scholarly journals Arctic smoke – aerosol characteristics during a record air pollution event in the European Arctic and its radiative impact

2007 ◽  
Vol 7 (1) ◽  
pp. 2275-2324 ◽  
Author(s):  
R. Treffeisen ◽  
P. Turnved ◽  
J. Ström ◽  
A. Herber ◽  
J. Bareiss ◽  
...  
Keyword(s):  
Air Pollution ◽  
Size Distribution ◽  
Climate Model ◽  
Atmospheric Stability ◽  
The Arctic ◽  
Aerosol Size Distribution ◽  
Geometric Standard Deviation ◽  
Transfer Model ◽  
Climatic Effects ◽  
Pollution Event

Abstract. In early May 2006 a record high air pollution event was observed at Ny-Ålesund, Spitsbergen. An atypical weather pattern established a pathway for the rapid transport of biomass burning aerosols from agricultural fires in Eastern Europe to the Arctic. Atmospheric stability was such that the smoke was constrained to low levels, within 2 km of the surface during the transport. A description of this smoke event in terms of transport and main aerosol characteristics can be found in Stohl et al. (2007). This study puts emphasis on the radiative effect of the smoke. The aerosol size distribution was characterized as having an accumulation mode centered at 165–185 nm and almost 1.6 for geometric standard deviation of the mode. Nucleation and small Aitken mode particles were almost completely suppressed within the smoke plume measured at Ny-Ålesund. Chemical and microphysical aerosol information obtained at Mt. Zeppelin (474 m.a.s.l) was used to derive input parameters for a one-dimensional radiation transfer model to explore the radiative effects of the smoke. The daily mean heating rate calculated on 2 May 2006 for the average size distribution and measured chemical composition reached 0.55 K day−1 at 0.5 km altitude for the assumed external mixture of the aerosols but showing much higher heating rates for an internal mixture (1.7 K day−1). In comparison a case study for March 2000 showed that the local climatic effects due to Arctic haze, using a regional climate model, HIRHAM, amounts to a maximum of 0.3 K day−1 of heating at 2 km altitude (Treffeisen et al., 2005).

scholarly journals Arctic smoke – aerosol characteristics during a record smoke event in the European Arctic and its radiative impact

2007 ◽  
Vol 7 (11) ◽  
pp. 3035-3053 ◽  
Author(s):  
R. Treffeisen ◽  
P. Tunved ◽  
J. Ström ◽  
A. Herber ◽  
J. Bareiss ◽  
...  
Keyword(s):  
Size Distribution ◽  
Climate Model ◽  
Regional Climate ◽  
Atmospheric Stability ◽  
The Arctic ◽  
Geometric Standard Deviation ◽  
Transfer Model ◽  
Heating Rates ◽  
Climatic Effects ◽  
Average Size

Abstract. In early May 2006 a record high air pollution event was observed at Ny-Ålesund, Spitsbergen. An atypical weather pattern established a pathway for the rapid transport of biomass burning aerosols from agricultural fires in Eastern Europe to the Arctic. Atmospheric stability was such that the smoke was constrained to low levels, within 2 km of the surface during the transport. A description of this smoke event in terms of transport and main aerosol characteristics can be found in Stohl et al. (2007). This study puts emphasis on the radiative effect of the smoke. The aerosol number size distribution was characterised by lognormal parameters as having an accumulation mode centered around 165–185 nm and almost 1.6 for geometric standard deviation of the mode. Nucleation and small Aitken mode particles were almost completely suppressed within the smoke plume measured at Ny-Ålesund. Chemical and microphysical aerosol information obtained at Mt. Zeppelin (474 m a.s.l) was used to derive input parameters for a one-dimensional radiation transfer model to explore the radiative effects of the smoke. The daily mean heating rate calculated on 2 May 2006 for the average size distribution and measured chemical composition reached 0.55 K day−1 at 0.5 km altitude for the assumed external mixture of the aerosols but showing much higher heating rates for an internal mixture (1.7 K day−1). In comparison a case study for March 2000 showed that the local climatic effects due to Arctic haze, using a regional climate model, HIRHAM, amounts to a maximum of 0.3 K day−1 of heating at 2 km altitude (Treffeisen et al., 2005).

scholarly journals The relationship between aerosol and cloud drop number concentrations in a global aerosol microphysics model

