scholarly journals The invigoration of deep convective clouds over the Atlantic: aerosol effect, meteorology or retrieval artifact?

2010 ◽  
Vol 10 (18) ◽  
pp. 8855-8872 ◽  
Author(s):  
I. Koren ◽  
G. Feingold ◽  
L. A. Remer
Keyword(s):  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Transport Model ◽  
Chemical Transport ◽  
Reanalysis Data ◽  
Cloud Fraction ◽  
Chemical Transport Model ◽  
Convective Clouds ◽  
Cloud Parameters ◽  
Cloud Properties

Abstract. Associations between cloud properties and aerosol loading are frequently observed in products derived from satellite measurements. These observed trends between clouds and aerosol optical depth suggest aerosol modification of cloud dynamics, yet there are uncertainties involved in satellite retrievals that have the potential to lead to incorrect conclusions. Two of the most challenging problems are addressed here: the potential for retrieved aerosol optical depth to be cloud-contaminated, and as a result, artificially correlated with cloud parameters; and the potential for correlations between aerosol and cloud parameters to be erroneously considered to be causal. Here these issues are tackled directly by studying the effects of the aerosol on convective clouds in the tropical Atlantic Ocean using satellite remote sensing, a chemical transport model, and a reanalysis of meteorological fields. Results show that there is a robust positive correlation between cloud fraction or cloud top height and the aerosol optical depth, regardless of whether a stringent filtering of aerosol measurements in the vicinity of clouds is applied, or not. These same positive correlations emerge when replacing the observed aerosol field with that derived from a chemical transport model. Model-reanalysis data is used to address the causality question by providing meteorological context for the satellite observations. A correlation exercise between the full suite of meteorological fields derived from model reanalysis and satellite-derived cloud fields shows that observed cloud top height and cloud fraction correlate best with model pressure updraft velocity and relative humidity. Observed aerosol optical depth does correlate with meteorological parameters but usually different parameters from those that correlate with observed cloud fields. The result is a near-orthogonal influence of aerosol and meteorological fields on cloud top height and cloud fraction. The results strengthen the case that the aerosol does play a role in invigorating convective clouds.

scholarly journals The invigoration of deep convective clouds over the Atlantic: aerosol effect, meteorology or retrieval artifact?

2010 ◽  
Vol 10 (2) ◽  
pp. 3893-3936 ◽  
Author(s):  
I. Koren ◽  
G. Feingold ◽  
L. A. Remer
Keyword(s):  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Transport Model ◽  
Chemical Transport ◽  
Cloud Fraction ◽  
Chemical Transport Model ◽  
Convective Clouds ◽  
Cloud Parameters ◽  
Aerosol Effect ◽  
Positive Correlations

Abstract. The effects of the aerosol on convective clouds in the tropical Atlantic Ocean are explored using satellite remote sensing, a chemical transport model, and a reanalysis of meteorological fields. Two of the most challenging problems are addressed: the potential for elements of the cloud field to be erroneously ascribed to aerosol optical depth; and the potential for correlations between aerosol and cloud parameters to be erroneously considered to be causal. Results show that there is a robust positive correlation between cloud fraction or cloud top height and the aerosol optical depth, regardless of whether a stringent filtering of aerosol measurements in the vicinity of clouds is applied, or not. These same positive correlations emerge when replacing the observed aerosol field with that derived from a chemical transport model. A correlation exercise between the full suite of meteorological fields derived from model reanalysis and satellite-derived cloud fields shows that observed cloud top height and cloud fraction correlate best with pressure updraft velocity and relative humidity. Observed aerosol optical depth does correlate with meteorological parameters but usually different parameters from those that correlate with observed cloud fields. The result is a near-orthogonal influence of aerosol and meteorological fields on cloud top height and cloud fraction. The results strengthen the case that the aerosol does play a role in invigorating convective clouds.

scholarly journals Estimated total emissions of trace gases from the Canberra wildfires of 2003: a new method using satellite measurements of aerosol optical depth and the MOZART chemical transport model

2010 ◽  
Vol 10 (1) ◽  
pp. 977-1004
Author(s):  
C. Paton-Walsh ◽  
L. K. Emmons ◽  
S. R. Wilson
Keyword(s):  
Carbon Monoxide ◽  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Transport Model ◽  
Trace Gases ◽  
Chemical Transport ◽  
New Method ◽  
Chemical Transport Model ◽  
Additional Tool ◽  
Vegetation Fires

