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1.
The biological pump is a central process in the ocean carbon cycle, and is a key factor controlling atmospheric carbon dioxide (CO2). However, whether the Arctic biological pump is enhanced or reduced by the recent loss of sea ice is still unclear. We examined if the effect was dependent on ocean circulation. Melting of sea ice can both enhance and reduce the biological pump in the Arctic Ocean, depending on ocean circulation. The biological pump is reduced within the Beaufort Gyre in the Canada Basin because freshwater accumulation within the gyre limits nutrient supply from deep layers and shelves hence inhibits the growth of large-bodied phytoplankton. Conversely, the biological pump is enhanced outside the Beaufort Gyre in the western Arctic Ocean because of nutrient supply from shelves and greater light penetration, enhancing photosynthesis, caused by the sea ice loss. The biological pump could also be enhanced by sea ice loss in the Eurasian Basin, where uplifted isohaline surfaces associated with the Transpolar Drift supply nutrients upwards from deep layers. New data on nitrate uptake rates are consistent with the pattern of enhancement and reduction of the Arctic biological pump. Our estimates indicate that the enhanced biological pump can be as large as that in other oceans when the sea ice disappears. Contrary to a recent conclusion based on data from the Canada Basin alone, our study suggests that the biological CO2 drawdown is important for the Arctic Ocean carbon sink under ice-free conditions.  相似文献   

2.
Intense studies of upper and deep ocean processes were carried out in the Northwestern Indian Ocean (Arabian Sea) within the framework of JGOFS and related projects in order to improve our understanding of the marine carbon cycle and the ocean’s role as a reservoir for atmospheric CO2. The results show a pronounced monsoon-driven seasonality with enhanced organic carbon fluxes into the deep-sea during the SW Monsoon and during the early and late NE Monsoon north of 10°N. The productivity is mainly regulated by inputs of nutrients from subsurface waters into the euphotic zone via upwelling and mixed layer-deepening. Deep mixing introduces light limitation by carrying photoautotrophic organisms below the euphotic zone during the peak of the NE Monsoon. Nevertheless, deep mixing and strong upwelling during the SW Monsoon provide an ecological advantage for diatoms over other photoautotrophic organisms by increasing the silica concentrations in the euphotic zone. When silica concentrations fall below 2 μmol l−1, diatoms lose their dominance in the plankton community. During diatom-dominated blooms, the biological pathway of uptake of CO2 (the biological pump) appears to be more efficient than during blooms of other organisms, as indicated by organic carbon to carbonate carbon (rain) ratios. Due to the seasonal alternation of diatom and non-diatom dominated exports, spatial variations of the annual mean rain ratios are hardly discernible along the main JGOFS transect.Data-based estimates of the annual mean impact of the biological pump on the fCO2 in the surface water suggest that the biological pump reduces the increase of fCO2 in the surface water caused by intrusion of CO2-enriched subsurface water by 50–70%. The remaining 30 to 50% are attributed to CO2 emissions into the atmosphere. Rain ratios up to 60% higher in river-influenced areas off Pakistan and in the Bay of Bengal than in the open Arabian Sea imply that riverine silica inputs can further enhance the impact of the biological pump on the fCO2 in the surface water by supporting diatom blooms. Consequently, it is assumed that reduced river discharges caused by the damming of major rivers increase CO2 emission by lowering silica inputs to the Arabian Sea; this mechanism probably operates in other regions of the world ocean also.  相似文献   

3.
Biological Pump in Northwestern North Pacific   总被引：1，自引：1，他引：1  
The northwestern North Pacific is considered to be one of the most productive areas in the global ocean. Although the marginal zones along the Japanese and Kuril islands, Kamchatka Peninsula, and Aleutian Islands are certainly productive, recent studies do not always show high primary production values in the western subarctic gyre (WSG). In addition, a recent analysis of the biological pump in the WSG showed that, in contrast to what was previously reported, the vertical change of the particulate organic carbon flux with depth is large. Nevertheless, the biological pump in the northwestern North Pacific may function to draw down the partial pressure of CO2 in the surface water because the ratio of the organic carbon flux to inorganic carbon flux (Corg/Cinorg), the export flux, and the export ratio from the surface water are higher than those in other oceans. This article also introduces recent research on changes to the biological pump that might have been caused by global warming. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

