scholarly journals Aerosol measurements at a high-elevation site: composition, size, and cloud condensation nuclei activity

2013 ◽  
Vol 13 (23) ◽  
pp. 11839-11851 ◽  
Author(s):  
B. Friedman ◽  
A. Zelenyuk ◽  
J. Beranek ◽  
G. Kulkarni ◽  
M. Pekour ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Single Particle ◽  
Temporal Evolution ◽  
Cloud Condensation Nuclei ◽  
High Elevation ◽  
Size Distributions ◽  
Condensation Nuclei ◽  
Particle Composition ◽  
Biomass Burning Particles ◽  
Aerosol Hygroscopicity

Abstract. Measurements of cloud condensation nuclei (CCN) concentrations, single particle composition and size distributions at a high-elevation research site from March 2011 are presented. The temporal evolution of detailed single particle composition is compared with changes in CCN activation on four days, two of which include new particle formation and growth events. Sulfate-containing particles dominated the single particle composition by number; biomass burning particles, sea salt particles, and particles containing organic components were also present. CCN activation largely followed the behavior of the sulfate-containing particle types; biomass burning particle types also likely contained hygroscopic material that impacted CCN activation. Newly formed particles also may contribute to CCN activation at higher supersaturation conditions. Derived aerosol hygroscopicity parameters from the size distribution and CCN concentration measurements are within the range of previous reports of remote continental kappa values.

scholarly journals Aerosol measurements at a high elevation site: composition, size, and cloud condensation nuclei activity

2013 ◽  
Vol 13 (7) ◽  
pp. 18277-18306 ◽  
Author(s):  
B. Friedman ◽  
A. Zelenyuk ◽  
J. Beránek ◽  
G. Kulkarni ◽  
M. Pekour ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Single Particle ◽  
Temporal Evolution ◽  
Cloud Condensation Nuclei ◽  
High Elevation ◽  
Size Distributions ◽  
Condensation Nuclei ◽  
Particle Composition ◽  
Biomass Burning Particles ◽  
Aerosol Hygroscopicity

Abstract. Measurements of cloud condensation nuclei (CCN) concentrations, single particle composition and size distributions at a high-elevation research site from March 2011 are presented. The temporal evolution of detailed single particle composition is compared with changes in CCN activation on four days, two of which include new particle formation and growth events. Sulfate-containing particles dominated the single particle composition by number; biomass burning particles, sea salt particles, and particles containing organic components also were present. CCN activation largely followed the behavior of the sulfate-containing particle types; biomass burning particle types also likely contained hygroscopic material that impacted CCN activation. Newly formed particles also may contribute to CCN activation at higher supersaturation conditions. Derived aerosol hygroscopicity parameters from the size distribution and CCN concentration measurements are within the range of previous reports of remote continental kappa values.

scholarly journals Aerosol hygroscopicity and cloud condensation nuclei activity during the AC<sup>3</sup>Exp campaign: implications for cloud condensation nuclei parameterization

2014 ◽  
Vol 14 (24) ◽  
pp. 13423-13437 ◽  
Author(s):  
F. Zhang ◽  
Y. Li ◽  
Z. Li ◽  
L. Sun ◽  
R. Li ◽  
...  
Keyword(s):  
Cloud Condensation Nuclei ◽  
Particle Diameter ◽  
Condensation Nuclei ◽  
Particle Composition ◽  
Particle Activation ◽  
Heavy Pollution ◽  
Pollution Events ◽  
Aerosol Hygroscopicity

Abstract. Aerosol hygroscopicity and cloud condensation nuclei (CCN) activity under background conditions and during pollution events are investigated during the Aerosol-CCN-Cloud Closure Experiment (AC3Exp) campaign conducted at Xianghe, China in summer 2013. A gradual increase in size-resolved activation ratio (AR) with particle diameter (Dp) suggests that aerosol particles have different hygroscopicities. During pollution events, the activation diameter (Da) measured at low supersaturation (SS) was significantly increased compared to background conditions. An increase was not observed when SS was > 0.4%. The hygroscopicity parameter (κ) was ~ 0.31–0.38 for particles in accumulation mode under background conditions. This range in magnitude of κ was ~ 20%, higher than κ derived under polluted conditions. For particles in nucleation or Aitken mode, κ ranged from 0.20–0.34 for background and polluted cases. Larger particles were on average more hygroscopic than smaller particles. The situation was more complex for heavy pollution particles because of the diversity in particle composition and mixing state. A non-parallel observation CCN closure test showed that uncertainties in CCN number concentration estimates ranged from 30–40%, which are associated with changes in particle composition as well as measurement uncertainties associated with bulk and size-resolved CCN methods. A case study showed that bulk CCN activation ratios increased as total condensation nuclei (CN) number concentrations (NCN) increased on background days. The background case also showed that bulk AR correlated well with the hygroscopicity parameter calculated from chemical volume fractions. On the contrary, bulk AR decreased with increasing total NCN during pollution events, but was closely related to the fraction of the total organic mass signal at m/z 44 (f44), which is usually associated with the particle's organic oxidation level. Our study highlights the importance of chemical composition in determining particle activation properties and underlines the significance of long-term observations of CCN under different atmospheric environments, especially regions with heavy pollution.

