Condensation Nuclei Concentrations Research Articles

The Association Between Cloud Droplet Number over the Summer Southern Ocean and Air Mass History

AbstractThe cloud properties and governing processes in Southern Ocean marine boundary layer clouds have emerged as a central issue in understanding the Earth's climate sensitivity. While our understanding of Southern Ocean cloud feedbacks have evolved in the most recent climate model intercomparison, the background properties of simulated summertime clouds in the Southern Ocean are not consistent with measurements due to known biases in simulating cloud condensation nuclei concentrations. This paper presents several case studies collected during the Capricorn 2 and Marcus campaigns held aboard Australian research vessels in the Austral Summer of 2018. Combining the surface‐observed cases with MODIS data along forward and backward air mass trajectories, we demonstrate the evolution of cloud properties with time. These cases are consistent with multi‐year statistics showing that long trajectories of air masses over the Antarctic ice sheet are critical to creating high droplet number clouds in the high latitude summer Southern Ocean. We speculate that secondary aerosol production via the oxidation of biogenically derived aerosol precursor gasses over the high actinic flux region of the high latitude ice sheets is fundamental to maintaining relatively high droplet numbers in Southern Ocean clouds during Summer.

Developing a climatological simplification of aerosols to enter the cloud microphysics of a global climate model

Abstract. Aerosol particles influence cloud formation and properties. Hence climate models that aim for a physical representation of the climate system include aerosol modules. In order to represent more and more processes and aerosol species, their representation has grown increasingly detailed. However, depending on one's modelling purpose, the increased model complexity may not be beneficial, for example because it hinders understanding of model behaviour. Hence we develop a simplification in the form of a climatology of aerosol concentrations. In one approach, the climatology prescribes properties important for cloud droplet and ice crystal formation, the gateways for aerosols to enter the model cloud microphysics scheme. Another approach prescribes aerosol mass and number concentrations in general. Both climatologies are derived from full ECHAM-HAM simulations and can serve to replace the HAM aerosol module and thus drastically simplify the aerosol treatment. The first simplification reduces computational model time by roughly 65 %. However, the naive mean climatological treatment needs improvement to give results that are satisfyingly close to the full model. We find that mean cloud condensation nuclei (CCN) concentrations yield an underestimation of cloud droplet number concentration (CDNC) in the Southern Ocean, which we can reduce by allowing only CCN at cloud base (which have experienced hygroscopic growth in these conditions) to enter the climatology. This highlights the value of the simplification approach in pointing to unexpected model behaviour and providing a new perspective for its study and model development.

Quantifying structural errors in cloud condensation nuclei activity from reduced representation of aerosol size distributions

Aerosol effects on clouds and radiation are a large source of uncertainty in our understanding of human impacts on the climate system. Uncertainty in aerosol effects results from uncertainty in parameter values, known as parametric uncertainty, and from uncertainty from the model’s structure, known as structural uncertainty. While previous studies have assessed the impact of parametric uncertainty on modeled forcing, structural errors from the numerical representation of particle distributions and their dynamics have not been well quantified. Here we present a framework for quantifying error in aerosol size distributions and cloud condensation nuclei activity, which we apply to the widely used 4-mode version of the Modal Aerosol Module (MAM4). Box model predictions from the MAM4 are evaluated against the Particle Monte Carlo Model for Simulating Aerosol Interactions and Chemistry (PartMC-MOSAIC), a benchmark model that tracks the evolution of individual particles. We show that size distributions simulated by MAM4 diverge from those simulated by PartMC-MOSAIC after only a few hours of aging by condensation and coagulation in polluted conditions, which leads to large errors in modeled cloud condensation nuclei concentrations. We find that differences between MAM4 and PartMC-MOSAIC are largest under polluted conditions, where the size distribution evolves rapidly though aging. These findings indicate that structural error in modeled aerosol properties is a key factor contributing to uncertainty in aerosol forcing.

