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Article

Analysis of Particulate Matter Concentration Variability and Origin in Selected Urban Areas in Poland

by
Izabela Sówka
1,*,
Anna Chlebowska-Styś
1,
Łukasz Pachurka
2,
Wioletta Rogula-Kozłowska
3 and
Barbara Mathews
4
1
Faculty of Environmental Engineering, Wroclaw University of Science and Technology, Wybrzeże Wyspiańskiego 27, 50-370 Wrocław, Poland
2
Galwanizer Ltd., Swidnicka Str. 38, 58-200 Dzierzoniow, Poland
3
The Main School of Fire Service, Słowackiego Str. 52/54, 01-629 Warsaw, Poland
4
Institute of Environmental Engineering, Polish Academy of Sciences in Zabrze, M. Skłodowskiej-Curie 34 Str., 41-819 Zabrze, Poland
*
Author to whom correspondence should be addressed.
Sustainability 2019, 11(20), 5735; https://0-doi-org.brum.beds.ac.uk/10.3390/su11205735
Submission received: 15 September 2019 / Revised: 6 October 2019 / Accepted: 14 October 2019 / Published: 16 October 2019
(This article belongs to the Special Issue Green Technologies in Air Treatment)

Abstract

:
The work presents the results of research and analyses related to measurements of concentration and chemical composition of three size fractions of particulate matter (PM), PM10, PM2.5 and PM1.0. The studies were conducted in the years 2014–2016 during both the heating and non-heating season in two Polish cities: Wrocław and Poznań. The studies indicate that in Wrocław and Poznań, the highest annual concentrations of particulate matter (PM1.0, PM2.5, and PM10) were observed in 2016, and the mean concentrations were respectively equal to 18.16 μg/m3, 30.88 μg/m3 and 41.08 μg/m3 (Wrocław) and 8.5 μg/m3, 30.8 μg/m3 and 32.9 μg/m3 (Poznań). Conducted analyses of the chemical composition of the particulate matter also indicated higher concentrations of organic and elemental carbon (OC and EC), and water-soluble ions in a measurement series which took place in the heating season were studied. Analyses with the use of principal component analysis (PCA) indicated a dominating percentage of fuel combustion processes as sources of particulate matter emission in the areas considered in this research. Acquired results from these analyses may indicate the influence of secondary aerosols on air quality. In the summer season, a significant role could be also played by an influx of pollutants—mineral dust—originating from outside the analyzed areas or from the resuspension of mineral and soil dust.

Graphical Abstract

1. Introduction

In the last few decades, concentrations of sulfur dioxide or nitrogen oxide within Europe, including Poland, decreased significantly [1]. However, there are many regions in Europe where standards established for particulate matter (PM) are still being exceeded, which negatively influences the health of people inhabiting those regions. Undesired effects are brought forth even by the mere presence of fine particles in the organism and in addition, their toxic influence is multiplied by heavy metals and polycyclic aromatic hydrocarbons, which are their carriers [2,3,4,5,6,7].
According to the European Environment Agency (EEA), in 2018, the standard permissible limit of days (in which the 24 hour average value of PM10 concentration is higher than 50 μg/m3 (the so called acceptable frequency of exceedance)), was exceeded in as many as 19 among 28 member states (19% of all measurement stations) [8]. The highest air pollution levels in Europe are observed in the eastern and central part of the European continent, which includes Poland [1,8,9]. In the years 2010–2014, the highest annual average concentrations of PM10 in the air were observed in the following Polish cities: Kraków, Poznań, Wrocław and Warszawa. The lowest concentrations of particulate matter were determined in the cities of northern Europe, such as Denmark or Copenhagen [9]. The problem of polluted air is counteracted by the majority of Polish metropolitan areas, while at the same time the higher pollution concentrations and more frequent occurrences of smog episodes are confirmed in the southern part of the country [10,11,12,13,14]. Moreover, in the case of Polish metropolitan areas, there is a clear seasonal variability in concentrations of particulate matter. [15]. The condition described above is influenced by the topography and meteorological factors, but a large role is played by methods used to heat dwellings (dwelling-adjacent individual boiler rooms with hard or brown coal used as fuel)—so called low-stack emissions from municipal and household sectors [11,13,14,16,17,18].
Metropolitan areas present not only seasonal variability in pollutant concentration, but also daily variability, which is influenced by the daily rhythm of inhabitants commuting to work or schools. In this case, a large influence on the air quality originates from traffic emissions. Intensive car traffic in the morning and noon hours undoubtedly influences the increase in pollutant emissions in those hours and also affects the composition of particulate matter [9,15,19,20,21]. In the year 2014 in Poland, road transport was responsible for 22% of the total emissions of particulate matter and 59% of the emissions originated from other stationary sources, which included low-stack emissions [9].
In Poland an entity responsible for monitoring the air, as a part of state environmental monitoring (SEM), is the Chief Inspectorate of Environmental Protection (CIEP). In standard air monitoring, the research on PM10 particulate matter composition in urbanized areas is limited to analyses of Cd, Ni, Pb, As and benzo(a)pyrene (BaP) [22], and in the case of the PM2.5 fraction, the measurement of its chemical composition is not carried out at urban background stations. It is a significant limitation, especially when it is necessary to determine the origins of the particulate matter in a specific urban area. Establishing the chemical composition of particulate matter enables us to indicate the sources of particulate matter emission, and as a consequence, it may aid efforts aiming to eliminate the problem of poor air quality.
Statistical methods find their use in the identification of emission sources through extraction of the most correlated factors, based on, among others, the concentrations of water-soluble ions, organic carbon (OC) and elemental carbon (EC), which subsequently enables us to classify specific factors and attribute them to a particular emission source (e.g., transport, power generation, industry). In this scope, statistical methods include, among others, principal component analysis (PCA) [23,24,25,26], which is one of the techniques used to determine the sources of particulate matter emission based on its chemical composition [14,27,28,29,30].
This work aimed to carry out a comparative analysis of the variability of concentration and composition of fine particulate matter in the area of Wrocław and Poznań city, as well as the identification of its sources. Wrocław and Poznań were selected due to the high population density and due to the fact that that little research has been done to date on the chemical characteristics of PM in these cities. In contrast to the areas of southern and central Poland, the areas of Lower Silesia and Greater Poland are regions where PM measurements are conducted, and their results are reported only to the extent necessary for routine air quality monitoring. In Poznań, chemical composition (macro components) of PM1 and PM2.5 is not recognized at all.

2. Area and Methodology of the Research

2.1. Research Time Periods and Characteristics of Measurement Points

In the case of our own studies carried out in Wrocław, the sample collection of PM10, PM2.5 and PM1 particulate matter took place at the measurement point located at Kosiby Street (Figure 1, Station 1) in the time periods: 26 June–26 July 2014 (summer 2014) and 7 January–7 February 2015 (winter 2015). Further studies of PM10, PM2.5 and PM1 were conducted in the time periods: 31 July–13 August 2015 (summer 2015), 9–26 January 2016 (winter 2016) and 9–23 May 2016 (spring 2016).
The remaining data used in this work originates from the Voivodship Inspectorate for Environmental Protection (VIEP) measurement stations in Wrocław. Data from the years 2014–2016 originates from the station located at Na Grobli Street (Figure 1, Station 2). A manual gravimetric measurement method with 2.5 µm fraction separation was used. At Wiśniowa Alley (Figure 1, Station 4), automatic measurement with 2.5 µm fraction separation was used. Data from the 2015–2016 period was measured at the station at J. Conrada–Korzeniowskiego Street (Figure 1, Station 3) using automatic measurement. For the PM10 fraction, data from the 2014–2016 period originated from the measurement stations located at Orzechowa Street (Figure 1, Station 5) and J. Conrada–Korzeniowskiego Street (Figure 1, Station 3). These measurements were done with the use of the manual gravimetric method with separation of the 10 µm fraction.
The measurement point in the studies representing urban background was stationed in the Biskupin estate in Wrocław at Kosiby 6/8 Street (Figure 1, Station 1) located in the southeastern part of the Śródmieście district, which encompasses a large number of green areas. The surroundings of the research station are an area of diverse character, which include parks, garden plots, low-rise buildings (semi-detached houses, villas) and high-rise buildings (blocks of flats). The measurement point was located about 5 km (in a straight line) from an electrical power and heating plant, about 0.1 km from the closest multi-family development (multi-family tenement house), about 180 m from another multi-family development (blocks of flats), and about 130 m from a road, whose traffic included passenger cars, trams, buses and bicycles.
The remaining measuring points are stations belonging to the VIEP in Wrocław and represent stations of urban background (Station 2, 3 and 5) and a station considered a road traffic station (Station 4). Stations 2 and 3 are located far from main traffic routes and are surrounded by green areas and multi-family dwellings. Station 4 at Wiśniowa Alley is located close to the main communication route in Wrocław, the intersection of Haller Street and Wiśniowa Alley, and is also located in the neighborhood of multi-family housings.
In the case of studies that took place in Poznań, two measurement campaigns were carried out: in the fall–winter season (25 October–22 November 2016) and in the summer season (5 June–2 July 2017) at three measurement stations (Figure 1, Stations 6–8).
Two measurement stations (at Szmanowskiego Street and at Polanka Street) belonged to the Provincial Environment Protection Inspector in Poznań; these were used as urban background stations. The station at Szymanowskiego Street (Station 6) borders with service and multi-family developments from the west, with multi-family buildings from the north and south and from the west and southwest directions, it is bordered by Podolany (a district of Poznań), which is characterized by single-family developments. At Podolany, only a manual measurement of PM10 particulate matter is carried out. The station at Polanka Street (Station 7) is surrounded by multi-family buildings, heated by local boiler rooms. Close to the north, there is also a man-made lake called Jezioro Maltańskie. From the east, there is a multi-family development heated by a district heating system and from the southwest, there is a large shopping mall. In the distance, about 800 m in the southeastern direction, there is a point emission source—the Malta-Décor company—which deals with the production of decorative paper. This work used the filters from the manual collection of PM2.5 from this station. Our own measurement station was located at Jana Pawła II 10 Street (Station 8). It is a divided street with separated tram trackage between the lanes. This segment is usually gridlocked. The selected location was supposed to reflect the influence of emissions from road traffic on air quality in this area. The area is directly bordered by the street. The device was installed at a distance of about 50 m from the street, on a green terrain belonging to the Poznan Supercomputing and Networking Center (PCSS). From the west, the station bordered directly with the street and right behind it is the Jezioro Maltańskie lake. From the north, the station bordered with green terrains, from the west with the Cybina river and from the south with the Poznan University of Technology Campus. At the station, the measurements were conducted manually by collection of three particulate matter fractions: PM10, PM2.5 and PM1.0.
The dates of measurements were intentionally planned for the heating season and the non-heating season in order to compare the chemical composition of particulate matter in two thermally different periods.

