| 1. |
- Kulmala, Markku, et al.
(författare)
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Direct Observations of Atmospheric Aerosol Nucleation
- 2013
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Ingår i: Science. - : American Association for the Advancement of Science (AAAS). - 0036-8075 .- 1095-9203. ; 339:6122, s. 943-946
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Tidskriftsartikel (refereegranskat)abstract
- Atmospheric nucleation is the dominant source of aerosol particles in the global atmosphere and an important player in aerosol climatic effects. The key steps of this process occur in the sub-2-nanometer (nm) size range, in which direct size-segregated observations have not been possible until very recently. Here, we present detailed observations of atmospheric nanoparticles and clusters down to 1-nm mobility diameter. We identified three separate size regimes below 2-nm diameter that build up a physically, chemically, and dynamically consistent framework on atmospheric nucleation-more specifically, aerosol formation via neutral pathways. Our findings emphasize the important role of organic compounds in atmospheric aerosol formation, subsequent aerosol growth, radiative forcing and associated feedbacks between biogenic emissions, clouds, and climate.
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| 2. |
- Chen, Dean, et al.
(författare)
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A modelling study of OH, NO3 and H2SO4 in 2007- 2018 at SMEAR II, Finland : Analysis of long-term trends
- 2021
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Ingår i: Environmental Science: Atmospheres. - : Royal Society of Chemistry (RSC). - 2634-3606. ; 1:6, s. 449-472
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Tidskriftsartikel (refereegranskat)abstract
- Major atmospheric oxidants (OH,O3 and NO3) dominate the atmospheric oxidation capacity, while H2SO4 is considered as a main driver for new particle formation. Although numerous studies have investigated the long-term trend of ozone in Europe, the trends of OH, NO3 and H2SO4 at specific sites are to a large extent unknown. The one-dimensional model SOSAA has been applied in several studies at the SMEAR II station and has been validated by measurements in several projects. Here, we applied the SOSAA model for the years 2007-2018 to simulate the atmospheric chemical components, especially the atmospheric oxidants OH and NO3, as well as H2SO4 at SMEAR II. The simulations were evaluated with observations from several shorter and longer campaigns at SMEAR II. Our results show that daily OH increased by 2.39% per year and NO3 decreased by 3.41% per year, with different trends of these oxidants during day and night. On the contrary, daytime sulfuric acid concentrations decreased by 2.78% per year, which correlated with the observed decreasing concentration of newly formed particles in the size range of 3- 25 nm with 1.4% per year at SMEAR II during the years 1997-2012. Additionally, we compared our simulated OH, NO3 and H2SO4 concentrations with proxies, which are commonly applied in case a limited number of parameters are measured and no detailed model simulations are available.
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| 3. |
- Hussein, Tareq, et al.
(författare)
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Observation of regional new particle formation in the urban atmosphere
- 2008
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Ingår i: Tellus. Series B, Chemical and physical meteorology. - : Stockholm University Press. - 0280-6509 .- 1600-0889. ; 60:4, s. 509-521
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Tidskriftsartikel (refereegranskat)abstract
- Long-term measurements of fine particle number-size distributions were carried out over 9.5 yr (May 1997-December 2006), in the urban background atmosphere of Helsinki. The total number of days was 3528 with about 91.9% valid data. A new particle formation event (NPF) is defined if a distinct nucleation mode of aerosol particles is observed below 25 nm for several hours, and it shows a growth pattern. We observed 185 NPF events, 111 d were clear non-events and most of the days (around 83.5%) were undefined. The observed events were regional because they were observed at Hyytiala (250 km north of Helsinki). The events occurred most frequently during spring and autumn. The observed formation rate was maximum during the spring and summer (monthly median 2.87 cm(-3) s(-1)) and the modal growth rate was maximum during late summer and Autumn (monthly median 6.55 mm h(-1)). The events were observed around noon, and the growth pattern often continued on the following day. The observation of weak NPF events was hindered due to pre-existing particles from both local sources. It is clear that regional NPF events have a clear influence oil the dynamic behaviour of aerosol particles in the urban atmosphere.
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| 4. |
- Kulmala, Markku, et al.
(författare)
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Measurement of the nucleation of atmospheric aerosol particles
- 2012
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Ingår i: Nature Protocols. - : Springer Science and Business Media LLC. - 1754-2189 .- 1750-2799. ; 7:9, s. 1651-1667
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Tidskriftsartikel (refereegranskat)abstract
- The formation of new atmospheric aerosol particles and their subsequent growth have been observed frequently at various locations all over the world. The atmospheric nucleation rate (or formation rate) and growth rate (GR) are key parameters to characterize the phenomenon. Recent progress in measurement techniques enables us to measure atmospheric nucleation at the size (mobility diameter) of 1.5 (+/- 0.4) nm. The detection limit has decreased from 3 to 1 nm within the past 10 years. In this protocol, we describe the procedures for identifying new-particle-formation (NPF) events, and for determining the nucleation, formation and growth rates during such events under atmospheric conditions. We describe the present instrumentation, best practices and other tools used to investigate atmospheric nucleation and NPF at a certain mobility diameter (1.5, 2.0 or 3.0 nm). The key instruments comprise devices capable of measuring the number concentration of the formed nanoparticles and their size, such as a suite of modern condensation particle counters (CPCs) and air ion spectrometers, and devices for characterizing the pre-existing particle number concentration distribution, such as a differential mobility particle sizer (DMPS). We also discuss the reliability of the methods used and requirements for proper measurements and data analysis. The time scale for realizing this procedure is 1 year.
