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1.
The global three-dimensional Lagrangian chemistry-transport model STOCHEM has been used to follow the changes in the tropospheric distributions of the two major radiatively-active trace gases, methane and tropospheric ozone, following the emission of pulses of the short-lived tropospheric ozone precursor species, methane, carbon monoxide, NOx and hydrogen. The radiative impacts of NOx emissionswere dependent on the location chosen for the emission pulse, whether at the surface or in the upper troposphere or whether in the northern or southern hemispheres. Global warming potentials were derived for each of the short-lived tropospheric ozone precursor species by integrating the methane and tropospheric ozone responses over a 100 year time horizon. Indirect radiative forcing due to methane and tropospheric ozone changes appear to be significant for all of the tropospheric ozone precursor species studied. Whereas the radiative forcing from methane changes is likely to be dominated by methane emissions, that from tropospheric ozone changes is controlled by all the tropospheric ozone precursor gases, particularly NOxemissions. The indirect radiative forcing impacts of tropospheric ozone changes may be large enough such that ozone precursors should be considered in the basket of trace gases through which policy-makers aim to combat global climate change.  相似文献   

2.
Oxidation by hydroxyl radicals is the main removal process for organic compounds in the troposphere. This oxidation acts as a source of ozone and as a removal process for hydroxyl and peroxy radicals, thereby reducing the efficiency of methane oxidation and promoting the build-up of methane. Emissions of organic compounds may therefore lead to the build-up of two important radiatively-active trace gases: methane and ozone. Emission pulses of 10 organic compounds were followed in a global 3-D Lagrangian chemistry-transport model to quantify their indirect greenhouse gas impacts through changes induced in the tropospheric distributions of methane and ozone. The main factors influencing the global warming potentials of the 10 organic compounds were found to be their spatial emission patterns, chemical reactivity and transport, molecular complexity and oxidation products formed. The indirect radiative forcing impacts of organic compounds may be large enough that ozone precursors should be considered in the basket of trace gases through which policy-makers aim to combat global climate change.  相似文献   

3.
The effect of anthropogenic emissions from China on global burdens of ozone, sulphate, organic carbon (OC) and black carbon (BC) aerosols is examined, using the three-dimensional chemistry transport model Oslo CTM2. Two model simulations were performed, the first with global present-day emissions and the second with the anthropogenic emissions from China set to their pre-industrial levels. The global radiative forcing for these species is then calculated. Industrial emissions from China are found to account for a 4–5% increase in the global burden of OC aerosol, the change in secondary organic aerosol being slightly less than that of primary organic aerosol. A 10% increase in the global sulphate aerosol burden is calculated, and the increase in BC is 23%. The global radiative forcing of aerosols from China was calculated to be −62, −3.7, −13 and 89 mW m−2, for sulphate, secondary organic, primary organic and BC aerosols, respectively. The increase in ozone causes a forcing of 77 mW m−2.  相似文献   

4.
We use recent advances in time series econometrics to estimate the relation among emissions of CO2 and CH4, the concentration of these gases, and global surface temperature. These models are estimated and specified to answer two questions; (1) does human activity affect global surface temperature and; (2) does global surface temperature affect the atmospheric concentration of carbon dioxide and/or methane. Regression results provide direct evidence for a statistically meaningful relation between radiative forcing and global surface temperature. A simple model based on these results indicates that greenhouse gases and anthropogenic sulfur emissions are largely responsible for the change in temperature over the last 130 years. The regression results also indicate that increases in surface temperature since 1870 have changed the flow of carbon dioxide to and from the atmosphere in a way that increases its atmospheric concentration. Finally, the regression results for methane hint that higher temperatures may increase its atmospheric concentration, but this effect is not estimated precisely.  相似文献   

