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    Satellite retrievals of dust aerosol over the Red Sea and the Persian Gulf (2005-2015)
    (Katlenburg-Lindau : EGU, 2017) Banks, Jamie R.; Brindley, Helen E.; Stenchikov, Georgiy; Schepanski, Kerstin
    The inter-annual variability of the dust aerosol presence over the Red Sea and the Persian Gulf is analysed over the period 2005-2015. Particular attention is paid to the variation in loading across the Red Sea, which has previously been shown to have a strong, seasonally dependent latitudinal gradient. Over the 11 years considered, the July mean 630 nm aerosol optical depth (AOD) derived from the Spinning Enhanced Visible and InfraRed Imager (SEVIRI) varies between 0.48 and 1.45 in the southern half of the Red Sea. In the north, the equivalent variation is between 0.22 and 0.66. The temporal and spatial pattern of variability captured by SEVIRI is also seen in AOD retrievals from the MODerate Imaging Spectroradiometer (MODIS), but there is a systematic offset between the two records. Comparisons of both sets of retrievals with ship-and land-based AERONET measurements show a high degree of correlation with biases of <0.08. However, these comparisons typically only sample relatively low aerosol loadings. When both records are stratified by AOD retrievals from the Multi-angle Imaging SpectroRadiometer (MISR), opposing behaviour is revealed at high MISR AODs (>1), with offsets of C0.19 for MODIS and 0.06 for SEVIRI. Similar behaviour is also seen over the Persian Gulf. Analysis of the scattering angles at which retrievals from the SEVIRI and MODIS measurements are typically performed in these regions suggests that assumptions concerning particle sphericity may be responsible for the differences seen.
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    Ship-based measurements of ice nuclei concentrations over the Arctic, Atlantic, Pacific and Southern oceans
    (Katlenburg-Lindau : EGU, 2020) Welti, André; Bigg, Keith E.; DeMott, Paul J.; Gong, Xianda; Hartmann, Markus; Harvey, Mike; Henning, Silvia; Herenz, Paul; Hill, Thomas C.J.; Hornblow, Blake; Leck, Caroline; Löffler, Mareike; McCluskey, Christina S.; Rauker, Anne Marie; Schmale, Julia; Tatzelt, Christian; van Pinxteren, Manuela; Stratmann, Frank
    Ambient concentrations of ice-forming particles measured during ship expeditions are collected and summarised with the aim of determining the spatial distribution and variability in ice nuclei in oceanic regions. The presented data from literature and previously unpublished data from over 23 months of ship-based measurements stretch from the Arctic to the Southern Ocean and include a circumnavigation of Antarctica. In comparison to continental observations, ship-based measurements of ambient ice nuclei show 1 to 2 orders of magnitude lower mean concentrations. To quantify the geographical variability in oceanic areas, the concentration range of potential ice nuclei in different climate zones is analysed by meridionally dividing the expedition tracks into tropical, temperate and polar climate zones. We find that concentrations of ice nuclei in these meridional zones follow temperature spectra with similar slopes but vary in absolute concentration. Typically, the frequency with which specific concentrations of ice nuclei are observed at a certain temperature follows a log-normal distribution. A consequence of the log-normal distribution is that the mean concentration is higher than the most frequently measured concentration. Finally, the potential contribution of ship exhaust to the measured ice nuclei concentration on board research vessels is analysed as function of temperature. We find a sharp onset of the influence at approximately 36 C but none at warmer temperatures that could bias ship-based measurements. © Author(s) 2020. This work is distributed under the Creative Commons Attribution 4.0 License.