Effects of a Vertical Cloud Condensation Nuclei Concentration Explosion in an Idealized Hailstorm Simulation

AbstractDetermination of the key vertical level for cloud condensation nuclei concentration (CCNC) explosions has been a long‐term issue in CCN‐cloud interaction studies. An idealized hailstorm is simulated with 37 sensitivity runs, including an initial CCNC grouping vertically from the ground to the cloud top, increasing from 100 to 3,000 mg−1. The results reveal a key zone from 750 to 800 hPa near the median boundary layer, where an explosion of CCNC plays a dominant role in the nonmonotonic response of the hail precipitation rate. The explosion of CCNC in this zone could initially result in the condensation of more water vapor into the clouds, which could be transported to a greater vertical extent to significantly affect the riming collection efficiency. However, the dominant zone for the total precipitation rate is wider at heights of 700–800 hPa due to the lower sensitivity of the riming collection efficiency.

Observational constraints on the parameterization of particle dry deposition over bare cropland

Dry deposition affects the removal rates and lifetimes of atmospheric particles. Bare cropland, a surface cover type representing cultivated land after harvesting and ploughing, is widespread around the world, but the parameterizations of dry deposition velocity for this land type have not been well constrained. In this study, we integrate existing observational data of particle dry deposition for bare cropland to constrain the corresponding parameterization scheme. Considering that strong disparities exist between the calculated dry deposition velocity from existing parameterizations and the observations, a range of empirical parameters employed are adjusted to best match the model simulations with the observations. The results from the revised parameterization match much more closely with the observations for the different particle sizes than those obtained when using the existing one. As a result, particles smaller than 0.5 μm in diameter exhibit a decrease in dry deposition velocity by roughly one order of magnitude, while that of larger particles increase. Among the processes contributing to the dry deposition, the impaction and interception are dominant for particles with aerodynamic diameters between 0.1 and 10 μm, due to the roughness characteristics and large clod size of bare cropland, in contrast to smooth bare soils. Applying our revised scheme in an atmospheric chemical transport model over the North China Plain leads to a general increase in PM2.5 mass concentrations across the domain, reaching up to 11.2% over the croplands. Particularly, the number concentrations of particle in Aitken and accumulation modes are increased by 12.9% and 16.8%, respectively. The associated increase in cloud condensation nuclei concentrations reaches as high as 39.6%.

High-resolution physicochemical dataset of atmospheric aerosols over the Tibetan Plateau and its surroundings

Abstract. Atmospheric aerosol in the Tibetan Plateau (TP) and its surroundings has attracted significant scientific interest in recent decades due to its notable impacts on regional climatic and cryospheric changes, ecological and environmental security, and the hydrological cycle. However, our understanding of the atmospheric aerosol in this remote region is highly limited by the scarcity of available datasets owing to the extremely harsh natural conditions. This challenge has been mitigated in recent decades by establishing field observatories at typical sites within the TP and its surroundings. A continuous project initiated in 2015 aims to explore the properties and sources of atmospheric aerosols, as well as their regional differences, through multiple short-term intensive observations obtained across this vast region utilizing a suite of high-time-resolution online instruments. This paper presents a systematic and hourly scale dataset of aerosol physicochemical and optical properties at eight sites across the TP and its surroundings that is derived from the project. It includes size-resolved chemical compositions of submicron aerosols, high-resolution mass spectra and sources of organic aerosols, size distributions of particle number concentrations, particle light-scattering and light-absorption coefficients, particle light absorptions attributed to different carbonaceous substances including black carbon and brown carbon, and number concentrations of cloud condensation nuclei. In brief, atmospheric aerosols in these remote sites were all well mixed and highly aged, reflecting their dominant regional transport sources. However, the southern TP region exhibited high contributions of carbonaceous organic aerosols, neutralized bulk submicron aerosols, and a relatively high light-absorption capacity, whereas in the northern TP region, secondary inorganic species were the main contributors to the overall acidic submicron aerosols. Beyond providing insights into the regional differences in aerosol sources and properties across the TP and its surroundings, the datasets will also benefit simulations of aerosol radiative forcing and evaluations of interactions among different Earth system components in numerical models for this region. The datasets are accessible through the National Cryosphere Desert Data Center, Chinese Academy of Sciences (https://doi.org/10.12072/ncdc.NIEER.db2200.2022; Xu, 2022).

Role of Iodine-Assisted Aerosol Particle Formation in Antarctica.

