Cloud condensation nuclei as a real source of ice forming nuclei in continental and marine air masses

1995 ◽  
Vol 38 (1-4) ◽  
pp. 351-359 ◽  
Author(s):  
J. Rosinski
Keyword(s):  
Cloud Condensation Nuclei ◽  
Condensation Nuclei ◽  
Air Masses ◽  
Marine Air

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 Biomass burning emissions of trace gases and particles in marine air at Cape Grim, Tasmania

2015 ◽  
Vol 15 (23) ◽  
pp. 13393-13411 ◽  
Author(s):  
S. J. Lawson ◽  
M. D. Keywood ◽  
I. E. Galbally ◽  
J. L. Gras ◽  
J. M. Cainey ◽  
...  
Keyword(s):  
Particle Size ◽  
Biomass Burning ◽  
Cloud Condensation Nuclei ◽  
Trace Gases ◽  
Particle Growth ◽  
Dominant Mode ◽  
Condensation Nuclei ◽  
Substantial Impact ◽  
Marine Air ◽  
Cape Grim

Abstract. Biomass burning (BB) plumes were measured at the Cape Grim Baseline Air Pollution Station during the 2006 Precursors to Particles campaign, when emissions from a fire on nearby Robbins Island impacted the station. Measurements made included non-methane organic compounds (NMOCs) (PTR-MS), particle number size distribution, condensation nuclei (CN) > 3 nm, black carbon (BC) concentration, cloud condensation nuclei (CCN) number, ozone (O3), methane (CH4), carbon monoxide (CO), hydrogen (H2), carbon dioxide (CO2), nitrous oxide (N2O), halocarbons and meteorology. During the first plume strike event (BB1), a 4 h enhancement of CO (max ~ 2100 ppb), BC (~ 1400 ng m-3) and particles > 3 nm (~ 13 000 cm-3) with dominant particle mode of 120 nm were observed overnight. A wind direction change lead to a dramatic reduction in BB tracers and a drop in the dominant particle mode to 50 nm. The dominant mode increased in size to 80 nm over 5 h in calm sunny conditions, accompanied by an increase in ozone. Due to an enhancement in BC but not CO during particle growth, the presence of BB emissions during this period could not be confirmed. The ability of particles > 80 nm (CN80) to act as CCN at 0.5 % supersaturation was investigated. The ΔCCN / ΔCN80 ratio was lowest during the fresh BB plume (56 ± 8 %), higher during the particle growth period (77 ± 4 %) and higher still (104 ± 3 %) in background marine air. Particle size distributions indicate that changes to particle chemical composition, rather than particle size, are driving these changes. Hourly average CCN during both BB events were between 2000 and 5000 CCN cm-3, which were enhanced above typical background levels by a factor of 6–34, highlighting the dramatic impact BB plumes can have on CCN number in clean marine regions. During the 29 h of the second plume strike event (BB2) CO, BC and a range of NMOCs including acetonitrile and hydrogen cyanide (HCN) were clearly enhanced and some enhancements in O3 were observed (ΔO3 / ΔCO 0.001–0.074). A short-lived increase in NMOCs by a factor of 10 corresponded with a large CO enhancement, an increase of the NMOC / CO emission ratio (ER) by a factor of 2–4 and a halving of the BC / CO ratio. Rainfall on Robbins Island was observed by radar during this period which likely resulted in a lower fire combustion efficiency, and higher emission of compounds associated with smouldering. This highlights the importance of relatively minor meteorological events on BB emission ratios. Emission factors (EFs) were derived for a range of trace gases, some never before reported for Australian fires, (including hydrogen, phenol and toluene) using the carbon mass balance method. This provides a unique set of EFs for Australian coastal heathland fires. Methyl halide EFs were higher than EFs reported from other studies in Australia and the Northern Hemisphere which is likely due to high halogen content in vegetation on Robbins Island. This work demonstrates the substantial impact that BB plumes can have on the composition of marine air, and the significant changes that can occur as the plume interacts with terrestrial, aged urban and marine emission sources.

scholarly journals Summer aerosol measurements over the East Antarctic seasonal ice zone

2021 ◽  
Vol 21 (12) ◽  
pp. 9497-9513
Author(s):  
Jack B. Simmons ◽  
Ruhi S. Humphries ◽  
Stephen R. Wilson ◽  
Scott D. Chambers ◽  
Alastair G. Williams ◽  
...  
Keyword(s):  
Southern Ocean ◽  
Atmospheric Circulation ◽  
Large Scale ◽  
Cloud Condensation Nuclei ◽  
Absolute Humidity ◽  
Condensation Nuclei ◽  
Atmospheric Measurements ◽  
Back Trajectories ◽  
Air Masses ◽  
Seasonal Ice Zone

