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1.
During CREAMS expeditions, fCO2 for surface waters was measured continuously along the cruise tracks. The fCO2 in surface waters in summer varied in the range 320–440 μatm, showing moderate supersaturation with respect to atmospheric CO2. In winter, however, fCO2 showed under-saturation of CO2 in most of the area, while varying in a much wider range from 180 to 520 μatm. Some very high fCO2 values observed in the northern East Sea (Japan Sea) appeared to be associated with the intensive convection system developed in the area. A gas-exchange model was developed for describing the annual variation of fCO2 and for estimating the annual flux of CO2 at the air-sea interface. The model incorporated annual variations in SST, the thickness of the mixed layer, gas exchange associated with wind velocity, biological activity and atmospheric concentration of CO2. The model shows that the East Sea releases CO2 into the atmosphere from June to September, and absorbs CO2 during the rest of the year, from October through May. The net annual CO2 flux at the air-sea interface was estimated to be 0.032 (±0.012) Gt-C per year from the atmosphere into the East Sea. Water column chemistry shows penetration of CO2 into the whole water column, supporting a short turnover time for deep waters in the East Sea. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

2.
More than 14,000 measurements of surface water xCO2 were obtained during two cruises, 3 weeks apart in June 2000, along 155°E between 34 and 44°N in the western North Pacific Ocean. Based on the distributions of salinity and sea surface temperature (SST), the region has been divided into 6 subregions; Oyashio, Oyashio front, Transition, Kuroshio front, and Kuroshio extension I and II zones, from north to south. The surface waters were always undersaturated with respect to atmospheric CO2. The Oyashio water was the least undersaturated: its xCO2 decreased slightly by 7 ppm, while SST increased by 2°C. The xCO2 normalized to a constant temperature decreased considerably. In the two frontal zones, a large drawdown of 30–40 ppm was observed after 18–19 days. In the Kuroshio extension zones, the xCO2 increased, but the normalized xCO2 decreased considerably. The Transition zone water may be somewhat affected by mixing with the subsurface water, as indicated by the smallest SST rise, an undecreased PO4 concentration, and a colder and less stable surface layer than the Oyashio front water. As the uncertainty derived from the air-sea CO2 flux was not large, the xCO2 data allowed us to calculate the net biological productivity. The productivities around 60 mmol C m−2d−1 outside the Transition zone indicate that the northwestern North Pacific, especially the two frontal zones, can be regarded as one of the most productive oceans in the world.  相似文献   

3.
The influence of the coastal ocean on global net annual air-sea CO2 fluxes remains uncertain. However, it is well known that air-sea pCO2 disequilibria can be large (ocean pCO2 ranging from ∼400 μatm above atmospheric saturation to ∼250 μatm below) in eastern boundary currents, and it has been hypothesized that these regions may be an appreciable net carbon sink. In addition it has been shown that the high productivity in these regions (responsible for the exceptionally low surface pCO2) can cause nutrients and inorganic carbon to become more concentrated in the lower layer of the water column over the shelf relative to adjacent open ocean waters of the same density. This paper explores the potential role of the winter season in determining the net annual CO2 flux in temperate zone eastern boundary currents, using the results from a box model. The model is parameterized and forced to represent the northernmost part of the upwelling region on the North American Pacific coast. Model results are compared to the few summer data that exist in that region. The model is also used to determine the effect that upwelling and downwelling strength have on the net annual CO2 flux. Results show that downwelling may play an important role in limiting the amount of CO2 outgassing that occurs during winter. Finally data from three distinct regions on the Pacific coast are compared to highlight the importance of upwelling and downwelling strength in determining carbon fluxes in eastern boundary currents and to suggest that other features, such as shelf width, are likely to be important.  相似文献   

