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1.
海洋对人为CO2吸收的三维模式研究   总被引：1，自引：0，他引：1  
文中用包含海洋化学过程和一个简单生物过程的三维碳循环模式模拟了海洋对大气CO2的吸收,并分析了碳吸收的纬度分布。模拟工业革命以来海洋对大气CO2的吸收表明:海洋碳吸收再加上大气CO2的增加只占由化石燃料燃烧、森林砍伐和土地利用的变化而释放到大气中的CO2的2/3。1980～1989年期间海洋年平均吸收2.05GtC。海洋人为CO2的吸收有明显的纬度特征。模式计算的海洋CO2的吸收在总量与纬度分布上与观测结果比较相符。  相似文献   

2.
A three-dimensional ocean carbon cycle model which is a general circulation model coupled with simple biogeochemical processes is used to simulate CO2 uptake by the ocean.The OGCM used is a modified version of the Geophysical Fluid Dynamics Laboratory modular ocean model(MOM2).The ocean chemistry and a simple ocean biota model are included.Principal variablesare total CO2,alkalinity and phosphate.The vertical profile of POC flux observed by sediment traps is adopted,the rain ratio,a ratio of production rate of calcite against that of POC,and the bio-production efficiency should be 0.06 and 2 per year,separately.The uptake of anthropogenic CO2 by the ocean is studied.Calculated oceanic uptake of anthropogenic CO2 during the 1980s is 2.05×1015g(Pg)per year.The regional distributions of global oceanic CO2 are discussed.  相似文献   

3.
Using a global carbon cycle model (GLOCO) that considers seven terrestrial biomes, surface and deep ocean layers based on the HILDA model and a single mixed atmosphere, we analyzed the response of atmospheric CO2 concentration and oceanic DIC and DOC depth profiles to additions of carbon to the atmosphere and ocean. The rate of transport of carbon to the deepest oceanic layers is rather insensitive to the atmosphereic-ocean surface gas exchange coefficient over a wide range, hence discrepancies between researchers on the precise global average value of this coefficient do not significantly affect predictions of atmospheric response to anthropogenic inputs. Upwelling velocity, on the other hand, amplifies oceanic response by increasing primary production in the upper ocean layers, resulting in a larger flux into DOC and sediments and increased carbon storage; experiments to reduce the uncertainty in this parameter would be valuable.The location of the carbon addition, whether it is released in the atmosphere or in the middle of the oceanic thermocline, has a significant impact on the maximum atmospheric CO2 concentration (pCO2) subsequently reached, suggesting that oceanic burial of a significant fraction of carbon emissions (e.g. via clathrate hydrides) may be an important management option for limiting pCO2 buildup. Our analysis indicates that the effectiveness of ocean burial decreases asymptotically below about 1000 m depth. With a constant emissions scenario (at 1990 levels), pCO2 at year 2100 is reduced from 501 ppmv considering all emissions go to the atmosphere, to 422 ppmv with ocean burial at a depth of 1000 m of 50% of the fossil fuel emissions. An alternative scenario looks at stabilizing pCO2 at 450 ppmv; with no ocean burial of fossil fuel emissions, the rate of emissions has to be cut drastically after the year 2010, whereas oceanic burial of 2 GtC/yr allows for a smoother transition to alternative energy sources.  相似文献   

4.
Empirical investigations have indicated that projections of future atmospheric carbon dioxide concentrations of a quality quite adequate for practical questions regarding the environmental threat of anthropogenic carbon dioxide emissions and its relationship to energy use policy could be made with the simple assumption that a constant fraction of these emissions would be retained by the atmosphere. By analysis of the structural behavior of equations describing the transfer of carbon and carbon dioxide between their several reservoirs we have been able to demonstrate that this characteristic can be explained to result from approximately linear behavior and exponentially growing carbon dioxide release rates, combined with fitting of carbon cycle model parameters to the last twenty years of observed atmospheric carbon dioxide growth. These conclusions are independent of the details of carbon cycle model structure for projections up to 100 years into the future as long as the growth in atmospheric carbon dioxide release rates is sufficiently high, of the order of 1.5% per annum or more, as referenced to p re-industrial (steady state) conditions. At low rates of growth, when the longer response times of the carbon cycling system become important, for most energy use projections the resultant CO2 induced climate changes are small and the uncertainties in predicted atmospheric carbon dioxide level are thus not important. A possible exception to this condition occurs for scenarios of future fossil fuel use rates designed to avoid atmospheric CO2 levels exceeding a chosen threshold. In this instance details of carbon cycle model structure could significantly affect conclusions that might be drawn concerning future energy use policies; however, it is possible that such a result stems from inappropriate specification of a criterion for an environmental threat, rather than from inherent inadequacy of current carbon cycle models. Recent carbon cycle model developments postulate transfer processes of carbon into the deep ocean, large carbon storage reservoir at rates much higher than in the models we have analysed. If the existence of such mechanisms is confirmed, and they are found to be sufficiently rapid and large, some of our conclusions regarding the use of the constant fractional retention assumption may have to be modified. Currently at the Gas Research Institute, 8600 West Bryn, Mawr Ave., Chicago, IL 60631, U.S.A.  相似文献   

