The connection of atmospheric new particle formation to fair-weather Earth-atmosphere electric field

2020 ◽  
Author(s):  
Xuemeng Chen ◽  
Susana Barbosa ◽  
Antti Mäkelä ◽  
Jussi Paatero ◽  
Catarina Monteiro ◽  
...  
Keyword(s):  
Electric Field ◽  
Aerosol Particles ◽  
Global Radiation ◽  
Weather Conditions ◽  
Particle Formation ◽  
Earth Atmosphere ◽  
New Particle Formation ◽  
Fair Weather ◽  
Air Ions ◽  
The Earth

<p>Atmospheric new particle formation (NPF) generates secondary aerosol particles into the lower atmosphere via gas-to-particle phase transition. Secondary aerosol particles dominate the total particle number concentration and are an important source for cloud condensation nuclei <sup>[1]</sup>. NPF typically begins with clustering among gaseous molecules. Once the newly formed clusters attain a size larger than the critical cluster size (~1.5 nm), their growth to larger sizes is energetically favoured and eventually they become nanoparticles <sup>[2]</sup>. NPF is often observed with the participation of air ions <sup>[3]</sup> and sometimes is induced by ions <sup>[4]</sup>. Air ions are a constituent of atmospheric electricity. The presence of the Earth-atmosphere electric field poses an electrical force on air ions. The earth-atmosphere electric field exhibits variability at different time scales under fair-weather conditions <sup>[5]</sup>. It is therefore interesting to understand whether the Earth-atmosphere electric field influences atmospheric new particle formation.</p><p>We analysed the Earth-atmosphere electric field together with the number size distribution data of air ions and aerosol particles under fair-weather conditions measured at Hyytiälä SMEAR II station in Southern Finland <sup>[6]</sup>. The electric field were measured by two Campbell CS 110 field mills in parallel. Air ion data were obtained with a Balance Scanning Mobility Analyser (BSMA) and a Neutral and Air Ion Spectrometer (NAIS), and aerosol particle data with a Differential Mobility Particle Sizer (DMPS). We used condensation Sinks (CS) derived from the DMPS measurement, air temperature, relative humidity, wind speed, global radiation as well as brightness derived from the global radiation measurement to assist the analysis. The measured earth-atmosphere electric field on NPF days was higher than on non-NPF days. We found that under low CS conditions, the electric field can enhance the formation of 1.7-3 nm air ions, but the concentration of 1.7-3 nm ions decreased with an increasing electric field under high CS conditions.</p><p>References:</p><p>[1]       Kerminen V.-M. et al., Environ. Res. Lett. <strong>2018</strong>, 13, 103003.</p><p>[2]       Kulmala M. et al., Science <strong>2013</strong>, 339, 943-946.</p><p>[3]       Manninen H. E. et al., Atmos. Chem. Phys. <strong>2010</strong>, 10, 7907-7927.</p><p>[4]       Jokinen T. et al., Science Advances <strong>2018</strong>, 4, eaat9744.</p><p>[5]       Bennett A. J., Harrison R. G., Journal of Physics: Conference Series <strong>2008</strong>, 142, 012046.</p><p>[6]       Hari P., Kulmala M., Boreal Environ. Res. <strong>2005</strong>, 10, 315-322.</p>

scholarly journals Concentrations and fluxes of aerosol particles during the LAPBIAT measurement campaign at Värriö field station

2007 ◽  
Vol 7 (14) ◽  
pp. 3683-3700 ◽  
Author(s):  
T. M. Ruuskanen ◽  
M. Kaasik ◽  
P. P. Aalto ◽  
U. Hõrrak ◽  
M. Vana ◽  
...  
Keyword(s):  
Kola Peninsula ◽  
Aerosol Particle ◽  
Aerosol Particles ◽  
Particle Formation ◽  
Nucleation Event ◽  
New Particle Formation ◽  
Air Ions ◽  
Field Station ◽  
Air Mass ◽  
Measurement Campaign

