海洋对人为CO2吸收的三维模式研究

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。     

海洋对人为CO2吸收的三维模式研究

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。1 980～ 1 989年期间海洋年平均吸收 2 .0 5Gt C。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。     

Estimates of anthropogenic CO<Subscript>2</Subscript> uptake in a global ocean model

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.     

Uptake and Storage of Anthropogenic CO2 in the Pacific Ocean Estimated Using Two Modeling Approaches

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.     

Ocean dynamics determine the response of oceanic CO2 uptake to climate change

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%).     

The Variability of Air-sea O2 Flux in CMIP6: Implications for Estimating Terrestrial and Oceanic Carbon Sinks

The measurement of atmospheric O₂ concentrations and related oxygen budget have been used to estimate terrestrial and oceanic carbon uptake. However, a discrepancy remains in assessments of O₂ exchange between ocean and atmosphere (i.e. air-sea O₂ flux), which is one of the major contributors to uncertainties in the O₂-based estimations of the carbon uptake. Here, we explore the variability of air-sea O₂ flux with the use of outputs from Coupled Model Intercomparison Project phase 6 (CMIP6). The simulated air-sea O₂ flux exhibits an obvious warming-induced upward trend (~1.49 Tmol yr^?2) since the mid-1980s, accompanied by a strong decadal variability dominated by oceanic climate modes. We subsequently revise the O₂-based carbon uptakes in response to this changing air-sea O₂ flux. Our results show that, for the 1990?2000 period, the averaged net ocean and land sinks are 2.10±0.43 and 1.14±0.52 GtC yr^?1 respectively, overall consistent with estimates derived by the Global Carbon Project (GCP). An enhanced carbon uptake is found in both land and ocean after year 2000, reflecting the modification of carbon cycle under human activities. Results derived from CMIP5 simulations also investigated in the study allow for comparisons from which we can see the vital importance of oxygen dataset on carbon uptake estimations.     

海洋中碳及营养物自然分布的数值模拟

用海洋生物化学环流模式（Ｂ－ ＧＣＭ） 模拟了工业化前碳及营养物在海洋中的分布, 并得到了较为合理的结果。模式考虑了海洋表面化学和一个简单的生物过程。模式的主要预报变量有总ＣＯ２ 、碱度和磷酸盐。决定生物化学物质分布的三个参数的取值为： ＰＯＣ 通量的垂直廓线的指数ａ 取观测值０－８５８ 、生物生产效率ｒ ＝ ２／ 年和下落比Ｒ＝ ０－０６ 。用Ｂ－ＧＣＭ 模拟出的结果与ＧＥＯＳＥＣＳ观测值基本相符。     

A simple carbon cycle representation for economic and policy analyses

Integrated Assessment Models (IAMs) that couple the climate system and the economy require a representation of ocean CO₂ uptake to translate human-produced emissions to atmospheric concentrations and in turn to climate change. The simple linear carbon cycle representations in most IAMs are not however physical at long timescales, since ocean carbonate chemistry makes CO₂ uptake highly nonlinear. No linearized representation can capture the ocean’s dual-mode behavior, with initial rapid uptake and then slow equilibration over ∽10,000 years. In a business-as-usual scenario followed by cessation of emissions, the carbon cycle in the 2007 version of the most widely used IAM, DICE (Dynamic Integrated model of Climate and the Economy), produces errors of ∽2^°C by the year 2300 and ∽6^°C by the year 3500. We suggest here a simple alternative representation that captures the relevant physics and show that it reproduces carbon uptake in several more complex models to within the inter-model spread. The scheme involves little additional complexity over the DICE model, making it a useful tool for economic and policy analyses.     

Estimates of Anthropogenic CO_2 Uptake in a Global Ocean Model

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 ...     

Factors influencing anthropogenic carbon dioxide uptake in the North Atlantic in models of the ocean carbon cycle

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.     

