Investigating the vertical extent and short-wave radiative effects of the ice phase in Arctic summertime low-level clouds

Low-level (cloud tops below 2 km) mixed-phase clouds are important in amplifying warming in the Arctic region through positive feedback in cloud fraction, water content and phase. In order to understand the cloud feedbacks in the Arctic region, good knowledge of the vertical distribution of the cloud water content, particle size and phase is required. Here we investigate the vertical extent of the cloud-phase and ice-phase optical properties in six case studies measured in the European Arctic during the ACLOUD campaign. Late spring- and summertime stratiform clouds were sampled in situ over pack ice, marginal sea ice zone and open-ocean surface, with cloud top temperatures varying between −15 and −1.5 ∘C. The results show that, although the liquid phase dominates the upper parts of the clouds, the ice phase was frequently observed in the lower parts down to cloud top temperatures as warm as −3.8 ∘C. In the studied vertical cloud profiles, the maximum of average liquid phase microphysical properties, droplet number concentration, effective radius and liquid water content, varied between 23 and 152 cm−3, 19 and 26 µm, 0.09 and 0.63 g m−3, respectively. The maximum of average ice-phase microphysical properties varied between 0.1 and 57 L−1 for the ice number concentration, 40 and 70 µm for the effective radius, and 0.005 and 0.08 g m−3 for the ice water content. The elevated ice crystal number concentrations and ice water paths observed for clouds, with cloud top temperatures between −3.8 and −8.7 ∘C can be likely attributed to secondary ice production through rime splintering. Low asymmetry parameters between 0.69 and 0.76 were measured for the mixed-phase ice crystals with a mean value of 0.72. The effect of the ice-phase optical properties on the radiative transfer calculations was investigated for the four cloud cases potentially affected by secondary ice production. Generally the choice of ice-phase optical properties only has a minor effect on the cloud transmissivity and albedo, except in a case where the ice phase dominated the upper cloud layer extinction. In this case, cloud albedo at solar wavelengths was increased by 10 % when the ice phase was given its measured optical properties instead of treating it as liquid phase. The presented results highlight the importance of accurate vertical information on cloud phase for radiative transfer and provide a suitable data set for testing microphysical parameterizations in models

Airborne investigation of black carbon interaction with low-level, persistent, mixed-phase clouds in the Arctic summer

Aerosol–cloud interaction is considered one of the largest sources of uncertainty in radiative forcing estimations. To better understand the role of black carbon (BC) aerosol as a cloud nucleus and the impact of clouds on its vertical distribution in the Arctic, we report airborne in situ measurements of BC particles in the European Arctic near Svalbard during the “Arctic CLoud Observations Using airborne measurements during polar Day” (ACLOUD) campaign held in the summer of 2017. BC was measured with a single-particle soot photometer aboard the Polar 6 research aircraft from the lowest atmospheric layer up to approximately 3500 m a.s.l (metres above sea level). During in-cloud flight transects, BC particles contained in liquid droplets (BC residuals) were sampled through a counterflow virtual impactor (CVI) inlet. Four flights, conducted in the presence of low-level, surface-coupled, inside-inversion, and mixed-phase clouds over sea ice, were selected to address the variability in BC above, below, and within the cloud layer. First, the increase in size and coating thickness of BC particles from the free troposphere to the cloud-dominated boundary layer confirmed that ground observations were not representative of upper atmospheric layers. Second, although only 1 % of liquid droplets contained a BC particle, the higher number concentration of BC residuals than BC particles sampled below cloud indicated that the totality of below-cloud BC was activated by nucleation scavenging but also that alternative scavenging processes such as the activation of free-tropospheric BC at the cloud top might occur. Third, the efficient exchange of aerosol particles at cloud bottom was confirmed by the similarity of the size distribution of BC residuals and BC particles sampled below cloud. Last, the increase in the BC residual number concentration (+31 %) and geometric mean diameter (+38 %) from the cloud top to the cloud bottom and the absolute enrichment in larger BC residuals compared with outside of the cloud supported the hypothesis of concomitant scavenging mechanisms but also suggested the formation of BC agglomerates caused by cloud processing. The vertical evolution of BC properties from inside the cloud and below the cloud indicated an efficient aerosol exchange at cloud bottom, which might include activation, cloud processing, and sub-cloud release of processed BC agglomerates. In the case of persistent low-level Arctic clouds, this cycle may reiterate multiple times, adding an additional degree of complexity to the understanding of cloud processing of BC particles in the Arctic

Assessing the role of anthropogenic and biogenic sources on PM₁ over southern West Africa using aircraft measurements