2009 ◽  
Vol 9 (1) ◽  
pp. 3207-3241 ◽  
Author(s):  
K. J. Pringle ◽  
K. S. Carslaw ◽  
D. V. Spracklen ◽  
G. M. Mann ◽  
M. P. Chipperfield
Keyword(s):  
Size Distribution ◽  
Cloud Droplet ◽  
Global Scale ◽  
Rate Of Change ◽  
The Arctic ◽  
Aerosol Size Distribution ◽  
Percentage Error ◽  
Empirical Relationships ◽  
Wide Range ◽  
Global Mean

Abstract. Empirical relationships that link cloud droplet number (CDN) to aerosol number or mass are commonly used to calculate global fields of CDN for climate forcing assessments. In this work we use a sectional global model of sulfate and sea-salt aerosol coupled to a mechanistic aerosol activation scheme to explore the limitations of this approach. We find that a given aerosol number concentration produces a wide range of CDN concentrations due to variations in the shape of the aerosol size distribution. On a global scale, the dependence of CDN on the size distribution results in regional biases in predicted CDN (for a given aerosol number). Empirical relationships between aerosol number and CDN are often derived from regional data but applied to the entire globe. In an analogous process, we derive regional "correlation-relations" between aerosol number and CDN and apply these regional relations to calculations of CDN on the global scale. The global mean percentage error in CDN caused by using regionally derived CDN-aerosol relations is 20 to 26%, which is about half the global mean percentage change in CDN caused by doubling the updraft velocity. However, the error is as much as 25–75% in the Southern Ocean, the Arctic and regions of persistent stratocumulus when an aerosol-CDN correlation relation from the North Atlantic is used. These regions produce much higher CDN concentrations (for a given aerosol number) than predicted by the globally uniform empirical relations. CDN-aerosol number relations from different regions also show very different sensitivity to changing aerosol. The magnitude of the rate of change of CDN with particle number, a measure of the aerosol efficacy, varies by a factor 4. CDN in cloud processed regions of persistent stratocumulus is particularly sensitive to changing aerosol number. It is therefore likely that the indirect effect will be underestimated in these important regions.

scholarly journals Arctic smoke – record high air pollution levels in the European Arctic due to agricultural fires in Eastern Europe

2006 ◽  
Vol 6 (5) ◽  
pp. 9655-9722 ◽  
Author(s):  
A. Stohl ◽  
T. Berg ◽  
J. F. Burkhart ◽  
A. M. Fjæraa ◽  
C. Forster ◽  
...  
Keyword(s):  
Air Pollution ◽  
Eastern Europe ◽  
Dispersion Model ◽  
Spatial Scales ◽  
Agricultural Waste ◽  
Particle Dispersion ◽  
The Arctic ◽  
Aerosol Size Distribution ◽  
Radiative Processes ◽  
European Arctic

Abstract. In spring 2006, the European Arctic was abnormally warm, setting new historical temperature records. During this warm period, smoke from agricultural fires in Eastern Europe intruded into the European Arctic and caused the most severe air pollution episodes ever recorded there. This paper confirms that biomass burning (BB) was indeed the source of the observed air pollution, studies the transport of the smoke into the Arctic, and presents an overview of the observations taken during the episode. Fire detections from the MODIS instruments aboard the Aqua and Terra satellites were used to estimate the BB emissions. The FLEXPART particle dispersion model was used to show that the smoke was transported to Spitsbergen and Iceland, which was confirmed by MODIS retrievals of the aerosol optical depth (AOD) and AIRS retrievals of carbon monoxide (CO) total columns. Concentrations of halocarbons, carbon dioxide and CO, as well as levoglucosan and potassium, measured at Zeppelin mountain near Ny Ålesund, were used to further corroborate the BB source of the smoke at Spitsbergen. The ozone (O3) and CO concentrations were the highest ever observed at the Zeppelin station, and gaseous elemental mercury was also enhanced. A new O3 record was also set at a station on Iceland. The smoke was strongly absorbing – black carbon concentrations were the highest ever recorded at Zeppelin –, and strongly perturbed the radiation transmission in the atmosphere: aerosol optical depths were the highest ever measured at Ny Ålesund. We furthermore discuss the aerosol chemical composition, obtained from filter samples, as well as the aerosol size distribution during the smoke event. Photographs show that the snow at a glacier on Spitsbergen became discolored during the episode and, thus, the snow albedo was reduced. Samples of this polluted snow contained strongly enhanced levels of potassium, sulphate, nitrate and ammonium ions, thus relating the discoloration to the deposition of the smoke aerosols. This paper shows that, to date, BB has been underestimated as a source of aerosol and air pollution for the Arctic, relative to emissions from fossil fuel combustion. Given its significant impact on air quality over large spatial scales and on radiative processes, the practice of agricultural waste burning should be banned in the future.