4.
Results from twin control simulations of the preindustrial CO2 gas exchange (natural flux of CO2) between the ocean and the atmosphere are presented here using the NASA-GISS climate model, in which the same atmospheric component (modelE2) is coupled to two different ocean models, the Russell ocean model and HYCOM. Both incarnations of the GISS climate model are also coupled to the same ocean biogeochemistry module (NOBM) which estimates prognostic distributions for biotic and abiotic fields that influence the air–sea flux of CO2. Model intercomparison is carried out at equilibrium conditions and model differences are contrasted with biases from present day climatologies. Although the models agree on the spatial patterns of the air–sea flux of CO2, they disagree on the strength of the North Atlantic and Southern Ocean sinks mainly because of kinematic (winds) and chemistry (pCO2) differences rather than thermodynamic (SST) ones. Biology/chemistry dissimilarities in the models stem from the different parameterizations of advective and diffusive processes, such as overturning, mixing and horizontal tracer advection and to a lesser degree from parameterizations of biogeochemical processes such as gravitational settling and sinking. The global meridional overturning circulation illustrates much of the different behavior of the biological pump in the two models, together with differences in mixed layer depth which are responsible for different SST, DIC and nutrient distributions in the two models and consequently different atmospheric feedbacks (in the wind, net heat and freshwater fluxes into the ocean).  相似文献   

5.
Most marginal seas in the North Pacific are fed by nutrients supported mainly by upwelling and many are undersaturated with respect to atmospheric CO2 in the surface water mainly as a result of the biological pump and winter cooling. These seas absorb CO2 at an average rate of 1.1 ± 0.3 mol C m−2yr−1 but release N2/N2O at an average rate of 0.07 ± 0.03 mol N m−2yr−1. Most of primary production, however, is regenerated on the shelves, and only less than 15% is transported to the open oceans as dissolved and particulate organic carbon (POC) with a small amount of POC deposited in the sediments. It is estimated that seawater in the marginal seas in the North Pacific alone may have taken up 1.6 ± 0.3 Gt (1015 g) of excess carbon, including 0.21 ± 0.05 Gt for the Bering Sea, 0.18 ± 0.08 Gt for the Okhotsk Sea; 0.31 ± 0.05 Gt for the Japan/East Sea; 0.07 ± 0.02 Gt for the East China and Yellow Seas; 0.80 ± 0.15 Gt for the South China Sea; and 0.015 ± 0.005 Gt for the Gulf of California. More importantly, high latitude marginal seas such as the Bering and Okhotsk Seas may act as conveyer belts in exporting 0.1 ± 0.08 Gt C anthropogenic, excess CO2 into the North Pacific Intermediate Water per year. The upward migration of calcite and aragonite saturation horizons due to the penetration of excess CO2 may also make the shelf deposits on the Bering and Okhotsk Seas more susceptible to dissolution, which would then neutralize excess CO2 in the near future. Further, because most nutrients come from upwelling, increased water consumption on land and damming of major rivers may reduce freshwater output and the buoyancy effect on the shelves. As a result, upwelling, nutrient input and biological productivity may all be reduced in the future. As a final note, the Japan/East Sea has started to show responses to global warming. Warmer surface layer has reduced upwelling of nutrient-rich subsurface water, resulting in a decline of spring phytoplankton biomass. Less bottom water formation because of less winter cooling may lead to the disappearance of the bottom water as early as 2040. Or else, an anoxic condition may form as early as 2200 AD. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

6.
Feasibility studies recently suggest that sequestration of anthropogenic CO2 in the deep ocean could help reduce the atmospheric CO2 concentration. However, implementation of this strategy could have a significant environmental impact on marine organisms. This has highlighted the urgent need of further studies concerning the biological impact of CO2 ocean sequestration. In this paper we summarize the recent literature reporting on the biological impact of CO2 and discuss the research work required for the future. Although fundamental research of the effect of CO2 on marine organisms before the practical consideration of CO2 ocean sequestration was limited, laboratory and field studies concerning biological impacts have been increasing after the first international workshop in 1991 discussing CO2 ocean sequestration. Acute impacts of CO2 ocean sequestration could be determined by laboratory and field experiments and assessed by simulation models as described by the following papers in this section. On the other hand, chronic effects of CO2 ocean sequestration, those directly related to the marine ecosystem, would be difficult to verify by means of experiments and to assess using ecosystem models. One of the practical solutions for this issue implies field experiments starting with controlled small scale and eventually to a large scale of CO2 injection intended to determine ecosystem alteration. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

