Relative radiative forcing consequences of global emissions of hydrocarbons, carbon monoxide and NOx from human activities estimated with a zonally-averaged two-dimensional model

A global two-dimensional (altitude-latitude) chemistry transport model is used to follow the changes in the tropospheric distribution of the two major radiatively active trace gases, methane and ozone, following step changes to the sustained emissions of the short-lived trace gases methane, carbon monoxide and non-methane hydrocarbons. The radiative impacts were dependent on the latitude chosen for the applied change in emissions. Step change global warming potentials (GWPs) were derived for a range of short-lived trace gases to describe their time-integrated radiative forcing impacts for unit emissions relative to that of carbon dioxide. The GWPs show that the tropospheric chemistry of the hydrocarbons can produce significant indirect radiative impacts through changing the tropospheric distributions of hydroxyl radicals, methane and ozone. For aircraft, the indirect radiative forcing impact of the NO _x emissions appears to be greater than that from their carbon dioxide emissions. Quantitative results from this two-dimensional model study must, however, be viewed against the known inadequacies of zonally-averaged models and their poor representation of many important tropospheric processes.     

Dynamic responses of atmospheric carbon dioxide concentration to global temperature changes between 1850 and 2010

Changes in Earth's temperature have significant impacts on the global carbon cycle that vary at different time scales, yet to quantify such impacts with a simple scheme is traditionally deemed difficult. Here, we show that, by incorporating a temperature sensitivity parameter(1.64 ppm yr~(-1) ?C~(-1)) into a simple linear carbon-cycle model, we can accurately characterize the dynamic responses of atmospheric carbon dioxide(CO_2) concentration to anthropogenic carbon emissions and global temperature changes between 1850 and 2010(r~2 0.96 and the root-mean-square error 1 ppm for the period from 1960onward). Analytical analysis also indicates that the multiplication of the parameter with the response time of the atmospheric carbon reservoir(～12 year) approximates the long-term temperature sensitivity of global atmospheric CO_2concentration(～15 ppm?C~(-1)), generally consistent with previous estimates based on reconstructed CO_2 and climate records over the Little Ice Age. Our results suggest that recent increases in global surface temperatures, which accelerate the release of carbon from the surface reservoirs into the atmosphere, have partially offset surface carbon uptakes enhanced by the elevated atmospheric CO_2 concentration and slowed the net rate of atmospheric CO_2 sequestration by global land and oceans by ～30%since the 1960 s. The linear modeling framework outlined in this paper thus provides a useful tool to diagnose the observed atmospheric CO_2 dynamics and monitor their future changes.     

Greenhouse Gas Emissions from Hydroelectric Reservoirs in Tropical Regions

This paper discusses emissions by power-dams in the tropics. Greenhouse gas emissions from tropical power-dams are produced underwater through biomass decomposition by bacteria. The gases produced in these dams are mainly nitrogen, carbon dioxide and methane. A methodology was established for measuring greenhouse gases emitted by various power-dams in Brazil. Experimental measurements of gas emissions by dams were made to determine accurately their emissions of methane (CH₄) and carbon dioxide (CO₂) gases through bubbles formed on the lake bottom by decomposing organic matter, as well as rising up the lake gradient by molecular diffusion.The main source of gas in power-dams reservoirs is the bacterial decomposition (aerobic and anaerobic) of autochthonous and allochthonous organic matter that basically produces CO₂ and CH₄. The types and modes of gas production and release in the tropics are reviewed.     

Emissions from Russian domestic civil aviation in 2000–2012 and integrated assessment of their impact on the climate system

Emissions from Russian domestic civil aviation for the period of 2000–2012 are assessed for the following gases: carbon dioxide, methane, nitrous oxide, carbon monoxide, nitrogen oxides, and sulfur dioxide. The integrated assessment of their impact on the climate system is performed using the values of the global warming potential. The CO₂ equivalent was used as a common measure of emissions. It is established that the modern impact of Russian civil aviation on the Earth climate is insignificant.     

