scholarly journals Quantifying the impact of aerosol scattering on the retrieval of methane from airborne remote sensing measurements

2020 ◽  
Author(s):  
Yunxia Huang ◽  
Vijay Natraj ◽  
Zhaocheng Zeng ◽  
Yuk L. Yung

Abstract. As a greenhouse gas with strong global warming potential, atmospheric methane (CH4) emissions have attracted a great deal of attention. Remote sensing measurements can provide information about CH4 sources and emissions. However, accurate assessment of CH4 emissions is challenging due to the influence of aerosol scattering in the atmosphere. In this study, imaging spectroscopic measurements from the Airborne Visible/Infrared Imaging Spectrometer–Next Generation (AVIRIS-NG) in the short-wave infrared are used to analyze the impact of aerosol scattering on CH4 retrievals. Using a numerically efficient two-stream-exact-single-scattering radiative transfer model, we also simulate AVIRIS-NG measurements for different scenarios and quantify the impact of aerosol scattering using two retrieval techniques – the traditional Matched Filter (MF) method and the Optimal Estimation (OE) method, which is a popular approach for trace gas retrievals. The results show that the MF method exhibits up to 50 % lower fractional retrieval bias compared to the OE method at high CH4 concentrations (> 100 % enhancement over typical background values) and is suitable for detecting strong CH4 emissions, while the OE method is an optimal technique for diffuse sources (

2020 ◽  
Vol 13 (12) ◽  
pp. 6755-6769
Author(s):  
Yunxia Huang ◽  
Vijay Natraj ◽  
Zhao-Cheng Zeng ◽  
Pushkar Kopparla ◽  
Yuk L. Yung

Abstract. As a greenhouse gas with strong global warming potential, atmospheric methane (CH4) emissions have attracted a great deal of attention. Although remote sensing measurements can provide information about CH4 sources and emissions, accurate retrieval is challenging due to the influence of atmospheric aerosol scattering. In this study, imaging spectroscopic measurements from the Airborne Visible/Infrared Imaging Spectrometer – Next Generation (AVIRIS-NG) in the shortwave infrared are used to compare two retrieval techniques – the traditional matched filter (MF) method and the optimal estimation (OE) method, which is a popular approach for trace gas retrievals. Using a numerically efficient radiative transfer model with an exact single-scattering component and a two-stream multiple-scattering component, we also simulate AVIRIS-NG measurements for different scenarios and quantify the impact of aerosol scattering in the two retrieval schemes by including aerosols in the simulations but not in the retrievals. The presence of aerosols causes an underestimation of CH4 in both the MF and OE retrievals; the biases increase with increasing surface albedo and aerosol optical depth (AOD). Aerosol types with high single-scattering albedo and low asymmetry parameter (such as water-soluble aerosols) induce large biases in the retrieval. When scattering effects are neglected, the MF method exhibits lower fractional retrieval bias compared to the OE method at high CH4 concentrations (2–5 times typical background values) and is suitable for detecting strong CH4 emissions. For an AOD value of 0.3, the fractional biases of the MF retrievals are between 1.3 % and 4.5 %, while the corresponding values for OE retrievals are in the 2.8 %–5.6 % range. On the other hand, the OE method is an optimal technique for diffuse sources (<1.5 times typical background values), showing up to 5 times smaller fractional retrieval bias (8.6 %) than the MF method (42.6 %) for the same AOD scenario. However, when aerosol scattering is significant, the OE method is superior since it provides a means to reduce biases by simultaneously retrieving AOD, surface albedo, and CH4. The results indicate that, while the MF method is good for plume detection, the OE method should be employed to quantify CH4 concentrations, especially in the presence of aerosol scattering.


2021 ◽  
Vol 14 (10) ◽  
pp. 6483-6507
Author(s):  
Zhao-Cheng Zeng ◽  
Vijay Natraj ◽  
Feng Xu ◽  
Sihe Chen ◽  
Fang-Ying Gong ◽  
...  