As part of the Dynamics-Aerosol-Chemistry-Cloud Interactions in West Africa (DACCIWA) project, an airborne campaign was designed to measure a large range of atmospheric constituents, focusing on the effect of anthropogenic emissions on regional climate. The presented study details results of the French ATR42 research aircraft, which aimed to characterize gas-phase, aerosol and cloud properties in the region during the field campaign carried out in June/July 2016 in combination with the German Falcon 20 and the British Twin Otter aircraft. The aircraft flight paths covered large areas of Benin, Togo, Ghana and Côte d\u27Ivoire, focusing on emissions from large urban conurbations such as Abidjan, Accra and Lomé, as well as remote continental areas and the Gulf of Guinea. This paper focuses on aerosol particle measurements within the boundary layer (<  2000 m), in particular their sources and chemical composition in view of the complex mix of both biogenic and anthropogenic emissions, based on measurements from a compact time-of-flight aerosol mass spectrometer (C-ToF-AMS) and ancillary instrumentation. Background concentrations (i.e. outside urban plumes) observed from the ATR42 indicate a fairly polluted region during the time of the campaign, with average concentrations of carbon monoxide of 131 ppb, ozone of 32 ppb, and aerosol particle number concentration ( >  15 nm) of 735 cm−3 stp. Regarding submicron aerosol composition (considering non-refractory species and black carbon, BC), organic aerosol (OA) is the most abundant species contributing 53 %, followed by SO4 (27 %), NH4 (11 %), BC (6 %), NO3 (2 %) and minor contribution of Cl (<  0.5 %). Average background PM1 in the region was 5.9 µg m−3 stp. During measurements of urban pollution plumes, mainly focusing on the outflow of Abidjan, Accra and Lomé, pollutants are significantly enhanced (e.g. average concentration of CO of 176 ppb, and aerosol particle number concentration of 6500 cm−3 stp), as well as PM1 concentration (11.9 µg m−3 stp). Two classes of organic aerosols were estimated based on C-ToF-AMS: particulate organic nitrates (pONs) and isoprene epoxydiols secondary organic aerosols (IEPOX–SOA). Both classes are usually associated with the formation of particulate matter through complex interactions of anthropogenic and biogenic sources. During DACCIWA, pONs have a fairly small contribution to OA (around 5 %) and are more associated with long-range transport from central Africa than local formation. Conversely, IEPOX–SOA provides a significant contribution to OA (around 24 and 28 % under background and in-plume conditions). Furthermore, the fractional contribution of IEPOX–SOA is largely unaffected by changes in the aerosol composition (particularly the SO4 concentration), which suggests that IEPOX–SOA concentration is mainly driven by pre-existing aerosol surface, instead of aerosol chemical properties. At times of large in-plume SO4 enhancements (above 5 µg m−3), the fractional contribution of IEPOX–SOA to OA increases above 50 %, suggesting only then a change in the IEPOX–SOA-controlling mechanism. It is important to note that IEPOX–SOA constitutes a lower limit to the contribution of biogenic OA, given that other processes (e.g. non-IEPOX isoprene, monoterpene SOA) are likely in the region. Given the significant contribution to aerosol concentration, it is crucial that such complex biogenic–anthropogenic interactions are taken into account in both present-day and future scenario models of this fast-changing, highly sensitive region

French Airborne Measurement Platform (PMA) cloud particle size distribution and volumic cloud particle scattering properties dataset near Svalbard for the HALO-AC3 measurement campaign in 2022

This data set is composed of in-situ measurement of arctic cloud microphysical properties (particle size distribution and volumic cloud particle scattering properties) observed during the HALO-AC3 campaign, which occurred between March 20th and April 10th 2022. These measurements were made using the 2D stereoscopic (2D-S, SPEC Inc.) and Polar Nephelometer (Gayet et al., 1997) probes from the airborne measurement platform of the Laboratoire de Météorologie Physique (CNRS/UCA, Aubière, France). There is one file per flight. All files are in NetCDF format, with a complete description of the parameters inside. A detailed list of the parameters present in the data set is added in a separate document (see "Further details" link)

French Airborne Measurement Platform (PMA) cloud particle size distribution and volumic cloud particle diffusion properties dataset near Svalbard for AFLUX measurement campaign with POLAR 5 in 2019

This data set is composed of in-situ measurement of arctic cloud microphysical properties (particle size distribution and volumic cloud particle diffusion properties) observed during the AFLUX-AC3 campaign, which occurred between 19 March and 11 April 2019. These measurements were made using the 2D stereoscopic (2D-S, SPEC Inc.) and Polar Nephelometer (Gayet et al., 1997) probes from the airborne measurement platform of the Laboratoire de Météorologie Physique (CNRS/UCA, Aubière, France). There is one file per flight. All files are in NetCDF format, with a complete description of the parameters inside. A detailed list of the parameters present in the data set is added in a separate document

