Profiles Of Aerosol Optical Properties Research Articles

Aerosol Vertical Structure and Optical Properties during Two Dust and Haze Episodes in a Typical Valley Basin City, Lanzhou of Northwest China

The vertical profiles of aerosol optical properties are vital to clarify their transboundary transport, climate forcing and environmental health influences. Based on synergistic measurements of multiple advanced detection techniques, this study investigated aerosol vertical structure and optical characteristics during two dust and haze events in Lanzhou of northwest China. Dust particles originated from remote deserts traveled eastward at different altitudes and reached Lanzhou on 10 April 2020. The trans-regional aloft (~4.0 km) dust particles were entrained into the ground, and significantly modified aerosol optical properties over Lanzhou. The maximum aerosol extinction coefficient (σ), volumetric depolarization ratio (VDR), optical depth at 500 nm (AOD500), and surface PM10 and PM2.5 concentrations were 0.4~1.5 km−1, 0.15~0.30, 0.5~3.0, 200~590 μg/m3 and 134 μg/m3, respectively, under the heavy dust event, which were 3 to 11 times greater than those at the background level. The corresponding Ångström exponent (AE440–870), fine-mode fraction (FMF) and PM2.5/PM10 values consistently persisted within the ranges of 0.10 to 0.50, 0.20 to 0.50, and 0.20 to 0.50, respectively. These findings implied a prevailing dominance of coarse-mode and irregular non-spherical particles. A severe haze episode stemming from local emissions appeared at Lanzhou from 30 December 2020 to 2 January 2021. The low-altitude transboundary transport aerosols seriously deteriorated the air quality level in Lanzhou, and aerosol loading, surface air pollutants and fine-mode particles strikingly increased during the gradual strengthening of haze process. The maximum AOD500, AE440–870nm, FMF, PM2.5 and PM10 concentrations, and PM2.5/PM10 were 0.65, 1.50, 0.85, 110 μg/m3, 180 μg/m3 and 0.68 on 2 January 2021, respectively, while the corresponding σ and VDR at 0.20–0.80 km height were maintained at 0.68 km−1 and 0.03~0.12, implying that fine-mode and spherical small particles were predominant. The profile of ozone concentration exhibited a prominent two-layer structure (0.60–1.40 km and 0.10–0.30 km), and both concentrations at two heights always remained at high levels (60~72 μg/m3) during the entire haze event. Conversely, surface ozone concentration showed a significant decrease during severe haze period, with the peak value of 20~30 μg/m3, which was much smaller than that before haze pollution (~80 μg/m3 on 30 December). Our results also highlighted that the vertical profile of aerosol extinction coefficient was a good proxy for evaluating mass concentrations of surface particulate matters under uniform mixing layers, which was of great scientific significance for retrieving surface air pollutants in remote desert or ocean regions. These statistics of the aerosol vertical profiles and optical properties under heavy dust and haze events in Lanzhou would contribute to investigate and validate the transboundary transport and radiative forcing of aloft aerosols in the application of climate models or satellite remote sensing.

Lidar Profiling of Aerosol Vertical Distribution in the Urbanized French Alpine Valley of Annecy and Impact of a Saharan Dust Transport Event

The vertical aerosol layering of the troposphere is poorly documented in mountainous regions, particularly in the Alpine valleys, which are influenced by valley and mountain winds. To improve our knowledge of particulate matter trapped in the Annecy valley, synergetic measurements performed by a ground-based meteorological Raman lidar and a Rayleigh-Mie lidar aboard an ultralight aircraft were implemented as part of the Lacustrine-Water vApor Isotope inVentory Experiment (L-WAIVE) over Lake Annecy. These observations were complemented by satellite observations and Lagrangian modeling. The vertical profiles of aerosol optical properties (e.g., aerosol extinction coefficient (AEC), lidar ratio (LR), particle linear depolarization ratio (PDR)) are derived from lidar measurements at 355 nm during the period between 13 and 22 June 2019. The background aerosol content with an aerosol optical thickness (AOT) of 0.10 ± 0.05, corresponding to local–regional conditions influenced by anthropogenic pollution, has been characterized over the entirety of Lake Annecy thanks to the mobile ultralight payload. The aerosol optical properties are shown to be particularly variable over time in the atmospheric column, with mean LRs (PDRs) varying between 40 ± 8 and 115 ± 15 sr (2 ± 1 and 35 ± 2%). Those conditions can be disturbed by air masses that have recirculated over the valley, as well as by contributions from neighboring valleys. We have observed an important disruption in the atmospheric aerosol profiles by the arrival of an exceptionally dry air mass (RH ~ 30%), containing aerosols identified as coming from the Great Western Erg (AOT ~ 0.5, LR = 65 ± 10 sr, PDR = 20–35%) in the Sahara. These desert dust particles are shown to influence the entire atmospheric column in the Annecy valley. Such an experimental approach, coupling upward and downward lidar and spaceborne observation/Lagrangian modelling, was shown to be of significant interest for the long-term monitoring of the evolution of aerosol loads over deep valleys. It allows a better understanding of the influence of dust storms in the presence of severe convective weather processes.

