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1.
Phytoplankton NH4+ and NO3 uptake was examined along the longitudinal salinity gradient of the Delaware Estuary over several seasonal cycles using 15N-tracer techniques. Saturated nitrogen uptake rates increased directly with water temperature and reached a maximum of 380 nmol Nl−1h−1 during summer. This temperature dependence was related primarily to changes in the rate of maximum chlorophyll specific uptake, which varied exponentially between 2 and 70 nmol N [μg Chl h]−1 over a temperature range of 2–28°C. Despite these high uptake rates, balanced growth (C:N7:1) could be maintained over the diel light cycle only by highly efficient nitrogen uptake at low light intensities and dark uptake below the photic zone and at night (dark UPTAKE=25% maximum uptake).Ammonium fulfilled 82% of the annual phytoplankton nitrogen demand in the estuary despite dominance of NO3 in the ambient dissolved inorganic nitrogen pool. The predominance of NH4+ uptake occurred because of the general suppression of NO3 assimilation at NH4+ concentrations in excess of 2 μ . This suppression, however, was not as universal as has been reported for other systems, and it is suggested that the extremely high NO3 concentrations found in the estuary contribute to this pattern. Nitrate was a significant source of nitrogen only during periods of high phytoplankton production in summer, and when NH4+ concentrations were low towards the end of the spring bloom.  相似文献   

2.
The magnitude of the exchange flux at the water–sediment interface was determined on the basis of the ammonia concentration gradient at the near-bottom water–interstitial interface and Fick's first law. It was established that in Puck Bay, ammonia almost always passes from the sediment to water. Ammonia flux varied from 5 to 1434 μmol NH4-N m−2 day−1. In total,c. 138·2 tonneammonia year−1pass from sediments of Internal Puck Bay to near-bottom water, the equivalent value for External Puck Bay being 686·9 tonne year−1. In total, about 825 tonne ammonia year−1passes from the sediment to near-bottom water of Puck Bay. In interstitial waters, ammonia occurred in concentrations varying over a wide range (3–1084 μmol NH4-N dm−3).The basic factors affecting the magnitude of ammonia concentration in interstitial waters included: oxidation of organic matter, type of sediment, and inflow of fresh underground waters to the region examined.This paper involves preliminary studies only and constitutes a continuation of the studies on ionic macrocomponents and phosphorus in interstitial waters of Puck Bay undertaken previously.  相似文献   

3.
Concentrations of bacteria, chlorophyll a, and several dissolved organic compounds were determined during 11 tidal cycles throughout the year in a high and a low elevation marsh of a brackish tidal estuary. Mean bacterial concentrations were slightly higher in flooding (7·1 × 106 cells ml−1) than in ebbing waters (6·5 × 106 cells ml−1), and there were no differences between marshes. Mean chlorophyll a concentrations were 36·7 μg l−1 in the low marsh and 20·4 μg l−1 in the high marsh. Flux calculations, based on tidal records and measured concentrations, suggested a small net import of bacterial and algal biomass into both marshes. Over the course of individual tidal cycles, concentrations of all parameters were variable and not related to tidal stage. Heterotrophic activity measured by the uptake of 3H-thymidine, was found predominantly in the smallest particle size fractions (< 1·0 μm). Thymidine uptake was correlated with temperature (r = 0·48, P < 0·01), and bacterial productivity was estimated to be 7 to 42 μg Cl−1 day−1.  相似文献   

