Ice Nucleating Particles Research Articles

Increasing Arctic dust suppresses the reduction of ice nucleation in the Arctic lower troposphere by warming

Ice nucleating particles (INPs) affect the cloud radiative budget in the rapidly warming Arctic by changing the cloud liquid/ice phase balance. Dust emitted in the Arctic (Arctic dust) has been suggested to be a major contributor to INPs in the Arctic lower troposphere. However, how Arctic dust and its impacts on ice nucleation change with Arctic warming has not been explored. Here we find that the simulated dust emission flux in the Arctic (>60°N) in global model simulations increases by 20% from 1981–1990 to 2011–2020. This increase weakens the sensitivity of ice nucleation in Arctic lower tropospheric clouds to warming by 40% compared to the case without considering Arctic dust emission increases. Our results demonstrate a better understanding of the counterbalancing feedbacks of Arctic dust (i.e., increasing emissions and decreasing ice nucleation efficiency) is needed for more accurate estimates of changes in ice nucleation in the rapidly changing Arctic climate.

Ice-nucleating particles active below −24 °C in a Finnish boreal forest and their relationship to bioaerosols

Abstract. Cloud properties are strongly influenced by ice formation; hence, we need to understand the sources of ice-nucleating particles (INPs) around the globe. Boreal forests are known as sources of bioaerosol, and recent work indicates that these dominate the INP spectra above −24 °C. To quantify the INP population at temperatures below −24 °C, we deployed a portable cloud expansion chamber (PINE) in a Finnish boreal forest from 13 March 2018 to 11 May 2018. Using the 6 min time resolution PINE data, we present several lines of evidence that INPs below −24 °C in this location are also from biological sources: (i) an INP parameterization developed for a pine forest site in Colorado, where many INPs were shown to be biological, produced a good fit to our measurements; a moderate correlation of INPs with aerosol concentration larger than 0.5 µm and the fluorescent bioaerosol concentration; (ii) a negative correlation with relative humidity that may relate to enhanced release of bioaerosol at low humidity from local sources such as the prolific lichen population in boreal forests; and (iii) the absence of correlation with ultra-fine particles (3.5 to 50 nm), indicating that new particle formation events are not sources of INPs. This study should motivate further work to establish whether the commonality in bioaerosol ice-nucleating properties between spring in Finland and summer in Colorado is more generally applicable to different coniferous forest locations and times and also to determine to what extent these bioaerosols are transported to locations where they may affect clouds.

Air mass history linked to the development of Arctic mixed-phase clouds

Abstract. Clouds formed during marine cold-air outbreaks (MCAOs) exhibit a distinct transition from stratocumulus decks near the ice edge to broken cumuliform fields further downwind. The mechanisms associated with ice formation are believed to be crucial in driving this transition, yet the factors influencing such formation remain unclear. Through Lagrangian trajectories collocated with satellite data, this study investigates the development of mixed-phase clouds using these outbreaks. Cloud formed in MCAOs are characterized by a swift shift from liquid to ice-containing states, contrasting with non-MCAO clouds also moving off the ice edge. These mixed-phase clouds are predominantly observed at temperatures below −20 °C near the ice edge. However, further into the outbreak, they become dominant at temperatures as high as −13 °C. This shift is consistent with the influence of biological ice-nucleating particles (INPs), which become more prevalent as the air mass ages over the ocean. The evolution of these clouds is closely linked to the history of the air mass, especially the length of time it spends over snow- and ice-covered surfaces – terrains may that be deficient in INPs. This connection also accounts for the observed seasonal variations in the development of Arctic clouds, both within and outside of MCAO events. The findings highlight the importance of understanding both local marine aerosol sources near the ice edge and the overarching INP distribution in the Arctic for modelling of cloud phase in the region.

