Continuous Flow Diffusion Chamber Research Articles

The Puy de Dôme ICe Nucleation Intercomparison Campaign (PICNIC): comparison between online and offline methods in ambient air

Abstract. Ice crystal formation in mixed-phase clouds is initiated by specific aerosol particles, termed ice-nucleating particles (INPs). Only a tiny fraction of all aerosol particles are INPs, providing a challenge for contemporary INP measurement techniques. Models have shown that the presence of INPs in clouds can impact their radiative properties and induce precipitation formation. However, for a qualified implementation of INPs in models, measurement techniques able to accurately detect the temperature-dependent INP concentration are needed. Here we present measurements of INP concentrations in ambient air under conditions relevant to mixed-phase clouds from a total of 10 INP methods over 2 weeks in October 2018 at the Puy de Dôme observatory in central France. A special focus in this intercomparison campaign was placed on having overlapping sampling periods. Although a variety of different measurement principles were used, the majority of the data show INP concentrations within a factor of 5 of one another, demonstrating the suitability of the instruments to derive model-relevant INP data. Lower values of comparability are likely due to instrument-specific features such as aerosol lamina spreading in continuous-flow diffusion chambers, demonstrating the need to account for such phenomena when interpreting INP concentration data from online instruments. Moreover, consistently higher INP concentrations were observed from aerosol filters collected on the rooftop at the Puy de Dôme station without the use of an aerosol inlet.

Low-temperature ice nucleation of sea spray and secondary marine aerosols under cirrus cloud conditions

Abstract. Sea spray aerosols (SSAs) represent one of the most abundant aerosol types on a global scale and have been observed at all altitudes including the upper troposphere. SSA has been explored in recent years as a source of ice-nucleating particles (INPs) in cirrus clouds due to the ubiquity of cirrus clouds and the uncertainties in their radiative forcing. This study expands upon previous works on low-temperature ice nucleation of SSA by investigating the effects of atmospheric aging of SSA and the ice-nucleating activity of newly formed secondary marine aerosols (SMAs) using an oxidation flow reactor. Polydisperse aerosol distributions were generated from a marine aerosol reference tank (MART) filled with 120 L of real or artificial seawater and were dried to very low relative humidity to crystallize the salt constituents of SSA prior to their subsequent freezing, which was measured using a continuous flow diffusion chamber (CFDC). Results show that for primary SSA (pSSA), as well as aged SSA and SMA (aSSA+SMA) at temperatures >220 K, homogeneous conditions (92 %–97 % relative humidity with respect to water – RHw) were required to freeze 1 % of the particles. However, below 220 K, heterogeneous nucleation occurs for both pSSA and aSSA+SMA at much lower RHw, where up to 1 % of the aerosol population freezes between 75 % and 80 % RHw. Similarities between freezing behaviors of the pSSA and aSSA+SMA at all temperatures suggest that the contributions of condensed organics onto the pSSA or alteration of functional groups in pSSA via atmospheric aging did not hinder the major heterogeneous ice nucleation process at these cirrus temperatures, which have previously been shown to be dominated by the crystalline salts. Occurrence of a 1 % frozen fraction of SMA, generated in the absence of primary SSA, was observed at or near water saturation below 220 K, suggesting it is not an effective INP at cirrus temperatures, similar to findings in the literature on other organic aerosols. Thus, any SMA coatings on the pSSA would only decrease the ice nucleation behavior of pSSA if the organic components were able to significantly delay water uptake of the inorganic salts, and apparently this was not the case. Results from this study demonstrate the ability of lofted primary sea spray particles to remain an effective ice nucleator at cirrus temperatures, even after atmospheric aging has occurred over a period of days in the marine boundary layer prior to lofting. We were not able to address aging processes under upper-tropospheric conditions.