scholarly journals Evaluation of the sectional aerosol microphysics module SALSA implementation in ECHAM5-HAM aerosol-climate model

2012 ◽  
Vol 5 (3) ◽  
pp. 845-868 ◽  
Author(s):  
T. Bergman ◽  
V.-M. Kerminen ◽  
H. Korhonen ◽  
K. J. Lehtinen ◽  
R. Makkonen ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Size Distribution ◽  
Black Carbon ◽  
Climate Model ◽  
Good Choice ◽  
Sea Salt ◽  
Aerosol Size Distribution ◽  
Chemical Compositions ◽  
Model Framework ◽  
Aerosol Properties

Abstract. We present the implementation and evaluation of a sectional aerosol microphysics module SALSA within the aerosol-climate model ECHAM5-HAM. This aerosol microphysics module has been designed to be flexible and computationally efficient so that it can be implemented in regional or global scale models. The computational efficiency has been achieved by minimising the number of variables needed to describe the size and composition distribution. The aerosol size distribution is described using 10 size classes with parallel sections which can have different chemical compositions. Thus in total, the module tracks 20 size sections which cover diameters ranging from 3 nm to 10 μm and are divided into three subranges, each with an optimised selection of processes and compounds. The implementation of SALSA into ECHAM5-HAM includes the main aerosol processes in the atmosphere: emissions, removal, radiative effects, liquid and gas phase sulphate chemistry, and the aerosol microphysics. The aerosol compounds treated in the module are sulphate, organic carbon, sea salt, black carbon, and mineral dust. In its default configuration, ECHAM5-HAM treats aerosol size distribution using the modal method. In this implementation, the aerosol processes were converted to be used in a sectional model framework. The ability of the module to describe the global aerosol properties was evaluated by comparing against (1) measured continental and marine size distributions, (2) observed variability of continental number concentrations, (3) measured sulphate, organic carbon, black carbon and sea-salt mass concentrations, (4) observations of aerosol optical depth (AOD) and other aerosol optical properties from satellites and AERONET network, (5) global aerosol budgets and concentrations from previous model studies, and (6) model results using M7, which is the default aerosol microphysics module in ECHAM5-HAM. The evaluation shows that the global aerosol properties can be reproduced reasonably well using a coarse resolution of 10 sections in size space. The simulated global aerosol budgets are within the range of previous studies. Surface concentrations of sulphate and carbonaceous species have an annual mean within a factor of two of the observations. The simulated sea-salt concentrations reproduce the observations within a factor of two, apart from the Southern Ocean over which the concentrations are within a factor of five. Regionally, AOD is in a relatively good agreement with the observations (within a factor of two). At mid-latitudes the observed AOD is captured well, while at high-latitudes as well as in some polluted and dust regions the modelled AOD is significantly lower than observed. Regarding most of the investigated aerosol properties, the SALSA and the modal aerosol module M7 perform comparably well against observations. However, SALSA reproduces the observed number concentrations and the size distribution of CCN sized particles much more accurately than M7, and is therefore a good choice for aerosol-cloud interaction studies in global models. Our study also shows that when activation type nucleation in the boundary layer is included, the observed concentration of particles under 50 nm in diameter are reproduced much better compared to when only binary nucleation in the free troposphere is assumed.

scholarly journals Uncertainty analysis for estimates of the first indirect aerosol effect

2005 ◽  
Vol 5 (4) ◽  
pp. 4507-4543 ◽  
Author(s):  
Y. Chen ◽  
J. E. Penner
Keyword(s):  
Size Distribution ◽  
Chemical Transport ◽  
Cloud Fraction ◽  
Radiative Transfer Model ◽  
Aerosol Size Distribution ◽  
Transfer Model ◽  
Transport Models ◽  
Aerosol Forcing ◽  
Chemical Transport Models ◽  
Indirect Forcing

Abstract. The IPCC has stressed the importance of producing unbiased estimates of the uncertainty in indirect aerosol forcing, in order to give policy makers as well as research managers an understanding of the most important aspects of climate change that require refinement. In this study, we use 3-D meteorological fields together with a radiative transfer model to examine the spatially-resolved uncertainty in estimates of the first indirect aerosol forcing. Uncertainties in the indirect forcing associated with aerosol and aerosol precursor emissions, aerosol mass concentrations from different chemical transport models, aerosol size distributions, the cloud droplet parameterization, the representation of the in-cloud updraft velocity, the relationship between effective radius and volume mean radius, cloud liquid water content, cloud fraction, and the change in the cloud drop single scattering albedo due to the presence of black carbon are calculated. The cloud fraction is found to be the most important source of uncertainty and causes an overestimation of the indirect forcing by almost 0.8 Wm−2 in the reference case. Uncertainties associated with aerosol and aerosol precursor emissions are the next most important uncertainty followed closely by uncertainties in the calculation of aerosol burden by chemical transport models and uncertainties in the representation of the aerosol size distribution (including the representation of the pre-industrial size distribution). There are significant regional differences in the uncertainty associated with the first indirect forcing with largest uncertainties in regions associated with the major biomass burning regions followed by uncertainties in Asia and Europe.

