Investigation of June 2020 giant Saharan dust storm using remote sensing observations and model reanalysis.

This paper investigates the characteristics and impact of a major Saharan dust storm during June 14th-19th 2020 on atmospheric radiative and thermodynamics properties over the Atlantic Ocean. The event witnessed the highest ever aerosol optical depth for June since 2002. The satellites and high-resolution model reanalysis products well captured the origin and spread of the dust storm. The Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) measured total attenuated backscatter and aerosol subtype profiles, lower angstrom exponent values (~ 0.12) from Modern-Era Retrospective Analysis for Research and Application-version 2 (MERRA-2) and higher aerosol index value from Ozone monitoring instrument (> 4) tracked the presence of elevated dust. It was found that the dust AOD was as much as 250-300% higher than their climatology resulting in an atmospheric radiative forcing ~ 200% larger. As a result, elevated warming (8-16%) was observed, followed by a drop in relative humidity (2-4%) in the atmospheric column, as evidenced by both in-situ and satellite measurements. Quantifications such as these for extreme dust events provide significant insights that may help in understanding their climate effects, including improvements to dust simulations using chemistry-climate models.

Chemical Characterization of Highly Functionalized Organonitrates Contributing to Night-Time Organic Aerosol Mass Loadings and Particle Growth.

Reactions of volatile organic compounds (VOC) with NO3 radicals and of reactive intermediates of oxidized VOC with NO x can lead to the formation of highly functionalized organonitrates (ON). We present quantitative and chemical information on ON contributing to high night-time organic aerosol (OA) mass concentrations measured during July-August 2016 in a rural area in southwest Germany. A filter inlet for gases and aerosols coupled to a high-resolution time-of-flight chemical ionization mass spectrometer (FIGAERO-HR-ToF-CIMS) was used to analyze the molecular composition of ON in both the gas and particle phase. We find larger contributions of ON to OA mass during the night. Identified ON are highly functionalized, with 4 to 12 oxygen atoms. The diel patterns of ON compounds with 5, 7, 10, or 15 carbon atoms per molecule vary, indicating a corresponding behavior of their potential precursor VOC. The temporal behavior of ON after sunset correlates with that of the number concentration of ultrafine particles, indicating a potential role of ON in night-time new particle formation (NPF) regularly observed at this location. We estimate an ON contribution of 18-25% to the mass increase of newly formed particles after sunset. Our study provides insights into the chemical composition of highly functionalized ON in the rural atmosphere and the role of anthropogenic emissions for night-time SOA formation in an area where biogenic VOC emissions dominate.