7.
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   

8.
Measurements of pCO2, pH and alkalinity in the surface waters of an iron fertilised patch of sub-Antarctic water were made during SAGE (SOLAS SAGE: Surface-Ocean Lower Atmosphere Studies Air-Sea Gas Experiment). The iron addition induced a minor phytoplankton bloom, however the patch dynamics were dominated by physical processes which suppressed and masked the biological effects. The Lagrangian nature of the experiment allowed the carbonate chemistry in the patch to be followed for 15.5 days, and the relative importance of the biological and physical factors influencing the surface water pCO2 was estimated. The pCO2 of the surface waters of the patch increased from 327 ??atm prior to iron addition to 338 ??atm on Day 14, effects of vertical and horizontal mixing offset the 15 ??atm drawdown that would have occurred had the induced biological uptake been the sole factor to influence the pCO2. The air-sea carbon flux calculated using the measured skin temperature and a piston velocity parameterisation determined during SAGE (Ho et al., 2006) was 98.5% of the flux determined using conventional bulk temperature measurement and the Wanninkhof (1992) piston velocity parameterisation. The skin temperature alone contributed to an 8% increase in the flux compared with that determined using bulk temperature.  相似文献   

9.
This article presents the results of long-term studies of the dynamics of carbonate parameters and air–sea carbon dioxide fluxes on the Chukchi Sea shelf during the summer. As a result of the interaction of physical and biological factors, the surface waters on the west of Chukchi Sea were undersaturated with carbon dioxide when compared with atmospheric air; the partial pressure of CO2 varied in the range from 134 to 359 μatm. The average value of CO2 flux in the Chukchi Sea per unit area varied in the range from–2.4 to–22.0 mmol /(m2 day), which is significantly higher than the average value of CO2 flux in the World Ocean. It has been estimated that the minimal mass of C absorbed by the surface of Chukchi Sea from the atmosphere during ice-free season is 13 × 1012 g; a great part of this carbon is transported to the deeper layers of sea and isolated from the atmosphere for a long period of time. The studies of the carbonate system of the Chukchi Sea, especially of its western part, will provide some new data on the fluxes of carbon dioxide in the Arctic Ocean and their changes. Our analysis can be used for an interpretation of the satellite assessment of CO2 fluxes and dissolved CO2 distribution in the upper layers of the ocean.  相似文献   

10.
The direct injection of CO2 in the deep ocean is a promising way to mitigate global warming. One of the uncertainties in this method, however, is its impact on marine organisms in the near field before CO2 is diluted widely in the ocean. Since field experiments cost enormously, computational simulations are expected to show detailed information on the dilution process near injection points and its impact on marine organisms. In general, the LC50 concept is widely applied for testing the acute impact of a toxic agent on organisms. As a biological impact model we therefore consider mortality, which reflects recent laboratory experiments on zooplankton at various concentrations of CO2. Here we regard the sigmoid-transformed mortality as a linear function of time in the logarithmic scale, and not just of the concentration of CO2 in the logarithmic scale. This model was installed in a computational simulation code for the reconstruction of small-scale ocean turbulence. The results suggest that the biological effect is not significant when the ship speed is 4 knots and CO2 is injected at 0.1 ton/sec in the form of a spray through 100 nozzles provided vertically on a pipe at 10 m intervals. It is therefore considered that the moving-ship method is effective for direct CO2 injection. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

11.
The Canadian Model of Ocean Carbon (CMOC) has been developed as part of a global coupled climate carbon model. In a stand-alone integration to preindustrial equilibrium, the model ecosystem and global ocean carbon cycle are in general agreement with estimates based on observations. CMOC reproduces global mean estimates and spatial distributions of various indicators of the strength of the biological pump; the spatial distribution of the air-sea exchange of CO2 is consistent with present-day estimates. Agreement with the observed distribution of alkalinity is good, consistent with recent estimates of the mean rain ratio that are lower than historic estimates, and with calcification occurring primarily in the lower latitudes. With anthropogenic emissions and climate forcing from a 1850-2000 climate model simulation, anthropogenic CO2 accumulates at a similar rate and with a similar spatial distribution as estimated from observations. A hypothetical scenario for complete elimination of iron limitation generates maximal rates of uptake of atmospheric CO2 of less than 1 PgC y−1, or about 11% of 2004 industrial emissions. Even a ‘perfect’ future of sustained fertilization would have a minor impact on atmospheric CO2 growth. In the long term, the onset of fertilization causes the ocean to take up an additional 77 PgC after several thousand years, compared with about 84 PgC thought to have occurred during the transition into the last glacial maximum due to iron fertilization associated with increased dust deposition.  相似文献   