5.
Data concerning carbon cycle variations on the earth's surface during the past 200,000 years are reviewed.The variations of the surface temperature (T) and concentration of carbon dioxide (CO2) in the atmosphere of Antarctica are compared to those of the isotopic ratios of oxygen 18O/16O (δ18O) and of carbon 13C/12C (°13C) of waters in the deep oceans for the two last glacial cycles. This comparison shows that the decrease of the atmospheric CO2 concentration is accompanied by a carbon transferase from the continental biosphere to the oceanic deep waters. At the glacial maximum this transfer is estimated to be about 500 GtC (1 GtC = 1015g of carbon) equivalent to 25% of the carbon storage of the biosphere. It occurs mainly in the high latitudes of the Southern Hemisphere by incorporation of CO2 into particulate matter during photosynthesis. It is shown that the mean oceanic productivity does not increase with a supplementary supply of ions such as phosphate (PO43−) or nitrate (NO3−) but that the intensity of the thermohaline circulation is certainly reduced. As the warming up of the oceans and the melting of the ice-sheet begin carbon transfer takes place to restore the continental biosphere.Another carbon transfer of a much more important intensity is also at work in the sea shore environment. Its intensity could be sufficient to renew the entire carbon of the continental biospheric, atmospheric and oceanic reservoirs in a length of time comparable to a glacial cycle. This fact shows the importance of studying the deposition of carbon in oceanic zones which are uncovered with drops in sea level. At the present time data on the coastal environment in relation to the global carbon cycle are very scarce and warrants more research in this area.  相似文献   

6.
A new complex earth system model consisting of an atmospheric general circulation model, an ocean general circulation model, a three-dimensional ice sheet model, a marine biogeochemistry model, and a dynamic vegetation model was used to study the long-term response to anthropogenic carbon emissions. The prescribed emissions follow estimates of past emissions for the period 1751–2000 and standard IPCC emission scenarios up to the year 2100. After 2100, an exponential decrease of the emissions was assumed. For each of the scenarios, a small ensemble of simulations was carried out. The North Atlantic overturning collapsed in the high emission scenario (A2) simulations. In the low emission scenario (B1), only a temporary weakening of the deep water formation in the North Atlantic is predicted. The moderate emission scenario (A1B) brings the system close to its bifurcation point, with three out of five runs leading to a collapsed North Atlantic overturning circulation. The atmospheric moisture transport predominantly contributes to the collapse of the deep water formation. In the simulations with collapsed deep water formation in the North Atlantic a substantial cooling over parts of the North Atlantic is simulated. Anthropogenic climate change substantially reduces the ability of land and ocean to sequester anthropogenic carbon. The simulated effect of a collapse of the deep water formation in the North Atlantic on the atmospheric CO2 concentration turned out to be relatively small. The volume of the Greenland ice sheet is reduced, but its contribution to global mean sea level is almost counterbalanced by the growth of the Antarctic ice sheet due to enhanced snowfall. The modifications of the high latitude freshwater input due to the simulated changes in mass balance of the ice sheet are one order of magnitude smaller than the changes due to atmospheric moisture transport. After the year 3000, the global mean surface temperature is predicted to be almost constant due to the compensating effects of decreasing atmospheric CO2 concentrations due to oceanic uptake and delayed response to increasing atmospheric CO2 concentrations before.  相似文献   

