scholarly journals New particle formation in coastal New Zealand with a focus on open ocean air masses

2021 ◽  
Author(s):  
Maija Peltola ◽  
Clémence Rose ◽  
Jonathan V. Trueblood ◽  
Sally Gray ◽  
Mike Harvey ◽  
...  
Keyword(s):  
New Zealand ◽  
Particle Concentration ◽  
Particle Number ◽  
Particle Formation ◽  
Open Ocean ◽  
New Particle Formation ◽  
Air Masses ◽  
Wind Speeds ◽  
Marine Air ◽  
Aerosol Properties

Abstract. Even though oceans cover the majority of the Earth, most aerosol measurements are from continental sites. We measured aerosol particle number size distribution at Baring Head, in coastal New Zealand, over a total period of 10 months to study aerosol properties and new particle formation, with a special focus on aerosol formation in open ocean air masses. Particle concentrations were higher in land-influenced air compared to clean marine air in all size classes from sub-10 nm to cloud condensation nuclei sizes. When classifying the particle number size distributions with traditional methods designed for continental sites, new particle formation was observed at the station throughout the year with an average event frequency of 23 %. While most of these traditional event days had some land-influence, we also observed particle growth starting from nucleation mode during 16 % of the data in clean marine air and at least part of this growth was connected to nucleation in the marine boundary layer. Sub-10 nm particles accounted for 29 % of the total aerosol number concentration of particles larger than 1 nm in marine air during the spring. This shows that nucleation in marine air is frequent enough to influence the total particle concentration. Particle formation in land-influenced air was more intense and had on average higher growth rates than what was found for marine air. Particle formation and primary emissions increased particle number concentrations as a function of time spent over land during the first 1–2 days spent over land. After this, nucleation seems to start getting suppressed by the pre-existing particle population, but accumulation mode particle concentration keeps increasing, likely due to primary particle emissions. Further work showed that traditional NPF events were favoured by sunny conditions with low relative humidity and wind speeds. In marine air, formation of sub-10 nm particles was favoured by low temperatures, relative humidity, and wind speeds and could happen even during the night. Our future work will study the mechanisms responsible for particle formation at Baring Head with a focus on different chemical precursor species. This study sheds light on both new particle formation in open ocean air masses coming from the Southern Ocean and local aerosol properties in New Zealand.

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 First long-term study of particle number size distributions and new particle formation events of regional aerosol in the North China Plain

2010 ◽  
Vol 10 (10) ◽  
pp. 25205-25242 ◽  
Author(s):  
X. J. Shen ◽  
J. Y. Sun ◽  
Y. M. Zhang ◽  
B. Wehner ◽  
A. Nowak ◽  
...  
Keyword(s):  
North China Plain ◽  
North China ◽  
Particle Number ◽  
Particle Formation ◽  
Mean Value ◽  
Size Distributions ◽  
New Particle Formation ◽  
Air Masses ◽  
Nucleation Mode ◽  
The North

Abstract. Atmospheric particle number size distributions (size range 0.003–10 μm) were measured between March 2008 and August 2009 at Shangdianzi (SDZ), a rural research station in the North China Plain. These measurements were made in an attempt to better characterize the tropospheric background aerosol in Northern China, one of the currently more polluted regions of the globe. The mean particle number concentrations of the total aerosol, as well as the nucleation, Aitken and accumulation modes were determined to 1.2±0.9×104, 3.6±7.9×103, 4.4±3.4×103 and 3.5±2.8×103 cm−3, respectively. A general finding is that the particle number concentrations were higher during spring compared to the other seasons. The air mass origin had an important effect on the particle number concentration and new particle formation events. Air masses from northwest (i.e. inner Asia) showed the highest concentrations of nucleation mode particles, while southeasterly air masses showed the highest concentrations of accumulation mode particles. Significant diurnal variations in particle number were observed, which could be linked to new particle formation events, i.e. gas-to-particle conversion. During particle formation events, the number concentration of the nucleation mode rose up to maximum values of 104 cm−3. New particle formation events were observed on 36% of the measurement days. The formation rate ranged between 0.7 and 72.7 cm−3 s−1, with a mean value of 8.0 cm−3 s−1. The values of the nucleation mode growth rate ranged between 0.3 and 14.5 nm h−1, with a mean value of 4.3 nm h−1. It is an essential observation that on many occasions, the nucleation mode was able to grow into the size of cloud condensation nuclei (CCN) within a matter of several hours. Furthermore, the new particle formation were usually followed by a measurable increase in total particle mass concentration and extinction coefficient, indicative of a high abundance of condensable vapors in the atmosphere under study.

