1. 

Introduction

Aerosol particles are ubiquitous in the atmosphere and important for the Earth radiative balance. They interact directly with radiation through scattering and absorption, and indirectly by acting as cloud condensation nuclei (CCN). The indirect aerosol radiative effect, through cloud formation, generally cools the Earth system, but can also cause local heating. According to the Intergovernmental Panel on Climate Change (IPCC, 2013), aerosol-cloud interactions currently represent the largest uncertainty in estimates of the anthropogenic perturbation of the Earth’s radiative budget. Removal by clouds and precipitation is also the major sink of atmospheric aerosol particles and therefore an important factor influencing regional scale air quality and aerosol climate effect (Theobald et al., 2019). To quantify aerosol indirect effects on climate and to better constrain the wet deposition mechanisms of particulate matter (PM), the complex interactions between atmospheric aerosol particles, clouds and precipitation need to be better understood (e.g. Ervens, 2015 and references therein).

The ability of an aerosol particle to act as CCN depends, in favourable meteorological conditions, on the size and chemical composition of the particle (Köhler, 1936; Hobbs, 1993; Seinfeld and Pandis, 2006; Ervens, 2015; Lowe et al., 2019). Therefore, the fraction of particles acting as CCN at a certain supersaturation and thus also taken up by clouds and precipitation can be predicted if the atmospheric aerosol size distribution and composition are known. Owing to the multitude of atmospheric aerosol sources, the aerosol population in the atmosphere is generally a mixture of particles with different sizes between a few nm and up to several µm with varying chemical composition. The chemical complexity is a particular challenge for the atmospheric aerosol organic fraction, as it contains thousands of different compounds with various molecular properties (Goldstein and Galbally, 2007; Jimenez et al., 2009). To develop general approaches for describing aerosol-cloud interactions in various climate or air quality applications, we need to systematically investigate the roles of the size-dependent chemical composition of aerosol particles and their number size distribution (e.g. Dusek et al., 2006), and simplify them accordingly without losing any necessary level of detail.

The scientific understanding of aerosol-cloud interactions is still limited by the lack of direct observational data on aerosol and cloud properties with sufficient resolution. This is true also for simultaneous observations of aerosol particle and cloud residual size distributions and chemical compositions. Besides, direct and simultaneous chemical characterisation of aerosol particles and cloud residuals, observations of volatility (see e.g. Häkkinen et al., 2012 and references therein) and hygroscopicity (see e.g. Rissler et al., 2006 and references therein) are useful in this regard. Besides being a proxy for particle composition, the volatility of aerosol constituents (related to saturation vapour pressure or -concentrations) governs phase transitions and condensational growth and is therefore needed in descriptions of the evolution of the size distribution of aerosol particles (Mohr et al., 2019). The hygroscopicity described by the parameter κ (Rissler et al., 2006; Petters and Kreidenweis, 2007), on the other hand, is a direct proxy of the ability of a given particle (or particle population) to take up water and act as CCN. Previous studies with simultaneous measurements of aerosol chemical composition, size distribution, volatility and hygroscopicity in- and out-of-cloud exist (e.g. Seifert et al., 2004; Drewnick et al., 2006; Ditas et al., 2012; Hao et al., 2013; Hammer et al., 2014; Kruger et al., 2014; Väisänen et al., 2016), and have generally demonstrated the importance of particle size in CCN activation: the size distributions of ambient aerosols contain generally more and on average larger particles than those observed in the interstitial aerosol. In particular, closure studies of particle number size distributions in- and out-of-cloud, including measurements of the cloud residuals, have provided as a valuable means to estimate water supersaturation conditions within clouds where direct measurements are extremely challenging. We are not, however, aware of any measurements coupling direct measurements of the volatility and hygroscopicity of atmospheric aerosol particles and cloud residuals (particles remaining after evaporating the cloud water) to corresponding observations of the ambient and residual size distribution and chemical composition. Such measurements can, however, shed light on the processes and properties governing (1) aerosol particle uptake by clouds; (2) transport and scavenging of chemical species via clouds and rain; (3) the potential aqueous phase processing of the species present in the particles (Targino et al., 2007).

Here we present simultaneous observations of the key physical and chemical properties of ambient aerosol and cloud residuals during the Cloud and Aerosol Experiment at Åre (CAEsAR 2014) campaign, which took place between summer and early autumn 2014 at a remote site on a mountaintop in central Sweden. We combine simultaneous (with time resolution of about 12 min or less) observations of aerosol particle size distributions, volatility, hygroscopicity and black carbon (BC) content with sampling and chemical analysis of the bulk PM and cloud water over much longer time scales. Using the collected data sets, we investigate the similarities and differences in the chemical composition, volatility and hygroscopicity of the aerosol particles and the cloud residuals, along with the influence of the clouds on the ambient particle size distribution. Finally, we compare the volatility and hygroscopicity estimated based on the bulk chemical compositions to those directly observed with the online techniques. This comparison is used to discuss the level of detail in aerosol size distribution and composition representations that is needed to reproduce the ability of aerosol particles to interact with clouds at a remote boreal site like Mt. Åreskutan.

