Emission characterization of size-resolved particles in a pre-school classroom in relation to children’s activities

2017 ◽  
Vol 28 (5) ◽  
pp. 659-676 ◽  
Author(s):  
Jihye Kim ◽  
Seongjun Park ◽  
Heegang Kim ◽  
Myoung Souk Yeo

The objective of this study was to investigate the effect of children’s daily activity patterns on the size-resolved indoor particles in a pre-school classroom, qualitatively and quantitatively. Real-time particle number size distribution data in conjunction with activity were collected experimentally in a pre-school classroom during two seasons: late spring and early winter. We divided daily activities into six groups: Arrival, Large Group, Small Group, Naptime, Dismissal and Unoccupied. The concentration variation forms of coarse particles were compared qualitatively among activity groups. The results indicated that noteworthy coarse particle concentration variations were observed during each activity group. These variations were caused by four factors: presence/absence of children, variation in the number of children, activity intensity and presence of sources. The emission rates were estimated to quantify the impact of activities. Time series emission rates were deduced from the piecewise-constant inputs and outputs model. The piecewise-constant emission rates were averaged for sequential parts to reduce noise and ensure daily repeated peaks were not missed. The sequential part-constant emission rates were consistent with previously described particle number concentration variation results and the predicted indoor particle number concentration data with sequential part-constant emission rates agreed well with measured data.

2021 ◽  
Vol 21 (22) ◽  
pp. 17185-17223
Author(s):  
Clémence Rose ◽  
Martine Collaud Coen ◽  
Elisabeth Andrews ◽  
Yong Lin ◽  
Isaline Bossert ◽  
...  

Abstract. Aerosol particles are a complex component of the atmospheric system which influence climate directly by interacting with solar radiation, and indirectly by contributing to cloud formation. The variety of their sources, as well as the multiple transformations they may undergo during their transport (including wet and dry deposition), result in significant spatial and temporal variability of their properties. Documenting this variability is essential to provide a proper representation of aerosols and cloud condensation nuclei (CCN) in climate models. Using measurements conducted in 2016 or 2017 at 62 ground-based stations around the world, this study provides the most up-to-date picture of the spatial distribution of particle number concentration (Ntot) and number size distribution (PNSD, from 39 sites). A sensitivity study was first performed to assess the impact of data availability on Ntot's annual and seasonal statistics, as well as on the analysis of its diel cycle. Thresholds of 50 % and 60 % were set at the seasonal and annual scale, respectively, for the study of the corresponding statistics, and a slightly higher coverage (75 %) was required to document the diel cycle. Although some observations are common to a majority of sites, the variety of environments characterizing these stations made it possible to highlight contrasting findings, which, among other factors, seem to be significantly related to the level of anthropogenic influence. The concentrations measured at polar sites are the lowest (∼ 102 cm−3) and show a clear seasonality, which is also visible in the shape of the PNSD, while diel cycles are in general less evident, due notably to the absence of a regular day–night cycle in some seasons. In contrast, the concentrations characteristic of urban environments are the highest (∼ 103–104 cm−3) and do not show pronounced seasonal variations, whereas diel cycles tend to be very regular over the year at these stations. The remaining sites, including mountain and non-urban continental and coastal stations, do not exhibit as obvious common behaviour as polar and urban sites and display, on average, intermediate Ntot (∼ 102–103 cm−3). Particle concentrations measured at mountain sites, however, are generally lower compared to nearby lowland sites, and tend to exhibit somewhat more pronounced seasonal variations as a likely result of the strong impact of the atmospheric boundary layer (ABL) influence in connection with the topography of the sites. ABL dynamics also likely contribute to the diel cycle of Ntot observed at these stations. Based on available PNSD measurements, CCN-sized particles (considered here as either >50 nm or >100 nm) can represent from a few percent to almost all of Ntot, corresponding to seasonal medians on the order of ∼ 10 to 1000 cm−3, with seasonal patterns and a hierarchy of the site types broadly similar to those observed for Ntot. Overall, this work illustrates the importance of in situ measurements, in particular for the study of aerosol physical properties, and thus strongly supports the development of a broad global network of near surface observatories to increase and homogenize the spatial coverage of the measurements, and guarantee as well data availability and quality. The results of this study also provide a valuable, freely available and easy to use support for model comparison and validation, with the ultimate goal of contributing to improvement of the representation of aerosol–cloud interactions in models, and, therefore, of the evaluation of the impact of aerosol particles on climate.


2017 ◽  
Vol 17 (2) ◽  
pp. 1529-1541 ◽  
Author(s):  
Clémence Rose ◽  
Karine Sellegri ◽  
Isabel Moreno ◽  
Fernando Velarde ◽  
Michel Ramonet ◽  
...  