Abstract. In this paper we describe a new method for estimating trace gas emissions from large vegetation fires using measurements of aerosol optical depth from the MODIS instruments onboard NASA's Terra and Aqua satellites, combined with the atmospheric chemical transport model MOZART. The model allows for an estimate of double counting of enhanced levels of aerosol optical depth in consecutive satellite overpasses. Using this method we infer an estimated total emission of 10±3 Tg of carbon monoxide from the Canberra fires of 2003. Emissions estimates for several other trace gases are also given. An assessment of the uncertainties in the new method is made and we show that our estimate agrees (within expected uncertainties) with estimates made using current conventional methods of multiplying together factors for the area burned, fuel load, the combustion efficiency and the emission factor for carbon monoxide. The new method for estimating emissions from large vegetation fires described in this paper has some significant uncertainties, but these are mainly quantifiable and largely independent of the uncertainties inherent in conventional techniques. Thus we conclude that the new method is a useful additional tool for characterising emissions from vegetation fires.

scholarly journals Estimated total emissions of trace gases from the Canberra Wildfires of 2003: a new method using satellite measurements of aerosol optical depth & the MOZART chemical transport model

2010 ◽  
Vol 10 (12) ◽  
pp. 5739-5748 ◽  
Author(s):  
C. Paton-Walsh ◽  
L. K. Emmons ◽  
S. R. Wilson
Keyword(s):  
Carbon Monoxide ◽  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Transport Model ◽  
Chemical Transport ◽  
New Method ◽  
Chemical Transport Model ◽  
Satellite Measurements ◽  
Additional Tool ◽  
Vegetation Fires

Abstract. In this paper we describe a new method for estimating trace gas emissions from large vegetation fires using satellite measurements of aerosol optical depth (AOD) at 550 nm, combined with an atmospheric chemical transport model. The method uses a threshold value to screen out normal levels of AOD that may be caused by raised dust, sea salt aerosols or diffuse smoke transported from distant fires. Using this method we infer an estimated total emission of 15±5 Tg of carbon monoxide, 0.05±0.02 Tg of hydrogen cyanide, 0.11±0.03 Tg of ammonia, 0.25±0.07 Tg of formaldehyde, 0.03±0.01 of acetylene, 0.10±0.03 Tg of ethylene, 0.03±0.01 Tg of ethane, 0.21±0.06 Tg of formic acid and 0.28±0.09 Tg of methanol released to the atmosphere from the Canberra fires of 2003. An assessment of the uncertainties in the new method is made and we show that our estimate agrees (within expected uncertainties) with estimates made using current conventional methods of multiplying together factors for the area burned, fuel load, the combustion efficiency and the emission factor for carbon monoxide. A simpler estimate derived directly from the satellite AOD measurements is also shown to be in agreement with conventional estimates, suggesting that the method may, under certain meteorological conditions, be applied without the complication of using a chemical transport model. The new method is suitable for estimating emissions from distinct large fire episodes and although it has some significant uncertainties, these are largely independent of the uncertainties inherent in conventional techniques. Thus we conclude that the new method is a useful additional tool for characterising emissions from vegetation fires.

Estimating long-term PM2.5 concentrations in China using satellite-based aerosol optical depth and a chemical transport model

2015 ◽  
Vol 166 ◽  
pp. 262-270 ◽  
Author(s):  
Guannan Geng ◽  
Qiang Zhang ◽  
Randall V. Martin ◽  
Aaron van Donkelaar ◽  
Hong Huo ◽  
...  
Keyword(s):  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Transport Model ◽  
Chemical Transport ◽  
Chemical Transport Model

scholarly journals Up/Down trend in the MODIS Aerosol Optical Depth and its relationship to the Sulfur Dioxide Emission Changes in China during 2000 and 2010

2011 ◽  
Vol 11 (8) ◽  
pp. 21971-21993 ◽  
Author(s):  
S. Itahashi ◽  
I. Uno ◽  
K. Yumimoto ◽  
H. Irie ◽  
K. Osada ◽  
...  
Keyword(s):  
East Asia ◽  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Power Plants ◽  
Transport Model ◽  
Chemical Transport ◽  
Chinese Government ◽  
Chemical Transport Model ◽  
So2 Emissions ◽  
So2 Emission