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| 5. |
- Kyro, Ella-Maria, et al.
(författare)
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Long-term Aerosol and Trace Gas Measurements in Eastern Lapland, Finland : The Impact of Kola Air Pollution to New Particle Formation
- 2013
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Ingår i: NUCLEATION AND ATMOSPHERIC AEROSOLS. - : American Institute of Physics (AIP). - 9780735411524 ; , s. 409-412
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Konferensbidrag (refereegranskat)abstract
- Sulfur emissions from the Kola Peninsula smelter industry have been decreasing over the past two decades. We investigated the effect of this to new particle formation at SMEAR I station in Eastern Lapland, Finland, using long-term measurements of trace gases and aerosol size distributions. We show that the number of events per year has decreased and can be linked with the decreasing sulfur emissions from Kola.
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| 6. |
- Nieminen, Tuomo, et al.
(författare)
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Global analysis of continental boundary layer new particle formation based on long-term measurements
- 2018
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Ingår i: Atmospheric Chemistry And Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 18:19, s. 14737-14756
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Tidskriftsartikel (refereegranskat)abstract
- Atmospheric new particle formation (NPF) is an important phenomenon in terms of global particle number concentrations. Here we investigated the frequency of NPF, formation rates of 10 nm particles, and growth rates in the size range of 10-25 nm using at least 1 year of aerosol number size-distribution observations at 36 different locations around the world. The majority of these measurement sites are in the Northern Hemisphere. We found that the NPF frequency has a strong seasonal variability. At the measurement sites analyzed in this study, NPF occurs most frequently in March-May (on about 30 % of the days) and least frequently in December-February (about 10 % of the days). The median formation rate of 10 nm particles varies by about 3 orders of magnitude (0.01-10 cm(-3) s(-1)) and the growth rate by about an order of magnitude (1-10 nm h(-1)). The smallest values of both formation and growth rates were observed at polar sites and the largest ones in urban environments or anthropogenically influenced rural sites. The correlation between the NPF event frequency and the particle formation and growth rate was at best moderate among the different measurement sites, as well as among the sites belonging to a certain environmental regime. For a better understanding of atmospheric NPF and its regional importance, we would need more observational data from different urban areas in practically all parts of the world, from additional remote and rural locations in North America, Asia, and most of the Southern Hemisphere (especially Australia), from polar areas, and from at least a few locations over the oceans.
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| 7. |
- Schobesberger, Siegfried, et al.
(författare)
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Airborne measurements over the boreal forest of southern Finland during new particle formation events in 2009 and 2010
- 2013
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Ingår i: Boreal environment research. - 1239-6095 .- 1797-2469. ; 18:2, s. 145-163
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Tidskriftsartikel (refereegranskat)abstract
- Schobesberger, S., Vaananen, R., Leino, K., Virkkula, A., Backman, J., Pohja, T., Siivola, E., Franchin, A., Mikkila, J., Paramonov, M., Aalto, P.P., Krejci, R., Petaja, T. & Kulmala, M. 2013: Airborne measurements over the boreal forest of southern Finland during new particle formation events in 2009 and 2010. Boreal Env. Res. 18: 145-163. We conducted airborne observations of aerosol physical properties over the southern Finland boreal forest environment. The aim was to investigate the lower tropospheric aerosol (up to 4-km altitude) over an area of 250 by 200 km, in particular during new particle formation (NPF) events, and to address the spatial variability of aerosol number concentration and number size distribution. The regional NPF events, detected both airborne and at the ground, with air masses originating from the Arctic or northern Atlantic Ocean were studied throughout the boundary layer and throughout the area covered. Three suitable case studies are presented in more detail. In two of these studies, the concentrations of nucleation mode particles (3-10 nm in diameter) were found considerably higher (up to a factor of 30) in the upper parts of the planetary boundary layer compared to ground-based measurements during the nucleation events. The observed vertical variation can be connected to boundary layer dynamics and interactions between the boundary layer and the lower free troposphere, likely yielding high concentrations of newly formed aerosol particles. Our results suggest that nucleation does not necessarily occur close to the surface. In one presented case we found evidence of NPF occurring in a limited area above cloud, in the complete absence of a regional NPF event.
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| 8. |
- Väänänen, Riikka, et al.
(författare)
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Analysis of particle size distribution changes between three measurement sites in Northern Scandinavia
- 2013
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Ingår i: Nucleation and Atmospheric Aerosols - 19th International Conference. - : AIP. - 1551-7616 .- 0094-243X. - 9780735411524 ; 1527, s. 531-534
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Konferensbidrag (refereegranskat)abstract
- Measured aerosol size distributions from three measurement stations and modeled air mass trajectory data were combined to study aerosol dynamics in the boreal forest zone in Northern Scandinavia. Three approaches were used: investigation of new particle formation events, analysis of air masses arriving from ocean to continent, and study of changes in the aerosol size distributions when air masses travel from one measurement site to another. The statistical analysis of air masses travelling either from the Atlantic Ocean to measurement sites or from one site to another showed that on average the condensational growth was present during the summer season, and it was not restricted only to the days when evident new particle formation was observed. The rate of this average apparent growth of particle diameter was 3-7 times smaller than the growth rate of nucleation mode particles during the new particle formation events.
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