Marc Mallet

The 7–13 March 2006 dust storm over West Africa: Generation, transport, and vertical stratification

Several studies have shown the importance of desert dust aerosols in weather forecast models. Nevertheless, desert dust has been poorly represented in such models and is the source of some prediction errors, in particular for tropical and subtropical regions. The purpose of this paper is to illustrate the formation and the three-dimensional transport of a severe dust storm which occurred in March 2006 over West Africa. An intense dust haze was transported southward over the Gulf of Guinea thereby generating an aerosol optical thickness (AOT) greater than 4 over Nigeria. The MesoNH mesoscale atmospheric model coupled with new dust parameterization schemes has been used to illustrate the three-dimensional transport of the dust plume and the vertical layering of this desert air mass above the lower atmosphere monsoon flux layer. It is modeled that more than 50 g m−2 of dust was emitted during this event from the surface by a strong Harmattan wind over the Sahel region. It is also shown that when the dust layer is located over the boundary layer, it can modify the atmospheric stability by as much as 9.5 K in terms of potential temperature in the lowest 2000 m of the atmosphere.

Direct and semi-direct aerosol radiative effect on the Mediterranean climate variability using a coupled regional climate system model

A fully coupled regional climate system model (CNRM-RCSM4) has been used over the Mediterranean region to investigate the direct and semi-direct effects of aerosols, but also their role in the radiation–atmosphere–ocean interactions through multi-annual ensemble simulations (2003–2009) with and without aerosols and ocean–atmosphere coupling. Aerosols have been taken into account in CNRM-RCSM4 through realistic interannual monthly AOD climatologies. An evaluation of the model has been achieved, against various observations for meteorological parameters, and has shown the ability of CNRM-RCSM4 to reproduce the main patterns of the Mediterranean climate despite some biases in sea surface temperature (SST), radiation and cloud cover. The results concerning the aerosol radiative effects show a negative surface forcing on average because of the absorption and scattering of the incident radiation. The SW surface direct effect is on average −20.9xa0Wm−2 over the Mediterranean Sea, −14.7xa0Wm−2 over Europe and −19.7xa0Wm−2 over northern Africa. The LW surface direct effect is weaker as only dust aerosols contribute (+4.8xa0Wm−2 over northern Africa). This direct effect is partly counterbalanced by a positive semi-direct radiative effect over the Mediterranean Sea (+5.7xa0Wm−2 on average) and Europe (+5.0xa0Wm−2) due to changes in cloud cover and atmospheric circulation. The total aerosol effect is consequently negative at the surface and responsible for a decrease in land (on average −0.4xa0°C over Europe, and −0.5xa0°C over northern Africa) and sea surface temperature (on average −0.5xa0°C for the Mediterranean SST). In addition, the latent heat loss is shown to be weaker (−11.0xa0Wm−2) in the presence of aerosols, resulting in a decrease in specific humidity in the lower troposphere, and a reduction in cloud cover and precipitation. Simulations also indicate that dust aerosols warm the troposphere by absorbing solar radiation, and prevent radiation from reaching the surface, thus stabilizing the troposphere. The comparison with the model response in atmosphere-only simulations shows that these feedbacks are attenuated if SST cannot be modified by aerosols, highlighting the importance of using coupled regional models over the Mediterranean. Oceanic convection is also strengthened by aerosols, which tends to reinforce the Mediterranean thermohaline circulation. In parallel, two case studies are presented to illustrate positive feedbacks between dust aerosols and regional climate. First, the eastern Mediterranean was subject to high dust aerosol loads in June 2007 which reduce land and sea surface temperature, as well as air–sea humidity fluxes. Because of northern wind over the eastern Mediterranean, drier and cooler air has been consequently advected from the sea to the African continent, reinforcing the direct dust effect over land. On the contrary, during the western European heat wave in June 2006, dust aerosols have contributed to reinforcing an important ridge responsible for dry and warm air advection over western Europe, and thus to increasing lower troposphere (+0.8xa0°C) and surface temperature (+0.5xa0°C), namely about 15xa0% of this heat wave.

Emission factors of trace gases and particles from tropical savanna fires in Australia

Savanna fires contribute significantly to global aerosol loading and hence to the earths radiative budget. Modelling of the climatic impact of these aerosols is made difficult due to a lack of knowledge of their size distribution. Australia is the third largest source of global carbon emissions from biomass burning, with emissions dominated by tropical savanna fires. Despite this, only a few previous studies have reported emission factors of trace gases from this important ecosystem and there are no previous published emission factors for the aerosol properties reported here for Australian savanna fires. In June 2014, the SAFIRED campaign (Savanna Fires in the Early Dry season) took place in the northern territory of Australia, with the purpose of investigating emissions and aging of aerosols from Australian savanna fires. This paper presents observed enhancement ratios and inferred emission factors of trace gases (CO2, CO, CH4, N2O and gaseous elemental mercury), particles over different size modes (Aitken and accumulation) and speciated aerosols components (organics, sulfate, nitrate, ammonium and chloride). Nine smoke events were identified from the data using large enhancements in CO and/or aerosol data to indicate biomass burning event. The results reported in this paper include the first emission factors for Aitken and accumulation mode aerosols from savanna fires, providing useful size information to enable better modelling of the climatic impact of this important source of global aerosols.

