Technical note: Absorption aerosol optical depth components from AERONET observations of mixed dust plumes

© Author(s) 2019.Absorption aerosol optical depth (AAOD) as obtained from sun–sky photometer measurements provides a measure of the light-absorbing properties of the columnar aerosol loading. However, it is not an unambiguous aerosol-type-specific parameter, particularly if several types of absorbing aerosols, for instance black carbon (BC) and mineral dust, are present in a mixed aerosol plume. The contribution of mineral dust to total aerosol light absorption is particularly important at UV wavelengths. In this study we refine a lidar-based technique applied to the separation of dust and non-dust aerosol types for the use with Aerosol Robotic Network (AERONET) direct sun and inversion products. We extend the methodology to retrieve AAOD related to non-dust aerosol (AAODnd) and BC (AAODBC). We test the method at selected AERONET sites that are frequently affected by aerosol plumes that contain a mixture of Saharan or Asian mineral dust and biomass-burning smoke or anthropogenic pollution, respectively. We find that aerosol optical depth (AOD) related to mineral dust as obtained with our methodology is frequently smaller than coarse-mode AOD. This suggests that the latter is not an ideal proxy for estimating the contribution of mineral dust to mixed dust plumes. We present the results of the AAODBC retrieval for the selected AERONET sites and compare them to coincident values provided in the Copernicus Atmosphere Monitoring System aerosol reanalysis.We find that modelled and AERONET AAODBC are most consistent for Asian sites or at Saharan sites with strong local anthropogenic sources.Peer reviewe

Nitric acid scavenging by mineral and biomass burning aerosols

The abundance of gas phase nitric acid in the upper troposphere is overestimated by global chemistry-transport models, especially during the spring and summer seasons. Recent aircraft data obtained over the central US show that mineral aerosols were abundant in the upper troposphere during spring. Chemical reactions on mineral dust may provide an important sink for nitric acid. In regions where the mineral dust abundance is low in the upper troposphere similar HNO3 removal processes may occur on biomass burning aerosols. We propose that mineral and biomass burning aerosols may provide an important global sink for gas phase nitric acid, particularly during spring and summer when aerosol composition in the upper troposphere may be greatly affected by dust storms from east Asia or tropical biomass burning plumes

Saharan dust and ice nuclei over Central Europe

Surface measurements of aerosol and ice nuclei (IN) at a Central European mountain site during an episode of dust transport from the Sahara are presented. Ice nuclei were sampled by electrostatic precipitation on silicon wafers and were analyzed in an isothermal static vapor diffusion chamber. The transport of mineral dust is simulated by the Eulerian regional dust model DREAM. Ice nuclei and mineral dust are significantly correlated, in particular IN number concentration and aerosol surface area. The ice nucleating characteristics of the aerosol as analyzed with respect to temperature and supersaturation are similar during the dust episode than during the course of the year. This suggests that dust may be a main constituent of ice nucleating aerosols in Central Europe

Occupational exposure to gases/fumes and mineral dust affect DNA methylation levels of genes regulating expression

Many workers are daily exposed to occupational agents like gases/fumes, mineral dust or biological dust, which could induce adverse health effects. Epigenetic mechanisms, such as DNA methylation, have been suggested to play a role. We therefore aimed to identify differentially methylated regions (DMRs) upon occupational exposures in never-smokers and investigated if these DMRs associated with gene expression levels. To determine the effects of occupational exposures independent of smoking, 903 never-smokers of the LifeLines cohort study were included. We performed three genome-wide methylation analyses (Illumina 450 K), one per occupational exposure being gases/fumes, mineral dust and biological dust, using robust linear regression adjusted for appropriate confounders. DMRs were identified using comb-p in Python. Results were validated in the Rotterdam Study (233 never-smokers) and methylation-expression associations were assessed using Biobank-based Integrative Omics Study data (n = 2802). Of the total 21 significant DMRs, 14 DMRs were associated with gases/fumes and 7 with mineral dust. Three of these DMRs were associated with both exposures (RPLP1 and LINC02169 (2x)) and 11 DMRs were located within transcript start sites of gene expression regulating genes. We replicated two DMRs with gases/fumes (VTRNA2-1 and GNAS) and one with mineral dust (CCDC144NL). In addition, nine gases/fumes DMRs and six mineral dust DMRs significantly associated with gene expression levels. Our data suggest that occupational exposures may induce differential methylation of gene expression regulating genes and thereby may induce adverse health effects. Given the millions of workers that are exposed daily to occupational exposures, further studies on this epigenetic mechanism and health outcomes are warranted

Using aircraft measurements to determine the refractive index of Saharan dust during the DODO Experiments

Much uncertainty in the value of the imaginary part of the refractive index of mineral dust contributes to uncertainty in the radiative effect of mineral dust in the atmosphere. A synthesis of optical, chemical and physical in-situ aircraft measurements from the DODO experiments during February and August 2006 are used to calculate the refractive index mineral dust encountered over West Africa. Radiative transfer modeling and measurements of broadband shortwave irradiance at a range of altitudes are used to test and validate these calculations for a specific dust event on 23 August 2006 over Mauritania. Two techniques are used to determine the refractive index: firstly a method combining measurements of scattering, absorption, size distributions and Mie code simulations, and secondly a method using composition measured on filter samples to apportion the content of internally mixed quartz, calcite and iron oxide-clay aggregates, where the iron oxide is represented by either hematite or goethite and clay by either illite or kaolinite. The imaginary part of the refractive index at 550 nm (ni550) is found to range between 0.0001 i to 0.0046 i, and where filter samples are available, agreement between methods is found depending on mineral combination assumed. The refractive indices are also found to agree well with AERONET data where comparisons are possible. ni550 is found to vary with dust source, which is investigated with the NAME model for each case. The relationship between both size distribution and ni550 on the accumulation mode single scattering albedo at 550 nm (ω0550) are examined and size distribution is found to have no correlation to ω0550, while ni550 shows a strong linear relationship with ω0550. Radiative transfer modeling was performed with different models (Mie-derived refractive indices, but also filter sampling composition assuming both internal and external mixing). Our calculations indicate that Mie-derived values of ni550 and the externally mixed dust where the iron oxide-clay aggregate corresponds to the goethite-kaolinite combination result in the best agreement with irradiance measurements. The radiative effect of the dust is found to be very sensitive to the mineral combination (and hence refractive index) assumed, and to whether the dust is assumed to be internally or externally mixed

