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Opis: Abstract. The geographical origin and source apportionment of submicron carbonaceous aerosols (organic aerosols, OAs, and black carbon, BC) have been investigated here for the first time, deploying high time-resolution measurements at an urban background site of Nicosia, the capital city of Cyprus, in the eastern Mediterranean. This study covers a half-year period, encompassing both the cold and warm periods with continuous observations of the physical and chemical properties of PM1 performed with an Aerosol Chemical Speciation Monitor (ACSM), an aethalometer, accompanied by a suite of various ancillary offline and online measurements. Carbonaceous aerosols were dominant during both seasons (cold and warm periods), with a contribution of 57 % and 48 % to PM1, respectively, and exhibited recurrent intense nighttime peaks (> 20–30 µg m−3) during the cold period, associated with local domestic heating. The findings of this study show that high concentrations of sulfate (close to 3 µg m−3) were continuously recorded, standing among the highest ever reported for Europe and originating from the Middle East region. Source apportionment of the OA and BC fractions was performed using the positive matrix factorization (PMF) approach and the combination of two models (aethalometer model and multilinear regression), respectively. Our study revealed elevated hydrocarbon-like organic aerosol (HOA) concentrations in Nicosia (among the highest reported for a European urban background site), originating from a mixture of local and regional fossil fuel combustion sources. Although air masses from the Middle East had a low occurrence and were observed mostly during the cold period, they were shown to strongly affect the mean concentrations levels of BC and OA in Nicosia during both seasons. Overall, the present study brings to our attention the need to further characterize primary and secondary carbonaceous aerosols in the Middle East, an undersampled region characterized by continuously increasing fossil fuel (oil and gas) emissions and extreme environmental conditions, which can contribute to photochemical ageing.
Ključne besede: PM1, BC, source apportionment, Cyprus, long range transport
Objavljeno v RUNG: 10.05.2024; Ogledov: 262; Prenosov: 2
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Opis: Measurements of PM2.5 concentrations in five major Greek cities over a two-year period using calibrated low-cost sensor-based particulate matter (PM) monitors (Purple Air PA-II) were combined with local meteorological parameters, synoptic patterns and air mass residence time models to investigate the factors controlling PM2.5 spatiotemporal variability over continental Greece. Fourteen sensors nodes in Athens, Patras, Ioannina, Xanthi, and Thermi (in the Metropolitan Area of Thessaloniki) were selected out of more than 100 of a countrywide network for detailed analysis. The cities have populations ranging from 65k to 3M inhabitants and cover different latitudes along the South-North axis. High correlations between the daily average PM2.5 levels were observed among all sites, indicating strong intra- and inter-city covariance of concentrations, both in cold and warm periods. Higher PM2.5 concentrations in all cities during the cold period were primarily associated with low temperatures and stagnant anticyclonic conditions, favoring the entrapment of residential heating emissions from biomass burning. Anticyclonic conditions were also connected to an increased frequency of PM2.5 episodes, exceeding the updated daily guideline value (15 μg m−3) of the World Health Organization (WHO). During the warm period, nearly uniform PM2.5 levels were encountered across continental Greece, independently of their population size. This uniformity strongly suggests the importance of long-range transport and regional secondary aerosol formation for PM2.5 during this period. Peak concentrations were associated mainly with regional northern air flows over Greece and the Balkan Peninsula. The use of the measurements from dense air quality sensor networks, provided that a robust calibration protocol and continuous data quality assurance practices are followed, appears to be an efficient tool to gain insights on the levels and variability of PM2.5 concentrations, underpinning the characterization of spatial and seasonal particularities and supporting real-time public information and warning.