Abstract. Remote sensing of greenhouse gases (GHGs) in cities, where high GHG emissions are typically associated with heavy aerosol loading, is challenging due to retrieval uncertainties caused by the imperfect characterization of scattering by aerosols. We investigate this problem by developing GFIT3, a full physics algorithm to retrieve GHGs (CO2 and CH4) by accounting for aerosol scattering effects in polluted urban atmospheres. In particular, the algorithm includes coarse- (including sea salt and dust) and fine- (including organic carbon, black carbon, and sulfate) mode aerosols in the radiative transfer model. The performance of GFIT3 is assessed using high-spectral-resolution observations over the Los Angeles (LA) megacity made by the California Laboratory for Atmospheric Remote Sensing Fourier transform spectrometer (CLARS-FTS). CLARS-FTS is located on Mt. Wilson, California, at 1.67 km a.s.l. overlooking the LA Basin, and it makes observations of reflected sunlight in the near-infrared spectral range. The first set of evaluations are performed by conducting retrieval experiments using synthetic spectra. We find that errors in the retrievals of column-averaged dry air mole fractions of CO2 (XCO2) and CH4 (XCH4) due to uncertainties in the aerosol optical properties and atmospheric a priori profiles are less than 1 % on average. This indicates that atmospheric scattering does not induce a large bias in the retrievals when the aerosols are properly characterized. The methodology is then further evaluated by comparing GHG retrievals using GFIT3 with those obtained from the CLARS-GFIT algorithm (used for currently operational CLARS retrievals) that does not account for aerosol scattering. We find a significant correlation between retrieval bias and aerosol optical depth (AOD). A comparison of GFIT3 AOD retrievals with collocated ground-based observations from AErosol RObotic NETwork (AERONET) shows that the developed algorithm produces very accurate results, with biases in AOD estimates of about 0.02. Finally, we assess the uncertainty in the widely used tracer–tracer ratio method to obtain CH4 emissions based on CO2 emissions and find that using the CH4/CO2 ratio effectively cancels out biases due to aerosol scattering. Overall, this study of applying GFIT3 to CLARS-FTS observations improves our understanding of the impact of aerosol scattering on the remote sensing of GHGs in polluted urban atmospheric environments. GHG retrievals from CLARS-FTS are potentially complementary to existing ground-based and spaceborne observations to monitor anthropogenic GHG fluxes in megacities.


2012 ◽  
Vol 5 (4) ◽  
pp. 5993-6035 ◽  
Author(s):  
F. Ernst ◽  
C. von Savigny ◽  
A. Rozanov ◽  
V. Rozanov ◽  
K.-U. Eichmann ◽  
...  

Abstract. Stratospheric aerosol extinction profiles are retrieved from SCIAMACHY/Envisat limb-scatter observations in the visible spectral range. The retrieval algorithm is based on a colour-index approach using the normalized limb-radiance profiles at 470 nm and 750 nm wavelength. The optimal estimation approach in combination with the radiative transfer model SCIATRAN is employed for the retrievals. This study presents a detailed description of the retrieval algorithm, and a sensitivity analysis investigating the impact of the most important parameters that affect the aerosol extinction profile retrieval accuracy. It is found that the parameter with the largest impact is surface albedo, particularly for SCIAMACHY observations in the Southern Hemisphere where the error in stratospheric aerosol extinction can be up to 50% if the surface albedo is not well known. The effect of errors in the assumed ozone and neutral density profiles on the aerosol profile retrievals is with generally less than 6% relatively small. The aerosol extinction profiles retrieved from SCIAMACHY are compared with co-located SAGE II solar occultation measurements of stratospheric aerosol extinction during the period 2003–2005. The mean aerosol extinction profiles averaged over all co-locations agree to within 20% between 15 and 35 km altitude. However, larger differences are observed at specific latitudes.