Abstract. The LAPBIAT measurement campaign took place in the Värriö SMEAR I measurement station located in Eastern Lapland in the spring of 2003 between 26 April and 11 May. In this paper we describe the measurement campaign, concentrations and fluxes of aerosol particles, air ions and trace gases, paying special attention to an aerosol particle formation event broken by a air mass change from a clean Arctic air mass with new particle formation to polluted one approaching from industrial areas of Kola Peninsula, Russia, lacking new particle formation. Aerosol particle number flux measurements show strong downward fluxes during that time. Concentrations of coarse aerosol particles were high for 1–2 days before the nucleation event (i.e. 28–29 April), very low immediately before and during the observed aerosol particle formation event (30 April) and increased moderately from the moment of sudden break of the event. In general particle deposition measurements based on snow samples show the same changes. Measurements of the mobility distribution of air ions showed elevated concentrations of intermediate air ions during the particle formation event. We estimated the growth rates in the nucleation mode size range. For particles <10 nm, the growth rate increases with size on 30 April. Dispersion modelling made with model SILAM support the conclusion that the nucleation event was interrupted by an outbreak of sulphate-rich air mass in the evening of 30 April that originated from the industry at Kola Peninsula, Russia. The results of this campaign highlight the need for detailed research in atmospheric transport of air constituents for understanding the aerosol dynamics.

scholarly journals Hygroscopic properties of ultrafine aerosol particles in the boreal forest: diurnal variation, solubility and the influence of sulfuric acid

2007 ◽  
Vol 7 (1) ◽  
pp. 211-222 ◽  
Author(s):  
M. Ehn ◽  
T. Petäjä ◽  
H. Aufmhoff ◽  
P. Aalto ◽  
K. Hämeri ◽  
...  
Keyword(s):  
Sulfuric Acid ◽  
Boreal Forest ◽  
Diurnal Variation ◽  
Gas Phase ◽  
Aerosol Particles ◽  
Particle Formation ◽  
Time Of Day ◽  
New Particle Formation ◽  
Hygroscopic Growth ◽  
Hygroscopic Properties

Abstract. The hygroscopic growth of aerosol particles present in a boreal forest was measured at a relative humidity of 88%. Simultaneously the gas phase concentration of sulfuric acid, a very hygroscopic compound, was monitored. The focus was mainly on days with new particle formation by nucleation. The measured hygroscopic growth factors (GF) correlated positively with the gaseous phase sulfuric acid concentrations. The smaller the particles, the stronger the correlation, with r=0.20 for 50 nm and r=0.50 for 10 nm particles. The increase in GF due to condensing sulfuric acid is expected to be larger for particles with initially smaller masses. During new particle formation, the changes in solubility of the new particles were calculated during their growth to Aitken mode sizes. As the modal diameter increased, the solubility of the particles decreased. This indicated that the initial particle growth was due to more hygroscopic compounds, whereas the later growth during the evening and night was mainly caused by less hygroscopic or even hydrophobic compounds. For all the measured sizes, a diurnal variation in GF was observed both during days with and without particle formation. The GF was lowest at around midnight, with a mean value of 1.12–1.24 depending on particle size and if new particle formation occurred during the day, and increased to 1.25–1.34 around noon. This can be tentatively explained by day- and nighttime gas-phase chemistry; different vapors will be present depending on the time of day, and through condensation these compounds will alter the hygroscopic properties of the particles in different ways.

scholarly journals Atmospheric electric field in the Atlantic marine boundary layer: first results from the SAIL project

2020 ◽  
Author(s):  
Susana Barbosa ◽  
Mauricio Camilo ◽  
Carlos Almeida ◽  
José Almeida ◽  
Guilherme Amaral ◽  
...  
Keyword(s):  
Boundary Layer ◽  
Electric Field ◽  
Marine Boundary Layer ◽  
Weather Conditions ◽  
Cape Verde ◽  
The Other ◽  
Atmospheric Electric Field ◽  
Fair Weather ◽  
Near Surface ◽  
First Results