5.
The concept of global warming potential was developed as a relative measure of the potential effects on climate of a greenhouse gas as compared to CO2. In this paper a series of sensitivity studies examines several uncertainties in determination of Global Warming Potentials (GWPs). For example, the original evaluation of GWPs for the Intergovernmental Panel on Climate Change (IPCC, 1990) did not attempt to account for the possible sinks of carbon dioxide (CO2) that could balance the carbon cycle and produce atmospheric concentrations of CO2 that match observations. In this study, a balanced carbon cycle model is applied in calculation of the radiative forcing from CO2. Use of the balanced model produces up to 21% enhancement of the GWPs for most trace gases compared with the IPCC (1990) values for time horizons up to 100 years, but a decreasing enhancement with longer time horizons. Uncertainty limits of the fertilization feedback parameter contribute a 20% range in GWP values. Another systematic uncertainty in GWPs is the assumption of an equilibrium atmosphere (one in which the concentration of trace gases remains constant) versus a disequilibrium atmosphere (one in which the concentration of trace gases varies with time). The latter gives GWPs that are 19 to 32% greater than the former for a 100 year time horizons, depending upon the carbon dioxide emission scenario chosen. Five scenarios are employed: constant-concentration, constant-emission past 1990 and the three IPCC (1992) emission scenarios. For the analysis of uncertainties in atmospheric lifetime (τ) the GWP changes in direct proportion toτ for short-lived gases, but to a lesser extent for gases withτ greater than the time horizontal for the GWP calculation.  相似文献   

6.
A sensitivity analysis is performed in order to study recently observed changes in atmospheric methane and carbon monoxide trends. For the analysis we have adapted a one-dimensional transport/chemistry model in order to comply with changes in vertical transport, stratosphere-troposphere flux of ozone, the water vapour cycle and the short-wave radiative transfer. In addition we have formulated an improved relationship which expresses the steady state OH concentration in terms of longer lived compounds which has a fair agreement with the one-dimensional model results. An analysis of the observed changes and trends in methane and carbon monoxide shows that both emissions and changes in global OH concentrations can be main causes for the observed changes. Average methane emissions have slowed down, particularly in the NH, in the last five years, though perhaps not very significantly. Carbon monoxide emissions are decreasing faster in the last couple of years than in the period 1983–1990. The study suggests that climate fluctuations (tropospheric water vapour, temperature and convective activity) and the stratospheric ozone depletion (tropospheric UV radiation) have a significant influence on tropospheric composition and thus on trends in methane and carbon monoxide concentrations.The IMAU is partner in the Netherlands Centre for Climate Research (CCR).  相似文献   

7.
Climate policies must consider radiative forcing from Kyoto greenhouse gases, as well as other forcing constituents, such as aerosols and tropospheric ozone that result from air pollutants. Non-Kyoto forcing constituents contribute negative, as well as positive forcing, and overall increases in total forcing result in increases in global average temperature. Non-Kyoto forcing modeling is a relatively new component of climate management scenarios. This paper describes and assesses current non-Kyoto radiative forcing modeling within five integrated assessment models. The study finds negative forcing from aerosols masking (offsetting) approximately 25 % of positive forcing in the near-term in reference non-climate policy projections. However, masking is projected to decline rapidly to 5–10 % by 2100 with increasing Kyoto emissions and assumed reductions in air pollution—with the later declining to as much as 50 % and 80 % below today’s levels by 2050 and 2100 respectively. Together they imply declining importance of non-Kyoto forcing over time. There are however significant uncertainties and large differences across models in projected non-Kyoto emissions and forcing. A look into the modeling reveals differences in base conditions, relationships between Kyoto and non-Kyoto emissions, pollution control assumptions, and other fundamental modeling. In addition, under climate policy scenarios, we find air pollution and resulting non-Kyoto forcing reduced to levels below those produced by air pollution policies alone—e.g., China sulfur emissions fall an additional 45–85 % by 2050. None of the models actively manage non-Kyoto forcing for climate implications. Nonetheless, non-Kyoto forcing may be influencing mitigation results, including allowable carbon dioxide emissions, and further evaluation is merited.  相似文献   

8.
A three-dimensional Lagrangian tropospheric chemistry modelis used toinvestigate the impact of human activities on the tropospheric distributionofozone and hydroxyl radicals. The model describes the behaviour of 50 speciesincluding methane, carbon monoxide, oxides of nitrogen, sulphur dioxide andnineorganic compounds emitted from human activities and a range of other sources.Thechemical mechanism involves about 100 chemical reactions of which 16 arephotochemical reactions whose diurnal dependence is treated in full. The modelutilises a five minute chemistry time step and a three hour advection timestepfor the 50,000 air parcels. Meteorological data for the winds, temperatures,clouds and so on are taken from the UK Meteorological Office global model for1994 onwards. The impacts of a 50% reduction in European NOXemissions onglobal ozone concentrations are assessed. Surface ozoneconcentrations decrease in summertime and rise in wintertime, but to differentextents.  相似文献   