2021 ◽  
Author(s):  
Zhao-Cheng Zeng ◽  
Vijay Natraj ◽  
Feng Xu ◽  
Sihe Chen ◽  
Fang-Ying Gong ◽  
...  

Abstract. Remote sensing of greenhouse gases (GHGs) in cities, where high GHG emissions are typically associated with heavy aerosol loading, is challenging due to retrieval uncertainties caused by imperfect characterization of scattering by aerosols. We investigate this problem by developing GFIT3, a full physics algorithm to retrieve GHGs (CO2 and CH4) by accounting for aerosol scattering effects in polluted urban atmospheres. In particular, the algorithm includes coarse (including sea salt and dust) and fine (including organic carbon, black carbon, and sulfate) mode aerosols in the radiative transfer model. The performance of GFIT3 is assessed using high spectral resolution observations over the Los Angeles (LA) megacity made by the California Laboratory for Atmospheric Remote Sensing–Fourier Transform Spectrometer (CLARS–FTS). CLARS–FTS is located on Mt. Wilson, California, at 1.67 km a.s.l. overlooking the LA basin, and makes observations of reflected sunlight in the near-infrared spectral range. The first set of evaluations are performed by conducting retrieval experiments using synthetic spectra. We find that errors in the retrievals of column-averaged dry air mole fractions of CO2 (XCO2) and CH4 (XCH4) due to uncertainties in the aerosol optical properties and atmospheric a priori profiles are less than 1 % on average. This indicates that atmospheric scattering does not induce a large bias in the retrievals when the aerosols are properly characterised. The methodology is then further evaluated by comparing GHG retrievals using GFIT3 with those obtained from the CLARS-GFIT algorithm (used for currently operational CLARS retrievals) that does not account for aerosol scattering. We find a significant correlation between retrieval bias and aerosol optical depth (AOD). Comparison of GFIT3 AOD retrievals with collocated ground-based observations from AERONET shows that the developed algorithm produces very accurate results, with biases in AOD estimates of about 0.02. Finally, we assess the uncertainty in the widely used tracer-tracer ratio method to obtain CH4 emissions based on CO2 emissions, and find that using the CH4 / CO2 ratio effectively cancels out biases due to aerosol scattering. Overall, this study of applying GFIT3 to CLARS-FTS observations improves our understanding of the impact of aerosol scattering on the remote sensing of GHGs in polluted urban atmospheric environments. GHG retrievals from CLARS-FTS are potentially complementary to existing ground-based and space-borne observations to monitor anthropogenic GHG fluxes in megacities.


2002 ◽  
Vol 80 (4) ◽  
pp. 469-481 ◽  
Author(s):  
C A McLinden ◽  
J C McConnell ◽  
K Strong ◽  
I C McDade ◽  
R L Gattinger ◽  
...  

The optical spectrograph and infrared imaging system (OSIRIS), launched in 2001, is a UV–visible diffraction-grating instrument designed to measure light scattered from the Earth's limb. Laboratory measurements of the OSIRIS diffraction-grating efficiency reveal a sensitivity to polarization including an anomalous structure of width 20–30 nm introduced into light polarized in a direction perpendicular to the grooves of the grating. A vector radiative-transfer model was used to generate synthetic OSIRIS spectra in an effort to examine the effect of this on radiances and trace-gas retrievals. Radiances that included grating effects were found to deviate by nearly 10% from those that did not and also contained the anomalous structure. Performing differential optical absorption spectroscopy (DOAS) on these spectra revealed errors in ozone apparent column densities of up to 80 DU. The size of the error was controlled mainly by the difference in polarization between the two DOAS spectra. Two possible correction methods were investigated. The first was to remove the grating effects by applying a correction factor to the raw radiances calculated using the vector radiative-transfer model. The second was to include the efficiency coefficient spectra in the DOAS fit. PACS Nos.: 42.68Mj, 98.55Qf


