Note: When clicking on a Digital Object Identifier (DOI) number, you will be taken to an external site maintained by the publisher.
Some full text articles may not yet be available without a charge during the embargo (administrative interval).
What is a DOI Number?
Some links on this page may take you to non-federal websites. Their policies may differ from this site.
-
Abstract. The role of secondary organic aerosol (SOA) in atmospheric ice nucleation is not well understood, limiting accurate predictions of aerosol indirect effects in global climate simulations. This article details experiments performed to characterize the ice-nucleating properties of proxy SOA. Experimental techniques in conditioning aerosol to glass transition temperatures (Tg) as low as −70 °C using a pre-cooling unit are described. Ice nucleation measurements of proxy organosulfates (i.e., methyl, ethyl, and dodecyl sulfates) and citric acid were performed using the SPectrometer for ice nucleation (SPIN), operating at conditions relevant to upper-tropospheric cirrus temperatures (−45 °C, −40 °C, −35 °C) and ice saturation ratios (1.0<1.6). Methyl, ethyl, and dodecyl sulfates did not nucleate ice, despite dodecyl sulfate possessing a Tg higher than ambient temperature. Citric acid nucleated ice heterogeneously at −45 and −40 °C (1.2<1.4) but required pre-cooling temperatures of −70 °C, notably colder than the lowest published Tg. A kinetic flux model was used to numerically estimate water diffusion timescales to verify experimental observations and predict aerosol phase state. Diffusion modeling showed rapid liquefaction of glassy methyl and ethyl sulfates due to high hygroscopicity, preventing heterogeneous ice nucleation. The modeling results suggest that citric acid nucleated ice heterogeneously via deposition freezing or immersion freezing after surface liquefaction. We conclude that Tg alone is not sufficient for predicting heterogeneous ice formation for proxy SOA using the SPIN.more » « lessFree, publicly-accessible full text available January 1, 2026
-
Abstract. New particle formation (NPF) events are defined as asudden burst of aerosols followed by growth and can impact climate bygrowing to larger sizes and under proper conditions, potentially formingcloud condensation nuclei (CCN). Field measurements relating NPF and CCN arecrucial in expanding regional understanding of how aerosols impactclimate. To quantify the possible impact of NPF on CCN formation, it isimportant to not only maintain consistency when classifying NPF events butalso consider the proper timeframe for particle growth to CCN-relevantsizes. Here, we analyze 15 years of direct measurements of both aerosol sizedistributions and CCN concentrations and combine them with novel methods toquantify the impact of NPF on CCN formation at Storm Peak Laboratory (SPL),a remote, mountaintop observatory in Colorado. Using the new automaticmethod to classify NPF, we find that NPF occurs on 50 % of all daysconsidered in the study from 2006 to 2021, demonstrating consistency withprevious work at SPL. NPF significantly enhances CCN during the winter by afactor of 1.36 and during the spring by a factor of 1.54, which, when combined withprevious work at SPL, suggests the enhancement of CCN by NPF occurs on aregional scale. We confirm that events with persistent growth are common inthe spring and winter, while burst events are more common in the summer andfall. A visual validation of the automatic method was performed in thestudy. For the first time, results clearly demonstrate the significantimpact of NPF on CCN in montane North American regions and the potential forwidespread impact of NPF on CCN.more » « less
-
Abstract. A new inlet for studying the aerosol particles andhydrometeor residuals that compose mixed-phase clouds – the phaSeseParation Inlet for Droplets icE residuals and inteRstitial aerosolparticles (SPIDER) – is described here. SPIDER combines a large pumpedcounterflow virtual impactor (L-PCVI), a flow tube evaporation chamber, anda pumped counterflow virtual impactor (PCVI) to separate droplets, icecrystals (∼3–25 µm), and interstitial aerosolparticles for simultaneous sampling. Laboratory verification tests of eachindividual component and the composite SPIDER system were conducted.Transmission efficiency, evaporation, and ice crystals' survival weredetermined to show the capability of the system. The experiments show theSPIDER system can separate distinct cloud elements and interstitial aerosolparticles for subsequent analysis. As a field instrument, SPIDER will helpexplore the properties of different cloud elements and interstitial aerosolparticles in mixed-phase clouds.more » « less
An official website of the United States government