Seasonal and Diurnal Characteristics of the Vertical Profile of Aerosol Optical Properties in Urban Beijing, 2017–2021

Seasonal and diurnal characteristics of the vertical profiles of aerosol properties are essential for detecting the regional transport and the climatic radiative effects of aerosol particles. We have studied the seasonal and diurnal characteristics of the vertical distribution of aerosols in urban Beijing from 2017 to 2021 based on long-term Raman–Mie LiDAR observations. The influence of the vertical distribution of aerosols, the meteorological conditions within the boundary layer, the optical–radiometric properties of aerosols, and their interconnections, were investigated during a heavy haze pollution event in Beijing from 8 to 15 February 2020 using both meteorological and sun photometer data. The aerosol extinction coefficient was highest in summer (0.4 km−1), followed by winter (0.35 km−1), and roughly equal in spring and autumn (0.3 km−1). The aerosol extinction coefficient showed clear daily variations and was different in different seasons as a result of the variation in the height of the boundary layer. During the haze pollution event, the particulate matter mainly consisted of scattered spherical fine particles and the accumulation time of pollutants measured via the AOD440nm and PM2.5 mass concentration was different as a result of the hygroscopic growth of the aerosol particles. This growth increased scattering and led to an increase in the aerosol optical depth. The vertical transport of particulate matter also contributed to the increase in the aerosol optical depth.

On the influence of VOCs on new particle growth in a Continental-Mediterranean region

A field campaign has been performed in the Madrid region to study the VOC influence in the growth of new particles in ambient air. A number of instruments have been deployed to characterize the main pollutant gases and particle properties and composition. The measurements were performed simultaneously at three sites (rural, urban background and urban traffic influenced) in the period 1–17 July 2019. The sites: Tres Cantos (rural), CIEMAT (urban background) and Leganés (urban traffic) were located within the Madrid airshed. Particle size distributions, mass concentrations at fractions PM10, PM2.5 and PM1, black carbon, VOCs species and gaseous pollutants (NOx and O3) were obtained in the sites. Some supplementary measurements were obtained in at least one of the sites: meteorological parameters, non-refractory submicron aerosol species and vertical profiles of aerosol optical properties. It has been observed that the new particle formation (NPF) events, nucleation and subsequent growth, happened at a regional scale, although differently among the sites. In the rural site, fewer events than expected were observed because of the high temperatures that affected the BVOC emissions. In the urban background site, the highest number of events was reached. In this station, it is common to receive air masses from the nearby forest and from the urban area, producing a mix of conditions with high BVOC and AVOC concentrations. In the urban traffic site, several NPF cases appeared, being a site dominated by AVOCs. Among the BVOCs measured in the three stations, the most common were α-Pinene and Limonene. Among the AVOCs measured, aromatics and linear hydrocarbon compounds for C10 and above were found. The linear group was found to be predominant during the NPF event days in the urban background site. This work provides new insights about the aerosol-forming precursors and growth of new particles in the Madrid region.