Abstract. Anthropogenic SO2 emissions increased alongside economic development in China at a rate of 12.7 % yr−1 from 2000 to 2005. However, under new Chinese government policy, SO2 emissions declined by 3.9 % yr−1 between 2005 and 2009. Between 2000 and 2010, we found that the variability in the fine-mode (submicron) aerosol optical depth (AOD) over the oceans adjacent to East Asia increased by 4–8 % yr−1 to a peak around 2005–2006 and subsequently decreased by 4–7 % yr−1, based on observations by the Moderate Resolution Imaging Spectroradiometer (MODIS) on board NASA's Terra satellite and simulations by a chemical transport model. This trend is consistent with ground-based observations of the number-size distribution of aerosol particles at a mountainous background observation site in central Japan. These fluctuations in SO2 emission intensity and AOD are thought to reflect the widespread installation of fuel-gas desulfurization (FGD) devices in power plants in China because aerosol sulfate is a major determinant of the AOD in East Asia. Using a chemical transport model, we confirmed that the above-mentioned fluctuation in AOD is mainly caused by changes in SO2 emission rather than by varying meteorological conditions in East Asia. High correlation was also found between satellite-retrieved SO2 vertical column density and bottom-up SO2 emissions, both of which were also consistent with observed AOD trends. We proposed a simplified approach for evaluating changes in SO2 emissions in China, combining the use of modeled sensitivity coefficients that describe the variation of AOD with changes in SO2 emissions and satellite retrieval. Satellite measurements of the AOD above Sea of Japan marked the 4.1 % yr−1 declining between 2007 and 2010, and this correspond to the SO2 emissions from China decreased by ~9 % yr−1 between the same period.

scholarly journals Interannual variation in the fine-mode MODIS aerosol optical depth and its relationship to the changes in sulfur dioxide emissions in China between 2000 and 2010

2012 ◽  
Vol 12 (5) ◽  
pp. 2631-2640 ◽  
Author(s):  
S. Itahashi ◽  
I. Uno ◽  
K. Yumimoto ◽  
H. Irie ◽  
K. Osada ◽  
...  
Keyword(s):  
East Asia ◽  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Transport Model ◽  
Chemical Transport ◽  
Chinese Government ◽  
Chemical Transport Model ◽  
So2 Emissions ◽  
So2 Emission ◽  
Fine Mode

Abstract. Anthropogenic SO2 emissions increased alongside economic development in China at a rate of 12.7% yr−1 from 2000 to 2005. However, under new Chinese government policy, SO2 emissions declined by 3.9% yr−1 between 2005 and 2009. Between 2000 and 2010, we found that the variability in the fine-mode (submicron) aerosol optical depth (AOD) over the oceans adjacent to East Asia increased by 3–8% yr−1 to a peak around 2005–2006 and subsequently decreased by 2–7% yr−1, based on observations by the Moderate Resolution Imaging Spectroradiometer (MODIS) on board NASA's Terra satellite and simulations by a chemical transport model. This trend is consistent with ground-based observations of aerosol particles at a mountainous background observation site in central Japan. These fluctuations in SO2 emission intensity and fine-mode AOD are thought to reflect the widespread installation of fuel-gas desulfurization (FGD) devices in power plants in China, because aerosol sulfate is a major determinant of the fine-mode AOD in East Asia. Using a chemical transport model, we confirmed that the contribution of particulate sulfate to the fine-mode AOD is more than 70% of the annual mean and that the abovementioned fluctuation in fine-mode AOD is caused mainly by changes in SO2 emission rather than by other factors such as varying meteorological conditions in East Asia. A strong correlation was also found between satellite-retrieved SO2 vertical column density and bottom-up SO2 emissions, both of which were also consistent with observed fine-mode AOD trends. We propose a simplified approach for evaluating changes in SO2 emissions in China, combining the use of modeled sensitivity coefficients that describe the variation of fine-mode AOD with changes in SO2 emissions and satellite retrieval. Satellite measurements of fine-mode AOD above the Sea of Japan marked a 4.1% yr−1 decline between 2007 and 2010, which corresponded to the 9% yr−1 decline in SO2 emissions from China during the same period.

scholarly journals The relevance of aerosol optical depth to cumulus fraction changes: a five-year climatology at the ACRF SGP site