2019 ◽  
Vol 11 (10) ◽  
pp. 1218 ◽  
Author(s):  
Federico Santini ◽  
Angelo Palombo

The enhanced spectral and spatial resolutions of the remote sensors have increased the need for highly performing preprocessing procedures. In this paper, a comprehensive approach, which simultaneously performs atmospheric and topographic corrections and includes second order corrections such as adjacency effects, was presented. The method, developed under the assumption of Lambertian surfaces, is physically based and uses MODTRAN 4 radiative transfer model. The use of MODTRAN 4 for the estimates of the radiative quantities was widely discussed in the paper and the impact on remote sensing applications was shown through a series of test cases.


2012 ◽  
Vol 5 (2) ◽  
pp. 2043-2075
Author(s):  
S. Noël ◽  
K. Bramstedt ◽  
H. Bovensmann ◽  
J. P. Burrows ◽  
C. Standfuss ◽  
...  

Abstract. The quality of trace gas products derived from measurements of a space-borne imaging spectrometer is affected by the inhomogeneity of the illumination of the instrument slit and thus by the heterogeneity of the observed scene. This paper aims to quantify this effect and summarise findings on how to mitigate the impact of inhomogeneous slit illumination on tropospheric O3, NO2, SO2 and HCHO columns derived from measurements of the Sentinel-4 UVN imaging spectrometer. For this purpose, spectra for inhomogeneous ground scenes have been simulated based on a combination of a radiative transfer model and spatially high resolved MODIS (Moderate Resolution Imaging Spectroradiometer) data. The resulting errors on tropospheric O3, NO2, SO2 and HCHO columns derived from these spectra have been determined via an optimal estimation approach. It could be concluded that inhomogeneous illumination results in significant errors in the data products if the natural inhomogeneity of the observed scenes is not accounted for. O3 columns are less affected than the other data products; largest errors occur for NO2 (mean absolute errors about 5%, maximum error exceeding 50%). These errors may be significantly reduced (by factors up to >10) by an appropriate wavelength calibration applied individually to each Earthshine radiance spectrum. With wavelength calibration the estimated mean absolute errors due to inhomogeneity are for all gases well below 1%; maximum errors are about 10% for NO2 and around 5% for the other gases.


2012 ◽  
Vol 5 (6) ◽  
pp. 1319-1331 ◽  
Author(s):  
S. Noël ◽  
K. Bramstedt ◽  
H. Bovensmann ◽  
K. Gerilowski ◽  
J. P. Burrows ◽  
...  

Abstract. The quality of trace gas products derived from measurements of a space-borne imaging spectrometer is affected by the inhomogeneity of the illumination of the instrument slit and thus by the heterogeneity of the observed scene. This paper aims to quantify this effect and summarise findings on how to mitigate the impact of inhomogeneous slit illumination on tropospheric O3, NO2, SO2 and HCHO columns derived from measurements of the Sentinel-4 UVN imaging spectrometer. For this purpose, spectra for inhomogeneous ground scenes have been simulated based on a combination of a radiative transfer model and spatially high resolved MODIS (Moderate Resolution Imaging Spectroradiometer) data. The resulting errors on tropospheric O3, NO2, SO2 and HCHO columns derived from these spectra have been determined via an optimal estimation approach. We conclude that inhomogeneous illumination results in significant errors in the data products if the natural inhomogeneity of the observed scenes are not accounted for. O3 columns are less affected than the other data products; largest errors occur for NO2 (mean absolute errors about 5%, maximum error exceeding 50%, standard deviation of the errors about 8%). These errors may be significantly reduced (by factors up to about 10) by an appropriate wavelength calibration applied individually to each Earthshine radiance spectrum. With wavelength calibration the estimated mean absolute errors due to inhomogeneity are for all gases well below 1%; standard deviations of the errors are 1.5% or lower; maximum errors are about 10% for NO2 and around 5% for the other gases.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Qinghong Zeng ◽  
Shengbo Chen ◽  
Yuanzhi Zhang ◽  
Yongling Mu ◽  
Rui Dai ◽  
...  