12.
Along with meteorological observations, complementary and systematic oceanographic observations of various physical, biological and chemical parameters have been made at Ocean Station P (OSP) (50°N, 145°W) since the early 1950s. These decadal time scale data have contributed to a better understanding of the physical, biological and chemical processes in the surface layer of the northeastern subarctic region of the Pacific Ocean. These data have demonstrated the importance of the North Pacific in the global carbon cycle and, in particular, the role of biological/chemical processes in the net exchange of CO2 across the air–sea interface. Although we do not fully comprehend how climatic variations influence marine communities or marine biogeochemistry, previous studies have provided some basic understanding of the mechanisms controlling the seasonal and inter-annual variations of biological and chemical parameters (such as phytoplankton, bacteria, nitrate/ammonium concentration) at OSP, and how they affect the carbon cycling in the subarctic North Pacific. In this study, we investigate how these mechanisms might alter the seasonal variations of these parameters at OSP under a 2XCO2 condition. We examine these influences using a new biological model calibrated by the climatological data from OSP. For the 2XCO2 simulation, the biological model is driven off line (i.e., no feedback to the ocean/atmospheric model components) by the climatology plus 2XCO2−1XCO2 outputs from a global surface ocean model and the Canadian GCM. Under the 2XCO2 condition, the upper layer ocean shows an increase in the entrainment rate at the bottom of the mixed layer for OSP during the late autumn and winter seasons, resulting in an increase in the f-ratio. Although there is an overall increase in the primary production (PP) by 3–18%, a decrease in the biomass of small phytoplankton and microzooplankton (due to mesozooplankton grazing) lowers the concentration of dissolved organic matter (DOM) by 4–25%. The model also predicts a significant increase in the concentrations of nitrate and ammonium, and in bacterial production during July and August. Doubling of the atmospheric CO2 from 330 to 660 ppm forces the marine pCO2 to increase by about 63%, much of which is driven by an increased flux of CO2 from the atmosphere to the oceans.  相似文献   

13.
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   

14.
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.  相似文献   

15.
《Marine Chemistry》2005,93(2-4):131-147
Data on the distribution of dissolved inorganic carbon (DIC) and partial pressure of CO2 (pCO2) were obtained during a cruise in the North Sea during late summer 2001. A 1° by 1° grid of 97 stations was sampled for DIC while the pCO2 was measured continuously between the stations. The surface distributions of these two parameters show a clear boundary located around 54°N. South of this boundary the DIC and pCO2 range from 2070 to 2130 μmol kg−1 and 290 to 490 ppm, respectively, whereas in the northern North Sea, values range between 1970 and 2070 μmol kg−1 and 190 to 350 ppm, respectively. The vertical profiles measured in the two different areas show that the mixing regime of the water column is the major factor determining the surface distributions. The entirely mixed water column of the southern North Sea is heterotrophic, whereas the surface layer of the stratified water column in the northern North Sea is autotrophic. The application of different formulations for the calculation of the CO2 air–sea fluxes shows that the southern North Sea acts as a source of CO2 for the atmosphere within a range of +0.8 to +1.7 mmol m−2 day−1, whereas the northern North Sea absorbs CO2 within a range of −2.4 to −3.8 mmol m−2 day−1 in late summer. The North Sea as a whole acts as a sink of atmospheric CO2 of −1.5 to −2.2 mmol m−2 day−1 during late summer. Compared to the Baltic and the East China Seas at the same period of the year, the North Sea acts a weak sink of atmospheric CO2. The anticlockwise circulation and the short residence time of the water in the North Sea lead to a rapid transport of the atmospheric CO2 to the deeper layer of the North Atlantic Ocean. Thus, in late summer, the North Sea exports 2.2×1012 g C month−1 to the North Atlantic Ocean via the Norwegian trench, and, at the same period, absorbs from the atmosphere a quantity of CO2 (0.4 1012 g C month−1) equal to 15% of that export, which makes the North Sea a continental shelf pump of CO2.  相似文献   