New particle formation via the ion-mediated sulfuric acid and ammonia molecular clustering mechanism remains the most widely observed and experimentally verified pathway. Recent laboratory and molecular level observations indicate iodine-driven nucleation as a potentially important source of new particles, especially in coastal areas. In this study, we assess the role of iodine species in particle formation using the best available molecular thermochemistry data and coupled to a detailed 1-d column model which is run along air mass trajectories over the Southern Ocean and the coast of Antarctica. In the air masses traversing the open ocean, ion-mediated SA-NH3 clustering appears insufficient to explain the observed particle size distribution, wherein the simulated Aitken mode is lacking. Including the iodine-assisted particle formation improves the modeled Aitken mode representation with an increase in the number of freshly formed particles. This implies that more particles survive and grow to Aitken mode sizes via condensation of gaseous precursors and heterogeneous reactions. Under certain meteorological conditions, iodine-assisted particle formation can increase cloud condensation nuclei concentrations by 20%-100%.

A cloud-by-cloud approach for studying aerosol–cloud interaction in satellite observations

Abstract. The effective radiative forcing (ERF) due to aerosol–cloud interactions (ACIs) and rapid adjustments (ERFaci) still causes the largest uncertainty in the assessment of climate change. It is understood only with medium confidence and is studied primarily for warm clouds. Here, we present a novel cloud-by-cloud (C×C) approach for studying ACI in satellite observations that combines the concentration of cloud condensation nuclei (nCCN) and ice nucleating particles (nINP) from polar-orbiting lidar measurements with the development of the properties of individual clouds by tracking them in geostationary observations. We present a step-by-step description for obtaining matched aerosol–cloud cases. The application to satellite observations over central Europe and northern Africa during 2014, together with rigorous quality assurance, leads to 399 liquid-only clouds and 95 ice-containing clouds that can be matched to surrounding nCCN and nINP respectively at cloud level. We use this initial data set for assessing the impact of changes in cloud-relevant aerosol concentrations on the cloud droplet number concentration (Nd) and effective radius (reff) of liquid clouds and the phase of clouds in the regime of heterogeneous ice formation. We find a Δln⁡Nd/Δln⁡nCCN of 0.13 to 0.30, which is at the lower end of commonly inferred values of 0.3 to 0.8. The Δln⁡reff/Δln⁡nCCN between −0.09 and −0.21 suggests that reff decreases by −0.81 to −3.78 nm per increase in nCCN of 1 cm−3. We also find a tendency towards more cloud ice and more fully glaciated clouds with increasing nINP that cannot be explained by the increasingly lower cloud top temperature of supercooled-liquid, mixed-phase, and fully glaciated clouds alone. Applied to a larger number of observations, the C×C approach has the potential to enable the systematic investigation of warm and cold clouds. This marks a step change in the quantification of ERFaci from space.

Effect of Long‐Range Transported Fire Aerosols on Cloud Condensation Nuclei Concentrations and Cloud Properties at High Latitudes

AbstractActive vegetation fires in south‐eastern (SE) Europe resulted in a notable increase in the number concentration of aerosols and cloud condensation nuclei (CCN) particles at two high latitude locations—the SMEAR IV station in Kuopio, Finland, and the Zeppelin Observatory in Svalbard, high Arctic. During the fire episode aerosol hygroscopicity κ slightly increased at SMEAR IV and at the Zeppelin Observatory κ decreased. Despite increased κ in high CCN conditions at SMEAR IV, the aerosol activation diameter increased due to the decreased supersaturation with an increase in aerosol loading. In addition, at SMEAR IV during the fire episode, in situ measured cloud droplet number concentration (CDNC) increased by a factor of ∼7 as compared to non‐fire periods which was in good agreement with the satellite observations (MODIS, Terra). Results from this study show the importance of SE European fires for cloud properties and radiative forcing in high latitudes.

Above-cloud concentrations of cloud condensation nuclei help to sustain some Arctic low-level clouds

Abstract. Previous studies have found that low-level Arctic clouds often persist for long periods even in the face of very low surface cloud condensation nuclei (CCN) concentrations. Here, we investigate whether these conditions could occur due to continuous entrainment of aerosol particles from the free troposphere (FT). We use an idealized large eddy simulation (LES) modeling framework, where aerosol concentrations are low in the boundary layer (BL) but increased up to 50× in the free troposphere. We find that the tests with higher tropospheric aerosol concentrations simulated clouds, which persisted for longer and maintained higher liquid water paths (LWPs). This is due to direct entrainment of the tropospheric aerosol into the cloud layer, which results in a precipitation suppression from the increase in cloud droplet number and in stronger cloud-top radiative cooling, which causes stronger circulations maintaining the cloud in the absence of surface forcing. Together, these two responses result in a more well-mixed boundary layer with a top that remains in contact with the tropospheric aerosol reservoir and can maintain entrainment of those aerosol particles. The surface aerosol concentrations, however, remained low in all simulations. The free-tropospheric aerosol concentration necessary to maintain the clouds is consistent with concentrations that are frequently seen in observations.

