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Dive into the research topics where Eija Asmi is active.

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Featured researches published by Eija Asmi.


Bulletin of the American Meteorological Society | 2016

BAECC: A Field Campaign to Elucidate the Impact of Biogenic Aerosols on Clouds and Climate

Tuukka Petäjä; Ewan J. O’Connor; Dmitri Moisseev; Victoria A. Sinclair; Antti Manninen; Riikka Väänänen; Annakaisa von Lerber; Joel A. Thornton; Keri Nicoll; Walt Petersen; V. Chandrasekar; James N. Smith; Paul M. Winkler; Olaf Krüger; Hannele Hakola; Hilkka Timonen; David Brus; Tuomas Laurila; Eija Asmi; Marja-Liisa Riekkola; Lucia Mona; Paola Massoli; Ronny Engelmann; M. Komppula; Jian Wang; Chongai Kuang; Jaana Bäck; Annele Virtanen; Janne Levula; Michael Ritsche

AbstractDuring Biogenic Aerosols—Effects on Clouds and Climate (BAECC), the U.S. Department of Energy’s Atmospheric Radiation Measurement (ARM) Program deployed the Second ARM Mobile Facility (AMF2) to Hyytiala, Finland, for an 8-month intensive measurement campaign from February to September 2014. The primary research goal is to understand the role of biogenic aerosols in cloud formation. Hyytiala is host to the Station for Measuring Ecosystem–Atmosphere Relations II (SMEAR II), one of the world’s most comprehensive surface in situ observation sites in a boreal forest environment. The station has been measuring atmospheric aerosols, biogenic emissions, and an extensive suite of parameters relevant to atmosphere–biosphere interactions continuously since 1996. Combining vertical profiles from AMF2 with surface-based in situ SMEAR II observations allows the processes at the surface to be directly related to processes occurring throughout the entire tropospheric column. Together with the inclusion of extensi...


Bulletin of the American Meteorological Society | 2016

International Arctic Systems for Observing the Atmosphere: An International Polar Year Legacy Consortium

Taneil Uttal; Sandra Starkweather; James R. Drummond; Timo Vihma; Alexander Makshtas; Lisa S. Darby; J. F. Burkhart; Christopher J. Cox; Lauren Schmeisser; Thomas Haiden; Marion Maturilli; Matthew D. Shupe; Gijs de Boer; Auromeet Saha; Andrey A. Grachev; Sara M. Crepinsek; Lori Bruhwiler; Barry Goodison; Bruce McArthur; Von P. Walden; E. J. Dlugokencky; P. Ola G. Persson; Glen Lesins; Tuomas Laurila; John A. Ogren; Robert S. Stone; Charles N. Long; Sangeeta Sharma; Andreas Massling; David D. Turner

AbstractInternational Arctic Systems for Observing the Atmosphere (IASOA) activities and partnerships were initiated as a part of the 2007–09 International Polar Year (IPY) and are expected to continue for many decades as a legacy program. The IASOA focus is on coordinating intensive measurements of the Arctic atmosphere collected in the United States, Canada, Russia, Norway, Finland, and Greenland to create synthesis science that leads to an understanding of why and not just how the Arctic atmosphere is evolving. The IASOA premise is that there are limitations with Arctic modeling and satellite observations that can only be addressed with boots-on-the-ground, in situ observations and that the potential of combining individual station and network measurements into an integrated observing system is tremendous. The IASOA vision is that by further integrating with other network observing programs focusing on hydrology, glaciology, oceanography, terrestrial, and biological systems it will be possible to under...