scholarly journals Toward a minimal representation of aerosols in climate models: description and evaluation in the Community Atmosphere Model CAM5

2012 ◽  
Vol 5 (3) ◽  
pp. 709-739 ◽  
Author(s):  
X. Liu ◽  
R. C. Easter ◽  
S. J. Ghan ◽  
R. Zaveri ◽  
P. Rasch ◽  
...  
Keyword(s):  
Developing Countries ◽  
Optical Properties ◽  
Size Distribution ◽  
Sea Salt ◽  
The Arctic ◽  
Aerosol Size Distribution ◽  
Model Version ◽  
Community Atmosphere Model ◽  
Atmosphere Model ◽  
Aerosol Module

Abstract. A modal aerosol module (MAM) has been developed for the Community Atmosphere Model version 5 (CAM5), the atmospheric component of the Community Earth System Model version 1 (CESM1). MAM is capable of simulating the aerosol size distribution and both internal and external mixing between aerosol components, treating numerous complicated aerosol processes and aerosol physical, chemical and optical properties in a physically-based manner. Two MAM versions were developed: a more complete version with seven lognormal modes (MAM7), and a version with three lognormal modes (MAM3) for the purpose of long-term (decades to centuries) simulations. In this paper a description and evaluation of the aerosol module and its two representations are provided. Sensitivity of the aerosol lifecycle to simplifications in the representation of aerosol is discussed. Simulated sulfate and secondary organic aerosol (SOA) mass concentrations are remarkably similar between MAM3 and MAM7. Differences in primary organic matter (POM) and black carbon (BC) concentrations between MAM3 and MAM7 are also small (mostly within 10%). The mineral dust global burden differs by 10% and sea salt burden by 30–40% between MAM3 and MAM7, mainly due to the different size ranges for dust and sea salt modes and different standard deviations of the log-normal size distribution for sea salt modes between MAM3 and MAM7. The model is able to qualitatively capture the observed geographical and temporal variations of aerosol mass and number concentrations, size distributions, and aerosol optical properties. However, there are noticeable biases; e.g., simulated BC concentrations are significantly lower than measurements in the Arctic. There is a low bias in modeled aerosol optical depth on the global scale, especially in the developing countries. These biases in aerosol simulations clearly indicate the need for improvements of aerosol processes (e.g., emission fluxes of anthropogenic aerosols and precursor gases in developing countries, boundary layer nucleation) and properties (e.g., primary aerosol emission size, POM hygroscopicity). In addition, the critical role of cloud properties (e.g., liquid water content, cloud fraction) responsible for the wet scavenging of aerosol is highlighted.

scholarly journals The relationship between aerosol and cloud drop number concentrations in a global aerosol microphysics model

2009 ◽  
Vol 9 (12) ◽  
pp. 4131-4144 ◽  
Author(s):  
K. J. Pringle ◽  
K. S. Carslaw ◽  
D. V. Spracklen ◽  
G. M. Mann ◽  
M. P. Chipperfield
Keyword(s):  
Size Distribution ◽  
Cloud Droplet ◽  
Global Scale ◽  
Rate Of Change ◽  
The Arctic ◽  
Aerosol Size Distribution ◽  
Percentage Error ◽  
Empirical Relationships ◽  
Wide Range ◽  
Global Mean