The impact of aerosols and model grid spacing on a supercell storm from Swabian MOSES 2021

AbstractThe supercell storm that occurred in southwestern Germany on June 23, 2021, had an exceptionally long lifetime of 7.5 hr, travelled a distance of nearly 190 km, and produced large amounts of hail. During that summer, the Swabian MOSES field campaign was held in that area, and several hydro‐meteorological measurements are available, as the storm passed directly over the main observation site. We present hindcasts of this event with the Icosahedral Non‐hydrostatic model using two horizontal grid spacings (i.e., 2 km, 1 km) with a single‐moment and an advanced double‐moment microphysics scheme. Numerical results show that all 2 km model realizations do not simulate convective precipitation at the correct location and time. For the 1 km grid spacing, changes in aerosol concentration resulted in large changes in convective precipitation. Only the 1 km run assuming a low cloud condensation nuclei (CCNs) concentration is able to realistically capture the storm, whereas no supercell is simulated in the more polluted scenarios. Observed aerosol particle concentrations indicate that CCNs values were the lowest of the month, which suggests that the low aerosol concentration is a reasonable assumption. The thermodynamic structure of the pre‐convective environment, as well as other observations, showed the best agreement to this model run as well, indicating that the good representation of the supercell was obtained for the right reason. The automatic tracking of individual clouds revealed that more convective cells with longer lifetimes are simulated at finer resolution. We also find a negative aerosol–precipitation effect that is not only due to a reduced collision–coalescence process, but also to weaker cold‐rain processes. These findings demonstrate the benefits of using an aerosol‐aware double‐moment microphysics scheme for convective‐scale predictability and that the use of different CCNs concentrations can determine whether a supercell is successfully simulated or not.

Cloud condensation nuclei concentrations derived from the CAMS reanalysis

Abstract. Determining number concentrations of cloud condensation nuclei (CCN) is one of the first steps in the chain in analysis of cloud droplet formation, the direct microphysical link between aerosols and cloud droplets, and a process key for aerosol–cloud interactions (ACI). However, due to sparse coverage of in situ measurements and difficulties associated with retrievals from satellites, a global exploration of their magnitude, source as well as temporal and spatial distribution cannot be easily obtained. Thus, a better representation of CCN numbers is one of the goals for quantifying ACI processes and achieving uncertainty-reduced estimates of their associated radiative forcing. Here, we introduce a new CCN dataset which is derived based on aerosol mass mixing ratios from the latest Copernicus Atmosphere Monitoring Service reanalysis (CAMSRA) in a diagnostic model that uses CAMSRA aerosol properties and a simplified kappa-Köhler framework suitable for global models. The emitted aerosols in CAMSRA are not only based on input from emission inventories using aerosol observations, they also have a strong tie to satellite-retrieved aerosol optical depth (AOD) as this is assimilated as a constraining factor in the reanalysis. Furthermore, the reanalysis interpolates for cases of poor or missing retrievals and thus allows for a full spatiotemporal quantification of CCN numbers. The derived CCN dataset captures the general trend and spatial and temporal distribution of total CCN number concentrations and CCN from different aerosol species. A brief evaluation with ground-based in situ measurements demonstrates the improvement of the modelled CCN over the sole use of AOD as a proxy for CCN as the overall correlation coefficient improved from 0.37 to 0.71. However, we find the modelled CCN from CAMSRA to be generally high biased and find a particular erroneous overestimation at one heavily polluted site which emphasises the need for further validation. The CCN dataset (https://doi.org/10.26050/WDCC/QUAERERE_CCNCAMS_v1, Block, 2023), which is now freely available to users, features 3-D CCN number concentrations of global coverage for various supersaturations and aerosol species covering the years 2003–2021 with daily frequency. This dataset is one of its kind as it offers lots of opportunities to be used for evaluation in models and in ACI studies.