Influence of the Neutralization Degree on the Ice Nucleation Ability of Ammoniated Sulfate Particles

AbstractPrevious laboratory measurements suggest that ammonium sulfate crystals (AS, (NH4)2SO4) are efficient ice‐nucleating particles under cirrus conditions. Sulfate particles not completely neutralized by ammonium are less well studied and include two other solids, ammonium bisulfate (AHS, NH4HSO4) and letovicite (LET, (NH4)3H(SO4)2). In this work, we have obtained the first comprehensive data set for the heterogeneous ice nucleation ability of crystallized particles in the AS–LET–AHS system as a function of their degree of neutralization at a temperature of about 220 K. Quantitative data on nucleation onsets, ice‐active fractions, and ice nucleation active surface site densities were derived from expansion cooling experiments in a large cloud chamber and measurements with two continuous flow diffusion chambers. We found a strong dependence of the efficiency and the mode of heterogenous ice nucleation on the degree of neutralization. Ice formation for AS, mixed AS/LET, and LET crystals occurred by the deposition nucleation or pore condensation and freezing mode. The lowest nucleation onset was observed for AS, where 0.1% of the particles became ice‐active at an ice saturation ratio of 1.25. This threshold gradually increased to 1.35 for LET, and abruptly further to 1.45 for mixed LET/AHS crystals, which partially deliquesced and induced ice formation via immersion freezing. Pure AHS crystals did not form due to the inhibition of efflorescence. Our data allow for a more sophisticated treatment of ice formation in the AS–LET–AHS system in future model simulations, which have so far only considered the available data for AS alone.

Development and characterization of the Portable Ice Nucleation Chamber 2 (PINCii)

Abstract. The Portable Ice Nucleation Chamber 2 (PINCii) is a newly developed continuous flow diffusion chamber (CFDC) for measuring ice nucleating particles (INPs). PINCii is a vertically oriented parallel-plate CFDC that has been engineered to improve upon the limitations of previous generations of CFDCs. This work presents a detailed description of the PINCii instrument and the upgrades that make it unique compared with other operational CFDCs. The PINCii design offers several possibilities for improved INP measurements. Notably, a specific icing procedure results in low background particle counts, which demonstrates the potential for PINCii to measure INPs at low concentrations (<10 L−1). High-spatial-resolution wall-temperature mapping enables the identification of temperature inhomogeneities on the chamber walls. This feature is used to introduce and discuss a new method for analyzing CFDC data based on the most extreme lamina conditions present within the chamber, which represent conditions most likely to trigger ice nucleation. A temperature gradient can be maintained throughout the evaporation section in addition to the main chamber, which enables PINCii to be used to study droplet activation processes or to extend ice crystal growth. A series of both liquid droplet activation and ice nucleation experiments were conducted at temperature and saturation conditions that span the spectrum of PINCii's operational conditions (-50≤ temperature ≤-15 ∘C and 100 ≤ relative humidity with respect to ice ≤160 %) to demonstrate the instrument's capabilities. In addition, typical sources of uncertainty in CFDCs, including particle background, particle loss, and variations in aerosol lamina temperature and relative humidity, are quantified and discussed for PINCii.

The Relationship of Aerosol Properties and Ice‐Nucleating Particle Concentrations in Beijing

AbstractThis paper investigates immersion mode ice‐nucleating particle (INP) concentrations measured with a continuous flow diffusion chamber at temperatures of −20°C, −25°C, and −30°C in Beijing from 4 May to 4 June 2018. Aerosol conditions in the experiment period are classified into four types: clean, light PM2.5 pollution, heavy PM2.5 pollution, and dust. The PM mass concentrations and the aerosol size distributions are distinctly different in the four aerosol conditions. INP concentration increases as temperature decreases from −20°C to −30°C for all the four aerosol conditions. At a given temperature, INP concentrations progressively increase as the aerosol condition changes from clean to light PM2.5 pollution and to heavy PM2.5 pollution condition. At −25°C and −30°C, the dust condition has a much higher INP concentration than the other aerosol conditions. The INP concentration is closely related to the number concentration of aerosols with diameters of 1.0–2.5 μm (). Using a similar method as in the previous parameterization of INP concentrations for global and fairly clean aerosol conditions, a new parameterization of the INP concentration based on is provided for the complicated aerosol conditions with high aerosol number concentrations in Beijing.