9.
Increases in chlorinated and brominated halocarbons are believed to be responsible for the depletion of stratospheric ozone observed over much of the globe in the past decade or so. Ozone depletion is in turn believed to lead to a negative radiative forcing, tending to cool the stratosphere and the surface. We show that the increasing atmospheric concentrations of ozone-depleting halocarbons and onset of related ozone depletion likely led to a negative forcing of the climate system in the 1980s that slowed significantly the rate of change of total anthropogenic radiative forcing due to the combined effect of all greenhouse gases over that decade. Within the next decade, emissions of these halocarbons are expected to rapidly decrease, with corresponding impacts on ozone and radiative forcing. As the emissions of ozone-depleting gases are reduced and eventually phased out, the rate of ozone depletion is expected to decrease and eventually reverse. All other things being equal, we show that the change from deepening ozone depletion in the 1980s to ozone increases in the future should lead to a pronounced increase in the decadal rate of change of anthropogenic greenhouse forcing of the next few decades, perhaps to levels unprecedented in this century.  相似文献   

10.
The radiative impact of greenhouse gases in warming the Earth varies significantly, depending on whether one considers the forcing at the tropopause or at the surface. Compared to the former, the surface forcing for some greenhouse gases is reduced by the interference of water vapour. Hence, we calculate alternative surface global warming potentials (SGWPs) that are derived from the surface forcing radiation of greenhouse gases for potential use in surface radiative energy balance models (SREBMs). For gases with a large water vapour overlap, the SGWPs are typically 30% smaller than current GWPs; for gases with relatively little overlap, the SGWPs are larger by more than 33%. These results may be used in conjunction with SREBMs as an additional means of calculating climate change, and may lead to an altered emissions budget compared to that outlined by the current Kyoto agreement.  相似文献   

11.
In this paper, we discuss the results of 2000?C2100 simulations following the emissions associated with the Representative Concentration Pathways (RCPs) with a chemistry-climate model, focusing on the changes in 1) atmospheric composition (troposphere and stratosphere) and 2) associated environmental parameters (such as nitrogen deposition). In particular, we find that tropospheric ozone is projected to decrease (RCP2.6, RCP4.5 and RCP6) or increase (RCP8.5) between 2000 and 2100, with variations in methane a strong contributor to this spread. The associated tropospheric ozone global radiative forcing is shown to be in agreement with the estimate used in the RCPs, except for RCP8.5. Surface ozone in 2100 is projected to change little compared from its 2000 distribution, a much-reduced impact from previous projections based on the A2 high-emission scenario. In addition, globally-averaged stratospheric ozone is projected to recover at or beyond pre-1980 levels. Anthropogenic aerosols are projected to strongly decrease in the 21st century, a reflection of their projected decrease in emissions. Consequently, sulfate deposition is projected to strongly decrease. However, nitrogen deposition is projected to increase over certain regions because of the projected increase in NH3 emissions.  相似文献   

12.
Global Warming Potentials: 2. Accuracy   总被引：1，自引：1，他引：0  
This paper exposes flaws in the mathematical structure of the Global Warming Potential (GWP) concept. These lead to errors when emissions changes in different greenhouse gases are compared. The most fundamental problem is that the unit impulse response functions from which GWPs, and many of their proposed alternatives, are constructed provide an incomplete representation of the relationship between emissions and radiative forcing. Additional errors occur when GWPs are used to compare finite-length emissions changes.  相似文献   

13.
100-year Global Warming Potentials (GWPs) are used almost universally to compare emissions of greenhouse gases in national inventories and reduction targets. GWPs have been criticised on several grounds, but little work has been done to determine global mitigation costs under alternative physics-based metrics . We used the integrated assessment model MESSAGE to compare emission pathways and abatement costs for fixed and time-dependent variants of the Global Temperature Change Potential (GTP) with those based on GWPs, for a policy goal of limiting the radiative forcing to a specified level in the year 2100. We find that fixed 100-year GTPs would increase global abatement costs (discounted and aggregated over the 21st century) under this policy goal by 5–20 % relative to 100-year GWPs, whereas time-varying GTPs would reduce costs by about 5 %. These cost differences are smaller than differences arising from alternative assumptions regarding agricultural mitigation potential and much smaller than those arising from alternative radiative forcing targets. Using the land-use model GLOBIOM, we show that alternative metrics affect food production differently in different world regions depending on regional characteristics of future land-use change to meet growing food demand. We conclude that under scenarios of complete participation, the choice of metric has a limited impact on global abatement costs but could be important for the political economy of regional and sectoral participation in collective mitigation efforts, in particular changing costs and gains over time for agriculture and energy-intensive sectors.  相似文献   

