scholarly journals Chemically speciated mass size distribution, particle effective density and origin of non-refractory PM<sub>1 </sub>measured at a rural background site in Central Europe

2021 ◽  
Author(s):  
Petra Pokorná ◽  
Naděžda Zíková ◽  
Radek Lhotka ◽  
Petr Vodička ◽  
Saliou Mbengue ◽  
...  
Keyword(s):  
Size Distribution ◽  
Long Range ◽  
Central Europe ◽  
Effective Density ◽  
Long Range Transport ◽  
Air Masses ◽  
Mass Size Distribution ◽  
Background Site ◽  
Range Transport ◽  
Mass Size

Abstract. The seasonal variability of non-refractory PM1 (NR-PM1) was studied at a rural background site (National Atmospheric Observatory Košetice – NAOK) in the Czech Republic to examine the impact of atmospheric regional and long-range transport in Central Europe. NR-PM1 measurements were performed by compact time-of-flight aerosol mass spectrometry (C-ToF-AMS), and the chemically speciated mass size distributions, effective density, and origin were discussed. The average PM1 concentrations, calculated as the sum of the NR-PM1 (after collection efficiency corrections – CE corrections of 0.4 and 0.33 in summer and winter, respectively) and the equivalent black carbon (eBC) concentrations measured by an aethalometer (AE), were 8.58 ± 3.70 μg m−3 in summer and 10.08 ± 8.04 μg m−3 in winter. Organics dominated during both campaigns (summer/winter: 4.97 ± 2.92/4.55 ± 4.40 μg m−3), followed by sulphate in summer (1.68 ± 0.81/1.36± 1.38 μg m−3) and nitrate in winter (0.67 ± 0.38/2.03 ± 1.71 μg m−3). The accumulation mode dominated the average mass size distribution during both seasons, with larger particles of all species measured in winter (mode diameters: Org: 334/413 nm, NO3−: 377/501 nm, SO42−: 400/547 nm, and NH4+: 489/515 nm) pointing to regional and long-range transport. However, since the winter aerosols were less oxidized than the summer aerosols (comparing fragments f44 and f43), the importance of local sources in the cold part of the year was not negligible. The average PM1 particle effective density, defined as the ratio of the mass to the volume of a particle, corresponded to higher inorganic contents during both seasons (summer: ∼ 1.30 g cm−3 and winter: ∼ 1.40 g cm−3). However, the effective densities during episodes of higher mass concentrations calculated based on the particle number (mobility diameter) and mass size distribution (vacuum aerodynamic diameter) were even higher, ranging from 1.40–1.60 g cm−3 in summer and from 1.40–1.75 g cm−3 in winter. Although aged continental air masses from the SE were rare in summer (7 %), they were connected with the highest concentrations of all NR-PM1 species, especially sulphate and ammonium. In winter, slow continental air masses from the SW (44 %) were linked to inversion conditions over Central Europe and were associated with the highest concentrations among all NR-PM1 measurements.

scholarly journals First simultaneous measurements of peroxyacetyl nitrate (PAN) and ozone at Nam Co in the central Tibetan Plateau: impacts from the PBL evolution and transport processes

2017 ◽  
Author(s):  
Xiaobin Xu ◽  
Hualong Zhang ◽  
Weili Lin ◽  
Ying Wang ◽  
Shihui Jia
Keyword(s):  
Long Range ◽  
Early Morning ◽  
Diurnal Variations ◽  
Long Range Transport ◽  
Nam Co ◽  
Monsoon Period ◽  
Air Masses ◽  
Upper Troposphere ◽  
Central Tibetan Plateau ◽  
Range Transport

