Jarno Ruusunen
University of Eastern Finland
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Featured researches published by Jarno Ruusunen.
Inhalation Toxicology | 2012
Maija Tapanainen; Pasi I. Jalava; Jorma Mäki-Paakkanen; Pasi Hakulinen; Heikki Lamberg; Jarno Ruusunen; Jarkko Tissari; Jorma Jokiniemi; Maija-Riitta Hirvonen
Context: Particulate matter (PM) has been identified as a major environmental pollutant causing severe health problems. Large amounts of the harmful particulate matter (PM) are emitted from residential wood combustion, but the toxicological properties of wood combustion particles are poorly known. Objective: To investigate chemical and consequent toxicological characteristics of PM1 emitted from different phases of batch combustion in four heating appliances. Materials and methods: Mouse RAW264.7 macrophages and human BEAS-2B bronchial epithelial cells were exposed for 24 h to different doses (15–300 µg/mL) of wood combustion particles. After the exposure, cytotoxicity, genotoxicity, production of the inflammatory mediators (TNF-α and MIP-2) and effects on the cell cycle were assessed. Furthermore, the detected toxicological responses were compared with the chemical composition of PM1 samples including PAHs, metals and ions. Results: All the wood combustion samples exerted high cytotoxicity, but only moderate inflammatory activity. The particles emitted from the inefficient phase of batch combustion in the sauna stove (SS) induced the most extensive cytotoxic and genotoxic responses in mammalian cells. Polycyclic aromatic hydrocarbons (PAHs) and other organic compounds in PM1 samples might have contributed to these effects. Instead, water-soluble metals seemed to participate in the cytotoxic responses triggered by the particles from more efficient batch combustion in the masonry heaters. Overall, the toxicological responses were decreased when the combustion phase was more efficient. Conclusion: Efficiency of batch combustion plays a significant role in the harmfulness of PM even under incomplete wood combustion processes.
Science of The Total Environment | 2018
Teemu J. Rönkkö; Pasi I. Jalava; Mikko S. Happo; Stefanie Kasurinen; Olli Sippula; Ari Leskinen; Hanna Koponen; Kari Kuuspalo; Jarno Ruusunen; Olli Väisänen; Liqing Hao; Antti Ruuskanen; Jürgen Orasche; Die Fang; Lei Zhang; K. E. J. Lehtinen; Yu Zhao; Cheng Gu; Qin'geng Wang; Jorma Jokiniemi; M. Komppula; Maija-Riitta Hirvonen
Ambient inhalable particulate matter (PM) is a serious health concern worldwide, but especially so in China where high PM concentrations affect huge populations. Atmospheric processes and emission sources cause spatial and temporal variations in PM concentration and chemical composition, but their influence on the toxicological characteristics of PM are still inadequately understood. In this study, we report an extensive chemical and toxicological characterization of size-segregated urban air inhalable PM collected in August and October 2013 from Nanjing, and assess the effects of atmospheric processes and likely emission sources. A549 human alveolar epithelial cells were exposed to day- and nighttime PM samples (25, 75, 150, 200, 300 μg/ml) followed by analyses of cytotoxicity, genotoxicity, cell cycle, and inflammatory response. PM10-2.5 and PM0.2 caused the greatest toxicological responses for different endpoints, illustrating that particles with differing size and chemical composition activate distinct toxicological pathways in A549 cells. PM10-2.5 displayed the greatest oxidative stress and genotoxic responses; both were higher for the August samples compared with October. In contrast, PM0.2 and PM2.5-1.0 samples displayed high cytotoxicity and substantially disrupted cell cycle; August samples were more cytotoxic whereas October samples displayed higher cell cycle disruption. Several components associated with combustion, traffic, and industrial emissions displayed strong correlations with these toxicological responses. The lower responses for PM1.0-0.2 compared to PM0.2 and PM2.5-1.0 indicate diminished toxicological effects likely due to aerosol aging and lower proportion of fresh emission particles rich in highly reactive chemical components in the PM1.0-0.2 fraction. Different emission sources and atmospheric processes caused variations in the chemical composition and toxicological responses between PM fractions, sampling campaigns, and day and night. The results indicate different toxicological pathways for coarse-mode particles compared to the smaller particle fractions with typically higher content of combustion-derived components. The variable responses inside PM fractions demonstrate that differences in chemical composition influence the induced toxicological responses.
