The present study investigates the mineral dust emissions and the occurrence of dust emission events over the Sahara desert from 1996 to 2001. Mineral dust emissions are simulated over a region extending from 16°N to 38°N and from 19°W to 40°E with a ° × ° spatial resolution. The input parameters required by the dust emission model are surface features data (aerodynamic roughness length, dry soil size distribution and texture for erodible soils), and meteorological surface data (mainly surface wind velocity and soil moisture). A map of the aerodynamic roughness lengths is established based on a composition of protrusion coefficients derived from the POLDER‐1 surface products. Soil dry size distribution and texture are derived from measurements performed on soil samples from desert areas, and from a soil map derived from a geomorphologic analysis of desert landscapes. Surface re‐analyzed meteorological databases (ERA‐40) of the European Centre for Medium range Weather Forecasts (ECMWF) are used. The influence of soil moisture on simulated dust emissions is quantified. The main Saharan dust sources identified during the 6‐year simulated period are in agreement with the previous studies based on in situ or satellite observations. The relevance of the simulated large dust sources and point sources (“hot spots”) is tested using aerosol indexes derived from satellite observations (TOMS Absorbing Aerosol Index and Infrared Dust Difference Index Meteosat). The Saharan dust emissions simulated from 1996 to 2001 range from 585 to 759 Tg a−1. The simulations show marked seasonal cycles with a maximum in summer for the western Sahara and in spring for the eastern Sahara. The interannual variability of dust emissions is pronounced in the eastern part of the Sahara while the emissions from the western Sahara are more regular over the studied period. The soil moisture does not noticeably affect the Saharan dust emissions, their seasonal cycle or their interannual variability, but it can partly control and limit the dust emissions in some parts of the northern desert margin, where the precipitation rates are higher. Our simulations also tend to confirm that the Sahara is the major terrestrial source of mineral dust.
Abstract. The Chemistry-Aerosol Mediterranean Experiment (ChArMEx; http://charmex.lsce.ipsl.fr) is a collaborative research program federating international activities to investigate Mediterranean regional chemistry-climate interactions. A special observing period (SOP-1a) including intensive airborne measurements was performed in the framework of the Aerosol Direct Radiative Impact on the regional climate in the MEDiterranean region (ADRIMED) project during the Mediterranean dry season over the western and central Mediterranean basins, with a focus on aerosol-radiation measurements and their modeling. The SOP-1a took place from 11 June to 5 July 2013. Airborne measurements were made by both the ATR-42 and F-20 French research aircraft operated from Sardinia (Italy) and instrumented for in situ and remote-sensing measurements, respectively, and by sounding and drifting balloons, launched in Minorca. The experimental setup also involved several ground-based measurement sites on islands including two ground-based reference stations in Corsica and Lampedusa and secondary monitoring sites in Minorca and Sicily. Additional measurements including lidar profiling were also performed on alert during aircraft operations at EARLINET/ACTRIS stations at Granada and Barcelona in Spain, and in southern Italy. Remote-sensing aerosol products from satellites (MSG/SEVIRI, MODIS) and from the AERONET/PHOTONS network were also used. Dedicated meso-scale and regional modeling experiments were performed in relation to this observational effort. We provide here an overview of the different surface and aircraft observations deployed during the ChArMEx/ADRIMED period and of associated modeling studies together with an analysis of the synoptic conditions that determined the aerosol emission and transport. Meteorological conditions observed during this campaign (moderate temperatures and southern flows) were not favorable to producing high levels of atmospheric pollutants or intense biomass burning events in the region. However, numerous mineral dust plumes were observed during the campaign, with the main sources located in Morocco, Algeria and Tunisia, leading to aerosol optical depth (AOD) values ranging between 0.2 and 0.6 (at 440 nm) over the western and central Mediterranean basins. One important point of this experiment concerns the direct observations of aerosol extinction onboard the ATR-42, using the CAPS system, showing local maxima reaching up to 150 M m −1 within the dust plume. Non-negligible aerosol extinction (about 50 M m −1 ) has also been observed within the marine boundary layer (MBL). By combining the ATR-42 extinction coefficient observations with absorption and scattering measurements, we performed a complete optical closure revealing excellent agreement with estimated optical properties. This additional information on extinction properties has allowed calculation of the dust single scattering albedo (SSA) with a high level of confidence over the western Mediterranean. Our results show a moderate variability from 0....
One of the principal findings of this paper is that a significant contribution to the aerosol load over the NIO is due to the advection of continental aerosols from India in a well-identified monsoon layer above the marine boundary layer. Moreover, it is suggested that the increase in biomass burning plays a significant role in the increasing trend in ACT during the winter dry monsoon season.
Aerosol absorption properties are of high importance to assess aerosol impact on regional climate. This study presents an analysis of aerosol absorption products obtained over the Mediterranean basin or land stations in the region from multi-year ground-based AERONET observations with a focus on the Absorbing Aerosol Optical Depth (AAOD), Single Scattering Albedo (SSA) and their spectral dependence. The AAOD and Absorption Angström Exponent (AAE) dataset is composed of daily averaged AERONET level 2 data from a total of 22 Mediterranean stations having long time series, mainly under the influence of urban-industrial aerosols and/or soil dust. This dataset covers the 17-yr period 1996–2012 with most data being from 2003–2011 (~89% of level-2 AAOD data). Since AERONET level-2 absorption products require a high aerosol load (AOD at 440 nm > 0.4), which is most often related to the presence of desert dust, we also consider level-1.5 SSA data, despite their higher uncertainty, and filter out data with an Angström exponent < 1.0 in order to study absorption by carbonaceous aerosols. The SSA dataset includes AERONET level-2 products. Sun-photometer observations show that values of AAOD at 440 nm vary between 0.024 ± 0.01 (resp. 0.040 ± 0.01) and 0.050 ± 0.01 (0.055 ± 0.01) for urban (dusty) sites. Analysis shows that the Mediterranean urban-industrial aerosols appear "moderately" absorbing with values of SSA close to ~0.94–0.95 ± 0.04 (at 440 nm) in most cases except over the large cities of Rome and Athens, where aerosol appears more absorbing (SSA ~0.89–0.90 ± 0.04). The aerosol Absorption Angström Exponent (AAE, estimated using 440 and 870 nm) is found to be larger than 1 for most sites over the Mediterranean, a manifestation of mineral dust (iron) and/or brown carbon producing the observed absorption. AERONET level-2 sun-photometer data indicate a possible East-West gradient, with higher values over the eastern basin (AAEEast = 1.39/AAEWest = 1.33). The North-South AAE gradient is more pronounced, especially over the western basin. Our additional analysis of AERONET level-1.5 data also shows that organic absorbing aerosols significantly affect some Mediterranean sites. These results indicate that current climate models treating organics as nonabsorbing over the Mediterranean certainly underestimate the warming effect due to carbonaceous aerosols
We have used one year (1999) of Meteosat observations to monitor the dust activity in the arid and semi‐arid areas surrounding the North Indian Ocean. The method is based on the IDDI product derived from the infrared channel of the satellite. Dust sources are located according to a threshold on the IDDI and another on the surface wind speed. The global features of the dust activity in this area are in a good agreement with previous studies. Main dust sources are located in the Nubian desert, the Arabian peninsula, Iran, Pakistan and Afghanistan, and North West India. It is found that Somalia is also an area of dust emission with a maximum of activity from May to October.
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