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    The impact of biomass burning and aqueous-phase processing on air quality: A multi-year source apportionment study in the Po Valley, Italy
    (Katlenburg-Lindau : EGU, 2020) Paglione, Marco; Gilardoni, Stefania; Rinaldi, Matteo; Decesari, Stefano; Zanca, Nicola; Sandrini, Silvia; Giulianelli, Lara; Bacco, Dimitri; Ferrari, Silvia; Poluzzi, Vanes; Scotto, Fabiana; Trentini, Arianna; Poulain, Laurent; Herrmann, Hartmut; Wiedensohler, Alfred; Canonaco, Francesco; Prévôt, André S.H.; Massoli, Paola; Carbone, Claudio; Facchini, Maria Cristina; Fuzzi, Sandro
    The Po Valley (Italy) is a well-known air quality hotspot characterized by particulate matter (PM) levels well above the limit set by the European Air Quality Directive and by the World Health Organization, especially during the colder season. In the framework of Emilia-Romagna regional project "Supersito", the southern Po Valley submicron aerosol chemical composition was characterized by means of high-resolution aerosol mass spectroscopy (HR-AMS) with the specific aim of organic aerosol (OA) characterization and source apportionment. Eight intensive observation periods (IOPs) were carried out over 4 years (from 2011 to 2014) at two different sites (Bologna, BO, urban background, and San Pietro Capofiume, SPC, rural background), to characterize the spatial variability and seasonality of the OA sources, with a special focus on the cold season. On the multi-year basis of the study, the AMS observations show that OA accounts for averages of 45 ± 8 % (ranging from 33 % to 58 %) and 46 ± 7 % (ranging from 36 % to 50 %) of the total non-refractory submicron particle mass (PM1-NR) at the urban and rural sites, respectively. Primary organic aerosol (POA) comprises biomass burning (23±13 % of OA) and fossil fuel (12±7 %) contributions with a marked seasonality in concentration. As expected, the biomass burning contribution to POA is more significant at the rural site (urban / rural concentration ratio of 0.67), but it is also an important source of POA at the urban site during the cold season, with contributions ranging from 14 % to 38 % of the total OA mass. Secondary organic aerosol (SOA) contributes to OA mass to a much larger extent than POA at both sites throughout the year (69 ± 16 % and 83 ± 16 % at the urban and rural sites, respectively), with important implications for public health. Within the secondary fraction of OA, the measurements highlight the importance of biomass burning aging products during the cold season, even at the urban background site. This biomass burning SOA fraction represents 14 %-44 % of the total OA mass in the cold season, indicating that in this region a major contribution of combustion sources to PM mass is mediated by environmental conditions and atmospheric reactivity. © 2020 Author(s).
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    North African mineral dust sources: New insights from a combined analysis based on 3D dust aerosol distributions, surface winds and ancillary soil parameters
    (Katlenburg-Lindau : EGU, 2020) Vandenbussche, Sophie; Callewaert, Sieglinde; Schepanski, Kerstin; De Mazière, Martine
    Mineral dust aerosol is a key player in the climate system. Determining dust sources and the spatio-temporal variability of dust emission fluxes is essential for estimating the impact of dust on the atmospheric radiation budget, cloud and precipitation formation processes, the bio-productivity and, ultimately, the carbon cycle. Although much effort has been put into determining dust sources from satellite observations, geo-locating active dust sources is still challenging and uncertainties in space and time are evident. One major source of uncertainty is the lack of clear differentiation between near-source dust aerosol and transported dust aerosol. In order to reduce this uncertainty, we use 3D information on the distribution of dust aerosol suspended in the atmosphere calculated from spectral measurements obtained by the Infrared Atmospheric Sounding Interferometer (IASI) by using the Mineral Aerosols Profiling from Infrared Radiance (MAPIR) algorithm. In addition to standard dust products from satellite observations, which provide 2D information on the horizontal distribution of dust, MAPIR allows for the retrieval of additional information on the vertical distribution of dust plumes. This ultimately enables us to separate between near-source and transported dust plumes. Combined with information on near-surface wind speed and surface properties, low-altitude dust plumes can be assigned to dust emission events and low-altitude transport regimes can be excluded. Consequently, this technique will reduce the uncertainty in automatically geo-locating active dust sources. The findings of our study illustrate the spatio-temporal distribution of North African dust sources based on 9 years of data, allowing for the observation of a full seasonal cycle of dust emissions, differentiating morning and afternoon/evening emissions and providing a first glance at long-term changes. In addition, we compare the results of this new method to the results from Schepanski et al. (2012), who manually identified dust sources from Spinning Enhanced Visible and InfraRed Imager (SEVIRI) red-green-blue (RGB) images. The comparison illustrates that each method has its strengths and weaknesses that must be taken into account when using the results. This study is of particular importance for understanding future environmental changes due to a changing climate. © Author(s) 2020