AbstractWe report on the mineralogical and chemical properties of materials investigated by the lunar rover Yutu-2, which landed on the Von Kármán crater in the pre-Nectarian South Pole–Aitken (SPA) basin. Yutu-2 carried several scientific payloads, including the Visible and Near-infrared Imaging Spectrometer (VNIS), which is used for mineral identification, offering insights into lunar evolution. We used 86 valid VNIS data for 21 lunar days, with mineral abundance obtained using the Hapke radiative transfer model and sparse unmixing algorithm and chemical compositions empirically estimated. The mineralogical properties of the materials at the Chang’E-4 (CE-4) site referred to as norite/gabbro, based on findings of mineral abundance, indicate that they may be SPA impact melt components excavated by a surrounding impact crater. We find that CE-4 materials are dominated by plagioclase and pyroxene and feature little olivine, with 50 of 86 observations showing higher LCP than HCP in pyroxene. In view of the effects of space weathering, olivine content may be underestimated, with FeO and TiO2 content estimated using the maturity-corrected method. Estimates of chemical content are 7.42–18.82 wt% FeO and 1.48–2.1 wt% TiO2, with a low-medium Mg number (Mg # ~ 55). Olivine-rich materials are not present at the CE-4 landing site, based on the low-medium Mg #. Multi-origin materials at the CE-4 landing site were analyzed with regard to concentrations of FeO and TiO2 content, supporting our conclusion that the materials at CE-4 do not have a single source but rather are likely a mixture of SPA impact melt components excavated by surrounding impact crater and volcanic product ejecta.


2016 ◽  
Vol 16 (2) ◽  
pp. 873-905 ◽  
Author(s):  
E. W. Butt ◽  
A. Rap ◽  
A. Schmidt ◽  
C. E. Scott ◽  
K. J. Pringle ◽  
...  

Abstract. Combustion of fuels in the residential sector for cooking and heating results in the emission of aerosol and aerosol precursors impacting air quality, human health, and climate. Residential emissions are dominated by the combustion of solid fuels. We use a global aerosol microphysics model to simulate the impact of residential fuel combustion on atmospheric aerosol for the year 2000. The model underestimates black carbon (BC) and organic carbon (OC) mass concentrations observed over Asia, Eastern Europe, and Africa, with better prediction when carbonaceous emissions from the residential sector are doubled. Observed seasonal variability of BC and OC concentrations are better simulated when residential emissions include a seasonal cycle. The largest contributions of residential emissions to annual surface mean particulate matter (PM2.5) concentrations are simulated for East Asia, South Asia, and Eastern Europe. We use a concentration response function to estimate the human health impact due to long-term exposure to ambient PM2.5 from residential emissions. We estimate global annual excess adult (>  30 years of age) premature mortality (due to both cardiopulmonary disease and lung cancer) to be 308 000 (113 300–497 000, 5th to 95th percentile uncertainty range) for monthly varying residential emissions and 517 000 (192 000–827 000) when residential carbonaceous emissions are doubled. Mortality due to residential emissions is greatest in Asia, with China and India accounting for 50 % of simulated global excess mortality. Using an offline radiative transfer model we estimate that residential emissions exert a global annual mean direct radiative effect between −66 and +21 mW m−2, with sensitivity to the residential emission flux and the assumed ratio of BC, OC, and SO2 emissions. Residential emissions exert a global annual mean first aerosol indirect effect of between −52 and −16 mW m−2, which is sensitive to the assumed size distribution of carbonaceous emissions. Overall, our results demonstrate that reducing residential combustion emissions would have substantial benefits for human health through reductions in ambient PM2.5 concentrations.


Sign in / Sign up

Export Citation Format

Share Document