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1.
We have carried out a series of in situ experiments to investigate the formation of a CO2 hydrate (CO2:5.75 H2O) for the purpose of evaluating scenarios for ocean fossil fuel CO2 disposal with a solid hydrate as the sequestered form. The experiments were carried out with a remotely operated vehicle in Monterey Bay at a depth of 619 m. pH measurements made in close proximity to the hydrate–seawater interface showed a wide range of values, depending upon the method of injection and the surface area of the hydrate formed. Rapid injection of liquid CO2 into an inverted beaker to form a flocculant mass of hydrate resulted in pH initially as low as 4.5 within a few centimeters of the interface, decaying slowly over 1–2 h towards normal seawater values as dense CO2 rich brine drained from the hydrate mass. In a second experiment, slower injection of the liquid CO2 to produce a simple two-layer system with a near planar interface of liquid CO2 with a thin hydrate film yielded pH values indistinguishable from the in situ ocean background level of 7.6. Both field and laboratory results now show that the dissolution rate of a mass of CO2 hydrate in seawater is slow but finite.  相似文献   

2.
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   

3.
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   

4.
A global ocean carbon cycle model based on the ocean general circulation model POP and the improved biogeochemical model OCMIP-2 is employed to simulate carbon cycle processes under the historically observed atmospheric CO 2 concentration and different future scenarios (called Rep- resentative Concentration Pathways, or RCPs). The RCPs in this paper follow the design of Inter- governmental Panel on Climate Change (IPCC) for the Fifth Assessment Report (AR5). The model results show that the ocean absorbs CO 2 from atmosphere and the absorbability will continue in the 21st century under the four RCPs. The net air-sea CO 2 flux increased during the historical time and reached 1.87 Pg/a (calculated by carbon) in 2005; however, it would reach peak and then decrease in the 21st century. The ocean absorbs CO 2 mainly in the mid latitude, and releases CO 2 in the equator area. However, in the Antarctic Circumpolar Current (ACC) area the ocean would change from source to sink under the rising CO 2 concentration, including RCP4.5, RCP6.0, and RCP8.5. In 2100, the anthropogenic carbon would be transported to the 40 S in the Atlantic Ocean by the North Atlantic Deep Water (NADW), and also be transported to the north by the Antarctic Bottom Water (AABW) along the Antarctic continent in the Atlantic and Pacific oceans. The ocean pH value is also simulated by the model. The pH decreased by 0.1 after the industrial revolution, and would continue to decrease in the 21st century. For the highest concentration sce- nario of RCP8.5, the global averaged pH would decrease by 0.43 to reach 7.73 due to the absorption of CO 2 from atmosphere.  相似文献   

5.
基于海洋环流模式POP和生物地球化学模型OCMIP-2,建立了全球海洋碳循环模式,并用于对全球海洋碳循环的模拟研究。该模式在大气CO2为283×10-6条件下,积分3 100 a,达到工业革命前的平衡态。在此基础上,用历史时期观测的大气CO2浓度进行强迫,模拟了历史时期的海洋碳循环。模拟的无机碳浓度、总碱度与基于观测得到的结果基本一致,模式能够较好地模拟全球碳循环过程。模拟结果表明,在北半球中高纬度和南半球的中纬度,海洋是大气CO2的主要汇区;在赤道南北纬20°之间和南大洋50°S以南,海洋表现为大气CO2的源区。在1980s海洋吸收CO2速率(以C计)为1.38 Pg/a,1990s为1.55 Pg/a。海洋中人为碳在北大西洋含量最大,向下到达海底并向南输运到30°N附近;在南极附近,浓度较小,深度达到3 000 m;在中纬度,人为碳被限制在温跃层以上。  相似文献   

