Model simulations of the changing distribution of Ozone and its radiative forcing of climate: past, present and future

A background tropospheric chemistry model that is coupled to the general circulation model ECHAM4 is used to calculate tropospheric ozone with preindustrial, present-day and future (IS92a) emission scenarios as boundary conditions. The model calculates separate contributions to tropospheric ozone levels from stratosphere-troposphere exchange (STE) and from photo- chemical production in the troposphere. In the preindustrial atmosphere, the simulated annual tropospheric ozone content is 190 Tg 03, of which about 110 Tg 03 originates from the strato- sphere. In the present-day simulation the ozone content is about 80 Tg 03 larger, mainly due to O3 precursor emissions from industrial processes in the NH and from biomass burning in trop- ical regions. In the next few decades, industrial growth is expected to occur mainly at NH (sub) tropical latitudes, leading to an additional increase of the tropospheric ozone budget by 60 Tg 03. We calculate a global and annual average radiative forcing by tropospheric ozone perturbations of 0.42 w m-2 creases in the next few decades of 0.31 W m-2 for the present-day simulation, and an additional forcing due to ozone in- The model results indicate that the amount of tropospheric ozone from stratospheric origin remains relatively unaffected by the changing pho- tochemistry

Prediction of the number of cloud droplets in the ECHAM GCM

In this paper a prognostic equation for the number of cloud droplets (CDNC) is introduced into the ECHAM general circulation model. The initial CDNC is based on the mechanistic model of Chuang and Penner [1995], providing a more realistical prediction of CDNC than the empirical method previously used. Cloud droplet nucleation is parameterized as a function of total aerosol number concentration, updraft velocity, and a shape parameter, which takes the aerosol composition and size distribution into account. The total number of aerosol particles is obtained as the sum of marine sulfate aerosols produced from dimethyl sulfide, hydrophylic organic and black carbon, submicron dust, and sea-salt aerosols. Anthropogenic sulfate aerosols only add mass to the preexisting aerosols but do not form new particles. The simulated annual mean liquid water path, column CDNC, and effective radius agree well with observations, as does the frequency distributions of column CDNC for clouds over oceans and the variations of cloud optical depth with effective radius

Emission-Induced Nonlinearities in the Global Aerosol System: Results from the ECHAM5-HAM Aerosol-Climate Model

In a series of simulations with the global ECHAM5-HAM aerosol-climate model, the response to changes in anthropogenic emissions is analyzed. Traditionally, additivity is assumed in the assessment of the aerosol climate impact, as the underlying bulk aerosol models are largely constrained to linearity. The microphysical aerosol module HAM establishes degrees of freedom for nonlinear responses of the aerosol system. In this study’s results, aerosol column mass burdens respond nonlinearly to changes in anthropogenic emissions, manifested in alterations of the aerosol lifetimes. Specific emission changes induce modifications of aerosol cycles with unaltered emissions, indicating a microphysical coupling of the aerosol cycles. Anthropogenic carbonaceous emissions disproportionately contribute to the accumulation mode numbers close to the source regions. In contrast, anthropogenic sulfuric emissions less than proportionally contribute to the accumulation mode numbers close to the source regions and disproportionately contribute in remote regions. The additivity of the aerosol system is analyzed by comparing the changes from a simulation with emission changes for several compounds with the sum of changes of single simulations, in each of which one of the emission changes was introduced. Close to the anthropogenic source regions, deviations from additivity are found at up to 30% and 15% for the accumulation mode number burden and aerosol optical thickness, respectively. These results challenge the traditional approach of assessing the climate impact of aerosols separately for each component and demand for integrated assessments and emission strategies

The evolution of the global aerosol system in a transient climate simulation from 1860 to 2100

The evolution of the global aerosol system from 1860 to 2100 is investigated through a transient atmosphere-ocean General Circulation Model climate simulation with interactively coupled atmospheric aerosol and oceanic biogeochemistry modules. The microphysical aerosol module HAM incorporates the major global aerosol cycles with prognostic treatment of their composition, size distribution, and mixing state. Based on an SRES A1B emission scenario, the global mean sulfate burden is projected to peak in 2020 while black carbon and particulate organic matter show a lagged peak around 2070. From present day to future conditions the anthropogenic aerosol burden shifts generally from the northern high-latitudes to the developing low-latitude source regions with impacts on regional climate. Atmospheric residence- and aging-times show significant alterations under varying climatic and pollution conditions. Concurrently, the aerosol mixing state changes with an increasing aerosol mass fraction residing in the internally mixed accumulation mode. The associated increase in black carbon causes a more than threefold increase of its co-single scattering albedo from 1860 to 2100. Mid-visible aerosol optical depth increases from pre-industrial times, predominantly from the aerosol fine fraction, peaks at 0.26 around the sulfate peak in 2020 and maintains a high level thereafter, due to the continuing increase in carbonaceous aerosols. The global mean anthropogenic top of the atmosphere clear-sky short-wave direct aerosol radiative perturbation intensifies to −1.1 W m^−2 around 2020 and weakens after 2050 to −0.6 W m^−2, owing to an increase in atmospheric absorption. The demonstrated modifications in the aerosol residence- and aging-times, the microphysical state, and radiative properties challenge simplistic approaches to estimate the aerosol radiative effects from emission projections