Atmospheric Fungal Spore Injection: A Promising Breakthrough for Challenging the Impacts of Climate Change Through Cloud Seeding and Weather Modification

Cloud seeding is a technique used to enhance precipitation in drought-prone areas, support agricultural productivity, ensure water supply for human consumption, improve hydropower generation from dams, lessen hurricanes, cool urban heat, and disperse fog in airports. Growing global population size and climate change are the biggest impetus for weather modification and cloud seeding operations. Currently, salt powders like silver iodide, potassium iodide, sodium chloride, calcium chloride, dry ice (solid carbon dioxide), and liquid propane are widely used as ice nucleating particles for cloud seeding purposes while in natural cloud formation, and precipitation particles from dust storms, mineral dust and biological aerosols (like spores, pollen, bacteria) are the dominant ice nucleators. Having this knowledge on hand and the ubiquitous nature of fungi on the other hand; it is feasible to exploit the ice nucleating ability of fungal spores and use it as potential candidates for cloud seeding and weather modification operations.

Simulated contrail-processed aviation soot aerosols are poor ice-nucleating particles at cirrus temperatures

Abstract. Aviation soot surrogates processed in contrails are believed to become potent ice nuclei at cirrus temperatures. This is not verified for real aviation soot, which can have vastly different physico-chemical properties. Here, we sampled soot particles from in-use commercial aircraft engines and quantified the effect of contrail processing on their ice nucleation ability at T< 228 K. We show that aviation soot becomes compacted upon contrail processing, but that does not change their ice nucleation ability in contrast to other soot types. The presence of H2SO4 condensed in soot pores, the highly fused nature of the soot primary particles and their arrangement are what limit the volume of pores generated upon contrail processing, in turn limiting sites for ice nucleation. Furthermore, we hypothesized that contrail-processed aviation soot particles emitted from alternative jet fuel would also be poor ice-nucleating particles if their emission sizes remain small (< 150 nm).

Surface warming in Svalbard may have led to increases in highly active ice-nucleating particles

The roles of Arctic aerosols as ice-nucleating particles remain poorly understood, even though their effects on cloud microphysics are crucial for assessing the climate sensitivity of Arctic mixed-phase clouds and predicting their response to Arctic warming. Here we present a full-year record of ice-nucleating particle concentrations over Svalbard, where surface warming has been anomalously faster than the Arctic average. While the variation of ice-nucleating particles active at around −30 °C was relatively small, those active at higher temperatures (i.e., highly active ice-nucleating particles) tended to increase exponentially with rising surface air temperatures when the surface air temperatures rose above 0 °C and snow/ice-free barren and vegetated areas appeared in Svalbard. The aerosol population relevant to their increase was largely characterized by dust and biological organic materials that likely originated from local/regional terrestrial sources. Our results suggest that highly active ice-nucleating particles could be actively released from Arctic natural sources in response to surface warming.

Biophysical evidence that frostbite is triggered on nanocrystals of biogenic magnetite in garlic cloves (Allium sativum)

Trace levels of biologically precipitated magnetite (Fe3O4) nanocrystals are present in the tissues of many living organisms, including those of plants. Recent work has also shown that magnetite nanoparticles are powerful ice nucleation particles (INPs) that can initiate heterogeneous freezing in supercooled water just below the normal melting temperature. Hence there is a strong possibility that magnetite in plant tissues might be an agent responsible for triggering frost damage, even though the biological role of magnetite in plants is not understood. To test this hypothesis, we investigated supercooling and freezing mortality in cloves of garlic (Allium sativum), a species which is known to have moderate frost resistance. Using superconducting magnetometry, we detected large numbers of magnetite INPs within individual cloves. Oscillating magnetic fields designed to torque magnetite crystals in situ and disturb the ice nucleating process produced significant effects on the temperature distribution of supercooling, thereby confirming magnetite’s role as an INP in vivo. However, weak oscillating fields increased the probability of freezing, whereas stronger fields decreased it, a result that predicts the presence of magnetite binding agents that are loosely attached to the ice nucleating sites on the magnetite crystals.