2. 

Method

2.1. 

The CAEsAR campaign at Mt. Åreskutan

Mount Åreskutan, Sweden (63°26N and 13°6E), is located in central Scandinavia, surrounded primarily by the boreal vegetation zone with no major cities nearby. It provides an opportunity to study aerosols of various origins as the station is located at an intersection of e.g. marine, boreal, polar and continental air masses (Ogren and Rodhe, 1986; Drewnick et al., 2006; Franke et al., 2017). At an elevation of 1250 m a.s.l., the station is most of the time located within the planetary boundary layer (PBL) but it is frequently encompassed in clouds (Franke et al., 2017). The closest potential source of PM and related precursors is the village of Åre down in the valley (∼400 m a.s.l.) with approximately 1500 inhabitants during the summer.

The CAEsAR campaign took place at Mt. Åreskutan from 27 June to 10 October 2014 (Franke et al., 2017; Vega et al., 2019). Aerosol particle size distributions of the ambient aerosol and cloud residuals were continually measured during the entire campaign, PM filter samples were collected 27 June–10 October (Franke et al., 2017) and cloud water samples 4 July–12 September (Vega et al., 2019). Additionally, the volatility (8–26 July) and hygroscopicity (1 August–21 September) of the ambient aerosol particles were measured with a VHTDMA (volatility–hygroscopicity tandem differential mobility analyser) system. Further details of the measurements used in this study are provided below.

2.2. 

Sampling setup and in-situ measurements

Figure 1 presents an overview of the experimental setup, with the two main aerosol inlets (the CVI [counterflow virtual impactor] with variable cut-off diameters as described below and the PM10 inlet with an aerodynamic particle cut-off diameter of 10 µm) along with the PM filter (with a cut-off diameter of 10 µm) and cloud water samplers. Hereafter, ambient aerosol and cloud residuals refer to atmospheric particulate phases sampled in-situ behind the CVI. The material collected on the filters and the cloud water samples were analysed offline in the laboratory, and are referred to as PM and cloud water. This is important to keep in mind since the CVI and PM10 inlets have different cut-off sizes and hence collect different parts of the atmospheric aerosol population.

Fig. 1. 

Inlet system and instrumental setup during the CAEsAR campaign. PM10 refers to particulate matter with aerodynamic diameters smaller than 10 µm and CVI to counterflow virtual impactor, which were the two main aerosol inlets. DMPS refers to differential mobility particle sizer, VHTDMA to volatility and hygroscopicity tandem differential mobility analyser, measuring at the initial diameter (Dinit.), MAAP to multi-angle absorption photometer, measuring the black carbon (BC) content at the wavelength (λ), and EM to elemental mass (an estimate of BC derived from EC).

A ground-based CVI (Bretchel Inc., GCVI, model 1205) was used to collect cloud residuals for size distribution measurements and in-situ volatility and hygroscopicity analysis. The CVI allows separation of aerosols and cloud elements by their inertia (Noone et al., 1988). In this experiment the aerodynamic particle cut-off diameter was 6.3 ± 0.8 µm (mean ± standard deviation) when the CVI was on, hence sampling hydrometeors and aerosol particles larger than this diameter. The measurements were corrected with a setting-dependent enrichment factor of EF = 8.5 ± 1.2 (see e.g. Shingler et al., 2012). After collection, the hydrometeors were quickly evaporated in the dry particle-free carrier air and transported to various instruments operating downstream of the CVI inlet. The CVI was controlled via a visibility sensor and turned on automatically during periods with visibilities below 1 km. During periods with visibilities above 1 km, the CVI inlet was operated as a normal total aerosol inlet, sampling the majority of the ambient aerosol population.

Size distributions of 10–600 nm ambient aerosol and cloud residual particles were measured with a time resolution of about 6 min using a differential mobility particle sizer (DMPS) located downstream the CVI. The sample flow was dried to relative humidity (RH) = 20.4 ± 9.6% using a combination of dried pressurised air and Nafion dryers (Perma Pure, model MD-110-12S-4), and brought to charge equilibrium using a Ni-63 source before entering the DMPS. The DMPS consists of a custom-built Vienna-type differential mobility analyser (DMA) operated at RH = 9.8 ± 2.9% (using Nafion dryers, Perma Pure, model PD-100T-12MSS), and a condensation particle counter (CPC; TSI, model 3010). The ambient aerosol particles and cloud residuals were also characterised for their BC content using a multi-angle absorption photometer (MAAP, Thermo Fisher Scientific Inc., model 5012). The MAAP measures the intensity of attenuated and scattered light (wavelength λ = 637 nm; Müller et al., 2011) by particles deposited on a glass micro-fibre filter, and derives the equivalent BC (hereafter referred to as BC) mass concentration using a fixed mass absorption coefficient with a time resolution of about 1 min. The ambient aerosol size distributions 10–500 nm were simultaneously sampled through a PM10 inlet with a second DMPS system, with a time resolution of about 10 min (see Franke et al., 2017 for a more detailed description). Size distributions measured with both DMPS systems were corrected for multiple charge effects and diffusion losses using the Particle Loss Calculator developed by von der Weiden et al. (2009). All measurements used in this study are given at ambient conditions.