Evidence for Anthropogenic Organic Aerosols Contributing to Ice Nucleation

AbstractThe role of organic aerosols (OA) as ice nucleating particles (INPs) deserves attention because of their high atmospheric abundance. The low concentration of INPs poses challenges in identifying the ice nucleation (IN) of OA among a mix of aerosol types in ambient environment. This study coupled a catalytic stripper system (350°C heating) with a continuous flow diffusion chamber to online investigate the immersion INPs of ambient particles at −30°C at a suburban site. Significant reduction (71 ± 25%) of INP concentrations after evaporation suggested that INPs can be significantly contributed by volatile OA. In addition, nonvolatile OA were more efficient INPs than black carbon. Oxygenated OA by photooxidation and lower ambient promoted the IN activity at noon, when the OA may be more viscous. These results hereby present the first field evidence that OA in anthropogenically influenced regions can be efficient INPs well above the homogeneous IN temperature.

Hygroscopicity and Ice Nucleation Properties of Dust/Salt Mixtures Originating from the Source of East Asian Dust Storms

Dust storms are common meteorological events that occur frequently in the late spring and early summer in arid and semi-arid areas. The resulting lofted dust and salt mixtures can impact atmospheric chemistry and climate systems through the many pathways represented by aerosol-cloud-climate interactions. In this study, dust/salt samples were collected from important sources of the East Asian dust storm, including the Badain Jaran Desert, the Tengger Desert and the Ulan Buh Desert in northwestern China. Ion chromatography (IC) measurements were performed to determine the concentrations of cations and anions. The ionic concentrations, pH and dissolvable fractions of sand samples show a positive correlation, indicating that the dissolved content is rich in alkaline ions. A positive matrix factorization (PMF) receptor model was employed to analyze the IC results, and from the PMF solutions non-obvious connections to local geography emerge. The results of hygroscopic experiments of sand samples which were measured by a vapor sorption analyzer indicate that the hygroscopicity may be related to the soluble content of samples, and the observed hygroscopic behavior can be well described by a thermodynamic model. The morphology of individual particles was chemically mapped by the synchrotron-based scanning transmission X-ray microscopy, and needle-shaped CaCO3 particles were observed to adhere to more irregular high K-containing particles. Moreover, a continuous flow diffusion chamber was used to investigate the ice nucleation abilities of typical salts, with both homogeneous freezing and deposition nucleation being observed. The results indicate that the salts primarily act as cloud condensation nuclei but can also act as ice nucleating particles at low temperatures.

Laboratory studies of ice nucleation onto bare and internally mixed soot–sulfuric acid particles

Abstract. Soot particles are potential candidates for ice-nucleating particles in cirrus cloud formation, which is known to exert a net-warming effect on climate. Bare soot particles, generally hydrophobic and fractal ones, mainly exist near emission sources. Coated or internally mixed soot particles are more abundant in the atmosphere and have a higher probability of impacting cloud formation and climate. However, the ice nucleation ability of coated soot particles is not as well understood as that of freshly produced soot particles. In this laboratory study, two samples, a propane flame soot and a commercial carbon black, were used as atmospheric soot surrogates and coated with varying wt % of sulfuric acid (H2SO4). The ratio of coating material mass to the mass of bare soot particles was controlled and progressively increased from less than 5 wt % to over 100 wt %. Both bare and coated soot particle ice nucleation activities were investigated with a continuous-flow diffusion chamber operated at mixed-phase and cirrus cloud conditions. The mobility diameter and mass distribution of size-selected soot particles with/without H2SO4 coating were measured by a scanning mobility particle sizer and a centrifugal particle mass analyser running in parallel. The mixing state and morphology of soot particles were characterized by scanning electron microscopy and transmission electron microscopy. In addition, the evidence of the presence of H2SO4 on a coated soot particle surface is shown by energy-dispersive X-ray spectroscopy. Our study demonstrates that H2SO4 coatings suppress the ice nucleation activity of soot particles to varying degrees depending on the coating thickness, but in a non-linear fashion. Thin coatings causing pore filling in the soot aggregate inhibits pore condensation and freezing. Thick coatings promote particle ice activation via droplet homogeneous freezing. Overall, our findings reveal that H2SO4 coatings will suppress soot particle ice nucleation abilities in the cirrus cloud regime, having implications for the fate of soot particles with respect to cloud formation in the upper troposphere.

