Measurement report : Long-term measurements of aerosol precursor concentrations in the Finnish subarctic boreal forest

• Published in: Atmospheric Chemistry and Physics
• Main Authors: Jokinen, Tuija, Lehtipalo, Katrianne, Thakur, Roseline Cutting, Ylivinkka, Ilona, Neitola, Kimmo, Sarnela, Nina, Laitinen, Totti, Kulmala, Markku, Petäjä, Tuukka, Sipilä, Mikko
• Other Authors: Institute for Atmospheric and Earth System Research (INAR), Polar and arctic atmospheric research (PANDA), Global Atmosphere-Earth surface feedbacks
• Format: Article in Journal/Newspaper
• Language: English
• Published: COPERNICUS GESELLSCHAFT MBH 2022
• Subjects: 114 Physical sciences; Arctic; Varrio; Subarctic
• Online Access: http://hdl.handle.net/10138/342819

Aerosol particles form in the atmosphere via the clustering of certain atmospheric vapors. After growing into larger particles by the condensation of low-volatility gases, they can affect the Earth's climate by scattering light and acting as cloud condensation nuclei (CCN). Observations of low-volatility aerosol precursor gases have been reported around the world, but longer-term measurement series and any Arctic data sets showing seasonal variation are close to nonexistent. Here, we present similar to 7 months of aerosol precursor gas measurements performed with a nitrate-based chemical ionization atmospheric pressure interface time-of-flight (CI-APi-TOF) mass spectrometer. We deployed our measurements similar to 150 km north of the Arctic Circle at the SMEAR I (Station for Measuring Ecosystem-Atmosphere Relations) continental Finnish subarctic field station, located in the Varrio strict nature reserve. We report concentration measurements of the most common compounds related to new particle formation (NPF): sulfuric acid (SA), methane sulfonic acid (MSA), iodic acid (IA) and the total concentration of highly oxygenated organic molecules (HOMs). At this remote measurement site, SA originates from both anthropogenic and biological sources and has a clear diurnal cycle but no significant seasonal variation. MSA shows a more distinct seasonal cycle, with concentrations peaking in the summer. Of the measured compounds, IA concentrations are the most stable throughout the measurement period, except in April during which time the concentration of IA is significantly higher than during the rest of the year. Otherwise, IA has almost identical daily maximum concentrations in spring, summer and autumn, and on NPF event or non-event days. HOMs are abundant during the summer months and low in the autumn months. Due to their low autumn concentrations and high correlation with ambient air temperature, we suggest that most HOMs are products of biogenic emissions, most probably monoterpene oxidation products. NPF events at ...