2.2. Collection of Samples and Determination of Particulate Matter Concentration

In order to collect PM1.0, PM2.5 and PM10 samples, Harvard type impactors (MS&T Area Samplers, Air Diagnostics and Engineering, Inc., Harrison, ME, USA) were used. The airflow was forced by ultra-silent, oil-free vacuum pumps (Air Diagnostics and Engineering, air sampling pump, SP-280E model, Harrison, USA). Quartz fiber filters-Whatman QM-A (Wathaman Healthcare UK Limited, Amersham Place, Little Chalfont, Buckinghamshire, UK)with diameter of 37 mm were used as a substrate. The flow rate during sample collection was respectively equal to: samples ≤1.0 µm—23 dm3/min, samples ≤2.5 µm and ≤10 µm—10 dm3/min. The volume of pumped air was controlled by an Actaris type flowmeter. The time of sample collection was 24 h. The measurement of particulate matter was carried out with use of the gravimetric method in accordance with the PN-EN 12341: 2014 standard.

2.3. Analysis of OC and EC Content in Particulate Matter Samples

In order to determine organic carbon (OC) and elemental carbon (EC) in particulate matter samples, a thermo-optic analyzer of organic and elemental carbon (Model 4L Main Oven Assembly, Sunset Laboratory Inc., Tigard, OR, USA) with flame ionization detection (FID) was used. Samples of particulate matter, in the form of quartz filter specimens with an area of 1 cm2, were subjected to an analysis composed of two stages. First, by the gradual heating of the sample in a stream of helium, the organic fraction (OC) was released from the filter. In the following stage, a specimen of the filter was heated in an oxidizing mixture of helium and oxygen in order to release elemental carbon (EC). The heating of the examined samples progressed in accordance with the parameters determined in a specific measurement protocol. Compounds separated from the sample during subsequent heating stages in the furnace, in oxidizing conditions and with the presence of magnesium oxide, were transformed in stoichiometric ratio in relation to CO2. Carbon dioxide produced during the analysis was further reduced in a methanizer, in the presence of a hydrogen and a nickel catalyst, to methane, which was measured with the use of FID. Based on transmittance measurement which was done during the thermo-optic analysis with the use of a red-light laser beam (thermal optical transmittance (TOT)), the corrections for the determined contents of OC and EC were made. The last stage of the measurement process was the inclusion of a fixed volume loop in order to inject an external standard at the end of each analysis, which enabled us to provide optimal and stable conditions for the measurement, increasing the repeatability of the whole analytical method.
With the use of the carbon analyzer, it is possible to take measurements in accordance with several standard temperature protocols, which differ from each other in the values of temperature thresholds, their number and duration. The analysis for this work was carried out using the “EUSAAR_2” protocol, which was designed as the suggested standard method for European measurement stations as a part of a European Supersites for Atmospheric Aerosol Research (EUSAAR) project.
Certified gases from Air Liquide (Cracow, Poland) were used to conduct analyses.
Validation parameters for the methods used are as follows:
  • Total measurement uncertainty of EC in PM2.5 particulate matter: 5%;
  • EC limit of detection (LOD): 0.1 μg/cm2;
  • Total measurement uncertainty of OC in PM2.5 particulate matter: 5%;
  • OC limit of detection (LOD): 0.47 μg/cm2.

2.4. Analysis of the Content of Ions Soluble in Water in Samples of Particulate Matter

Determination of water-soluble ions in samples of particulate matter deposited on filters consisted of extracting anions and cations from particulate matter and in deionized water and later determining their content in water extracts. The extraction of ions was performed with the use of a vortexer (12 h) in a cold room (≤18 °C) at 60 cycles per minute. Moreover, before the agitation process, the samples of particulate matter were subjected to ultrasound for 1 h in a water bath (at ≤27 °C). After the agitation process, acquired extracts were cleansed with the use of micropore polyethersulfone (PES) syringe filters.
The content of ions acquired from water extracts was determined with the use of the ion chromatography method. In order to determine anions (F, Cl, NO3, PO43−, SO42−) and cations (Na+, NH4+, K+, Ca2+, Mg2+) in samples of particulate matter, authors used chromatographs of Dionex ICS 1100 type (Thermo Scientific company, USA) with a dual piston serial pump, automatic electrolytic suppression, and vacuum eluent degassing before the guard column and thermostating columns.
Chromeleon®SE (version 7, Thermo Scientific company, USA) dedicated software was used in order to operate the chromatograph. Only reagents with purity of at least p.a. grade were used in the analysis and the solutions for the preparation of calibration curves and control samples were done based on LGC standards of known uncertainty and concentration equal to 1 g/l.
Limits of detections were at the following levels: 0.01 mg/dm3 for NH4+, 0.20 mg/dm3 for Na+ and Mg2+, 0.22 mg/dm3 for Ca2+, 0.25 mg/dm3 for K+, 0.06 mg/dm3 for NO3, 0.07 mg/dm3 for F and Cl, 0.10 mg/dm3 for SO42− and PO43−.

2.5. Analysis of Main Components

This work presents the results of the PCA analyses carried out based on the determination of concentrations of organic carbon, elemental carbon, the following anions: F, Cl, NO3, PO43−, SO42− and the following cations: Na+, NH4+, K+, Mg2+, Ca2+ for measurements done at the stations at Kosiby Street in Wrocław (Station 1), Polanka Street (Station 7) and Jana Pawła II Street (Station 8) in Poznań, which respectively represent urban background stations and traffic stations. The calculations assumed varimax normalized rotation and that the factor loadings exceeding 0.7 are the most significant for each principal component [31]. Because of the short time of measurement campaigns carried out in Wrocław, acquired measurement data was merged into seasons with a similar period of concluded measurements, e.g., spring–summer season (non-heating season: Series 1 (summer) 2014; Series 3 (summer) 2015; Series 5 (spring) 2016) and fall–winter season (heating season: Series 2 (winter) 2015; Series 4 (winter) 2016). In the case of Poznań, the analysis was performed for two measurement stations with separation for two thermal seasons.

