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

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

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

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

Modeling cosmogenic radionuclides 10Be and 7Be during the Maunder Minimum using the ECHAM5-HAM general circulation model

All existing 10Be records from Greenland and Antarctica show increasing concentrations during the Maunder Minimum period (MM), 1645–1715, when solar activity was very low and the climate was colder (little ice age). In detail, however, the 10Be records deviate from each other. We investigate to what extent climatic changes influence the 10Be measured in ice by modeling this period using the ECHAM5-HAM general circulation model. Production calculations show that during the MM the mean global 10Be production was higher by 32% than at present due to lower solar activity. Our modeling shows that the zonally averaged modeled 10Be deposition flux deviates by only ~8% from the average increase of 32%, indicating that climatic effects are much smaller than the production change. Due to increased stratospheric production, the 10Be content in the downward fluxes is larger during MM, leading to larger 10Be deposition fluxes in the subtropics, where stratosphere-troposphere exchange (STE) is strongest. In polar regions the effect is small. In Greenland the deposition change depends on latitude and altitude. In Antarctica the change is larger in the east than in the west. We use the 10Be/7Be ratio to study changes in STE. We find larger change between 20° N–40° N during spring, pointing to a stronger STE in the Northern Hemisphere during MM. In the Southern Hemisphere the change is small. These findings indicate that climate changes do influence the 10Be deposition fluxes, but not enough to significantly disturb the production signal. Climate-induced changes remain small, especially in polar regions

Meridional transport and deposition of atmospheric 10Be

10Be concentrations measured in ice cores exhibit larger temporal variability than expected based on theoretical production calculations. To investigate whether this is due to atmospheric transport a general circulation model study is performed with the 10Be production divided into stratospheric, tropospheric tropical, tropospheric subtropical and tropospheric polar sources. A control run with present day 10Be production rate is compared with a run during a geomagnetic minimum. The present 10Be production rate is 4–5 times higher at high latitudes than in the tropics whereas during a period of no geomagnetic dipole field it is constant at all latitudes. The 10Be deposition fluxes, however, show a very similar latitudinal distribution in both the present day and the geomagnetic minimum run indicating that 10Be is well mixed in the atmosphere before its deposition. This is also confirmed by the fact that the contribution of 10Be produced in the stratosphere is dominant (55%–70%) and relatively constant at all latitudes. The contribution of stratospheric 10Be is approximately 70% in Greenland and 60% in Antarctica reflecting the weaker stratosphere-troposphere air exchange in the Southern Hemisphere

Impact of regional climate and substance properties on the fate and atmospheric long-range transport of persistent organic pollutants - examples of DDT and g-HCH

A global multicompartment model which is based on a 3-D atmospheric general circulation model (ECHAM5) coupled to 2-D soil, vegetation and sea surface mixed layer reservoirs, is used to simulate the atmospheric transports and total environmental fate of dichlorodiphenyltrichloroethane (DDT) and γ-hexachlorocyclohexane (γ-HCH, lindane). Emissions into the model world reflect the substance's agricultural usage in 1980 and 1990 and same amounts in sequential years are applied. Four scenarios of DDT usage and atmospheric decay and one scenario of γ-HCH are studied over a decade. The global environment is predicted to be contaminated by the substances within ca. 2a (years). DDT reaches quasi-steady state within 3-4a in the atmosphere and vegetation compartments, ca. 6a in the sea surface mixed layer and near to or slightly more than 10a in soil. Lindane reaches quasi-steady state in the atmosphere and vegetation within 2a, in soils within 8 years and near to or slightly more than 10a and in the sea surface mixed layer. The substances' differences in environmental behaviour translate into differences in the compartmental distribution and total environmental residence time, τoverall. τoverall≈0.8a for γ-HCH's and ≈1.0-1.3 a for the various DDT scenarios. Both substances' distributions are predicted to migrate in northerly direction, 5-12° for DDT and 6.7° for lindane between the first and the tenth year in the environment. Cycling in various receptor regions is a complex superposition of influences of regional climate, advection, and the substance's physico-chemical properties. As a result of these processes the model simulations show that remote boreal regions are not necessarily less contaminated than tropical receptor regions. Although the atmosphere accounts for only 1% of the total contaminant burden, transport and transformation in the atmosphere is key for the distribution in other compartments. Hence, besides the physico-chemical properties of pollutants the location of application (entry) affects persistence and accumulation emphasizing the need for georeferenced exposure models

Long-range transport and multimedia partitioning of semivolatile organic compounds: A case study on two modern agrochemicals

The global environmental fate of two modern pesticides was studied using a multimedia model based on a three- dimensional atmosphere general circulation model. The emissions are predicted dynamically based on agricultural application inventories. The insecticide methyl parathion, when assuming properties at the high mobility end of the respective data uncertainties, was found to be distributed on continental and even global scales. This finding implies that based on present knowledge one cannot exclude that methyl parathion reaches regions as far from the sources as e.g. the Arctic. Two scenarios of the environmental cycling of the herbicide atrazine were studied which reflect a lower and an upper estimate of the substance’ mobility. Atrazine largely remains in the source (application) regions and the neighbouring seas. But also atrazine seems to have an albeit limited potential for long-range transport. The findings on substance mobilities are quantified by indicators which address spatial range in the zonal direction in individual media. The seasonal variability of the total environmental burden of both pesticides is governed by the degradation in soil and vegetation which together host 73 % of methyl parathion and 90-99 % of atrazine. Also, the cycling between compartments was studied. Methyl parathion undergoes more deposition and re-emission cycles than atrazine, a characteristics of the environmental fate of semivolatile substances. Persistence is addressed by determination of global total environmental decay times during periods without introduction of new substance into the environment. These are in the range 4-7 months. It is found that the seasonal variability of persistence is pronounced