Abstract. Global models predict that new particle formation (NPF) is, in some environments, responsible for a substantial fraction of the total atmospheric particle number concentration and subsequently contributes significantly to cloud condensation nuclei (CCN) concentrations. NPF events were frequently observed at the highest atmospheric observatory in the world, on Chacaltaya (5240 m a.s.l.), Bolivia. The present study focuses on the impact of NPF on CCN population. Neutral cluster and Air Ion Spectrometer and mobility particle size spectrometer measurements were simultaneously used to follow the growth of particles from cluster sizes down to ∼ 2 nm up to CCN threshold sizes set to 50, 80 and 100 nm. Using measurements performed between 1 January and 31 December 2012, we found that 61 % of the 94 analysed events showed a clear particle growth and significant enhancement of the CCN-relevant particle number concentration. We evaluated the contribution of NPF, relative to the transport and growth of pre-existing particles, to CCN size. The averaged production of 50 nm particles during those events was 5072, and 1481 cm−3 for 100 nm particles, with a larger contribution of NPF compared to transport, especially during the wet season. The data set was further segregated into boundary layer (BL) and free troposphere (FT) conditions at the site. The NPF frequency of occurrence was higher in the BL (48 %) compared to the FT (39 %). Particle condensational growth was more frequently observed for events initiated in the FT, but on average faster for those initiated in the BL, when the amount of condensable species was most probably larger. As a result, the potential to form new CCN was higher for events initiated in the BL (67 % against 53 % in the FT). In contrast, higher CCN number concentration increases were found when the NPF process initially occurred in the FT, under less polluted conditions. This work highlights the competition between particle growth and the removal of freshly nucleated particles by coagulation processes. The results support model predictions which suggest that NPF is an effective source of CCN in some environments, and thus may influence regional climate through cloud-related radiative processes.


2016 ◽  
Author(s):  
C. Rose ◽  
K. Sellegri ◽  
I. Moreno ◽  
F. Velarde ◽  
M. Ramonet ◽  
...  

Abstract. Global models predict that new particle formation (NPF) is, in some environments, responsible for a substantial fraction of the total atmospheric particle number concentration and subsequently contribute significantly to cloud condensation nuclei (CCN) concentrations. NPF events were frequently observed at the highest atmospheric observatory in the world, Chacaltaya (5240 m a.s.l.), Bolivia. The present study focuses on the impact of NPF on CCN population. Neutral cluster and Air Ion Spectrometer and mobility particle size spectrometer measurements were simultaneously used to follow the growth of particles from cluster sizes down to ~ 2 nm up to CCN threshold sizes set to 50, 80 and 100 nm. Using measurements performed between January 1 and December 31 2012, we found that 61% of the 94 analysed events showed a clear particle growth and significant enhancement of the CCN-relevant particle number concentration. We evaluated the contribution of NPF events relative to the transport of pre-existing particles to the site. The averaged production of 50 nm particles during those events was 5072 cm−3, and 1481 cm−3 for 100 nm particles, with a larger contribution of NPF compared to transport, especially during the wet season. The data set was further segregated into boundary layer (BL) and free troposphere (FT) conditions at the site. The NPF frequency of occurrence was higher in the BL (48 %) compared to the FT (39 %). Particle condensational growth was more frequently observed for events initiated in the FT, but on average faster for those initiated in the BL, when the amount of condensable species was most probably larger. As a result, the potential to form new CCN was higher for events initiated in the BL (67 % against 56 % in the FT). In contrast, higher CCN number concentration increases were found when the NPF process initially occurred in the FT, under less polluted conditions. This work highlights the competition between particle growth and the removal of freshly nucleated particles by coagulation processes. The results support model predictions which suggest that NPF is an effective source of CCN in some environments, and thus may influence regional climate through cloud related radiative processes.


2019 ◽  
Author(s):  
Stina Ausmeel ◽  
Axel Eriksson ◽  
Erik Ahlberg ◽  
Adam Kristensson

Abstract. Ship traffic is a major source of aerosol particles, particularly near shipping lanes and harbours. In order to estimate the contribution to exposure downwind of a shipping lane, it is important to be able to measure the ship emission contribution at various distances from the source. We report on measurements of atmospheric particles, 7–20 km downwind of a shipping lane in the Baltic Sea Sulphur Emission Control Area (SECA) at a coastal location in southern Sweden during a winter and a summer campaign. Each ship plume was linked to individual ship passages using a novel method based on wind field data and Automatic ship Identification System data (AIS), where varying wind speeds and directions were applied to calculate a plume trajectory. In a situation where AIS data is not matching measured plumes well or if AIS data is missing, we provide an alternative method with particle number concentration data. The shipping lane contribution to the particle number concentration in Falsterbo was estimated by subtracting background concentrations from the ship plume concentrations, and more than 150 plumes were analysed. We have also extrapolated the contribution to seasonal averages and provide recommendations for future similar measurements. Averaged over a season, the contribution to particle number concentration was about 18 % during the winter and 10 % during the summer, including those periods with wind directions when the shipping lane was not affecting the station. The corresponding contribution to equivalent black carbon was 1.4 %.