3. Result and Discussion

3.1. Analysis of Variability in Concentration of Particulate Matter in Wrocław and Poznań

Analysis of annual average values of concentrations acquired as a part of SEM in the years 2014–2016 in Wrocław and Poznań, alongside averaged values for the heating season (December–March) and the non-heating season (April–September) are presented in Figure 2. Pursuant to the regulation of the Minister for Environmental Protection [22], the permissible annual average concentration of PM2.5 in the air is equal to 25 µg/m3; in 2014 the applicable margin of tolerance was equal to 1 µg/m3. In the case of PM10 particulate matter, the law sets out two permissible values: annual average value equal to 40 µg/m3 and permissible number of days with 24 h average value exceeding 50 µg/m3. In accordance with the numbers described above, in 2014–2016, the analysis of data indicates that the standard for PM2.5 particulate matter was exceeded three-fold in Wrocław (each time at the station at Wiśniowa Alley—Station 4). In Poznań, the limits were not exceeded. However, the annual average values were closing in on the permissible value threshold. In Poznań as in Wrocław, significantly higher values of particulate matter were observed in the heating season. The values were twice as high than in the summer season. A similar situation occurs in other Polish urban areas [10,18,32,33].
The analyses of the studies carried out in Wrocław (Station 1) indicate that the largest concentrations of PM10 particulate matter were recorded during the studies carried out in the heating season in the winter of 2016. The maximum concentration of the PM10 fraction at that time was equal to 97.81 µg/m3 (Table 1). Moreover, for the fraction studied in that research period, the authors observed the highest standard deviation (± 22.98) for specific concentration values of the analyzed period. A large standard deviation (± 10.66) was recorded for PM1.0 particulate matter. The results acquired in that measurement series for the studied fraction (PM1.0) were contained within the range of 2.84–38.20 μg/m3 [34].
In the case of Poznań, the average concentration of PM10 in the winter season was higher at the Szymanowskiego Street station. However, during the measurement series, the concentration levels at both stations were at a similar level (Table 2). For the station at Jana Pawła II Street (Station 8), an average concentration of PM10 in the summer season was 35% lower than in the first measurement series; moreover, in the case of the station at Szymanowskiego Street (Station 6), the concentration in the second measurement series was lower than the average concentration in the first measurement series by as much as 55%. Perhaps this phenomenon is related to the phenomenon of low-stack emissions. The surroundings of the station at Szymanowskiego Street are composed mainly of single-family buildings, and the method of heating these houses in the heating season affects the air quality in this case. However, it must be noted that the average concentration of PM10 in the summer season at the station at Szymanowskiego Street was lower than at the station at Jana Pawła II Street. This situation also confirms that elimination of this factor (heating of the buildings) affects the air quality in a given area. The levels of PM10 pollution at both stations were close to the concentrations of PM10 observed in the same time periods in the previous years of measurements carried out by VIEP in the cities of Wielkopolska, with the exception of Kalisz (where there are specific conditions for the dispersion of pollutants) [17,32]. Concentrations of PM2.5 during the first measurements series ranged from 2.2 µg/m3 to 39.9 µg/m3 at the station at Jana Pawła II Street (Station 8). At the station at Polanka Street (Station 7), the concentrations ranged from 7.2 µg/m3 to 88.5 µg/m3. The average concentration was respectively equal to 15.2 µg/m3 for the station at Jana Pawła II Street and 30.8 µg/m3 for the station at Polanka Street. Concentrations noted during the second measurement series (summer period) were lower and ranged from 1.2 µg/m3 to 40.3 µg/m3 at the station at Jana Pawła II Street (Station 8) and from 7.2 µg/m3 to 17.1 µg/m3 at the station at Polanka Street (Station 7). The average concentrations of PM2.5 during the second measurement series at both stations were very similar and equal to 10.4 µg/m3 at Jana Pawła II Street and 11.0 µg/m3 at Polanka Street. Thus, the average concentration of PM2.5 at Jana Pawła II Street, in the summer season, was 32% lower than in the winter season, and at the station at Polanka Street, the concentration was lower by as much as 64%. At the station at Jana Pawła II Street, which is treated as a so-called road traffic station and was established to determine how emission from road traffic influences the air quality, we did not observe as distinctive differences in the concentrations of PM10 and PM2.5 between seasons, as we did for the two remaining background stations. However, it should be highlighted that the levels of particulate matter concentration in the winter season at every station were considerably higher than concentrations determined by World Health Organization (WHO) as safe for the health and life of people (PM10—20 µg/m3, PM2.5—10 µg/m3) [35].
Twenty-four-hour concentrations of PM1.0 in the winter season ranged from 2.47 µg/m3 to 22.87 µg/m3 and in the summer season from 2.72 µg/m3 to 10.35 µg/m3. The average concentration in the winter season was equal to 8.50 µg/m3 and in the summer season it was lower by 33% and equal to 5.72 µg/m3. The differences in PM1.0 concentrations between seasons are not as large as in the case of remaining two fractions; however, in the winter season, the concentrations are generally higher which is related to the origins of the finest ambient particles emitted primarily from fossil fuel (solid and liquid) and biomass combustion [36]. It is confirmed that in the winter season, there is an increase in the emission of gaseous precursors of PM1.0; therefore, it is obvious that the concentration of the finest ambient particles is increasing simultaneously. The concentrations of PM1.0 in Poznań are comparable to concentrations measured in other Polish cities and also higher than in the countries of western Europe [35,37]. High concentrations of PM1.0 in cities are related to the presence of many emission sources in those areas. It is however necessary to mention that high concentrations of PM1.0 in Poland are also confirmed in rural and suburban stations. This is most likely related to the process of transportation of PM1.0 from other areas, often very distant ones. The finest fraction of particulate matter may be present in the atmosphere for a long time; therefore, it may be transported a long distance [38]. Higher concentrations of particulate matter in the heating season in Poland are confirmed by numerous studies [29,39,40].
Studies carried out in Wrocław and Poznań confirmed that concentrations of all PM fractions are higher in the heating period than in the non-heating period.

3.2. Analysis of Variability in Concentrations of Elemental/Organic Carbon and Selected Ions

Table 3 presents values of concentrations of selected anions, cations, OC and EC, along with descriptive statistics in specific measurement series for PM2.5 and PM10 fractions in Wrocław. These studies took place in Wrocław both in the heating and non-heating seasons, and high concentrations of PO43− and SO42 ions were measured. In the heating season for Series 4 and in the non-heating season for Series 5, the average concentration of total carbon (TC) (TC = EC + OC) was respectively equal to 4.90 μg/m3 and 1.53 μg/m3. The highest values of organic carbon in PM2.5 were measured in Series 4 (winter 2016) and the value was equal to 17.13 μg/m3. For the 2016 winter season, the average concentration of OC was equal to 7.96 µg/m3, with daily average concentrations values contained in the range of 2.00 µg/m3 to 17.13 µg/m3. The concentration of EC was lower than the content of OC in all measurement series carried out in Wrocław at Kosiby Street. The highest average value of EC for the winter period in 2016 (Series 4) was equal to 1.83 µg/m3, and the daily average concentrations ranged from 0.46 µg/m3 to 4.06 µg/m3. Analysis of the composition of PM2.5 in Wrocław in the winter season of 2015 revealed that among the determined cations, dominating concentrations were observed for NH4+ (2.20 µg/m3) and Na+ (1.14 µg/m3). The daily average concentration of NH4+ in atmospheric air ranged from 0.30 µg/m3 to 5.29 µg/m3. The daily average concentration of Na+ ranged from 0.64 µg/m3 to 8.12 µg/m3. Among the determined anions, for the winter season, a dominating concentration was noted for SO42−, NO3 and Cl. Sulfate anion content in the samples ranged from 4.75 µg/m3 to 11.34 µg/m3. The range of concentrations of NO3 in the air was from 1.14 μg/m3 to 18.56 µg/m3. Concentrations of Cl ions ranged from 0.57 μg/m3 to 10.51 µg/m3. The concentration of OC determined in PM2.5 at the station at Kosiby Street ranged between 1.22 µg/m3 and 16.48 µg/m3, with the average value for measurement period at the level of 5.79 µg/m3. In the summer season, the dominating percentage in the total weight of ions determined in PM during Series 3 was SO42− (2.28 µg/m3), NO3 (0.69 µg/m), NH4+ (2.44 µg/m3) and Ca2+ (2.25 µg/m3). In the case of EC and OC, the maximum daily concentration was respectively at the level of 0.63 µg/m3 (Series 1) and 4.26 µg/m3 (Series 3). In the non-heating season, the higher content of NO3, SO42− and also OC and EC in the composition of PM2.5 may indicate an influence of fuel combustion on the composition of particulate matter and, moreover, the higher content of Na+ and Cl ions may indicate the influence of salt spread on roads in the winter season [12,44,45].
The analysis of the composition of PM2.5 in Poznań in the fall–winter season revealed that among the determined cations, the dominating percentage belonged to (Table 3): Na+ (at both stations), NH4+ (Polanka—Station 7), and Ca2+ (Jana Pawła II Street—Station 8) ions. Concentrations of Na+ in the samples originating from the Polanka Street station ranged from 0.451 µg/m3 to 1.053 µg/m3 and in samples from Jana Pawła II Street station, concentrations ranged from 0.619 µg/m3 to 2.896 µg/m3. The concentration of NH4+ in samples collected at the station at Polanka Street was twice as high as in samples collected at the second station and range from 0.050 µg/m3 to 2.540 µg/m3 with an average value of 1.102 µg/m3. Furthermore, in the samples collected at the station at Jana Pawła II Street (Station 8) a three-fold higher concentration of Ca2+ (average: 0.730 µg/m3) was observed in relation to the concentration measured at the station at Polanka Street (0.197 µg/m3). Among the determined anions, the dominating percentage belonged to SO42−, NH3 and F ions. The content of sulfate anions in samples taken at the stations at Polanka Street ranged from 0.940 µg/m3 to 7.939 µg/m3 and in samples collected at Jana Pawła II station, the content ranged from 0.889 µg/m3 to 6.043 µg/m3. The percentage of NO3 in the samples was relatively high and equal to 0.870–21.816 µg/m3 in the samples from Polanka Street station (Station 7) and 0.638–8.607 µg/m3 from Jana Pawła II Street station (Station 8). The concentrations of F ions ranged from 0.757–6.317 µg/in samples collected at Polanka Street and 1.988–10.508 µg/m3 in samples collected at the Jana Pawła II Street station. The determined range of concentrations of nitrate in samples collected at both measurement stations is similar to concentrations determined for other locations in Poland, which could indicate its high percentage in the general background of the country. Values of concentrations of sulfate anions at Polanka Street are similar to concentrations determined in the air of Katowice, and at the same time, higher than in other regions in the country (Gdańsk, Puszcza Borecka) [46,47]. It may be assumed that the air quality in Poznań is affected by the same factors as in south of the country; i.e., primarily combustion of hard and brown coal. The daily average concentrations of OC determined in PM2.5 at the station at Polanka Street ranged from 2.91 µg/m3 to 37.94 µg/m3 with an average value for the measurement period equal to 13.52 µg/m3. In the case of the station located at Jana Pawła II Street, the concentrations of OC ranged from 2.35 µg/m3 to 26.66 µg/m3 with an average value equal to 8.36 µg/m3. The concentrations of EC in the air were lower than the concentrations of OC and ranged respectively from 1.14 µg/m3 to 6.22 µg/m3 for PM2.5 measured at station at Polanka Street and 0.83–6.64 µg/m3 for PM2.5 at the station at Jana Pawła II Street. In the summer season, the concentrations of all analyzed ions at both stations were at a very similar level; however, they were much lower in comparison to the fall–winter season for most of the ions. The dominating percentage in the sum of ions determined in PM in the summer season belonged to PO43− (0.328 µg/m3 at the station at Jana Pawła II Street and 0.363 µg/m3 at the station at Polanka Street), SO42− (0.290 µg/m3 at the station at Jana Pawła II Street and 0.86 µg/m3 at the station at Polanka Street) and Na+ (0.465 µg/m3 at both of the stations). At the station at Polanka Street, the concentrations of F (99%), Cl (63%), NO3 (74%) and K+ (84%) and Ca2+ (80%) determined in PM2.5 particulate matter in the summer season were lower than in the winter season. Furthermore, concentrations of Mg2+ bound to PM2.5 in the air at the station at Polanka Street, were twice as high than in the summer season. In the case of the station at Jana Pawła II Street, the concentration of ions bound with PM2.5 in the summer season was lower than in the winter season. For F, these concentrations were lower than 99%, (Cl = 81%; NO3 = 64%; PO43− = 43%; SO42− = 68%; Na+ = 25%; NH4+ = 83%; K+ = 97%; Mg2+ = 89% and Ca2+ = 68%). A lower content of PO43−, SO42− and NH4+ ions in the sum of the ions determined in PM2.5 in the non-heating season may indicate the influence of fossil fuel and biomass combustion on the composition of particulate matter. Cl and Na+ ions may indicate the influence of salting and sanding in the winter season [12,44,45]. The content of OC and EC in PM2.5 particulate matter at both of the stations in the summer season were at a similar level, however it was about four times lower than the content in the winter season. Higher concentrations of OC, EC and selected ions during the heating period are also observed in other Polish and European cities (Table 4).