&lt;p&gt;&lt;span&gt;The study of the electrical properties of the atmospheric marine boundary layer is important as the effect of natural radioactivity in driving near surface ionisation is significantly reduced over the ocean, and the concentration of aerosols is also typically lower than over continental areas, allowing a clearer examination of space-atmosphere interactions. Furthermore, cloud cover over the ocean is dominated by low-level clouds and most of the atmospheric charge lies near the earth surface, at low altitude cloud tops. &lt;/span&gt;&lt;/p&gt;&lt;p&gt;&lt;span&gt;The relevance of electric field observations in the marine boundary layer is enhanced by the the fact that the electrical conductivity of the ocean air is clearly linked to global atmospheric pollution and aerosol content. The increase in aerosol pollution since the original observations made in the early 20th century by the survey ship Carnegie is a pressing and timely motivation for modern measurements of the atmospheric electric field in the marine boundary layer. Project SAIL (Space-Atmosphere-Ocean Interactions in the marine boundary Layer) addresses this challenge by means of an unique monitoring campaign on board the ship-rigged sailing ship NRP Sagres during its 2020 circumnavigation expedition. &lt;/span&gt;&lt;/p&gt;&lt;p&gt;&lt;span&gt;The Portuguese Navy ship NRP Sagres departed from Lisbon on January 5th in a journey around the globe that will take 371 days. Two identical field mill sensors (CS110, Campbell Scientific) are installed &lt;/span&gt;&lt;span&gt;o&lt;/span&gt;&lt;span&gt;n the mizzen mast, one at a height of 22 m, and the other at a height of 5 meters. &lt;/span&gt;&lt;span&gt;A visibility sensor (SWS050, Biral) was also set-up on the same mast in order to have measurements of the extinction coefficient of the atmosphere and assess fair-weather conditions.&lt;/span&gt;&lt;span&gt; Further observations include gamma radiation measured with a NaI(Tl) scintillator from 475 keV to 3 MeV, cosmic radiation up to 17 MeV, and atmospheric ionisation from a cluster ion counter (Airel). The&lt;/span&gt;&lt;span&gt; 1 Hz measurements of the atmospheric electric field&lt;/span&gt;&lt;span&gt; and from all the other sensors&lt;/span&gt;&lt;span&gt; are &lt;/span&gt;&lt;span&gt;linked to the same rigorous temporal reference frame and precise positioning through kinematic GNSS observations. &lt;/span&gt;&lt;/p&gt;&lt;p&gt;&lt;span&gt;Here the first results of the SAIL project will be presented, focusing on fair-weather electric field over the Atlantic. The observations obtained in the first three sections of the circumnavigation journey, including Lisbon (Portugal) - Tenerife (Spain), from 5 to 10 January, Tenerife - Praia (Cape Verde) from 13 to 19 January, and across the Atlantic from Cape Verde to Rio de Janeiro (Brasil), from January 22nd to February 14th, will be presented and discussed.&lt;/span&gt;&lt;/p&gt;

scholarly journals New insights into nocturnal nucleation

2012 ◽  
Vol 12 (9) ◽  
pp. 4297-4312 ◽  
Author(s):  
I. K. Ortega ◽  
T. Suni ◽  
M. Boy ◽  
T. Grönholm ◽  
H. E. Manninen ◽  
...  
Keyword(s):  
Quantum Chemical ◽  
Aerosol Particles ◽  
Particle Formation ◽  
Nucleation And Growth ◽  
Oxidation Products ◽  
New Particle Formation ◽  
Aerosol Dynamics ◽  
Different Types ◽  
Consistent Manner ◽  
Dynamics Models