14.
Global Warming Potentials: 1. Climatic Implications of Emissions Reductions   总被引：1，自引：1，他引：0  
The use of Global Warming Potentials (GWPs) to calculate equivalent carbon dioxide emissions reductions in the climate change context is examined. We find that GWPs are accurate only for short time horizons. Over long time horizons their use implicitly leads to tradeoffs between near-term and long-term climate change. For one of the most policy-relevant cases, comparing reductions in methane and carbon dioxide, the long-term effect on climate of reducing methane emissions is relatively small, at variance with the common perception based on published GWP values.  相似文献   

15.
Hydrogen is named as possible energy carrier for future energy systems. However, the impact of large-scale hydrogen use on the atmosphere is uncertain. Application of hydrogen in clean fuel cells reduces emissions of air pollutants, but emissions from hydrogen production and leakages of molecular hydrogen could influence atmospheric chemistry. This paper combines a global energy system model and a global atmospheric model to explore the range of impacts of hydrogen on atmospheric chemistry. We found that emissions of molecular hydrogen may range from 0.2 up to 10% (or 25-167 Tg hydrogen/yr) for a global hydrogen energy system. The lower end of this range would in fact be equal to current emissions from fossil fuel combustion. Hydrogen energy use leads to a clear decrease in emissions of carbon monoxide, nitrogen oxides and sulphur dioxide, but large-scale hydrogen production from coal may lead to net increase in emissions of nitrous oxide and volatile organic compound. Compared to a reference scenario, this would lead to positive impacts on surface concentrations of carbon monoxide, nitrogen oxides and ozone. However, if hydrogen leakage would not be minimised it leads to an increase in methane lifetimes and a decrease in stratospheric ozone concentrations.  相似文献   

16.
We summarize an on-line coupled meteorological–emissions–photochemical modelling system that allows feedback from air-quality/chemistry to meteorology via radiative forcing. We focus on the radiative-forcing impacts (direct effects) of ozone. We present an application of the coupled modelling system to the episode of 23–31 July 1998 in Portland, Oregon, U.S.A. Results suggest that the inclusion of radiative-forcing feedback produces small but accountable impacts. For this region and episode, stand-alone radiative transfer simulations, i.e., evaluating the effects of radiative forcing independently of changes in meteorology or emissions, suggest that a change of 1 ppb in ground-level ozone is approximately equivalent to a change of 0.017 W m−2 in radiative forcing. In on-line, coupled, three-dimensional simulations, where the meteorological dependencies are accounted for, domain-wide peak ozone concentrations were higher by 2–4 ppb (relative to a simulated peak of 119.4 ppb) when including the effects of radiative-forcing feedback. A scenario of 10% reduction in anthropogenic emissions produced slightly larger decreases in ozone, an additional 1 ppb in local-peak reductions, relative to scenarios without feedback.  相似文献   

17.
Min WEI 《大气科学进展》2005,22(6):798-806
The Asian summer monsoon is an important part of the climate system. Investigating the response of the Asian summer monsoon to changing concentrations of greenhouse gases and aerosols will be meaningful to understand and predict climate variability and climate change not only in Asia but also globally. In order to diagnose the impacts of future anthropogenic emissions on monsoon climates, a coupled general circulation model of the atmosphere and the ocean has been used at the Max-Planck-Institute for Meteorology. In addition to carbon dioxide, the major well mixed greenhouse gases such as methane, nitrous oxide, several chlorofluorocarbons, and CFC substitute gases are prescribed as a function of time. The sulfur cycle is simulated interactively, and both the direct aerosol effect and the indirect cloud albedo effect are considered. Furthermore, changes in tropospheric ozone have been pre-calculated with a chemical transport model and prescribed as a function of time and space in the climate simulations. Concentrations of greenhouse gases and anthropogenic emissions of sulfur dioxide are prescribed according to observations （1860-1990） and projected into the future （1990-2100） according to the Scenarios A2 and B2 in Special Report on Emissions Scenarios （SRES, Nakcenovic et al., 2000） developed by the Intergovernmental Panel on Climate Change （IPCC）. It is found that the Indian summer monsoon is enhanced in the scenarios in terms of both mean precipitation and interannual variability. An increase in precipitation is simulated for northern China but a decrease for the southern part. Furthermore, the simulated future increase in monsoon variability seems to be linked to enhanced ENSO variability towards the end of the scenario integrations.  相似文献   

