) were observed, at which concentrations were higher than in the overlying water. This was also true for nitrate (NO₃⁻) and nitrite (NO₂⁻) profiles, suggesting that the transport of oxic overlying water to the depth through faunal burrows induced in situ N₂O production depending on nitrification. In the summer of Koaziro Bay, sediment concentrations of N₂O, NO₃⁻ and NO₂⁻ were lower than in the overlying water. In most East China Sea sediments, both N₂O and NO₃⁻ decreased sharply in the top 0.5–2 cm oxic layer (oxygen: 15–130 μM), which may have indicated N₂O and NO₃⁻ consumption by denitrification at anoxic microsites. N₂O peaks at subsurface depth (0.5–6.5 cm) implied in situ production of N₂O and/or its supply from the overlying water through faunal burrows. However, the occurrence of the latter process was not confirmed by the profiles of other constituents. In the central Pacific Ocean, the accumulation of N₂O and NO₃⁻ in the sediments likely resulted from nitrification. Nitrous oxide fluxes from the sediments, calculated using its gradient at the sediment–water interface and the molecular diffusion coefficient, were −45 to 6.9 nmolN m⁻² h⁻¹ in Koaziro Bay in the spring, −29 to −21 nmolN m⁻² h⁻¹ in the summer, −46 to 37 nmolN m⁻² h⁻¹ in the East China Sea, 0.17 to 0.23 nmolN m⁻² h⁻¹ in the equatorial Pacific, and <±0.2 nmolN m⁻² h⁻¹ in the subtropical North Pacific, respectively.     

Carbon and nitrogen primary productivity in three North Carolina estuaries

Uptake of inorganic carbon and ammonium by the plankton community of three North Carolina estuaries was measured using ¹⁴C and ¹⁵N isotope methods. At 0% light, C appeared to be lost via respiration, and at increasing light levels uptake of inorganic carbon increased linearly, saturated (mean I_k = 358±30 μEin m⁻² s⁻¹), and frequently showed inhibition at the highest light intensities. At 0% light NH₄⁺ uptake was significantly greater than zero and was frequently equivalent to uptake in the light (light independent); at increasing light levels NH₄⁺ uptake saturated (mean I_k = 172±44 μEin m⁻² s⁻¹) and frequently indicated strong inhibition. Light-saturated uptake rates of inorganic carbon and NH₄⁺ were a function of chlorophyll a (r² = 0·7−0·9); average assimilation numbers were 625 nmol CO₂ (μg chl. a)⁻¹ h⁻¹ and 12·9 nmol NH₄⁺ (μg chl. a)⁻¹ h⁻¹ and were positively correlated with temperature (r² = 0·3−0·7). The ratio of dark to light-saturated NH₄⁺ uptake tended to be near 1·0 for large algal populations at low NH₄⁺ concentrations, indicating near light independence of uptake; whereas the ratio was lower for the opposite conditions. These data are interpreted as indicative of nitrogen stress, and it is suggested that uptake of NH₄⁺ deep in the euphotic zone and at night are mechanisms for balancing the C:N of cellular pools. A 24-h study using summed short-term incubations confirmed this; the cumulative C:N of CO₂ and NH₄⁺ uptake during the daylight period was 10–20, whereas over the 24-h period the ratio was 6 due to dark NH₄⁺ uptake. Annual carbon and nitrogen primary productivity were respectively estimated as 24 and 4·0 mol m⁻² year⁻¹ for the South River estuary, 42 and 7·3 mol m⁻² year⁻¹ for the Neuse River estuary, and 9·6 and 1·6 mol m⁻² year⁻¹ for the Newport River estuary.     