Particle emissions from a modern heavy-duty diesel engine as ice nuclei in immersion freezing mode: a laboratory study on fossil and renewable fuels

Abstract. We studied ice-nucleating abilities of particulate emissions from a modern heavy-duty diesel engine using three different types of fuel. The polydisperse particle emissions were sampled during engine operation and introduced to a continuous-flow diffusion chamber (CFDC) instrument at a constant relative humidity RHwater=110 %, while the temperature was ramped between −43 and −32 ∘C (T scan). The tested fuels were EN 590 compliant low-sulfur fossil diesel, hydrotreated vegetable oil (HVO), and rapeseed methyl ester (RME); all were tested without blending. Sampling was carried out at different stages in the engine exhaust aftertreatment system, with and without simulated atmospheric processing using an oxidation flow reactor. In addition to ice nucleation experiments, we used supportive instrumentation to characterize the emitted particles for their physicochemical properties and presented six parameters. We found that the studied emissions contained no significant concentrations of ice-nucleating particles likely to be of atmospheric relevance. The substitution of fossil diesel with renewable fuels, using different emission aftertreatment systems such as a diesel oxidation catalyst, and photochemical aging of total exhaust had only minor effect on their ice-nucleating abilities.

Immersion Freezing Ability of Freshly Emitted Soot with Various Physico-Chemical Characteristics

The immersion freezing ability of soot particles has in previous studies been reported in the range of low/insignificant to very high. The aims of this study were to: (i) perform detailed physico-chemical characterisation of freshly produced soot particles with very different properties, (ii) investigate the immersion freezing ability of the same particles, and (iii) investigate the potential links between physico-chemical particle properties and ice-activity. A miniCAST soot generator was used to produce eight different soot samples representing a wide range of physico-chemical properties. A continuous flow diffusion chamber was used to study each sample online in immersion mode over the temperature (T) range from −41 to −32 °C, at a supersaturation of about 10% with respect to liquid water. All samples exhibited low to no heterogeneous immersion freezing. The most active sample reached ice-activated fractions (AF) of 10−3 and 10−4 at temperatures of 1.7 and 1.9 K , respectively, above the homogeneous freezing temperature. The samples were characterized online with respect to a wide range of physico-chemical properties including effective particle density, optical properties, particle surface oxidation and soot maturity. We did observe indications of increasing immersion freezing ice-activity with increasing effective particle density and increasing particulate PAH fraction. Hence, those properties, or other properties co-varying with those, could potentially enhance the immersion freezing ice-activity of the studied soot particle types. However, we found no significant correlation between the physico-chemical properties and the observed ice-nucleating ability when the particle ensemble was extended to include previously published results including more ice-active biomass combustion soot particles. We conclude that it does not appear possible in general and in any straightforward way to link observed soot particle physico-chemical properties to the ice-nucleating ability using the online instrumentation included in this study. Furthermore, our observations support that freshly produced soot particles with a wide range of physico-chemical properties have low to insignificant immersion freezing ice-nucleating ability.

Is Ice Formation by Sea Spray Particles at Cirrus Temperatures Controlled by Crystalline Salts?

The ice nucleating ability of sea spray aerosols (SSA) has been explored in recent years due to the abundance of SSA in the atmosphere. The role of SSA in ice nucleation extends to cirrus clouds, due to processes that loft SSA to the upper troposphere. This is of special relevance because of the frequent occurrence of cirrus in the atmosphere, their role in the Earth’s radiative balance, and uncertainties regarding how aerosols may affect their formation and evolution. In this study, a continuous flow diffusion chamber (CFDC) is used to investigate the ice nucleating ability of size-selected particle distributions of SSA and its primary constituent sodium chloride (NaCl) at temperatures < 235 K. Results show that above ~220 K, the majority of SSA and NaCl particles fully deliquesce and freeze via homogeneous nucleation at or below water relative humidities, RHw, of ~ 95%. However, below 220 K, the onset RHw of freezing for NaCl and SSA is much lower, at ~75%, where strong heterogeneous freezing of 10% of the aerosol population occurs. Similar heterogeneous freezing behavior for NaCl and SSA aerosols, occurring near their predicted deliquescence RHw, points towards SSA freezing at the lowest temperatures being controlled by the crystalline salts. Finally, calculations of ice nucleation active surface site densities show that particle size does not dictate the efficiency of freezing for NaCl and SSA. These results indicate SSA as a potentially significant source of ice nucleating particles at cirrus temperatures, with the ability to contribute to cirrus-mediated climate impacts if sea spray emission and transport scenarios change in the future.

