More Than Emissions and Chemistry: Fire Size, Dilution, and Background Aerosol Also Greatly Influence Near‐Field Biomass Burning Aerosol Aging

2019 ◽  
Vol 124 (10) ◽  
pp. 5589-5611 ◽  
Author(s):  
A. L. Hodshire ◽  
Q. Bian ◽  
E. Ramnarine ◽  
C. R. Lonsdale ◽  
M. J. Alvarado ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Near Field ◽  
Fire Size ◽  
Biomass Burning Aerosol ◽  
Aerosol Aging

scholarly journals Characterising Brazilian biomass burning emissions using WRF-Chem with MOSAIC sectional aerosol

2015 ◽  
Vol 8 (3) ◽  
pp. 549-577 ◽  
Author(s):  
S. Archer-Nicholls ◽  
D. Lowe ◽  
E. Darbyshire ◽  
W. T. Morgan ◽  
M. M. Bela ◽  
...  
Keyword(s):  
Organic Matter ◽  
Tropical Forest ◽  
Biomass Burning ◽  
Burned Area ◽  
Plume Rise ◽  
Fire Size ◽  
Aerosol Composition ◽  
Fire Emissions ◽  
Biomass Burning Aerosol ◽  
Flight Measurements

Abstract. The South American Biomass Burning Analysis (SAMBBA) field campaign took detailed in situ flight measurements of aerosol during the 2012 dry season to characterise biomass burning aerosol and improve understanding of its impacts on weather and climate. Developments have been made to the Weather Research and Forecast model with chemistry (WRF-Chem) model to improve the representation of biomass burning aerosol in the region, by coupling a sectional aerosol scheme to the plume-rise parameterisation. Brazilian Biomass Burning Emissions Model (3BEM) fire emissions are used, prepared using PREP-CHEM-SRC, and mapped to CBM-Z and MOSAIC species. Model results have been evaluated against remote sensing products, AERONET sites, and four case studies of flight measurements from the SAMBBA campaign. WRF-Chem predicted layers of elevated aerosol loadings (5–20 μg sm−3) of particulate organic matter at high altitude (6–8 km) over tropical forest regions, while flight measurements showed a sharp decrease above 2–4 km altitude. This difference was attributed to the plume-rise parameterisation overestimating injection height. The 3BEM emissions product was modified using estimates of active fire size and burned area for the 2012 fire season, which reduced the fire size. The enhancement factor for fire emissions was increased from 1.3 to 5 to retain reasonable aerosol optical depths (AODs). The smaller fire size lowered the injection height of the emissions, but WRF-Chem still showed elevated aerosol loadings between 4–5 km altitude. Over eastern cerrado (savannah-like) regions, both modelled and measured aerosol loadings decreased above approximately 4 km altitude. Compared with MODIS satellite data and AERONET sites, WRF-Chem represented AOD magnitude well (between 0.3–1.5) over western tropical forest fire regions in the first half of the campaign, but tended to over-predict them in the second half, when precipitation was more significant. Over eastern cerrado regions, WRF-Chem tended to under-predict AODs. Modelled aerosol loadings in the east were higher in the modified emission scenario. The primary organic matter to black carbon ratio was typically between 8–10 in WRF-Chem. This was lower than the western flight measurements (interquartile range of 11.6–15.7 in B734, 14.7–24.0 in B739), but similar to the eastern flight B742 (8.1–10.4). However, single scattering albedo was close to measured over the western flights (0.87–0.89 in model; 0.86–0.91 in flight B734, and 0.81–0.95 in flight B739 measurements) but too high over the eastern flight B742 (0.86–0.87 in model, 0.79–0.82 in measurements). This suggests that improvements are needed to both modelled aerosol composition and optical properties calculations in WRF-Chem.

scholarly journals Characterising Brazilian biomass burning emissions using WRF-Chem with MOSAIC sectional aerosol

2014 ◽  
Vol 7 (5) ◽  
pp. 6061-6131
Author(s):  
S. Archer-Nicholls ◽  
D. Lowe ◽  
E. Darbyshire ◽  
W. T. Morgan ◽  
M. M. Bela ◽  
...  
Keyword(s):  
Organic Matter ◽  
Tropical Forest ◽  
Biomass Burning ◽  
Burned Area ◽  
Plume Rise ◽  
Fire Size ◽  
Aerosol Composition ◽  
Fire Emissions ◽  
Biomass Burning Aerosol ◽  
Flight Measurements