scholarly journals Regional New Particle Formation over the Eastern Mediterranean and Middle East

Atmosphere ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 13
Author(s):  
Panayiotis Kalkavouras ◽  
Aikaterini BougiatiotI ◽  
Tareq Hussein ◽  
Nikos Kalivitis ◽  
Iasonas Stavroulas ◽  
...  
Keyword(s):  
Dynamic Characteristics ◽  
Particle Number ◽  
Eastern Mediterranean ◽  
Particle Formation ◽  
Urban Environments ◽  
Urban Site ◽  
Simultaneous Occurrence ◽  
New Particle Formation ◽  
Air Masses ◽  
Background Site

Atmospheric new particle formation (NPF) events taking place over large distances between locations, featuring similar characteristics, have been the focus of studies during the last decade. The exact mechanism which triggers NPF still remains indefinable, so are the circumstances under which simultaneous occurrence of such events take place in different environments, let alone in environments which are parted by over 1200 km. In this study, concurrent number size distribution measurements were conducted in the urban environments of Athens (Greece) and Amman (Jordan) as well as the regional background site of Finokalia, Crete, all located within a distance of almost 1300 km for a 6-month period (February–July 2017). During the study period Athens and Finokalia had similar occurrence of NPF (around 20%), while the occurrence in Amman was double. When focusing on the dynamic characteristics at each site, it occurs that formation and growth rates at Amman are similar to those at Finokalia, while lower values in Athens can be ascribed to a higher pre-existing particle number at this urban site. By comparing common NPF events there are 5 concomitant days between all three sites, highly related to air masses origin. Additionally, for another 19 days NPF takes place simultaneously between Finokalia and Amman, which also share common meteorological characteristics, adding to a total of 60% out of 41 NPF events observed at Finokalia, also simultaneously occurring in Amman.

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

2011 ◽  
Vol 11 (9) ◽  
pp. 25709-25750 ◽  
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 First long-term study of particle number size distributions and new particle formation events of regional aerosol in the North China Plain

2011 ◽  
Vol 11 (4) ◽  
pp. 1565-1580 ◽  
Author(s):  
X. J. Shen ◽  
J. Y. Sun ◽  
Y. M. Zhang ◽  
B. Wehner ◽  
A. Nowak ◽  
...  
Keyword(s):  
North China Plain ◽  
North China ◽  
Particle Number ◽  
Particle Formation ◽  
Mean Value ◽  
Number Concentration ◽  
New Particle Formation ◽  
Air Masses ◽  
Nucleation Mode ◽  
The North

Abstract. Atmospheric particle number size distributions (size range 0.003–10 μm) were measured between March 2008 and August 2009 at Shangdianzi (SDZ), a rural research station in the North China Plain. These measurements were made in an attempt to better characterize the tropospheric background aerosol in Northern China. The mean particle number concentrations of the total particle, as well as the nucleation, Aitken, accumulation and coarse mode were determined to be 1.2 ± 0.9 × 104, 3.6 ± 7.9 × 103, 4.4 ± 3.4 × 103, 3.5 ± 2.8 × 103 and 2 ± 3 cm−3, respectively. A general finding was that the particle number concentration was higher during spring compared to the other seasons. The air mass origin had an important effect on the particle number concentration and new particle formation events. Air masses from northwest (i.e. inner Asia) favored the new particle formation events, while air masses from southeast showed the highest particle mass concentration. Significant diurnal variations in particle number were observed, which could be linked to new particle formation events, i.e. gas-to-particle conversion. During particle formation events, the number concentration of the nucleation mode rose up to maximum value of 104 cm−3. New particle formation events were observed on 36% of the effective measurement days. The formation rate ranged from 0.7 to 72.7 cm−3 s−1, with a mean value of 8.0 cm−3 s−1. The value of the nucleation mode growth rate was in the range of 0.3–14.5 nm h−1, with a mean value of 4.3 nm h−1. It was an essential observation that on many occasions the nucleation mode was able to grow into the size of cloud condensation nuclei (CCN) within a matter of several hours. Furthermore, the new particle formation was regularly followed by a measurable increase in particle mass concentration and extinction coefficient, indicative of a high abundance of condensable vapors in the atmosphere under study.