Terrestrial or marine – indications towards the origin of ice-nucleating particles during melt season in the European Arctic up to 83.7° N

Abstract. Ice-nucleating particles (INPs) initiate the primary ice formation in clouds at temperatures above ca. −38 ∘C and have an impact on precipitation formation, cloud optical properties, and cloud persistence. Despite their roles in both weather and climate, INPs are not well characterized, especially in remote regions such as the Arctic. We present results from a ship-based campaign to the European Arctic during May to July 2017. We deployed a filter sampler and a continuous-flow diffusion chamber for offline and online INP analyses, respectively. We also investigated the ice nucleation properties of samples from different environmental compartments, i.e., the sea surface microlayer (SML), the bulk seawater (BSW), and fog water. Concentrations of INPs (NINP) in the air vary between 2 to 3 orders of magnitudes at any particular temperature and are, except for the temperatures above −10 ∘C and below −32 ∘C, lower than in midlatitudes. In these temperature ranges, INP concentrations are the same or even higher than in the midlatitudes. By heating of the filter samples to 95 ∘C for 1 h, we found a significant reduction in ice nucleation activity, i.e., indications that the INPs active at warmer temperatures are biogenic. At colder temperatures the INP population was likely dominated by mineral dust. The SML was found to be enriched in INPs compared to the BSW in almost all samples. The enrichment factor (EF) varied mostly between 1 and 10, but EFs as high as 94.97 were also observed. Filtration of the seawater samples with 0.2 µm syringe filters led to a significant reduction in ice activity, indicating the INPs are larger and/or are associated with particles larger than 0.2 µm. A closure study showed that aerosolization of SML and/or seawater alone cannot explain the observed airborne NINP unless significant enrichment of INP by a factor of 105 takes place during the transfer from the ocean surface to the atmosphere. In the fog water samples with −3.47 ∘C, we observed the highest freezing onset of any sample. A closure study connecting NINP in fog water and the ambient NINP derived from the filter samples shows good agreement of the concentrations in both compartments, which indicates that INPs in the air are likely all activated into fog droplets during fog events. In a case study, we considered a situation during which the ship was located in the marginal sea ice zone and NINP levels in air and the SML were highest in the temperature range above −10 ∘C. Chlorophyll a measurements by satellite remote sensing point towards the waters in the investigated region being biologically active. Similar slopes in the temperature spectra suggested a connection between the INP populations in the SML and the air. Air mass history had no influence on the observed airborne INP population. Therefore, we conclude that during the case study collected airborne INPs originated from a local biogenic probably marine source.

A new method for operating a continuous-flow diffusion chamber to investigate immersion freezing: assessment and performance study

Abstract. Glaciation in mixed-phase clouds predominantly occurs through the immersion-freezing mode where ice-nucleating particles (INPs) immersed within supercooled droplets induce the nucleation of ice. Model representations of this process currently are a large source of uncertainty in simulating cloud radiative properties, so to constrain these estimates, continuous-flow diffusion chamber (CFDC)-style INP devices are commonly used to assess the immersion-freezing efficiencies of INPs. This study explored a new approach to operating such an ice chamber that provides maximum activation of particles without droplet breakthrough and correction factor ambiguity to obtain high-quality INP measurements in a manner that previously had not been demonstrated to be possible. The conditioning section of the chamber was maintained at −20 ∘C and water relative humidity (RHw) conditions of 113 % to maximize the droplet activation, and the droplets were supercooled with an independently temperature-controlled nucleation section at a steady cooling rate (0.5 ∘C min−1) to induce the freezing of droplets and evaporation of unfrozen droplets. The performance of the modified compact ice chamber (MCIC) was evaluated using four INP species: K-feldspar, illite-NX, Argentinian soil dust, and airborne soil dusts from an arable region that had shown ice nucleation over a wide span of supercooled temperatures. Dry-dispersed and size-selected K-feldspar particles were generated in the laboratory. Illite-NX and soil dust particles were sampled during the second phase of the Fifth International Ice Nucleation Workshop (FIN-02) campaign, and airborne soil dust particles were sampled from an ambient aerosol inlet. The measured ice nucleation efficiencies of model aerosols that had a surface active site density (ns) metric were higher but mostly agreed within 1 order of magnitude compared to results reported in the literature.