7.
Summary A series of sensitivity runs have been performed with a coupled climate–carbon cycle model. The climatic component consists of the climate model of intermediate complexity IAP RAS CM. The carbon cycle component is formulated as a simple zero-dimensional model. Its terrestrial part includes gross photosynthesis, and plant and soil respirations, depending on temperature via Q 10-relationships (Lenton, 2000). Oceanic uptake of anthropogenic carbon is formulated is a bi-linear function of tendencies of atmospheric concentration of CO2 and globally averaged annual mean sea surface temperature. The model is forced by the historical industrial and land use emissions of carbon dioxide for the second half of the 19th and the whole of the 20th centuries, and by the emission scenario SRES A2 for the 21st century. For the standard set of the governing parameters, the model realistically captures the main features of the Earth’s observed carbon cycle. A large number of simulations have been performed, perturbing the governing parameters of the terrestrial carbon cycle model. In addition, the climate part is perturbed, either by zeroing or artificially increasing the climate model sensitivity to the doubling of the atmospheric CO2 concentration. Performing the above mentioned perturbations, it is possible to mimic most of the range found in the C4MIP simulations. In this way, a wide range of the climate–carbon cycle feedback strengths is obtained, differing even in the sign of the feedback. If the performed simulations are subjected to the constraints of a maximum allowed deviation of the simulated atmospheric CO2 concentration (pCO2(a)) from the observed values and correspondence between simulated and observed terrestrial uptakes, it is possible to narrow the corresponding uncertainty range. Among these constraints, considering pCO2(a) and uptakes are both important. However, the terrestrial uptakes constrain the simulations more effectively than the oceanic ones. These constraints, while useful, are still unable to rule out both extremely strong positive and modest negative climate–carbon cycle feedback.  相似文献   

8.
Ocean iron fertilization has been proposed as a method to mitigate anthropogenic climate change, and there is continued commercial interest in using iron fertilization to generate carbon credits. It has been further speculated that ocean iron fertilization could help mitigate ocean acidification. Here, using a global ocean carbon cycle model, we performed idealized ocean iron fertilization simulations to place an upper bound on the effect of iron fertilization on atmospheric CO2 and ocean acidification. Under the IPCC A2 CO2 emission scenario, at year 2100 the model simulates an atmospheric CO2 concentration of 965 ppm with the mean surface ocean pH 0.44 units less than its pre-industrial value of 8.18. A globally sustained ocean iron fertilization could not diminish CO2 concentrations below 833 ppm or reduce the mean surface ocean pH change to less than 0.38 units. This maximum of 0.06 unit mitigation in surface pH change by the end of this century is achieved at the cost of storing more anthropogenic CO2 in the ocean interior, furthering acidifying the deep-ocean. If the amount of net carbon storage in the deep ocean by iron fertilization produces an equivalent amount of emission credits, ocean iron fertilization further acidifies the deep ocean without conferring any chemical benefit to the surface ocean.  相似文献   

9.
The increase of atmospheric CO2 concentrations due to anthropogenic activities is substantially damped by the ocean, whose CO2 uptake is determined by the state of the ocean, which in turn is influenced by climate change. We investigate the mechanisms of the ocean’s carbon uptake within the feedback loop of atmospheric CO2 concentration, climate change and atmosphere/ocean CO2 flux. We evaluate two transient simulations from 1860 until 2100, performed with a version of the Max Planck Institute Earth System Model (MPI-ESM) with the carbon cycle included. In both experiments observed anthropogenic CO2 emissions were prescribed until 2000, followed by the emissions according to the IPCC Scenario A2. In one simulation the radiative forcing of changing atmospheric CO2 is taken into account (coupled), in the other it is suppressed (uncoupled). In both simulations, the oceanic carbon uptake increases from 1 GT C/year in 1960 to 4.5 GT C/year in 2070. Afterwards, this trend weakens in the coupled simulation, leading to a reduced uptake rate of 10% in 2100 compared to the uncoupled simulation. This includes a partial offset due to higher atmospheric CO2 concentrations in the coupled simulation owing to reduced carbon uptake by the terrestrial biosphere. The difference of the oceanic carbon uptake between both simulations is primarily due to partial pressure difference and secondary to solubility changes. These contributions are widely offset by changes of gas transfer velocity due to sea ice melting and wind changes. The major differences appear in the Southern Ocean (?45%) and in the North Atlantic (?30%), related to reduced vertical mixing and North Atlantic meridional overturning circulation, respectively. In the polar areas, sea ice melting induces additional CO2 uptake (+20%).  相似文献   