Investigating the contribution of grown new particles to cloud condensation nuclei with largely varying preexisting particles – Part 1: Observational data analysis

Abstract. This study employed multiple techniques to investigate the contribution of grown new particles to the number concentration of cloud condensation nuclei (CCN) at various supersaturation (SS) levels at a rural mountain site in the North China Plain from 29 June to 14 July 2019. On 8 new particle formation (NPF) days, the total particle number concentrations (Ncn) were 8.4 ± 6.1×103 cm−3, which was substantially higher compared to 4.7 ± 2.6×103 cm−3 on non-NPF days. However, the CCN concentration (Nccn) at 0.2 % SS and 0.4 % SS on the NPF days was significantly lower than those observed on non-NPF days (p<0.05). This was due to the lower cloud activation efficiency of preexisting particles resulting from organic vapor condensation and smaller number concentrations of preexisting particles on NPF days. A case-by-case examination showed that the grown new particles only yielded a detectable contribution to Nccn at 0.4 % SS and 1.0 % SS during the NPF event on 1 July 2019, accounting for 12 % ± 11 % and 23 % ± 12 % of Nccn, respectively. The increased Nccn during two other NPF events and at 0.2 % SS on 1 July 2019 were detectable but determined mainly by varying preexisting particles rather than grown new particles. In addition, the hygroscopicity parameter values, concentrations of inorganic and organic particulate components, and surface chemical composition of different sized particles were analyzed in terms of chemical drivers to grow new particles. The results showed that the grown new particles via organic vapor condensation generally had no detectable contribution to Nccn but incidentally did. However, this conclusion was drawn from a small size of observational data, leaving more observations, particularly long-term observations and the growth of preexisting particles to the CCN required size, needed for further investigation.

Detection of dilution due to turbulent mixing vs. precipitation scavenging effects on biomass burning aerosol concentrations using stable water isotope ratios during ORACLES

Abstract. The interaction between biomass burning aerosols and clouds remains challenging to accurately determine, in part because of difficulties using direct observations to account for influences on aerosol concentrations from precipitation scavenging and dilution due to air mass mixing and separating those signals from source contributions. The prevalence of mixing versus precipitation processes in air laden with biomass burning aerosol (BBA) in the southeast Atlantic lower free troposphere (FT) and marine boundary layer (MBL) is assessed during three observation periods (September 2016, August 2017, and October 2018) during the NASA ORACLES (ObseRvations of Aerosols above CLouds and their intEractionS) campaign. Significant sources of BBAs over the African continent combined with regional circulation patterns result in BBA-laden air flowing from the continent over the southeast Atlantic in the lower FT, then subsiding onto the semi-permanent stratocumulus cloud deck, and entraining into the MBL. This study is broken into two parts, first analyzing hydrologic histories of the BBA air in the lower FT and then carrying out a similar assessment in the underlying MBL. Both analyses leverage joint measurements of water concentration and its heavy isotope ratio, interpreted in the previously established (q, δD) phase space framework. For the lower-FT analysis, in situ observations (water concentration, water isotope ratios) in the lower FT are combined with satellite and Modern-Era Retrospective analysis for Research and Applications, Version 2 (MERRA-2), global reanalysis data into simple analytical models to constrain hydrologic histories. We find that even simple models are capable of detecting and constraining the primary processes at play, e.g., distinguishing air masses that experienced moist convection and precipitation (likely over the continent) from those that underwent dry convection and turbulent mixing. Regression of the aircraft data onto a simple model of convective detrainment is used to develop a metric of total precipitation for the in situ measurements and then compared to an aerosol metric of black carbon scavenging also derived from the in situ measurements (the ratio of black carbon to carbon monoxide, BC/CO). There is a strong correlation between the two, suggesting black carbon scavenging has been detected and partially quantified, if only in a relative manner. In comparison, weak correlation is found between BC/CO and the total water concentration itself. The above method is expanded to test for entrainment and precipitation influences on BBA concentrations in the MBL. This is more difficult than the FT analysis since signals are subtle and limited by imperfect knowledge of the water and isotope ratios of the entrained air mass at cloud top. For some of the MBLs observed during 2016 and 2018, lower cloud condensation nuclei (CCN) concentrations occur in the sub-cloud layer coincident with isotopic evidence of precipitation, indicating aerosol scavenging, but more complex models are needed to produce definitive conclusions. For the 2017 observation period, with the highest sub-cloud CCN concentrations, there is no connection between precipitation signals and CCN concentrations, likely indicating the importance of different geographic sampling and air mass history in that year. Nonetheless, these findings along with the FT analysis suggest that utilizing isotope ratio signals may be an aid in addressing cloud–aerosol challenges. Especially for the FT case, these findings support the pursuit of more complex models combined with targeted in situ data to constrain BC scavenging coefficients in a manner which can guide model parameterizations, leading to improvements in the accuracy of simulated BC concentrations and lifetimes in climate models.