The ice-nucleating activity of Arctic sea surface microlayer samples and marine algal cultures

Abstract. In recent years, sea spray as well as the biological material it contains has received increased attention as a source of ice-nucleating particles (INPs). Such INPs may play a role in remote marine regions, where other sources of INPs are scarce or absent. In the Arctic, these INPs can influence water–ice partitioning in low-level clouds and thereby the cloud lifetime, with consequences for the surface energy budget, sea ice formation and melt, and climate. Marine aerosol is of a diverse nature, so identifying sources of INPs is challenging. One fraction of marine bioaerosol (phytoplankton and their exudates) has been a particular focus of marine INP research. In our study we attempt to address three main questions. Firstly, we compare the ice-nucleating ability of two common phytoplankton species with Arctic seawater microlayer samples using the same instrumentation to see if these phytoplankton species produce ice-nucleating material with sufficient activity to account for the ice nucleation observed in Arctic microlayer samples. We present the first measurements of the ice-nucleating ability of two predominant phytoplankton species: Melosira arctica, a common Arctic diatom species, and Skeletonema marinoi, a ubiquitous diatom species across oceans worldwide. To determine the potential effect of nutrient conditions and characteristics of the algal culture, such as the amount of organic carbon associated with algal cells, on the ice nucleation activity, Skeletonema marinoi was grown under different nutrient regimes. From comparison of the ice nucleation data of the algal cultures to those obtained from a range of sea surface microlayer (SML) samples obtained during three different field expeditions to the Arctic (ACCACIA, NETCARE, and ASCOS), we found that they were not as ice active as the investigated microlayer samples, although these diatoms do produce ice-nucleating material. Secondly, to improve our understanding of local Arctic marine sources as atmospheric INPs we applied two aerosolization techniques to analyse the ice-nucleating ability of aerosolized microlayer and algal samples. The aerosols were generated either by direct nebulization of the undiluted bulk solutions or by the addition of the samples to a sea spray simulation chamber filled with artificial seawater. The latter method generates aerosol particles using a plunging jet to mimic the process of oceanic wave breaking. We observed that the aerosols produced using this approach can be ice active, indicating that the ice-nucleating material in seawater can indeed transfer to the aerosol phase. Thirdly, we attempted to measure ice nucleation activity across the entire temperature range relevant for mixed-phase clouds using a suite of ice nucleation measurement techniques – an expansion cloud chamber, a continuous-flow diffusion chamber, and a cold stage. In order to compare the measurements made using the different instruments, we have normalized the data in relation to the mass of salt present in the nascent sea spray aerosol. At temperatures above 248 K some of the SML samples were very effective at nucleating ice, but there was substantial variability between the different samples. In contrast, there was much less variability between samples below 248 K. We discuss our results in the context of aerosol–cloud interactions in the Arctic with a focus on furthering our understanding of which INP types may be important in the Arctic atmosphere.

Solid Ammonium Nitrate Aerosols as Efficient Ice Nucleating Particles at Cirrus Temperatures

AbstractRecent satellite observations and high‐altitude aircraft measurements have demonstrated the presence of solid ammonium nitrate particles in the Asian monsoon upper troposphere. Most likely, these particles are formed by a heterogeneous crystallization mechanism, given that efflorescence is strongly inhibited for pure ammonium nitrate solution droplets. Crystallization can be induced by the presence of ammonium sulfate, which more easily crystallizes and serves as a heterogeneous nucleus for the crystallization of ammonium nitrate. In the present study, we have investigated this crystallization pathway for different amounts of ammonium sulfate admixed to ammonium nitrate solution droplets and measured the heterogeneous ice nucleation ability of the crystallized particles at cirrus temperatures in a cloud chamber and with a continuous flow diffusion chamber. We found that an admixture of only 0.6 mol% of ammonium sulfate was sufficient to induce the crystallization of ammonium nitrate at 223 K and 22% RHw. These almost pure, crystalline ammonium nitrate particles showed the same temperature‐dependent ice nucleation behavior as observed for other inorganic salts like ammonium sulfate and sodium chloride. At temperatures above 230 K, the crystalline ammonium nitrate particles first deliquesced and nucleated ice homogeneously at ice saturation ratios between about 1.45 and 1.50. Below 230 K, heterogeneous ice nucleation was observed to start at an ice saturation ratio as low as 1.13. The deduced ice nucleation active surface site densities were in the range from 1010–1011 m−2 at ice saturation ratios between 1.2 and 1.4, thus similar in magnitude to those of desert dust particles.