Estimates of the Climate Response to Aircraft CO2 and NO x Emissions Scenarios

A combination of linear response models is used to estimate the transient changes in the global means of carbon dioxide (CO₂) concentration, surface temperature, and sea level due to aviation. Apart from CO₂, the forcing caused by ozone (O₃) changes due to nitrogen oxide (NO_x) emissions from aircraft is also considered. The model is applied to aviation using several CO₂ emissions scenarios, based on reported fuel consumption in the past and scenarios for the future, and corresponding NO_x emissions. Aviation CO₂ emissions from the past until 1995 enlarged the atmospheric CO₂ concentration by 1.4 ppmv (1.7% of the anthropogenic CO₂ increase since 1800). By 1995, the global mean surface temperature had increased by about 0.004 K, and the sea level had risen by 0.045 cm. In one scenario (Fa1), which assumes a threefold increase in aviation fuel consumption until 2050 and an annual increase rate of 1% thereafter until 2100, the model predicts a CO₂ concentration change of 13 ppmv by 2100, causing temperature increases of 0.01, 0.025, 0.05 K and sea level increases of 0.1, 0.3, and 0.5 cm in the years 2015, 2050, and 2100, respectively. For other recently published scenarios, the results range from 5 to 17 ppmv for CO₂ concentration increase in the year 2050, and 0.02 to 0.05 K for temperature increase. Under the assumption that present-day aircraft-induced O₃ changes cause an equilibrium surface warming of 0.05 K, the transient responses amount to 0.03 K in surface temperature for scenario Fa1 in 1995. The radiative forcing due to an aircraft-induced O₃ increase causes a larger temperature change than aircraft CO₂ forcing. Also, climate reacts more promptly to changes in O₃ than to changes in CO₂ emissions from aviation. Finally, even under the assumption of a rather small equilibrium temperature change from aircraft-induced O₃ (0.01 K for the 1992 NO_x emissions), a proposed new combustor technology which reduces specific NO_x emissions will cause a smaller temperature change during the next century than the standard technology does, despite a slightly enhanced fuel consumption. Regional effects are not considered here, but may be larger than the global mean responses.     

Carbon dioxide and methane in the Arctic atmosphere

Fifty flask air samples were taken during April 1986 from a NOAA WP-3D Orion aircraft which flew missions across a broad region of the Arctic as part of the second Arctic Gas and Aerosol Sampling Program (AGASP II). The samples were subsequently analyzed for both carbon dioxide (CO₂) and methane (CH₄). The samples were taken in well-defined layers of Arctic haze, in the background troposphere where no haze was detected, and from near the surface to the lower stratosphere. Vertical profiles were specifically measured in the vicinity of Barrow, Alaska to enable comparisons with routine surface measurements made at the NOAA/GMCC observatory. Elevated levels of both methane and carbon dioxide were found in haze layers. For samples taken in the background troposphere we found negative vertical gradients (lower concentrations aloft) for both gases. For the entire data set (including samples collected in the haze layers) we found a strong positive correlation between the methane and carbon dioxide concentrations, with a linear regression slope of 17.5 ppb CH₄/ppm CO₂, a standard error of 0.6, and a correlation coefficient (r²) of 0.95. This correlation between the two gases seen in the aircraft samples was corroborated by in situ surface measurements of these gases made at the Barrow observatory during March and April 1986. We also find a similar relationship between methane and carbon dioxide measured concurrenty for a short period in the moderately polluted urban atmosphere of Boulder, Colorado. We suggest that the strong correlation between methane and carbon dioxide concentrations reflects a common source region for both, with subsequent long-range transport of the polluted air to the Arctic.     

Carbon Sequestration in Arable Soils is Likely to Increase Nitrous Oxide Emissions,Offsetting Reductions in Climate Radiative Forcing

Strategies for mitigating the increasing concentration of carbon dioxide (CO₂) in the atmosphere include sequestering carbon (C) in soils and vegetation of terrestrial ecosystems. Carbon and nitrogen (N) move through terrestrial ecosystems in coupled biogeochemical cycles, and increasing C stocks in soils and vegetation will have an impact on the N cycle. We conducted simulations with a biogeochemical model to evaluate the impact of different cropland management strategies on the coupled cycles of C and N, with special emphasis on C-sequestration and emission of the greenhouse gases methane (CH₄) and nitrous oxide (N₂O). Reduced tillage, enhanced crop residue incorporation, and farmyard manure application each increased soil C-sequestration, increased N₂O emissions, and had little effect on CH₄ uptake. Over 20 years, increases in N₂O emissions, which were converted into CO₂-equivalent emissions with 100-year global warming potential multipliers, offset 75–310% of the carbon sequestered, depending on the scenario. Quantification of these types of biogeochemical interactions must be incorporated into assessment frameworks and trading mechanisms to accurately evaluate the value of agricultural systems in strategies for climate protection.     