On the Impact of a Dry Intrusion Driving Cloud-Regime Transitions in a Midlatitude Cold-Air Outbreak

Abstract Marine cold-air outbreaks (CAOs) occur in the postfrontal sector of midlatitude storms, usually accompanied by dry intrusions (DIs) shaping the free-tropospheric (FT) air aloft. Substantial rain initiates overcast to broken regime transitions in marine boundary layer (MBL) cloud decks that form where cold air first meets relatively high sea surface temperatures. An exemplary CAO in the northwest Atlantic shows earlier transitions (corresponding to reduced extents of overcast clouds) closer to the low pressure center. We hypothesize that gradients in the meteorological pattern imposed by the prevailing DI induced a variability in substantial rain onset and thereby transition. We compile satellite observations, reanalysis fields, and Lagrangian large-eddy simulations (LES) translating along MBL trajectories to show that postfrontal trajectories closer to the low pressure center are more favorable to rain formation (and thereby cloud transitions) because of 1) weaker FT subsidence rates, 2) greater FT humidity, 3) stronger MBL winds, and 4) a colder MBL with reduced lower-tropospheric stability. LES confirms the observed variability in transitions, with substantial rain appearing earlier where there is swifter reduction of cloud condensation nucleus (CCN) concentration and increase of liquid water path (LWP). Prior to substantial rain, CCN budgets indicate dominant loss terms from FT entrainment and hydrometeor collisions. LWP-enhancing cloud thickness increases more rapidly for weaker large-scale subsidence that enables faster MBL deepening. Mere MBL warming and moistening cannot explain cloud thickness increases. The generality of such a DI-imposed cloud transition pattern merits further investigation with more cases that may additionally be convoluted by onshore aerosol gradients. Significance Statement Cold-air outbreaks (CAOs) lead to marine boundary layer (MBL) clouds that commonly undergo rain-initiated overcast to broken cloud regime transitions that can drastically impact reflected solar radiation. We aim to better understand what mechanisms control these transitions. For a CAO event in the northwest Atlantic that shows earlier transitions closer to the low pressure center, we find the transition timing to be largely governed by the coinciding dry intrusion that imposes an inhomogeneous large-scale meteorological pattern onto the overlying free troposphere and thereby affects MBL rain formation. Our findings update conceptual understanding of extratropical cyclones and motivate analyzing observations and conducting simulations for more postfrontal cases through a Lagrangian perspective as done here for one case, to assess the generality of our findings.

Drivers of Cloud Condensation Nuclei in the Eastern North Atlantic as Observed at the ARM Site

AbstractSeven years of data collected at the Atmospheric Radiation Measurement's Eastern North Atlantic (ENA) site are analyzed to understand the controls of Cloud Condensation Nuclei (CCN) concentrations in the region. Day‐night differences in the aerosol data as segregated by wind direction demonstrate the aerosol observations to be impacted by local emissions when the wind direction (wdir) is between 90° and 310° (measured clockwise from the North where air is coming from). Data collected during marine conditions (wdir <90° or wdir >310°) show the CCN concentrations to be higher in the summer months as compared to the winter months. CCN budget analysis revealed advection and precipitation scavenging being primarily responsible for modulating the CCN concentrations at the site on monthly timescales, with rain rates driving the precipitation scavenging term. High (greater than 75th percentile) and low (lower than 25th percentile) CCN events were identified for each month to characterize the sub‐monthly variability of CCN concentrations. Low CCN events had thicker clouds, stronger rain rates, and lower reanalysis reported free‐tropospheric aerosol pseudo number concentration at the ENA site as compared to the high CCN events. Analysis of satellite data of air‐parcels 48 hr prior to their arrival at the ENA site demonstrated the air parcels during low CCN events to encounter higher cloudiness, stronger rain rates, and higher cloud top heights as compared to the high CCN events. The results presented herein provide key constraints for model evaluation studies and climatological studies conducted at the ENA site.