scholarly journals In Situ Chemical Characterization of Aged Biomass-Burning Aerosols Impacting Cold Wave Clouds

2010 ◽  
Vol 67 (8) ◽  
pp. 2451-2468 ◽  
Author(s):  
Kerri A. Pratt ◽  
Andrew J. Heymsfield ◽  
Cynthia H. Twohy ◽  
Shane M. Murphy ◽  
Paul J. DeMott ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Biomass Burning ◽  
Single Particle ◽  
Cloud Condensation Nuclei ◽  
Chemical Characterization ◽  
Cloud Droplet ◽  
Cloud Microphysics ◽  
Particle Mass ◽  
Cold Wave ◽  
Biomass Burning Particles

Abstract During the Ice in Clouds Experiment–Layer Clouds (ICE-L), aged biomass-burning particles were identified within two orographic wave cloud regions over Wyoming using single-particle mass spectrometry and electron microscopy. Using a suite of instrumentation, particle chemistry was characterized in tandem with cloud microphysics. The aged biomass-burning particles comprised ∼30%–40% by number of the 0.1–1.0-μm clear-air particles and were composed of potassium, organic carbon, elemental carbon, and sulfate. Aerosol mass spectrometry measurements suggested these cloud-processed particles were predominantly sulfate by mass. The first cloud region sampled was characterized by primarily homogeneously nucleated ice particles formed at temperatures near −40°C. The second cloud period was characterized by high cloud droplet concentrations (∼150–300 cm−3) and lower heterogeneously nucleated ice concentrations (7–18 L−1) at cloud temperatures of −24° to −25°C. As expected for the observed particle chemistry and dynamics of the observed wave clouds, few significant differences were observed between the clear-air particles and cloud residues. However, suggestive of a possible heterogeneous nucleation mechanism within the first cloud region, ice residues showed enrichments in the number fractions of soot and mass fractions of black carbon, measured by a single-particle mass spectrometer and a single-particle soot photometer, respectively. In addition, enrichment of biomass-burning particles internally mixed with oxalic acid in both the homogeneously nucleated ice and cloud droplets compared to clear air suggests either preferential activation as cloud condensation nuclei or aqueous phase cloud processing.

scholarly journals Hygroscopic properties and cloud condensation nuclei activity of atmospheric aerosols under the influences of Asian continental outflow and new particle formation at a coastal site in eastern Asia

2020 ◽  
Vol 20 (10) ◽  
pp. 5911-5922 ◽  
Author(s):  
Hing Cho Cheung ◽  
Charles Chung-Kuang Chou ◽  
Celine Siu Lan Lee ◽  
Wei-Chen Kuo ◽  
Shuenn-Chin Chang
Keyword(s):  
Chemical Composition ◽  
Cloud Condensation Nuclei ◽  
Particle Formation ◽  
Number Concentration ◽  
Pollution Sources ◽  
New Particle Formation ◽  
Condensation Nuclei ◽  
Air Masses ◽  
Hygroscopic Properties ◽  
Aerosol Hygroscopicity

Abstract. The chemical composition of fine particulate matter (PM2.5), the size distribution and number concentration of aerosol particles (NCN), and the number concentration of cloud condensation nuclei (NCCN) were measured at the northern tip of Taiwan during an intensive observation experiment from April 2017 to March 2018. The parameters of aerosol hygroscopicity (i.e., activation ratio, activation diameter and kappa of CCN) were retrieved from the measurements. Significant variations were found in the hygroscopicity of aerosols (kappa – κ – of 0.18–0.56, for water vapor supersaturation – SS – of 0.12 %–0.80 %), which were subject to various pollution sources, including aged air pollutants originating in eastern and northern China and transported by the Asian continental outflows and fresh particles emitted from local sources and distributed by land–sea breeze circulations as well as produced by processes of new particle formation (NPF). Cluster analysis was applied to the back trajectories of air masses to investigate their respective source regions. The results showed that aerosols associated with Asian continental outflows were characterized by lower NCN and NCCN values and by higher kappa values of CCN, whereas higher NCN and NCCN values with lower kappa values of CCN were observed in the aerosols associated with local air masses. Besides, it was revealed that the kappa value of CCN exhibited a decrease during the early stage of an event of new particle formation, which turned to an increasing trend over the later period. The distinct features in the hygroscopicity of aerosols were found to be consistent with the characteristics in the chemical composition of PM2.5. This study has depicted a clear seasonal characteristic of hygroscopicity and CCN activity under the influence of a complex mixture of pollutants from different regional and/or local pollution sources. Nevertheless, the mixing state and chemical composition of the aerosols critically influence the aerosol hygroscopicity, and further investigations are necessary to elucidate the atmospheric processing involved in the CCN activation in coastal areas.