Effects of black carbon aerosol on air quality and vertical meteorological factors in early summer in Beijing

Black carbon (BC) aerosols have effects on the atmospheric thermal vertical structure due to its radiation absorption characteristics, hereby influencing the boundary layer characteristics and pollutant diffusion. This study focuses on the BC effects under different atmospheric conditions on air quality and vertical meteorological conditions. Four days flight observation combined with surface wind profiler radar data were used to investigate the vertical profiles of BC and wind speed over Beijing urban area in early summer. The vertical profiles of BC concentration and wind speed in the boundary layer had a negative correlation, both having abrupt changes near the boundary layer height under stagnant weather conditions. The chemical transport model showed the increase of BC under stagnant conditions could cause aggravation of the stability of the boundary layer, thereby increasing the accumulation of pollutants. In particular, BC leads to the changes in the temperature profile, which will modify relative humidity and indirectly lead to the changes in the vertical profile of aerosol optical properties. However, if the early accumulation of BC was absent under more turbulent conditions, the effects of BC on air quality and meteorological conditions were limited.

A Decade of Poland-AOD Aerosol Research Network Observations

The Poland-AOD aerosol research network was established in 2011 to improve aerosol–climate interaction knowledge and provide a real-time and historical, comprehensive, and quantitative database for the aerosol optical properties distribution over Poland. The network consists of research institutions and private owners operating 10 measurement stations and an organization responsible for aerosol model transport simulations. Poland-AOD collaboration provides observations of spectral aerosol optical depth (AOD), Ångstrom Exponent (AE), incoming shortwave (SW) and longwave (LW) radiation fluxes, vertical profiles of aerosol optical properties and surface aerosol scattering and absorption coefficient, as well as microphysical particle properties. Based on the radiative transfer model (RTM), the aerosol radiative forcing (ARF) and the heating rate are simulated. In addition, results from GEM-AQ and WRF-Chem models (e.g., aerosol mass mixing ratio and optical properties for several particle chemical components), and HYSPLIT back-trajectories are used to interpret the results of observation and to describe the 3D aerosol optical properties distribution. Results of Poland-AOD research indicate progressive improvement of air quality and at mospheric turbidity during the last decade. The AOD was reduced by about 0.02/10 yr (at 550 nm), which corresponds to positive trends in ARF. The estimated clear-sky ARF trend is 0.34 W/m2/10 yr and 0.68 W/m2/10 yr, respectively, at TOA and at Earth’s surface. Therefore, reduction in aerosol load observed in Poland can significantly contribute to climate warming.

The Unmanned Systems Research Laboratory (USRL): A New Facility for UAV-Based Atmospheric Observations

The Unmanned Systems Research Laboratory (USRL) of the Cyprus Institute is a new mobile exploratory platform of the EU Research Infrastructure Aerosol, Clouds and Trace Gases Research InfraStructure (ACTRIS). USRL offers exclusive Unmanned Aerial Vehicle (UAV)-sensor solutions that can be deployed anywhere in Europe and beyond, e.g., during intensive field campaigns through a transnational access scheme in compliance with the drone regulation set by the European Union Aviation Safety Agency (EASA) for the research, innovation, and training. UAV sensor systems play a growing role in the portfolio of Earth observation systems. They can provide cost-effective, spatial in-situ atmospheric observations which are complementary to stationary observation networks. They also have strong potential for calibrating and validating remote-sensing sensors and retrieval algorithms, mapping close-to-the-ground emission point sources and dispersion plumes, and evaluating the performance of atmospheric models. They can provide unique information relevant to the short- and long-range transport of gas and aerosol pollutants, radiative forcing, cloud properties, emission factors and a variety of atmospheric parameters. Since its establishment in 2015, USRL is participating in major international research projects dedicated to (1) the better understanding of aerosol-cloud interactions, (2) the profiling of aerosol optical properties in different atmospheric environments, (3) the vertical distribution of air pollutants in and above the planetary boundary layer, (4) the validation of Aeolus satellite dust products by utilizing novel UAV-balloon-sensor systems, and (5) the chemical characterization of ship and stack emissions. A comprehensive overview of the new UAV-sensor systems developed by USRL and their field deployments is presented here. This paper aims to illustrate the strong scientific potential of UAV-borne measurements in the atmospheric sciences and the need for their integration in Earth observation networks.