4.
We have carried out a small-scale (∼20 l) CO2 sequestration experiment off northern California (684 m depth, ∼5°C, background ocean pH ∼7.7) designed as an initial investigation of the effects of physical forcing of the fluid, and the problem of sensing the formation of a low pH plume. The buoyant CO2 was contained in a square frame 1.2 m high, exposing 0.21 m2 to ocean flow. Two pH electrodes attached to the frame recorded the signal; a second frame placed 1.9 m south of the CO2 pool was also equipped with two recording pH electrodes. An additional pH electrode was held in the ROV robotic arm to probe the fluid interface. Local water velocities of up to 40 cm sec−1 were encountered, creating significant eddies within the CO2 box, and forcing wavelets at the fluid interface. This resulted in rapid CO2 dissolution, with all CO2 being depleted in a little more than 2 days. The pH record from the sensor closest (∼10 cm) to the CO2 showed many spikes of low pH water, the extreme value being ∼5.9. The sensor 1 m immediately below this showed no detectable response. The electrodes placed 1.9 m distant from the source also recorded very small perturbations. The results provide important clues for the design of future experiments for CO2 disposal and biogeochemical impact studies. These include the need for dealing with the slow CO2 hydration kinetics, better understanding of the fluid dynamics of the CO2-water interface, and non-point source release designs to provide more constant, controlled local CO2 enrichments within the experimental area. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

5.
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.  相似文献   

6.
We observed the partial pressure of oceanic CO2, pCO2 sea, and related surface properties in the westernmost region of the subarctic North Pacific, seasonally from 1998 to 2001. The pCO2 sea in the Oyashio region showed a large decrease from winter to spring. In winter, pCO2 sea was higher than 400 μatm in the Oyashio region and this region was a source of atmospheric CO2. In spring, pCO2 sea decreased to extremely low values, less than 200 μatm (minimum, 139 μatm in 2001), around the Oyashio region with low surface salinity and this region turned out to be a strong sink. The spatial variations of pCO2 sea were especially large in spring in this region. The typical Oyashio water with minimal mixing with subtropical warm water was extracted based on the criterion of potential alkalinity. The contribution of main oceanic processes to the changes in pCO2 sea from winter to spring was estimated from the changes in the concentrations of dissolved inorganic carbon and nutrients, total alkalinity, temperature and salinity observed in surface waters in respective years. These quantifications indicated that photosynthesis made the largest contribution to the observed pCO2 sea decreases in all years and its magnitude was variable year by year. These year-to-year differences in spring biological contribution could be linked to those in the development of the density stratification due to the decrease in surface salinity. Thus, the changes in the surface physical structure could induce those in pCO2 sea in the Oyashio region in spring. Furthermore, it is suggested that the direction and magnitude of the air-sea CO2 flux during this season could be controlled significantly by the onset time of the spring bloom. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

7.
Observations of primary productivity, 234Th, and particulate organic carbon (POC) were made from west to east across the northern North Pacific Ocean (from station K2 to Ocean Station Papa) during September–October 2005. Primary productivities in this region varied longitudinally from approximately 236 to 444 mgC m−2d−1 and clearly indicate the West High East Low (WHEL) trend. We estimated east-west variations in the POC flux from the surface layer (0–100 m) by using 234Th as a tracer. POC fluxes in the western region (44–53 mgC m−2d−1) were higher than those in the eastern region (21–34 mgC m−2d−1). However, the export ratios (e-ratios) ranged from approximately 8% to 16% and did not show the WHEL trend. Contrary to our expectation, no relation between POC flux (or e-ratio) and diatom biomass (or dominance) was apparent in autumn in the northern North Pacific.  相似文献   

8.
In order to examine temporal variations of the surface oceanic and atmospheric fCO2 and the DIC concentration, we analyzed air and seawater samples collected during the period May 1992–June 1996 in the northwestern North Pacific, about 30 km off the coast of the main island of Japan. The atmospheric CO2 concentration has increased secularly at a rate of 1.9 ppmv yr−1, and it showed a clear seasonal cycle with a maximum in spring and a minimum late in summer, produced mainly by seasonally-dependent terrestrial biospheric activities. DIC also showed a prominent seasonal cycle in the surface ocean; the minimum and maximum values of the cycle appeared in early fall and in early spring, respectively, due primarily to the seasonally-dependent activities of marine biota and partly to the vertical mixing of seawater and the coastal upwelling. The oceanic fCO2 values were almost always lower than those of the atmospheric fCO2, suggesting that this area of the ocean acts as a sink for atmospheric CO2. Values varied seasonally, mainly reflecting seasonal changes of SST and DIC, with a secular increase at a rate of 3.7 μatm yr−1. The average values of the annual net CO2 flux between the ocean and the atmosphere calculated by using the different bulk equations ranged between −0.8 and −1.7 mol m−2yr−1, and its magnitude was enhanced and reduced late in spring and mid-summer, respectively, due mainly to the seasonally varying oceanic fCO2.  相似文献   