scholarly journals Estimating cloud condensation nuclei number concentrations using aerosol optical properties: role of particle number size distribution and parameterization

2019 ◽  
Vol 19 (24) ◽  
pp. 15483-15502 ◽  
Author(s):  
Yicheng Shen ◽  
Aki Virkkula ◽  
Aijun Ding ◽  
Krista Luoma ◽  
Helmi Keskinen ◽  
...  
Keyword(s):  
Optical Properties ◽  
Size Distribution ◽  
Cloud Condensation Nuclei ◽  
Size Distributions ◽  
Condensation Nuclei ◽  
Aerosol Optical Properties ◽  
Average Bias ◽  
Angstrom Exponent ◽  
Ångström Exponent ◽  
Ångstrom Exponent

Abstract. The concentration of cloud condensation nuclei (CCN) is an essential parameter affecting aerosol–cloud interactions within warm clouds. Long-term CCN number concentration (NCCN) data are scarce; there are a lot more data on aerosol optical properties (AOPs). It is therefore valuable to derive parameterizations for estimating NCCN from AOP measurements. Such parameterizations have already been made, and in the present work a new parameterization is presented. The relationships between NCCN, AOPs, and size distributions were investigated based on in situ measurement data from six stations in very different environments around the world. The relationships were used for deriving a parameterization that depends on the scattering Ångström exponent (SAE), backscatter fraction (BSF), and total scattering coefficient (σsp) of PM10 particles. The analysis first showed that the dependence of NCCN on supersaturation (SS) can be described by a logarithmic fit in the range SS <1.1 %, without any theoretical reasoning. The relationship between NCCN and AOPs was parameterized as NCCN≈((286±46)SAE ln(SS/(0.093±0.006))(BSF − BSFmin) + (5.2±3.3))σsp, where BSFmin is the minimum BSF, in practice the 1st percentile of BSF data at a site to be analyzed. At the lowest supersaturations of each site (SS ≈0.1 %), the average bias, defined as the ratio of the AOP-derived and measured NCCN, varied from ∼0.7 to ∼1.9 at most sites except at a Himalayan site where the bias was >4. At SS >0.4 % the average bias ranged from ∼0.7 to ∼1.3 at most sites. For the marine-aerosol-dominated site Ascension Island the bias was higher, ∼1.4–1.9. In other words, at SS >0.4 % NCCN was estimated with an average uncertainty of approximately 30 % by using nephelometer data. The biases were mainly due to the biases in the parameterization related to the scattering Ångström exponent (SAE). The squared correlation coefficients between the AOP-derived and measured NCCN varied from ∼0.5 to ∼0.8. To study the physical explanation of the relationships between NCCN and AOPs, lognormal unimodal particle size distributions were generated and NCCN and AOPs were calculated. The simulation showed that the relationships of NCCN and AOPs are affected by the geometric mean diameter and width of the size distribution and the activation diameter. The relationships of NCCN and AOPs were similar to those of the observed ones.

scholarly journals Classification of aerosol population type and cloud condensation nuclei properties in a coastal California littoral environment using an unsupervised cluster model

2019 ◽  
Author(s):  
Samuel A. Atwood ◽  
Sonia M. Kreidenweis ◽  
Paul J. DeMott ◽  
Markus D. Petters ◽  
Gavin C. Cornwell ◽  
...  
Keyword(s):  
Cluster Model ◽  
Particle Number ◽  
Cloud Condensation Nuclei ◽  
Sea Breeze ◽  
Northern Coast ◽  
Size Distributions ◽  
Condensation Nuclei ◽  
Entire Study ◽  
Total Particle Number ◽  
Total Particle