Aerosol Science and Technology | 2015
Jarno Ruusunen; Jouni Pyykönen; Mika Ihalainen; P. Tiitta; Tiina Torvela; Tommi Karhunen; Olli Sippula; Qi Hang Qin; Sebastiaan van Dijken; Jorma Joutsensaari; Anna Lähde; Jorma Jokiniemi
A novel porous tube reactor that combines simultaneous reactions and continuous dilution in a single-stage gas-phase process was designed for nanoparticle synthesis. The design is based on the atmospheric pressure chemical vapor synthesis (APCVS) method. In comparison to the conventional hot wall chemical vapor synthesis reactor, the APCVS method offers an effective process for the synthesis of ultrafine metal particles with controlled oxidation. In this study, magnetic iron and maghemite were synthesized using iron pentacarbonyl as a precursor. Morphology, size, and magnetic properties of the synthesized nanoparticles were determined. The X-ray diffraction results show that the porous tube reactor produced nearly pure iron or maghemite nanoparticles with crystallite sizes of 24 and 29 nm, respectively. According to the scanning mobility particle sizer data, the geometric number mean diameter was 110 nm for iron and 150 nm for the maghemite agglomerates. The saturation magnetization value of iron was 150 emu/g and that of maghemite was 12 emu/g, measured with superconducting quantum interference device (SQUID) magnetometry. A computational fluid dynamics (CFD) simulation was used to model the temperature and flow fields and the decomposition of the precursor as well as the mixing of the precursor vapor and the reaction gas in the reactor. An in-house CFD model was used to predict the extent of nucleation, coagulation, sintering, and agglomeration of the iron nanoparticles. CFD simulations predicted a primary particle size of 36 nm and an agglomerate size of 134 nm for the iron nanoparticles, which agreed well with the experimental data. Copyright 2015 American Association for Aerosol Research
Science of The Total Environment | 2019
Mirella Miettinen; Ari Leskinen; Gülcin Abbaszade; Jürgen Orasche; Maija Sainio; Santtu Mikkonen; Hanna Koponen; Teemu J. Rönkkö; Jarno Ruusunen; Kari Kuuspalo; P. Tiitta; Pasi I. Jalava; Liqing Hao; Die Fang; Qin'geng Wang; Cheng Gu; Yu Zhao; Bernhard Michalke; Jürgen Schnelle-Kreis; K. E. J. Lehtinen; Ralf Zimmermann; M. Komppula; Jorma Jokiniemi; Maija-Riitta Hirvonen; Olli Sippula
Industrial processes, coal combustion, biomass burning (BB), and vehicular transport are important sources of atmospheric fine particles (PM2.5) and contribute to ambient air concentrations of health-hazardous species, such as heavy metals, polycyclic aromatic hydrocarbons (PAH), and oxygenated-PAHs (OPAH). In China, emission controls have been implemented to improve air quality during large events, like the Youth Olympic Games (YOG) in August 2014 in Nanjing. In this work, six measurement campaigns between January 2014 and August 2015 were undertaken in Nanjing to determine the effects of emission controls and meteorological factors on PM2.5 concentration and composition. PAHs, OPAHs, hopanes, n‑alkanes, heavy metals, and several other inorganic elements were measured. PM2.5 and potassium concentrations were the highest in May-June 2014 indicating the prevalence of BB plumes in Nanjing. Emission controls substantially reduced concentrations of PM2.5 (31%), total PAHs (59%), OPAHs (37%), and most heavy metals (44-89%) during the YOG compared to August 2015. In addition, regional atmospheric transport and meteorological parameters partly explained the observed differences between the campaigns. The most abundant PAHs and OPAHs were benzo[b,k]fluoranthenes, fluoranthene, pyrene, chrysene, 1,8‑naphthalic anhydride, and 9,10‑anthracenedione in all campaigns. Carbon preference index and the contribution of wax n‑alkanes indicated mainly biogenic sources of n‑alkanes in May-June 2014 and anthropogenic sources in the other campaigns. Hopane indexes pointed to vehicular transport as the major source of hopanes, but contribution of coal combustion was detected in winter 2015. The results provide evidence to the local government of the impacts of the air protection regulations. However, differences between individual components were observed, e.g., concentrations of potentially more harmful OPAHs decreased less than concentrations of PAHs. The results suggest that the proportions of hazardous components in the PM2.5 may also change considerably due to emission control measures.
Atmospheric Environment | 2011
Heikki Lamberg; Kati Nuutinen; Jarkko Tissari; Jarno Ruusunen; Pasi Yli-Pirilä; Olli Sippula; Maija Tapanainen; Pasi I. Jalava; Ulla Makkonen; Kimmo Teinilä; Karri Saarnio; Risto Hillamo; Maija-Riitta Hirvonen; Jorma Jokiniemi
Journal of Nanoparticle Research | 2012
Jani Leskinen; Jorma Joutsensaari; Jussi Lyyränen; J. Koivisto; Jarno Ruusunen; Merja Järvelä; Timo Tuomi; Kaarle Hämeri; Ari Auvinen; Jorma Jokiniemi
Atmospheric Environment | 2011
Maija Tapanainen; Pasi I. Jalava; Jorma Mäki-Paakkanen; Pasi Hakulinen; Mikko S. Happo; Heikki Lamberg; Jarno Ruusunen; Jarkko Tissari; Kati Nuutinen; Pasi Yli-Pirilä; Risto Hillamo; Raimo O. Salonen; Jorma Jokiniemi; Maija-Riitta Hirvonen
Analytical and Bioanalytical Chemistry | 2011
Jarno Ruusunen; Maija Tapanainen; Olli Sippula; Pasi I. Jalava; Heikki Lamberg; Kati Nuutinen; Jarkko Tissari; Mika Ihalainen; Kari Kuuspalo; Jorma Mäki-Paakkanen; Pasi Hakulinen; Arto Pennanen; Kimmo Teinilä; Ulla Makkonen; Raimo O. Salonen; Risto Hillamo; Maija-Riitta Hirvonen; Jorma Jokiniemi
Atmospheric Environment | 2013
Anna Lähde; Sigurbjörg Sæunn Gudmundsdottir; Jorma Joutsensaari; Unto Tapper; Jarno Ruusunen; Mika Ihalainen; Tommi Karhunen; Tiina Torvela; Jorma Jokiniemi; Kristiina Järvinen; Sigurður Reynir Gíslason; Haraldur Briem; Sveinbjörn Gizurarson
Atmospheric Environment | 2015
Pasi I. Jalava; Qingeng Wang; Kari Kuuspalo; Jarno Ruusunen; Liqing Hao; Die Fang; Olli Väisänen; Antti Ruuskanen; Olli Sippula; Mikko S. Happo; Oskari Uski; Stefanie Kasurinen; Tiina Torvela; Hanna Koponen; K. E. J. Lehtinen; M. Komppula; Cheng Gu; Jorma Jokiniemi; Maija-Riitta Hirvonen