Abstract. Both peroxyacetyl nitrate (PAN) and ozone (O3) are key photochemical products in the atmosphere. Most of the previous in-situ observations of both gases have been made in polluted regions and at low altitude sites. Here we present first simultaneous measurements of PAN and O3 at Nam Co (NMC, 90°57′ E, 30°46′ N, 4745 m  a.s.l.), a remote site in the central Tibetan Plateau (TP). The observations were made during summer periods in 2011 and 2012. The PAN concentrations averaged 0.36 ppb (range: 0.11–0.76 ppb) and 0.44 ppb (range: 0.21–0.99 ppb) during 16–25 August 2011 and 15 May to 13 July 2012, respectively. The O3 concentration varied from 27.9 ppb to 96.4 ppb, with an average of 60.0 ppb. Profound diurnal cycles of PAN and O3 were observed, with minimum values around 05:00 LT, steep rises in the early morning, and broader platforms of high values during 09:00–20:00 LT. We find that the evolution of planetary boundary layer (PBL) played a key role in shaping the diurnal patterns of both gases, particularly the rapid increases of PAN and O3 in the early morning. Air entrainment from the free troposphere into the PBL seemed to cause the early morning increase and be a key factor of sustaining the daytime high concentrations of both gases. The days with higher daytime PBL (about 3 km) showed stronger diurnal variations of both gases and were mainly distributed in the drier pre-monsoon period, while those with shallower daytime PBL (about 2 km) showed minor diurnal variations of both gases and were mainly distributed in the humid monsoon period. Episodes of higher PAN levels were observed occasionally at NMC. These PAN episodes were caused either by rapid downward transport of air masses from the middle/upper troposphere or by long-range transport of PAN plumes from North India. The PAN level in the downward transport cases ranged from 0.5 ppb to 0.7 ppb and may indicate the PAN abundance in the middle/upper troposphere. In the long-range transport case, the PAN level varied in the range of 0.6–1.0 ppb. This long-range transport process influenced most of the western and central TP region for about a week in early June 2012. Our results suggest that polluted air masses from South Asia can significantly enhance the PAN level over the TP. As PAN act as a reservoir of NOx, the impacts of pollution transport from South Asia on tropospheric photochemistry over the TP region deserve further studies.

Radioactivity measurements in the atmosphere and water column of Rogoznica Lake (central Adriatic)

2021 ◽  
Author(s):  
Ivana Tucaković ◽  
Sarah Mateša ◽  
Ivana Coha ◽  
Marija Marguš ◽  
Milan Čanković ◽  
...  
Keyword(s):  
Water Column ◽  
Long Range ◽  
Lake Water ◽  
Dry Deposition ◽  
Long Range Transport ◽  
Atmospheric Input ◽  
Air Masses ◽  
Activity Concentrations ◽  
Range Transport ◽  
Radionuclide Activity

&lt;p&gt;Croatian Science Foundation MARRES project (MARine lake (Rogoznica) as a model for EcoSystem functioning in a changing environment) aims to investigate the unique environment (slow exchange of seawater with the sea; atmospheric input is the only source of freshwater) of the marine lake which is an example of highly stratified (permanent anoxia bellow 9 m depth), and by climate changes affected marine system in the middle of the eastern Adriatic coast (43.53&amp;#176; N, 15.95&amp;#176; E). The area of the lake is characterized by the extensive tourism and mariculture, and the low impact of local industrial activities. It is also affected by the combined influence of long-range transport of air masses and local emissions (open-fire events).&lt;/p&gt;&lt;p&gt;An important part of the project is focused on the exchange and interaction between atmosphere, water column and sediment by measuring the atmospheric input (wet and dry deposition) of sulphur compounds, organic carbon, trace metals and radionuclides (Be-7, Pb-210).&lt;/p&gt;&lt;p&gt;This work for the first time will present the current state of the measurements of radioactivity in the Rogoznica lake area, including samples of aerosol particulate matter, PM2.5 &lt; 2.5 um, rainwater and lake water column. Namely, the concentrations of Be-7 and Pb-210 in PM2.5 are measured to determine and correlate the dynamics of particle transport, meteorological information, especially origin of air masses and seasonal variation of PM2.5. While presence of Be-7 indicates the recent wet or dry deposition from the upper parts of the atmosphere, Pb-210 may be used as a tracer for continental air masses. Therefore, it can also indicate the influence of the pollution induced by human activity. Regarding that, special attention will be paid to compare results before and during the Covid-19 lockdown periods.&lt;/p&gt;&lt;p&gt;So far, preliminary results do not show significant difference in PM2.5 masses and measured radionuclide activity concentrations for the lockdown period. Be-7 and Pb-210 were regularly detected in aerosols collected on a glass fiber filters during a one-week sampling periods with the air flow rate of 2.3 m&lt;sup&gt;3&lt;/sup&gt;/h. Their activity concentrations are determined by gamma spectrometry using High Purity Germanium detectors. The results are found to be correlated with PM2.5 masses, ranging from 2.9 to 12.2 Bq/m&lt;sup&gt;3&lt;/sup&gt; for Be-7 and from 0.5 to 2.5 Bq/m&lt;sup&gt;3&lt;/sup&gt; for Pb-210. First analyses show that the highest values can be related to the long-range transport of air masses and to the recorded near open-fire event. As expected, Be-7 is also detected in almost every rainwater sample (event), with the activity concentration up to 5.6 Bq/L, while low activities of Pb-210 are detected only sporadically. Related to that, Be-7 is detected in lake water column as well, but only in the surface layer and in samples collected during, or immediately after the rain events.&amp;#160;&lt;/p&gt;&lt;p&gt;Dynamics and seasonal variation of radionuclide activity concentrations in here studied samples will be discussed, and the relationships with some meteorological parameters (temperature, wind speed, relative humidity, precipitation level) as well as local and long-range transport and physico-chemical conditions in the lake water column will be established.&lt;/p&gt;