Direct Online Mass Spectrometry Measurements of Ice Nucleating Particles at a California Coastal Site

AbstractThe formation of ice in clouds can strongly impact cloud properties and precipitation processes during storms, including atmospheric rivers. Sea spray aerosol (SSA) particles are relatively inefficient as ice nucleating particles (INPs) compared to mineral dust. However, due to the vast coverage of the Earth's surface by the oceans, a number of recent studies have focused on identifying sources of marine INPs, particularly in regions lacking a strong influence from dust. This study describes the integration, validation, and application of a system coupling a continuous flow diffusion chamber with a single particle mass spectrometer using a pumped counterflow virtual impactor to remove nonnucleated particles and selectively measure the composition of INPs with a detection efficiency of 3.10 × 10−4. In situ measurements of immersion freezing INP composition were made at a coastal site in California using the integrated system. Mineral dust particles were the most abundant ice crystal residual type during the sampling period and found to be ice active despite having undergone atmospheric processing. SSA were more abundant in ambient measurements but represented only a minor fraction of the ice crystal residual population at −31 °C. Notably, the SSA particles that activated were enriched with organic nitrogen species that were likely transferred from the ocean. Calculations of ice nucleation active site densities were within good agreement with previous studies of mineral dust and SSA.

Characteristics of Ice Nucleating Particles in and Around California Winter Storms

AbstractA major component of California's yearly precipitation comes from wintertime atmospheric river events which bring large amounts of moisture from the tropics up to the midlatitudes. Understanding these systems, specifically the effects of aerosol particles on precipitation associated with these storms, was a major focus of the 2015 Atmospheric Radiation Measurement Cloud Aerosol Precipitation Experiment, which was part of the wintertime California Water 2015 campaign. The measurement campaign provided sampling platforms on four aircraft, including the Atmospheric Radiation Measurement Aerial Facility G‐1, as well as the National Oceanic and Atmospheric Administration Ronald H. Brown research vessel and at a ground station in Bodega Bay, CA. Measurements of ice nucleating particles (INPs) were made with the Colorado State University Continuous Flow Diffusion Chamber aboard the G‐1, and aerosol filters were collected on the G‐1, at the Bodega Bay site and on the Ronald H. Brown for postprocessing via immersion freezing in the Colorado State University Ice Spectrometer. Aerosol composition was measured aboard the G‐1 with the Aerosol Time‐of‐Flight Mass Spectrometer. Here we present INP concentrations and aerosol chemical compositions during the course of the aircraft campaign. During the atmospheric river event, we found that marine aerosol was the main aerosol type and that marine INPs were dominant at cloud activation temperatures, which is in stark contrast to the dominance of dust INPs during the atmospheric river events in the California Water 2011 campaign.

Laboratory study of the heterogeneous ice nucleation on black-carbon-containing aerosol