Abstract. Formation of new aerosol particles by nucleation and growth is a significant source of aerosols in the atmosphere. New particle formation events usually take place during daytime, but in some locations they have been observed also at night. In the present study we have combined chamber experiments, quantum chemical calculations and aerosol dynamics models to study nocturnal new particle formation. All our approaches demonstrate, in a consistent manner, that the oxidation products of monoterpenes play an important role in nocturnal nucleation events. By varying the conditions in our chamber experiments, we were able to reproduce the very different types of nocturnal events observed earlier in the atmosphere. The exact strength, duration and shape of the events appears to be sensitive to the type and concentration of reacting monoterpenes, as well as the extent to which the monoterpenes are exposed to ozone and potentially other atmospheric oxidants.

Studying new particle formation from chemical emissions from sea surface using  ship-borne air-sea-interaction tanks

2021 ◽  
Author(s):  
Maija Peltola ◽  
Manon Rocco ◽  
Neill Barr ◽  
Erin Dunne ◽  
James Harnwell ◽  
...  
Keyword(s):  
Marine Biology ◽  
Cloud Condensation Nuclei ◽  
Aerosol Particles ◽  
Chemical Species ◽  
Particle Formation ◽  
Biological Properties ◽  
The European Union ◽  
New Particle Formation ◽  
Aerosol Formation ◽  
Horizon 2020

&lt;p&gt;Even though oceans cover over 70% of the Earth&amp;#8217;s surface, the ways in which oceans interact with climate are not fully known. Marine micro-organisms such as phytoplankton can play an important role in regulating climate by releasing different chemical species into air. In air these chemical species can react and form new aerosol particles. If grown to large enough sizes, aerosols can influence climate by acting as cloud condensation nuclei which influence the formation and properties of clouds. Even though a connection of marine biology and climate through aerosol formation was first proposed already over 30 years ago, the processes related to this connection are still uncertain.&lt;/p&gt;&lt;p&gt;To unravel how seawater properties affect aerosol formation and to identify which chemical species are responsible for aerosol formation, we built two Air-Sea-Interaction Tanks (ASIT) that isolate 1000 l of seawater and 1000 l of air directly above the water. The used seawater was collected from different locations during a ship campaign on board the R/V Tangaroa in the South West Pacific Ocean, close to Chatham Rise, east of New Zealand. Seawater from one location was kept in the tanks for 2-3 days and then changed. By using seawater collected from different locations, we could obtain water with different biological populations. To monitor the seawater, we took daily samples to determine its chemical and biological properties.&lt;/p&gt;&lt;p&gt;The air in the tanks was continuously flushed with particle filtered air. This way the air had on average 40 min to interact with the seawater surface before being sampled. Our air sampling was continuous and consisted of aerosol and air chemistry measurements. The instrumentation included measurements of aerosol number concentration from 1 to 500 nm and&amp;#160; chemical species ranging from ozone and sulphur dioxide to volatile organic compounds and chemical composition of molecular clusters.&lt;/p&gt;&lt;p&gt;Joining the seawater and atmospheric data together can give us an idea of what chemical species are emitted from the water into the atmosphere and whether these species can form new aerosol particles. Our preliminary results show a small number of particles in the freshly nucleated size range of 1-3 nm in the ASIT headspaces, indicating that new aerosol particles can form in the ASIT headspaces. In this presentation, we will also explore which chemical species could be responsible for aerosol formation and which plankton groups could be related to the emissions of these species. Combining these results with ambient data and modelling work can shed light on how important new particle formation from marine sources is for climate.&lt;/p&gt;&lt;p&gt;Acknowledgements: Sea2Cloud project is funded by European Research Council (ERC) under the European Union&amp;#8217;s Horizon 2020 research and innovation programme (Grant agreement No. 771369).&lt;/p&gt;

scholarly journals Formation and characteristics of ions and charged aerosol particles in a native Australian Eucalypt forest