Particulate matter (PM10) was also collected over intervals of 72 h on micro-quartz fibre filters (Munktell and Filtrak GmbH, model T293, 47 mm, heated at 800 °C for 12 h before sampling) using a low-volume reference sampler (Leckel GmbH, model LVS3 Small Filter Device). The substrates were stored at +4 °C until chemical analysis was performed (Franke et al., 2017). Cloud water samples were collected using a custom-built single-stage Caltech Active Strand Cloudwater Collector (see e.g. Demoz et al., 1996; Vega et al., 2019). At RH > 80%, a fan was turned on causing a flow through the system trapping cloud droplets on Teflon strings through inertial impaction. The cloud droplets were then collected in pre-cleaned glass bottles (Vega et al., 2019), and the collected cloud water was further filtered into glass bottles through micro-quartz fibre filters and stored at −20 °C until chemical analysis. The sampling periods varied between 23 and 395 h depending on the amount of collected water.

2.3. 

Chemical analysis of PM and cloud water samples

The chemical composition of the PM10 filter samples was characterised using a combination of a thermo-optical transmission (TOT) method (Sunset Laboratory B.V, see Birch and Cary, 1996; Wallén et al., 2010 for more detailed descriptions) and ion chromatography (IC, Thermo Scientific, model Dionex ICS-2000) to determine the organic carbon (OC) and elemental carbon (EC) content and inorganic mass (IM, here the sum of the dominant inorganic ions; Na+, NH4+, K+, Ca2+, Mg2+, Cl, NO3, SO42‒), respectively. The chemical composition measurement and analysis of the PM filters are described in detail by Franke et al. (2017). The PM characterised by the TOT and IC corresponded to about 80% of the total PM10 mass, the rest being likely mineral dust from local sources (Franke et al., 2017).

The cloud water samples were filtrated through micro-quartz fibre filters to separate the water-soluble organic carbon (WSOC) from the water-insoluble organic carbon (WINSOC) and EC. The filtrates were analysed for WSOC using a total OC analyser (Shimadzu, model TOC-LCPH), which determines the non-purgeable organic carbon (NPOC) with infrared gas detection after acidification, sparging and high-temperature catalytic combustion (Campos et al., 2007). The IM (here the sum of the dominant inorganic ions; Na+, NH4+, K+, Ca2+, Mg2+, Cl, NO3, SO42‒) was analysed using IC (Metrohm, model ProfIC850, Vega et al., 2019). The material left on the filters was considered to solely consist of WINSOC and EC, whose concentrations were determined using the TOT.

The OC and EC concentrations of the PM10 and cloud water samples were converted to total organic mass (OM) and elemental mass (EM) (the latter of which is an estimate of BC based on the EC concentration) and added to IM to determine the total analysed mass and the corresponding mass fractions of the analysed species. Concentrations were multiplied with the following conversion factors to account for atoms other than carbon, where water-soluble organic mass (WSOM) was assumed to contain more heteroatoms than water-insoluble organic mass (WINSOM): EM = 1.05 × EC, WINSOM = 1.3 × WINSOC, TOM = 1.8 × TOC and WSOM = 2.1 × WSOC (Turpin and Lim, 2001; Franke et al., 2017). The EM concentration determined from the chemical analysis might be representative of somewhat different material than the BC measured using the MAAP which can, for instance, include also non-elemental absorbing material (Andreae and Gelencser, 2006).

2.4. 

Volatility and hygroscopicity tandem DMA

The tandem differential mobility analyser (TDMA, first introduced by Liu et al., 1978), is a commonly used technique for measuring a change in particle size due to physical or chemical processes. The custom-built TDMA used in this work combines evaporation and humidification to characterise particle volatility and hygroscopicity (VHTDMA, see e.g. Tritscher et al., 2011) and was measuring ambient aerosols and cloud residuals downstream of the CVI (see Fig. 1). Before the sample flow entered the VHTDMA system, the particles were brought into charge equilibrium using a Ni-63 source. The first DMA selected a monodisperse aerosol at RH = 11.7 ± 2.7% (using Nafion driers, Perma Pure, Model PD-100T-12MSS), with a time resolution of 12 min and the median electrical mobility diameter set to either 100, 200 and 300 nm, hereafter referred to as D100, D200, D300, respectively. The monodisperse aerosol was then either heated to 300 ± 3 °C in a 30 cm long custom-built thermodenuder (TD) with a residence time of 1.6 s, or humidified to RH = 80–95% using a custom-built humidifier combining Gore-tex tubing and Nafion driers (Perma Pure, model PD-100T-12MSS). The resulting size distribution was measured using a second DMPS system (one for volatility and one for hygroscopicity each). From the change in particle diameter, distributions of the aerosol volume fraction remaining (VFR) or hygroscopic growth factor (GF) were obtained as:

((1))
VFR (D, T, Dinit)=D(T)3Dinit.3
((2))
GF (D, RH, Dinit)=D(RH)Dinit.
where Dinit. is the initial diameter, and D(T) and D(RH) are the measured and humidified particle diameters. The RH in the HTDMA was calibrated using ammonium sulphate (AS) particles (Topping et al., 2005). The geometric mean mode diameters of the heated and humidified size distributions were estimated by using a bimodal lognormal fit function, and used for the VFR and GF calculations as values representative of the whole heated or humidified size distribution.

Quantitative estimates of the volatility of the PM were obtained using a kinetic model that simulates the evaporation of monodisperse aerosol particles in a TD (Riipinen et al., 2010; Häkkinen et al., 2012; Hong et al., 2017). The analysed PM and cloud water composition along with the initial particle diameters D100, D200 and D300 were used as the model inputs. The saturation concentration c* (in µg m−3) of the organic fraction was then estimated by matching the measured and calculated VFR, assuming AS to represent the inorganic components present in the mixture (see Franke et al., 2017) with its c* estimated in the same manner as in Hong et al. (2017). EM was assumed to be completely non-volatile.

The measured GF was used to determine the hygroscopicity parameter κ (Petters and Kreidenweis, 2007):

((3))
κ=(GF31)(1S)Sexp(4σs/aMwRTρwDd)
where σs/a is the surface tension of the surface/air interface, Mw is the molecular weight of water, R is the universal gas constant, T is the temperature, ρw is the density of water, Dd is the droplet diameter and saturation ratio S = RH/100%. The exponential Kelvin term can be omitted for diameters larger than about 100 nm and was not included in the present analysis. Using the determined κ values, the HTDMA scans (with RH = 80–95%) were then converted back to RH = 90% for comparisons. The hygroscopicity of the PM and cloud residuals was also estimated using the analysed chemical composition of the PM and cloud water samples. The total hygroscopicity was estimated for each sample as
((4))
κ=iεiκi
where εi and κi are the mass fraction and hygroscopicity parameter of each chemical component i. The IM fraction of aerosol particle- and cloud water samples was dominated by AS, so κAS = 0.53 was used to represent the IM hygroscopicity parameter (Franke et al., 2017). The OM and EM were represented by κorg. = 0.01–0.3 and κEM = 0, respectively (Petters and Kreidenweis, 2007).

3. 

Results and discussion

3.1. 

Physical and chemical properties of aerosol particles, PM and cloud water during the CAEsAR campaign

An overview of the physical and chemical properties of the aerosol particles and cloud water during the CAEsAR campaign is presented in Fig. 2, together with information on when the station was engulfed in clouds as well as the data availability from the VHTDMA. The total particle number concentrations for particles with diameter above 10 nm were 342–817 cm‒3 (quartiles) with a median concentration of 584 cm‒3. The size distributions generally consisted of accumulation and/or Aitken modes, with occasions of nucleation mode linked to new particle formation (NPF) events (on e.g. 17 August, see Fig. 2a).

Fig. 2. 

Overview of the ambient particle size distribution and chemical composition of PM10 and cloud water during the CAEsAR campaign. (a) Ambient size distribution measured behind the PM10 inlet; (b) and (c) the chemical composition of the analysed fraction of PM10 (inidicated by the black lines, see below) and cloud water, respectively. The analysed chemical composition is comprised of total organic mass (TOM, with water-soluble and water-insoluble OM for the liquid phase), elemental mass (EM) and inorganic mass (IM). The black lines represent the total mass concentrations inferred from the sum of analysed chemical species, and the purple line the total (sub-10 µm) PM mass inferred from the particle size distribution measurements assuming a particle density of 1500 kg m−3. Blue circles above panel (a) mark the times when the station engulfed in cloud and the CVI inlet was on. The red and blue lines below panel (c) mark the times when the VHTDMA was running in volatility and hygroscopicity mode, respectively.

The average total PM concentration analysed from the filter samples during the CAeSAR campaign was 2.5 ± 1.9 µg m−3, and OM dominated the aerosol composition with the exception of the period at the end of the campaign when IM was a major aerosol component (Fig. 2b, Table 1). Franke et al. (2017) used back trajectories to identify several pollution events during which air masses arrived from central Europe, such as 3–12 July. The second highest mass concentration measured during the campaign, 2–5 August, originated from a major wildfire outbreak in the county of Västmanland (Lidskog and Sjödin, 2016). During 22–28 September, the air masses originated over the Atlantic ocean, bringing emissions from the degassing of the Bardarbunga volcano on Iceland (Grahn et al., 2015) and coinciding with a dominant Aitken mode (Fig. 2a) and distinct NPF events as a result of the increased sulphuric acid concentrations (Olenius et al., 2018).