4.
We examined the effect of light on water column and benthic fluxes in the Pensacola Bay estuary, a river-dominated system in the northeastern Gulf of Mexico. Measurements were made during the summers of 2003 and 2004 on 16 dates distributed along depth and salinity gradients. Dissolved oxygen fluxes were measured on replicate sediment and water column samples exposed to a gradient of photosynthetically active radiation. Sediment inorganic nutrient (NH4+, NO3, PO43−) fluxes were measured. The response of dissolved oxygen fluxes to variation in light was fit to a photosynthesis–irradiance model and the parameter estimates were used to calculate daily integrated production in the water column and the benthos. The results suggest that shoal environments supported substantial benthic productivity, averaging 13.6 ± 4.7 mmol O2 m−2 d−1, whereas channel environments supported low benthic productivity, averaging 0.5 ± 0.3 mmol O2 m−2 d−1SE). Estimates of baywide microphytobenthic productivity ranged from 8.1 to 16.5 mmol O2 m−2 d−1, comprising about 16–32% of total system productivity. Benthic and water column dark respiration averaged 15.2 ± 3.2 and 33.6 ± 3.7 mmol O2 m−2 d−1, respectively Inorganic nutrient fluxes were generally low compared to relevant estuarine literature values, and responded minimally to light exposure. Across all stations, nutrient fluxes from sediments to the water column averaged 1.11 ± 0.98 mmol m−2 d−1 for NH4+, 0.58 ± 1.08 mmol m−2 d−1 for NO3, 0.01 ± 0.09 mmol m−2 d−1 for PO43−. The results of this study illustrate how light reaching the sediments is an important modulator of benthic nutrient and oxygen dynamics in shallow estuarine systems.  相似文献   

5.
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.  相似文献   

6.
Phytoplankton community composition, productivity and biomass characteristics of the mesohaline lower Neuse River estuary were assessed monthly from May 1988 to February 1990. An incubation method which considered water-column mixing and variable light exposure was used to determine phytoplankton primary productivity. The summer productivity peaks in this shallow estuary were stimulated by increases in irradiance and temperature. However, dissolved inorganic nitrogen loading was the major factor controlling ultimate yearly production. Dynamic, unpredictable rainfall events determined magnitudes of seasonal production pulses through nitrogen loading, and helped determine phytoplankton species composition. Dinoflagellates occasionally bloomed but were otherwise present in moderate numbers; rainfall events produced large pulses of cryptomonads, and dry seasons and subsequent higher salinity led to dominance by small centric diatoms. Daily production was strongly correlated (r = 0·82) with nitrate concentration and inversely correlated (r = −0·73) with salinity, while nitrate and salinity were inversely correlated (r = −0·71), emphasizing the importance of freshwater input as a nutrient-loading source to the lower estuary. During 1989 mean daily areal phytoplankton production was 938 mgC m−2, mean chlorophyll a was 11·8 mg m−3, and mean phytoplankton density was 1·56 × 103 cells ml−1. Estimated 1989 annual areal phytoplankton production for the lower estuary was 343 gC m−2.  相似文献   

7.
Seasonal and diurnal reduced sulfur gas emissions were measured along a salinity gradient in Louisiana Gulf Coast salt, brackish and freshwater marshes. Reduced sulfur gas emission was strongly associated with habitat and salinity gradient. The dominant emission component was dimethyl sulfide (average: 57·3 μg S m−2 h−1) in saltmarsh with considerable seasonal (max: 144·03 μg S m−2 h−1; min: 1·47 μg S m−2 h−1) and diurnal (max: 83·58 μg S m−2 h−1; min: 69·59 μg S m−2 h−1) changes in flux rates. Hydrogen sulfide was dominant (average: 21·2 μg S m−2 h−1, max: 79·2 μg S m−2 h−1; min: 5·29 μg S m−2 h−1) form in brackishmarsh and carbonyl sulfide (average: 1·09 μg S m−2 h−1; max: 3·42 μg S m−2 h−1; min: 0·32 μg S m−2 h−1) was dominant form in freshwater marsh. A greater amount of H2S was evolved from brackishmarsh (21·22 μg S m−2 h−1) as compared to the saltmarsh (2·46 μg S m−2 h−1) and freshwater marsh (0·30 μg S m−2 h−1). Emission of total reduced sulfur gases decreased with decrease in salinity and distance inland from the coast. Emission of total reduced sulfur gases over the study averaged 73·3 μg S m−2 h−1 for the saltmarsh, 32·1 μg S m−2 h−1 for brackishmarsh and 2·76 μg S m−2 h−1 for the freshwater marsh.  相似文献   