Abstract. Soot and black carbon (BC) particles are generated in the incomplete combustion of fossil fuels, biomass, and biofuels. These airborne particles affect air quality, human health, aerosol–cloud interactions, precipitation formation, and climate. At present, the climate effects of BC particles are not well understood. Their role in cloud formation is obscured by their chemical and physical variability and by the internal mixing states of these particles with other compounds. Ice nucleation in field studies is often difficult to interpret. Nonetheless, most field studies seem to suggest that BC particles are not efficient ice-nucleating particles (INPs). On the other hand, laboratory measurements show that in some cases, BC particles can be highly active INPs under certain conditions. By working with well-characterized BC particles, our aim is to systematically establish the factors that govern the ice nucleation activity of BC. The current study focuses on laboratory measurements of the effectiveness of BC-containing aerosol in the formation of ice crystals in temperature and ice supersaturation conditions relevant to cirrus clouds. We examine ice nucleation on BC particles under water-subsaturated cirrus cloud conditions, commonly understood as deposition-mode ice nucleation. We study a series of well-characterized commercial carbon black particles with varying morphologies and surface chemistries as well as ethylene flame-generated combustion soot. The carbon black particles used in this study are proxies for atmospherically relevant BC aerosols. These samples were characterized by electron microscopy, mass spectrometry, and optical scattering measurements. Ice nucleation activity was systematically examined in temperature and saturation conditions in the ranges of 217≤T≤235 K and 1.0≤Sice≤1.5 and 0.59≤Swater≤0.98, respectively, using a SPectrometer for Ice Nuclei (SPIN) instrument, which is a continuous-flow diffusion chamber coupled with instrumentation to measure light scattering and polarization. To study the effect of coatings on INPs, the BC-containing particles were coated with organic acids found in the atmosphere, namely stearic acid, cis-pinonic acid, and oxalic acid. The results show significant variations in ice nucleation activity as a function of size, morphology, and surface chemistry of the BC particles. The measured ice nucleation activity dependencies on temperature, supersaturation conditions, and the physicochemical properties of the BC particles are consistent with an ice nucleation mechanism of pore condensation followed by freezing. Coatings and surface oxidation modify the initial formation efficiency of pristine ice crystals on BC-containing aerosol. Depending on the BC material and the coating, both inhibition and enhancement in INP activity were observed. Our measurements at low temperatures complement published data and highlight the capability of some BC particles to nucleate ice under low ice supersaturation conditions. These results are expected to help refine theories relating to soot INP activation in the atmosphere.

Measurements of Ice Nucleating Particles in Beijing, China

AbstractHeterogeneous ice nucleating particle (INP) concentrations are reported for a site on the eastern margin of Beijing, China, during the period 4 May to 4 June 2018. INP concentrations were measured continuously at −20, −25, and −30 °C in a repeating cycle by a newly developed, automated continuous flow diffusion chamber, and reached concentrations as high as 2800 sL−1 during dust‐impacted periods. Study average concentrations were 70 ± 70, 230 ± 290, and 430 ± 500 sL−1 at −20, −25, and −30 °C. There was no clear relationship between pollution periods, identified based on fine‐mode particle concentration increases, and INP concentrations or characteristics. Other anthropogenic emissions, such as non‐combustion industrial or agricultural activities play an unresolved role.

A high-speed particle phase discriminator (PPD-HS) for the classification of airborne particles, as tested in a continuous flow diffusion chamber

Abstract. A new instrument, the High-speed Particle Phase Discriminator (PPD-HS), developed at the University of Hertfordshire, for sizing individual cloud hydrometeors and determining their phase is described herein. PPD-HS performs an in situ analysis of the spatial intensity distribution of near-forward scattered light for individual hydrometeors yielding shape properties. Discrimination of spherical and aspherical particles is based on an analysis of the symmetry of the recorded scattering patterns. Scattering patterns are collected onto two linear detector arrays, reducing the complete 2-D scattering pattern to scattered light intensities captured onto two linear, one-dimensional strips of light sensitive pixels. Using this reduced scattering information, we calculate symmetry indicators that are used for particle shape and ultimately phase analysis. This reduction of information allows for detection rates of a few hundred particles per second. Here, we present a comprehensive analysis of instrument performance using both spherical and aspherical particles generated in a well-controlled laboratory setting using a vibrating orifice aerosol generator (VOAG) and covering a size range of approximately 3–32 µm. We use supervised machine learning to train a random forest model on the VOAG data sets that can be used to classify any particles detected by PPD-HS. Classification results show that the PPD-HS can successfully discriminate between spherical and aspherical particles, with misclassification below 5 % for diameters &gt;3 µm. This phase discrimination method is subsequently applied to classify simulated cloud particles produced in a continuous flow diffusion chamber setup. We report observations of small, near-spherical ice crystals at early stages of the ice nucleation experiments, where shape analysis fails to correctly determine the particle phase. Nevertheless, in the case of simultaneous presence of cloud droplets and ice crystals, the introduced particle shape indicators allow for a clear distinction between these two classes, independent of optical particle size. From our laboratory experiments we conclude that PPD-HS constitutes a powerful new instrument to size and discriminate the phase of cloud hydrometeors. The working principle of PPD-HS forms a basis for future instruments to study microphysical properties of atmospheric mixed-phase clouds that represent a major source of uncertainty in aerosol-indirect effect for future climate projections.