This study investigates the changes in January diurnal temperature range(DTR) in China during 1961-2000.The observed DTR changes during 1981-2000 relative to 1961-80 are first analyzed based on the daily temperature data at 546 weather stations.These observed DTR changes are classified into six cases depending on the changes in daily maximum and minimum temperatures,and then the occurrence frequency and magnitude of DTR change in each case are presented.Three transient simulations are then performed to understand the impact of greenhouse gases(GHGs) and aerosol direct forcing on DTR change:one without anthropogenic radiative forcing,one with anthropogenic GHGs,and another one with the combined forcing of GHGs and five species of anthropogenic aerosols.The predicted daily DTR changes during the years 1981-2000 are also classified into six cases and are compared with the observations.Results show that the previously proposed reason for DTR reduction,a stronger nocturnal warming than a daytime warming,explains only 19.8%of the observed DTR reduction days.DTR reductions are found to generally occur in northeastern China,coinciding with significant regional warming.The simulation with GHG forcing alone reproduces this type of DTR reduction with an occurrence frequency of 32.9%,which is larger than the observed value.Aerosol direct forcing reduces DTR mainly by daytime cooling.Consideration of aerosol cooling improves the simulation of occurrence frequencies of different types of DTR changes as compared to the simulation with GHGs alone,but it cannot improve the prediction of the magnitude of DTR changes.
Lightning is one of the most important natural sources of atmospheric NOx.The authors investigate the2000–2050 changes in NOx emissions from lightning using the global three-dimensional Goddard Earth Observing System chemical transport model(GEOS-Chem)driven by meteorological fields from the Goddard Institute for Space Studies(GISS)general circulation model(GCM)3.Projected changes in climate over 2000–2050are based on the Intergovernmental Panel on Climate Change(IPCC)A1B scenario.The global NOx emission from lightning is simulated to be 4.8 Tg N in present day and to increase by about 16.7%over 2000–2050 as a result of the future climate change.The largest present-day emissions and climate-induced changes are found in the upper troposphere in the tropics.Regionally in eastern China(20–55 N,98–125 E),NOx emissions from lighting is simulated to be 0.3 Tg N(6.3%of the global total emission)in present day and to increase by 26.7%over2000–2050.The simulated changes in NOx from lightening correspond well with the projected future changes in convective precipitation.
This study estimates direct radiative forcing by tropospheric ozone and all aerosols between the years 1850 and 2000, using the new IPCC AR5 （the Intergovernmental Panel on Climate Change Fifth Assessment Report） emissions inventories and a fully coupled chemistry-aerosol general circulation model. As compared to the previous Global Emissions Inventory Activity （GEIA） data, that have been commonly used for forcing estimates since 1990, the IPCC AR5 emissions inventories report lower anthropogenic emissions of organic carbon and black carbon aerosols and higher sulfur and NOx emissions. The simulated global and annual mean burdens of sulfate, nitrate, black carbon （BC）, primary organic aerosol （POA）, secondary organic aerosol （SOA）, and ozone were 0.79, 0.35, 0.05, 0.49, 0.34, and 269 Tg, respectively, in the year 1850, and 1.90, 0.90, 0.11, 0.71, 0.32, and 377 Tg, respectively, in the year 2000. The estimated annual mean top of the atmosphere （TOA） direct radiative forcing of all anthropogenic aerosols based on the AR5 emissions inventories is -0.60 W m^-2 on a global mean basis from 1850 to 2000. However, this is -2.40 W m-2 when forcing values are averaged over eastern China （18-45°N and 95-125°E）. The value for tropospheric ozone is 0.17 W m^-1 on a global mean basis and 0.24 W m^-2 over eastern China. Forcing values indicate that the climatic effect of aerosols over eastern China is much more significant than the globally averaged effect.
A unified chemistry-aerosol-climate model is applied in this work to compare climate responses to changing concentrations of long-lived greenhouse gases （GHGs, CO2, CH4, N2O）, tropospheric O3, and aerosols during the years 1951-2000. Concentrations of sulfate, nitrate, primary organic carbon （POA）, secondary organic carbon （SOA）, black carbon （BC） aerosols, and tropospheric 03 for the years 1950 and 2000 are obtained a priori by coupled chemistry-aerosol-GCM simulations, and then monthly concentrations are interpolated linearly between 1951 and 2000. The annual concentrations of GHGs are taken from the IPCC Third Assessment Report. BC aerosol is internally mixed with other aerosols. Model results indicate that the sinmlated climate change over 1951-2000 is sensitive to anthropogenic changes in atmospheric components. The predicted year 2000 global mean surface air temperature can differ by 0.8℃ with different forcings. Relative to the climate simulation without changes in GHGs, O3, and aerosols, anthropogenic forcings of SO4^2-, BC, BC＋SO4^2-, BC＋SO4^2- ＋POA, BC＋SO4^2- ＋POA＋SOA＋NO3^-, O3, and GHGs are predicted to change the surface air temperature averaged over 1971-2000 in eastern China, respectively, by -0.40℃, ＋0.62℃, ＋0.18℃, ＋0.15℃, -0.78℃, ＋0.43℃, and ＋0.85℃, and to change the precipitation, respectively, by -0.21, ＋0.07, -0.03, ＋0.02, -0.24, -0.08, and ＋0.10 mm d^-1. The authors conclude that all major aerosols are as important as GHGs in influencing climate change in eastern China, and tropospheric O3 also needs to be included in studies of regional climate change in China.