陆表自然和人文要素相互作用——“全球变化及应对”重点专项研究进展

在国家重点研发计划支持下,项目提出了陆表不均一性检测和订正的新方法,解决了渐变型不均一性检测和订正的难题,构建了中国地表太阳辐射、气温、地温、风速和降水等参数均一化站点和格点数据集,修订了关于中国地表风速变化趋势、增温格局及其形成机制的结论。融合多源数据,构建并验证了千米级、流域级或县域级的电厂、人口、生物质能、取水量、氮排放、二氧化碳排放等影响自然系统的关键人文要素历史和未来预估数据集。构建了未来关键人文要素情景,研制了碳中和目标下甲烷和氧化亚氮排放情景和用于驱动全球模式的未来情景,预估了中国碳中和战略的实施对全球变暖的减缓作用,发现中国碳中和对远期和中期全球变暖的减缓作用显著。给出了中国各省份水体氮排放安全阈值及超越时间,阐明了中国粮食产量与氮施肥的关系,提出了在保障粮食安全的前提下减少水体氮排放的有效途径,指出重构城乡养分循环体系是同时保障粮食安全和恢复水质的必要途径。发现全球饱和水汽压差的年际变化与大气二氧化碳浓度上升速率的年际变化显著相关,阐明了饱和水汽压差变化在调控生态系统生产力中的重要角色以及多因素耦合作用在生态系统生产力变化中的复杂影响。建议更全面细致地评估中国各种碳中...     

Adjustment of the natural ocean carbon cycle to negative emission rates

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.     

Biotic Feedbacks in the Warming of the Earth

A positive correlation exists between temperature and atmospheric concentrations of carbon dioxide and methane over the last 220,000 years of glacial history, including two glacial and three interglacial periods. A similar correlation exists for the Little Ice Age and for contemporary data. Although the dominant processes responsible may be different over the three time periods, a warming trend, once established, appears to be consistently reinforced through the further accumulation of heat-trapping gases in the atmosphere; a cooling trend is reinforced by a reduction in the release of heat-trapping gases. Over relatively short periods of years to decades, the correspondence between temperature and greenhouse gas concentrations may be due largely to changes in the metabolism of terrestrial ecosystems, whose respiration, including microbial respiration in soils, responds more sensitively, and with a greater total effect, to changes in temperature than does gross photosynthesis. Despite the importance of positive feedbacks and the recent rise in surface temperatures, terrestrial ecosystems seem to have been accumulating carbon over the last decades. The mechanisms responsible are thought to include increased nitrogen mobilization as a result of human activities, and two negative feedbacks: CO₂ fertilization and the warming of the earth, itself, which is thought to lead to an accumulation of carbon on land through increased mineralization of nutrients and, as a result, increased plant growth. The relative importance of these mechanisms is unknown, but collectively they appear to have been more important over the last century than a positive feedback through warming-enhanced respiration. The recent rate of increase in temperature, however, leads to concern that we are entering a new phase in climate, one in which the enhanced greenhouse effect is emerging as the dominant influence on the temperature of the earth. Two observations support this concern. One is the negative correlation between temperature and global uptake of carbon by terrestrial ecosystems. The second is the positive correlation between temperature and the heat-trapping gas content of the atmosphere. While CO₂ fertilization or nitrogen mobilization (either directly or through a warming-enhanced mineralization) may partially counter the effects of a warming-enhanced respiration, the effect of temperature on the metabolism of terrestrial ecosystems suggests that these processes will not entirely compensate for emissions of carbon resulting directly from industrial and land-use practices and indirectly from the warming itself. The magnitude of the positive feedback, releasing additional CO₂, CH₄, and N₂O, is potentially large enough to affect the rate of warming significantly.     