10.
Climate change mitigation via a reduction in the anthropogenic emissions of carbon dioxide (CO2) is the principle requirement for reducing global warming, its impacts, and the degree of adaptation required. We present a simple conceptual model of anthropogenic CO2 emissions to highlight the trade off between delay in commencing mitigation, and the strength of mitigation then required to meet specific atmospheric CO2 stabilization targets. We calculate the effects of alternative emission profiles on atmospheric CO2 and global temperature change over a millennial timescale using a simple coupled carbon cycle-climate model. For example, if it takes 50 years to transform the energy sector and the maximum rate at which emissions can be reduced is ?2.5% $\text{year}^{-1}$ , delaying action until 2020 would lead to stabilization at 540 ppm. A further 20 year delay would result in a stabilization level of 730 ppm, and a delay until 2060 would mean stabilising at over 1,000 ppm. If stabilization targets are met through delayed action, combined with strong rates of mitigation, the emissions profiles result in transient peaks of atmospheric CO2 (and potentially temperature) that exceed the stabilization targets. Stabilization at 450 ppm requires maximum mitigation rates of ?3% to ?5% $\text{year}^{-1}$ , and when delay exceeds 2020, transient peaks in excess of 550 ppm occur. Consequently tipping points for certain Earth system components may be transgressed. Avoiding dangerous climate change is more easily achievable if global mitigation action commences as soon as possible. Starting mitigation earlier is also more effective than acting more aggressively once mitigation has begun.  相似文献   

11.
Carbon dioxide removal (CDR) is the only geoengineering technique that allows negative emissions and the reduction of anthropogenic carbon in the atmosphere. Since the time scales of the global carbon cycle are largely driven by the exchanges with the natural oceanic stocks, the implementation of CDR actions is anticipated to create outgassing from the ocean that may reduce their efficiency. The adjustment of the natural carbon cycle to CDR was studied with a numerical Earth System Model, focusing on the oceanic component and considering two idealized families of CDR policies, one based on a target atmospheric concentration and one based on planned negative emissions. Results show that both actions are anticipated to release the anthropogenic carbon stored in the surface ocean, effectively increasing the required removal effort. The additional negative emissions are expected to be lower when the CDR policy is driven by planned removal rates without prescribing a target atmospheric CO2 concentration.  相似文献   

12.
A global ocean general circulation model (L30T63) is employed to study the uptake and distribution of anthropogenic CO2 in the ocean. A subgrid-scale mixing scheme called GM90 is used in the model. There are two main GM90 parameters including isopycnal diffusivity and skew (thickness) diffusivity. Sensitivities of the ocean circulation and the redistribution of dissolved anthropogenic CO2 to these two parameters are examined. Two runs estimate the global oceanic anthropogenic CO2 uptake to be 1.64 and 1.73 Pg C yr-1 for the 1990s, and that the global ocean contained 86.8 and 92.7 Pg C of anthropogenic CO2 at the end of 1994, respectively. Both the total inventory and uptake from our model are smaller than the data-based estimates. In this presentation, the vertical distributions of anthropogenic CO2 at three meridional sections are discussed and compared with the available data-based estimates. The inventory in the individual basins is also calculated. Use of large isopycnal diffusivity can generally improve the simulated results, including the exchange flux, the vertical distribution patterns, inventory, storage, etc. In terms of comparison of the vertical distributions and column inventory, we find that the total inventory in the Pacific Ocean obtained from our model is in good agreement with the data-based estimate, but a large difference exists in the Atlantic Ocean, particularly in the South Atlantic. The main reasons are weak vertical mixing and that our model generates small exchange fluxes of anthropogenic CO2 in the Southern Ocean. Improvement in the simulation of the vertical transport and sea ice in the Southern Ocean is important in future work.  相似文献   

13.
The contribution of deforestation in Russia to the anthropogenic emission of carbon dioxide (CO2) in 1990–2013 is estimated using the methods of computational monitoring. It is found that since 1990 the area of deforestation and forest conversion to other land-use categories is equal to 628.4 x 103 ha. The respective CO2 emissions from deforestation in Russia for the whole analyzed period are estimated at 142200 kt CO2 with the average annual value of 5900 + 2270 kt CO2/year. The largest contribution to the total losses is made by the changes in soil carbon stock (41.6%) and biomass carbon losses (28.8%). CO2 emissions from deforestation make an insignificant contribution to the total anthropogenic CO2 emission in the country (0.2%). Among the CO2 sources in the land use, land-use change, and forestry sector (LULUCF), the emission from deforestation is the lowest with the average for 1990–2013 contribution of about 0.6%.  相似文献   