Glaciation of mixed-phase clouds: insights from bulk model and bin-microphysics large-eddy simulation informed by laboratory experiment

Abstract. Mixed-phase clouds affect precipitation and radiation differently from liquid and ice clouds, posing greater challenges to their representation in numerical simulations. Recent laboratory experiments using the Pi Cloud Chamber explored cloud glaciation conditions based on increased injection of ice-nucleating particles. In this study, we use two approaches to reproduce the results of the laboratory experiments: a bulk scalar mixing model and large-eddy simulation (LES) with bin microphysics. The first approach assumes a well-mixed domain to provide an efficient assessment of the mean cloud properties for a wide range of conditions. The second approach resolves the energy-carrying turbulence, the particle size distribution, and their spatial distribution to provide more details. These modeling approaches enable a separate and detailed examination of liquid and ice properties, which is challenging in the laboratory. Both approaches demonstrate that, with an increased ice number concentration, the flow and microphysical properties exhibit the same changes in trends. Additionally, both approaches show that the ice integral radius reaches the theoretical glaciation threshold when the cloud is subsaturated with respect to liquid water. The main difference between the results of the two approaches is that the bulk model allows for the complete glaciation of the cloud. However, LES reveals that, in a dynamic system, the cloud is not completely glaciated as liquid water droplets are continuously produced near the warm lower boundary and subsequently mixed into the chamber interior. These results highlight the importance of the ice mass fraction in distinguishing the mixed-phase clouds and ice clouds.

Decreased dust particles amplify the cloud cooling effect by regulating cloud ice formation over the Tibetan Plateau.

Ice-nucleating particles (INPs) can initiate cloud ice formation, influencing cloud radiative effects (CRE) and climate. However, the knowledge of INP sources, concentrations, and their impact on CRE over the Tibetan Plateau (TP)-a highly climate-sensitive region-remains largely hypothetical. Here, we integrated data from multisource satellite observations and snowpack samples collected from five glaciers to demonstrate that dust particles constitute primary INP sources over the TP. The springtime dust influxes lead to seasonally elevated ice concentrations in mixed-phase clouds. Furthermore, the decadal reduction in dustiness from 2007 to 2019 results in decreased springtime dust INPs, thereby amplifying the cooling effect of clouds over the TP, with a 1.98 ± 0.39-watt per square meter reduction in surface net CRE corresponding to a 0.01 decrease in dust optical depth. Our findings elucidate previously unidentified pathways of climate feedback from an atmospheric INP perspective, especially highlighting the crucial role of dust in aerosol-cloud interactions.

Biological and dust aerosols as sources of ice-nucleating particles in the eastern Mediterranean: source apportionment, atmospheric processing and parameterization

Abstract. Aerosol–cloud interactions in mixed-phase clouds (MPCs) are one of the most uncertain drivers of the hydrological cycle and climate change. A synergy of in situ, remote-sensing and modelling experiments were used to determine the source of ice-nucleating particles (INPs) for MPCs at Mount Helmos in the eastern Mediterranean. The influences of boundary layer turbulence, vertical aerosol distributions and meteorological conditions were also examined. When the observation site is in the free troposphere (FT), approximately 1 in ×106 aerosol particles serve as INPs around −25 °C. The INP abundance spans 3 orders of magnitude and increases in the following order: marine aerosols; continental aerosols; and, finally, dust plumes. Biological particles are important INPs observed in continental and marine aerosols, whereas they play a secondary, although important, role during Saharan dust events. Air masses in the planetary boundary layer (PBL) show both enriched INP concentrations and a higher proportion of INPs to total aerosol particles, compared with cases in the FT. The presence of precipitation/clouds enriches INPs in the FT but decreases INPs in the PBL. Additionally, new INP parameterizations are developed that incorporate the ratio of fluorescent-to-nonfluorescent or coarse-to-fine particles and predict >90 % of the observed INPs within an uncertainty range of a factor of 10; these new parameterizations exhibit better performance than current widely used parameterizations and allow ice formation in models to respond to variations in dust and biological particles. The improved parameterizations can help MPC formation simulations in regions with various INP sources or different regions with prevailing INP sources.

TAMU TRACER: Targeted Mobile Measurements to Isolate the Impacts of Aerosols and Meteorology on Deep Convection