Meridional carbon dioxide transport in the northern North Atlantic

Combination of estimated water transport and accurate measurements of total carbon dioxide (TCO₂) on a hydrographic section at 58 °N allows the assessment of meridional inorganic carbon transport in the northern North Atlantic Ocean. The transport has been decomposed into contributions from the large-scale baroclinic overturning, the Ekman transport, baroclinic and a barotropic eddy terms, and an estimated contribution of the East Greenland Current. These terms are −0.27 · 10⁶, +0.03 · 10⁶, +0.03 · 10⁶, +0.10 · 10⁶, and +0.05 · 10⁶ mol s⁻¹, respectively, which result in a total southward inorganic carbon transport of only −0.06 · 10⁶ mol s⁻¹. An order of magnitude estimate of the meridional transport of dissolved organic carbon (DOC) has shown that in general this term cannot be ignored in the total carbon flux, this being +0.04 · 10⁶ to +0.16 · 10⁶ mol s⁻¹ at 58 °N. A simple carbon budget has been formulated for the temperate North Atlantic, using our flux estimates as well as those of Brewer et al. (1989). This budget shows that the divergence of the meridional carbon flux, connected with the freshwater balance of the ocean may be of the same order of magnitude as the divergence of the total inorganic carbon flux. For an accurate estimate of the total carbon budget of the ocean it will be necessary to take both the DOC transport and the effects of the freshwater balance into account.     

Short-term variability of fCO2 in seawater and air–sea CO2 fluxes in a coastal upwelling system (Ría de Vigo, NW Spain)

Coastal upwelling systems are regions with highly variable physical processes and very high rates of primary production and very little is known about the effect of these factors on the short-term variations of CO₂ fugacity in seawater (fCO₂^w). This paper presents the effect of short-term variability (<1 week) of upwelling–downwelling events on CO₂ fugacity in seawater (fCO₂^w), oxygen, temperature and salinity fields in the Ría de Vigo (a coastal upwelling ecosystem). The magnitude of fCO₂^w values is physically and biologically modulated and ranges from 285 μatm in July to 615 μatm in October. There is a sharp gradient in fCO₂^w between the inner and the outer zone of the Ría during almost all the sampling dates, with a landward increase in fCO₂^w.CO₂ fluxes calculated from local wind speed and air–sea fCO₂ differences indicate that the inner zone is a sink for atmospheric CO₂ in December only (−0.30 mmol m⁻² day⁻¹). The middle zone absorbs CO₂ in December and July (−0.05 and −0.27 mmol·m⁻² day⁻¹, respectively). The oceanic zone only emits CO₂ in October (0.36 mmol·m⁻² day⁻¹) and absorbs at the highest rate in December (−1.53 mmol·m⁻² day⁻¹).     

Simultaneous determination of dissolved organic carbon and total dissolved nitrogen in seawater by high temperature catalytic oxidation: conditions for precise shipboard measurements

Appropriate conditions have been achieved for the accurate, rapid, and highly precise shipboard simultaneous determination of dissolved organic carbon and total dissolved nitrogen in seawater by high temperature catalytic oxidation. A nitrogen-specific Antek 705D chemiluminescence detector and a CO₂-specific LiCor Li6252 IRGA have been coupled in-series with a Shimadzu TOC-5000 organic carbon analyser. Precision of both simultaneous measurements is ≤1.5%, i.e. ±1 μmol C l⁻¹ and ±0.3 μmol N l⁻¹, respectively. Quality of analysis is not compromised by vibrations associated with ocean going research vessels.     

Eutrophication and the rate of net nitrification in a coastal marine ecosystem

Rates of net nitrification were calculated for four large (13 m³) estuarine-based microcosms that had been subjected to inorganic nutrient enrichment. Calculated rates were based on two years of weekly nitrate and nitrite measurements and ranged from a maximum of 0·55 μmol NO₂₊₃⁻ produced l⁻¹ day⁻¹ in the control tank (no enrichment) to over 13 μmol NO₂₊₃⁻ produced l⁻¹ day⁻¹ in the most enriched tank (receiving 18·6 μmol NH₄ l⁻¹ day⁻¹). Almost all NO₂₊₃⁻ production was pelagic, little was benthic. Net NO₃⁻ production or net NO₂⁻ production dominated the net nitrification rates during different seasons. Good correlations were found between various oxidation rates and substrate concentrations. The calculated net nitrite production rates were 10 to 1000 times higher than previously reported rates for open ocean systems, demonstrating the potential importance of nitrification to estuarine systems.