3.3. Identification of the Sources of Origin of Particulate Matter in Wrocław and Poznań

Table 5 and Figure 3 present, respectively, the results of the PCA analysis factors for the PM2.5 fraction and linear dependence of the sum of PM2.5-bound cations vs. the sum of PM2.5-bound anions obtained for the heating and non-heating season and for the two selected cities under study.
In the case of Wrocław, the conducted analyses (Table 4) enabled the identification of four main components in the heating season. In the Principal Component (PC) 1 (Factor 1), for the heating season, there was a correlation between the main component and F and Cl anions, and Na+, K+ and Mg2+ cations. Such a relationship was strengthened by the correlation between the main component and Ca2+ cations in the PC 2 and NH4+, OC and EC in the PC 3. This proves the influence of combustion processes and soil resuspension as sources of PM2.5 particulate matter [58]. In the non-heating season, there was a correlation for Mg2+, SO42− and NH4+ identified in the PC 1 that indicates the influence of emissions originating from fuel combustion processes and also the influence of secondary aerosols [48,58,59]. For stations located in Poznań, the analysis revealed that in the winter season at the station at Polanka Street (Station 7), the most significant for the first PC were OC, EC, F, Cl and K+, whereas at the station at Jana Pawła II (Station 8), the most important for the first PC were: F, Cl, SO42−, K+, Mg2+ and Ca2+, which indicates combustion processes as the source of the considered pollutants. A high percentage of Na+ and Cl in the fourth PC may also indicate the influence of salting (in the winter season) on the composition of particulate matter at the given station [60]. PC 2, singled out in the analysis for the station at Polanka Street, indicates the existence of mineral dust and vegetal fragments in the content of PM2.5 particulate matter. PC 3, similarly to the case of PC 2, indicates the influence of emissions originating from fuel combustion processes in the analysis for the station at Jana Pawła II Street. In this case, the influence of road transport emissions indicates a high correlation coefficient for OC and EC. PC 4, in the case of the station at Polanka Street, as well as PC 3 from the station at Jana Pawła II Street, are related to the emission of the secondary aerosol NH4NO3, whose presence proves the that there are high concentrations of its precursors in atmospheric air [33,46]. In the case of Poznań, their presence may be attributed to both road transport and gas heating, which is used by the downtown inhabitants. In the summer season, four main PCs were singled out for both of the analyzed stations. At the station at Jana Pawła II Street, it was found that the most important components for the first PC were SO42− and NH4+, and it confirms the influence of fuel combustion on the air quality in Poznań. In the second factor, a high correlation coefficient was characteristic for Ca2+, Mg2+ and PO43−, and in the third factor, a high correlation coefficient was characteristic for F. This indicates the influence of mineral dust and vegetal fragments on the composition of particulate matter in the summer season at that station [61,62]. At the station at Polanka Street, in the two first factors, the main components that were singled out were characteristic for both liquid and solid fuel combustion. In the third and fourth factors, the main components that were singled out were characteristic of mineral dust presence. The influence on this condition in the summer season may be attributed to the floating of mineral particles originating from the surface of roads and parking lots and also to the influx of air from the Saharan terrains [48]. Nonetheless, it is possible to observe a difference between the origin of particulate matter in the heating and non-heating seasons. In the winter season, fuel combustion remains a dominating source of emissions and at the same time a factor influencing the composition of particulate matter. In the summer season, the presence of mineral dust, which often flows from distant areas [46,60], is very important.
From analyzing the linear dependence sum of PM2.5-bound cations vs. the analyses sum of PM2.5-bound anions in all cases (locations and seasons), a statistically significant (p < 0.05) linear relationship of Σcations and Σanions was observed (Figure 3). Generally, it can be seen that the Σcations/Σanions ratio reached values below one in the winter season and higher than one in the summer season. Specifically, in Poznań, the average values of the Σcations/Σanions ratio in winter and summer were at 0.33 and 2 at Polanka Street, and 2 and 1.1 at John Paul II Street, respectively. In the case of Wrocław, at Kosiby Street, the average values of the Σcations/Σanions ratio were at 1.4, and 0.74 in winter. It can be stated that in winter seasons in the studied atmospheric aerosol, both in Poznań and Wrocław, mainly sulfate and nitrogen anions forming inorganic secondary aerosols predominated. In the summer season, in both considered urban locations, mineral aerosol components (calcium, potassium and magnesium) had a clear contribution. During this period, the aerosol probably have an alkaline characteristic, and the emission of mineral dusts (road dust, soil) can definitely contribute to the PM2.5 concentration.

4. Summary

In the analyzed measuring period, the concentrations of particulate matter were high; the highest PM2.5 concentration in Wrocław was found in the winter of 2016 (70.12 µg/m3) and in Poznań in the autumn–winter of 2016 (88.5 µg/m3). Organic and elemental carbon were macro elements in both locations regardless of the measurement season. Among the ions determined, the highest concentrations were generally recorded for PO43−, SO42−, Na+, NH4+ and F.
It has been shown that the primary sources of fine PM emissions in both areas are the burning of fossil fuels, biomass and liquid fuels in automotive engines. In addition, in the measurement campaign conducted in Poznań, a clear impact of gaseous transformations of PM precursors on PM concentrations in the air was observed. In both locations, in selected seasons, a possible contribution of mineral matter (road and soil dust) in PM was also revealed.

Author Contributions

Conceptualization, I.S.; Data curation, A.C.-S., Ł.P., B.M. and W.R.-K.; Formal analysis, I.S. and W.R.-K.; Investigation, I.S., A.C.-S., Ł.P., B.M. and W.R.-K.; Methodology, I.S., A.C.-S., B.M. and W.R.-K.; Supervision, I.S.; Validation, W.R.-K.; Visualization, A.C.-S.; Writing – original draft, I.S., A.C.-S. and Ł.P.; Writing – review & editing, I.S. and W.R.-K.

Funding

Research was co-financed from funds No. 0402/0209/15 and 0402/0088/16 from a special purpose grant awarded to the Faculty of Environmental Engineering of the Wrocław University of Science and Technology (W-7) by the Minister of Science and Higher Education for conducting scientific research or development works and related tasks development of young scientists and doctoral students.