2007 ◽  
Vol 7 (4) ◽  
pp. 11797-11837 ◽  
Author(s):  
E. I. Kassianov ◽  
L. K. Berg ◽  
C. Flynn ◽  
S. McFarlane
Keyword(s):  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Great Plains ◽  
Value Added ◽  
Cloud Fraction ◽  
Satellite Observations ◽  
Time Dependent ◽  
Size Dependent ◽  
Cloud Properties ◽  
Moderate Resolution Imaging Spectroradiometer

Abstract. The objective of this study is to investigate, by observational means, the magnitude and sign of the actively discussed relationship between cloud fraction N and aerosol optical depth τa. Collocated and coincident ground-based measurements and Terra/Aqua satellite observations at the Atmospheric Radiation Measurement (ARM) Climate Research Facility (ACRF) Southern Great Plains (SGP) site form the basis of this study. The N–τa relationship occurred in a specific 5-year dataset of fair-weather cumulus (FWC) clouds and mostly non-absorbing aerosols. To reduce possible contamination of the aerosols on the cloud properties estimation (and vice versa), we use independent datasets of τa and N obtained from the Multi-filter Rotating Shadowband Radiometer (MFRSR) measurements and from the ARM Active Remotely Sensed Clouds Locations (ARSCL) value-added product, respectively. Optical depth of the FWC clouds τcld and effective radius of cloud droplets re are obtained from the MODerate resolution Imaging Spectroradiometer (MODIS) data. We found that relationships between cloud properties (N,τcld, re) and aerosol optical depth are time-dependent (morning versus afternoon). Observed time-dependent changes of cloud properties, associated with aerosol loading, control the variability of surface radiative fluxes. In comparison with pristine clouds, the polluted clouds are more transparent in the afternoon due to smaller cloud fraction, smaller optical depth and larger droplets. As a result, the corresponding correlation between the surface radiative flux and τa is positive (warming effect of aerosol). Also we found that relationship between cloud fraction and aerosol optical depth is cloud size dependent. The cloud fraction of large clouds (larger than 1 km) is relatively insensitive to the aerosol amount. In contrast, cloud fraction of small clouds (smaller than 1 km) is strongly positively correlated with τa. This suggests that an ensemble of polluted clouds tends to be composed of smaller clouds than a similar one in a pristine environment. One should be aware of these time- and size-dependent features when qualitatively comparing N–τa relationships obtained from the satellite observations, surface measurements, and model simulations.

scholarly journals Estimating ground-level PM<sub>2.5</sub> in Eastern China using aerosol optical depth determined from the GOCI Satellite Instrument

2015 ◽  
Vol 15 (12) ◽  
pp. 17251-17281 ◽  
Author(s):  
J. Xu ◽  
R. V. Martin ◽  
A. van Donkelaar ◽  
J. Kim ◽  
M. Choi ◽  
...  
Keyword(s):  
Organic Matter ◽  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Transport Model ◽  
Eastern China ◽  
Ground Level ◽  
East China ◽  
Chemical Transport Model ◽  
Near Surface ◽  
Significant Agreement

Abstract. We determine and interpret fine particulate matter (PM2.5) concentrations in East China for January to December 2013 at a horizontal resolution of 6 km from aerosol optical depth (AOD) retrieved from the Korean Geostationary Ocean Color Imager (GOCI) satellite instrument. We implement a set of filters to minimize cloud contamination in GOCI AOD. Evaluation of filtered GOCI AOD with AOD from the Aerosol Robotic Network (AERONET) indicates significant agreement with mean fractional bias (MFB) in Beijing of 6.7 % and northern Taiwan of −1.2 %. We use a global chemical transport model (GEOS-Chem) to relate the total column AOD to the near-surface PM2.5. The simulated PM2.5/AOD ratio exhibits high consistency with ground-based measurements (MFB = −0.52–8.0 %). We evaluate the satellite-derived PM2.5 vs. the ground-level PM2.5 in 2013 measured by the China Environmental Monitoring Center. Significant agreement is found between GOCI-derived PM2.5 and in-situ observations in both annual averages (r = 0.81, N = 494) and monthly averages (MFB = 13.1 %), indicating GOCI provides valuable data for air quality studies in Northeast Asia. The GEOS-Chem simulated chemical speciation of GOCI-derived PM2.5 reveals that secondary inorganics (SO42−, NO3−, NH4+) and organic matter are the most significant components. Biofuel emissions in northern China for heating are responsible for an increase in the concentration of organic matter in winter. The population-weighted GOCI-derived PM2.5 over East China for 2013 is 53.8 μg m−3, threatening the health and life expectancy of its 600 million residents.

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