Abstract. Aerosol particle and cloud condensation nuclei (CCN) measurements from a littoral location on the northern coast of California at Bodega Bay Marine Laboratory (BML) are presented for approximately six weeks of observations during the CalWater-2015 field campaign. A combination of aerosol microphysical and meteorological parameters was used to classify variability in the properties of the BML surface aerosol using a K-means cluster model. Eight aerosol population types were identified that were associated with a range of impacts from both marine and terrestrial sources. Average measured total particle number concentrations, size distributions, hygroscopicities, and activated fraction spectra between 0.08 % and 1.1 % supersaturation are given for each of the identified aerosol population types, along with meteorological observations and transport pathways during time periods associated with each type. Five terrestrially influenced aerosol population types represented different degrees of aging of the continental outflow from the coast and interior of California and their appearance at the BML site was often linked to changes in wind direction and transport pathway. In particular, distinct aerosol populations, associated with diurnal variations in source region induced by land/sea-breeze shifts, were classified by the clustering technique. A terrestrial type representing fresh emissions, and/or a recent new particle formation event, occurred in approximately 10 % of the observations. Over the entire study period, three marine influenced population types were identified that typically occurred when the regular diurnal land/sea-breeze cycle collapsed and BML was continuously ventilated by air masses from marine regions for multiple days. These marine types differed from each other primarily in the degree of cloud processing evident in the size distributions, and in the presence of an additional large-particle mode for the type associated with the highest wind speeds. One of the marine types was associated with a multi-day period during which an atmospheric river made landfall at BML. The generally higher total particle number concentrations but lower activated fractions of four of the terrestrial types yielded similar CCN number concentrations to two of the marine types for supersaturations below about 0.4 %. Despite quite different activated fraction spectra, the two remaining marine and terrestrial types had CCN spectral number concentrations very similar to each other, due in part to higher number concentrations associated with the terrestrial type.

scholarly journals Simultaneous measurements of aerosol size distributions at three sites in the European high Arctic

2019 ◽  
Vol 19 (11) ◽  
pp. 7377-7395 ◽  
Author(s):  
Manuel Dall'Osto ◽  
David C. S. Beddows ◽  
Peter Tunved ◽  
Roy M. Harrison ◽  
Angelo Lupi ◽  
...  
Keyword(s):  
Cluster Analysis ◽  
Cloud Condensation Nuclei ◽  
High Arctic ◽  
The Arctic ◽  
Research Station ◽  
Size Distributions ◽  
Aerosol Formation ◽  
Condensation Nuclei ◽  
Main Mode ◽  
Accumulation Mode

Abstract. Aerosols are an integral part of the Arctic climate system due to their direct interaction with radiation and indirect interaction through cloud formation. Understanding aerosol size distributions and their dynamics is crucial for the ability to predict these climate relevant effects. When of favourable size and composition, both long-range-transported – and locally formed particles – may serve as cloud condensation nuclei (CCN). Small changes of composition or size may have a large impact on the low CCN concentrations currently characteristic of the Arctic environment. We present a cluster analysis of particle size distributions (PSDs; size range 8–500 nm) simultaneously collected from three high Arctic sites during a 3-year period (2013–2015). Two sites are located in the Svalbard archipelago: Zeppelin research station (ZEP; 474 m above ground) and the nearby Gruvebadet Observatory (GRU; about 2 km distance from Zeppelin, 67 m above ground). The third site (Villum Research Station at Station Nord, VRS; 30 m above ground) is 600 km west-northwest of Zeppelin, at the tip of north-eastern Greenland. The GRU site is included in an inter-site comparison for the first time. K-means cluster analysis provided eight specific aerosol categories, further combined into broad PSD classes with similar characteristics, namely pristine low concentrations (12 %–14 % occurrence), new particle formation (16 %–32 %), Aitken (21 %–35 %) and accumulation (20 %–50 %). Confined for longer time periods by consolidated pack sea ice regions, the Greenland site GRU shows PSDs with lower ultrafine-mode aerosol concentrations during summer but higher accumulation-mode aerosol concentrations during winter, relative to the Svalbard sites. By association with chemical composition and cloud condensation nuclei properties, further conclusions can be derived. Three distinct types of accumulation-mode aerosol are observed during winter months. These are associated with sea spray (largest detectable sizes, >400 nm), Arctic haze (main mode at 150 nm) and aged accumulation-mode (main mode at 220 nm) aerosols. In contrast, locally produced particles, most likely of marine biogenic origin, exhibit size distributions dominated by the nucleation and Aitken mode during summer months. The obtained data and analysis point towards future studies, including apportioning the relative contribution of primary and secondary aerosol formation processes and elucidating anthropogenic aerosol dynamics and transport and removal processes across the Greenland Sea. In order to address important research questions in the Arctic on scales beyond a singular station or measurement events, it is imperative to continue strengthening international scientific cooperation.

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