Conflicts of Interest

The authors declare no conflict of interest

References

  1. European Environment Agency. Air Quality in Europe—2016 Report; Publications Office of the European Union: Luxemburg, 2016. [Google Scholar]
  2. Oberdörster, G.; Sharp, Z.; Atudorei, V.; Elder, A.; Gelein, R.; Lunts, A.; Kreyling, W.; Cox, C. Extrapulmonary translocation of ultrafine carbon particles following whole-body inhalation exposure of rats. J. Toxicol. Environ. Health Part A 2002, 65, 1531–1543. [Google Scholar] [CrossRef] [PubMed]
  3. Wilson, M. Interactions between Ultrafine Particles and Transition Metals in Vivo and in Vitro. Toxicol. Appl. Pharm. 2002, 184, 172–179. [Google Scholar] [CrossRef]
  4. Gwinn, M.R.; Vallyathan, V. Nanoparticles. Health effects—Pros and cons. Environ. Health Perspect. 2006, 114, 1818. [Google Scholar] [CrossRef] [PubMed]
  5. Lu, S.; Zhang, W.; Zhang, R.; Liu, P.; Wang, Q.; Shang, Y.; Wu, M.; Donaldson, K.; Wang, Q. Comparison of cellular toxicity caused by ambient ultrafine particles and engineered metal oxide nanoparticles. Part. Fibre Toxicol. 2015, 12, 5. [Google Scholar] [CrossRef]
  6. Corsini, E.; Vecchi, R.; Marabini, L.; Fermo, P.; Becagli, S.; Bernardoni, V.; Caruso, D.; Corbella, L.; Dell’Acqua, M.; Galli, C.L.; et al. The chemical composition of ultrafine particles and associated biological effects at an alpine town impacted by wood burning. Sci. Total Environ. 2017, 587, 223–231. [Google Scholar] [CrossRef]
  7. Widziewicz, K.; Rogula-Kozłowska, W. Urban environment as a factor modulating metals deposition in the respiratory track and associated cancer risk. Atmos. Pollut. Res. 2017, 9, 399–410. [Google Scholar] [CrossRef]
  8. European Environment Agency. Air Quality in Europe—2018 Report; Publications Office of the European Union: Luxemburg, 2018. [Google Scholar] [CrossRef]
  9. Chlebowska-Styś, A.; Kobus, D.; Pachurka, Ł.; Sówka, I. Analysis of concentrations trends and origins of PM 10 in selected European cities. E3S Web Conf. 2017, 17, 13. [Google Scholar] [CrossRef] [Green Version]
  10. Chlebowska-Styś, A.; Sówka, I.; Pachurka, Ł. Analysis of air quality in selected polish cities. In Człowiek a Środowisko: Wzajemne Oddziaływanie = Man vs Environment: Interaction; Chmielewski, J., Żeber-Dzikowska, I., Gworek, B., Eds.; Instytut Ochrony Środowiska, Państwowy Instytut Badawczy: Warszawa, Poland, 2016; pp. 103–120. (In Polish) [Google Scholar]
  11. Błaszczak, B.; Rogula-Kozłowska, W.; Mathews, B.; Juda-Rezler, K.; Klejnowski, K.; Rogula-Kopiec, P. Chemical Compositions of PM2.5 at Two Non-Urban Sites from the Polluted Region in Europe. Aerosol Air Qual. Res. 2016, 16, 2333–2348. [Google Scholar] [CrossRef] [Green Version]
  12. Rogula-Kozłowska, W.; Majewski, G.; Czechowski, P.O.; Rogula-Kopiec, P. Analysis of the data set from a two-year observation of the ambient water-soluble ions bound to four particulate matter fractions in an urban background site in southern Poland. Environ. Prot. Eng. 2017, 43, 137–149. [Google Scholar] [CrossRef]
  13. Czarnecka, M.; Kalbarczyk, R. Weather conditions determining variability of suspended particulate matter concentration in Pomerania. Acta Agroph 2008, 11, 357–368. [Google Scholar]
  14. Juda-Rezler, K.; Reizer, M.; Oudinet, J.-P. Determination and analysis of PM10 source apportionment during episodes of air pollution in Central Eastern European urban areas: The case of wintertime 2006. Atmos. Environ. 2011, 45, 6557–6566. [Google Scholar] [CrossRef]
  15. Chlebowska-Styś, A.; Kobus, D.; Zathey, M.; Sówka, I. The impact of road transport on air quality in selected Polish cities. E3S Web Conf. 2017, 22, 1–8. [Google Scholar]
  16. Rogula-Kozłowska, W. Size-segregated urban particulate matter: Mass closure, chemical composition, and primary and secondary matter content. Air Qual. Atmos. Health 2016, 9, 533–550. [Google Scholar] [CrossRef]
  17. Cembrzyńka, J.; Krakowiak, E.; Brewczyński, P.Z. Zanieczyszczenie powietrza pyłem zawieszonym PM10 oraz PM2,5 w warunkach silnej antropopresji na przykładzie miasta Sosnowiec. Med. Środowiskowa Environ. Med. 2012, 15, 31–38. [Google Scholar]
  18. Chlebowska-Styś, A.; Sówka, I.; Pachurka, Ł. Analiza składu pyłu zawieszonego PM10 na stacji tła miejskiego w Pile. In Interdyscyplinarne Zagadnienia w Inżynierii i Ochronie Środowiska; Kaźmierczak, B., Kotowski, A., Piekarska, K., Eds.; Oficyna Wydawnicza Politechniki Wrocławskiej: Wrocław, Poland, 2016; pp. 36–53. (In Polish) [Google Scholar]
  19. Jeong, C.H.J.; Jon, M.; Wang, J.M.; Greg, J.; Evans, G.J. Source apportionment of particulate matter in Europe: A review of methods and results. J. Aerosol Sci. 2008, 39, 827–849. [Google Scholar] [CrossRef]
  20. Kozielska, B.; Kozłowska, W.R.; Pastuszka, J.S. Traffic emission effects on ambient air pollution by PM2.5-related PAH in Upper Silesia, Poland. Int. J. Environ. Pollut. 2013, 53, 245. [Google Scholar] [CrossRef]
  21. Rogula-Kozłowska, W.; Kuskowska, K.; Ogrodnik, P.; Penkała, M. Traffic-generated changes in the elemental profile of urban coarse dust at a highway and crossroads. E3S Web Conf. 2018, 45, 00074. [Google Scholar] [CrossRef] [Green Version]
  22. Polish Journal of Laws 2012, item 1031: Regulation of the Minister of the Environment of 24 August 2012 on the Levels of Certain Substances in the Air. Available online: http://prawo.sejm.gov.pl/isap.nsf/DocDetails.xsp?id=WDU20120001031 (accessed on 10 September 2019).
  23. Almeida, S.M.; Pio, C.; Freitas, M.; Reis, M.; Trancoso, M.; Pio, C.; Reis, M. Approaching PM2.5 and PM2.5−10 source apportionment by mass balance analysis, principal component analysis and particle size distribution. Sci. Total Environ. 2006, 368, 663–674. [Google Scholar] [CrossRef]
  24. Almeida, S.M.; Pio, C.; Freitas, M.; Reis, M.A.; Trancoso, M. Source apportionment of fine and coarse particulate matter in a sub-urban area at the Western European Coast. Atmos. Environ. 2005, 39, 3127–3138. [Google Scholar] [CrossRef]
  25. Masiol, M.; Squizzato, S.; Ceccato, D.; Rampazzo, G.; Pavoni, B. A chemometric approach to determine local and regional sources of PM10 and its geochemical composition in a coastal area. Atmos. Environ. 2012, 54, 127–133. [Google Scholar] [CrossRef] [Green Version]
  26. Samek, L.; Zwoździak, A.; Sówka, I. Chemical characterization and source identification of particulate matter PM10 in rural and urban site in Poland. Environ. Prot. Eng. 2013, 4, 91–103. [Google Scholar] [CrossRef]
  27. Vianaab, M.; Querolb, X.; Alastueyb, A.; Gilc, J.I.; Menéndezc, M. Identification of PM sources by principal component analysis (PCA) coupled with wind direction data. Chemosphere 2006, 65, 2411–2418. [Google Scholar] [CrossRef]
  28. Majewski, G.; Rogula-Kozłowska, W.; Czechowski, P.O.; Badyda, A.; Brandyk, A. The Impact of Selected Parameters on Visibility: First Results from a Long-Term Campaign in Warsaw, Poland. Atmosphere 2015, 6, 1154–1174. [Google Scholar] [CrossRef] [Green Version]
  29. Rogula-Kozłowska, W.; Majewski, G.; Czechowski, P.O. The size distribution and origin of elements bound to ambient particles: A case study of a Polish urban area. Environ. Monit. Assess. 2015, 187, 240. [Google Scholar] [CrossRef]
  30. Majewski, G.; Rogula-Kozłowska, W. The elemental composition and origin of fine ambient particles in the largest Polish conurbation: First results from the short-term winter campaign. Theor. Appl. Climatol. 2016, 125, 79–92. [Google Scholar] [CrossRef]
  31. Dragon, K.; Jażdzewska, J. Analiza czynnikowa jako metoda identyfikacji procesów kształtujących skład chemiczny wód podziemnych. Przegląd Geol. 2015, 63, 688–693. (In Polish) [Google Scholar]
  32. Chlebowska-Styś, A.; Sówka, I. Trendy zmian stężeń pyłów (PM10 i PM2.5) oraz benzo(a)pirenu na przykładzie wybranych miast Wielkopolski. In Interdyscyplinarne Zagadnienia w Inżynierii i Ochronie Środowiska; Kotowski, A., Piekarska, K., Kaźmierczak, B., Eds.; Oficyna Wydawnicza Politechniki Wrocławskiej: Wrocław, Poland, 2015; pp. 40–53. (In Polish) [Google Scholar]