Tellus B | 2016

Coupling an aerosol box model with one-dimensional flow: a tool for understanding observations of new particle formation events

Niku Kivekäs; Jimmie Carpman; Pontus Roldin; Johannes Leppä; Ewan J. O'Connor; Adam Kristensson; Eija Asmi

Field observations of new particle formation and the subsequent particle growth are typically only possible at a fixed measurement location, and hence do not follow the temporal evolution of an air parcel in a Lagrangian sense. Standard analysis for determining formation and growth rates requires that the time-dependent formation rate and growth rate of the particles are spatially invariant; air parcel advection means that the observed temporal evolution of the particle size distribution at a fixed measurement location may not represent the true evolution if there are spatial variations in the formation and growth rates. Here we present a zero-dimensional aerosol box model coupled with one-dimensional atmospheric flow to describe the impact of advection on the evolution of simulated new particle formation events. Wind speed, particle formation rates and growth rates are input parameters that can vary as a function of time and location, using wind speed to connect location to time. The output simulates measurements at a fixed location; formation and growth rates of the particle mode can then be calculated from the simulated observations at a stationary point for different scenarios and be compared with the ‘true’ input parameters. Hence, we can investigate how spatial variations in the formation and growth rates of new particles would appear in observations of particle number size distributions at a fixed measurement site. We show that the particle size distribution and growth rate at a fixed location is dependent on the formation and growth parameters upwind, even if local conditions do not vary. We also show that different input parameters used may result in very similar simulated measurements. Erroneous interpretation of observations in terms of particle formation and growth rates, and the time span and areal extent of new particle formation, is possible if the spatial effects are not accounted for.


Tellus B: Chemical and Physical Meteorology | 2018

Primary sources control the variability of aerosol optical properties in the Antarctic Peninsula

Eija Asmi; Kimmo Neitola; Kimmo Teinilä; Edith Rodriguez; Aki Virkkula; John Backman; Matthew Bloss; Jesse Jokela; Heikki Lihavainen; Gerrit de Leeuw; Jussi Paatero; V. Aaltonen; Miguel Mei; Gonzalo Gambarte; Gustavo Copes; Marco Albertini; Germán Pérez Fogwill; Jonathan Ferrara; María Elena Barlasina; Ricardo Sánchez

Abstract Aerosol particle optical properties were measured continuously between years 2013–2015 at the Marambio station in the Antarctic Peninsula. Annual cycles of particle scattering and absorption were studied and explained using measured particle chemical composition and the analysis of air mass transport patterns. The particle scattering was found elevated during the winter but the absorption did not show any clear annual cycle. The aerosol single scattering albedo at nm was on average 0.96 0.10, with a median of 0.99. Aerosol scattering Ångström exponent increased during summer, indicating an increasing fraction of fine mode particles. The aerosol was mainly composed of sea salt, sulphate and crustal soil minerals, and most of the particle mass were in the coarse mode. Both the particle absorption and scattering were increased during high wind speeds. This was explained by the dominance of the primary marine sea-spray and wind-blown soil dust sources. In contrast, the back-trajectory analysis suggested that long-range transport has only a minor role as a source of absorbing aerosol at the peninsula.


Tellus B: Chemical and Physical Meteorology | 2018

Anthropogenic fine aerosols dominate the wintertime regime over the northern Indian Ocean

K.B. Budhavant; Srinivas Bikkina; August Andersson; Eija Asmi; John Backman; Jutta Kesti; H. Zahid; S. K. Satheesh; Örjan Gustafsson

Abstract This study presents and evaluates the most comprehensive set to date of chemical, physical and optical properties of aerosols in the outflow from South Asia covering a full winter (Nov. 2014 – March 2015), here intercepted at the Indian Ocean receptor site of the Maldives Climate Observatory in Hanimaadhoo (MCOH). Cluster analysis of air-mass back trajectories for MCOH, combined with AOD and meteorological data, demonstrate that the wintertime northern Indian Ocean is strongly influenced by aerosols transported from source regions with three major wind regimes, originating from the Indo-Gangetic Plain (IGP), the Bay of Bengal (BoB) and the Arabian Sea (AS). As much as 97 ± 3% of elemental carbon (EC) in the PM10 was also found in the fine mode (PM2.5). Other mainly anthropogenic constituents such as organic carbon (OC), non-sea-salt (nss) -K+, nss-SO42− and NH4+ were also predominantly in the fine mode (70–95%), particularly in the air masses from IGP. The combination at this large-footprint receptor observatory of consistently low OC/EC ratio (2.0 ± 0.5), strong linear relationships between EC and OC as well as between nss-K+ and both OC and EC, suggest a predominance of primary sources, with a large biomass burning contribution. The particle number-size distributions for the air masses from IGP and BoB exhibited clear bimodal shapes within the fine fraction with distinct accumulation (0.1 μm < d < 1 μm) and Aitken (0.025 μm < d < 0.10 μm) modes. This study also supports that IGP is a key source region for the wider South Asia and nearby oceans, as defined by the criteria that anthropogenic AODs exceed 0.3 and absorption AOD > 0.03. Taken together, the aerosol pollution over the northern Indian Ocean in the dry season is dominated by a well-mixed long-range transported regime of the fine-mode aerosols largely from primary combustion origin.