Abstract. Aerosol measurements over the Southern Ocean have been identified as critical to an improved understanding of aerosol–radiation and aerosol–cloud interactions, as there currently exists significant discrepancies between model results and measurements in this region. The atmosphere above the Southern Ocean provides crucial insight into an aerosol regime relatively free from anthropogenic influence, yet its remoteness ensures atmospheric measurements are relatively rare. Here we present observations from the Polar Cell Aerosol Nucleation (PCAN) campaign, hosted aboard the RV Investigator during a summer (January–March) 2017 voyage from Hobart, Australia, to the East Antarctic seasonal sea ice zone. A median particle number concentration (condensation nuclei > 3 nm; CN3) of 354 (95 % CI 345–363) cm−3 was observed from the voyage. Median cloud condensation nuclei (CCN) concentrations were 167 (95 % CI 158–176) cm−3. Measured particle size distributions suggested that aerosol populations had undergone significant cloud processing. To understand the variability in aerosol observations, measurements were classified by meteorological variables. Wind direction and absolute humidity were used to identify different air masses, and aerosol measurements were compared based on these identifications. CN3 concentrations measured during SE wind directions (median 594 cm−3) were higher than those measured during wind directions from the NW (median 265 cm−3). Increased frequency of measurements from these wind directions suggests the influence of large-scale atmospheric transport mechanisms on the local aerosol population in the boundary layer of the East Antarctic seasonal ice zone. Modelled back trajectories imply different air mass histories for each measurement group, supporting this suggestion. CN3 and CCN concentrations were higher during periods where the absolute humidity was less than 4.3 gH2O/m3, indicative of free tropospheric or Antarctic continental air masses, compared to other periods of the voyage. Increased aerosol concentration in air masses originating close to the Antarctic coastline have been observed in numerous other studies. However, the smaller changes observed in the present analyses suggest seasonal differences in atmospheric circulation, including lesser impact of synoptic low-pressure systems in summer. Further measurements in the region are required before a more comprehensive picture of atmospheric circulation in this region can be captured and its influence on local aerosol populations understood.

scholarly journals Marine productivity and synoptic meteorology drive summer-time variability in Southern Ocean aerosols

2020 ◽  
Vol 20 (13) ◽  
pp. 8047-8062
Author(s):  
Joel Alroe ◽  
Luke T. Cravigan ◽  
Branka Miljevic ◽  
Graham R. Johnson ◽  
Paul Selleck ◽  
...  
Keyword(s):  
Southern Ocean ◽  
Cloud Condensation Nuclei ◽  
Large Diameter ◽  
Convective Transport ◽  
Sea Spray ◽  
Strong Wind ◽  
Condensation Nuclei ◽  
Air Mass ◽  
Air Masses ◽  
High Concentrations

Abstract. Cloud–radiation interactions over the Southern Ocean are not well constrained in climate models, in part due to uncertainties in the sources, concentrations, and cloud-forming potential of aerosol in this region. To date, most studies in this region have reported measurements from fixed terrestrial stations or a limited set of instrumentation and often present findings as broad seasonal or latitudinal trends. Here, we present an extensive set of aerosol and meteorological observations obtained during an austral summer cruise across the full width of the Southern Ocean south of Australia. Three episodes of continental-influenced air masses were identified, including an apparent transition between the Ferrel atmospheric cell and the polar cell at approximately 64∘ S, and accompanied by the highest median cloud condensation nuclei (CCN) concentrations, at 252 cm−3. During the other two episodes, synoptic-scale weather patterns diverted air masses across distances greater than 1000 km from the Australian and Antarctic coastlines, respectively, indicating that a large proportion of the Southern Ocean may be periodically influenced by continental air masses. In all three cases, a highly cloud-active accumulation mode dominated the size distribution, with up to 93 % of the total number concentration activating as CCN. Frequent cyclonic weather conditions were observed at high latitudes and the associated strong wind speeds led to predictions of high concentrations of sea spray aerosol. However, these modelled concentrations were not achieved due to increased aerosol scavenging rates from precipitation and convective transport into the free troposphere, which decoupled the air mass from the sea spray flux at the ocean surface. CCN concentrations were more strongly impacted by high concentrations of large-diameter Aitken mode aerosol in air masses which passed over regions of elevated marine biological productivity, potentially contributing up to 56 % of the cloud condensation nuclei concentration. Weather systems were vital for aerosol growth in biologically influenced air masses and in their absence ultrafine aerosol diameters were less than 30 nm. These results demonstrate that air mass meteorological history must be considered when modelling sea spray concentrations and highlight the potential importance of sub-grid-scale variability when modelling atmospheric conditions in the remote Southern Ocean.