The cloud water composition follows the temporal variation of the analysed PM composition. Overall, there is little difference in the bulk chemical composition between PM and cloud water (Fig. 2 and Table 1), in line with earlier studies at Mt. Åreskutan (Drewnick et al., 2006), except for EM, which is enriched in the PM. This is in agreement with the general low hygroscopicity of EM (Liu et al., 2013), but could also indicate an enrichment of EC in the Aitken mode. The small differences in the chemical composition indicate that (a) the average aerosol particle chemical composition represents also the average chemical composition of the cloud residuals, and therefore is also related to the composition of particles acting as CCN; (b) most of the analysed particulate mass can be taken up and scavenged by clouds and thereafter potentially also deposited by precipitation. The similarity of the chemical signature of the cloud water and the ambient particles is most likely linked to the remote nature of the measurement site and hence the aerosol being relatively aged and therefore e.g. subject to previous cloud processing.

Interestingly, WINSOM is present in a significant proportion in the cloud water (Table 1), indicating that even compounds with extremely low water solubility can enter the cloud phase. This observation could be explained by recent results on phase separation behaviour (Rastak et al., 2017) and surface activity (e.g. Ruehl et al., 2016) of secondary organic aerosol (SOA) from monoterpene oxidation, which show that compounds of low solubility can be present on the droplet surfaces, hence lowering the surface tension and enhancing CCN activation (e.g. Ruehl et al., 2016; Ovadnevaite et al., 2017). Monoterpene oxidation products are expected to be the dominant SOA compounds present at the Åre station (Tunved et al., 2006). In general, the organic fraction can be deemed representative of a boreal background station, albeit with influence from anthropogenic activities, marine air and even forest fires and volcanic emissions in the overall chemical composition (Jimenez et al., 2009; Grahn et al., 2015; Lidskog and Sjödin, 2016; Hong et al., 2017).

3.2. 

Aerosol particle and cloud residual number size distributions

The change in the ambient aerosol size distributions as a result of presence of clouds at the station during 8 July–22 September is presented in Fig. 3. The figure also includes the size distribution of cloud residuals, based on in total 197 h of in-cloud measurements behind the CVI.

Fig. 3. 

Median size distributions, with shaded areas presenting the quartiles, of the ambient aerosol (a) 2 h before and (b) 2 h after cloud events together with (c) the median size distribution of the cloud residuals (rightmost y-axis, marked in blue) measured behind the CVI. The overall median ambient aerosol particle size distribution is presented as the dotted line in all three panels. Numbers in parentheses mark the number of DMPS scans included in each median and the black dash-dotted lines mark the diameters analysed in the VHTDMA.

The overall median size distribution (the black dotted distribution in Fig. 3) was generally monodisperse with the mode around 100 nm, based on a total of 823 h sampling time (8232 DMPS scans). Before the cloud events, the aerosol particle size distribution (green line in Fig. 3a) resembled the average ambient aerosol particle size distribution (dotted lines in Fig. 3) with also comparable total number concentration of particles. After the cloud events, the ambient aerosol size distribution changed shape towards a bimodal distribution with an Aitken mode around 50 nm and an accumulation mode around 100 nm, in line with the expected size dependence of CCN activation and previous measurements at Mt. Åreskutan (Drewnick et al., 2006). The appearance of the distinct Aitken mode after cloud cover may, however, also be related to the ability of clouds to clean the air from larger particles and hence enhance the effect of NPF along the trajectory of the airmass arriving at the station. As expected for size-limited CCN activation, the measured size distribution of the cloud residuals is shifted towards larger particle sizes as compared with the average ambient distribution (Fig. 3c). The results are qualitatively consistent with previous literature reporting measurements of aerosol particle size distributions in- and out-of-cloud at a number of European background sites (e.g. Ditas et al., 2012; Hammer et al., 2014; Kruger et al., 2014). While these studies have investigated interstitial aerosol instead of direct measurements of cloud residuals, they also show the enrichment of smaller particles in the interstitial aerosol as compared with the overall particle population, and report average CCN activation diameters between roughly 50–150 nm depending on conditions – which is also generally consistent with our observed cloud residual size distributions (see Fig. 3c). We observe, however, a small contribution of very small (<50 nm in diameter) Aitken mode particles in the cloud residual size distribution. Aitken-mode particles within cloud residuals have been observed previously by e.g. Schwarzenboeck et al. (2000) and are also theoretically confirmed to be plausible CCN at low particle concentrations or high updrafts (e.g. Gérémy et al., 2000; Korhonen et al., 2008). At Mt Åreskutan, Targino et al. (2007) also previously observed cloud residuals smaller than 25 nm which were believed to originate from biogenic organic aerosol sources.

