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The formation of ice particles in Earth's atmosphere strongly influences the dynamics and optical properties of clouds and their impacts on the climate system. Ice formation in clouds is often triggered heterogeneously by ice-nucleating particles (INPs) that represent a very low number of particles in the atmosphere. To date, many sources of INPs, such as mineral and soil dust, have been investigated and identified in the low and mid latitudes. Although less is known about the sources of ice nucleation at high latitudes, efforts have been made to identify the sources of INPs in the Arctic and boreal environments. In this study, we investigate the INP emission potential from high-latitude boreal forests in the mixed-phase cloud regime. We introduce the HyICE-2018 measurement campaign conducted in the boreal forest of Hyytiälä, Finland, between February and June 2018. The campaign utilized the infrastructure of the Station for Measuring Ecosystem-Atmosphere Relations (SMEAR) II, with additional INP instruments, including the Portable Ice Nucleation Chamber I and II (PINC and PINCii), the SPectrometer for Ice Nuclei (SPIN), the Portable Ice Nucleation Experiment (PINE), the Ice Nucleation SpEctrometer of the Karlsruhe Institute of Technology (INSEKT) and the Microlitre Nucleation by Immersed Particle Instrument (µ L-NIPI), used to quantify the INP concentrations and sources in the boreal environment. In this contribution, we describe the measurement infrastructure and operating procedures during HyICE-2018, and we report results from specific time periods where INP instruments were run in parallel for inter-comparison purposes. Our results show that the suite of instruments deployed during HyICE-2018 reports consistent results and therefore lays the foundation for forthcoming results to be considered holistically. In addition, we compare measured INP concentrations to INP parameterizations, and we observe good agreement with the parameterization developed from measurements conducted in a ponderosa pine forest ecosystem in Colorado, USA. [ABSTRACT FROM AUTHOR]

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 RH water=110 %, while the temperature was ramped between -4 3 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. [ABSTRACT FROM AUTHOR]

We investigate the effect of water content and oxidative age on ice nucleation using 100 nm monodisperse particles of boreal forest secondary organic aerosol (SOA) surrogates. Ice nucleation experiments are conducted in the temperature range between 210 and 240 K and from ice to water saturation using the Spectrometer for Ice Nuclei (SPIN). The effect of the particle water content on the ice nucleation process is tested by preconditioning α -pinene SOA at different humidities (40 %, 10 % and <1 % RHW). The influence of the particle oxidative age is tested by varying their O:C ratio (oxygen-to-carbon ratio, O:C ∼0.45 , 0.8, 1.1). To assess the suitability of α -pinene as a model compound to study the ice nucleation properties of boreal forest SOA and to confirm the atmospheric relevance of our findings, we compare them to measurements of SOA using pine-needle oil or Scots pine tree emissions as precursors. The ice nucleation measurements show that surrogates of boreal forest SOA particles promote only homogeneous ice formation. An effect of preconditioning humidity on homogeneous ice nucleation could be observed. Contrary to the expected behavior, homogeneous freezing is suppressed for SOA particles with high water content (preconditioned at 40 % RHW) and was only observed for SOA preconditioned at low RHW (≤10 %). No dependence of homogeneous freezing on the SOA oxidative age was observed. The results can be explained by a significant change of particulate water diffusivity as a function of humidity (from 10 % to 40 % RHW) at 293 K , where the aerosol is preconditioned. The measurements suggest that at low temperatures, water diffusion into dry SOA particles is slow enough to form a core-shell morphology. The liquid outer layer can equilibrate within the timescale of the experiment and freeze homogeneously. On SOA particles with higher water content, water diffuses faster into the particle, delaying equilibration at the particle surface and preventing the formation of a diluted shell, which can delay homogeneous freezing. We propose that the partial water vapor pressure to which the particles are exposed prior to an experiment can serve as an indicator of whether a core-shell structure is developing. [ABSTRACT FROM AUTHOR]