Regional and Transported A erosols in Ambient A tmosphere of Raipur,India, during W inter

2021 ◽  
Vol 30 (1) ◽  
pp. 7-17
Author(s):  
Manas Kanti Deb ◽  
Mithlesh Mahilang ◽  
Jayant Nirmalkar
Keyword(s):  
Size Distribution ◽  
Long Range ◽  
Fine Particles ◽  
Characteristic Size ◽  
Long Range Transport ◽  
Bimodal Size Distribution ◽  
Entire Study ◽  
Coarse Mode ◽  
Range Transport ◽  
Air Trajectory

Size fractionated atmospheric aerosols were collected using cascade impactor sampler on quartz flter substrate during October 2015 to February 2016 in campus of Pt Ravishankar Shukla University of Raipur Chhattisgarh. The size of aerosol particles is of crucial importance to several processes in the atmosphere. The relative concentrations in both modes are responsible for the variability observed in the shape of the size distribution. Characteristic size distributions of measured aerosol over central India showed identifcation of three main behaviour types during entire study period: (i) month in which bimodal size distribution dominated in coarse mode (October 2015, 5 December 2015 and January, 2016), (ii) those months in which bimodal distribution equally intense in both one, and coarse modes (November, 2015) and (iii) those which were mainly dominated within fine (February, 2016, December, 2015). The two-subsequent month namely November 2015 and December 2015 shows bimodal size distribution with dominance in fine size range in comparison to coarse mode, possibly these high loading of one particles is due to long range transport. The peculiar observation of air trajectory shows that there is increase in fine particles concentration during December 2015, although there in increase in temperature and wind speed. The reason for this high concentration is long range transport of air masses. However, January has normal trend in particular matter concentration. The important finding of the present study based on characteristic size distribution and air trajectory plots accomplishes that fine particles are obtained through long range transport whereas coarse particles are mainly from local origin.

Metal contamination of natural surface soils from long-range atmospheric transport: Existing and missing knowledge

2006 ◽  
Vol 14 (3) ◽  
pp. 169-186 ◽  
Author(s):  
Eiliv Steinnes ◽  
Andrew J Friedland
Keyword(s):  
Organic Matter ◽  
Long Range ◽  
Atmospheric Transport ◽  
Long Range Transport ◽  
Surface Soils ◽  
Air Masses ◽  
Range Transport ◽  
Zinc Cadmium ◽  
Lead Zinc ◽  
Temporal And Spatial

This review focuses on the long-range atmospheric transport of metals to organic-rich surface soils (mostly 50–90% organic matter) in the temperate, coniferous, and boreal zones of North America and Europe. From various air-pollution related measurements (air, precipitation, moss, peat cores) Pb and Zn are known to be transported long distances in the air in large amounts. Arsenic, Cd, Hg, Sb, and Se are also typical representatives of long-range transported air masses, and there is evidence that Ag, Bi, In, Mo, Tl, and W belong to this group of elements. Through the use of “environmental archives” such as ice and peat cores it has become evident that long-range transport of pollutants and associated contamination of natural surfaces is not just a recent phenomenon. There is compelling evidence for widespread enrichment of surface soil horizons in Pb from long-range transport, and many studies support enrichment of Zn. Mercury is also generally elevated by anthropogenic emissions over natural levels in organic-rich surface soils, whereas results for Cd are less conclusive. There is evidence that As, Se, Ag, Mo, In, Sb, W, Tl, and Bi all are subject to some enrichment in organic-rich surface soils from long-range atmospheric transport, but studies are still few for most of these elements. With the exception of Pb, little is known about residence times of the elements in the organic-rich surface horizon, and more research is needed on this topic. Further studies are desirable on the temporal and spatial trends in supply of the above elements, which are poorly known in large parts of the northern temperate zone.Key words: natural soils, metals, long-range atmospheric transport, organic matter, lead, zinc, cadmium, mercury.