6.
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   

7.
One proposal for ameliorating global warming is to sequester large amounts of carbon dioxide in the deep ocean, but the environmental consequences of sequestration for sediment-dwelling animals are poorly known. In a previous publication, we reported that ∼80% of benthic copepods were killed in an experimental release of CO2 off northern California at 3262 m. The effects of this release on nematodes are reported here. We examined samples of nematodes taken inside two ‘corrals’ into which CO2 was directly injected (providing an extreme endpoint for CO2 exposure) and taken near to and far from this CO2 source. After 30 days, pore-water pH was unchanged (∼7.8) at the sediment–water interface far (∼40 m) from corrals, but pH profiles were reduced by ∼0.75 near (∼2 m) corrals. Corral pH was highly acidic (5.4 in a measurement from a subsequent experiment). Fifty randomly selected nematodes from each of four vertical layers from the 14 cores were photographed. They were assigned to a tail group (based on morphology), and individual biovolume was estimated from measurements of body length and width. Although nematode abundance (expressed as total nematodes and by tail group) was not affected, length, width, and individual biovolume significantly differed between near and far samples. Median nematode biovolume examined across tail group and core layer increased by ∼48% inside and near corrals. Differences between near and corral samples were always less than differences between near and far samples. However, nematode length:width ratio did not differ between near and far, and the shapes of length, width, and biovolume frequency distributions were similar in all samples. We postulate that the nematode community throughout the upper 3 cm suffered a high rate of mortality after exposure to CO2, and that nematodes were larger because postmortem expansions in body length and width occurred. Decomposition rates were probably low and corpses did not disintegrate in 30 days. The observable effects of a reduction in pH to about 7.0 after 30 days were as great as an extreme pH reduction (5.4), suggesting that ‘moderate’ CO2 exposure, compared to the range of exposures possible following CO2 release, causes high mortality rates in the two most abundant sediment-dwelling metazoans (nematodes and copepods).  相似文献   

8.
Comprehensive sea surface surveys of the partial pressure of carbon dioxide (pCO2) have been made in the upwelling system of the coastal (0–200 km from shore) southeastern tropical Pacific since 2004. The shipboard data have been supplemented by mooring and drifter based observations. Air–sea flux estimates were made by combining satellite derived wind fields with the direct sea surface pCO2 measurements. While there was considerable spatial heterogeneity, there was a significant flux of CO2 from the ocean to the atmosphere during all survey periods in the region between 4° and 20° south latitude. During periods of strong upwelling the average flux out of the ocean exceeded 10 moles of CO2 per square meter per year. During periods of weaker upwelling and high productivity the CO2 evasion rate was near 2.5 mol/m2/yr. The average annual fluxes exceed 5 mol/m2/yr. These findings are in sharp contrast to results obtained in mid-latitude upwelling systems along the west coast of North America where the average air–sea CO2 flux is low and can often be from the atmosphere into the ocean. In the Peruvian upwelling system there are several likely factors that contribute to sea surface pCO2 levels that are well above those of the atmosphere in spite of elevated primary productivity: (1) the upwelling source waters contain little pre-formed nitrate and are affected by denitrification, (2) iron limitation of primary production enhanced by offshore upwelling driven by the curl of the wind stress and (3) rapid sea surface warming. The combined carbon, nutrient and oxygen dynamics of this region make it a candidate site for studies of global change.  相似文献   

9.
The ocean captures a large part of the anthropogenic carbon dioxide emitted to the atmosphere. As a result of the increase in CO2 partial pressure the ocean pH is lowered as compared to pre-industrial times and a further decline is expected. Ocean acidification has been proposed to pose a major threat for marine organisms, particularly shell-forming and calcifying organisms. Here we show, on the basis of meta-analysis of available experimental assessments, differences in organism responses to elevated pCO2 and propose that marine biota may be more resistant to ocean acidification than expected. Calcification is most sensitive to ocean acidification while it is questionable if marine functional diversity is impacted significantly along the ranges of acidification predicted for the 21st century. Active biological processes and small-scale temporal and spatial variability in ocean pH may render marine biota far more resistant to ocean acidification than hitherto believed.  相似文献   