Radiative effects of long-range-transported Saharan air layers as determined from airborne lidar measurements

Abstract. The radiative effect of long-range-transported Saharan air layers is investigated on the basis of simultaneous airborne high-spectral-resolution and differential-absorption lidar measurements in the vicinity of Barbados. Within the observed Saharan air layers, increased water vapor concentrations compared to the dry trade wind atmosphere are found. The measured profiles of aerosol optical properties and water vapor mixing ratios are used to characterize the atmospheric composition in radiative transfer calculations, to calculate radiative effects of moist Saharan air layers and to determine radiative heating rate profiles. An analysis based on three case studies reveals that the observed enhanced amounts of water vapor within Saharan air layers have a much stronger impact on heating rate calculations than mineral dust aerosol. Maximum mineral dust short-wave heating and long-wave cooling rates are found at altitudes of highest dust concentration (short wave: +0.5 K d−1; long wave: −0.2 K d−1; net: +0.3 K d−1). However, when considering both aerosol concentrations and measured water vapor mixing ratios in radiative transfer calculations, the maximum heating/cooling rates shift to the top of the dust layer (short wave: +2.2 K d−1; long wave: −6.0 to −7.0 K d−1; net: −4.0 to −5.0 K d−1). Additionally, the net heating rates decrease with height – indicating a destabilizing effect in the dust layers. Long-wave counter-radiation of Saharan air layers is found to reduce cooling at the tops of the subjacent marine boundary layers and might lead to less convective mixing in these layers. The overall short-wave radiative effect of mineral dust particles in Saharan air layers indicates a maximum magnitude of −40 W m−2 at surface level and a maximum of −25 W m−2 at the top of the atmosphere.

In situ vertical characteristics of optical properties and heating rates of aerosol over Beijing

Abstract. Characterizing vertical profiles of aerosol optical properties is important because relying on only the surface or column-integrated measurements cannot unambiguously constrain the radiative impacts of aerosol. This study presents series of vertical profiles of in situ measured multi-wavelength optical properties of aerosols during three pollution events from November to December 2016 over the Beijing region. For all pollution events, the clean periods (CPs) before pollution initialization showed a higher scattering Ångström exponent (SAE) and a smaller asymmetry parameter (g) with relatively uniform vertical structures. The heavy pollution periods (HPs) showed an increased particle size, causing these parameters to vary in the opposite way. During the transition periods (TPs), regional transport of aged aerosols at higher altitudes was found. The Aerosol Robotic Network (AERONET) aerosol optical depth (AOD) matched the in situ measurements within 10 %; however the AERONET absorption optical depth (AAOD) was 10 %–20 % higher than the in situ measurements, and this positive discrepancy increased to 30 % at shorter wavelengths. The absorption of brown carbon (BrC) was identified by the increased-absorption Ångström exponent (AAE), and the heating rate of black carbon (BC) and BrC was estimated by computing the spectral absorption coefficient and actinic flux calculated by a radiative transfer model. BC and BrC had a heating rate of up to 0.18 and 0.05 K h−1 in the planetary boundary layer (PBL), respectively, during the pollution period. The fraction of BrC absorption increased from 12 % to 40 % in the PBL from the CP to the HP. Notably, a higher contribution of BrC heating was found above the PBL under polluted conditions. This study paints a full picture of shortwave heating impacts of carbonaceous aerosols during different stages of pollution events and highlights the increased contribution of BrC absorption especially at higher altitudes during pollution.

Lidar Overlap Function Determination Using the Raman Lidar Signals

The determination of vertical distribution of optical properties of clouds and aerosols using the lidar system is affected by the incomplete overlap between the field of view of transmitter i.e. laser beam & the receiver in the near‐field range. Thus, the study of vertical profiles of aerosol optical properties in the lower atmosphere is erroneous without the correction of lidar overlap function. Here we have analysed the effect of overlap using a simple technique proposed by Ansmann and Wandinger to determine overlap function. We have determined the overlap factor for 5 different days of June 2016 and then calculated the mean overlap profile and determined the relative deviation of each day with respect to mean overlap factor. Results reveal that the complete overlap was achieved beyond 300 meters.