3.3. 

Volatility of ambient aerosol particles and cloud residuals

The temporal evolution of the volatility of ambient aerosols and cloud residuals is presented in Fig. 4. The VFR distributions for D100, D200, D300 (Fig. 4a‒c) generally displayed a monomodal shape, indicating internal mixing of the particles. The median VFR values corresponding to the fitted mode diameters were 0.036–0.053 for the ambient aerosol populations and 0.036–0.046 for the cloud residuals (Table 2). VFR increased, hence volatility decreased, with increasing Dinit. for the ambient aerosols. In contrast, the average VFR of the cloud residuals slightly decreased for increasing Dinit. Both of these trends, however, are within the standard deviations of the recorded VFR values. The temporal variation in the VFR of the ambient aerosols was relatively small (see black lines in Fig. 4), and consistent among the three diameters. The VFR never dropped below 0.01 and exhibited less variability with increasing particle size, indicating some contribution from essentially non-volatile material (e.g. BC, Fig. 4d) throughout the campaign. One clear bimodal event was identified in the early morning on 13 July. The event appeared simultaneously for all Dinit. and coincided with a brief bimodal event in the ambient size distribution (not visible in Fig. 2a due to the time resolution), indicating externally mixed aerosols due to a shift in the local wind direction. The observed values of the VFR are in a reasonable agreement with the studies by Häkkinen et al. (2012) and Hong et al. (2014), which report a VFR of about 0.05–0.09 for boreal forest summer aerosol for a comparable BC fraction of about 0.04 but somewhat lower TD temperature of 280 °C.

Fig. 4. 

Measured VFR distributions as a function of time and Dinit. (a–c) together with the (d) BC mass fraction from the MAAP. The black lines represent the median VFR and the white circles mark cloud events (CVI in operation, VFR of cloud residuals). BC fraction of the cloud residuals during the longer cloud event are marked with a blue rectangle in panel d.

In general, only few cloud events took place at the measuring site during the month of July. However, one long-lasting stratiform cloud event occurred on the 14 July. During 22 h, the station was covered in clouds the measured VFR of the cloud residuals decreased simultaneously for all Dinit., by 52%, 50% and 59% for D100, D200 and D300, respectively. There are several potential explanations for the increasing volatility for the cloud residuals during this cloud event. The most likely explanation is the decreasing fraction of BC in the cloud residuals during the cloud event, coinciding with the drop in the VFR. Other potential explanations are increased evaporation rates due to fragmentation as a result of heterogeneous chemistry in the cloud droplet (Romonosky et al., 2017), or co-condensation of semi-volatile vapours during the evolution of the cloud (Topping et al., 2013), or that the more volatile fraction is more efficiently taken up by the clouds due to e.g. size-dependent chemical composition. It is unclear however why this would result in the time-dependent change in the volatility instead of a consistent difference between cloud residuals and ambient aerosols.

Figure 5 presents the VFR calculated from the PM composition as a function of Dinit. and fitted c* (see Section 2.4) together with the measured VFR. The measured and calculated VFR are systematically higher than the EM mass fraction throughout the period, indicating that while EM is an important component explaining the fraction remaining after the TD, it does not account for all of the non-volatile material. Since the inorganics in the submicron fraction are expected to evaporate at temperatures lower than used in this experiment (e.g. ammonium nitrate and AS are reported to fully evaporate at 60 and 180 °C, respectively, Villani et al., 2007), the remaining part is assigned to organics. The temporal evolution of the VFR predicted from the PM composition captures the measured decreasing trend during the first half of the period remarkably well, while it slightly overestimates VFR in the end of the period, indicating that the overall volatility of the organic fraction decreased somewhat over the course of the measurement period. The organic saturation concentrations corresponding to the measured VFR were c*(D100) = 1.9 × 10−4 µg m−3, c*(D200) = 4.1 × 10−4 µg m−3 and c*(D300) = 6.5 × 10−4 µg m−3. These values correspond to those of extremely low volatile organic compounds (ELVOC) and low volatile organic compounds (LVOC), expected to originate from boreal forests (Mohr et al., 2019). During 22 h, cloud event on 14 July the change in the VFR was equal to, or even smaller than, the change in BC – suggesting that the observed trend in VFR could result from a corresponding trend in BC.

Fig. 5. 

Predicted VFR as a function of time and Dinit. Dashed lines represent the measured VFR as a function of time and Dinit. The black line illustrates the EM mass fraction in the PM10 and the dashed black line the BC mass fraction behind the CVI.

3.4. 

