scholarly journals Is there a bias in AERONET retrievals of aerosol light absorption at low AOD conditions?

Author(s):  
Elisabeth Andrews ◽  
John Ogren ◽  
Stefan Kinne ◽  
Bjorn Samset

Abstract. Here we present new results comparing aerosol absorption optical depth (AAOD) and column single scattering albedo (SSA) obtained from in-situ vertical profile measurements with AERONET ground-based remote sensing from two rural continental sites in the US. The profiles are closely matched in time (within +/-3 h) and space (within 15 km) with the AERONET retrievals. These direct comparisons of in-situ-derived to AERONET-retrieved AAOD (or SSA) reveal that AERONET retrievals yield higher aerosol absorption for the low aerosol optical depth (AOD) conditions prevalent at the two study sites. The tendency of AERONET inversions to overestimate absorption at low AOD values is generally consistent with other published comparisons. We conclude that scaling modelled black carbon concentrations upwards to match AERONET retrievals of AAOD may lead to aerosol absorption overestimates in regions of low AOD.

2017 ◽  
Vol 17 (9) ◽  
pp. 6041-6072 ◽  
Author(s):  
Elisabeth Andrews ◽  
John A. Ogren ◽  
Stefan Kinne ◽  
Bjorn Samset

Abstract. Here we present new results comparing aerosol optical depth (AOD), aerosol absorption optical depth (AAOD) and column single scattering albedo (SSA) obtained from in situ vertical profile measurements with AERONET ground-based remote sensing from two rural, continental sites in the US. The profiles are closely matched in time (within ±3 h) and space (within 15 km) with the AERONET retrievals. We have used Level 1.5 inversion retrievals when there was a valid Level 2 almucantar retrieval in order to be able to compare AAOD and column SSA below AERONET's recommended loading constraint (AOD > 0.4 at 440 nm). While there is reasonable agreement for the AOD comparisons, the direct comparisons of in situ-derived to AERONET-retrieved AAOD (or SSA) reveal that AERONET retrievals yield higher aerosol absorption than obtained from the in situ profiles for the low aerosol optical depth conditions prevalent at the two study sites. However, it should be noted that the majority of SSA comparisons for AOD440 > 0.2 are, nonetheless, within the reported SSA uncertainty bounds. The observation that, relative to in situ measurements, AERONET inversions exhibit increased absorption potential at low AOD values is generally consistent with other published AERONET–in situ comparisons across a range of locations, atmospheric conditions and AOD values. This systematic difference in the comparisons suggests a bias in one or both of the methods, but we cannot assess whether the AERONET retrievals are biased towards high absorption or the in situ measurements are biased low. Based on the discrepancy between the AERONET and in situ values, we conclude that scaling modeled black carbon concentrations upwards to match AERONET retrievals of AAOD should be approached with caution as it may lead to aerosol absorption overestimates in regions of low AOD. Both AERONET retrievals and in situ measurements suggest there is a systematic relationship between SSA and aerosol amount (AOD or aerosol light scattering) – specifically that SSA decreases at lower aerosol loading. This implies that the fairly common assumption that AERONET SSA values retrieved at high-AOD conditions can be used to obtain AAOD at low-AOD conditions may not be valid.


2020 ◽  
Author(s):  
Lucia Timea Deaconu ◽  
Duncan Watson-Parris ◽  
Philip Stier ◽  
Lindsay Lee

<p>Absorbing aerosols affect the climate system (radiative forcing, cloud formation, precipitation and more) by strongly absorbing solar radiation, particularly at ultraviolet and visible wavelengths. The environmental impacts of an absorbing aerosol layer are influenced by its single scattering albedo (SSA), the albedo of the underlying surface, and also by the atmospheric residence time and column concentration of the aerosols.</p><p>Black-carbon (BC), the collective term used for strongly absorbing, carbonaceous aerosols, emitted by incomplete combustion of fossil fuel, biofuel and biomass, is a significant contributor to atmospheric absorption and probably a main-driver in inter-model differences and large uncertainties in estimating the aerosol radiative forcing due to aerosol-radiation interaction (RFari). Estimates of BC direct radiative forcing suggest a positive effect of +0.71 Wm<sup>-2</sup> (Bond and Bergstrom (2006)) with large uncertainties [+0.08, +1.27] Wm<sup>-2</sup>. These uncertainties result from poor estimates of BC atmospheric burden (emissions and removal rates) and its radiative properties. The uncertainty in the burden is due to the uncertainty in emissions (7.5 [2, 29] Tg yr<sup>-1</sup>) and lifetime (removal rates). In comparison with the available observations, global climate models (GCMs) tend to under-predict absorption near source (e.g. at AERONET stations), and over-predict concentrations in remote regions (e.g. as measured by aircraft campaigns). This may be due to GCM’s weak emissions at the source, but longer lifetime of aerosols in the atmosphere.</p><p>This study aims to address the parametric uncertainty of GCMs and constrain the direct radiative forcing using a perturbed parameter ensemble (PPE) and a collection of observations, from remote sensing to in-situ measurements. Total atmospheric aerosol extinction is quantified using satellite observations that provide aerosol optical depth (AOD), while the SSA is constrained by the use of high-temporal resolution aerosol absorption optical depth (AAOD) measured with AERONET sun-photometers (for near-source columnar information of aerosol absorption) and airborne black-carbon in-situ measurements collected and synthesised in the Global Aerosol Synthesis and Science Project (GASSP) (for properties of long-range transported aerosols). Measurements from the airborne campaigns ATOM and HIPPO are valuable for constraining aerosol absorption in remote areas, while CLARIFY and ORACLES, that were employed over Southeast Atlantic, are considered in our study for near source observations of biomass burning aerosols transported over the bright surface of stratocumulus clouds.</p><p>Using the PPE to explore the uncertainties in the aerosol absorption as well as the dominant emission and removal processes, and by comparing with a variety of observations we have confidence to better constrain the aerosol direct radiative forcing.</p>


