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Abstract. The methodology of analysing the biomass burning events recorded in the database of the European Aerosol Research Lidar Network in the framework of the Aerosol, Clouds and Trace Gases Research Infrastructure is presented. The period of 2008–2017 was chosen to analyse all of the events stored in the database under the Forest Fire category for a total of 14 stations available. The data provided ranged from complete datasets (particle backscatter, extinction and linear depolarization ratio profiles) to single profiles (particle backscatter coefficient profile). Smoke layers geometry was evaluated and the mean optical properties within each layer were computed. The back-trajectory technique was used to double-check the source of all pollution layers. The biomass burning layers were identified by taking into account the presence of the fires along the back trajectory. The biomass burning events are analysed by the means of the intensive parameters. The analysis was structured in three directions: (I) common biomass burning source (fire) recorded by at least two stations, (II) long-range transport from North America, and (III) analysis over four geographical regions (south-eastern Europe, north-eastern Europe, central Europe, and south-western Europe). Based on back-trajectory calculations and fire locations, the lidar measurements can be labelled either as measurements of a “single fire” or “mixed fires” (case I), measurements of North American fires, or measurements of mixed North American and local fires (case II). The histogram of the fire locations reveals the smoke sources for each region. For each region, statistics on intensive parameters are performed. The source origin of the intensive parameters is categorized based on the continental origin of the air mass (European, African, Asian, North American, or a combination of them). The methodology presented here is meant to provide a perspective to explore a large number of lidar data and deliver novel approaches to analyse the intensive parameters based on the assigned biomass burning sources. A thorough consideration of all potential fire sources reveals that most of the time the lidar measurements characterize the smoke from a mixture of fires. A comprehensive discussion of all the results (based on the intensive parameters and the source locations) will be given in a companion paper submitted to the ACP EARLINET special issue.
Abstract. The methodology of analysing the biomass burning events recorded in the database of the European Aerosol Research Lidar Network in the framework of the Aerosol, Clouds and Trace Gases Research Infrastructure is presented. The period of 2008–2017 was chosen to analyse all of the events stored in the database under the Forest Fire category for a total of 14 stations available. The data provided ranged from complete datasets (particle backscatter, extinction and linear depolarization ratio profiles) to single profiles (particle backscatter coefficient profile). Smoke layers geometry was evaluated and the mean optical properties within each layer were computed. The back-trajectory technique was used to double-check the source of all pollution layers. The biomass burning layers were identified by taking into account the presence of the fires along the back trajectory. The biomass burning events are analysed by the means of the intensive parameters. The analysis was structured in three directions: (I) common biomass burning source (fire) recorded by at least two stations, (II) long-range transport from North America, and (III) analysis over four geographical regions (south-eastern Europe, north-eastern Europe, central Europe, and south-western Europe). Based on back-trajectory calculations and fire locations, the lidar measurements can be labelled either as measurements of a “single fire” or “mixed fires” (case I), measurements of North American fires, or measurements of mixed North American and local fires (case II). The histogram of the fire locations reveals the smoke sources for each region. For each region, statistics on intensive parameters are performed. The source origin of the intensive parameters is categorized based on the continental origin of the air mass (European, African, Asian, North American, or a combination of them). The methodology presented here is meant to provide a perspective to explore a large number of lidar data and deliver novel approaches to analyse the intensive parameters based on the assigned biomass burning sources. A thorough consideration of all potential fire sources reveals that most of the time the lidar measurements characterize the smoke from a mixture of fires. A comprehensive discussion of all the results (based on the intensive parameters and the source locations) will be given in a companion paper submitted to the ACP EARLINET special issue.