8.
Concentrations of Hg0 in surface waters and atmosphere of the Scheldt estuary and the North Sea are presented and their relationship with biological processes is discussed. Hg0 concentrations in the Scheldt estuary range from 0.1 to 0.38 pmol·l−1 in the winter and from 0.24 to 0.65 pmol·l−1 in the summer and show a positive relationship with phytoplankton pigments. In the North Sea Hg0 concentrations range from 0.06 to 0.8 pmol·l−1 and are higher in coastal stations. Transfer velocities across the air–sea interface were calculated using a classical shear turbulence model. Volatilization fluxes of Hg0 were calculated for the Scheldt estuary and the North Sea. For the Scheldt estuary the fluxes range from 226–284 pmol·m−2·d−1 in winter and 500–701 pmol·m−2·d−1 in summer and for the North Sea the fluxes range from 59–1110 pmol·m−2·d−1 for an average windspeed of 8.1 m·s−1. These fluxes are comparable to the wet and dry depositional fluxes to the North Sea. Hg0 formation rates necessary to balance the volatilization fluxes vary from 0.2 to 4% d−1.  相似文献   

9.
The effect of a sudden increase in salinity from 10 to 37 in porewater concentration and the benthic fluxes of ammonium, calcium and dissolved inorganic carbon were studied in sediments of a small coastal lagoon, the Albufera d'Es Grau (Minorca Island, Spain). The temporal effects of the changes in salinity were examined over 17 days using a single diffusion-reaction model and a mass-balance approach. After the salinity change, NH4+-flux to the water and Ca-flux toward sediments increased (NH4+-flux: 5000–3000 μmol m−2 d−1 in seawater and 600/250 μmol m−2 d−1 in brackish water; Ca-flux: −40/−76 meq m−2 d−1 at S=37 and −13/−10 meq m−2 d−1 at S=10); however, later NH4+-flux decreased in seawater, reaching values lower than in brackish water. In contrast, Ca-flux presented similar values in both conditions. The fluxes of dissolved inorganic carbon, which were constant at S=10 (55/45 mmol m−2 d−1), increased during the experiment at S=37 (from 30 mmol m−2 d−1 immediately after salinity increase to 60 mmol m−2 d−1 after 17 days).In brackish conditions, NH4+ and Ca2+ fluxes were consistent with a single diffusion-reaction model that assumes a zero-order reaction for NH4+ production and a first-order reaction for Ca2+ production. In seawater, this model explained the Ca-flux observed, but did not account for the high initial flux of NH4+.The mass balance for 17 days indicated a higher retention of NH4+ in porewater in the littoral station in seawater conditions (9.5 mmol m−2 at S=37 and 1.6 mmol m−2 at S=10) and a significant reduction in the water consumption at both sites (5 mmol m−2 at S=37; 35/23 mmol m−2 at S=10). In contrast, accumulation of dissolved inorganic carbon in porewater was lower in seawater incubations (−10/−1 meq m−2 at S=37; 50/90 meq m−2 at S=10) and was linked to a higher efflux of CO2 to the atmosphere, because of calcium carbonate precipitation in water (675/500 meq m−2). These results indicate that increased salinity in shallow coastal waters could play a major role in the global carbon cycle.  相似文献   