scholarly journals Transformation of marine air masses in the Fennoscandian Boreal forest – changes in aerosol, humidity, and clouds

2021 ◽  
Author(s):  
Meri Räty ◽  
Larisa Sogacheva ◽  
Helmi-Marja Keskinen ◽  
Veli-Matti Kerminen ◽  
Tuukka Petäjä ◽  
...  
Keyword(s):  
Boreal Forest ◽  
Water Vapour ◽  
Cloud Condensation Nuclei ◽  
Source Region ◽  
Cloud Formation ◽  
Condensation Nuclei ◽  
Forest Environment ◽  
Transport Time ◽  
Air Mass ◽  
Air Masses

<p>Fennoscandian boreal forest is a region with commonly occurring particle formation, which benefits from the abundance of biogenic volatile organic compounds emitted by the vegetation. The same vegetation also regulates the exchange of water vapour between the ecosystem and the atmosphere. Thus, as the forest has the potential to provide the two components needed in cloud formation, i.e. condensation nuclei and humidity, there is reason to suspect consequent changes in air masses that are influenced by the forest below.</p><p>We investigated the link between boreal forest air mass transport and cloud related properties in air masses that arrived to the SMEAR II station (61°10’N, 24°17’E, 170m a.s.l.), Finland, from between western and norther directions. These selected air masses were originally marine and travelled only across a land area with relatively minor anthropogenic emissions sources, allowing us to focus on biogenic influences. The source region and the time each air mass spent above land before arrival, were determined from 96-hour long air mass back trajectories. We used a long-term comprehensive data sets, spanning up to 11 growing seasons (April-September, 2006-2016).</p><p>Air masses with short transport times over the forest, often coincided with measurements of particles in smaller size ranges. Higher numbers of larger cloud condensation nuclei sized particles became more common in air masses with longer transport times over the forest. Similarly, air masses that spent little time over land, were often relatively cool and carried less water vapour. Whereas, higher specific humidities were more likely in air masses with longer times spent over land, as associated warming had most likely facilitated an increased uptake of water vapour from plant evapotranspiration. We also observed corresponding moderate increases in satellite observed cloud optical thickness and in-situ measured precipitation. Air masses with very short transport times over land were an exception, as these fast-moving air masses are likely to be connected to weather fronts and therefore also have a high probability for clouds and precipitation. The reported differences between air masses more or less disappeared when the transport time over land reached approximately 60 hours, and any further increase in land transport time no longer caused a substantial change. This appears to be the time scale in which most of the forest environment’s influence on these cloud related properties is realised and a balance is reached.</p>

scholarly journals Air mass physiochemical characteristics over New Delhi: impacts on aerosol hygroscopicity and cloud condensation nuclei (CCN) formation

2020 ◽  
Vol 20 (11) ◽  
pp. 6953-6971 ◽  
Author(s):  
Zainab Arub ◽  
Sahil Bhandari ◽  
Shahzad Gani ◽  
Joshua S. Apte ◽  
Lea Hildebrandt Ruiz ◽  
...  
Keyword(s):  
Chemical Composition ◽  
Size Distribution ◽  
Cloud Condensation Nuclei ◽  
Chemical Properties ◽  
Industrial Emissions ◽  
Condensation Nuclei ◽  
Aerosol Composition ◽  
Time Resolved ◽  
Air Mass ◽  
Air Masses