scholarly journals Open ocean and coastal new particle formation from sulfuric acid and amines around the Antarctic Peninsula

2021 ◽  
Author(s):  
James Brean ◽  
Manuel Dall’Osto ◽  
Rafel Simó ◽  
Zongbo Shi ◽  
David C. S. Beddows ◽  
...  
Keyword(s):  
Sulfuric Acid ◽  
Antarctic Peninsula ◽  
Particle Formation ◽  
Open Ocean ◽  
New Particle Formation ◽  
The Antarctic

Impact of Urban Pollution on Organic-Mediated New-Particle Formation and Particle Number Concentration in the Amazon Rainforest

2021 ◽  
Vol 55 (8) ◽  
pp. 4357-4367
Author(s):  
Bin Zhao ◽  
Jerome D. Fast ◽  
Neil M. Donahue ◽  
Manish Shrivastava ◽  
Meredith Schervish ◽  
...  
Keyword(s):  
Particle Number ◽  
Urban Pollution ◽  
Particle Formation ◽  
Number Concentration ◽  
Amazon Rainforest ◽  
Particle Number Concentration ◽  
New Particle Formation

scholarly journals Modeling particle nucleation and growth over northern California during the 2010 CARES campaign

2015 ◽  
Vol 15 (21) ◽  
pp. 12283-12313 ◽  
Author(s):  
A. Lupascu ◽  
R. Easter ◽  
R. Zaveri ◽  
M. Shrivastava ◽  
M. Pekour ◽  
...  
Keyword(s):  
Size Distribution ◽  
Particle Number ◽  
Particle Formation ◽  
Number Concentration ◽  
Aerosol Size Distribution ◽  
Particle Nucleation ◽  
Particle Number Concentration ◽  
New Particle Formation ◽  
Organic Vapors ◽  
Diurnal Variability

Abstract. Accurate representation of the aerosol lifecycle requires adequate modeling of the particle number concentration and size distribution in addition to their mass, which is often the focus of aerosol modeling studies. This paper compares particle number concentrations and size distributions as predicted by three empirical nucleation parameterizations in the Weather Research and Forecast coupled with chemistry (WRF-Chem) regional model using 20 discrete size bins ranging from 1 nm to 10 μm. Two of the parameterizations are based on H2SO4, while one is based on both H2SO4 and organic vapors. Budget diagnostic terms for transport, dry deposition, emissions, condensational growth, nucleation, and coagulation of aerosol particles have been added to the model and are used to analyze the differences in how the new particle formation parameterizations influence the evolving aerosol size distribution. The simulations are evaluated using measurements collected at surface sites and from a research aircraft during the Carbonaceous Aerosol and Radiative Effects Study (CARES) conducted in the vicinity of Sacramento, California. While all three parameterizations captured the temporal variation of the size distribution during observed nucleation events as well as the spatial variability in aerosol number, all overestimated by up to a factor of 2.5 the total particle number concentration for particle diameters greater than 10 nm. Using the budget diagnostic terms, we demonstrate that the combined H2SO4 and low-volatility organic vapor parameterization leads to a different diurnal variability of new particle formation and growth to larger sizes compared to the parameterizations based on only H2SO4. At the CARES urban ground site, peak nucleation rates are predicted to occur around 12:00 Pacific (local) standard time (PST) for the H2SO4 parameterizations, whereas the highest rates were predicted at 08:00 and 16:00 PST when low-volatility organic gases are included in the parameterization. This can be explained by higher anthropogenic emissions of organic vapors at these times as well as lower boundary-layer heights that reduce vertical mixing. The higher nucleation rates in the H2SO4-organic parameterization at these times were largely offset by losses due to coagulation. Despite the different budget terms for ultrafine particles, the 10–40 nm diameter particle number concentrations from all three parameterizations increased from 10:00 to 14:00 PST and then decreased later in the afternoon, consistent with changes in the observed size and number distribution. We found that newly formed particles could explain up to 20–30 % of predicted cloud condensation nuclei at 0.5 % supersaturation, depending on location and the specific nucleation parameterization. A sensitivity simulation using 12 discrete size bins ranging from 1 nm to 10 μm diameter gave a reasonable estimate of particle number and size distribution compared to the 20 size bin simulation, while reducing the associated computational cost by ~ 36 %.

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