10.
We proposed an empirical equation of sea surface dimethylsulfide (DMS, nM) using sea surface temperature (SST, K), sea surface nitrate (SSN, μM) and latitude (L, °N) to reconstruct the sea surface flux of DMS over the North Pacific between 25°N and 55°N: ln DMS = 0.06346 · SST  0.1210 · SSN  14.11 · cos(L)  6.278 (R2 = 0.63, p < 0.0001). Applying our algorithm to climatological hydrographic data in the North Pacific, we reconstructed the climatological distributions of DMS and its flux between 25 °N and 55 °N. DMS generally increased eastward and northward, and DMS in the northeastern region became to 2–5 times as large as that in the southwestern region. DMS in the later half of the year was 2–4 times as large as that in the first half of the year. Moreover, applying our algorithm to hydrographic time series datasets in the western North Pacific from 1971 to 2000, we found that DMS in the last three decades has shown linear increasing trends of 0.03 ± 0.01 nM year− 1 in the subpolar region, and 0.01 ± 0.001 nM year− 1 in the subtropical region, indicating that the annual flux of DMS from sea to air has increased by 1.9–4.8 μmol m− 2 year− 1. The linear increase was consistent with the annual rate of increase of 1% of the climatological averaged flux in the western North Pacific in the last three decades.  相似文献   

11.
The first estimates of uptake kinetic parameters for NH4+, NO3, and urea in the Ross Sea, Antarctica were measured on three cruises during austral late winter–early spring 1996 (pre-bloom), late spring 1997 (bloom development), and summer 1997 (bloom decline). Nitrogen (N) uptake experiments were conducted with water collected at the 50% light penetration depth using trace-metal clean protocols and 15N tracer techniques. At all sites, ambient NO3 concentrations ranged from 5.8 to 30.5 μg-at N l−1 and silicic acid concentrations were greater than 62.0 μg-at Si l−1. The following trends were observed. First, based on maximum uptake rates (Vmax), apparent N utilization followed the order NO3>NH4+>urea during the pre-bloom and bloom development cruises. During the summer cruise, as the bloom was declining, the apparent order of utilization was NH4+>NO3>urea. Second, evidence for possible repression of NO3 uptake by elevated NH4+ concentrations was only observed at one site. Third, the kinetic parameters of NH4+ uptake rates corrected for isotope dilution were compared with the kinetic parameters determined from uncorrected rates. In this comparison, the measure of substrate affinity, α (α=Vmax/Ks) increased by an average of 4.6-fold when rates were corrected for isotope dilution, but values of Vmax remained unchanged. Fourth, using bacterial production data, the magnitude of bacterial N uptake was estimated. Assuming that all bacterial N demands were met with NH4+, the estimated bacterial portion of NH4+ uptake ranged from <1%, when the ratio of bacteria to autotrophic biomass was low, to 35%, when bacterial abundance and biomass were highest. Finally, dramatic changes in NH4+ uptake capacity were observed at one station (Stn. O), where kinetic parameters were measured during all three cruises. We hypothesize that a mutualistic relationship exists between phytoplankton and heterotrophic bacteria, and that the creation of microzones of high NH4+ concentrations contributed to the changes seen at this station.  相似文献   

12.
Macroalgae biomass and concentrations of nitrogen, phosphorus and chlorophyll a were determined weekly or biweekly in water and sediments, during the spring-summer of 1985 in a hypertrophic area of the lagoon of Venice. Remarkable biomass production (up to 286 g m−2 day−1, wet weight), was interrupted during three periods of anoxia, when macroalgal decomposition (rate: up to 1000 g m−2 day−1) released extraordinary amounts of nutrients. Depending on the macroalgae distribution in the water column, the nutrients released in water varied from 3·3 to 19·1 μg-at litre−1 for total inorganic nitrogen and from 1·8 to 2·7 μg-at litre−1 for reactive phosphorus. Most nutrients, however, accumulated in the surficial sediment (up to 0·640 and to 3·06 mg g−1 for P and N respectively) redoubling the amounts already stored under aerobic conditions, Phytoplankton, systematically below 5 mg m−3 as Chl. a, sharply increased up to 100 mg m−3 only after the release of nutrients in water by anaerobic macroalgal decomposition. During the algal growth periods, the N:P atomic ratio in water decreased to 0·7, suggesting that nitrogen is a growth-limiting factor. This ratio for surficial sediment was between 6·6 and 13·1, similar to that of macroalgae (8·6–12·0).  相似文献   