A Complex Approach for the Estimation of Carbonaceous Emissions from Wildfires in Siberia

A complex approach is considered to the estimation of emissions of carbon gases formed during wildfires in the middle taiga subzone in the Yenisei region of Siberia. Based on the large-scale Siberian wildfires in 2012, the relative contribution of emissions to the values of background concentration of carbon gases (CO₂, CH₄, CO) in the atmospheric boundary layer measured at the 300-m ZOTTO tall tower is assessed. The degree of ecosystem damage caused by wildfires is estimated depending on their intensity and combustion phase (flame or flameless). Emission factors are calculated for the major carbon gases in wildfire plumes which are the key component for assessing wildfire emissions to the atmosphere.     

Transient Behaviour of Tropospheric Ozone Precursors in a Global 3-D CTM and Their Indirect Greenhouse Effects

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, NO_x and hydrogen. The radiative impacts of NO_x 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 NO_xemissions. 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.     

Changes in Heat Index Associated with CO2-Induced Global Warming

Changes in Heat Index (a combined measure of temperature and humidity) associated with global warming are evaluated based on the output from four extended integrations of the GFDL coupled ocean-atmosphere climate model. The four integrations are: a control with constant levels of atmospheric carbon dioxide (CO₂), a second integration in which an estimate of the combined radiative forcing of greenhouse gases and sulfate aerosols over the period 1765–2065 is used to force the model, and a third (fourth) integration in which atmospheric CO₂$ increases at the rate of 1% per year to double (quadruple) its initial value, and is held constant thereafter. While the spatial patterns of the changes in Heat Index are largely determined by the changes in surface air temperature, increases in atmospheric moisture can substantially amplify the changes in Heat Index over regions which are warm and humid in the Control integration. The regions most prone to this effect include humid regions of the Tropics and summer hemisphere extra-tropics, including the southeastern United States, India, southeast Asia and northern Australia.     

Substitution of Natural Gas for Coal: Climatic Effects of Utility Sector Emissions

Substitution of natural gas for coal is one means of reducing carbon dioxide (CO₂) emissions. However, natural gas and coal use also results in emissions of other radiatively active substances including methane (CH₄), sulfur dioxide (SO₂), a sulfate aerosolprecursor, and black carbon (BC) particles. Will switching from coal to gas reduce the net impact of fossil fuel use on global climate? Using the electric utility sector as an example, changes in emissions of CO₂, CH₄,SO₂ and BC resulting from the replacement of coal by natural gas are evaluated, and their modeled net effect on global mean-annual temperature calculated. Coal-to-gas substitution initially produces higher temperatures relative to continued coal use. This warming is due to reduced SO₂ emissionsand possible increases in CH₄ emissions, and can last from 1 to 30years, depending on the sulfur controls assumed. This is followed by a net decrease in temperature relative to continued coal use, resulting from lower emissions of CO₂ and BC. The length of this period and the extent of the warming or cooling expected from coal-to-gas substitution is found to depend on key uncertainties and characteristics of the substitutions, especially those related to: (1) SO₂ emissions and consequentsulphate aerosol forcing; and (2) the relative efficiencies of the power plantsinvolved in the switch.     

Emission scenarios for a global hydrogen economy and the consequences for global air pollution

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.     

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.     