Abstract Difficulty in using observations to isolate the impacts of aerosols from meteorology on deep convection often stems from the inability to resolve the spatiotemporal variations in the environment serving as the storm’s inflow region. During the U.S. Department of Energy (DOE) Tracking Aerosol Convection interactions Experiment (TRACER) in June–September 2022, a Texas A&M University (TAMU) team conducted a mobile field campaign to characterize the meteorological and aerosol variability in air masses that serve as inflow to convection across the ubiquitous mesoscale boundaries associated with the sea and bay breezes in the Houston, Texas, region. These boundaries propagate inland over the fixed DOE Atmospheric Radiation Measurement (ARM) sites. However, convection occurs on either or both the continental or maritime sides or along the boundary. The maritime and continental air masses serving as convection inflow may be quite distinct, with different meteorological and aerosol characteristics that fixed-site measurements cannot simultaneously sample. Thus, a primary objective of TAMU TRACER was to provide mobile measurements similar to those at the fixed sites, but in the opposite air mass across these moving mesoscale boundaries. TAMU TRACER collected radiosonde, lidar, aerosol, cloud condensation nuclei (CCN), and ice nucleating particle (INP) measurements on 29 enhanced operations days covering a variety of maritime, continental, outflow, and prefrontal air masses. This paper summarizes the TAMU TRACER deployment and measurement strategy, instruments, and available datasets and provides sample cases highlighting differences between these mobile measurements and those made at the ARM sites. We also highlight the exceptional TAMU TRACER undergraduate student participation in high-impact learning activities through forecasting and field deployment opportunities.

The Abundance and Sources of Ice Nucleating Particles Within Alaskan Ice Fog

AbstractThe Alaskan Layered Pollution and Chemical Analysis (ALPACA) field campaign included deployment of a suite of atmospheric measurements in January–February 2022 with the goal of better understanding atmospheric processes and pollution under cold and dark conditions in Fairbanks, Alaska. We report on measurements of particle composition, particle size, ice nucleating particle (INP) composition, and INP size during an ice fog period (29 January–3 February). During this period, coarse particulate matter (PM10) concentrations increased by 150% in association with a decrease in air temperature, a stronger temperature inversion, and relatively stagnant conditions. Results also show a 18%–78% decrease in INPs during the ice fog period, indicating that particles had activated into the ice fog via nucleation. Peroxide and heat treatments performed on INPs indicated that, on average, the largest contributions to the INP population were heat‐labile (potentially biological, 63%), organic (31%), then inorganic (likely dust, 6%). Measurements of levoglucosan and bulk and single‐particle composition corroborate the presence of dust and aerosols from combustion sources. Heat‐labile and organic INPs decreased during the peak period of the ice fog, indicating those were preferentially activated, while inorganic INPs increased, suggesting they remained as interstitial INPs. In general, INP concentrations were unexpectedly high in Fairbanks compared to other locations in the Arctic during winter. The fact that these INPs likely facilitated ice fog formation in Fairbanks has implications for other high latitude locations subject to the hazards associated with ice fog.

Single particle characteristics and ice nucleation potential of particles collected during Asian dust storms in 2021

Dust storms have great impacts on air quality and climate. Dust can influence cloud microphysical properties and determine their radiative forcing and precipitation. Asian dust storms (ADS) are important sources of global aerosol. However, the physiochemical characteristics of dust from ADS at a single particle level are less understood, and the exact particles that can serve as ice nucleating particles (INPs) remain unclear. Here, we present the physicochemical properties and ice nucleation ability of dust particles collected in Beijing during two major ADS in March 2021. The particles from two ADS were classified into Illite, Kaolinite, Feldspar, Quartz, Chlorite, Mixed-dust, and Non-dust particles, which contributed 28.6 % ± 3.3 %, 20.0 % ± 3.9 %, 12.3 % ± 2.3 %, 11.1 % ± 2.8 %, 9.8 % ± 0.8 %, 13.7 % ± 1.8 %, and 4.4 % ± 1.7 % in number, respectively. On average, the ADS particles formed ice crystals via deposition ice nucleation from relative humidity with respect to ice (RHice) of 112 % ± 1 % at 250 K to 154 % ± 15 % RHice at 205 K. Part of the samples also formed ice via immersion freezing between 230 K and 250 K. Among the 149 identified INPs, Clay-like particles (Chlorite, Illite, and Kaolinite) contributed 71.1 % ± 6.2 % in number and followed by Mixed-dust-like particles (16.9 % ± 8.7 %) and Feldspar-like particles (10.4 % ± 6.3 %). Enrichment factor of each particle type in INPs is calculated as the ratio of its number fractions in INPs and the aerosol population. It ranges from 0.6 ± 0.7 to 1.3 ± 2.2. The contribution of each particle type to INP was correlated with its fraction in the population. These results imply that each particle type can serve as INP. Clay-like particles are the dominant INPs during the ADS. We conducted ice nucleation kinetic analysis and provided parameterizations of heterogeneous ice nucleation rate coefficient and contact angle for ADS. These parameterizations can be used in the modeling study to evaluate the impact of ADS in atmospheric ice crystal formation in clouds.