2008 ◽  
Vol 8 (1) ◽  
pp. 129-139 ◽  
Author(s):  
T. Suni ◽  
M. Kulmala ◽  
A. Hirsikko ◽  
T. Bergman ◽  
L. Laakso ◽  
...  
Keyword(s):  
Growth Rates ◽  
Aerosol Particles ◽  
Particle Formation ◽  
Cluster Ions ◽  
Native Forest ◽  
New Particle Formation ◽  
Aerosol Formation ◽  
Eucalypt Forest ◽  
The World ◽  
Strong Source

Abstract. Biogenic aerosol formation is likely to contribute significantly to the global aerosol load. In recent years, new-particle formation has been observed in various ecosystems around the world but hardly any measurements have taken place in the terrestrial Southern Hemisphere. Here, we report the first results of atmospheric ion and charged particle concentrations as well as of new-particle formation in a Eucalypt forest in Tumbarumba, South-East Australia, from July 2005 to October 2006. The measurements were carried out with an Air Ion Spectrometer (AIS) with a size range from 0.34 to 40 nm. The Eucalypt forest was a very strong source of new aerosol particles. Daytime aerosol formation took place on 52% of days with acceptable data, which is 2–3 times as often as in the Nordic boreal zone. Average growth rates for negative/positive 1.5–3 nm particles during these formation events were 2.89/2.68 nmh−1, respectively; for 3-7 nm particles 4.26/4.03, and for 7–20 nm particles 8.90/7.58 nmh−1, respectively. The growth rates for large ions were highest when the air was coming from the native forest which suggests that the Eucalypts were a strong source of condensable vapours. Average concentrations of cluster ions (0.34–1.8 nm) were 2400/1700 cm−3 for negative/positive ions, very high compared to most other measurements around the world. One reason behind these high concentrations could be the strong radon efflux from the soils around the Tumbarumba field site. Furthermore, comparison between night-time and daytime concentrations supported the view that cluster ions are produced close to the surface within the boundary layer also at night but that large ions are mostly produced in daytime. Finally, a previously unreported phenomenon, nocturnal aerosol formation, appeared in 32% of the analysed nights but was clustered almost entirely within six months from summer to autumn in 2006. From January to May, nocturnal formation was 2.5 times as frequent as daytime formation. Therefore, it appears that in summer and autumn, nocturnal production was the major mechanism for aerosol formation in Tumbarumba.

scholarly journals Identification and classification of the formation of intermediate ions measured in boreal forest

2007 ◽  
Vol 7 (1) ◽  
pp. 201-210 ◽  
Author(s):  
A. Hirsikko ◽  
T. Bergman ◽  
L. Laakso ◽  
M. Dal Maso ◽  
I. Riipinen ◽  
...  
Keyword(s):  
Boreal Forest ◽  
Aerosol Particle ◽  
Size Range ◽  
Aerosol Particles ◽  
Charged Particles ◽  
Negative Ions ◽  
Particle Formation ◽  
Air Ions ◽  
Charged Aerosol ◽  
Positively Charged

Abstract. We have measured the size distributions of air ions (0.42–7.5 nm in diameter) with the Balanced Scanning Mobility Analyzer in boreal forest, in Southern Finland since spring 2003. The size range covers the size range of cluster ions (approximately 0.42–1.6 nm) and naturally charged nanometre aerosol particles (1.6–7.5 nm) or intermediate air ions. Based on the measurements from April 2003 to March 2006 we studied the characteristics of charged aerosol particle formation by classifying each day either as a particle formation event, undefined or non-event day. The principal of the classification, as well as the statistical description of the charged aerosol particle formation events are given. We found in total 270 (26% of the analysed days) and 226 (22% of the analysed days) particle formation days for negative and positive intermediate ions, respectively. For negatively charged particles we classified 411 (40% of the analysed days) undefined and 348 (34% of the analysed days) non-event days whereas for positively charged particles 343 (33% of the analysed days) undefined and 460 (45% of the analysed days) non-event days. The results were compared with the ordinary classification based on the Differential Mobility Particle Sizer (DMPS) measurements carried out at the same place. The above-presented values differed slightly from that found from the DMPS data, with a lower particle diameter of 3 nm. In addition, we have found the rain-induced intermediate ion bursts frequently. The rain effect was detected on 163 days by means of negative ions and on 105 days by positive ones. Another interesting phenomenon among the charged aerosol particles was the appearance and existence of intermediate ions during the snowfall. We observed this phenomenon 24 times with negatively charged particles and 21 times with positively charged ones during winter months (October–April). These intermediate air ions were seen during the snowfall and may be caused by ice crystals, although the origin of these intermediate ions is unclear at the moment.