2018 ◽  
Vol 176 ◽  
pp. 08005 ◽  
Author(s):  
Alexandra Tsekeri ◽  
Vassilis Amiridis ◽  
Anton Lopatin ◽  
Eleni Marinou ◽  
Eleni Giannakaki ◽  
...  

Aerosol absorption profiling is crucial for radiative transfer calculations and climate modelling. Here, we utilize the synergy of lidar with sun-photometer measurements to derive the absorption coefficient and single scattering albedo profiles during the ACTRIS-2 campaigns held in Germany, Greece and Cyprus. The remote sensing techniques are compared with in situ measurements in order to harmonize and validate the different methodologies and reduce the absorption profiling uncertainties.


2019 ◽  
Author(s):  
Mohanan R. Manoj ◽  
Sreedharan K. Satheesh ◽  
Krishnaswamy K. Moorthy ◽  
Hugh Coe

Abstract. Vertical structures of aerosol single scattering albedo (SSA), from near the surface through the free troposphere, have been estimated for the first time at distinct geographical locations over the Indian mainland and adjoining oceans, using in-situ measurements of aerosol scattering and absorption coefficients aboard the FAAM BAe-146 aircraft during the South West Asian Aerosol Monsoon Interactions (SWAAMI) campaign from June to July 2016. These are used to examine the spatial variation of SSA profiles and also to characterize its transformation from just prior to the onset of Indian Summer Monsoon (June 2016) to its active phase (July 2016). Very strong aerosol absorption, with SSA values as low as 0.7, persisted in the lower altitudes (


2019 ◽  
Vol 12 (2) ◽  
pp. 1365-1373 ◽  
Author(s):  
Apoorva Pandey ◽  
Nishit J. Shetty ◽  
Rajan K. Chakrabarty

Abstract. Mass absorption cross section (MAC) measurements of atmospherically relevant aerosols are required to quantify their effect on Earth's radiative budget. Estimating aerosol light absorption from transmittance and/or reflectance measurements through filter deposits is an attractive option because of their ease of deployment in field settings, low cost, and the ability to revisit previously analyzed samples. These measurements suffer from artifacts that depend on a given filter measurement system and aerosol optics. Empirical correction algorithms are available for commercial instruments equipped with optically thick fiber filters, but optically thin filter media have not been characterized in detail. Here, we present empirical relationships between particle light absorption optical depth – measured using multiwavelength integrated photoacoustic spectrometers – and filter optical depth measurements for polytetrafluoroethylene (PTFE) membrane filter samples of carbonaceous aerosols generated from combustion of diverse biomass fuels and kerosene (surrogate for fossil fuel combustion). Through radiative transfer modeling, we assessed the suitability of three measures of filter-based optical depth for robustly describing particulate-phase light absorption over a range of single scattering albedo (SSA) values: (1) ODs – a measure of transmission of the fraction of incident radiation that is not backscattered by the filter system – which utilizes transmittance and reflectance of the sample side of the filter; (2) the commonly used ODc, which uses transmittance and reflectance of the clean side of the filter; and (3) ATN or the Beer–Lambert attenuation. Modeling results were also validated experimentally, with ODs showing the least variability around the mean in this multidimensional parameter space. We establish a simple, wavelength-independent formulation for calculating aerosol MAC and absorption coefficients from measurements of ODs. We find the ratio between in situ particulate absorption optical depth and ODs to be inversely proportional to aerosol SSA. Our findings underscore that ODs is a better optical depth measure than ODc for applying appropriate correction factors when estimating particle-phase light absorption from filter-based techniques.


2014 ◽  
Vol 14 (4) ◽  
pp. 2139-2153 ◽  
Author(s):  
S. Crumeyrolle ◽  
G. Chen ◽  
L. Ziemba ◽  
A. Beyersdorf ◽  
L. Thornhill ◽  
...  