Abstract. The South American Biomass Burning Analysis (SAMBBA) field campaign took detailed in-situ flight measurements of aerosol during the 2012 dry season to characterise biomass burning aerosol and improve understanding of its impacts on weather and climate. Developments have been made to the Weather research and Forecast model with chemistry (WRF-Chem) model to improve the representation of biomass burning aerosol in the region by coupling a sectional aerosol scheme to the plume rise parameterisation. Brazilian Biomass Burning Emissions Model (3BEM) fire emissions are used, prepared using PREP-CHEM-SRC, and mapped to CBM-Z and MOSAIC species. Model results have been evaluated against remote sensing products, AERONET sites, and four case studies of flight measurements from the SAMBBA campaign. WRF-Chem predicted layers of elevated aerosol loadings (5–20 μg sm−3) of particulate organic matter at high altitude (6–8 km) over tropical forest regions, while flight measurements showed a sharp decrease above 2–4 km altitude. This difference was attributed to the plume-rise parameterisation overestimating injection height. The 3BEM emissions product was modified using estimates of active fire size and burned area for the 2012 fire season, which reduced the fire size. The enhancement factor for fire emissions was increased from 1.3 to 5 to retain reasonable aerosol optical depths (AOD). The smaller fire size lowered the injection height of the emissions, but WRF-Chem still showed elevated aerosol loadings between 4–5 km altitude. Over eastern Cerrado (savannah-like) regions, both modelled and measured aerosol loadings decreased above approximately 4 km altitude. Compared with MODIS satellite data and AERONET sites, WRF-Chem represented AOD magnitude well (between 0.3–1.5) over western tropical forest fire regions in the first half of the campaign, but tended to over-predict them in the second half, when precipitation was more significant. Over eastern Cerrado regions, WRF-Chem tended to under-predict AOD. Modeled aerosol loadings in the east were higher in the modified emission scenario. The primary organic matter to black carbon ratio was typically between 8–10 in WRF-Chem. This was lower than western flights measurements (interquartile range of 11.6–15.7 in B734, 14.7–24.0 in B739), but similar to the eastern flight B742 (8.1–10.4). However, single scattering albedo was close to measured over the western flights (0.87–0.89 in model; 0.88–0.91 in flight B734, and 0.86–0.95 in flight B739 measurements) but too high over the eastern flight B742 (0.86–0.87 in model, 0.81–0.84 in measurements). This suggests that improvements are needed to both modeled aerosol composition and optical properties calculations in WRF-Chem.

scholarly journals Aerosol Characterization during the Summer 2017 Huge Fire Event on Mount Vesuvius (Italy) by Remote Sensing and In Situ Observations

2021 ◽  
Vol 13 (10) ◽  
pp. 2001
Author(s):  
Antonella Boselli ◽  
Alessia Sannino ◽  
Mariagrazia D’Emilio ◽  
Xuan Wang ◽  
Salvatore Amoruso
Keyword(s):  
Remote Sensing ◽  
Biomass Burning ◽  
Ground Level ◽  
Large Area ◽  
Fire Event ◽  
Near Surface ◽  
Mean Values ◽  
Microphysical Properties ◽  
Observational Site ◽  
Biomass Burning Aerosol

During the summer of 2017, multiple huge fires occurred on Mount Vesuvius (Italy), dispersing a large quantity of ash in the surrounding area ensuing the burning of tens of hectares of Mediterranean scrub. The fires affected a very large area of the Vesuvius National Park and the smoke was driven by winds towards the city of Naples, causing daily peak values of particulate matter (PM) concentrations at ground level higher than the limit of the EU air quality directive. The smoke plume spreading over the area of Naples in this period was characterized by active (lidar) and passive (sun photometer) remote sensing as well as near-surface (optical particle counter) observational techniques. The measurements allowed us to follow both the PM variation at ground level and the vertical profile of fresh biomass burning aerosol as well as to analyze the optical and microphysical properties. The results evidenced the presence of a layer of fine mode aerosol with large mean values of optical depth (AOD > 0.25) and Ångstrom exponent (γ > 1.5) above the observational site. Moreover, the lidar ratio and aerosol linear depolarization obtained from the lidar observations were about 40 sr and 4%, respectively, consistent with the presence of biomass burning aerosol in the atmosphere.

scholarly journals Analysis of incoming biomass burning aerosol plumes over southern Brazil

2016 ◽  
Vol 17 (11) ◽  
pp. 577-585 ◽  
Author(s):  
Aline Macedo de Oliveira ◽  
Glauber Lopes Mariano ◽  
Marcelo Félix Alonso ◽  
Ericka Voss Chagas Mariano
Keyword(s):  
Biomass Burning ◽  
Southern Brazil ◽  
Biomass Burning Aerosol

scholarly journals High-Resolution Biomass Burning Aerosol Transport Simulations in the Tropics