Abstract. Delhi is a megacity subject to high local anthropogenic emissions and long-range transport of pollutants. This work presents for the first time time-resolved estimates of hygroscopicity parameter (κ) and cloud condensation nuclei (CCN), spanning for more than a year, derived from chemical composition and size distribution data. As a part of the Delhi Aerosol Supersite (DAS) campaign, the characterization of aerosol composition and size distribution was conducted from January 2017 to March 2018. Air masses originating from the Arabian Sea (AS), Bay of Bengal (BB), and southern Asia (SA) exhibited distinct characteristics of time-resolved sub-micron non-refractory PM1 (NRPM1) species, size distributions, and CCN number concentrations. The SA air mass had the highest NRPM1 loading with high chloride and organics, followed by the BB air mass, which was more contaminated than AS, with a higher organic fraction and nitrate. The primary sources were identified as biomass-burning, thermal power plant emissions, industrial emissions, and vehicular emissions. The average hygroscopicity parameter (κ), calculated by the mixing rule, was approximately 0.3 (varying between 0.13 and 0.77) for all the air masses (0.32±0.06 for AS, 0.31±0.06 for BB, and 0.32±0.10 for SA). The diurnal variations in κ were impacted by the chemical properties and thus source activities. The total, Aitken, and accumulation mode number concentrations were higher for SA, followed by BB and AS. The mean values of estimated CCN number concentration (NCCN; 3669–28926 cm−3) and the activated fraction (af; 0.19–0.87), for supersaturations varying from 0.1 % to 0.8 %, also showed the same trend, implying that these were highest in SA, followed by those in BB and then those in AS. The size turned out to be more important than chemical composition directly, and the NCCN was governed by either the Aitken or accumulation modes, depending upon the supersaturation (SS) and critical diameter (Dc). af was governed mainly by the geometric mean diameter (GMD), and such a high af (0.71±0.14 for the most dominant sub-branch of the SA air mass – R1 – at 0.4 % SS) has not been seen anywhere in the world for a continental site. The high af was a consequence of very low Dc (25–130 nm, for SS ranging from 0.1 % to 0.8 %) observed for Delhi. Indirectly, the chemical properties also impacted CCN and af by impacting the diurnal patterns of Aitken and accumulation modes, κ and Dc. The high-hygroscopic nature of aerosols, high NCCN, and high af can severely impact the precipitation patterns of the Indian monsoon in Delhi, impact the radiation budget, and have indirect effects and need to be investigated to quantify this impact.

scholarly journals Secondary new particle formation in Northern Finland Pallas site between the years 2000 and 2010

2011 ◽  
Vol 11 (24) ◽  
pp. 12959-12972 ◽  
Author(s):  
E. Asmi ◽  
N. Kivekäs ◽  
V.-M. Kerminen ◽  
M. Komppula ◽  
A.-P. Hyvärinen ◽  
...  
Keyword(s):  
Growth Rates ◽  
Cloud Condensation Nuclei ◽  
Cloud Droplet ◽  
Detailed Examination ◽  
Particle Formation ◽  
New Particle Formation ◽  
Air Masses ◽  
Event Frequency ◽  
Marine Air

Abstract. Secondary new particle formation affects atmospheric aerosol and cloud droplet numbers and thereby, the aerosol effects on climate. In this paper, the frequency of nucleation events and the associated particle formation and growth rates, along with their seasonal variation, was analysed based on over ten years of aerosol measurements conducted at the Pallas GAW station in northern Finland. The long-term measurements also allowed a detailed examination of factors possibly favouring or suppressing particle formation. Effects of meteorological parameters and air mass properties as well as vapour sources and sinks for particle formation frequency and event parameters were inspected. In addition, the potential of secondary particle formation to increase the concentration of cloud condensation nuclei (CCN) sized particles was examined. Findings from these long-term measurements confirmed previous observations: event frequency peaked in spring and the highest growth rates were observed in summer, affiliated with increased biogenic activity. Events were almost exclusively observed in marine air masses on sunny cloud-free days. A low vapour sink by the background particle population as well as an elevated sulphuric acid concentration were found to favour particle formation. These were also conditions taking place most likely in marine air masses. Inter-annual trend showed a minimum in event frequency in 2003, when also the smallest annual median of growth rate was observed. This gives further evidence of the importance and sensitivity of particle formation for the condensing vapour concentrations at Pallas site. The particle formation was observed to increase CCN80 (>80 nm particle number) concentrations especially in summer and autumn seasons when the growth rates were the highest. When the growing mode exceeded the selected 80 nm limit, on average in those cases, 211 ± 114% increase of CCN80 concentrations was observed.

scholarly journals Aerosol properties associated with air masses arriving into the North East Atlantic during the 2008 Mace Head EUCAARI intensive observing period: an overview