Development of a High Spectral Resolution Lidar for day-time measurements of aerosol extinction

Lidar technique is the most performing way to obtain the atmospheric vertical profile of aerosol optical properties with high space-time resolution. With elastic scattering lidars, the retrieval of aerosol optical properties (as the extinction profile) is realizable only with assumptions on aerosol extinction-to-backscatter ratio or with Raman measurement achievable in night-time. In order to overcome these problems, the High Spectral Resolution Lidar (HSRL) technique has been examined. In this paper we present an innovative prototype of High Spectral Resolution Lidar realized at Physics Department of University “Federico II” of Naples for the LISA (LIdar for Space study of the Atmosphere) project in the framework of the China-Italy international cooperation between CNISM and BRIT. The prototype which represents a first step of a spaceborne HSRL, is based on a laser source at 1064nm and 532nm with high spectral resolution ability at 532nm. The separation between the molecular and the aerosol components was obtained through the use of a confocal Fabry-Perot interferometer (CFPI) cavity.

Aerosol profiling during the large scale field campaign CINDI-2

For the validation of space borne observations of NO2 and other trace gases from hyperspectral imagers, ground based instruments based on the MAXDOAS technique are an excellent choice, since they rely on similar retrieval techniques as the observations from orbit. To ensure proper traceability of the MAXDOAS observations, a thorough validation and intercomparison is mandatory. Advanced MAXDOAS observation and retrieval techniques enable inferring vertical structure of trace gases and aerosols. These techniques and their results need validation by e.g. lidar techniques. For the proper understanding of the results from passive remote sensing techniques, independent observations are needed that include parameters needed to understand the light paths, i.e. in-situ aerosol observations of optical and microphysical properties, and essential are in particular the vertical profiles of aerosol optical properties by (Raman) lidar. The approach used in the CINDI-2 campaign held in Cabauw in 2016 is presented in this paper and the results will be discussed in the presentation at the conference.

Vertical profiles of aerosol optical properties and the solar heating rate estimated by combining sky radiometer and lidar measurements

Abstract. The SKYLIDAR algorithm was developed to estimate vertical profiles of aerosol optical properties from sky radiometer (SKYNET) and lidar (AD-Net) measurements. The solar heating rate was also estimated from the SKYLIDAR retrievals. The algorithm consists of two retrieval steps: (1) columnar properties are retrieved from the sky radiometer measurements and the vertically mean depolarization ratio obtained from the lidar measurements and (2) vertical profiles are retrieved from the lidar measurements and the results of the first step. The derived parameters are the vertical profiles of the size distribution, refractive index (real and imaginary parts), extinction coefficient, single-scattering albedo, and asymmetry factor. Sensitivity tests were conducted by applying the SKYLIDAR algorithm to the simulated sky radiometer and lidar data for vertical profiles of three different aerosols, continental average, transported dust, and pollution aerosols. The vertical profiles of the size distribution, extinction coefficient, and asymmetry factor were well estimated in all cases. The vertical profiles of the refractive index and single-scattering albedo of transported dust, but not those of transported pollution aerosol, were well estimated. To demonstrate the performance and validity of the SKYLIDAR algorithm, we applied the SKYLIDAR algorithm to the actual measurements at Tsukuba, Japan. The detailed vertical structures of the aerosol optical properties and solar heating rate of transported dust and smoke were investigated. Examination of the relationship between the solar heating rate and the aerosol optical properties showed that the vertical profile of the asymmetry factor played an important role in creating vertical variation in the solar heating rate. We then compared the columnar optical properties retrieved with the SKYLIDAR algorithm to those produced with the more established scheme SKYRAD.PACK, and the surface solar irradiance calculated from the SKYLIDAR retrievals was compared with pyranometer measurement. The results showed good agreements: the columnar values of the SKYLIDAR retrievals agreed with reliable SKYRAD.PACK retrievals, and the SKYLIDAR retrievals were sufficiently accurate to evaluate the surface solar irradiance.