Ice-nucleating particles (INPs) trigger the formation of cloud ice crystals in the atmosphere. Therefore, they strongly influence cloud microphysical and optical properties and precipitation and the life cycle of clouds. Improving weather forecasting and climate projection requires an appropriate formulation of atmospheric INP concentrations. This remains challenging as the global INP distribution and variability depend on a variety of aerosol types and sources, and neither their short-term variability nor their long-term seasonal cycles are well covered by continuous measurements. Here, we provide the first year-long set of observations with a pronounced INP seasonal cycle in a boreal forest environment. Besides the observed seasonal cycle in INP concentrations with a minimum in wintertime and maxima in early and late summer, we also provide indications for a seasonal variation in the prevalent INP type. We show that the seasonal dependency of INP concentrations and prevalent INP types is most likely driven by the abundance of biogenic aerosol. As current parameterizations do not reproduce this variability, we suggest a new mechanistic description for boreal forest environments which considers the seasonal variation in INP concentrations. For this, we use the ambient air temperature measured close to the ground at 4.2 m height as a proxy for the season, which appears to affect the source strength of biogenic emissions and, thus, the INP abundance over the boreal forest. Furthermore, we provide new INP parameterizations based on the Ice Nucleation Active Surface Site (INAS) approach, which specifically describes the ice nucleation activity of boreal aerosols particles prevalent in different seasons. Our results characterize the boreal forest as an important but variable INP source and provide new perspectives to describe these new findings in atmospheric models. [ABSTRACT FROM AUTHOR]

The SPectrometer for Ice Nuclei (SPIN) has been modified to access ice nucleation at low temperatures. The modification consists of a reconfiguration of components from SPIN's cooling system to provide refrigerant with a low boiling point to the chamber. We describe the setup modification and determine the temperature and humidity range accessible to experiments. The modification extends the measurement range of SPIN to 208 K , which enables measurements in the temperature regime relevant for ice formation in cirrus clouds. This addition of low-temperature capability allows for far more comprehensive measurements of the temperature- and humidity-dependent ice nucleation of test substances, to investigate fundamentals of ice nucleation mechanisms. We present exemplary data of heterogeneous ice nucleation on silver iodide and homogeneous ice nucleation in solution droplets to demonstrate the usefulness of the modified SPIN setup for precision measurements to detect discrepancies between experiments and widely used theories. [ABSTRACT FROM AUTHOR]

This research was part of the Salutary Umeå Study of Aerosols in Biomass Cookstove Emissions (SUSTAINE) laboratory experiment campaign. We studied ice-nucleating abilities of particulate emissions from solid-fuel-burning cookstoves, using a portable ice nuclei counter, Spectrometer Ice Nuclei (SPIN). These emissions were generated from two traditional cookstove types commonly used for household cooking in sub-Saharan Africa and two advanced gasifier stoves under research to promote sustainable development alternatives. The solid fuels studied included biomass from two different African tree species, Swedish softwood and agricultural residue products relevant to the region. Measurements were performed with a modified version of the standard water boiling test on polydisperse samples from flue gas during burning and size-selected accumulation mode soot particles from a 15 m 3 aerosol-storage chamber. The studied soot particle sizes in nanometers were 250, 260, 300, 350, 400, 450 and 500. From this chamber, the particles were introduced to water-supersaturated freezing conditions (- 32 to - 43 ∘ C) in the SPIN. Accumulation mode soot particles generally produced an ice-activated fraction of 10 -3 in temperatures 1–1.5 ∘ C higher than that required for homogeneous freezing at fixed RH w=115 %. In five special experiments, the combustion performance of one cookstove was intentionally modified. Two of these exhibited a significant increase in the ice-nucleating ability of the particles, resulting in a 10 -3 ice activation at temperatures up to 5.9 ∘ C higher than homogeneous freezing and the observed increased ice-nucleating ability. We investigated six different physico-chemical properties of the emission particles but found no clear correlation between them and increasing ice-nucleating ability. We conclude that the freshly emitted combustion aerosols form ice via immersion and condensation freezing at temperatures only moderately above homogeneous freezing conditions. [ABSTRACT FROM AUTHOR]

Deposition ice nucleation on lead, copper and silver oxides has been studied bothexperimentally and theoretically. Experimental data of activated fractions of PbO, PbO2,CuO, CuO2, and Ag2O particles were measured as a function of ice supersaturation andtemperature using the SPIN instrument at temperatures between 228 and 252 K. The mainmotivation for choosing to study the metal oxide particles is their chemical and physicalhomogeneity. Experimental ice nucleation data on atmospherically relevant particle typesoften contain features which might be explained by different types of external heterogeneitieswithin the particle population (i.e. variations in particle chemical compositions ormorphologies), or by chemical or physical heterogeneities of individual particles. Therefore,comparison of the metal oxide deposition nucleation data with data from morecomplex particle types might reveal whether or not various experimental featuresoriginate from such heterogeneities. In addition, simple ice nuclei types enable morestraightforward comparisons with different ice nucleation theories. Here, we compare theexperimental results with the recently developed adsorption nucleation theory, andwith the classical nucleation theory. To get input data for the theories, we havemeasured adsorption isotherms and contact angles of water on the metal oxides. [ABSTRACT FROM AUTHOR]