Diverse sources and aging change the mixing state and ice nucleation properties of aerosol particles over the western Pacific and Southern Ocean

Abstract. Atmospheric particles can impact cloud formation and play a critical role in regulating cloud properties. However, particle characteristics at the single-particle level and their ability to act as ice-nucleating particles (INPs) over the marine atmosphere are poorly understood. In this study, we present micro-spectroscopic characterizations and ice nucleation properties of particles collected during a cruise from South Korea to Antarctica in 2019. Most of the samples were dominated by fresh sea salt, aged sea salt, and sea salt mixed with sulfate particles, with total number percentages ranging from 48 % to 99 % over the western Pacific and the Southern Ocean. The mixing-state index of the particle population ranged from 50 % to 95 % over the Northern Hemisphere and Southern Hemisphere. Multiphase processes on sea salt particles resulted in chlorine deficiency. This selective aging process made the marine particle population more externally mixed. Ice nucleation onset conditions primarily for the deposition mode were measured and the investigated particles showed diverse ice nucleation abilities. The fresh sea salt particles with organic coatings exhibited the highest ice nucleation ability at a relative humidity with respect to ice as low as 121 %. The sea salt mixed sulfate particle was enriched in INPs by a factor of 1.9. Aging processes affected both the mixing state of the particles and their ice nucleation abilities. Our analysis shows that assuming an internally mixed particle population in the marine atmosphere can lead to errors of several orders of magnitude in predicting ice nucleation rates.

Simulations of primary and secondary ice production during an Arctic mixed-phase cloud case from the Ny-Ålesund Aerosol Cloud Experiment (NASCENT) campaign

Abstract. The representation of Arctic clouds and their phase distributions, i.e., the amount of ice and supercooled water, influences predictions of future Arctic warming. Therefore, it is essential that cloud phase is correctly captured by models in order to accurately predict the future Arctic climate. Ice crystal formation in clouds happens through ice nucleation (primary ice production) and ice multiplication (secondary ice production). In common weather and climate models, rime splintering is the only secondary ice production process included. In addition, prescribed number concentrations of cloud condensation nuclei or cloud droplets and ice-nucleating particles are often overestimated in Arctic environments by standard model configurations. This can lead to a misrepresentation of the phase distribution and precipitation formation in Arctic mixed-phase clouds, with important implications for the Arctic surface energy budget. During the Ny-Ålesund Aerosol Cloud Experiment (NASCENT), a holographic probe mounted on a tethered balloon took in situ measurements of number and mass concentrations of ice crystals and cloud droplets in Svalbard, Norway, during fall 2019 and spring 2020. In this study, we choose one case study from this campaign that shows evidence of strong secondary ice production and use the Weather Research and Forecasting (WRF) model to simulate it at a high vertical and spatial resolution. We test the performance of different microphysical parametrizations and apply a new state-of-the-art secondary ice parametrization. We find that agreement with observations highly depends on the prescribed cloud condensation nuclei/cloud droplet and ice-nucleating particle concentrations and requires an enhancement of secondary ice production processes. Lowering mass mixing ratio thresholds for rime splintering inside the Morrison microphysics scheme is crucial to enable secondary ice production and thereby match observations for the right reasons. In our case, rime splintering is required to initiate collisional breakup. The simulated contribution from collisional breakup is larger than that from droplet shattering. Simulating ice production correctly for the right reasons is a prerequisite for reliable simulations of Arctic mixed-phase cloud responses to future temperature or aerosol perturbations.

