Seasonal Variability of the Ion Composition, Phase State, and Mass Concentration of Aerosol in the Rural and Urban Atmosphere over Belgium (2001–2003)

2020 ◽  
Vol 45 (3) ◽  
pp. 185-192
Author(s):  
A. N. Yermakov ◽  
A. E. Aloyan ◽  
V. O. Arutyunyan
Atmosphere ◽  
2021 ◽  
Vol 12 (3) ◽  
pp. 384
Author(s):  
Yaroslav Bezyk ◽  
Izabela Sówka ◽  
Maciej Górka ◽  
Jan Blachowski

Understanding the magnitude and distribution of the mixes of the near-ground carbon dioxide (CO2) components spatially (related to the surface characteristics) and temporally (over seasonal timescales) is critical to evaluating present and future climate impacts. Thus, the application of in situ measurement approaches, combined with the spatial interpolation methods, will help to explore variations in source contribution to the total CO2 mixing ratios in the urban atmosphere. This study presents the spatial characteristic and temporal trend of atmospheric CO2 levels observed within the city of Wroclaw, Poland for the July 2017–August 2018 period. The seasonal variability of atmospheric CO2 around the city was directly measured at the selected sites using flask sampling with a Picarro G2201-I Cavity Ring-Down Spectroscopy (CRDS) technique. The current work aimed at determining the accuracy of the interpolation techniques and adjusting the interpolation parameters for estimating the magnitude of CO2 time series/seasonal variability in terms of limited observations during the vegetation and non-vegetation periods. The objective was to evaluate how different interpolation methods will affect the assessment of air pollutant levels in the urban environment and identify the optimal sampling strategy. The study discusses the schemes for optimization of the interpolation results that may be adopted in areas where no observations are available, which is based on the kriging error predictions for an appropriate spatial density of measurement locations. Finally, the interpolation results were extended regarding the average prediction bias by exploring additional experimental configurations and introducing the limitation of the future sampling strategy on the seasonal representation of the CO2 levels in the urban area.


2015 ◽  
Vol 15 (8) ◽  
pp. 11495-11524 ◽  
Author(s):  
Z. J. Wu ◽  
J. Zheng ◽  
D. J. Shang ◽  
Z. F. Du ◽  
Y. S. Wu ◽  
...  

Abstract. Simultaneous measurements of particle number size distribution, particle hygroscopic properties, and size-resolved chemical composition were made during the summer of 2014 in Beijing, China. During the measurement period, the median hygroscopicity parameters (κ) of 50, 100, 150, 200, and 250 nm particles are respectively 0.15, 0.19, 0.22, 0.27, and 0.29, showing an increasing trend with increasing particle size. When PM2.5 mass concentration is greater than 50 μg m−3, the fractions of the hydrophilic mode for 150, 250, 350 nm particles increased towards 1 as PM2.5 mass concentration increased. This indicates that aged particles dominated during severe pollution periods in the atmosphere of Beijing. Particle hygroscopic growth can be well predicted using high time-resolution size-resolved chemical composition derived from AMS measurement on a basis of ZSR mixing rule. An empirical relationship between κ of organic fraction (κorg) and oxygen to carbon ratio (O : C) (κorg= 0.08·O : C+0.02) is obtained. During new particle formation event associating with strongly active photochemistry, the hygroscopic growth factor or κ of newly formed particles is greater than for particle with the same sizes during non-NPF periods. A quick transformation from external mixture to internal mixture for pre-existing particles (for example 250 nm particle) was observed. Such transformations can modify the state of mixture of pre-exiting particles and thus modify properties such as the light absorption coefficient and cloud condensation nuclei activation.


2020 ◽  
Vol 13 (9) ◽  
pp. 4973-4994
Author(s):  
Laurent Poulain ◽  
Gerald Spindler ◽  
Achim Grüner ◽  
Thomas Tuch ◽  
Bastian Stieger ◽  
...  