Analysis of Saharan dust intrusions into the Carpathian Basin (Central Europe) over the period of 1979–2011

Aeolian dust particles and dust storms play substantial role in climatic and other environmental processes of the Earth system. The largest and most important dust source areas are situated in the Sahara, from where several hundred thousand tons of mineral dust is emitted each year and transported towards the European continent. Here we show that 130 Saharan dust events (SDEs) reached the atmosphere of the Carpathian Basin from 1979 to 2011 by using the NASA's daily TOMS Aerosol Index data, satellite images and backward trajectory calculations of NOAA HYSPLIT model. Monthly trends of dust events demonstrate that the main period of dust transportation is in the spring, with a secondary maximum in the summer (in July and August). This seasonal distribution match well the seasonality of Saharan dust emissions. However synoptic meteorological conditions govern primarily the occurrence of long-range dust transport towards Central Europe. Based on their different meteorological backgrounds (geopotential field, wind vector and meridional flow), SDEs were classified into three main types. By using composite mean maps of synoptic situations and backward trajectories, the possible source areas have also been identified for the different types of events. Finally, we provide a short discussion on how the African mineral dust could contribute to the local aeolian sedimentation of the Carpathian Basin during the Plio-Pleistocene

Light scattering and absorption properties of dust particles retrieved from satellite measurements

We use the radiative transfer model and chemistry transport model to improve our retrievals of dust optical properties from satellite measurements. The optical depth and absorbing optical depth of mineral dust can be obtained from our improved retrieval algorithm. The solar radiative forcing of dust aerosols has also been calculated using refined optical model and radiative transfer model

Glacial/interglacial changes in mineral dust and sea-salt records in polar ice cores: sources, transport, and deposition

Sea salt and mineral dust records as represented by Na+ and Ca2+ concentrations, respectively, in Greenland and Antarctic ice cores show pronounced glacial/interglacial variations. For the Last Glacial Maximum (LGM) mineral dust (sea salt) concentrations in Greenland show an increase of a factor of approximately 80 (15) compared to the Holocene and significant shifts by a factor of 15 (5) during Dansgaard Oeschger events. In Antarctica, the dust (sea salt) flux is enhanced by a factor of 15 (3) during the LGM compared to the Holocene and variations by approximately a factor of 8 (1-2) exist in parallel to Antarctic warm events. Primary glacial dust sources are the Asian deserts for Greenland and Patagonia for Antarctica. Ice core evidence and model results show that both changes in source strength as well as atmospheric transport and lifetime contributed to the observed changes in Greenland ice cores. In Antarctica changes in ice core fluxes are in large parts related to source variations both for sea salt and dust, where the formation of sea salt aerosol from sea ice may play a pivotal role. Summarizing our latest estimates on changes in sources, transport and deposition these processes are roughly able to explain the glacial increase in sea salt in both polar regions while they fall short by at least a factor of 4-7 for mineral dust. Future improvements in model resolution and in the formulation of source and transport processes together with new ice core records, e.g. on dust size distributions, will eventually allow to converge models and observations

Technical Note: High-resolution mineralogical database of dust-productive soils for atmospheric dust modeling

Dust storms and associated mineral aerosol transport are driven primarily by meso- and synoptic-scale atmospheric processes. It is therefore essential that the dust aerosol process and background atmospheric conditions that drive dust emissions and atmospheric transport are represented with sufficiently well-resolved spatial and temporal features. The effects of airborne dust interactions with the environment determine the mineral composition of dust particles. The fractions of various minerals in aerosol are determined by the mineral composition of arid soils; therefore, a high-resolution specification of the mineral and physical properties of dust sources is needed. <br></br> Several current dust atmospheric models simulate and predict the evolution of dust concentrations; however, in most cases, these models do not consider the fractions of minerals in the dust. The accumulated knowledge about the impacts of the mineral composition in dust on weather and climate processes emphasizes the importance of including minerals in modeling systems. Accordingly, in this study, we developed a global dataset consisting of the mineral composition of the current potentially dust-producing soils. In our study, we (a) mapped mineral data to a high-resolution 30 s grid, (b) included several mineral-carrying soil types in dust-productive regions that were not considered in previous studies, and (c) included phosphorus

Climate models miss most of the coarse dust in the atmosphere.

Coarse mineral dust (diameter, ≥5 μm) is an important component of the Earth system that affects clouds, ocean ecosystems, and climate. Despite their significance, climate models consistently underestimate the amount of coarse dust in the atmosphere when compared to measurements. Here, we estimate the global load of coarse dust using a framework that leverages dozens of measurements of atmospheric dust size distributions. We find that the atmosphere contains 17 Tg of coarse dust, which is four times more than current climate models simulate. Our findings indicate that models deposit coarse dust out of the atmosphere too quickly. Accounting for this missing coarse dust adds a warming effect of 0.15 W·m-2 and increases the likelihood that dust net warms the climate system. We conclude that to properly represent the impact of dust on the Earth system, climate models must include an accurate treatment of coarse dust in the atmosphere