10.
Marine environments with naturally high CO2 concentrations have become important research sites for studying the impacts of future ocean acidification on biological processes. We conducted high temporal resolution pH and temperature measurements in and around a shallow (2.5-3 m) CO2 vent site off Ischia, Italy in May and June 2008. Loggers were deployed at five stations to monitor water at both the surface and benthos. Our reference station, 500 m from the CO2 vent, had no noticeable vent influence. It had a naturally high and stable benthic pH (mean 8.16, inter-quartile range (IQ): 8.14-8.18) fluctuating with diel periodicity, presumably driven by community photosynthesis and respiration. A principal component analysis (PCA) revealed that the pH of this station was well constrained by meteorological parameters. In contrast, a station positioned within the vent zone, had a low and very variable benthic mean pH of 7.11 (IQ: 6.91-7.62) with large pH fluctuations not well constrained by a PCA. Any stations positioned within 20 m of the main vent zone had lowered pH, but suffered from abnormally large pH fluctuations making them unsuitable representatives to predict future changes to a shallow coastal environment. Between these extremes, we identified a benthic area with a lower pH of 7.84 (IQ: 7.83-7.88) that retained many of the characteristics of the reference station such as a natural diel pH periodicity and low variability. Our results indicate that a range of pH environments maybe commonplace near CO2 vents due to their characteristic acidification of benthic water over a wide area. Such environments could become invaluable natural laboratories for ocean acidification research, closely mimicking future CO2 conditions in a natural setting.  相似文献   

11.
The ocean is an important sink for carbon and heat, yet high-resolution measurements of biogeochemical properties relevant to global climate change are being made only sporadically in the ocean at present. There is a growing need for automated, real-time, long-term measurements of CO2 in the ocean using a network of sensors, strategically placed on ships, moorings, free-drifting buoys and autonomous remotely operated vehicles. The ground-truthing of new sensor technologies is a vital component of present and future efforts to monitor changes in the ocean carbon cycle and air–sea exchange of CO2.A comparison of a moored Carbon Interface Ocean Atmosphere (CARIOCA) buoy and shipboard fugacity of CO2 (fCO2) measurements was conducted in the western North Atlantic during two extended periods (>1 month) in 1997. The CARIOCA buoy was deployed on the Bermuda Testbed Mooring (BTM), which is located 5 km north of the site of the US Joint Global Ocean Flux Study (JGOFS) Bermuda Atlantic Time-series Study (BATS). The high frequency of sampling revealed that temperature and fCO2 responded to physical forcing by the atmosphere on timescales from diurnal to 4–8 days. Concurrent with the deployments of the CARIOCA buoy, frequent measurements of surface fCO2 were made from the R/V Weatherbird II during opportunistic visits to the BTM and BATS sites, providing a direct calibration of the CARIOCA buoy fCO2 data. Although, the in situ ground-truthing of the CARIOCA buoy was complicated by diurnal processes, sub-mesoscale and fine-scale variability, the CARIOCA buoy fCO2 data was accurate within 3±6 μatm of shipboard fCO2 data for periods up to 50 days. Longer-term assessments were not possible due to the CARIOCA buoy breaking free of the BTM and drifting into waters with different fCO2-temperature properties. Strategies are put forward for future calibration of other in situ sensors.  相似文献   

12.
Effects of CO<Subscript>2</Subscript> Enrichment on Marine Phytoplankton   总被引：1，自引：0，他引：1  
Rising atmospheric CO2 and deliberate CO2 sequestration in the ocean change seawater carbonate chemistry in a similar way, lowering seawater pH, carbonate ion concentration and carbonate saturation state and increasing dissolved CO2 concentration. These changes affect marine plankton in various ways. On the organismal level, a moderate increase in CO2 facilitates photosynthetic carbon fixation of some phytoplankton groups. It also enhances the release of dissolved carbohydrates, most notably during the decline of nutrient-limited phytoplankton blooms. A decrease in the carbonate saturation state represses biogenic calcification of the predominant marine calcifying organisms, foraminifera and coccolithophorids. On the ecosystem level these responses influence phytoplankton species composition and succession, favouring algal species which predominantly rely on CO2 utilization. Increased phytoplankton exudation promotes particle aggregation and marine snow formation, enhancing the vertical flux of biogenic material. A decrease in calcification may affect the competitive advantage of calcifying organisms, with possible impacts on their distribution and abundance. On the biogeochemical level, biological responses to CO2 enrichment and the related changes in carbonate chemistry can strongly alter the cycling of carbon and other bio-active elements in the ocean. Both decreasing calcification and enhanced carbon overproduction due to release of extracellular carbohydrates have the potential to increase the CO2 storage capacity of the ocean. Although the significance of such biological responses to CO2 enrichment becomes increasingly evident, our ability to make reliable predictions of their future developments and to quantify their potential ecological and biogeochemical impacts is still in its infancy. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