Journal of The Air & Waste Management Association | 2018

Characteristics of particle emissions and their atmospheric dilution during co-combustion of coal and wood pellets in a large combined heat and power plant

Fanni Mylläri; Liisa Pirjola; Heikki Lihavainen; Eija Asmi; Erkka Saukko; Tuomas Laurila; Ville Vakkari; Ewan J. O’Connor; Jani Rautiainen; Anna Häyrinen; Ville Niemelä; Joni Maunula; Risto Hillamo; Jorma Keskinen; Topi Rönkkö

Abstract Coal combustion is one of the most significant anthropogenic CO2 and air pollution sources globally. This paper studies the atmospheric emissions of a power plant fuelled with a mixture of industrial pellets (10.5%) and coal (89.5%). Based on the stack measurements, the solid particle number emission, which was dominated by sub-200 nm particles, was 3.4×1011 MJ-1 for the fuel mixture when electrostatic precipitator (ESP) was cleaning the flue gas. The emission factor was 50 mg MJ-1 for particulate mass and 11 740 ng MJ-1 for the black carbon with the ESP. In the normal operation situation of the power plant, i.e., including the flue-gas desulphurisation and fabric filters (FGD and FF), the particle number emission factor was 1.7×108 MJ-1, particulate mass emission factor 2 mg MJ-1 and black carbon emission factor 14 ng MJ-1. Transmission electron microscopy (TEM) analysis supported the particle number size distribution measurement in terms of particle size and the black carbon concentration. The TEM images of the particles showed variability of the particle sizes, morphologies and chemical compositions. The atmospheric measurements, conducted in the flue-gas plume, showed that the flue-gas dilutes closed to background concentrations in 200 sec. However, an increase in particle number concentration was observed when the flue gas aged. This increase in particle number concentration was interpret as formation of new particles in the atmosphere. In general, the study highlights the importance of detailed particle measurements when utilizing new fuels in existing power plants. Implications: CO2 emissions of energy production decrease when substituting coal with biofuels. The effects of fuels changes on particle emission characteristics have not been studied comprehensively. In this study conducted for a real-scale power plant, co-combustion of wood pellets and coal caused elevated black carbon emissions. However, it was beneficial from the total particle number and particulate mass emission point of view. Flue-gas cleaning can significantly decrease the pollutant concentrations but also changes the characteristics of emitted particles. Atmospheric measurements implicated that the new particle formation in the atmospheric flue-gas plume should be taken into account when evaluating all effects of fuel changes.” Are implication statements part of the manuscript?


Geography, Environment, Sustainability | 2018

PAN-EURASIAN EXPERIMENT (PEEX) PROGRAM: AN OVERVIEW OF THE FIRST 5 YEARS IN OPERATION AND FUTURE PROSPECTS

Hanna K. Lappalainen; Nuria Altimir; Veli-Matti Kerminen; Tuukka Petäjä; R. Makkonen; Pavel Alekseychik; Nina Zaitseva; Irina Bashmakova; Joni Kujansuu; Antti Lauri; Päivi Haapanala; Stephany Buenrostro Mazon; Alla Borisova; Pavel Konstantinov; Sergej Chalov; Tuomas Laurila; Eija Asmi; Heikki Lihavainen; Jaana Bäck; Michael Arshinov; Alexander Mahura; Steven Arnold; Timo Vihma; Petteri Uotila; Gerrit de Leeuw; Ilmo T. Kukkonen; Svetlana Malkhazova; Veli-Pekka Tynkkynen; Irina Fedorova; Hans Hansson