14.
A basin-wide ocean general circulation model(OGCM) of the Pacific Ocean is employed to estimate the uptake and storage of anthropogenic CO 2 using two different simulation approaches.The simulation(named BIO) makes use of a carbon model with biological processes and full thermodynamic equations to calculate surface water partial pressure of CO 2,whereas the other simulation(named PTB) makes use of a perturbation approach to calculate surface water partial pressure of anthropogenic CO 2.The results from the two simulations agree well with the estimates based on observation data in most important aspects of the vertical distribution as well as the total inventory of anthropogenic carbon.The storage of anthropogenic carbon from BIO is closer to the observation-based estimate than that from PTB.The Revelle factor in 1994 obtained in BIO is generally larger than that obtained in PTB in the whole Pacific,except for the subtropical South Pacific.This,to large extent,leads to the difference in the surface anthropogenic CO 2 concentration between the two runs.The relative difference in the annual uptake between the two runs is almost constant during the integration processes after 1850.This is probably not caused by dissolved inorganic carbon(DIC),but rather by a factor independent of time.In both runs,the rate of change in anthropogenic CO 2 fluxes with time is consistent with the rate of change in the growth rate of atmospheric partial pressure of CO 2.  相似文献   

15.
The simulation model accounts for four major compartments in the global carbon cycle: atmosphere, ocean, terrestrial biosphere and fossil carbon reservoir. The ocean is further compartmentalized into a high and a low latitude surface layer, and into 10 deep sea strata. The oceanic carbon fluxes are caused by massflow of descending and upwelling water, by precipitation of organic material and by diffusion exchange.The biosphere is horizontally subdivided into six ecosystems and vertically into leaves, branches, stemwood, roots, litter, young humus and stable soil carbon. Deforestation, slash and burn agriculture, rangeland burning and shifts in land use have been included. The atmosphere is treated as one well mixed reservoir. Fossil fuel consumption is simulated with historic data, and with IIASA scenario's for the future. Using the low IIASA scenario an atmospheric CO2 concentration of 431 ppmv is simulated for 2030 AD. A sensitivity analysis shows the importance of different parameters and of human behaviour. Notwithstanding the large size of the biosphere fluxes, the atmospheric CO2 concentration in the next century will be predominantly determined by the growth rate of fossil fuel consumption.  相似文献   

16.
The uptake and storage of anthropogenic carbon in the North Atlantic is investigated using different configurations of ocean general circulation/carbon cycle models. We investigate how different representations of the ocean physics in the models, which represent the range of models currently in use, affect the evolution of CO2 uptake in the North Atlantic. The buffer effect of the ocean carbon system would be expected to reduce ocean CO2 uptake as the ocean absorbs increasing amounts of CO2. We find that the strength of the buffer effect is very dependent on the model ocean state, as it affects both the magnitude and timing of the changes in uptake. The timescale over which uptake of CO2 in the North Atlantic drops to below preindustrial levels is particularly sensitive to the ocean state which sets the degree of buffering; it is less sensitive to the choice of atmospheric CO2 forcing scenario. Neglecting physical climate change effects, North Atlantic CO2 uptake drops below preindustrial levels between 50 and 300 years after stabilisation of atmospheric CO2 in different model configurations. Storage of anthropogenic carbon in the North Atlantic varies much less among the different model configurations, as differences in ocean transport of dissolved inorganic carbon and uptake of CO2 compensate each other. This supports the idea that measured inventories of anthropogenic carbon in the real ocean cannot be used to constrain the surface uptake. Including physical climate change effects reduces anthropogenic CO2 uptake and storage in the North Atlantic further, due to the combined effects of surface warming, increased freshwater input, and a slowdown of the meridional overturning circulation. The timescale over which North Atlantic CO2 uptake drops to below preindustrial levels is reduced by about one-third, leading to an estimate of this timescale for the real world of about 50 years after the stabilisation of atmospheric CO2. In the climate change experiment, a shallowing of the mixed layer depths in the North Atlantic results in a significant reduction in primary production, reducing the potential role for biology in drawing down anthropogenic CO2.  相似文献   