13.
14.
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.  相似文献   

15.
The multiple-parameter linear regression method (Monitoring global ocean carbon inventories. Ocean Observing System Development Panel, Texas A&M University, College Station, TX, 1995, 54pp; Global Biogeochem. Cycles 13 (1999) 179) is used to compare inorganic carbon data from the GEOSECS CO2 survey in the Pacific Ocean in 1973 to the WOCE/JGOFS global CO2 survey in the 1990s. A model of total dissolved inorganic carbon (DIC) as a function of five variables (AOU, θ, S, Si, and PO4) has been developed from the recent CO2 survey data (namely CGC91 and CGC96) in the Pacific Ocean. After correcting for a systematic DIC offset of −30.3±7 μmol kg−1 from the GEOSECS data, the residual DIC based on this model as computed from GEOSECS data has been used to estimate the anthropogenic CO2 penetration in the Pacific Ocean. In the Northeast Pacific, we obtained an increase of CO2 of 21.3±7.9 mol m−2 over the period from GEOSECS in 1973 to CGC91 in 1991. This gives a mean anthropogenic CO2 uptake rate of 1.3±0.5 mol m−2 yr−1 over this 17 year time period. In the South Pacific, north of 50°S between 180° and 120°W region, the integrated anthropogenic CO2 inventory is estimated to be 19.7±5.7 mol m−2 over the period from GEOSECS in 1974 to CGC96 in 1996. The equivalent mean CO2 uptake rate is estimated to be 0.9±0.3 mol m−2 yr−1 over the 22 years. These results are compared with the isopycnal method (Nature 396 (1998) 560) to estimate the anthropogenic CO2 signal in the Northeast Pacific (30°N, 152°W) at the crossover region between CGC91 and GEOSECS. The results of the isopycnal method are consistent with those derived from the MLR method. Both methods show an increase in anthropogenic CO2 inventory in the ocean over two decades that is consistent with the increase expected if the ocean uptake has kept pace with the atmospheric CO2 increase.  相似文献   

16.
The Loire estuary has been surveyed from 1982 to 1985 by 13 isochronous longitudinal profiles realized at low tide. Nutrient (SiO2, NO3, NH4+, PO3−4, particulate organic carbon or POC) patterns are very variable depending on the season, the estuarine section [river, upper-inner estuary, upstream of the fresh-water-saline-water interphase FSI, the lower-inner estuary characterized by the high turbidity zone (HTZ), the outer estuary] and the river discharge. Biological processes are dominant. In the eutrophied River Loire (summer pigment > 100 μg l−1), the high algal productivity (algal POC > 3 mg l−1) results in severe depletion of SiO2, PO43−, NO3. The enormous biomass (55 000 ton algal POC/year) is degraded in the HTZ where bacterial activity is intense. As a result, there is generally a regeneration of dissolved SiO2 and PO43−, a marked NH4+ maximum, while NO3 is conservative or depleted when the HTZ is nearly anoxic. Other processes can be considered including pollution from fertilizer plans (PO43−, NH4+) and from a hydrothermal power plant (NH4+). In the less turbid outer estuary, nutrients are generally conservative. Major variations of concentrations are observed in the lowest chlorinity section (Cl < 1 g kg) and also upstream the FSI, defined here as a 100% increase in Cl. Nutrient inputs to the ocean are not significantly modified for SiO2 and NO2, but are increased by 70% and 180% for PO43− and NH4+ and depleted by 60% for POC. Odd hydrological events, especially some floods, may perturbate or even mask the usual seasonal pattern observed in profiles.  相似文献   