  33. Rogula-Kozłowska, W.; Pastuszka, J.S.; Talik, E. Influence of Vehicular Traffic on Concentration and Particle Surface Composition of PM10 and PM2.5 in Zabrze, Poland. Pol. J. Environ. Stud. 2008, 17, 539–548. [Google Scholar]
  34. Pachurka, Ł.; Sówka, I.; Rogula-Kozłowska, W.; Mathews, B.; Chlebowska-Styś, A.; Zwoździak, A. Analiza składu chemicznego i pochodzenia pyłu zawieszonego na wybranym obszarze miasta Wrocławia wraz z określeniem potencjalnego wpływu na zdrowie mieszkańców. In Determinanty Zdrowia = Health Determinants; Chmielewski, J., Florek-Łuszczki, M., Szpringer, M., Eds.; Instytut Ochrony Środowiska, Państwowy Instytut Badawczy: Warszawa, Poland, 2016; pp. 133–141. (In Polish) [Google Scholar]
  35. World Health Organization. Health Risk Assessment of Air Pollution—General Principles; WHO Regional Office for Europe: Copenhagen, Denmark, 2016. [Google Scholar]
  36. Chłopek, Z. Identyfikacja Modeli Imisji Cząstek Stałych PM2.5 i PM1; Zeszyty Naukowe Instytutu Pojazdów: Warsaw, Poland, 2012; pp. 157–164. [Google Scholar]
  37. Rogula-Kozłowska, W.; Klejnowski, K. Submicrometer Aerosol in Rural and Urban Backgrounds in Southern Poland: Primary and Secondary Components of PM1. Bull. Environ. Contam. Toxicol. 2013, 90, 103. [Google Scholar] [CrossRef]
  38. Allen, A.; Nemitz, E.; Shi, J.; Harrison, R.; Greenwood, J. Size distributions of trace metals in atmospheric aerosols in the United Kingdom. Atmos. Environ. 2001, 35, 4581–4591. [Google Scholar] [CrossRef]
  39. Rogula-Kozłowska, W.; Klejnowski, K.; Rogula-Kopiec, P.; Ośródka, L.; Krajny, E.; Błaszczak, E.; Mathews, B. Spatial and seasonal variability of the mass concentration and chemical composition of PM2.5 in Poland. Air Qual. Atmos. Health 2014, 7, 41–58. [Google Scholar] [CrossRef]
  40. Rogula-Kozłowska, W.; Majewski, G.; Błaszczak, B.; Klejnowski, K.; Rogula-Kopiec, P. Origin-Oriented Elemental Profile of Fine Ambient Particulate Matter in Central European Suburban Conditions. Int. J. Environ. Res. Public Health 2016, 13, 715. [Google Scholar] [CrossRef] [PubMed]
  41. Pachurka, Ł.; Sówka, I.; Rogula-Kozłowska, W.; Chlebowska-Styś, A.; Zwoździak, A. Assessment of the health risks associated with inhalation exposure to cadmium, arsenic and nickel in selected cities of Lower Silesia. In Proceedings of the Ukrainian-Polish Conference: The Problems of Air Pollution and Purification: Control, Monitoring, Catalytic, Photocatalytic and Sorption Methods of Treatment, Kyiv, Ukraine, 6–8 November 2016. [Google Scholar]
  42. Pachurka, Ł.; Rogula-Kozłowska, W.; Chlebowska-Styś, A.; Nych, A.; Zwoździak, A. Exposure of urban agglomeration population to the selected components of PM1emitted from low emission sources. E3S Web Conf. 2017, 17, 71. [Google Scholar] [CrossRef] [Green Version]
  43. Pachurka, Ł.; Sówka, I. Wpływ zanieczyszczeń powietrza pyłem zawieszonym na ryzyko potencjalnej utraty zdrowia mieszkańców Wrocławia. In Środowiskowe i Zawodowe Zagrożenia Zdrowia—Wiedza i Praktyka = Environmental and Occupational Health Hazards—Knowledge and Practice; Chmielewski, J., Pawlas, N., Szpringer, M., Eds.; Zakład Poligraficzno-Wydawniczy “Magraf”: Kielce, Poland, 2016; pp. 43–56. (In Polish) [Google Scholar]
  44. Majewski, G.; Rogula-Kozłowska, W.; Rozbicka, K.; Rogula-Kopiec, P.; Mathews, B.; Brandyk, A. Concentration, Chemical Composition and Origin of PM1: Results from the First Long-term Measurement Campaign in Warsaw (Poland). Aerosol Air Qual. Res. 2018, 18, 636–654. [Google Scholar] [CrossRef]
  45. Rogula-Kozłowska, W.; Kozielska, B.; Klejnowski, K. Hazardous Compounds in Urban Pm in the Central Part of Upper Silesia (Poland) in Winter. Arch. Environ. Prot. 2013, 39, 53–65. [Google Scholar] [CrossRef]
  46. Institute of Environmental Engineering of the Polish Academy of Sciences; Institute of Ecology of Industrial Areas; Institute of Meteorology and Water Management PIB; Institute of Environmental Protection PIB. Analysis of the State of Air Pollution with Dust PM10 and PM2.5 Taking into Account the Chemical Composition of Dust and the Impact of Natural Sources—A Synthetic Report; Inspection for Environmental Protection; Institute of Environmental Protection PIB: Zabrze, Poland, 2011. (In Polish) [Google Scholar]
  47. Lewandowska, A.; Falkowska, L.; Jóźwik, J. Factors determining the fluctuation of fluoride concentrations in PM10 aerosols in the urbanized coastal area of the Baltic Sea (Gdynia, Poland). Environ. Sci. Pollut. Res. 2013, 20, 6109–6118. [Google Scholar] [CrossRef] [Green Version]
  48. AirBase Official Website. Available online: https://www.eea.europa.eu/data-and-maps/data/airbase-theeuropean-air-quality-database-7 (accessed on 25 August 2017).
  49. Schwarz, J.; Cusack, M.; Karban, J.; Chalupníˇcková, E.; Havránek, V.; Smolík, J.; Ždímal, V. PM2.5 chemical composition at a rural background site in Central Europe, including correlation and air mass back trajectory analysis. Atmos. Res. 2016, 176–177, 108–120. [Google Scholar] [CrossRef]
  50. EBAS Database. Available online: http://ebas.nilu.no (accessed on 25 February 2014).
  51. Rogula-Kozłowska, W.; Klejnowski, K.; Rogula-Kopiec, P.; Mathews, B.; Szopa, S. A Study on the Seasonal Mass Closure of Ambient Fine and Coarse Dusts in Zabrze, Poland. Bull. Environ. Contam. Toxicol. 2012, 88, 722–729. [Google Scholar] [CrossRef]
  52. Makkonen, U.; Virkkula, A.; Mäntykenttä, J.; Hakola, H.; Keronen, P.; Vakkari, V.; Aalto, P.P. Semi-continuous gas and inorganic aerosol measurements at a Finnish urban site: Comparisons with filters, nitrogen in aerosol and gas phases, and aerosol acidity. Atmos. Chem. Phys. Discuss. 2012, 12, 5617–5631. [Google Scholar] [CrossRef]
  53. Ravindra, K.; Stranger, M.; Van Grieken, R.; Grieken, R. Chemical characterization and multivariate analysis of atmospheric PM2.5 particles. J. Atmos. Chem. 2008, 59, 199–218. [Google Scholar] [CrossRef] [Green Version]
  54. Kfoury, A.; LeDoux, F.; Roche, C.; Delmaire, G.; Roussel, G.; Courcot, D. PM2.5 source apportionment in a French urban coastal site under steelworks emission influences using constrained non-negative matrix factorization receptor model. J. Environ. Sci. 2016, 40, 114–128. [Google Scholar] [CrossRef]
  55. Szigeti, T.; Óvári, M.; Dunster, C.; Kelly, F.J.; Lucarelli, F.; Záray, G. Changes in chemical composition and oxidative potential of urban PM2.5 between 2010 and 2013 in Hungary. Sci. Total Environ. 2015, 518, 534–544. [Google Scholar] [CrossRef] [PubMed]
  56. Tolis, E.I.; Saraga, D.E.; Lytra, M.K.; Papathanasiou, A.C.; Bougaidis, P.N.; Prekas-Patronakis, O.E.; Ioannidis, I.I.; Bartzis, J.G. Concentration and chemical composition of PM2.5 for a one-year period at Thessaloniki, Greece: A comparison between city and port area. Atmos. Environ. 2015, 113, 197–207. [Google Scholar] [CrossRef]
  57. Mirante, F.; Salvador, P.; Pio, C.; Alves, C.; Artíñano, B.; Caseiro, A.; Revuelta, M.A. Size fractionated aerosol composition at roadside and background environments in the Madrid urban atmosphere. Atmos. Res. 2014, 138, 278–292. [Google Scholar] [CrossRef]
  58. Rogula-Kozłowska, W.; Rogula-Kopiec, P.; Mathews, B.; Klejnowski, K. Effects of road traffic on the ambient concentrations of three PM fractions and their main components in a large Upper Silesian city. Annals of Warsaw University of Life Sciences-SGGW. Land Reclam. 2013, 45, 243–253. [Google Scholar]
  59. Klejnowski, K.; Rogula-Kopiec, P.; Rogula-Kozłowska, W. Ocena zawartości wtórnego węgla organicznego w drobnym pyle zawieszonym w wybranych obszarach województwa śląskiego. Przegląd Nauk. Inżynieria Kształtowanie Środowiska Sci. Rev. Eng. Environ. Sci. 2014, 66, 347–359. [Google Scholar]