Abstract. The scattering and backscattering enhancement factors (f(RH) and fb(RH)) describe how aerosol particle light scattering and backscattering, respectively, change with relative humidity (RH). They are important parameters in estimating direct aerosol radiative forcing (DARF). In this study we use the dataset presented in Burgos et al. (2019) that compiles f(RH) and fb(RH) measurements at three wavelengths (i.e., 450, 550 and 700 nm) performed with tandem nephelometer systems at multiple sites around the world. We present an overview of f(RH) and fb(RH) based on both long-term and campaign observations from 23 sites representing a range of aerosol types. The scattering enhancement shows a strong variability from site to site, with no clear pattern with respect to the total scattering coefficient. In general, higher f(RH) is observed at Arctic and marine sites, while lower values are found at urban and desert sites, although a consistent pattern as a function of site type is not observed. The backscattering enhancement fb(RH) is consistently lower than f(RH) at all sites, with the difference between f(RH) and fb(RH) increasing for aerosol with higher f(RH). This is consistent with Mie theory, which predicts higher enhancement of the light scattering in the forward than in the backward direction as the particle takes up water. Our results show that the scattering enhancement is higher for PM1 than PM10 at most sites, which is also supported by theory due to the change in scattering efficiency with the size parameter that relates particle size and the wavelength of incident light. At marine-influenced sites this difference is enhanced when coarse particles (likely sea salt) predominate. For most sites, f(RH) is observed to increase with increasing wavelength, except at sites with a known dust influence where the spectral dependence of f(RH) is found to be low or even exhibit the opposite pattern. The impact of RH on aerosol properties used to calculate radiative forcing (e.g., single-scattering albedo, ω0, and backscattered fraction, b) is evaluated. The single-scattering albedo generally increases with RH, while b decreases. The net effect of aerosol hygroscopicity on radiative forcing efficiency (RFE) is an increase in the absolute forcing effect (negative sign) by a factor of up to 4 at RH = 90 % compared to dry conditions (RH < 40 %). Because of the scarcity of scattering enhancement measurements, an attempt was made to use other more commonly available aerosol parameters (i.e., ω0 and scattering Ångström exponent, αsp) to parameterize f(RH). The majority of sites (75 %) showed a consistent trend with ω0 (higher f(RH = 85 %) for higher ω0), while no clear pattern was observed between f(RH = 85 %) and αsp. This suggests that aerosol ω0 is more promising than αsp as a surrogate for the scattering enhancement factor, although neither parameter is ideal. Nonetheless, the qualitative relationship observed between ω0 and f(RH) could serve as a constraint on global model simulations.
Abstract. For the radiative impact of individual climate forcings, most previous studies focused on the global mean values at the top of the atmosphere (TOA), and less attention has been paid to surface processes, especially for black carbon (BC) aerosols. In this study, the surface radiative responses to five different forcing agents were analyzed by using idealized model simulations. Our analyses reveal that for greenhouse gases, solar irradiance, and scattering aerosols, the surface temperature changes are mainly dictated by the changes of surface radiative heating, but for BC, surface energy redistribution between different components plays a more crucial role. Globally, when a unit BC forcing is imposed at TOA, the net shortwave radiation at the surface decreases by -5.87±0.67 W m−2 (W m−2)−1 (averaged over global land without Antarctica), which is partially offset by increased downward longwave radiation (2.32±0.38 W m−2 (W m−2)−1 from the warmer atmosphere, causing a net decrease in the incoming downward surface radiation of -3.56±0.60 W m−2 (W m−2)−1. Despite a reduction in the downward radiation energy, the surface air temperature still increases by 0.25±0.08 K because of less efficient energy dissipation, manifested by reduced surface sensible (-2.88±0.43 W m−2 (W m−2)−1) and latent heat flux (-1.54±0.27 W m−2 (W m−2)−1), as well as a decrease in Bowen ratio (-0.20±0.07 (W m−2)−1). Such reductions of turbulent fluxes can be largely explained by enhanced air stability (0.07±0.02 K (W m−2)−1), measured as the difference of the potential temperature between 925 hPa and surface, and reduced surface wind speed (-0.05±0.01 m s−1 (W m−2)−1). The enhanced stability is due to the faster atmospheric warming relative to the surface, whereas the reduced wind speed can be partially explained by enhanced stability and reduced Equator-to-pole atmospheric temperature gradient. These rapid adjustments under BC forcing occur in the lower atmosphere and propagate downward to influence the surface energy redistribution and thus surface temperature response, which is not observed under greenhouse gases or scattering aerosols. Our study provides new insights into the impact of absorbing aerosols on surface energy balance and surface temperature response.
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