18.
Climate change alone influences future levels of tropospheric ozone and their precursors through modifications of gas-phase chemistry, transport, removal, and natural emissions. The goal of this study is to determine at what extent the modes of variability of gas-phase pollutants respond to different climate change scenarios over Europe. The methodology includes the use of the regional modeling system MM5 (regional climate model version)-CHIMERE for a target domain covering Europe. Two full-transient simulations covering from 1991–2050 under the SRES A2 and B2 scenarios driven by ECHO-G global circulation model have been compared. The results indicate that the spatial patterns of variability for tropospheric ozone are similar for both scenarios, but the magnitude of the change signal significantly differs for A2 and B2. The 1991–2050 simulations share common characteristics for their chemical behavior. As observed from the NO2 and α-pinene modes of variability, our simulations suggest that the enhanced ozone chemical activity is driven by a number of parameters, such as the warming-induced increase in biogenic emissions and, to a lesser extent, by the variation in nitrogen dioxide levels. For gas-phase pollutants, the general increasing trend for ozone found under A2 and B2 forcing is due to a multiplicity of climate factors, such as increased temperature, decreased wet removal associated with an overall decrease of precipitation in southern Europe, increased photolysis of primary and secondary pollutants as a consequence of lower cloudiness and increased biogenic emissions fueled by higher temperatures.  相似文献   

19.
本文首先对中国PM2.5和近地面臭氧浓度的观测进行了简要的综述;并利用2010-2013年全球对流层臭氧的卫星观测数据给出了对流层臭氧浓度在全球和中国地区的分布特征,其平均值分别为29.78 DU和33.97 DU。然后,利用一个气溶胶大气化学-全球气候双向耦合模式模拟了中国地区PM2.5的浓度分布和季节变化,其年平均值为0.51×10-8 kg/m3。在此基础上又分析了5种典型气溶胶对PM2.5总浓度在不同季节的贡献。结合IPCC第五次评估报告（AR5）,讨论了气溶胶和温室气体及其前体物的排放与辐射强迫的联系,以及减排大气臭氧前体物和气溶胶颗粒物质（PM）对气候变化的可能影响。指出减排臭氧前体物对气候的影响还不完全清楚,对短寿命的温室气体和黑碳气溶胶的减排是一种短期（未来50年）的辅助措施;为了保证全球平均温度增长不超过2℃,减少二氧化碳的排放仍是我们需要坚持的长期战略。短期和长期的减排战略对于保护环境和减缓气候变化都是至关重要的。  相似文献   

20.
The global three-dimensional Lagrangian chemistry-transport model STOCHEM has been used to follow changes in the tropospheric distributions of methane CH4 and ozone O3 following the emission of pulses of the oxides of nitrogen NO x . Month-long emission pulses of NO x produce deficits in CH4 mixing ratios that bring about negative radiative forcing (climate cooling) and decay away with e-folding times of 10–15 years. They also produce short-term excesses in O3 mixing ratios that bring about positive radiative forcing (climate warming) that decay over several months to produce deficits, with their attendant negative radiative forcing (climate cooling) that decays away in step with the CH4 deficits. Total time-integrated net radiative forcing is markedly influenced by cancellation between the negative CH4 and long-term O3 contributions and the positive short-term O3 contribution to leave a small negative residual. Consequently, total net radiative forcing from NO x emission pulses and the global warming potentials derived from them, show a strong dependence on the magnitudes, locations and seasons of the emissions. These dependences are illustrated using the Asian continent as an example and demonstrate that there is no simple robust relationship between continental-scale NO x emissions and globally-integrated radiative forcing. We find that the magnitude of the time-integrated radiative forcing from NO x -driven CH4 depletion tends to approach and outweigh that from ozone enhancement, leaving net time-integrated radiative forcings and global warming potentials negative (climate cooling) in contrast to the situation for aircraft NO x (climate warming). Control of man-made surface NO x emissions alone may lead to positive radiative forcing (climate warming).  相似文献   

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