Managing atmospheric CO2

A coupled carbon cycle-climate model is used to compute global atmospheric CO₂ and temperature variation that would result from several future CO₂ emission scenarios. The model includes temperature and CO₂ feedbacks on the terrestrial biosphere, and temperature feedback on the oceanic uptake of CO₂. The scenarios used include cases in which fossil fuel CO₂ emissions are held constant at the 1986 value or increase by 1% yr^–1 until either 2000 or 2020, followed by a gradual transition to a rate of decrease of 1 or 2% yr^–1. The climatic effect of increases in non-CO₂ trace gases is included, and scenarios are considered in which these gases increase until 2075 or are stabilized once CO₂ emission reductions begin. Low and high deforestation scenarios are also considered. In all cases, results are computed for equilibrium climatic sensitivities to CO₂ doubling of 2.0 and 4.0 °C.Peak atmospheric CO₂ concentrations of 400–500 ppmv and global mean warming after 1980 of 0.6–3.2 °C occur, with maximum rates of global mean warming of 0.2–0.3 °C decade^–1. The peak CO₂ concentrations in these scenarios are significantly below that commonly regarded as unavoidable; further sensitivity analyses suggest that limiting atmospheric CO₂ to as little as 400 ppmv is a credible option.Two factors in the model are important in limiting atmospheric CO₂: (1) the airborne fraction falls rapidly once emissions begin to decrease, so that total emissions (fossil fuel + land use-induced) need initially fall to only about half their present value in order to stabilize atmospheric CO₂, and (2) changes in rates of deforestation have an immediate and proportional effect on gross emissions from the biosphere, whereas the CO₂ sink due to regrowth of forests responds more slowly, so that decreases in the rate of deforestation have a disproportionately large effect on net emission.If fossil fuel emissions were to decrease at 1–2% yr^–1 beginning early in the next century, emissions could decrease to the rate of CO₂ uptake by the predominantly oceanic sink within 50–100 yrs. Simulation results suggest that if subsequent emission reductions were tied to the rate of CO₂ uptake by natural CO₂ sinks, these reductions could proceed more slowly than initially while preventing further CO₂ increases, since the natural CO₂ sink strength decreases on time scales of one to several centuries. The model used here does not account for the possible effect on atmospheric CO₂ concentration of possible changes in oceanic circulation. Based on past rates of atmospheric CO₂ variation determined from polar ice cores, it appears that the largest plausible perturbation in ocean-air CO₂ flux due to changes of oceanic circulation is substantially smaller than the permitted fossil fuel CO₂ emissions under the above strategy, so tieing fossil fuel emissions to the total sink strength could provide adequate flexibility for responding to unexpected changes in oceanic CO₂ uptake caused by climatic warming-induced changes of oceanic circulation.     

Long-term variations of long-wave radiation in Moscow

Using the data of long-term (1958–2012) actinometric and meteorological observations of the Meteorological Observatory of Lomonosov Moscow State University, the observed and computed long-wave fluxes and the factors defining their variability are estimated. Obtained are the normals and determined are the limits of variability of effective radiation. Analyzed are the peculiarities of atmospheric back radiation. Demonstrated is the trend towards the decrease (in absolute value) in effective radiation caused by the increase in the atmospheric back radiation flux (E _a). The trend towards the increase in the atmospheric back radiation is determined by the increase in the values of meteorological parameters: cloudiness, atmospheric moisture content, and temperature. The content of aerosol and carbon dioxide does not affect the long-term variations of E _a registered in Moscow. Derived empirical formulae can be recommended for estimating the atmospheric back radiation and effective radiation of the Earth surface using meteorological observations.     

A simple model for estimating methane concentration and lifetime variations

A simple methane model is presented in which lifetime changes are expressed as a function of CH₄ concentration and emissions of NO_x CO and NMHCs. The model parameters define the relative sensitivities of lifetime to these determining factors. The parameterized model is fitted to results from five more complex atmospheric chemistry models and to 1990 IPCC concentration projections. The IPCC data and four of the five models are well fitted, implying that the models have similar relative sensitivities. However, overall sensitivities of lifetime to changes in atmospheric composition vary widely from model to model. The parameterized model is used to estimate the history of past methane emissions, lifetime changes and OH variations, with estimates of uncertainties. The pre-industrial lifetime is estimated to be 15–34% lower than today. This implies that 23–55% of past concentration changes are due to lifetime changes. Pre-industrial emissions are found to be much higher (220–330 TgCH₄/y) than the best estimate of present natural emissions (155 TgCH₄/y). The change in emissions since pre-industrial times is estimated to lie in the range 160–260 TgCH₄/y, compared with the current best guess for anthropogenic emissions of 360 TgCH₄/y. These results imply either that current estimates of anthropogenic emissions are too high and/or that there have been large changes in natural emissions. 1992 IPCC emissions scenarios are used to give projections of future concentration and lifetime changes, together with their uncertainties. For any given emissions scenario, these uncertainties are large. In terms of future radiative forcing and global-mean temperature changes over 1990–2100 they correspond to uncertainties of at least ±0.2 Wm^–2 and ± 0.1° C, respectively.