scholarly journals Ozone and carbon monoxide over India during the summer monsoon: regional emissions and transport

2016 ◽  
Vol 16 (5) ◽  
pp. 3013-3032 ◽  
Author(s):  
Narendra Ojha ◽  
Andrea Pozzer ◽  
Armin Rauthe-Schöch ◽  
Angela K. Baker ◽  
Jongmin Yoon ◽  
...  
Keyword(s):  
Carbon Monoxide ◽  
Long Range ◽  
Summer Monsoon ◽  
Lower Troposphere ◽  
Southern India ◽  
Long Range Transport ◽  
Minor Role ◽  
Air Masses ◽  
Range Transport ◽  
Regional Emissions

Abstract. We compare in situ measurements of ozone (O3) and carbon monoxide (CO) profiles from the CARIBIC program with the results from the regional chemistry transport model (WRF-Chem) to investigate the role of local and regional emissions and long-range transport over southern India during the summer monsoon of 2008. WRF-Chem successfully reproduces the general features of O3 and CO distributions over the South Asian region. However, absolute CO concentrations in the lower troposphere are typically underestimated. Here we investigate the influence of local relative to remote emissions through sensitivity simulations. The influence of 50 % increased CO emissions over South Asia leads to a significant enhancement (upto 20 % in July) in upper tropospheric CO in the northern and central Indian regions. Over Chennai in southern India, this causes a 33 % increase in surface CO during June. However, the influence of enhanced local and regional emissions is found to be smaller (5 %) in the free troposphere over Chennai, except during September. Local to regional emissions are therefore suggested to play a minor role in the underestimation of CO by WRF-Chem during June–August. In the lower troposphere, a high pollution (O3: 146.4 ± 12.8, CO: 136.4 ± 12.2 nmol mol−1) event (15 July 2008), not reproduced by the model, is shown to be due to transport of photochemically processed air masses from the boundary layer in southern India. A sensitivity simulation combined with backward trajectories indicates that long-range transport of CO to southern India is significantly underestimated, particularly in air masses from the west, i.e., from Central Africa. This study highlights the need for more aircraft-based measurements over India and adjacent regions and the improvement of global emission inventories.

scholarly journals Concentration Trajectory Route of Air pollution with an Integrated Lagrangian model (C-TRAIL model v1.0) derived from the Community Multiscale Air Quality Modeling (CMAQ model v5.2)

2020 ◽  
Author(s):  
Arman Pouyaei ◽  
Yunsoo Choi ◽  
Jia Jung ◽  
Bavand Sadeghi ◽  
Chul Han Song
Keyword(s):  
Air Pollution ◽  
Air Quality ◽  
Long Range ◽  
Lagrangian Model ◽  
Long Range Transport ◽  
Air Masses ◽  
Range Transport ◽  
Potential Sources ◽  
Model C ◽  
Co Concentrations

Abstract. This paper introduces a reliable and comprehensive Lagrangian output (Concentration Trajectory Route of Air pollution with Integrated Lagrangian model, C-TRAIL version 1.0) from an Eulerian air quality model for validating the source-receptor link by following real polluted air masses. To investigate the concentrations and trajectories of air masses simultaneously, we implement the trajectory-grid (TG) Lagrangian advection scheme in the CMAQ (Community Multiscale Air Quality) Eulerian model version 5.2. The TG algorithm follows the concentrations of representative air packets of species along trajectories determined by the wind field. The generated output from C-TRAIL accurately identifies the origins of pollutants. For validation, we analyzed the results of C-TRAIL during the KORUS-AQ campaign over South Korea. Initially, we implemented C-TRAIL in a simulation of CO concentrations with an emphasis on the long- and short-range transport effect. The output from C-TRAIL reveals that local trajectories were responsible for CO concentrations over Seoul during the stagnant period (May 17–22, 2016) and during the extreme pollution period (May 25–28, 2016), highly polluted air masses from China were distinguished as sources of CO transported to the Seoul Metropolitan Area (SMA). We conclude that long-range transport played a crucial role in high CO concentrations over the receptor area during this period. Furthermore, for May 2016, we find that the potential sources of CO over that SMA were the result of either local transport or long-range transport from the Shandong Peninsula and, in some cases, from north of the SMA. By identifying the trajectories of CO concentrations, one can use the results from C-TRAIL to directly link strong potential sources of pollutants to a receptor in specific regions during various time frames.

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