Abstract. Empirical relationships that link cloud droplet number (CDN) to aerosol number or mass are commonly used to calculate global fields of CDN for climate forcing assessments. In this work we use a sectional global model of sulfate and sea-salt aerosol coupled to a mechanistic aerosol activation scheme to explore the limitations of this approach. We find that a given aerosol number concentration produces a wide range of CDN concentrations due to variations in the shape of the aerosol size distribution. On a global scale, the dependence of CDN on the size distribution results in regional biases in predicted CDN (for a given aerosol number). Empirical relationships between aerosol number and CDN are often derived from regional data but applied to the entire globe. In an analogous process, we derive regional "correlation-relations" between aerosol number and CDN and apply these regional relations to calculations of CDN on the global scale. The global mean percentage error in CDN caused by using regionally derived CDN-aerosol relations is 20 to 26%, which is about half the global mean percentage change in CDN caused by doubling the updraft velocity. However, the error is as much as 25–75% in the Southern Ocean, the Arctic and regions of persistent stratocumulus when an aerosol-CDN correlation relation from the North Atlantic is used. These regions produce much higher CDN concentrations (for a given aerosol number) than predicted by the globally uniform empirical relations. CDN-aerosol number relations from different regions also show very different sensitivity to changing aerosol. The magnitude of the rate of change of CDN with particle number, a measure of the aerosol efficacy, varies by a factor 4. CDN in cloud processed regions of persistent stratocumulus is particularly sensitive to changing aerosol number. It is therefore likely that the indirect effect will be underestimated in these important regions.

scholarly journals Using MODIS and AERONET to Determine GCM Aerosol Size

2006 ◽  
Vol 63 (4) ◽  
pp. 1338-1347 ◽  
Author(s):  
Glen Lesins ◽  
Ulrike Lohmann
Keyword(s):  
Size Distribution ◽  
Aerosol Optical Depth ◽  
Optical Depth ◽  
General Circulation ◽  
Climate Model ◽  
General Circulation Models ◽  
Aerosol Size Distribution ◽  
Error Source ◽  
Fine Mode ◽  
Fine Mode Aerosol

Abstract Aerosol size is still a poorly constrained quantity in general circulation models (GCMs). By using the modal radii of the coarse and fine mode retrieved from 103 stations in the Aerosol Robotic Network (AERONET) and the fine mode aerosol optical depth fraction derived from both the Moderate Resolute Imaging Spectroradiometer (MODIS) Terra and AERONET, a globally and monthly averaged aerosol size distribution dataset was computed assuming internally mixed aerosols. Different methods were employed in creating the size distribution datasets that were input to the ECHAM4 climate model giving a globally averaged aerosol optical depth (AOD) at 500 nm that ranged from 0.11 to 0.20 depending on the method. This translates into a globally averaged direct aerosol top-of-atmosphere forcing range from −1.6 to −3.9 W m−2. Reducing the uncertainty in the aerosol sizes is important when using AOD to validate models since mass burden errors can then be assumed to be the main AOD error source. This paper explores a procedure that can help achieve this goal.

scholarly journals An aerosol activation metamodel of v1.2.0 of the pyrcel cloud parcel model: development and offline assessment for use in an aerosol–climate model

2017 ◽  
Vol 10 (4) ◽  
pp. 1817-1833 ◽  
Author(s):  
Daniel Rothenberg ◽  
Chien Wang
Keyword(s):  
Size Distribution ◽  
Relative Error ◽  
Climate Model ◽  
Cloud Condensation Nuclei ◽  
Full Range ◽  
Model Development ◽  
Cloud Droplet ◽  
Aerosol Size Distribution ◽  
Mean Relative Error ◽  
Distribution Parameters

Abstract. We describe an emulator of a detailed cloud parcel model which has been trained to assess droplet nucleation from a complex, multimodal aerosol size distribution simulated by a global aerosol–climate model. The emulator is constructed using a sensitivity analysis approach (polynomial chaos expansion) which reproduces the behavior of the targeted parcel model across the full range of aerosol properties and meteorology simulated by the parent climate model. An iterative technique using aerosol fields sampled from a global model is used to identify the critical aerosol size distribution parameters necessary for accurately predicting activation. Across the large parameter space used to train them, the emulators estimate cloud droplet number concentration (CDNC) with a mean relative error of 9.2 % for aerosol populations without giant cloud condensation nuclei (CCN) and 6.9 % when including them. Versus a parcel model driven by those same aerosol fields, the best-performing emulator has a mean relative error of 4.6 %, which is comparable with two commonly used activation schemes also evaluated here (which have mean relative errors of 2.9 and 6.7 %, respectively). We identify the potential for regional biases in modeled CDNC, particularly in oceanic regimes, where our best-performing emulator tends to overpredict by 7 %, whereas the reference activation schemes range in mean relative error from −3 to 7 %. The emulators which include the effects of giant CCN are more accurate in continental regimes (mean relative error of 0.3 %) but strongly overestimate CDNC in oceanic regimes by up to 22 %, particularly in the Southern Ocean. The biases in CDNC resulting from the subjective choice of activation scheme could potentially influence the magnitude of the indirect effect diagnosed from the model incorporating it.

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