Air pollution and cloud-interaction over Europe in 1985 and today

Author(s):  
Roland Schrödner ◽  
Christa Genz ◽  
Bernd Heinold ◽  
Holger Baars ◽  
Silvia Henning ◽  
...  

<p>Aerosol concentrations over Europe and Germany were simulated for the years 1985 and 2013 using the aerosol-chemistry transport model COSMO-MUSCAT. The aerosol fields from the two simulations were used in a high-resolution meteorological model for a sensitivity study on cloud properties. The modelled aerosol and cloud variables were compared to a variety of available observations, including satellites, remote sensing and in-situ observations. Finally, the radiative forcing of the aerosol could be estimated from the different sensitivity simulations.</p><p>Due to reduction of emissions the ambient aerosol mass and number in Europe was strongly decreased since the 1980s. Hence, today’s number of particles in the CCN size range is smaller. The HD(CP)<sup>2</sup> (High Definition Clouds and Precipitation for Climate Prediction) project amongst others aimed at analysing the effect of the emission reduction on cloud properties.</p><p>As a pre-requiste, the aerosol mass, number, and composition over Germany were simulated for 1985 and 2013 using the regional chemistry-transport-model COSMO-MUSCAT. The EDGAR emission inventory was used for both years.</p><p>The model results were compared to observations from the two HD(CP)<sup>2</sup> campaigns that took place in 2013 (HOPE, HOPE-Melpitz) as well as the AVHRR aerosol optical thickness product, which is available from 1981 onwards. Despite the fact, that emissions of the 1980s are very uncertain, the modelled AOD is in good agreement with observations. The modelled mean CCN number concentration in 1985 is a factor of 2-4 higher than in 2013.</p><p>Within HD(CP)<sup>2</sup>, the ICON weather forecast model was applied in a configuration allowing for large-eddy simulations. In these simulations, the time-varying CCN fields for the year 1985 and 2013 calculated with COSMO-MUSCAT were used as input for ICON-LEM. In the present-day simulation, the cloud droplet number agrees with observations, whereas the perturbed (1985) simulation does not with droplet numbers about twice as high as in 2013. Also, for other cloud variables systematic changes between the two scenarios were observed.</p>

2017 ◽  
Author(s):  
Duseong S. Jo ◽  
Rokjin J. Park ◽  
Jaein I. Jeong ◽  
Gabriele Curci ◽  
Hyung-Min Lee ◽  
...  

Abstract. Single Scattering Albedo (SSA), the ratio of scattering efficiency to total extinction efficiency, is an essential parameter used to estimate the Direct Radiative Forcing (DRF) of aerosols. However, SSA is one of the large contributors to the uncertainty of DRF estimations. In this study, we examined the sensitivity of SSA calculations to the physical properties of absorbing aerosols, in particular, Black Carbon (BC), Brown Carbon (BrC), and dust. We used GEOS-Chem 3-D global chemical transport model (CTM) simulations and a post-processing tool for the aerosol optical properties (FlexAOD). The model and input parameters were evaluated by comparison against the observed aerosol mass concentrations and the Aerosol Optical Depth (AOD) values obtained from global surface observation networks such as the global Aerosol Mass Spectrometer (AMS) dataset, the Surface Particulate Matter Network (SPARTAN), and the Aerosol Robotic Network (AERONET). The model was generally successful in reproducing the observed variability of both the Particulate Matter 2.5 μm (PM2.5) and AOD (R ~ 0.76) values, although it underestimated the magnitudes by approximately 20 %. Our sensitivity tests of the SSA calculation revealed that the aerosol physical parameters, which have generally received less attention than the aerosol mass loadings, can cause large uncertainties in the resulting DRF estimation. For example, large variations in the calculated BC absorption may result from slight changes of the geometric mean radius, geometric standard deviation, real and imaginary refractive indices, and density. The inclusion of BrC and observationally-constrained dust size distributions also significantly affected the SSA, and resulted in a remarkable improvement for the simulated SSA at 440 nm (bias was reduced by 44–49 %) compared with the AERONET observations. Based on the simulations performed during this study, we found that the global aerosol direct radiative effect was increased by 10 % after the SSA bias was reduced.