Atmosphere ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 91
Author(s):  
Nurzahziani ◽  
Chinnawat Surussavadee ◽  
Thanchanok Noosook
Keyword(s):  
High Resolution ◽  
Biomass Burning ◽  
Mean Squared Error ◽  
Dry Mass ◽  
Northern Region ◽  
Emission Model ◽  
Aerosol Transport ◽  
Monthly Average ◽  
Biomass Burning Aerosol ◽  
The Tropics

This study evaluates the performance of the Weather Research and Forecasting Model with Chemistry (WRF-Chem) for simulating biomass burning aerosol transport at high resolution in the tropics using two different biomass burning emission inventories. Hourly, daily, and monthly average PM10 dry mass concentrations at 5 km resolution—simulated separately using the Brazilian Biomass Burning Emission Model (WRF-3BEM) and the Fire Inventory from NCAR (WRF-FINN) and their averages (WRF-AVG) for 3 months from February to April—are evaluated, using measurements from ground stations distributed in northern Thailand for 2014 and 2015. Results show that WRF-3BEM agrees well with observations and performs much better than WRF-FINN and WRF-AVG. WRF-3BEM simulations are almost unbiased, while those of WRF-FINN and WRF-AVG are significantly overestimated due to significant overestimates of FINN emissions. WRF-3BEM and the measured monthly average PM10 concentrations for all stations and both years are 89.22 and 87.20 μg m−3, respectively. The root mean squared error of WRF-3BEM simulated monthly average PM10 concentrations is 72.00 and 47.01% less than those of WRF-FINN and WRF-AVG, respectively. The correlation coefficient of WRF-3BEM simulated monthly PM10 concentrations and measurements is 0.89. WRF-3BEM can provide useful biomass burning aerosol transport simulations for the northern region of Thailand.

scholarly journals Insights into the aging of biomass burning aerosol from satellite observations and 3D atmospheric modeling: evolution of the aerosol optical properties in Siberian wildfire plumes

2021 ◽  
Vol 21 (1) ◽  
pp. 357-392
Author(s):  
Igor B. Konovalov ◽  
Nikolai A. Golovushkin ◽  
Matthias Beekmann ◽  
Meinrat O. Andreae
Keyword(s):  
Optical Properties ◽  
Long Range ◽  
Biomass Burning ◽  
Organic Aerosol ◽  
Satellite Observations ◽  
Long Range Transport ◽  
Aerosol Optical Properties ◽  
Smoke Plumes ◽  
Range Transport ◽  
Aerosol Aging

Abstract. Long-range transport of biomass burning (BB) aerosol from regions affected by wildfires is known to have a significant impact on the radiative balance and air quality in receptor regions. However, the changes that occur in the optical properties of BB aerosol during long-range transport events are insufficiently understood, limiting the adequacy of representations of the aerosol processes in chemistry transport and climate models. Here we introduce a framework to infer and interpret changes in the optical properties of BB aerosol from satellite observations of multiple BB plumes. Our framework includes (1) a procedure for analysis of available satellite retrievals of the absorption and extinction aerosol optical depths (AAOD and AOD) and single-scattering albedo (SSA) as a function of the BB aerosol photochemical age and (2) a representation of the AAOD and AOD evolution with a chemistry transport model (CTM) involving a simplified volatility basis set (VBS) scheme with a few adjustable parameters. We apply this framework to analyze a large-scale outflow of BB smoke plumes from Siberia toward Europe that occurred in July 2016. We use AAOD and SSA data derived from OMI (Ozone Monitoring Instrument) satellite measurements in the near-UV range along with 550 nm AOD and carbon monoxide (CO) columns retrieved from MODIS (Moderate Resolution Imaging Spectroradiometer) and IASI (Infrared Atmospheric Sounding Interferometer) satellite observations, respectively, to infer changes in the optical properties of Siberian BB aerosol due to its atmospheric aging and to get insights into the processes underlying these changes. Using the satellite data in combination with simulated data from the CHIMERE CTM, we evaluate the enhancement ratios (EnRs) that allow isolating AAOD and AOD changes due to oxidation and gas–particle partitioning processes from those due to other processes, including transport, deposition, and wet scavenging. The behavior of EnRs for AAOD and AOD is then characterized using nonlinear trend analysis. It is found that the EnR for AOD strongly increases (by about a factor of 2) during the first 20–30 h of the analyzed evolution period, whereas the EnR for AAOD does not exhibit a statistically significant increase during this period. The increase in AOD is accompanied by a statistically significant enhancement of SSA. Further BB aerosol aging (up to several days) is associated with a strong decrease in EnRs for both AAOD and AOD. Our VBS simulations constrained by the observations are found to be more consistent with satellite observations of strongly aged BB plumes than “tracer” simulations in which atmospheric transformations of BB organic aerosol were disregarded. The simulation results indicate that the upward trends in EnR for AOD and in SSA are mainly due to atmospheric processing of secondary organic aerosol (SOA), leading to an increase in the mass scattering efficiency of BB aerosol. Evaporation and chemical fragmentation of the SOA species, part of which is assumed to be absorptive (to contain brown carbon), are identified as likely reasons for the subsequent decrease in the EnR for both AAOD and AOD. Hence, our analysis reveals that the long-range transport of smoke plumes from Siberian fires is associated with major changes in BB aerosol optical properties and chemical composition. Overall, this study demonstrates the feasibility of using available satellite observations for evaluating and improving representations in atmospheric models of the BB aerosol aging processes in different regions of the world at much larger temporal scales than those typically addressed in aerosol chamber experiments.