长江三角洲地区净生态系统二氧化碳通量及浓度的数值模拟

净生态系统碳通量(NEE)的计算对于准确模拟区域碳通量和大气CO₂浓度的时空变化至关重要。本文利用中尺度大气-温室气体耦合模式WRF-GHG(Weather Research and Forecasting Model with Greenhouse Gases Module),对2010年7月28日至2010年8月2日期间影响长江三角洲地区大气CO₂浓度及时空分布的各种过程进行了详尽模拟。结果表明,植被光合呼吸模型(VPRM)能模拟不同植被下垫面NEE的日变化;WRF-GHG模拟的大气CO₂浓度日变化与观测相吻合,但低估了大气CO₂浓度5~15 ppm(ppm表示10-6),这可能与人为排放源的低估、VPRM参数的不确定性以及气象场模拟的不准确性有关。太湖和植被覆盖较好的地区如浙江北部山区是该地区的主要碳汇,而城市为CO₂的主要排放源。太湖和陆地生态系统对区域内碳循环起到一定的调节作用,减缓区域大气CO₂浓度的升高。此外,局地气象条件如湖陆风对太湖周边地区大气CO₂浓度有显著影响。     

Learning about the ocean carbon cycle from observational constraints and model simulations of multiple tracers

A key question in studies of the potential for reducing uncertainty in climate change projections is how additional observations may be used to constrain models. We examine the case of ocean carbon cycle models. The reliability of ocean models in projecting oceanic CO₂ uptake is fundamentally dependent on their skills in simulating ocean circulation and air–sea gas exchange. In this study we demonstrate how a model simulation of multiple tracers and utilization of a variety of observational data help us to obtain additional information about the parameterization of ocean circulation and air–sea gas exchange, relative to approaches that use only a single tracer. The benefit of using multiple tracers is based on the fact that individual tracer holds unique information with regard to ocean mixing, circulation, and air–sea gas exchange. In a previous modeling study, we have shown that the simulation of radiocarbon enables us to identify the importance of parameterizing sub-grid scale ocean mixing processes in terms of diffusive mixing along constant density surface (isopycnal mixing) and the inclusion of the effect of mesoscale eddies. In this study we show that the simulation of phosphate, a major macronutrient in the ocean, helps us to detect a weak isopycnal mixing in the upper ocean that does not show up in the radiocarbon simulation. We also show that the simulation of chlorofluorocarbons (CFCs) reveals excessive upwelling in the Southern Ocean, which is also not apparent in radiocarbon simulations. Furthermore, the updated ocean inventory data of man-made radiocarbon produced by nuclear tests (bomb ¹⁴C) enable us to recalibrate the rate of air–sea gas exchange. The progressive modifications made in the model based on the simulation of additional tracers and utilization of updated observational data overall improve the model’s ability to simulate ocean circulation and air–sea gas exchange, particularly in the Southern Ocean, and has great consequence for projected CO₂ uptake. Simulated global ocean uptake of anthropogenic CO₂ from pre-industrial time to the present day by both previous and updated models are within the range of observational-based estimates, but with substantial regional difference, especially in the Southern Ocean. By year 2100, the updated model estimated CO₂ uptake are 531 and 133 PgC (1PgC?=?10¹⁵ gram carbon) for the global and Southern Ocean respectively, whereas the previous version model estimated values are 540 and 190 PgC.     

Oceanic transport and storage of carbon emissions

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.     

On the response of the oceanic wind-driven circulation to atmospheric CO2 increase

A global, flux-corrected climate model is employed to predict the surface wind stress and associated wind-driven oceanic circulation for climate states corresponding to a doubling and quadrupling of the atmospheric CO₂ concentration in a simple 1% per year CO₂ increase scenario. The model indicates that in response to CO₂ increase, the position of zero wind stress curl in the mid-latitudes of the Southern Hemisphere shifts poleward. In addition, the wind stress intensifies significantly in the mid-latitudes of the Southern Hemisphere. As a result, the rate of water circulation in the subpolar meridional overturning cell in the Southern Ocean increases by about 6 Sv (1 Sv=10⁶ m³ s⁻¹) for doubled CO₂ and by 12 Sv for quadrupled CO₂, implying an increase of deep water upwelling south of the circumpolar flow and an increase of Ekman pumping north of it. In addition, the changes in the wind stress and wind stress curl translate into changes in the horizontal mass transport, leading to a poleward expansion of the subtropical gyres in both hemispheres, and to strengthening of the Antarctic Circumpolar Current. Finally, the intensified near-surface winds over the Southern Ocean result in a substantial increase of mechanical energy supply to the ocean general circulation.     