Ključne besede: particulate matter, PM2.5, biomass burning, low-cost sensors, purple air PA-II, concentration weighted trajectory, potential source contribution function
Objavljeno v RUNG: 10.05.2024; Ogledov: 279; Prenosov: 2
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Ključne besede: ACSM, PMF, cooking organic aerosol, meat charbroiling
Objavljeno v RUNG: 10.05.2024; Ogledov: 277; Prenosov: 0
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Opis: Vertical profiling of aerosol particles was performed during the PANhellenic infrastructure for Atmospheric Composition and climatE chAnge (PANACEA) winter campaign (10 January 2020–7 February 2020) over the city of Ioannina, Greece (39.65° N, 20.85° E, 500 m a.s.l.). The middle-sized city of Ioannina suffers from wintertime air pollution episodes due to biomass burning (BB) domestic heating activities. The lidar technique was applied during the PANACEA winter campaign on Ioannina city, to fill the gap of knowledge of the spatio-temporal evolution of the vertical mixing of the particles occurring during these winter-time air pollution episodes. During this campaign the mobile single-wavelength (532 nm) depolarization Aerosol lIdAr System (AIAS) was used to measure the spatio-temporal evolution of the aerosols’ vertical profiles within the Planetary Boundary Layer (PBL) and the lower free troposphere (LFT; up to 4 km height a.s.l.). AIAS performed almost continuous lidar measurements from morning to late evening hours (typically from 07:00 to 19:00 UTC), under cloud-free conditions, to provide the vertical profiles of the aerosol backscatter coefficient (baer) and the particle linear depolarization ratio (PLDR), both at 532 nm. In this study we emphasized on the vertical profiling of very fresh (~hours) biomass burning (BB) particles originating from local domestic heating activities in the area. In total, 33 out of 34 aerosol layers in the lower free troposphere were characterized as fresh biomass burning ones of local origin, showing a mean particle linear depolarization value of 0.04 ± 0.02 with a range of 0.01 to 0.09 (532 nm) in a height region 1.21–2.23 km a.s.l. To corroborate our findings, we used in situ data, particulate matter (PM) concentrations (PM2.5) from a particulate sensor located close to our station, and the total black carbon (BC) concentrations along with the respective contribution of the fossil fuel (BCff) and biomass/wood burning (BCwb) from the Aethalometer. The PM2.5 mass concentrations ranged from 5.6 to 175.7 μg/m3, while the wood burning emissions from residential heating were increasing during the evening hours, with decreasing temperatures. The BCwb concentrations ranged from 0.5 to 17.5 μg/m3, with an extremely high mean contribution of BCwb equal to 85.4%, which in some cases during night-time reached up to 100% during the studied period.
Ključne besede: lidar, depolarization ratio, fresh biomass burning aerosols, domestic heating, black carbon, PM2.5
Objavljeno v RUNG: 10.05.2024; Ogledov: 288; Prenosov: 3
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Opis: Offline aerosol mass spectrometer (AMS) measurements can provide valuable information about ambient organic aerosols in areas and periods in which online AMS measurements are not available. However, these offline measurements have a low temporal resolution, as they are based on filter samples usually collected over 24 h. In this study, we examine whether and how this low time resolution affects source apportionment results. We used a five-month period (November 2016–March 2017) of online measurements in Athens, Greece, and performed positive matrix factorization (PMF) analysis to both the original dataset, which consists of 30 min measurements, and to time averages from 1 up to 24 h. The 30 min results indicated that five factors were able to represent the ambient organic aerosol (OA): a biomass burning organic aerosol factor (BBOA), which contributed 16 % of the total OA; hydrocarbon-like OA (HOA) (29 %); cooking OA (COA) (20 %); more-oxygenated OA (MO-OOA) (18 %); and less-oxygenated OA (LO-OOA) (17 %). Use of the daily averages resulted in estimated average contributions that were within 8 % of the total OA compared with the high-resolution analysis for the five-month period. The most important difference was for the BBOA contribution, which was overestimated (25 % for low resolution versus 17 % for high resolution) when daily averages were used. The estimated secondary OA varied from 35 % to 28 % when the averaging interval varied between 30 min and 24 h. The high-resolution results are expected to be more accurate, both because they are based on much larger datasets and because they are based on additional information about the temporal source variability. The error for the low-resolution analysis was much higher for individual days, and its results for high-concentration days in particular are quite uncertain. The low-resolution analysis introduces errors in the determined AMS profiles for the BBOA and LO-OOA factors but determines the rest relatively accurately (theta angle around 10∘ or less).
Ključne besede: AMS, offline PMF, ACSM, organic aerosols
Objavljeno v RUNG: 10.05.2024; Ogledov: 325; Prenosov: 3
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