Maximum Supersaturation in the Marine Boundary Layer Clouds Over the North Atlantic

AbstractThe maximum supersaturation (Sx) in clouds is a key parameter affecting the cloud's microphysical and radiative properties. We investigate the Sx of the marine boundary layer clouds by combining airborne and surface observations in the Eastern North Atlantic. The cloud droplet number concentration (Nc) in the least diluted cloud cores agrees well with the number concentration of particles larger than the Hoppel Minimum (HM) (N>HM) below clouds, indicating that the HM represents the average size threshold above which particles are activated to form cloud droplets. The Sx values derived from surface observations vary from 0.10% to 0.50% from June 2017 to June 2018, with a clear seasonal variation exhibiting higher values during winter. Most of the Sx variance (∼60%) can be explained by the cloud condensation nuclei (CCN) concentration and updraft velocity (w), with the CCN concentration playing a more important role than w in explaining the variation of Sx. The influence of CCN concentration on Sx leads to a buffered response of Nc to aerosol perturbations. The response of Nc to low aerosol concentration during winter is further buffered by the high w. The global Community Earth System Model (CESM) simulated Sx values in the Azores have a positive bias compared to measured Sx, likely due to overestimated w and underestimated CCN concentration. The CESM simulated Sx exhibits higher values further north over the North Atlantic Ocean, which is attributed to stronger w. The suppression of Sx by aerosol is also evident in regions with high CCN concentrations.

New particle formation leads to enhanced cloud condensation nuclei concentrations on the Antarctic Peninsula

Abstract. Few studies have investigated the impact of new particle formation (NPF) on cloud condensation nuclei (CCN) in remote Antarctica, and none has elucidated the relationship between NPF and CCN production. To address that knowledge gap, we continuously measured the number size distribution of 2.5–300 nm particles and CCN number concentrations at King Sejong Station on the Antarctic Peninsula from 1 January to 31 December 2018. Ninety-seven NPF events were detected throughout the year. Clear annual and seasonal patterns of NPF were observed: high concentration and frequency of nucleation-mode particles in summer (December–February: 53 NPF cases) and undetected nucleation-mode particles in winter (June–August: no NPF cases). We estimated the spatial scale of NPF by multiplying the time during which a distinct nucleation mode can be observed at the sampling site by the locally measured wind speed. The estimated median spatial scale of NPF around the Antarctic Peninsula was found to be approximately 155 km, indicating the large scale of NPF events. Air back-trajectory analysis revealed that 80 cases of NPF events were associated with air masses originating over the ocean, followed by sea-ice (12 cases), multiple (3 cases), and land (2 cases) regions. We present and discuss three major NPF categories: (1) marine NPF, (2) sea-ice NPF, and (3) multiple NPF. Satellite estimates for sea-surface dimethylsulfoniopropionate (DMSP; a precursor of gaseous dimethyl sulfide) data showed that the production of oceanic biogenic precursors could be a key component in marine NPF events, whereas halogen compounds released from ice-covered areas could contribute to sea-ice NPF events. Terrestrial sources (wildlife colonies, vegetation, and meltwater ponds) from Antarctica could affect aerosol production in multiple air masses. Out of 97 observed NPF events, 83 cases were characterized by the simultaneous increase in the CCN concentration by 2 %–270 % (median 44 %) in the following 1 to 36 h (median 8 h) after NPF events. Overall, Antarctic NPF events were found to be a significant source of particles with different physical characteristics and related to biogenic sources in and around the Antarctic Peninsula, which subsequently grew to cloud condensation nuclei.