Emissions of Selected Semivolatile Organic Chemicals from Forest and Savannah Fires

The emission factors (EFs) for a broad range of semivolatile organic chemicals (SVOCs) from subtropical eucalypt forest and tropical savannah fires were determined for the first time from in situ investigations. Significantly higher (t test, P < 0.01) EFs (μg kg-1 dry fuel, gas + particle-associated) for polycyclic aromatic hydrocarbons (∑13 PAHs) were determined from the subtropical forest fire (7,000 ± 170) compared to the tropical savannah fires (1,600 ± 110), due to the approximately 60-fold higher EFs for 3-ring PAHs from the former. EF data for many PAHs from the eucalypt forest fire were comparable with those previously reported from pine and fir forest combustion events. EFs for other SVOCs including polychlorinated biphenyl (PCB), polychlorinated naphthalene (PCN), and polybrominated diphenyl ether (PBDE) congeners as well as some pesticides (e.g., permethrin) were determined from the subtropical eucalypt forest fire. The highest concentrations of total suspended particles, PAHs, PCBs, PCNs, and PBDEs, were typically observed in the flaming phase of combustion. However, concentrations of levoglucosan and some pesticides such as permethrin peaked during the smoldering phase. Along a transect (10-150-350 m) from the forest fire, concentration decrease for PCBs during flaming was faster compared to PAHs, while levoglucosan concentrations increased.

Sea spray aerosol in the Great Barrier Reef and the presence of nonvolatile organics

Sea spray aerosol (SSA) particles produced from the ocean surface in regions of biological activity can vary greatly in size, number and composition and in their influence on cloud formation. Algal species such as phytoplankton can alter the SSA composition. Numerous studies have investigated nascent SSA properties, but all of these have focused on aerosol particles produced by seawater from non-coral related phytoplankton and in coastal regions. Bubble chamber experiments were performed with seawater samples taken from the reef flat around Heron Island in the Great Barrier Reef during winter 2011. Here we show that the SSA from these samples was comprised of an internal mixture of varying fractions of sea salt, semi-volatile organics as well as non-volatile (below 550°C) organics. A relatively constant volume fraction of semi-volatile organics of 10%-13% was observed while non-volatile organic volume fractions varied from 29%-49% for 60 nm SSA. SSA organic fractions were estimated to reduce the activation ratios of SSA to cloud condensation nuclei by up to 14% when compared with artificial sea salt. Additionally, a sea salt calibration was applied so that a compact Time-of-Flight Aerosol Mass Spectrometer could be used to quantify the contribution of sea salt to sub-micron SSA, which yielded organic volume fractions of 3%-6%. Overall, these results indicate a high fraction of organics associated with wintertime Aitken mode SSA generated from Great Barrier Reef seawater. Further work is required to fully distinguish any differences coral reefs have on SSA composition when compared to open oceans.

Contribution of EARLINET/ACTRIS to the summer 2013 Special Observing Period of the ChArMEx project: monitoring of a Saharan dust event over the western and central Mediterranean

ABSTRACT In the framework of the Chemistry-Aerosol Mediterranean Experiment (ChArMEx; http://charmex.lsce.ipsl.fr/) initiative, a field campaign took place in the western Mediterranean Basin between 10 June and 5 July 2013 within the ADRIMED (Aerosol Direct Radiative Impact on the regional climate in the MEDiterranean region) project. The scientific objectives of ADRIMED are the characterization of the most common ‘Mediterranean aerosols’ and their direct radiative forcing (column closure and regional scale). During 15–24 June a multi-intrusion dust event took place over the western and central Mediterranean Basin. Extra measurements were carried out by some EARLINET/ACTRIS (European Aerosol Research Lidar Network /Aerosols, Clouds, and Trace gases Research InfraStructure Network, http://www.actris.net/) lidar stations in Spain and Italy, in particular on 22 June in support to the flight over southern Italy of the Falcon 20 aircraft involved in the campaign. This article describes the physical and optical properties of dust observed at the different lidar stations in terms of dust plume centre of mass, optical depth, lidar ratio, and particle depolarization ratio. To link the differences found in the origin of dust plumes, the results are discussed on the basis of back-trajectories and air- and space-borne lidars. This work puts forward the collaboration between a European research infrastructure (ACTRIS) and an international project (ChArMEx) on topics of interest for both parties, and more generally for the atmospheric community.

Interactions aérosols-rayonnement-climat en région méditerranéenne : Impact de l'effet radiatif direct sur le cycle de l'eau

An experimental campaign, coupled with three-dimensional modeling, was conducted in the western Mediterranean during the summer of 2013 to study the impact of aerosols on the radiative balance and climate of this region. In situ observations were obtained on the ground, aboard two research aircraft and balloons to characterize the physico-chemical and optical properties of particles and their vertical stratification. This campaign was mainly characterized by moderate events of desert aerosols. During these episodes, strong vertical stratification was observed and the measurements of the optical properties reveal moderate absorbing particles in the visible spectrum. Climate simulations indicate a significant impact of aerosols in particular by changing the surface temperature of the sea, the ocean-atmosphere fluxes and consequently seasonal precipitation.

Marine Aerosol Hygroscopicity and Volatility, Measured on the Chatham Rise (New Zealand)

The Surface Ocean Aerosol Production (SOAP) study was undertaken in February/March 2012 in the biologically active waters of the Chatham Rise, NZ. Aerosol hygroscopicity and volatility were examined with a volatility hygroscopicity tandem differential mobility analyser. These observations confirm results from other hygroscopicity-based studies that the dominant fraction of the observed remote marine particles were non-sea salt sulfates. Further observations are required to clarify the influences of seawater composition, meteorology and analysis techniques seasonally across different ocean basins.