16.
Iron fertilization of nutrient-rich surface waters of the ocean is one possible way to help slow the rising levels of atmospheric CO2 by sequestering it in the oceans via biological carbon export. Here, I use an ocean general circulation model to simulate a patch of nutrient depletion in the subpolar northwest Pacific under various scenarios. Model results confirm that surface fertilization is an inefficient way to sequester carbon from the atmosphere (Gnanadesikan et al., 2003), since only about 20% of the exported carbon comes initially from the atmosphere. Fertilization reduces future production and thus CO2 uptake by utilizing nutrients that would otherwise be available later. Effectively, this can be considered as leakage when compared to a control run. This “effective” leakage and the actual leakage of sequestered CO2 cause a significant, rapid decrease in carbon retention (only 30–45% retained after 10 years and less than 20% after 50 years). This contrasts markedly with the almost 100% retention efficiency for the same duration using the same model, when carbon is disposed directly into the northwest Pacific (Matsumoto and Mignone, 2005). As a consequence, the economic effectiveness of patch fertilization is poor in two limiting cases of the future price path of carbon. Sequestered carbon in patch fertilization is lost to the atmosphere at increasingly remote places as time passes, which would make monitoring exceedingly difficult. If all organic carbon from one-time fertilization reached the ocean bottom and remineralized there, acidification would be about −0.05 pH unit with O2 depletion about −20 μmol kg−1. These anomalies are probably too small to seriously threaten deep sea biota, but they are underestimated in the model because of its large grid size. The results from this study offer little to advocate purposeful surface fertilization as a serious means to address the anthropogenic carbon problem.  相似文献   

17.
High resolution measurements of carbon dioxide and oxygen were made in surface waters of the central Arkona Sea (Baltic Sea) from May 2003 to September 2004. Sensors for CO2 partial pressure (pCO2w) and oxygen (O2) concentration were mounted in 7 m depth on a moored platform which is used for hydrographic and meteorological monitoring. The pCO2w data were obtained in half hour intervals and O2 was measured each hour as an average of a 10 min measurement. To check the performance of the sensors, pCO2w and O2 were determined by shipboard measurements on a research vessel which visited the site in 1–2 month intervals. In addition, pCO2w was measured on a “volunteer observing ship” (VOS) passing the platform each second day at a distance of about 25 km. Minima of 220 to 250 μatm of pCO2w were observed at the time of the spring bloom and a cyanobacteria bloom in mid-summer. During winter the pCO2w was mostly close to equilibrium with the atmosphere but maxima of 430 to 530 μatm were also observed. The seasonality of oxygen and pCO2w showed an opposing pattern. From a multiple regression analysis, we concluded that two processes primarily controlled pCO2w during our study: biological turnover and mixing. A parameterization, based on apparent oxygen utilisation (AOU) and salinity (S) only (pCO2w = 1.23 AOU + 43 S), reproduced the seasonality of pCO2w in surface water reasonably well. Based on our pCO2, salinity, and temperature data set, we attempted to separate processes changing total inorganic carbon concentrations (CT) by using an alkalinity–salinity relation for the area. The contribution of CO2 gas exchange and mixing were calculated and from this the biological turnover was deduced to reveal the calculated CT changes.The net annual uptake of CO2 in the central Arkona Sea was estimated to be about 1.5 Tg (1.5·1012 g) which was approximately balanced by a net oxygen release considering the uncertainties of the flux calculations. Near-coast CO2 emission due to episodic upwelling partly compensated the uptake of the central part of the Arkona Sea reducing the overall magnitude of the CO2 uptake.  相似文献   