  60. Degórska, A. Sources of air pollution with dust. In Fine dust in the atmosphere. In Compendium of Knowledge about Air Pollution in Particulate Matter in Poland; Juda-Rezler, K., Toczko, B., Eds.; Chief Inspectorate for Environmental Protection: Warsaw, Poland, 2016; pp. 22–30. (In Polish) [Google Scholar]
  61. Engelbrecht, J.P.; Moosmüller, H.; Pincock, S.; Jayanty, R.K.M.; Lersch, T.; Casuccio, G. Technical note: Mineralogical, chemical, morphological, and optical. Atmos. Chem. Phys. 2016, 16, 10809–10830. [Google Scholar] [CrossRef]
  62. Karydis, V.A.; Tsimpidi, A.P.; Pozzer, A.; Astitha, M.; Lelieveld, J. Effects of mineral dust on global atmospheric nitrate concentrations. Atmos. Chem. Phys. Discuss. 2016, 16, 1491–1509. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Localization of measurement points (source: own elaboration with use of Google Maps map backgrounds, access date: 28 August 2019).
Figure 1. Localization of measurement points (source: own elaboration with use of Google Maps map backgrounds, access date: 28 August 2019).
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Figure 2. Mean annual concentration of particulate matter (PM) (PM2.5 and PM10), averaged for the heating and non-heating seasons in Wrocław and Poznań, calculated on the basis of measurements carried out as a part of state environmental monitoring (SEM) (measurement points 2–7) (source: own elaboration based on Chief Inspectorate of Environmental Protection (CIEP) data).
Figure 2. Mean annual concentration of particulate matter (PM) (PM2.5 and PM10), averaged for the heating and non-heating seasons in Wrocław and Poznań, calculated on the basis of measurements carried out as a part of state environmental monitoring (SEM) (measurement points 2–7) (source: own elaboration based on Chief Inspectorate of Environmental Protection (CIEP) data).
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Figure 3. Sum of cations (Σcations in μeq m−3) vs. sum of anions (Σanions in μeq m−3) and a trendline equation (the result of linear regression is described using R2; the coefficient of determination) in Wroclaw at Kosiby Street in spring–summer (a); at Kosiby Street in winter (b); in Poznań at Polanka Street in winter (c); at Jana Pawla II Street in winter (d); at Polanka Street in summer (e); at Jana Pawla II Street in summer (f).
Figure 3. Sum of cations (Σcations in μeq m−3) vs. sum of anions (Σanions in μeq m−3) and a trendline equation (the result of linear regression is described using R2; the coefficient of determination) in Wroclaw at Kosiby Street in spring–summer (a); at Kosiby Street in winter (b); in Poznań at Polanka Street in winter (c); at Jana Pawla II Street in winter (d); at Polanka Street in summer (e); at Jana Pawla II Street in summer (f).
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Table 1. Descriptive statistics calculated for PM10, PM2.5 and PM1.0 concentrations for measurement point 1 located in Wrocław [34,41,42,43]. All values in this table are given in μg/m3.
Table 1. Descriptive statistics calculated for PM10, PM2.5 and PM1.0 concentrations for measurement point 1 located in Wrocław [34,41,42,43]. All values in this table are given in μg/m3.
Year201420152016
PM1.0PM2.5PM10PM1.0PM2.5PM10PM1.0PM2.5PM10
Descriptive StatisticsHeating Season (Winter)
Minimum---3.584.58-2.842.0911.58
Maximum---19.5244.45-38.2070.1297.81
Mean---9.7617.93-18.1630.8841.08
Median---9.7614.85-15.5131.1337.50
Standard deviation---4.3810.80-10.6614.6522.98
Descriptive StatisticsNon-Heating Season (Spring/Summer)
Minimum2.816.18-0.734.104.713.442.415.97
Maximum14.0719.75-11.9622.1024.5111.5314.2532.32
Mean7.6610.79-7.3413.2613.778.056.4616.72
Median7.559.90-12.5412.5314.878.365.1916.77
Standard deviation2.923.75-7.345.735.672.883.536.72
Table 2. Descriptive statistics calculated for PM10, PM2,5 and PM1.0 concentrations for measurement points 6, 7 and 8 located in Poznan. All values in this table are given in μg/m3.
Table 2. Descriptive statistics calculated for PM10, PM2,5 and PM1.0 concentrations for measurement points 6, 7 and 8 located in Poznan. All values in this table are given in μg/m3.
Heating Season (25 October–22 November 2016)Non-Heating Season (05 June–02 July 2017)
PM10
Descriptive StatisticsJana Pawła II St.Szymanowskiego St.Jana Pawła II St.Szymanowskiego St.
Minimum9.48.75.21.0
Maximum68.669.642.822.6
Mean25.432.916.614.7
Median21.534.515.115.7
Standard deviation14.615.58.55.2
PM2.5
Descriptive StatisticsJana Pawła II St.Szymanowskiego St.Jana Pawła II St.Szymanowskiego St.
Minimum2.27.21.27.2
Maximum39.988.540.317.1
Mean15.230.810.411.0
Median12.927.28.710.9
Standard deviation10.019.19.12.5
PM1.0
Descriptive StatisticsJana Pawła II St.-Jana Pawła II St.-
Minimum2.47-2.72-
Maximum22.87-10.35-
Mean8.50-5.72-
Median7.65-5.36-
Standard deviation5.27-1.95-
Table 3. Concentrations of PM2.5-bound anions, cations, organic carbon (OC) and elemental carbon (EC) at the selected measuring stations. All values in this table are given in μg/m3.
Table 3. Concentrations of PM2.5-bound anions, cations, organic carbon (OC) and elemental carbon (EC) at the selected measuring stations. All values in this table are given in μg/m3.
FClNO3PO43−SO42−Na+NH4+K+Mg2+Ca2+OCEC
Wrocław, Kosiby St. Series 1 (26 June–26 July 2014; Summer 2014)
No. of samples272727272727272727272727
Mean0.060.130.320.041.420.180.350.070.000.043.230.63
Minimum<dl0.080.13<dl0.660.050.15<dl<dl<dl2.12<dl
Maximum0.190.4492.470.353.080.860.800.660.000.214.971.64
Median0.050.100.170.001.240.080.340.000.000.003.070.59
Standard deviation0.040.080.450.110.650.210.170.180.000.190.740.34
Wrocław, Kosiby St. Series 2 (7 January–7 February 2015; Winter 2015)
No. of samples323232323232323232323232
Mean0.131.764.200.077.771.142.200.190.060.025.791.42
Minimum0.050.571.14<dl4.750.640.30<dl<dl<dl1.220.45
Maximum1.3610.518.561.4811.348.125.290.432.000.3716.482.77
Median0.091.343.870.006.910.801.660.090.000.004.731.19
Standard deviation0.231.842.460.272.061.311.620.410.070.353.690.67
Wrocław, Kosiby St. Series 3 (31 July–13 August 2015; Summer 2015)
No. of samples141414141414141414141414
Mean0.080.390.690.035.280.392.440.360.152.254.260.62
Minimum0.050.100.300.021.760.130.590.160.090.502.76<dl
Maximum0.171.561.300.059.421.324.540.780.387.936.471.12
Median0.080.260.630.035.300.282.510.300.121.084.330.62
Standard deviation0.030.390.240.012.170.311.040.170.092.370.970.25
Wrocław, Kosiby St. Series 4 (9–26 January 2016; Winter 2016)
No. of samples181818181818181818181818
Mean0.052.971.010.074.070.744.160.560.161.027.961.83
Minimum0.021.520.03<dl2.240.310.020.280.090.512.000.46
Maximum0.185.802.000.516.332.209.401.240.353.1317.134.06
Median0.080.481.080.004.090.504.840.440.140.767.971.61
Standard deviation0.041.130.480.161.130.572.810.300.070.633.690.82
Wrocław, Kosiby St. Series 5 (9–23 May 2016; Spring 2016)
No. of samples151515151515151515151515
Mean0.031.270.150.192.670.551.080.150.050.882.700.36
Minimum0.021.160.02<dl1.760.20<dl0.070.030.231.410.12
Maximum0.051.510.580.544.041.063.110.210.137.453.980.80
Median0.031.250.080.042.560.470.960.150.040.332.750.35
Standard deviation0.010.100.180.210.670.230.910.040.021.830.730.18
Poznań, Jana Pawła II St. (25 October–22 November 2016; Autumn 2016)
No. of samples282828282828282828282828
Mean1.9880.6890.6380.6300.8890.6190.0470.0770.0440.2368.362.53
Minimum10.5084.2018.6071.0926.0432.8961.8090.5860.2896.4852.350.83
Maximum3.0881.1602.6320.7842.1070.8860.5530.1590.0680.73026.666.64
Median2.7410.9292.1620.7521.8320.7680.4650.1310.0560.4167.142.32
Standard deviation1.6570.6831.8930.1051.0980.4180.4530.0970.0461.1775.161.39
Polanka St. (25 October–22 November 2016; Autumn 2016)
No. of samples282828282828282828282828
Mean0.7570.3830.8700.3780.9400.4510.0500.0490.0250.12214.773.26
Minimum6.3173.85821.8160.9517.9391.0532.5400.5280.4390.3842.911.14