Seasonal Variations, Origin, and Parameterization of Ice‐Nucleating Particles at a Mountain Station in Central France

AbstractIdentifying how aerosol particles interact with atmospheric water is critical to understand climate and precipitation. Ice‐nucleating particles (INP) trigger the formation of atmospheric ice crystals at higher temperatures than pure water. They are difficult to characterize because of their scarce occurrence, and variability, in the atmosphere, especially at temperatures above −20°C. It has been demonstrated that at these temperatures, biological aerosol particles can contribute significantly to INP number concentration. This study incorporates a series of offline, size‐segregated measurements of INPs collected at the Puy de Dôme station (PUY, 1,465 m a.s.l.) over a 6 month period from October to May, covering the transitions from autumn, winter, to spring. These measurements show a general trend of decreasing particle number concentrations during the winter months and higher concentration during autumn and spring. INP concentrations measured in the range of −5 and −18°C, had concentrations of 0.001 INP/Lair at the warmest temperatures, and between 0.01 and 0.1 INP/Lair at the coldest temperatures. The majority of INP measured at temperatures warmer than −15°C were heat labile, suggesting a biological or organic origin. The INP variability was compared with collocated aerosol physical and chemical properties, allowing us to associate highest INP concentrations with local and marine origins. Following these comparisons, we use aerosol total number concentration to develop a new parameterization. In addition, this parameterization is specifically optimized for warmer temperature INP measurements, and demonstrated a good performance when tested on independent data sets.

Characteristics of Atmospheric Ice Nucleation during Spring: A Case Study on Huangshan

Atmospheric ice nucleation particles (INPs) play a crucial role in influencing cloud formation and microphysical properties, which in turn impact precipitation and Earth’s radiation budget. However, the influence of anthropogenic activities on the properties and concentrations of INPs remains an area of significant uncertainty. This study investigated the physical and chemical characteristics of atmospheric ice nucleation particles in Huangshan, China during the May Day labor holiday period (spanning 8 days, from April 27th to May 5th). INP concentrations were measured at temperatures from −17 °C to −26 °C and relative humidities (RHw) from 95% to 101%. Average INP concentrations reached 13.7 L−1 at −26 °C and 101% RH, 137 times higher than at −17 °C and 95% RH. INP concentrations showed exponential increases with decreasing temperature and exponential increases with increasing RH. Concentration fluctuations were observed over time, with a peak of ~30 L−1 (t = −26 °C, RHw = 101%) around the start and end of the holiday period. Aerosol number concentrations were monitored simultaneously. The peak in aerosols larger than 0.5 μm aligned with the peak in INP concentrations, suggesting a link between aerosol levels and INPs. Chemical composition analysis using SEM–EDX revealed the distinct elemental makeup of INPs based on the activation temperature. INPs active at warmer temperatures contained N, Na, and Cl, indicating possible biomass and sea salt origins, while those active at colder temperatures contained crustal elements like Al and Ca.

Simulations of the impact of cloud condensation nuclei and ice-nucleating particles perturbations on the microphysics and radar reflectivity factor of stratiform mixed-phase clouds

Abstract. In this research, we delve into the influence of cloud condensation nuclei (CCN) and ice-nucleating particle (INP) concentrations on the morphology and abundance of ice particles in mixed-phase clouds, emphasizing the consequential impact of ice particle shape, number, and size on cloud dynamics and microphysics. Leveraging the synergy of the Advanced Microphysics Prediction System (AMPS) and the Kinematic Driver (KiD) model, we conducted simulations to capture cloud microphysics across diverse CCN and INP concentrations. The Passive and Active Microwave radiative TRAnsfer (PAMTRA) radar forward simulator further augmented our study, offering insights into how the concentrations of CCN and INPs affect radar reflectivities. Our experimental framework encompassed CCN concentrations ranging from 10 to 5000 cm−3 and INP concentrations from 0.001 to 10 L−1. Central to our findings is the observation that higher INP concentrations yield smaller ice particles, while an increase in CCN concentrations leads to a subtle growth in their dimensions. Consistent with existing literature, our results spotlight oblate-like crystals as dominant between temperatures of −20 and −16 °C. Notably, high-INP scenarios unveiled a significant prevalence of irregular polycrystals. The aspect ratio (AR) of ice particles exhibited a decline with the rise in both CCN and INP concentrations, highlighting the nuanced interrelation between CCN levels and ice particle shape, especially its ramifications on the riming mechanism. The forward-simulated radar reflectivities, spanning from −11.83 dBZ (low INP, 0.001 L−1) to 4.65 dBZ (high INP, 10 L−1), elucidate the complex dynamics between CCN and INPs in determining mixed-phase cloud characteristics. Comparable differences in radar reflectivity were also reported from observational studies of stratiform mixed-phase clouds in contrasting aerosol environments. Our meticulous analysis of KiD-AMPS simulation outputs, coupled with insights into aerosol-driven microphysical changes, thus underscores the significance of this study in refining our ability to understand and interpret observations and climate projections.