2010 ◽  
Vol 10 (23) ◽  
pp. 11459-11470 ◽  
Author(s):  
B. S. Grandey ◽  
P. Stier

Abstract. Analysing satellite datasets over large regions may introduce spurious relationships between aerosol and cloud properties due to spatial variations in aerosol type, cloud regime and synoptic regime climatologies. Using MODerate resolution Imaging Spectroradiometer data, we calculate relationships between aerosol optical depth τa derived liquid cloud droplet effective number concentration Ne and liquid cloud droplet effective radius re at different spatial scales. Generally, positive values of dlnNedlnτa are found for ocean regions, whilst negative values occur for many land regions. The spatial distribution of dlnredlnτa shows approximately the opposite pattern, with generally postive values for land regions and negative values for ocean regions. We find that for region sizes larger than 4° × 4°, spurious spatial variations in retrieved cloud and aerosol properties can introduce widespread significant errors to calculations of dlnNedlnτa and dlnredlnτa. For regions on the scale of 60° × 60°, these methodological errors may lead to an overestimate in global cloud albedo effect radiative forcing of order 80% relative to that calculated for regions on the scale of 1° × 1°.


2018 ◽  
Vol 18 (3) ◽  
pp. 2035-2047 ◽  
Author(s):  
Daniel T. McCoy ◽  
Frida A.-M. Bender ◽  
Daniel P. Grosvenor ◽  
Johannes K. Mohrmann ◽  
Dennis L. Hartmann ◽  
...  

Abstract. Cloud droplet number concentration (CDNC) is the key state variable that moderates the relationship between aerosol and the radiative forcing arising from aerosol–cloud interactions. Uncertainty related to the effect of anthropogenic aerosol on cloud properties represents the largest uncertainty in total anthropogenic radiative forcing. Here we show that regionally averaged time series of the Moderate-Resolution Imaging Spectroradiometer (MODIS) observed CDNC of low, liquid-topped clouds is well predicted by the MERRA2 reanalysis near-surface sulfate mass concentration over decadal timescales. A multiple linear regression between MERRA2 reanalyses masses of sulfate (SO4), black carbon (BC), organic carbon (OC), sea salt (SS), and dust (DU) shows that CDNC across many different regimes can be reproduced by a simple power-law fit to near-surface SO4, with smaller contributions from BC, OC, SS, and DU. This confirms previous work using a less sophisticated retrieval of CDNC on monthly timescales. The analysis is supported by an examination of remotely sensed sulfur dioxide (SO2) over maritime volcanoes and the east coasts of North America and Asia, revealing that maritime CDNC responds to changes in SO2 as observed by the ozone monitoring instrument (OMI). This investigation of aerosol reanalysis and top-down remote-sensing observations reveals that emission controls in Asia and North America have decreased CDNC in their maritime outflow on a decadal timescale.


2011 ◽  
Vol 4 (7) ◽  
pp. 1491-1514 ◽  
Author(s):  
P. Valks ◽  
G. Pinardi ◽  
A. Richter ◽  
J.-C. Lambert ◽  
N. Hao ◽  
...  

Abstract. This paper presents the algorithm for the operational near real time retrieval of total and tropospheric NO2 columns from the Global Ozone Monitoring Experiment (GOME-2). The retrieval is performed with the GOME Data Processor (GDP) version 4.4 as used by the EUMETSAT Satellite Application Facility on Ozone and Atmospheric Chemistry Monitoring (O3M-SAF). The differential optical absorption spectroscopy (DOAS) method is used to determine NO2 slant columns from GOME-2 (ir)radiance data in the 425–450 nm range. Initial total NO2 columns are computed using stratospheric air mass factors, and GOME-2 derived cloud properties are used to calculate the air mass factors for scenarios in the presence of clouds. To obtain the stratospheric NO2 component, a spatial filtering approach is used, which is shown to be an improvement on the Pacific reference sector method. Tropospheric air mass factors are computed using monthly averaged NO2 profiles from the MOZART-2 chemistry transport model. An error analysis shows that the random error in the GOME-2 NO2 slant columns is approximately 0.45 × 1015 molec cm−2. As a result of the improved quartz diffuser plate used in the GOME-2 instrument, the systematic error in the slant columns is strongly reduced compared to GOME/ERS-2. The estimated uncertainty in the GOME-2 tropospheric NO2 column for polluted conditions ranges from 40 to 80 %. An end-to-end ground-based validation approach for the GOME-2 NO2 columns is illustrated based on multi-axis MAXDOAS measurements at the Observatoire de Haute Provence (OHP). The GOME-2 stratospheric NO2 columns are found to be in good overall agreement with coincident ground-based measurements at OHP. A time series of the MAXDOAS and the GOME-2 tropospheric NO2 columns shows that pollution episodes at OHP are well captured by GOME-2. Monthly mean tropospheric columns are in very good agreement, with differences generally within 0.5 × 1015 molec cm−2.


2021 ◽  
Author(s):  
Edward Gryspeerdt ◽  
Daniel T. McCoy ◽  
Ewan Crosbie ◽  
Richard H. Moore ◽  
Graeme J. Nott ◽  
...  