Maximum2.2871.1545.8010.5333.5060.6121.1020.2150.0490.19743.216.22
Median1.8820.7534.8020.4303.3140.5621.1070.1880.0330.17212.072.84
Standard deviation1.1720.8594.7010.2091.8220.1300.6370.1260.0740.07010.591.46
Jana Pawła II St. (5 June–2 July 2017; Summer 2017)
No. of samples282828282828282828282828
Mean0.0100.1230.1500.3280.2900.4650.0080.0200.0520.0763.610.63
Minimum0.1550.5631.3844.5922.2022.3700.0460.0820.4775.3250.820.12
Maximum0.0480.4420.7132.3481.3532.0290.0160.0480.2422.5245.071.22
Median0.0290.4530.6931.7911.4002.0780.0110.0480.2572.6113.580.57
Standard deviation0.0410.0980.2321.1220.4060.3330.0110.0140.1051.4920.830.34
Polanka St. (5 June–2 July 2017; Summer 2017)
No. of samples282828282828282828282828
Mean0.0040.1330.2280.3630.860.4650.0080.0200.0520.0763.880.81
Minimum0.1300.3821.8452.6683.7042.2210.0930.0690.1081.7092.600.45
Maximum0.0450.1990.6180.9921.6791.0980.0360.0400.0810.6115.751.60
Median0.0460.1770.3890.5061.6520.6220.0340.0390.0810.4133.860.71
Standard deviation0.0330.0630.4310.7970.5510.7580.0170.0110.0150.4760.850.28
<dl-below detection limit.
Table 4. Concentrations of PM2.5 and its main chemical constituents (μg/m3) recorded at selected stations in Europe.
Table 4. Concentrations of PM2.5 and its main chemical constituents (μg/m3) recorded at selected stations in Europe.
LocationPeriod Concentration
PM2.5FClNO3PO43−SO42−Na+NH4+K+Mg2+Ca2+OCEC
Wroclaw (PL), Kosiby Street, BNH 26 June–26 July 201410.790.060.130.320.041.420.180.350.070.000.043.230.63
H 7 January–7 February 201517.930.131.764.200.077.771.142.200.190.060.025.791.42
NH 31 July–13 August 201513.260.080.390.690.035.280.392.440.360.152.254.260.62
H 9–26 January 201641.080.052.971.010.074.070.744.160.560.161.027.961.83
NH 9–23 May 20166.460.031.270.150.192.670.551.080.150.050.882.700.36
Poznan (PL), Polanka Street, BH 25 October–22 November 201630.800.7570.3830.8700.3780.9400.4510.0500.0490.0250.12214.773.26
NH 5 June–2 July 201711.000.0040.1330.2280.3630.860.4650.0080.0200.0520.0763.880.81
Racibórz (PL), C [39]2011, 201231.56-1.353.06-3.640.281.661.350.030.0412.081.96
H 2011, 201255.36-3.015.50-5.360.493.310.250.030.0522.543.59
NH 2011, 201214.76-0.181.34-2.430.120.500.020.030.044.700.80
Puszcza Borecka (PL), B [48]201112.79-0.141.43-2.110.300.780.110.020.083.420.58
H 201116.49-0.152.89-2.690.561.160.180.020.084.410.84
NH 20119.79-0.040.37-1.690.100.500.060.020.082.620.36
Zielonka (PL), A [48]201116.07-0.141.46-1.780.121.080.100.010.104.250.88
H 201120.49-0.232.47-2.150.131.660.150.010.085.591.25
NH 201111.97-0.050.54-1.440.110.540.060.010.123.020.53
Košetice (CZ), B [49]February 2009–April 201015.7-0.042.20-2.850.041.520.09<0.01-4.070.61
February 2009–April 201022.5-0.052.83-3.860.041.920.15<0.01-6.000.80
February 2009–April 20109.7-0.010.55-2.300.030.960.03<0.01-2.120.36
Üto (FI), B [50]20116.55-0.050.28-0.330.280.240.230.220.02--
H 20116.58-0.050.12-0.370.350.290.050.040.02--
NH 20116.53-0.060.44-0.300.200.190.410.410.02--
Neuglobsow (DE), B [48]201210.31-0.132.06-1.950.171.240.090.020.032.520.32
H 201213.14-0.213.59-2.110.221.710.120.020.033.020.45
NH 20127.47-0.060.53-1.790.120.760.050.010.022.050.20
Cabauw-Zijdeweg (NL), A [48]201115.25-0.203.93-2.270.251.690.100.040.062.300.56
H 201118.56-0.314.91-2.590.262.070.140.040.062.830.72
NH 201111.97-0.082.88-1.920.251.280.070.040.061.750.39
Iskrba (Sl), B [50]201011.61-0.040.08-0.880.040.820.120.020.073.380.38
H 201013.22-0.050.12-0.910.050.850.170.020.083.770.53
NH 201010.07-0.030.04-0.850.040.790.080.020.062.990.23
Ispra (IT), B [48]201017.92-0.550.83-0.750.111.390.330.0020.065.881.27
H 201026.52-0.321.41-0.710.101.960.590.020.019.031.91
NH 20109.02-0.790.17-0.780.110.840.070.030.102.710.65
Katowice (PL), U [39]H 201063.04-2.634.06-5.380.923.270.270.060.277.9113.57
NH 201022.73-0.811.13-3.781.461.590.200.120.453.324.47
Poznan (PL), Jana Pawla II Street, UH 25 October–22 November 201615.201.9880.6890.6380.6300.8890.6190.0470.0770.0440.2368.362.53
NH 5 June–2 July 201710.400.0100.1230.1500.3280.2900.4650.0080.0200.0520.0763.610.63
Zabrze (PL), U [51]January–March 200966.85-1.533.12-5.380.452.010.40.140.479.919.34
July–November 200918.44-0.040.51-3.780.240.530.14--4.214.12
Helsinki (FI), U [52]November 2009–February 2010--0.12.27-3.180.050.740.040.040.26--
March–May 2013--0.041.14-1.640.040.460.010.050.18--
Menen (BE), U [53]Winter 200317-0.895.28-4.99-1.880.250.030.07--
Summer 2003-0.254.17-3.23-1.920.130.020.06--
Dunkerque (FR), U [54]November–December 201024.9-0.585.71-2.52-1.91----6.2
March–April 201133.2-0.5411.06-2.85-2.31----4.73
Budapest (HU), U [55]June 2010–March 201321-0.112.14-2.840.221.330.180.050.165.422.02
Winter: June 2010–March 201328.7-0.23.9-2.540.31.80.30.040.128.232
Summer: June 2010–March 201314-0.030.26-30.130.90.090.040.12.871.88
Thessaloniki (GR), U [56]April 2011–May 201237.7-0.392.4-3.960.293.80.140.071.436.621.29
H: April 2011–May 201241.9-0.373.07-3.960.144.850.120.051.68.841.5
NH: April 2011–May 201232.9-0.41.61-3.960.472.580.160.091.254.061.05
Madrid (ES), U [57]January–February 201113.8-0.151.16-0.610.170.480.050.010.11.21.53
June 200916.6-0.160.69-1.020.20.270.050.030.212.710.94
Country abbreviations (codes ISO 3166 Country Codes): PL-Poland; CZ-Czech Republic; FI-Finland; DE-Germany; BE-Belgium; NL-Netherlands; FR-France; HU-Hungary; GR-Greece; IT-Italy; Sl-Slovenia; ES-Spain. Designations of stations: A-rural background station; B-regional background station; U-urban background station. H-heating season (months: January–March and October–December); NH-non-heating season (months: April–September).
Table 5. Main factors and their values extracted during principal component analysis (PCA) for PM2.5 fractions.
Table 5. Main factors and their values extracted during principal component analysis (PCA) for PM2.5 fractions.
Measurement PointSeason/DateFactor 1Factor 2Factor 3Factor 4
Wroclaw, Kosiby StreetSpring–Summer
26 June–26 July 2014
31 July–13 August 2015
9–23 May 2016
SO42− (0.93)
NH4+ (0.92)
Mg2+ (0.83)
Cl (0.82)
Na+ (0.85)
F (0.86)
NO3 (0.80)
-
Wroclaw, Kosiby StreetWinter
7 January–7 February 2015
9–26. January 2016
F (0.95)
Cl (0.83)
Na+ (0.97)
Mg2+ (0.97)
NO3 (0.91)
SO42− (0.93)
Ca2+ (−0.77)
NH4+ (0.83)
OC (0.91)
EC (0.85)
PO43− (0.95)
Poznan, Polanka StreetWinter
25 October–22 November 2016
F (0.85)
Cl (0.84)
OC (0.91)
EC (0.90)
PO43− (0.96)
Ca2+ (0.82)
Mg2+ (0.87)NO3 (0.88)
SO42− (0.81)
NH4+ (0.89)
Poznan, Jana Pawla II StreetWinter
25 October–22 November 2016
F (0.89)
Cl (0.92)
SO42− (0.72)
Na+ (0.98)
K+ (0.92)
Mg2+ (0.95)
Ca2+ (0.95)
OC (0.95)
EC (0.98)
NO3 (0.94)
NH4+ (0.87)
-
Poznan, Polanka StreetSummer
5 June–2 July 2017
Cl (0.88)
NO3 (0.91)
PO43− (0.93)
Na+ (0.93)
SO42− (0.93)
NH4+ (0.91)
OC (0.80)
Ca2+ (0.84)F (0.72)
Mg2+ (0.88)
Poznan, Jana Pawla II StreetSummer
5 June–2 July 2017
SO42− (0.85)
NH4+ (0.96)
PO43− (0.88)
Mg2+ (0.81)
Ca2+ (0.83)
F (0.95)Cl (0.73)
Na+ (0.93)

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Sówka, I.; Chlebowska-Styś, A.; Pachurka, Ł.; Rogula-Kozłowska, W.; Mathews, B. Analysis of Particulate Matter Concentration Variability and Origin in Selected Urban Areas in Poland. Sustainability 2019, 11, 5735. https://0-doi-org.brum.beds.ac.uk/10.3390/su11205735

AMA Style

Sówka I, Chlebowska-Styś A, Pachurka Ł, Rogula-Kozłowska W, Mathews B. Analysis of Particulate Matter Concentration Variability and Origin in Selected Urban Areas in Poland. Sustainability. 2019; 11(20):5735. https://0-doi-org.brum.beds.ac.uk/10.3390/su11205735

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Sówka, Izabela, Anna Chlebowska-Styś, Łukasz Pachurka, Wioletta Rogula-Kozłowska, and Barbara Mathews. 2019. "Analysis of Particulate Matter Concentration Variability and Origin in Selected Urban Areas in Poland" Sustainability 11, no. 20: 5735. https://0-doi-org.brum.beds.ac.uk/10.3390/su11205735

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