Impact of sulfate aerosols on albedo and lifetime of clouds: A sensitivity study with the ECHAM4 GCM

A coupled sulfur chemistry-cloud microphysics scheme (COUPL) is used to study the impact of sulfate aerosols on cloud lifetime and albedo. The cloud microphysics scheme includes precipitation formation, which depends on the cloud droplet number concentration (CDNC) and on the liquid water content. On the basis of different observational data sets, CDNC is proportional to the sulfate aerosol mass, which is calculated by the model. Cloud cover is a function of relative humidity only. Additional sensitivity experiments with another cloud cover parameterization (COUPL-CC), which also depends on cloud water, and with a different autoconversion rate of cloud droplets (COUPL-CC-Aut) are conducted to investigate the range of the indirect effect due to uncertainties in cloud physics. For each experiment, two simulations, one using present-day and one using preindustrial sulfur emissions are carried out. The increase in liquid water path, cloud cover, and shortwave cloud forcing due to anthropogenic sulfur emissions depends crucially upon the parameterization of cloud cover and autoconversion of cloud droplets. In COUPL the liquid water path increases by 17 and cloud cover increases by 1 because of anthropogenic sulfur emissions, yielding an increase in shortwave cloud forcing of-1.4 W m-2. In COUPL-CC the liquid water path increases by 32, cloud cover increases by 3 and thus shortwave cloud forcing increases by -4.8 W m-2. This large effect is caused by the strong dependence of cloud cover on cloud water and of the autoconversion rate on CDNC, cloud water, and cloud cover. Choosing a different autoconversion rate (COUPL-CC-Aut) with a reduced dependence on CDNC and cloud water results in an increase of liquid water path by only 11 and of cloud cover by 1 , and the increase in shortwave cloud forcing amounts to -2.2 W m-2. These results clearly show that the uncertainties linked to the indirect aerosol effect are higher than was previously suggested. Copyright 1997 by the American Geophysical Union

Aerosol activation and cloud processing in the global aerosol-climate model ECHAM5-HAM

A parameterization for cloud processing is presented that calculates activation of aerosol particles to cloud drops, cloud drop size, and pH-dependent aqueous phase sulfur chemistry. The parameterization is implemented in the global aerosol-climate model ECHAM5-HAM. The cloud processing parameterization uses updraft speed, temperature, and aerosol size and chemical parameters simulated by ECHAM5-HAM to estimate the maximum supersaturation at the cloud base, and subsequently the cloud drop number concentration (CDNC) due to activation. In-cloud sulfate production occurs through oxidation of dissolved SO2 by ozone and hydrogen peroxide. The model simulates realistic distributions for annually averaged CDNC although it is underestimated especially in remote marine regions. On average, CDNC is dominated by cloud droplets growing on particles from the accumulation mode, with smaller contributions from the Aitken and coarse modes. The simulations indicate that in-cloud sulfate production is a potentially important source of accumulation mode sized cloud condensation nuclei, due to chemical growth of activated Aitken particles and to enhanced coalescence of processed particles. The strength of this source depends on the distribution of produced sulfate over the activated modes. This distribution is affected by uncertainties in many parameters that play a direct role in particle activation, such as the updraft velocity, the aerosol chemical composition and the organic solubility, and the simulated CDNC is found to be relatively sensitive to these uncertainties

Properties of the main trough of the F region derived from Dynamic Explorer 2 data

In winter and equinoctial season nights, the main trough of the F region is an important stable structure of the ionosphere at the border between mid and high latitudes. Therefore it has to be taken into account in modelling and mapping approaches. Werner and Prölss (1995) derived a model for the position of the trough minimum which has found wide acceptance. The model is based on in-situ electron density data measured aboard the low orbiting Dynamic Explorer satellite DE 2 (1981-1986). We present results for other properties of the main trough derived from the same data set. These results are sufficiently good for modelling purposes which need reliable information on the depth, the equatorward and poleward width and the steepness of the walls of the trough. Because of the eccentric orbit of DE 2 (orbit height between about 300-1000 km) it was necessary to «project» observed electron densities to the peak of the F 2 layer. This was done by means of the electron density model COSTprof. The database was restricted to those cases for which the height of DE 2 was below 700 km. Examples are shown for «typical» troughs observed under various conditions

The Effect of Peer Group Overlap in Executives’ RPE Contracts on Competitive Aggressiveness

We investigate how peer group overlap within executives’ relative performance evaluation (RPE) contracts influences firms’ competitive aggressiveness. Conditional on using RPE, we hypothesize and find that if two firms have each other as peers in their respective RPE contracts, this creates a strategic interaction, which in turn increases their competitive aggressiveness. Specifically, firms in growing industries act aggressively by taking more frequent competitive actions, while firms in mature industries act aggressively through taking more complex actions. This also holds for a sample of exogenous changes in peer group overlap and when we compare it to non-RPE firms