scholarly journals The biomass burning aerosol influence on precipitation over the Central Amazon: an observational study

2014 ◽  
Vol 14 (13) ◽  
pp. 18879-18904 ◽  
Author(s):  
W. A. Gonçalves ◽  
L. A. T. Machado ◽  
P.-E. Kirstetter
Keyword(s):  
Biomass Burning ◽  
Climate Model ◽  
Regional Climate ◽  
Droplet Size Distribution ◽  
Particulate Material ◽  
Climate Change Scenarios ◽  
Aggregate Information ◽  
Wet Scavenging ◽  
Biomass Burning Aerosol ◽  
Climate Model Simulations

Abstract. Understanding the aerosol influence on clouds and precipitation is an important key to reduce uncertainties in simulations of climate change scenarios with regards to deforestation fires. Here, we associate rainfall characteristics obtained by an S-Band radar in the Amazon with in situ measurements of biomass burning aerosols for the entire year of 2009. The most important results were obtained during the dry semester (July–December). The results indicate that the aerosol influence on precipitating systems is modulated by the atmospheric instability degree. For stable atmospheres, the higher the aerosol concentration, the lower the precipitation over the region. On the other hand, for unstable cases, higher concentrations of particulate material are associated with more precipitation, elevated presence of ice and larger rain cells, which suggests an association with long lived systems. The results presented were statistically significant. However, due to the limitation imposed by the dataset used, some important features such as wet scavenging and droplet size distribution need further clarification. Regional climate model simulations in addition with new field campaigns could aggregate information to the aerosol/precipitation relationship.

scholarly journals Modelling the optical properties of fresh biomass burning aerosol produced in a smoke chamber: results from the EFEU campaign

2007 ◽  
Vol 7 (4) ◽  
pp. 12657-12686 ◽  
Author(s):  
K. Hungershöfer ◽  
K. Zeromskiene ◽  
Y. Iinuma ◽  
G. Helas ◽  
J. Trentmann ◽  
...  
Keyword(s):  
Optical Properties ◽  
Biomass Burning ◽  
Atmospheric Chemistry ◽  
Absorption Efficiency ◽  
Max Planck ◽  
Fresh Biomass ◽  
Biomass Burning Aerosol ◽  
Smoke Chamber ◽  
The Impact ◽  
Mass Absorption Efficiency

Abstract. A better characterisation of the optical properties of biomass burning aerosol as a function of the burning conditions is required in order to quantify their effects on climate and atmospheric chemistry. Controlled laboratory combustion experiments with different fuel types were carried out at the combustion facility of the Max Planck Institute for Chemistry (Mainz, Germany) as part of the 'Impact of Vegetation Fires on the Composition and Circulation of the Atmosphere' (EFEU) project. Using the measured size distributions as well as mass scattering and absorption efficiencies, Mie calculations provided mean effective refractive indices of 1.60−0.010i and 1.56−0.010i (λ=0.55 μm) for smoke particles emitted from the combustion of savanna grass and an African hardwood (musasa), respectively. The relatively low imaginary parts suggest that the light-absorbing carbon of the investigated fresh biomass burning aerosol is only partly graphitized, resulting in strongly scattering and less absorbing particles. While the observed variability in mass scattering efficiencies was consistent with changes in particle size, the changes in the mass absorption efficiency can only be explained, if the chemical composition of the particles varies with combustion conditions.

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