17.
Laboratory exposures of the urchin Lytechinus pictus to sediment dosed with varying concentrations of hydrogen sulfide (H2S), but without elevated organic material, were conducted. Changes in mortality, behavior, growth and gonad production were measured during 49 days' flow through exposures. Hydrogen sulfide concentrations of 165·8 μ liter−1 in pore water caused significant changes in all parameters measured. Concentrations as low as 32·9 μ liter−1 caused significant decreases in wet weight and male gonad production. A concentration of 91·8 μ liter−1 caused the mortality rate to increase 100-fold over control exposures (0·63 μ liter−1). Sublethal effects on growth and gonad production could have been caused by either direct biochemical inhibition by H2S or secondarily through behavioral modifications. Hydrogen sulfide concentrations above 165·8 μ liter−1 are common near sewage outfalls and could contribute to changes in species composition and sediment toxicity that occur there.  相似文献   

18.
Concentrations of total recoverable inorganic tin (TRISn), monomethyltin (MeSn3+), dimethyltin (Me2Sn2+), trimethyltin (Me3Sn+) and (3-dimethylsulphonio)propionate (DMSP) were determined in leaves of Spartina alterniflora from three sites in the Great Bay estuary (NH) from 8 May to 15 September 1989. Total methyltin concentration increased from 8·9 ng g−1 (fresh weight) on 8 May to 472 ng g−1 on 23 May, decreased to 52 ng g−1 on 7 June and 16ng g−1 on 20 June, and remained low until the last sample on 18 September. Statistical calculations showed that methyltin concentrations varied significantly with sampling week, but not with site. DMSP concentrations showed very different behaviour. During the same sampling period DMSP concentrations varied only from 7·5 to 26 μmol g−1 (fresh weight). DMSP concentrations varied significantly for site, but not sampling week.  相似文献   

19.
Benthic fluxes of dissolved inorganic nitrogen (NO3 and NH4+), dissolved organic nitrogen (DON), N2 (denitrification), O2 and TCO2 were measured in the tidal reaches of the Bremer River, south east Queensland, Australia. Measurements were made at three sites during summer and winter. Fluxes of NO3 were generally directed into the sediments at rates of up to −225 μmol N m−2 h−1. NH4+ was mostly taken up by the sediments at rates of up to −52 μmol N m−2 h−1, its ultimate fate probably being denitrification. DON fluxes were not significant during winter. During summer, fluxes of DON were observed both into (−105 μmol m−2 h−1) and out of (39 μmol m−2 h−1) the sediments. Average N2 fluxes at all sampling sites were similar during summer (162 μmol N m−2 h−1) and winter (153 μmol N m−2 h−1). Denitrification was fed both by nitrification within the sediment and NO3 from the water column. Sediment respiration rates played an important role in the dynamics of nitrification and denitrification. NO3 fluxes were significantly related to TCO2 fluxes (p<0.01), with a release of NO3 from the sediment only occurring at respiration rates below 1000 μmol C m−2 h−1. Rates of denitrification increased with respiration up to TCO2 fluxes of 1000 μmol C m−2 h−1. At sediment respiration rates above 1000 μmol C m−2 h−1, denitrification rates increased less rapidly with respiration in winter and declined during summer. On a monthly basis denitrification removed about 9% of the total nitrogen and 16% of NO3 entering the Bremer River system from known point sources. This is a similar magnitude to that estimated in other tidal river systems and estuaries receiving similar nitrogen loads. During flood events the amount of NO3 denitrified dropped to about 6% of the total river NO3 load.  相似文献   

20.
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 (fCO2w). This paper presents the effect of short-term variability (<1 week) of upwelling–downwelling events on CO2 fugacity in seawater (fCO2w), oxygen, temperature and salinity fields in the Ría de Vigo (a coastal upwelling ecosystem). The magnitude of fCO2w values is physically and biologically modulated and ranges from 285 μatm in July to 615 μatm in October. There is a sharp gradient in fCO2w between the inner and the outer zone of the Ría during almost all the sampling dates, with a landward increase in fCO2w.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).  相似文献   

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