Simulation of ~(14)C in IAP/LASG L30T63 Ocean Model

1. Introduction14C is a radioactive isotope of carbon, whose halftime is about 5730 yr. Under natural circumstance,14C comes into being in the stratosphere because of thenitrogen explosion of cosmic radial. 14C is mixed inthe atmosphere, absorbed by oceans, and then trans-ported into deep ocean. 14C radioactively reduces asits age increases. The reduction process of 14C canuncover the evolvement process of sea water's age andrenewal time.14 C content is usually described with one in athousan…     

Projected impact of deep ocean carbon dioxide discharge on atmospheric CO2 concentrations

An evaluation of oceanic containment strategies for anthropogenic carbon dioxide is presented. Energy conservation is also addressed through an input hydrocarbon-fuel consumption function. The effectiveness of the proposed countermeasures is determined from atmospheric CO₂ concentration predictions. A previous box model with a diffusive deep ocean is adapted and applied to the concept of fractional CO₂ injection in 500 m deep waters. Next, the contributions of oceanic calcium carbonate sediment dissolution, and of deep seawater renewal, are included. Numerical results show that for CO₂ direct removal measures to be effective, large fractions of anthropogenic carbon dioxide have to be processed. This point favors fuel pre-processing concepts. The global model also indicates that energy conservation, i.e. a hydrocarbon-fuel consumption slowdown, remains the most effective way to mitigate the greenhouse effect, because it offers mankind a substantial time delay to implement new energy production alternatives.     

A global ocean biogeochemistry general circulation model and its simulations

An ocean biogeochemistry model was developed and incorporated into a global ocean general circulation model (LICOM) to form an ocean biogeochemistry general circulation model (OBGCM). The model was used to study the natural carbon cycle and the uptake and storage of anthropogenic CO2 in the ocean. A global export production of 12.5 Pg C yr-1 was obtained. The model estimated that in the pre-industrial era the global equatorial region within 15o of the equator released 0.97 Pg C yr-1 to the atmosphere, which was balanced by the gain of CO2 in other regions. The post-industrial air-sea CO2 flux indicated the oceanic uptake of CO2 emitted by human activities. An increase of 20－50 mol kg-1 for surface dissolved inorganic carbon (DIC) concentrations in the 1990s relative to pre-industrial times was obtained in the simulation, which was consistent with data-based estimates. The model generated a total anthropogenic carbon inventory of 105 Pg C as of 1994, which was within the range of estimates by other researchers. Various transports of both natural and anthropogenic DIC as well as labile dissolved organic carbon (LDOC) were estimated from the simulation. It was realized that the Southern Ocean and the high-latitude region of the North Pacific are important export regions where accumulative air-sea CO2 fluxes are larger than the DIC inventory, whereas the subtropical regions are acceptance regions. The interhemispheric transport of total natural carbon (DIC+LDOC) was found to be northward (0.11 Pg C yr-1), which was just balanced by the gain of carbon from the atmosphere in the Southern Hemisphere.     

Long-term effects of anthropogenic CO<Subscript>2</Subscript> emissions simulated with a complex earth system model

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.     

Can ocean iron fertilization mitigate ocean acidification?

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.     

Detection of Anthropogenic CO2 Emission Signatures with TanSat CO2 and with Copernicus Sentinel-5 Precursor (S5P) NO2 Measurements: First Results

China’s first carbon dioxide(CO₂) measurement satellite mission, TanSat, was launched in December 2016. This paper introduces the first attempt to detect anthropogenic CO₂ emission signatures using CO₂ observations from TanSat and NO₂ measurements from the TROPOspheric Monitoring Instrument(TROPOMI) onboard the Copernicus Sentinel-5 Precursor(S5P) satellite. We focus our analysis on two selected cases in Tangshan, China and Tokyo, Japan.We found that t...