LIVAS: a 3-D multi-wavelength aerosol/cloud database based on CALIPSO and EARLINET

Abstract. We present LIVAS (LIdar climatology of Vertical Aerosol Structure for space-based lidar simulation studies), a 3-D multi-wavelength global aerosol and cloud optical database, optimized to be used for future space-based lidar end-to-end simulations of realistic atmospheric scenarios as well as retrieval algorithm testing activities. The LIVAS database provides averaged profiles of aerosol optical properties for the potential spaceborne laser operating wavelengths of 355, 532, 1064, 1570 and 2050 nm and of cloud optical properties at the wavelength of 532 nm. The global database is based on CALIPSO observations at 532 and 1064 nm and on aerosol-type-dependent backscatter- and extinction-related Ångström exponents, derived from EARLINET (European Aerosol Research Lidar Network) ground-based measurements for the UV and scattering calculations for the IR wavelengths, using a combination of input data from AERONET, suitable aerosol models and recent literature. The required spectral conversions are calculated for each of the CALIPSO aerosol types and are applied to CALIPSO backscatter and extinction data corresponding to the aerosol type retrieved by the CALIPSO aerosol classification scheme. A cloud optical database based on CALIPSO measurements at 532 nm is also provided, neglecting wavelength conversion due to approximately neutral scattering behavior of clouds along the spectral range of LIVAS. Averages of particle linear depolarization ratio profiles at 532 nm are provided as well. Finally, vertical distributions for a set of selected scenes of specific atmospheric phenomena (e.g., dust outbreaks, volcanic eruptions, wild fires, polar stratospheric clouds) are analyzed and spectrally converted so as to be used as case studies for spaceborne lidar performance assessments. The final global data set includes 4-year (1 January 2008–31 December 2011) time-averaged CALIPSO (Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations) data on a uniform grid of 1° × 1° with the original high vertical resolution of CALIPSO in order to ensure realistic simulations of the atmospheric variability in lidar end-to-end simulations.

Multi-wavelength Raman LIDAR for Use in Determining the Microphysical, Optical, and Radiative Properties of Mixed Aerosols

The Multi-wavelength Raman LIDAR (MRL) system was developed to enable a better understanding of the complex properties of aerosols in the atmosphere. In this study, the microphysical, optical, and radiative properties of mixed aerosols were retrieved using the discrete aerosol observation products from the MRL. The dust mixing ratio, which is the proportion of dust particles to the total mixed, was derived using the particle depolarization ratio. It was employed in the retrieval of backscattering and extinction coefficient profiles for dust and non-dust particles. The vertical profiles of aerosol optical properties were then used as input parameters in the inversion algorithm for the retrieval of microphysical parameters including the effective radius, refractive index, and the single scattering albedo (SSA). Those products were successfully applied to an analysis of radiative flux using a radiative transfer model. The relationship between the MRL derived extinction and aerosol radiative forcing (ARF) in short-wavelength was assessed over Gwangju, Korea. The results clearly demonstrate that the MRL-derived extinction profiles are a good surrogate for use in the estimation of optical, microphysical, and radiative properties of aerosols. It is considered that the analytical results shown in this study can be used to provide a better understanding of air quality and the variation of local radiative effects due to aerosols.

Comparison of AOD between CALIPSO and MODIS: significant differences over major dust and biomass burning regions

Abstract. Cloud–Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) provide global vertical profiles of aerosol optical properties for the first time. In this study, we employed about 6 yr (2006–2011) of CALIPSO level 3 monthly mean gridded aerosol optical depth (AOD) products (daytime and nighttime) for cloud-free conditions, to compare with the Moderate Resolution Imaging Spectroradiometer (MODIS) Terra/Aqua level 3 monthly mean AOD dataset for the same time period. While the spatial distribution and seasonal variability of CALIPSO AOD is generally consistent with that of MODIS, CALIPSO is overall lower than MODIS as MODIS has higher frequency than CALIPSO for most bins of AOD. The correlation between MODIS and CALIPSO is better over ocean than over land. We focused on four regions that have large systematic differences: two over dust regions (the Sahara and Northwest China) and two over biomass burning regions (South Africa and South America). It is found that CALIPSO AOD is significantly lower than MODIS AOD over dust regions during the whole time period, with a maximum difference of 0.3 over the Saharan region and 0.25 over Northwest China. For biomass burning regions, CALIPSO AOD is significantly higher than MODIS AOD over South Africa, with a maximum difference of 0.25. Additionally CALIPSO AOD is slightly higher than MODIS AOD over South America for most of the time period, with a few exceptions in 2006, 2007, and 2010, when biomass burning is significantly stronger than during other years. We analyzed the impact of the satellite spatial and temporal sampling issue by using level 2 CALIPSO and MODIS products, and these systematic differences can still be found. The results of this study indicate that systematic differences of CALIPSO relative to MODIS are closely associated with aerosol types, which vary by location and season. Large differences over dust and biomass burning regions may suggest that assumptions made in satellite retrievals, such as the assumed lidar ratios for CALIPSO retrievals over dust and biomass burning regions or the surface reflectance information and/or the aerosol model utilized by the MODIS algorithm, are not appropriate.