Hygroscopicity of ambient aerosol particles and cloud residuals

The temporal evolution of the hygroscopic GF of the ambient aerosols and cloud residuals for D100, D200 and D300 is presented in Fig. 6, with the mean and median GF and κ values given in Table 3. The GF distributions were generally monomodal, indicating internally mixed aerosol populations, with median ambient aerosol GF and corresponding κ value ranging 1.35–1.47 and 0.16–0.24. The hygroscopicity of the cloud residuals falls within the same GF- and κ-ranges (Table 3). The hygroscopicity is slightly higher in cloud residuals compared to the ambient aerosols for D100, but lower in cloud residuals for D200 and identical for D300 (see Table 3). These results could support the idea that chemical composition and hygroscopicity play a more important role for the activation of smaller particles as compared with the more CCN-active larger particles (Fig. 3 and e.g. Dusek et al., 2006). However, all values are within the standard deviation for both the measured GF and κ values, indicating the differences between the cloud residuals and ambient aerosol particles to be small – much like the differences between the chemical composition of the PM and cloud water (Table 1).

Fig. 6. 

Measured hygroscopic GF as a function of time and Dinit. (a‒c). The black line represents the median GF and the white circles mark the cloud events (CVI in operation, GF of cloud residuals).

The overall temporal evolution of GF reveals no clear trends, apart from a few specific events. For instance, the GF was lower than average (around 1.2 for all sizes) on 7 August, when the station was influenced by the fire plume, and higher than average (around 1.5–1.6) on 10–16 September, when IM concentrations increased as a result of the volcanic emissions.

The average κ values of the ambient aerosols, κ(D100) = 0.18, κ(D200) = 0.26 and κ(D300) = 0.24 (see Table 3), agree relatively well with a study in the boreal forest in Hyytiälä, Finland, performed by Hong et al. (2014) who report κ values of 0.17, 0.28 and 0.22 for 70, 102 and 203 nm. The results are also at least qualitatively consistent with the study by Väisänen et al. (2016), who infer the hygroscopicity of the cloud residuals based on the difference between the hygroscopicity of ambient aerosol (out-of-cloud) and interstitial aerosol at a semi-urban site at Puijo, Eastern Finland. While we observe primarily monomodal aerosol size and hygroscopicity distributions, Väisänen et al. (2016) report the presence of a more and a less hygroscopic mode, assigning the less hygroscopic particles to local anthropogenic influence. While our aerosol is somewhat less hygroscopic (with median κ values of 0.16–0.24 for 100–200 nm particles, see Table 3) than the hygroscopic mode observed by Väisänen et al. (2016) who report typical κ values of about 0.3–0.4 for 120–150 nm particles, both studies observe only minor differences in the hygroscopicity of ambient aerosols and cloud residuals.

Figure 7 presents the time series of κ values predicted from the PM and cloud water chemical composition (Equation (4)) together with the κ values calculated from the measured GF(Dinit.) of the ambient aerosol and cloud residuals. The measured κ values are independent of Dinit. at the beginning of the period, indicating relatively homogeneous hygroscopicity with particle size. After the 17 August, the hygroscopicity becomes different for D100 resulting in lower κ values, lasting for the rest of the period. Overall, the κ values calculated from the PM composition capture the trend in the measured κ values rather well, hence corroborating the assumption that the organic fraction is representative of aged boreal forest SOA – in line with what was observed with the volatility as well. The chemical composition of the cloud water resulted in slightly higher κ values compared to the values derived from the PM. This is due to the lower EM but mainly due to higher IM fractions compared to the aerosol particles (see Table 1). On the 14 August, the predicted κ values of the particle samples decreased while the predicted κ value of the cloud sample remained high, suggesting that the more hygroscopic material (IM) was scavenged by the cloud leaving the less hygroscopic fraction (OM and EM) in the particle phase. This was a period of persistent cloud cover at the measurement station (see Figs. 2b,c).

Fig. 7. 

Hygroscopicity parameter, κ, determined from measured GF as a function time and Dinit. (red, blue and green dashed lines for D100, D200 and D300, respectively) together with the κ values predicted with Equation (4) based on the chemical composition of the PM10 and cloud water samples (orange and grey solid lines, respectively).

3.5. 

Comparing the observed VFR and κ values to those predicted from PM and cloud water composition

A comparison of measured VFR and κ values with those predicted from the PM (for VFR and κ) and cloud water (for κ only) composition (Table 1) are presented in Fig. 8. The measured κ value was derived from the observed GF. A weak to intermediate linear correlation between predicted and measured volatility and hygroscopicity is observed (cf. Figs. 4 and 7), with R2 = 0.27 for VFR, R2 = 0.39 for κ (ambient aerosol vs. PM) and R2 = 0.60 for κ (cloud residuals vs. cloud water).

Fig. 8. 

(a) Predicted versus measured VFR, separated by Dinit. and coloured according to time of observation (see legend), were the error bars present the variability in the measurements and uncertainty of the predicted c*. (b) Predicted versus measurement-based κ value, separated in ambient aerosols and cloud residuals, where the error bars represent the variability of κorg. = 0.01–0.3. Dashed lines display the 1:1 line.