2010 ◽  
Vol 10 (17) ◽  
pp. 8413-8435 ◽  
Author(s):  
M. Dall'Osto ◽  
D. Ceburnis ◽  
G. Martucci ◽  
J. Bialek ◽  
R. Dupuy ◽  
...  
Keyword(s):  
Chemical Composition ◽  
Cloud Microphysics ◽  
Water Soluble ◽  
Research Station ◽  
Hygroscopic Growth ◽  
Condensation Nuclei ◽  
Air Masses ◽  
North East ◽  
Marine Air ◽  
Aerosol Properties

Abstract. As part of the EUCAARI Intensive Observing Period, a 4-week campaign to measure aerosol physical, chemical and optical properties, atmospheric structure, and cloud microphysics was conducted from mid-May to mid-June, 2008 at the Mace Head Atmospheric Research Station, located at the interface of Western Europe and the N. E. Atlantic and centered on the west Irish coastline. During the campaign, continental air masses comprising both young and aged continental plumes were encountered, along with polar, Arctic and tropical air masses. Polluted-continental aerosol concentrations were of the order of 3000 cm−3, while background marine air aerosol concentrations were between 400–600 cm−3. The highest marine air concentrations occurred in polar air masses in which a 15 nm nucleation mode, with concentration of 1100 cm−3, was observed and attributed to open ocean particle formation. Continental air submicron chemical composition (excluding refractory sea salt) was dominated by organic matter, closely followed by sulphate mass. Although the concentrations and size distribution spectral shape were almost identical for the young and aged continental cases, hygroscopic growth factors (GF) and cloud condensation nuclei (CCN) to total condensation nuclei (CN) concentration ratios were significantly less in the younger pollution plume, indicating a more oxidized organic component to the aged continental plume. The difference in chemical composition and hygroscopic growth factor appear to result in a 40–50% impact on aerosol scattering coefficients and Aerosol Optical Depth, despite almost identical aerosol microphysical properties in both cases, with the higher values been recorded for the more aged case. For the CCN/CN ratio, the highest ratios were seen in the more age plume. In marine air, sulphate mass dominated the sub-micron component, followed by water soluble organic carbon, which, in turn, was dominated by methanesulphonic acid (MSA). Sulphate concentrations were highest in marine tropical air – even higher than in continental air. MSA was present at twice the concentrations of previously-reported concentrations at the same location and the same season. Both continental and marine air exhibited aerosol GFs significantly less than ammonium sulphate aerosol pointing to a significant organic contribution to all air mass aerosol properties.

scholarly journals New Particle Formation at a High Altitude Site in India: Impact of Fresh Emissions and Long Range Transport

2018 ◽  
Author(s):  
Vyoma Singla ◽  
Subrata Mukherjee ◽  
Adam Kristensson ◽  
Govindan Pandithurai ◽  
Kundan K. Dani ◽  
...  
Keyword(s):  
High Altitude ◽  
Cloud Condensation Nuclei ◽  
Particle Formation ◽  
Western India ◽  
New Particle Formation ◽  
Condensation Nuclei ◽  
Air Masses ◽  
North East ◽  
The North ◽  
Inorganic Species

Abstract. There is a lack of characterization of the aerosol population in Western India, how it is affected by meteorological parameters, and new particle formation and the influence on cloud condensation nuclei (CCN). For this reason, measurements of particle number size distribution, aerosol chemical composition, meteorology and cloud condensation nuclei number concentration were monitored at High Altitude Cloud Physics Laboratory (HACPL) in Mahabaleshwar mountain town in Western India between November 2016 and February 2017. Most air masses in this period originated from the Indian continent to the north-east of HACPL. New particle formation (NPF) events were observed on 47 days and mainly associated with these north-easterly air masses and high SO2 emissions and biomass burning activities, while weaker or non-NPF days were associated with westerly air masses and relatively higher influence of local air pollution. The growth of newly formed particles enhanced the mass concentration of secondary organic and inorganic species of aerosol particles. The mean growth rate, formation rate, condensation sink and coagulation loss for the 13 strongest events was found to be 2.58 ± 0.38 nm h−1, 2.82 ± 1.37 cm−3 s−1, 22.3 ± 2.87 * 10-3 s−1 and 1.62 ± 1.04 cm−3 s−1 respectively. A closer examination of 5 events showed that low relative humidity and solar radiation favoured new particle formation. These NPF events lead to a significant increase in CCN concentration (mean ~ 53 ± 36 %). The NanoMap method revealed that NPF took place up to several hundred kilometers upwind and to the north-east of HACPL.

Sign in / Sign up

Export Citation Format

Share Document