Vertical profiles of aerosol optical properties over central Illinois and comparison with surface and satellite measurements

Abstract. Between June 2006 and September 2009, an instrumented light aircraft measured over 400 vertical profiles of aerosol and trace gas properties over eastern and central Illinois. The primary objectives of this program were to (1) measure the in situ aerosol properties and determine their vertical and temporal variability and (2) relate these aircraft measurements to concurrent surface and satellite measurements. The primary profile location was within 15 km of the NOAA/ESRL surface aerosol monitoring station near Bondville, Illinois. Identical instruments at the surface and on the aircraft ensured that the data from both platforms would be directly comparable and permitted a determination of how representative surface aerosol properties were of the lower column. Aircraft profiles were also conducted occasionally at two other nearby locations to increase the frequency of A-Train satellite underflights for the purpose of comparing in situ and satellite-retrieved aerosol data. Measurements of aerosol properties conducted at low relative humidity over the Bondville site compare well with the analogous surface aerosol data and do not indicate any major sampling issues or that the aerosol is radically different at the surface compared with the lowest flyby altitude of ~ 240 m above ground level. Statistical analyses of the in situ vertical profile data indicate that aerosol light scattering and absorption (related to aerosol amount) decreases substantially with increasing altitude. Parameters related to the nature of the aerosol (e.g., single-scattering albedo, Ångström exponent, etc.), however, are relatively constant throughout the mixed layer, and do not vary as much as the aerosol amount throughout the profile. While individual profiles often showed more variability, the median in situ single-scattering albedo was 0.93–0.95 for all sampled altitudes. Several parameters (e.g., submicrometer scattering fraction, hemispheric backscattering fraction, and scattering Ångström exponent) suggest that the fraction of smaller particles in the aerosol is larger near the surface than at high altitudes. The observed dependence of scattering on size, wavelength, angular integration range, and relative humidity, together with the spectral dependence of absorption, show that the aerosol at higher altitudes is larger, less hygroscopic, and more strongly absorbing at shorter wavelengths, suggesting an increased contribution from dust or organic aerosols. The aerosol profiles show significant differences among seasons. The largest amounts of aerosol (as determined by median light extinction profile measurements) throughout most of the sampled column were observed during summer, with the lowest amounts in the winter and intermediate values in the spring and fall. The highest three profile levels (3.1, 3.7, 4.6 km), however, showed larger median extinction values in the spring, which could reflect long-range transport of dust or smoke aerosols. The aerosols in the mixed layer were darkest (i.e., lowest single-scattering albedo) in the fall, in agreement with surface measurements at Bondville and other continental sites in the US. In situ profiles of aerosol radiative forcing efficiency showed little seasonal or vertical variability. Underflights of the CALIPSO satellite show reasonable agreement in a majority of retrieved profiles between aircraft-measured extinction at 532 nm (adjusted to ambient relative humidity) and CALIPSO-retrieved extinction, and suggest that routine aircraft profiling programs can be used to better understand and validate satellite retrieval algorithms. CALIPSO tended to overestimate the aerosol extinction at this location in some boundary layer flight segments when scattered or broken clouds were present, which could be related to problems with CALIPSO cloud screening methods. The in situ aircraft-collected aerosol data suggest extinction thresholds for the likelihood of aerosol layers being detected by the CALIOP lidar. In this study, aerosol layers with light extinction (532 nm) values > 50 Mm−1 were detected by CALIPSO ~ 95% of the time, while aerosol layers with extinction values lower than 10 Mm−1 had a detection efficiency of < 2%. For all collocated comparison cases, a 50% probability of detection falls at an in situ extinction level of 20–25 Mm−1. These statistical data offer guidance as to the likelihood of CALIPSO's ability to retrieve aerosol extinction at various locations around the globe.