9.
Concentration and stable isotopic compositions (δ 18O) of dissolved O2 were measured in seawater samples collected from the Philippine Sea in June 2006. The in-situ O2 consumption rate and the isotopic fractionation factor (α r ) during dissolved O2 consumption were obtained from field observations by applying a vertical one-dimensional advection diffusion model to the deep water mass of about 1000–4000 m. The average O2 consumption rate and α r were, respectively, 0.11 ± 0.07 μmol kg−1yr−1 and 0.990 ± 0.001. These estimated values agree well with values from earlier estimations of Pacific deep water. The in-situ O2 consumption rates are two or more times higher north of 20°N, although the value of α r was not significantly different between the north and south. Its levels varied rapidly in the water mass of less about 2000 m depth. These results suggest that organic matter from the continent imparts a meaningful contribution to the upper water in the northern part of the area; it might produce the strong O2 minimum that is evident in the water mass from about 1000–2000 m in the northern part of the Philippine Sea.  相似文献   

10.
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 (fCO2SW) 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 fCO2SW in the summer of 2015.  相似文献   

11.
We have developed new systems capable of profiling to >1000 m for measuring in situ pH and fugacity of CO2 (fCO2) in the ocean using spectrophotometric analysis (pH and CO2 profilers). The in situ pH is determined by detecting the color change of the pH indicator (m-cresol purple). It can withstand ambient pressure to 1000 m depth. The CO2 profiler analyzed in situ fCO2 by detecting the change of pH in an inner solution, equilibrated with the seawater through a gas permeable membrane. It can be operated to 2500 m depth. We used an amorphous fluoropolymer tubing form of AF-2400 for the gas permeable membrane due to its high gas permeability coefficients. The inner solution was a mixture of 2 μM bromocresol purple (BCP) and 5 μM sodium hydroxide. This system gave us a response time of 1 minute, which is twice as fast as previous systems. The precisions of pH and CO2 profilers were within 0.002 and 2.5% respectively. We have used these profilers to study the North Pacific, obtaining good agreement with the difference between the data from profilers and a discrete bottle of 0.002 ± 0.005 pH (SE, n = 25) and −0.4 ± 3 μatm (SE, n = 31).  相似文献   

12.
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 fCO2sea ranged about 185–335 μatm. The maximum of fCO2sea in the summer was primarily due to the change of water temperature. The minimum of fCO2sea 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 fCO2sea (water temperature, salinity, and biological activity), we carried out a sensitivity analysis of these effects on the variation of fCO2sea. In spring, the biological effect had the largest effect for the minimum of fCO2sea (40%). In summer, the water temperature effect had the largest effect for the maximum of fCO2sea (25%). In fall, the water temperature effect had the largest effect for the minimum of fCO2sea (53%). In winter, the biological effect had the largest effect for the minimum of fCO2sea (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 fCO2sea 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 fCO2sea, thus as the maximum trend of each variable on fCO2sea 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 fCO2sea. 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.  相似文献   

13.
The habitat quality of Chub mackerel (Scomber japonicus) in the East China Sea has been a subject of concern in the last 10 years due to large fluctuations in annual catches of this stock. For example, the Chinese light-purse seine fishery recorded 84000 tons in 1999 compared to 17000 tons in 2006. The fluctuations have been attributed to variability in habitat quality. The habitat suitability Index (HSI) has been widely used to describe fish habitat quality and in fishing ground forecasting. In this paper we use catch data and satellite derived environmental variables to determine habitat suitability indices for Chub mackerel during July to September in the East China Sea. More than 90% of the total catch was found to come from the areas with sea surface temperature of 28.0°–29.4°C, sea surface salinity of 33.6–34.2 psu, chlorophyll-a concentration of 0.15–0.50 mg/m3 and sea surface height anomaly of −0.1–1.1 m. Of the four conventional models of HSI, the Arithmetic Mean Model (AMM) was found to be most suitable according to Akaike Information Criterion analysis. Based on the estimation of AMM in 2004, the monthly HSIs in the waters of 123°–125°E and 27°30′–28°00′ N were more than 0.6 during July to September, which coincides with the catch distribution in the same time period. This implies that AMM can yield a reliable prediction of the Chub mackerel’s habitat in the East China Sea.  相似文献   