The volatility displayed a systematic change in predicted VFR with time (Figs. 5 and 8a), changing from over- to underestimation in the volatility from the beginning to the end of the period, suggesting a change in the chemical composition. However, if this change was to be explained by a changing volatility of the organic PM fraction, the corresponding difference turns out to be c*(D100) = 1.7–2.0 × 10−4 µg m−3, c*(D200) = 3.6–4.4 × 10−4 µg m−3, c*(D300) = 5.6–7.1 × 10−4 µg m−3, which still remains in the ELVOC range (vertical error bars in Fig. 8a). No significant changes in the IM composition were evident either (see Franke et al., 2017).

Figure 8b reveals a general overestimation in the hygroscopicity derived from the chemical composition as compared with the measured κ value. The most plausible explanation to these discrepancies is probably an uncertainty in the pure component hygroscopicity and the different time resolution between the chemical sampling and the VHTDMA measurement. The least well-known component of the PM composition is the organic matter, which can contain species with highly varying water solubility. The expected κorg. at Mt. Åreskutan could range from about 0.05 (corresponding to e.g. monoterpene SOA in sub-saturated conditions) up to as high as 0.2 (see e.g. Mikhailov et al., 2013; Pajunoja et al., 2015; Rastak et al., 2017). However, uncertainty in κorg. is not likely to explain the overprediction – as the κorg. values required to match the observations would be well below 0.05 assuming the composition of the PM. Uncertainty in the IM hygroscopicity is also an unlikely explanation to the missing low-hygroscopity material, as the IM throughout the campaign was dominated by AS (Franke et al., 2017), whose hygroscopicity is well known. A plausible explanation for the missing low-hygroscopicity material could be an enrichment of the EM (or the OM) in the submicron particle range as compared with the larger particles, therefore resulting in larger insoluble mass fractions at the size range covered by the VHTDMA than in the bulk sample. Another potential explanation could be mineral dust, which has been shown to likely to contribute to the overall undetermined fraction of the total particulate composition (Koehler et al., 2009; Franke et al., 2017).

As a summary, the general agreement between the measured VFR and κ and the values derived from bulk chemical composition measurements is promising. There is, however, still room for improvement in (1) understanding the exact properties of the various chemical components; (2) measuring the chemical composition of the aerosol particles and cloud hydrometeors – especially on time resolutions higher than achievable here.

4. 

Summary and conclusions

The size distributions, volatility and hygroscopicity of ambient aerosol particles and cloud residuals have been characterised as part of the CAEsAR campaign, performed at Mt. Åreskutan during summer to early autumn in 2014. These observations were compared with chemical analysis of PM filter samples and cloud water collected at the same site. Located in central Scandinavia, the measurement site is a good representation of the remote boreal background, albeit with some influence of airmasses of various origins. This was manifested in e.g. organic compounds dominating the chemical composition and a monomodal average size, volatility and hygroscopicity distributions, which were interpreted as a sign of internally mixed aerosol that had been subjected to atmospheric aging. The volatility and hygroscopicity of the organic aerosol fraction were representative of biogenic SOA found in the boreal region.

The station was frequently covered in clouds, which was followed by a shift in the ambient size distributions towards smaller particles sizes, with the larger particles being more efficiently scavenged to cloud droplets. However, also Aitken-mode particles were frequently observed as cloud residuals. The composition of the cloud water, however, was very similar to the composition of the PM mass, apart from a slight EM enrichment in the latter. Interestingly, a significant portion of WINSOC was present in the cloud water, indicating that also compounds with very low water solubility can enter the cloud phase. The average volatility and hygroscopicity of 100–300 nm ambient aerosol particles and cloud residuals were also very similar with only subtle differences, in line with the observed similar compositions. EC could explain a large part of the non-volatile fraction of the ambient aerosol, while the remaining fraction was found to be consistent with ELVOC and LVOC known to be present in the boreal SOA. While a clear effect of the clouds on the aerosol number size distributions was observed, our results do not show indications of the importance of size-dependent chemical composition for CCN activation nor significant cloud-phase chemical processing at Mt. Åreskutan in the time scales captured.

Our results indicate that in environments with aged homogeneous aerosol such as Mt. Åreskutan, relatively simple approximations of aerosol composition based on the overall aerosol mass and only a few chemical species are sufficient to capture the volatility and hygroscopicity of the particles. Furthermore, the chemical composition of the PM seems to be representative of the chemical composition of the cloud residuals. The number size distribution and the influence of cloud processing on it, however, needs to be represented with more detail to capture the evolution of aerosol particle populations, CCN and eventually cloud droplet numbers. The overall magnitude and trends in volatility and hygroscopicity could be captured relatively well with the simple approach of assuming bulk composition for the whole aerosol population. Higher resolution observations (both temporally but also chemically) of the chemical composition are, however, warranted to investigate processes taking place on shorter time- and smaller size scales. Such future studies might reveal unexpected subtleties in the processes taking place in the aerosol-cloud continuum.