scholarly journals New particle formation events observed at King Sejong Station, Antarctic Peninsula – Part 1: Physical characteristics and contribution to cloud condensation nuclei

2018 ◽  
Author(s):  
Jaeseok Kim ◽  
Young Jun Yoon ◽  
Yeontae Gim ◽  
Jin Hee Choi ◽  
Hyo Jin Kang ◽  
...  
Keyword(s):  
Antarctic Peninsula ◽  
Cloud Condensation Nuclei ◽  
Aerosol Particles ◽  
Particle Formation ◽  
Physical Characteristics ◽  
Weddell Sea ◽  
New Particle Formation ◽  
Condensation Nuclei ◽  
Source Rate ◽  
The Mean

Abstract. The physical characteristics of aerosol particles during a particle burst observed at King Sejong Station in Antarctic Peninsula from March 2009 to December 2016 were analyzed. This study focuses on the seasonal variation in parameters related to particle formation such as the occurrence, formation rate (FR) and growth rate (GR), condensation sink (CS), and source rate of condensable vapor. The number concentrations during new particle formation (NPF) events varied from 1707 cm−3 to 83 120 cm−3, with an average of 20 649 ± 9290 cm−3, and the duration of the NPF events ranged from 0.6 h to 14.4 h, with a mean of 4.6 ± 1.5 h. The NPF event dominantly occurred during austral summer period (~ 72 %). The mean values of FR and GR of the aerosol particles were 2.79 ± 1.05 cm−3 s−1 and 0.68 ± 0.27 nm h−1, respectively showing enhanced rates in the summer season. The mean value of FR at King Sejong Station was higher than that at other sites in Antarctica, at 0.002–0.3 cm−3 s−1, while those of growth rates was relatively similar results observed by precious studies, at 0.4~4.3 nm h−1. The average values of CS and source rate of condensable vapor were (6.04 ± 2.74) × 10−3 s−1 and (5.19 ± 3.51) × 104 cm−3 s−1, respectively. The contribution of particle formation to cloud condensation nuclei (CCN) concentration was also investigated. The CCN concentration during the NPF period increased approximately 9 % compared with the background concentration. In addition, the effects of the origin and pathway of air masses on the characteristics of aerosol particles during a NPF event were determined. The FRs were similar regardless of the origin and pathway, whereas the GRs of particles originating from the Antarctic Peninsula and the Bellingshausen Sea, at 0.77 ± 0.25 nm h−1 and 0.76 ± 0.30 nm h−1, respectively, were higher than those of particles originating from the Weddell Sea (0.41 ± 0.15 nm h−1).

scholarly journals Evaluation of the contribution of new particle formation to cloud droplet in urban atmosphere

2021 ◽  
Author(s):  
Sihui Jiang ◽  
Fang Zhang ◽  
Jingye Ren ◽  
Lu Chen ◽  
Xing Yan ◽  
...  
Keyword(s):  
Water Vapor ◽  
Cloud Condensation Nuclei ◽  
Aerosol Particles ◽  
Cloud Droplet ◽  
Particle Formation ◽  
Urban Atmosphere ◽  
Primary Sources ◽  
New Particle Formation ◽  
Multiple Sources ◽  
Considerable Impact