14.
We found a simple function of pH that relates to sea surface temperature (SST, K) and chlorophyll-a (Chl, µg l−1) using measured surface seawater pH, SST and Chl data sets over the North Pacific: pH (total hydrogen scale at 2°C) = 0.01325 SST − 0.0253 Chl + 4.150 (R2 = 0.95, p < 0.0001, n = 483). Moreover, evaluating the seasonal variation of pH based on this algorithm, we compared the measured pH with the predicted pH at the observational time series stations in subpolar and subtropical regions. The average of ΔpH (measured - predicted, n = 52) was 0.006 ± 0.022 pH. Therefore, the combination of SST and Chl can allow us to determine the spatiotemporal distribution of pH over the North Pacific. Using the climatological data sets of SST and Chl with our pH algorithms, we have described the seasonal distributions of pH at 25°C (pH(25)) and pH in situ temperature (pH(T)) over the North Pacific surface water.  相似文献   

15.
Partial pressure of CO2 in surface sea water (pCO2) was measured continuously off Sanriku in May, 1997 by a new pCO2 measurement system. We have examined the relation of pCO2 to physical factors such as temperature, salinity and density, chemical and biological factors such as nutrients and carbonate system and chlorophylla. In the Kuroshio region pCO2 was not correlated to physical, chemical and biological factors in the range of 260 to 290 μatom. In transition water (Tr1) between Kuroshio and the Oyashio second branch, pCO2 was weakly correlated to physical factors and strongly correlated to nutrients. In transition water (Tr2) between the Oyashio first and second branches, pCO2 was highly correlated to temperature (SD: 10.9 μatom) and salinity (SD: 8.6 μatom) and also to nutrients. In transition water (Tr1+Tr2), pCO2 was highly multivariately correlated to temperature (T), salinity (S), chlorophylla (CH) (or nitrate+nitrite (N)) as follows, pCO2(μatom)= 10.8×T(°C)+27.7×S+2.57CH(μg/1) −769, R2= 0.86, SD = 20.9, or pCO2(μatom)= 3.9×T(°C)+25.5×S+16.0NO3(μM) −686, R2= 0.99, SD = 6.4. Moreover, pCO2 was predicted by only two factors, one physical (S) and the other chemical/biological (N) as follows: pCO2 (μatom)=32.8×S+19.4N−908, R2=0.97, SD=8.4. The pH measured at 25°C was well correlated with normalized pCO2 at a fixed temperature. In the Oyashio region pCO2 was decreased to 160 μatom, probably because of spring bloom, but was not correlated linearly to chlorophylla. The results obtained showed the possibility of estimating pCO2 of the Oyashio and transition regions in May by satellite remote sensing of SST, but the problem of estimation of pCO2 in Kuroshio water remains to be solved.  相似文献   

16.
Purposeful deep-sea carbon dioxide sequestration by direct injection of liquid CO2 into the deep waters of the ocean has the potential to mitigate the rapid rise in atmospheric levels of greenhouse gases. One issue of concern for this carbon sequestration option is the impact of changes in seawater chemistry caused by CO2 injection on deep-sea ecosystems. The effects of deep-sea carbon dioxide injection on infaunal deep-sea organisms were evaluated during a field experiment in 3600 m depth off California, in which liquid CO2 was released on the seafloor. Exposure to the dissolution plume emanating from the liquid CO2 resulted in high rates of mortality for flagellates, amoebae, and nematodes inhabiting sediments in close proximity to sites of CO2 release. Results from this study indicate that large changes in seawater chemistry (i.e. pH reductions of ∼0.5–1.0 pH units) near CO2 release sites will cause high mortality rates for nearby infaunal deep-sea communities. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