Annual cycle of aerosol properties over the central Arctic during MOSAiC 2019–2020 – light-extinction, CCN, and INP levels from the boundary layer to the tropopause

Abstract. The MOSAiC (Multidisciplinary drifting Observatory for the Study of Arctic Climate) expedition was the largest Arctic field campaign ever conducted. MOSAiC offered the unique opportunity to monitor and characterize aerosols and clouds with high vertical resolution up to 30 km height at latitudes from 80 to 90∘ N over an entire year (October 2019 to September 2020). Without a clear knowledge of the complex aerosol layering, vertical structures, and dominant aerosol types and their impact on cloud formation, a full understanding of the meteorological processes in the Arctic, and thus advanced climate change research, is impossible. Widespread ground-based in situ observations in the Arctic are insufficient to provide these required aerosol and cloud data. In this article, a summary of our MOSAiC observations of tropospheric aerosol profiles with a state-of-the-art multiwavelength polarization Raman lidar aboard the icebreaker Polarstern is presented. Particle optical properties, i.e., light-extinction profiles and aerosol optical thickness (AOT), and estimates of cloud-relevant aerosol properties such as the number concentration of cloud condensation nuclei (CCN) and ice-nucleating particles (INPs) are discussed, separately for the lowest part of the troposphere (atmospheric boundary layer, ABL), within the lower free troposphere (around 2000 m height), and at the cirrus level close to the tropopause. In situ observations of the particle number concentration and INPs aboard Polarstern are included in the study. A strong decrease in the aerosol amount with height in winter and moderate vertical variations in summer were observed in terms of the particle extinction coefficient. The 532 nm light-extinction values dropped from >50 Mm−1 close to the surface to <5 Mm−1 at 4–6 km height in the winter months. Lofted, aged wildfire smoke layers caused a re-increase in the aerosol concentration towards the tropopause. In summer (June to August 2020), much lower particle extinction coefficients, frequently as low as 1–5 Mm−1, were observed in the ABL. Aerosol removal, controlled by in-cloud and below-cloud scavenging processes (widely suppressed in winter and very efficient in summer) in the lowermost 1–2 km of the atmosphere, seems to be the main reason for the strong differences between winter and summer aerosol conditions. A complete annual cycle of the AOT in the central Arctic could be measured. This is a valuable addition to the summertime observations with the sun photometers of the Arctic Aerosol Robotic Network (AERONET). In line with the pronounced annual cycle in the aerosol optical properties, typical CCN number concentrations (0.2 % supersaturation level) ranged from 50–500 cm−3 in winter to 10–100 cm−3 in summer in the ABL. In the lower free troposphere (at 2000 m), however, the CCN level was roughly constant throughout the year, with values mostly from 30 to 100 cm−3. A strong contrast between winter and summer was also given in terms of ABL INPs which control ice production in low-level clouds. While soil dust (from surrounding continents) is probably the main INP type during the autumn, winter, and spring months, local sea spray aerosol (with a biogenic aerosol component) seems to dominate the ice nucleation in the ABL during the summer months (June–August). The strong winter vs. summer contrast in the INP number concentration by roughly 2–3 orders of magnitude in the lower troposphere is, however, mainly caused by the strong cloud temperature contrast. A unique event of the MOSAiC expedition was the occurrence of a long-lasting wildfire smoke layer in the upper troposphere and lower stratosphere. Our observations suggest that the smoke particles frequently triggered cirrus formation close to the tropopause from October 2019 to May 2020.

Measurements of aerosol microphysical and chemical properties in the central Arctic atmosphere during MOSAiC

The Arctic environment is transforming rapidly due to climate change. Aerosols’ abundance and physicochemical characteristics play a crucial, yet uncertain, role in these changes due to their influence on the surface energy budget through direct interaction with solar radiation and indirectly via cloud formation. Importantly, Arctic aerosol properties are also changing in response to climate change. Despite their importance, year-round measurements of their characteristics are sparse in the Arctic and often confined to lower latitudes at Arctic land-based stations and/or short high-latitude summertime campaigns. Here, we present unique aerosol microphysics and chemical composition datasets collected during the year-long Multidisciplinary drifting Observatory for the Study of Arctic Climate (MOSAiC) expedition, in the central Arctic. These datasets, which include aerosol particle number concentrations, size distributions, cloud condensation nuclei concentrations, fluorescent aerosol concentrations and properties, and aerosol bulk chemical composition (black carbon, sulfate, nitrate, ammonium, chloride, and organics) will serve to improve our understanding of high-Arctic aerosol processes, with relevance towards improved modelling of the future Arctic (and global) climate.