Abstract. New particle formation (NPF) is a large source of cloud condensation nuclei (CCN) and cloud droplet in the troposphere. In this study, we quantified the contribution of NPF to cloud droplet number concentration (CDNC, or Nd) at typical updraft velocities (V) in clouds using a field campaign data of aerosol number size distribution and chemical composition observed on May 25–June 18, 2017 in urban Beijing. We show that the NPF drives the variations of CCN and cloud droplet and increases Nd by 30–33 % at V = 0.3–3 m s−1 in urban atmosphere. A markedly reduction in Nd is observed due to water vapor competition with consideration of actual environmental updraft velocity, decreasing by 11.8 ± 5.0 % at V = 3 m s−1 and 19.0 ± 4.5 % at V = 0.3 m s−1 compared to that from a prescribed supersaturation. The effect of water vapor competition becomes smaller at larger V that can provide more sufficient water vapor. Essentially, water vapor competition led to the reduction in Nd by decreasing the environmental maximum supersaturation (Smax) for the activation of aerosol particles. It is shown that Smax was decreased by 14.5–11.7 % for V = 0.3–3 m s−1. Particularly, the largest suppression of cloud droplet formation due to the water vapor competition is presented at extremely high aerosol particle number concentrations. As a result, although a larger increase of CCN-size particles by NPF event is derived on clean NPF day when pre-existing background aerosol particles are very low, there is no large discrepancy in the enhancement of Nd by NPF between the clean and polluted NPF day. We finally show a considerable impact of the primary sources when evaluating the NPF contribution to cloud droplet based on a case study. Our study highlights the importance of fully consideration of both the environmental meteorological conditions and multiple sources (i.e. secondary and primary) to evaluate the NPF effect on clouds and the associated climate effects in polluted regions.

scholarly journals Investigating the importance of sub-grid particle formation in point source plumes over eastern China using IAP-AACM v1.0 with a sub-grid parameterization

2021 ◽  
Vol 14 (7) ◽  
pp. 4411-4428
Author(s):  
Ying Wei ◽  
Xueshun Chen ◽  
Huansheng Chen ◽  
Yele Sun ◽  
Wenyi Yang ◽  
...  
Keyword(s):  
Point Source ◽  
Transport Model ◽  
Aerosol Particles ◽  
Eastern China ◽  
Regional Scale ◽  
Chemical Transport ◽  
Particle Formation ◽  
Point Sources ◽  
Formation Processes ◽  
New Particle Formation

Abstract. The influence of sub-grid particle formation (SGPF) in point source plumes on aerosol particles over eastern China was firstly illustrated by implementing an SGPF scheme into a global–regional nested chemical transport model with an aerosol microphysics module. The key parameter in the scheme was optimized based on the observations in eastern China. With the parameterization of SGPF, the spatial heterogeneity and diurnal variation in particle formation processes in sub-grid scale were well resolved. The SGPF scheme can significantly improve the model performance in simulating aerosol components and new particle formation processes at typical sites influenced by point sources. The comparison with observations at Beijing, Wuhan and Nanjing showed that the normal mean bias (NMB) of sulfate and ammonium could be reduced by 23 %–27 % and 12 %–14 %, respectively. When wind fields are well reproduced, the correlation of sulfate between simulation and observation can be increased by 0.13 in Nanjing. Considering the diurnal cycle of new particle formation, the SGPF scheme can greatly reduce the overestimation of particle number concentration in nucleation and Aitken mode at night caused by fixed-fraction parameterization of SGPF. On the regional scale, downwind areas of point source experienced an increase in sulfate concentration of 25 %–50 %. The results of this study indicate the significant effects of SGPF on aerosol particles over areas with the point source and the necessity of a reasonable representation of SGPF processes in chemical transport models.

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