13.
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14.
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   

15.
Carbon dioxide flux techniques performed during GasEx-98   总被引：2，自引：0，他引：2  
A comprehensive study of air–sea interactions focused on improving the quantification of CO2 fluxes and gas transfer velocities was performed within a large open ocean CO2 sink region in the North Atlantic. This study, GasEx-98, included shipboard measurements of direct covariance CO2 fluxes, atmospheric CO2 profiles, atmospheric DMS profiles, water column mass balances of CO2, and measurements of deliberate SF6–3He tracers, along with air–sea momentum, heat, and water vapor fluxes. The large air–sea differences in partial pressure of CO2 caused by a springtime algal bloom provided high signals for accurate CO2 flux measurements. Measurements were performed over a wind speed range of 1–16 m s−1 during the three-week process study. This first comparison between the novel air-side and more conventional water column measurements of air–sea gas transfer show a general agreement between independent air–sea gas flux techniques. These new advances in open ocean air–sea gas flux measurements demonstrate the progress in the ability to quantify air–sea CO2 fluxes on short time scales. This capability will help improve the understanding of processes controlling the air–sea fluxes, which in turn will improve our ability to make regional and global CO2 flux estimates.  相似文献   

16.
The effects of low-pH, high-pCO2 conditions on deep-sea organisms were examined during four deep-sea CO2 release experiments simulating deep-ocean C sequestration by the direct injection of CO2 into the deep sea. We examined the survival of common deep-sea, benthic organisms (microbes; macrofauna, dominated by Polychaeta, Nematoda, Crustacea, Mollusca; megafauna, Echinodermata, Mollusca, Pisces) exposed to low-pH waters emanating as a dissolution plume from pools of liquid carbon dioxide released on the seabed during four abyssal CO2-release experiments. Microbial abundance in deep-sea sediments was unchanged in one experiment, but increased under environmental hypercapnia during another, where the microbial assemblage may have benefited indirectly from the negative impact of low-pH conditions on other taxa. Lower abyssal metazoans exhibited low survival rates near CO2 pools. No urchins or holothurians survived during 30–42 days of exposure to episodic, but severe environmental hypercapnia during one experiment (E1; pH reduced by as much as ca. 1.4 units). These large pH reductions also caused 75% mortality for the deep-sea amphipod, Haploops lodo, near CO2 pools. Survival under smaller pH reductions (ΔpH<0.4 units) in other experiments (E2, E3, E5) was higher for all taxa, including echinoderms. Gastropods, cephalopods, and fish were more tolerant than most other taxa. The gastropod Retimohnia sp. and octopus Benthoctopus sp. survived exposure to pH reductions that episodically reached −0.3 pH units. Ninety percent of abyssal zoarcids (Pachycara bulbiceps) survived exposure to pH changes reaching ca. −0.3 pH units during 30–42 day-long experiments.  相似文献   

17.
Strong seasonal patterns in upper ocean total carbon dioxide (TCO2), alkalinity (TA) and calculated pCO2 were observed in a time series of water column measurements collected at the US Joint Global Ocean Flux Study (JGOFS) BATS site (31 °50′N, 64 °10′W) in the Sargasso Sea. TA distribution was a conservative function of salinity. However, in February 1992, a non-conservative decrease in TA was observed, with maximum depletion of 25–30 μmoles kg−1 occuring in the surface layer and at the depth of the chlorophyll maximum (˜ 80–100 m). Mixed-layer TCO2 also decreased, while surface pCO2 increased by 25–30 μatm. We suggest these changes in carbon dioxide species resulted from open-ocean calcification by carbonate-secreting organisms rather than physical processes. Coccolithophore calcification is the most likely cause of this event although calcification by foraminifera or pteropods cannot be ruled out. Due to the transient increase in surface pCO2, the net annual transfer of CO2 into the ocean at BATS was reduced. These observations demonstrate the potential importance of open-ocean calcification and biological community structure in the biogeochemical cycling of carbon.  相似文献   

18.
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   

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.
An increase in the level of atmospheric carbon dioxide (CO2) and the resultant rise in CO2 in seawater alter the inorganic carbon concentrations of seawater. This change, known as ocean acidification, ...  相似文献   

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