Abstract. Cloud droplet number concentration (Nd) is of central importance to observation-based estimates of aerosol indirect effects, being used to quantify both the cloud sensitivity to aerosol and the base state of the cloud. However, the derivation of Nd from satellite data depends on a number of assumptions about the cloud and the accuracy of the retrievals of the cloud properties from which it is derived, making it prone to systematic biases. A number of sampling strategies have been proposed to address these biases by selecting the most accurate Nd retrievals in the satellite data. This work compares the impact of these strategies on the accuracy of the satellite retrieved Nd, using a selection of insitu measurements. In stratocumulus regions, the MODIS Nd retrieval is able to achieve a high precision (r2 of 0.5–0.8). This is lower in other cloud regimes, but can be increased by appropriate sampling choices. Although the Nd sampling can have significant effects on the Nd climatology, it produces only a 20 % variation in the implied radiative forcing from aerosol-cloud interactions, with the choice of aerosol proxy driving the overall uncertainty. The results are summarised into recommendations for using MODIS Nd products and appropriate sampling.


2016 ◽  
Author(s):  
Régis Briant ◽  
Paolo Tuccella ◽  
Adrien Deroubaix ◽  
Dmitry Khvorostyanov ◽  
Laurent Menut ◽  
...  

Abstract. The presence of airborne aerosols affects the meteorology as it induces a perturbation in the radiation budget, the number of cloud condensation nuclei and the cloud micro-physics. Those effects are difficult to model at regional scale as several distinct models are usually involved. In this paper, the coupling of the CHIMERE chemistry-transport model with the WRF meteorological model using the OASIS3-MCT coupler is presented. WRF meteorological fields along with CHIMERE aerosol optical properties are exchanged through the coupler at a high frequency in order to model the aerosol direct and semidirect effects. The WRF-CHIMERE online model has a higher computational burden than both models ran separately in offline mode (up to 42 % higher). This is mainly due to some additional computations made within the models such as more frequent calls to meteorology treatment routines or calls to optical properties computations routines. On the other hand, the overall time required to perform the OASIS3-MCT exchanges is not significant compared to the total duration of the simulations. The impact of the coupling is evaluated on a case study over Europe, northern Africa, Middle East and western Asia during the Summer 2012, through comparisons of the offline and two online simulations (with and without the aerosol optical properties feedback) to observations of temperature, Aerosol Optical Depth (AOD) and surface PM10 (particulate matter with diameters lower than 10 µm) concentrations. Result shows that using the optical properties feedback induces a radiative forcing (average forcing of −4.8 W.m−2) which creates a perturbation in the average surface temperatures over desert areas (up to 2.6° locally) along with an increase of both AOD and PM10 concentrations.


2014 ◽  
Vol 14 (19) ◽  
pp. 10601-10618 ◽  
Author(s):  
S. K. Ebmeier ◽  
A. M. Sayer ◽  
R. G. Grainger ◽  
T. A. Mather ◽  
E. Carboni

Abstract. The impact of volcanic emissions, especially from passive degassing and minor explosions, is a source of uncertainty in estimations of aerosol indirect effects. Observations of the impact of volcanic aerosol on clouds contribute to our understanding of both present-day atmospheric properties and of the pre-industrial baseline necessary to assess aerosol radiative forcing. We present systematic measurements over several years at multiple active and inactive volcanic islands in regions of low present-day aerosol burden. The time-averaged indirect aerosol effects within 200 km downwind of island volcanoes are observed using Moderate Resolution Imaging Spectroradiometer (MODIS, 2002–2013) and Advanced Along-Track Scanning Radiometer (AATSR, 2002–2008) data. Retrievals of aerosol and cloud properties at Kīlauea (Hawai'i), Yasur (Vanuatu) and Piton de la Fournaise (la Réunion) are rotated about the volcanic vent to be parallel to wind direction, so that upwind and downwind retrievals can be compared. The emissions from all three volcanoes – including those from passive degassing, Strombolian activity and minor explosions – lead to measurably increased aerosol optical depth downwind of the active vent. Average cloud droplet effective radius is lower downwind of the volcano in all cases, with the peak difference ranging from 2–8 μm at the different volcanoes in different seasons. Estimations of the difference in Top of Atmosphere upward Short Wave flux upwind and downwind of the active volcanoes from NASA's Clouds and the Earth's Radiant Energy System (CERES) suggest a downwind elevation of between 10 and 45 Wm−2 at distances of 150–400 km from the volcano, with much greater local (< 80 km) effects. Comparison of these observations with cloud properties at isolated islands without degassing or erupting volcanoes suggests that these patterns are not purely orographic in origin. Our observations of unpolluted, isolated marine settings may capture processes similar to those in the pre-industrial marine atmosphere.


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