French Airborne Measurement Platform (PMA) cloud particle size distribution and volumic cloud particle diffusion properties dataset near Svalbard for MOSAIC-ACA measurement campaign in 2020

This data set is composed of in-situ measurement of arctic cloud microphysical properties (particle size distribution and volumic cloud particle diffusion properties) observed during the MOSAIC-ACA campaign, which occurred between August 30th and September 13th 2020. These measurements were made using the 2D stereoscopic (2D-S, SPEC Inc.) and Polar Nephelometer (Gayet et al., 1997) probes from the airborne measurement platform of the Laboratoire de Météorologie Physique (CNRS/UCA, Aubière, France). There is one file per flight. All files are in NetCDF format, with a complete description of the parameters inside. A detailed list of the parameters present in the data set is added in a separate document

CDP, CIP and PIP In-situ arctic cloud microphysical properties observed during ACLOUD-AC3 campaign in June 2017

This data set is composed of in-situ measurement of arctic cloud microphysical properties observed during the ACLOUD-AC3 campaign which occurred during June 2017. These measurements were made using the CDP, CIP and PIP probes from the airborne measurement platform of the Laboratoire de Météorologie Physique (CNRS/UCA, Aubière, France). There is one file per flight. All files are in NetCDF format with a complete description of the parameters inside. A detailed description of the data processing will be done in an upcoming data paper

Volcanic sulphate and arctic dust plumes over the North Atlantic Ocean

High time resolution aerosol mass spectrometry measurements were conducted during a field campaign at Mace Head Research Station, Ireland, in June 2007. Observations on one particular day of the campaign clearly indicated advection of aerosol from volcanoes and desert plains in Iceland which could be traced with NOAA Hysplit air mass back trajectories and satellite images. In conjunction with this event, elevated levels of sulphate and light absorbing particles were encountered at Mace Head. While sulphate concentration was continuously increasing, nitrate levels remained low indicating no significant contribution from anthropogenic pollutants. Sulphate concentration increased about 3.8 µg m-3 in comparison with the background conditions. Corresponding sulphur flux from volcanic emissions was estimated to about 0.3 TgS yr-1, suggesting that a large amount of sulphur released from Icelandic volcanoes may be distributed over distances larger than 1000 km. Overall, our results corroborate that transport of volcanogenic sulphate and dust particles can significantly change the chemical composition, size distribution, and optical properties of aerosol over the North Atlantic Ocean and should be considered accordingly by regional climate models.SF

Investigating the vertical extent and short-wave radiative effects of the ice phase in Arctic summertime low-level clouds

International audienceLow-level (cloud tops below 2 km) mixed-phase clouds are important in amplifying warming in the Arctic region through positive feedback in cloud fraction, water content and phase. In order to understand the cloud feedbacks in the Arctic region, good knowledge of the vertical distribution of the cloud water content, particle size and phase is required. Here we investigate the vertical extent of the cloud-phase and ice-phase optical properties in six case studies measured in the European Arctic during the ACLOUD campaign. Late spring- and summertime stratiform clouds were sampled in situ over pack ice, marginal sea ice zone and open-ocean surface, with cloud top temperatures varying between −15 and −1.5 ∘C. The results show that, although the liquid phase dominates the upper parts of the clouds, the ice phase was frequently observed in the lower parts down to cloud top temperatures as warm as −3.8 ∘C. In the studied vertical cloud profiles, the maximum of average liquid phase microphysical properties, droplet number concentration, effective radius and liquid water content, varied between 23 and 152 cm−3, 19 and 26 µm, 0.09 and 0.63 g m−3, respectively. The maximum of average ice-phase microphysical properties varied between 0.1 and 57 L−1 for the ice number concentration, 40 and 70 µm for the effective radius, and 0.005 and 0.08 g m−3 for the ice water content. The elevated ice crystal number concentrations and ice water paths observed for clouds, with cloud top temperatures between −3.8 and −8.7 ∘C can be likely attributed to secondary ice production through rime splintering. Low asymmetry parameters between 0.69 and 0.76 were measured for the mixed-phase ice crystals with a mean value of 0.72. The effect of the ice-phase optical properties on the radiative transfer calculations was investigated for the four cloud cases potentially affected by secondary ice production. Generally the choice of ice-phase optical properties only has a minor effect on the cloud transmissivity and albedo, except in a case where the ice phase dominated the upper cloud layer extinction. In this case, cloud albedo at solar wavelengths was increased by 10 % when the ice phase was given its measured optical properties instead of treating it as liquid phase. The presented results highlight the importance of accurate vertical information on cloud phase for radiative transfer and provide a suitable data set for testing microphysical parameterizations in models