ATMOSPHERIC LIDAR NOISE REDUCTION BASED ON ENSEMBLE EMPIRICAL MODE DECOMPOSITION

Abstract. As an active remote sensing instrument, lidar provides a high spatial resolution vertical profile of aerosol optical properties. But the effective range and data reliability are often limited by various noises. Performing a proper denoising method will improve the quality of the signals obtained. The denoising method based on ensemble empirical mode decomposition (EEMD) is introduced, but the denoised results are difficult to evaluated. A dual field-of-view lidar for observing atmospheric aerosols is described. The backscattering signals obtained from two channels have different signal-to-noise ratios (SNR). To overcome the drawback of the simulation experiment, the performance of noise reduction can be investigated by comparing the high SNR signal and the denoised low SNR signal. With this approach, some parameters of the denoising method based on EEMD can be determined effectively. The experimental results show that the EEMD-based method with proper parameters can effectively increase the atmospheric lidar observing ability.

Seasonal differences in the vertical profiles of aerosol optical properties over rural Oklahoma

Abstract. A small airplane made 597 aerosol optical property (light absorption and light scattering) vertical profile measurements over a rural Oklahoma site between March 2000 and December 2007. The aerosol profiles obtained during these 8 yr of measurements suggest significant seasonal differences in aerosol loading (scattering and absorption). The highest amounts of scattering and absorbing aerosol are observed during the summer and the lowest loading occurs during the winter. The relative contribution of aerosol absorption is highest in the winter (i.e., single scattering albedo is lowest in winter), particularly aloft. Aerosol absorption generally decreased with altitude below ~1.5 km and then was relatively constant or decreased more gradually above that. Aerosol scattering decreased sharply with altitude below ~1.5 km but, unlike absorption, also decreased at higher altitudes, albeit less sharply. Scattering Ångström exponents suggest that the aerosol was dominated by sub-micron aerosol during the summer at all altitudes, but that larger particles were present, especially in the spring and winter above 1 km. The seasonal variability observed for aerosol loading is consistent with AERONET aerosol optical depth (AOD) although the AOD values calculated from in situ adjusted to ambient conditions and matching wavelengths are up to a factor of two lower than AERONET AOD values depending on season. The column averaged single scattering albedo derived from in situ airplane measurements are similar in value to the AERONET single scattering albedo inversion product but the seasonal patterns are different – possibly a consequence of the strict constraints on obtaining single scattering albedo from AERONET data. A comparison of extinction Ångström exponent and asymmetry parameter from the airplane and AERONET platforms suggests similar seasonal variability with smaller particles observed in the summer and fall and larger particles observed in spring and winter. The observed seasonal cycle of aerosol loading corresponds with changes in air mass back trajectories: the aerosol scattering was higher when transport was from polluted areas (e.g., the Gulf Coast) and lower when the air came from cleaner regions and/or the upper atmosphere.

Dual-aureole and sun spectrometer system for airborne measurements of aerosol optical properties

We have designed an airborne spectrometer system for the simultaneous measurement of the direct sun irradiance and the aureole radiance in two different solid angles. The high-resolution spectral radiation measurements are used to derive vertical profiles of aerosol optical properties. Combined measurements in two solid angles provide better information about the aerosol type without additional and elaborate measuring geometries. It is even possible to discriminate between absorbing and nonabsorbing aerosol types. Furthermore, they allow to apply additional calibration methods and simplify the detection of contaminated data (e.g., by thin cirrus clouds). For the characterization of the detected aerosol type a new index is introduced that is the slope of the aerosol phase function in the forward scattering region. The instrumentation is a flexible modular setup, which has already been successfully applied in airborne and ground-based field campaigns. We describe the setup as well as the calibration of the instrument. In addition, example vertical profiles of aerosol optical properties--including the aureole measurements--are shown and discussed.