The impact of aerosols as ice nucleating particle on microphysics and electrification in the cumulus model

Here, a heterogeneous ice nucleation parameterization associated with aerosol acting as ice nucleating particle (INP) was implanted into a two-dimensional numerical cumulus model. To explore the impact of INP on microphysical and electrical processes, a comparison was conducted with the original approach, which employs an empirical formula. Simulation results indicate that INP greatly impacted microphysical evolution in the heterogeneous ice nucleation process, reducing total liquid precipitation amounts and causing a slight precipitation delay, as well as increasing the diameter and mixing ratio of ice crystals and the expansion of the vertical distribution of ice crystals. This led to a notable change in electrification in thunderstorms. The increase of ice crystal diameter was the dominant contributor to the enhancement of electrification using the new parameterization. Additionally, unlike the structure of thunderclouds in a mature stage, which always retains a normal dipole structure adopting the empirical formula, a tripole structure developed a lower positive charge, and the polarity inversion with upper negative and lower positive charges occurred when the new parameterization was adopted. This predominately was the result of abundant ice crystals present below the reversal temperature. The electrification characteristics of thunderstorms may have a close connection with lightning activity. It has been found that charge structure changed significantly in the two cases, with the tripolar charge structure facilitating the production of inverted intra-cloud (IC) flashes and negative Cloud-to-ground (CG) flashes simulated by the new parameterization; additionally, clouds simulated using the empirical formula may be able to develop normal IC lightning and positive CG flashes. Therefore, it will be very meaningful to obtain greater insight into the characteristics of thunderstorms electrification in cumulus model with aerosols.

Aerosols in the central Arctic cryosphere: satellite and model integrated insights during Arctic spring and summer

Abstract. The central Arctic cryosphere is influenced by the Arctic amplification (AA) and is warming faster than the lower latitudes. AA affects the formation, loss, and transport of aerosols. Efforts to assess the underlying processes determining aerosol variability are currently limited due to the lack of ground-based and space-borne aerosol observations with high spatial coverage in this region. This study addresses the observational gap by making use of total aerosol optical depth (AOD) datasets retrieved by the AEROSNOW algorithm over the vast cryospheric region of the central Arctic during Arctic spring and summer. GEOS-Chem (GC) simulations combined with AEROSNOW-retrieved data are used to investigate the processes controlling aerosol loading and distribution at different temporal and spatial scales. For the first time, an integrated study of AOD over the Arctic cryosphere during sunlight conditions was possible with the AEROSNOW retrieval and GC simulations. The results show that the spatial patterns observed by AEROSNOW differ from those simulated by GC. During spring, which is characterized by long-range transport of anthropogenic aerosols in the Arctic, GC underestimates the AOD in the vicinity of Alaska in comparison with AEROSNOW retrieval. At the same time, it overestimates the AOD along the Bering Strait, northern Europe, and the Siberian central Arctic sea-ice regions, with differences of −12.3 % and 21.7 %, respectively. By contrast, GC consistently underestimates AOD compared with AEROSNOW in summer, when transport from lower latitudes is insignificant and local natural processes are the dominant source of aerosol, especially north of 70° N. This underestimation is particularly pronounced over the central Arctic sea-ice region, where it is −10.6 %. Conversely, GC tends to overestimate AOD along the Siberian and Greenland marginal sea-ice zones by 19.5 % but underestimates AOD along the Canadian Archipelago by −9.3 %. The differences in summer AOD between AEROSNOW data products and GC-simulated AOD highlight the need to integrate improved knowledge of the summer aerosol process into existing models in order to constrain its effects on cloud condensation nuclei, on ice nucleating particles, and on the radiation budget over the central Arctic sea ice during the developing AA period.