18.
In the summers of 1999 and 2003, the 1st and 2nd Chinese National Arctic Research Expeditions measured the partial pressure of CO2 in the air and surface waters (pCO2) of the Bering Sea and the western Arctic Ocean. The lowest pCO2 values were found in continental shelf waters, increased values over the Bering Sea shelf slope, and the highest values in the waters of the Bering Abyssal Plain (BAP) and the Canadian Basin. These differences arise from a combination of various source waters, biological uptake, and seasonal warming. The Chukchi Sea was found to be a carbon dioxide sink, a result of the increased open water due to rapid sea-ice melting, high primary production over the shelf and in marginal ice zones (MIZ), and transport of low pCO2 waters from the Bering Sea. As a consequence of differences in inflow water masses, relatively low pCO2 concentrations occurred in the Anadyr waters that dominate the western Bering Strait, and relatively high values in the waters of the Alaskan Coastal Current (ACC) in the eastern strait. The generally lower pCO2 values found in mid-August compared to at the end of July in the Bering Strait region (66–69°N) are attributed to the presence of phytoplankton blooms. In August, higher pCO2 than in July between 68.5 and 69°N along 169°W was associated with higher sea-surface temperatures (SST), possibly as an influence of the ACC. In August in the MIZ, pCO2 was observed to increase along with the temperature, indicating that SST plays an important role when the pack ice melts and recedes.  相似文献   

19.
The integrity of the caprock of a storage formation is the most crucial parameter for the long-term performance of a geological CO2 storage site. The Sleipner area in the Southern Viking Graben hosts the first and longest operating industrial scale CO2 storage project, where CO2 is injected in a saline aquifer of the Utsira Formation. Time-lapse seismic monitoring shows neither that CO2 has left the Utsira Formation nor indications for fracturing of the caprock by the CO2 injection activity, which is in agreement with previous numerical simulations. However, large chimney structures as close as 7 km from the injection point indicate that the caprock has been breached in the geological past, which may raise questions about the integrity of the caprock above the Sleipner CO2 storage site. Here, we present seismically constrained numerical fluid flow simulations that evaluate the influence of chimney structures on the long-term performance of the CO2 storage operation at Sleipner. The simulation could reproduce the spreading of the Sleipner CO2 plume, which is controlled by the anisotropic permeability field of the Utsira Formation and the regional dip of the formation top. We have performed long-term plume evolution simulations, which show that the injected CO2 will not reach the existing chimney structures assuming a realistic injection duration of 30 years. Our simulations indicate that an unrealistically long injection period between 92 and 140 years would be required for the CO2 to reach the existing chimney structures. In this case, a comparably low chimney permeability of 10 mD may be sufficient to facilitate CO2 migration from the storage formation to the seafloor, once the CO2 has reached a chimney structure. However, the simulations indicate that it is very unlikely that the CO2 may migrate along existing chimney structures at Sleipner. Our results highlight that the reconstruction of palaeo fluid flow systems and the identification of focused fluid conduits should be considered in the assessment of CO2 storage sites.  相似文献   

20.
The seasonal variability of the carbon dioxide (CO2) system in the Southern Ocean, south of 50°S, is analysed from observations obtained in January and August 2000 during OISO cruises conducted in the Indian Antarctic sector. In the seasonal ice zone, SIZ (south of 58°S), surface ocean CO2 concentrations are well below equilibrium during austral summer. During this season, when sea-ice is not obstructing gas exchange at the air–sea interface, the oceanic CO2 sink ranges from −2 to −4 mmol/m2/d in the SIZ. In the permanent open ocean zone, POOZ (50–58°S), surface oceanic fugacity fCO2 increases from summer to winter. The seasonal fCO2 variations (from 10 to 30 μatm) are relatively low compared to seasonal amplitudes observed in the subtropics or the subantarctic zones. However, these variations in the POOZ are large enough to cross the atmospheric level from summer to winter. Therefore, this region is neither a permanent CO2 sink nor a permanent CO2 source. In the POOZ, air–sea CO2 fluxes calculated from observations are about −1.1 mmol/m2/d in January (a small sink) and 2.5 mmol/m2/d in August (a source). These estimates obtained for only two periods of the year need to be extrapolated on a monthly scale in order to calculate an integrated air–sea CO2 flux on an annual basis. For doing this, we use a biogeochemical model that creates annual cycles for nitrate, inorganic carbon, total alkalinity and fCO2. The changing pattern of ocean CO2 summer sink and winter source is well reproduced by the model. It is controlled mainly by the balance between summer primary production and winter deep vertical mixing. In the POOZ, the annual air–sea CO2 flux is about −0.5 mol/m2/yr, which is small compared to previous estimates based on oceanic observations but comparable to the small CO2 sink deduced from atmospheric inverse methods. For reducing the uncertainties attached to the global ocean CO2 sink south of the Polar Front the regional results presented here should be synthetized with historical and new observations, especially during winter, in other sectors of the Southern Ocean.  相似文献   

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