Abstract. During the NASA DISCOVER-AQ campaign over the US Baltimore, MD–Washington, D.C., metropolitan area in July 2011, the NASA P-3B aircraft performed extensive profiling of aerosol optical, chemical, and microphysical properties. These in situ profiles were coincident with ground-based remote sensing (AERONET) and in situ (PM2.5) measurements. Here, we use this data set to study the correlation between the PM2.5 observations at the surface and the column integrated measurements. Aerosol optical depth (AOD550 nm) calculated with the extinction (550 nm) measured during the in situ profiles was found to be strongly correlated with the volume of aerosols present in the boundary layer (BL). Despite the strong correlation, some variability remains, and we find that the presence of aerosol layers above the BL (in the buffer layer – BuL) introduces significant uncertainties in PM2.5 estimates based on column-integrated measurements (overestimation of PM2.5 by a factor of 5). This suggests that the use of active remote sensing techniques would dramatically improve air quality retrievals. Indeed, the relationship between the AOD550 nm and the PM2.5 is strongly improved by accounting for the aerosol present in and above the BL (i.e., integrating the aerosol loading from the surface to the top of the BuL). Since more than 15% of the AOD values observed during DISCOVER-AQ are dominated by aerosol water uptake, the f(RH)amb (ratio of scattering coefficient at ambient relative humidity (RH) to scattering coefficient at low RH; see Sect. 3.2) is used to study the impact of the aerosol hygroscopicity on the PM2.5 retrievals. The results indicate that PM2.5 can be predicted within a factor up to 2 even when the vertical variability of the f(RH)amb is assumed to be negligible. Moreover, f(RH = 80%) and RH measurements performed at the ground may be used to estimate the f(RH)amb during dry conditions (RHBL < 55%).


2007 ◽  
Vol 7 (23) ◽  
pp. 5937-5943 ◽  
Author(s):  
R. W. Bergstrom ◽  
P. Pilewskie ◽  
P. B. Russell ◽  
J. Redemann ◽  
T. C. Bond ◽  
...  

Abstract. We have determined the solar spectral absorption optical depth of atmospheric aerosols for specific case studies during several field programs (three cases have been reported previously; two are new results). We combined airborne measurements of the solar net radiant flux density and the aerosol optical depth with a detailed radiative transfer model for all but one of the cases. The field programs (SAFARI 2000, ACE Asia, PRIDE, TARFOX, INTEX-A) contained aerosols representing the major absorbing aerosol types: pollution, biomass burning, desert dust and mixtures. In all cases the spectral absorption optical depth decreases with wavelength and can be approximated with a power-law wavelength dependence (Absorption Angstrom Exponent or AAE). We compare our results with other recent spectral absorption measurements and attempt to briefly summarize the state of knowledge of aerosol absorption spectra in the atmosphere. We discuss the limitations in using the AAE for calculating the solar absorption. We also discuss the resulting spectral single scattering albedo for these cases.


2020 ◽  
Author(s):  
Bonan Li ◽  
Stephen P. Good

Abstract. NASA's Soil Moisture Active-Passive (SMAP) mission characterizes global spatiotemporal patterns in surface soil moisture using dual L-band microwave retrievals of horizontal, TBh, and vertical, TBv, polarized microwave brightness temperatures through a modeled relationship between vegetation opacity and surface scattering albedo (i.e. tau-omega model). Although this model has been validated against in situ soil moisture measurements across sparse validations sites, there is lack of systematic characterization of where and why SMAP estimates deviate from the in situ observations. Here, soil moisture observations from the US Climate Reference Network are used within a mutual information framework to decompose the overall retrieval uncertainty from SMAPs Modified Dual Channel Algorithm (MDCA) into random uncertainty derived from raw data itself and model uncertainty derived from the model’s inherent structure. The results shown that, on average, 12 % of the uncertainty in SMAP soil moisture estimates is caused by the loss of information in the MDCA model itself while the remainder is induced by inadequacy of TBh and TBv observations. We find the fraction of algorithm induced uncertainty is negatively correlated (pearson r of −0.48) with correlations between in-situ observations and MDCA estimates. A decomposition of mutual information between TBh, TBv and MDCA soil moisture shows that on average 55 % of the mutual information is redundantly shared by TBh and TBv, while the information provided uniquely from both TBh and TBv is 15 %. The fraction of information redundantly provided by TBh and TBv was found to be tightly correlated (pearson r = −0.7) to how well the MDCA output correlated to in situ observations. Thus, MDCA overall quality improves as TBh and TBv provide more redundant information for the MDCA. This suggests the informational redundancy between these remotely sensed observations can be used as independent metric to assess the overall quality of algorithms using these data streams. This study provides a baseline approach that can also be applied to evaluate other remote sensing models and understand informational loss as satellite retrievals are translated to end user products.


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