17.
The drivers of Chinese CO2 emissions from 1980 to 2030   总被引：4，自引：0，他引：4  
China's energy consumption doubled within the first 25 years of economic reforms initiated at the end of the 1970s, and doubled again in the past 5 years. It has resulted of a threefold CO2 emissions increase since early of 1980s. China's heavy reliance on coal will make it the largest emitter of CO2 in the world. By combining structural decomposition and input–output analysis we seek to assess the driving forces of China's CO2 emissions from 1980 to 2030. In our reference scenario, production-related CO2 emissions will increase another three times by 2030. Household consumption, capital investment and growth in exports will largely drive the increase in CO2 emissions. Efficiency gains will be partially offset the projected increases in consumption, but our scenarios show that this will not be sufficient if China's consumption patterns converge to current US levels. Relying on efficiency improvements alone will not stabilize China's future emissions. Our scenarios show that even extremely optimistic assumptions of widespread installation of carbon dioxide capture and storage will only slow the increase in CO2 emissions.  相似文献   

18.
The ongoing human-induced emission of carbon dioxide (CO2) threatens to change the earth's climate. One possible way of decreasing CO2 emissions is to apply CO2 removal, which involves recovering of carbon dioxide from energy conversion processes and storing it outside the atmosphere. Since the 1980's, the possibilities for recovering CO2 from thermal power plants received increasing attention.In this study possible techniques of recovering CO2 from large-scale industrial processes are assessed.In some industrial processes, e.g. ammonia production, CO2 is recovered from the process streams to prevent it from interfering with the production process. The CO2 thus recovered can easily be dehydrated and compressed, at low cost. In the iron and steel industry, carbon dioxide can be recovered from blast furnace gas. In the petrochemical industry CO2 can be recovered from flue gases, using low-temperature heat for the separation process.Carbon dioxide can be recovered from large-scale industrial processes and in some cases the cost of recovery is significantly less than CO2 recovery from thermal power plants. Therefore this option should be studied further and should be considered if carbon dioxide removal is introduced on a wide scale.  相似文献   

19.
Presented is the assessment of the contribution that such major types of the land use in Russia as arable lands, forage lands, settlements, and peatery make to anthropogenic fluxes of carbon dioxide CO2, methane CH4, and nitrogen oxide N2O, The assessment is based on the methods of computation monitoring carried out in the period from 2000 to 2011. The results of the study demonstrated that every year arable lands cause the emission of CO2 and N2O of about 117.0 and 74.9 million t CO2 equiv, and peatery, 0.54 and 105.4 thousand t CO2 equiv, respectively. The balance of soil carbon in hayfields and pastures is close to zero. The average emissions of CH4 and N2O from the manure of pasture animals amount to 0.2 and 5.0 million t CO2 equiv/year, and those from grass fires, 276.1 and 372.5 thousand t CO2 equiv/year, respectively. The carbon balance in permanent soils of settlements is also almost close to zero, and newly built-up lands are the source of CO2 (9.5 million t/year). The natural overgrowing of fallow lands leads to the accumulation of the soil carbon (about 92.4 million t CO2/year). It was revealed that the intensity of CO2 emission is defined by the soil carbon balance and that of other gases, by the amount of nitrogen fertilizers, plant residues, and manure coming to the soil. The total emission from the land use is 106.9 million t CO2 equiv/year that makes up 4.9% of the total anthropogenic emission of greenhouse gases in the Russian Federation.  相似文献   

20.
We present several equilibrium runs under varying atmospheric CO2 concentrations using the University of Victoria Earth System Climate Model (UVic ESCM). The model shows two very different responses: for CO2 concentrations of 400 ppm or lower, the system evolves into an equilibrium state. For CO2 concentrations of 440 ppm or higher, the system starts oscillating between a state with vigorous deep water formation in the Southern Ocean and a state with no deep water formation in the Southern Ocean. The flushing events result in a rapid increase in atmospheric temperatures, degassing of CO2 and therefore an increase in atmospheric CO2 concentrations, and a reduction of sea ice cover in the Southern Ocean. They also cool the deep ocean worldwide. After the flush, the deep ocean warms slowly again and CO2 is taken up by the ocean until the stratification becomes unstable again at high latitudes thousands of years later. The existence of a threshold in CO2 concentration which places the UVic ESCM in either an oscillating or non-oscillating state makes our results intriguing. If the UVic ESCM captures a mechanism that is present and important in the real climate system, the consequences would comprise a rapid increase in atmospheric carbon dioxide concentrations of several tens of ppm, an increase in global surface temperature of the order of 1–2°C, local temperature changes of the order of 6°C and a profound change in ocean stratification, deep water temperature and sea ice cover.  相似文献   

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