The Pan-Eurasian Experiment (PEEX) program was initiated as a bottom-up approach by the researchers coming fromFinlandandRussiain October 2012. The PEEX China kick off meeting was held in November 2013. During its five years in operation, the program has established a governance structure and delivered a science plan for the Northern Eurasian region. PEEX has also introduced a concept design for a modelling platform and ground-based in situ observation systems for detecting land-atmosphere and ocean-atmosphere interactions. Today, PEEX has an extensive researcher’s network representing research communities coming from the Nordic countries,RussiaandChina. PEEX is currently carrying out its research activities on a project basis, but is looking for more coordinated funding bases, especially inRussiaand inChina. The near-future challenge in implementing the PEEX research agenda is to achieve a successful integration and identification of the methodological approaches of the socio-economic research to environmental sciences. Here we give insight into these issues and provide an overview on the main tasks for the upcoming years.


NUCLEATION AND ATMOSPHERIC AEROSOLS: 19th International Conference | 2013

Charged and neutral binary nucleation of sulfuric acid in free troposphere conditions

Jonathan Duplissy; Joonas Merikanto; Karine Sellegri; C. Rose; Eija Asmi; Evelyn Freney; Heikki Juninen; Mikko Sipilä; Hanna Vehkamäki; Markku Kulmala

We present a data set of binary nucleation of sulfuric acid and water, measured in the CLOUD chamber at CERN during the CLOUD3 and CLOUD5 campaigns. Four parameters have been varied to cover neutral and ion-induced binary nucleation processes: Sulfuric acid concentration (1e5 to 1e8 molecules per cm^(−3)), relative humidity (10% to 80%), temperature (208-293K) and ion concentration (0-4000 ions per cm^(−3)). In addition, classical nucleation theory implemented with hydrates and ion induced nucleation is compared with the data set. Our model and data are also compared with nucleation rates measured at Puy de Dome in the tropopause.


Atmospheric Measurement Techniques | 2010

Mobility particle size spectrometers: harmonization of technical standards and data structure to facilitate high quality long-term observations of atmospheric particle number size distributions

A. Wiedensohler; W. Birmili; A. Nowak; A. Sonntag; K. Weinhold; M. Merkel; B. Wehner; T. Tuch; S. Pfeifer; Markus Fiebig; A. M. Fjäraa; Eija Asmi; K. Sellegri; R. Depuy; H. Venzac; P. Villani; P. Laj; Pasi Aalto; John A. Ogren; Erik Swietlicki; Paul Williams; Pontus Roldin; P. Quincey; Christoph Hüglin; R. Fierz-Schmidhauser; M. Gysel; E. Weingartner; Francesco Riccobono; Sebastiao Martins-Dos Santos; C. Grüning


Atmospheric Chemistry and Physics | 2010

EUCAARI ion spectrometer measurements at 12 European sites – analysis of new particle formation events

H. E. Manninen; Tuomo Nieminen; Eija Asmi; S. Gagné; S. A. K. Hakkinen; Katrianne Lehtipalo; Pasi Aalto; Marko Vana; A. Mirme; Sander Mirme; Urmas Hõrrak; C. Plass-Dülmer; G. Stange; Gyula Kiss; A. Hoffer; N. Törő; M.M. Moerman; Bas Henzing; G. de Leeuw; M. Brinkenberg; G. Kouvarakis; A. Bougiatioti; N. Mihalopoulos; Colin D. O'Dowd; Darius Ceburnis; Almut Arneth; Birgitta Svenningsson; Erik Swietlicki; L. Tarozzi; S. Decesari

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Heikki Lihavainen

Finnish Meteorological Institute

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Markku Kulmala

Finnish Meteorological Institute

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Pasi Aalto

University of Helsinki

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Tuomas Laurila

Finnish Meteorological Institute

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John Backman

Finnish Meteorological Institute

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Aki Virkkula

Finnish Meteorological Institute

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Niku Kivekäs

Finnish Meteorological Institute

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