Abstract. The aerosol chemical speciation monitor (ACSM) is nowadays widely used to identify and quantify the main components of fine particles in ambient air. As such, its deployment at observatory platforms is fully incorporated within the European Aerosol, Clouds and Trace Gases Research Infrastructure (ACTRIS). Regular intercomparisons are organized at the Aerosol Chemical Monitoring Calibration Center (ACMCC; part of the European Center for Aerosol Calibration, Paris, France) to ensure the consistency of the dataset, as well as instrumental performance and variability. However, in situ quality assurance remains a fundamental aspect of the instrument's stability. Here, we present and discuss the main outputs of long-term quality assurance efforts achieved for ACSM measurements at the research station Melpitz (Germany) since 2012 onwards. In order to validate the ACSM measurements over the years and to characterize seasonal variations, nitrate, sulfate, ammonium, organic, and particle mass concentrations were systematically compared against the collocated measurements of daily offline high-volume PM1 and PM2.5 filter samples and particle number size distribution (PNSD) measurements. Mass closure analysis was made by comparing the total particle mass (PM) concentration obtained by adding the mass concentration of equivalent black carbon (eBC) from the multi-angle absorption photometer (MAAP) to the ACSM chemical composition, to that of PM1 and PM2.5 during filter weighing, as well as to the derived mass concentration of PNSD. A combination of PM1 and PM2.5 filter samples helped identifying the critical importance of the upper size cutoff of the ACSM during such exercises. The ACSM–MAAP-derived mass concentrations systematically deviated from the PM1 mass when the mass concentration of the latter represented less than 60 % of PM2.5, which was linked to the transmission efficiency of the aerodynamic lenses of the ACSM. The best correlations are obtained for sulfate (slope =0.96; R2=0.77) and total PM (slope =1.02; R2=0.90). Although, sulfate did not exhibit a seasonal dependency, total PM mass concentration revealed a small seasonal variability linked to the increase in non-water-soluble fractions. The nitrate suffers from a loss of ammonium nitrate during filter collection, and the contribution of organo-nitrate compounds to the ACSM nitrate signal make it difficult to directly compare the two methods. The contribution of m∕z 44 (f44) to the total organic mass concentration was used to convert the ACSM organic mass (OM) to organic carbon (OC) by using a similar approach as for the aerosol mass spectrometer (AMS). The resulting estimated OCACSM was compared with the measured OCPM1 (slope =0.74; R2=0.77), indicating that the f44 signal was relatively free of interferences during this period. The PM2.5 filter samples use for the ACSM data quality might suffer from a systematic bias due to a size truncation effect as well as to the presence of chemical species that cannot be detected by the ACSM in coarse mode (e.g., sodium nitrate and sodium sulfate). This may lead to a systematic underestimation of the ACSM particle mass concentration and/or a positive artifact that artificially decreases the discrepancies between the two methods. Consequently, ACSM data validation using PM2.5 filters has to be interpreted with extreme care. The particle mass closure with the PNSD was satisfying (slope =0.77; R2=0.90 over the entire period), with a slight overestimation of the mobility particle size spectrometer (MPSS)-derived mass concentration in winter. This seasonal variability was related to a change on the PNSD and a larger contribution of the supermicrometer particles in winter. This long-term analysis between the ACSM and other collocated instruments confirms the robustness of the ACSM and its suitability for long-term measurements. Particle mass closure with the PNSD is strongly recommended to ensure the stability of the ACSM. A near-real-time mass closure procedure within the entire ACTRIS–ACSM network certainly represents an optimal quality control and assurance of both warranting the quality assurance of the ACSM measurements as well as identifying cross-instrumental biases.


2015 ◽  
Vol 15 (17) ◽  
pp. 23587-23612 ◽  
Author(s):  
L. Ammoura ◽  
I. Xueref-Remy ◽  
F. Vogel ◽  
V. Gros ◽  
A. Baudic ◽  
...  

Abstract. We propose a new approach to estimate urban emission ratios that takes advantage of the enhanced local urban signal in the atmosphere at low wind speed. We apply it to estimate monthly ratios between CO2, CO and some VOCs from several atmospheric concentration measurement datasets acquired in the centre of Paris between 2010 and 2014. We find that this approach is little sensitive to the regional background level definition and that, in the case of Paris, it samples all days (weekdays and weekends) and all hours of the day evenly. A large seasonal variability of the ΔCO/ΔCO2 ratio in Paris is shown, with a difference of around 60 % between the extreme values and a strong anti-correlation (r2 = 0.75) with atmospheric temperature. The comparison of the ratios obtained for two short measurement campaigns conducted in two different districts and two different periods (fall and winter) shows differences ranging from −120 to +63 %. A comparison with a highly resolved regional emission inventory suggests some spatial variations of the ratio within the city, although most of these differences seem to be rather driven by the seasonal variability.


2013 ◽  
Vol 7 (1) ◽  
pp. 41-58 ◽  
Author(s):  
Wioletta Rogula-Kozłowska ◽  
Krzysztof Klejnowski ◽  
Patrycja Rogula-Kopiec ◽  
Leszek Ośródka ◽  
Ewa Krajny ◽  
...  

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