17.
In the southwestern Okhotsk Sea off Hokkaido we observed chemical components related to the carbonate system for 1 year from August 1997 to June 1998. Using the conservative components salinity and water temperature, we confirmed the existence of two water masses flowing into the intermediate layer of the Okhotsk Sea, the East Sakhalin Current Water (ESCW) which becomes denser by mixing of brine water, and the Forerunner of Soya Warm Current Water (FSWW) which becomes denser due to cooling of the saline Kuroshio water. The ΔNTCx values were calculated by comparing the ESCW and the FSWW with the Pacific Deep Water (PDW). The ΔNTCx values obtained are 100–110 μmol/kg and 70–100 μmol/kg for the ESCW and the FSWW off Hokkaido, respectively, which are considerably larger than that of the Kuroshio water. These large ΔNTCx values may be due to both low DIC concentration in the surface water and intense gas exchange under the cold and stormy winter conditions for the ESCW and the cooling of the FSWW as it flows northward. Since the flow rates of dense waters concerned with the ESCW and the FSWW have previously been estimated as 0.9 Sv and 0.2 Sv, respectively, the amount of atmospheric CO2 absorbed and transported to the intermediate layer turns out to be 3.9−4.1 × 1013 gC/yr. This flux is small on a global scale, but the flux divided by the surface layer of the Okhotsk Sea is 30 gC/m2/yr, which is 5 times greater than the mean absorption flux of anthropogenic CO2 in the world's oceans. It is thus considered that atmospheric CO2 is efficiently absorbed in the Okhotsk Sea. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

18.
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.  相似文献   

19.
Ocean acidification damages calcareous organisms, such as calcifying algae, foraminifera, corals, and shells. In this study, we made a device equipped with a Clark-type oxygen electrode and a pH-stat to examine how the most abundant calcifying phytoplankton, the coccolithophorid Emiliania huxleyi, responded to acidification and alkalization of the seawater medium. When E. huxleyi was incubated at pH 8.2, close to oceanic pH, the medium was alkalized during photosynthesis, and the alkalization rate [determined as μmol HCl added (mg Chl)−1 h−1] was identical to the activity of photosynthesis [determined as μmol O2 evolved (mg Chl)−1 h−1]. When pH was maintained at 7.2 by the pH-stat, alkalization activity was stimulated and exceeded photosynthetic activity, resulting in an increase in the ratio of alkalization to photosynthesis (Alk/PS). On the other hand, no alkalization and photosynthesis were observed at pH 9.2. In contrast, acidification of seawater was observed in the dark because of the release of respiratory CO2 from cells at pH 8.2–9.2, but not at pH 7.2. When orthophosphate was rapidly depleted within a day in the batch culture, intracellular calcification gradually increased, and both photosynthesis and alkalization decreased gradually. During the period the Alk/PS ratio also decreased gradually. These results indicate that E. huxleyi possesses an ability to compensate for the acidification of seawater when photosynthesis is more actively driven than respiration. These results suggest that the E. huxleyi cells may not be severely damaged by oceanic acidification during photosynthesis because of their homeostatic function to avoid negative effects on cellular activity. Finally, we concluded that E. huxleyi cells possess a buffering ability to reduce acidification effects when photosynthesis is actively driven.  相似文献   

20.
This study explores the changes in the surface water fugacity of carbon dioxide (fCO2) and biological carbon uptake in two Southern Ocean iron fertilisation experiments with different hydrographic regimes. The Southern Ocean Iron Release Experiment (SOIREE) experiment was carried out south of the Antarctic Polar Front (APF) at 61°S, 141°E in February 1999 in a stable hydrographic setting. The EisenEx experiment was conducted in a cyclonic eddy north of the APF at 48°S, 21°E in November 2000 and was characterised by a rapid succession of low to storm-force wind speeds and dynamic hydrographic conditions. The iron additions promoted algal blooms in both studies. They alleviated algal iron limitation during the 13-day SOIREE experiment and probably during the first 12 days of EisenEx. The fCO2 in surface water decreased at a constant rate of 3.8 μatm day−1 from 4 to 5 days onwards in SOIREE. The fCO2 reduction was 35 μatm after 13 days. The evolution of surface water fCO2 in the iron-enriched waters (or ‘patch’) displayed a saw tooth pattern in EisenEx, in response to algal carbon uptake in calm conditions and deep mixing and horizontal dispersion during storms. The maximum fCO2 reduction was 18–20 μatm after 12 and 21 days with lower values in between. The iron-enriched waters in EisenEx absorbed four times more atmospheric CO2 than in SOIREE between 5 and 12 days, as a result of stronger winds. The total biological uptake of inorganic carbon across the patch was 1389 ton C (±10%) in SOIREE and 1433 ton C (±27%) in EisenEx after 12 days (1 ton=106 g). This similarity probably reflects the comparable size of the iron additions, as well as algal growth at a similar near-maximum growth rate in these regions. The findings imply that the different mixing regimes had less effect on the overall biological carbon uptake across the iron-enriched waters than suggested by the evolution of fCO2 in surface water.  相似文献   

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