2016 ◽  
Vol 16 (7) ◽  
pp. 4481-4495 ◽  
Author(s):  
Mattia Righi ◽  
Johannes Hendricks ◽  
Robert Sausen

Abstract. We use the EMAC (ECHAM/MESSy Atmospheric Chemistry) global climate–chemistry model coupled to the aerosol module MADE (Modal Aerosol Dynamics model for Europe, adapted for global applications) to simulate the impact of aviation emissions on global atmospheric aerosol and climate in 2030. Emissions of short-lived gas and aerosol species follow the four Representative Concentration Pathways (RCPs) designed in support of the Fifth Assessment Report of the Intergovernmental Panel on Climate Change. We compare our findings with the results of a previous study with the same model configuration focusing on year 2000 emissions. We also characterize the aviation results in the context of the other transport sectors presented in a companion paper. In spite of a relevant increase in aviation traffic volume and resulting emissions of aerosol (black carbon) and aerosol precursor species (nitrogen oxides and sulfur dioxide), the aviation effect on particle mass concentration in 2030 remains quite negligible (on the order of a few ng m−3), about 1 order of magnitude less than the increase in concentration due to other emission sources. Due to the relatively small size of the aviation-induced aerosol, however, the increase in particle number concentration is significant in all scenarios (about 1000 cm−3), mostly affecting the northern mid-latitudes at typical flight altitudes (7–12 km). This largely contributes to the overall change in particle number concentration between 2000 and 2030, which also results in significant climate effects due to aerosol–cloud interactions. Aviation is the only transport sector for which a larger impact on the Earth's radiation budget is simulated in the future: the aviation-induced radiative forcing in 2030 is more than doubled with respect to the year 2000 value of −15 mW m−2 in all scenarios, with a maximum value of −63 mW m−2 simulated for RCP2.6.


2021 ◽  
Author(s):  
Clémence Rose ◽  
Martine Collaud Coen ◽  
Elisabeth Andrews ◽  
Yong Lin ◽  
Isaline Bossert ◽  
...  

Abstract. Aerosol particles are a complex component of the atmospheric system that influences climate directly by interacting with solar radiation, and indirectly by contributing to cloud formation. The variety of their sources, as well as the multiple transformations they may undergo during their transport, result in significant spatial and temporal variability of their properties. Documenting this variability is essential to provide a proper representation of aerosols and cloud condensation nuclei (CCN) in climate models. Using measurements conducted in 2016 or 2017 at 62 ground based stations around the world, this study provides the most up-to-date picture of the spatial distribution of particle number concentration (Ntot) and number size distribution (PNSD, from 39 sites). A sensitivity study was first performed to assess the impact of data availability on Ntot's annual and seasonal statistics, as well as on the analysis of its diel cycle. Thresholds of 50 % and 60 % were set at the seasonal and annual scale, respectively, for the study of the corresponding statistics, and a slightly higher coverage (75 %) was required to document the diel cycle. Although some observations are common to a majority of sites, the variety of environments characterizing these stations made it possible to highlight contrasting findings, which, among other factors, seem to be significantly related to the level of anthropogenic influence. The concentrations measured at polar sites are the lowest (~102 cm−3) and show a clear seasonality, which is also visible in the shape of the PNSD, while diel cycles are in general barely marked, due notably to the absence of a regular day-night cycle in some seasons. In contrast, the concentrations characteristic of urban environments are the highest (~103–104 cm−3) and do not show pronounced seasonal variations, whereas diel cycles tend to be very regular over the year at these stations. The remaining sites, including mountain and non-urban continental and coastal stations, do not exhibit as obvious common behaviour as polar and urban sites and display, on average, intermediate Ntot (~102–103 cm−3). Particle concentrations measured at mountain sites, however, are generally lower compared to nearby lowland sites, and tend to exhibit somewhat more pronounced seasonal variations as a likely result of the strong impact of the atmospheric boundary layer (ABL) influence in connection with the topography of the sites. ABL dynamics also likely contribute to the diel cycle of Ntot observed at these stations. Based on available PNSD measurements, CCN-sized particles (i.e. > 50–100 nm) can represent from a few percent to almost all of Ntot, corresponding to seasonal medians in the order of ~10 to 1000 cm−3, with seasonal patterns and a hierarchy of the site types broadly similar to those observed for Ntot. Overall, this work illustrates the importance of in-situ measurements, in particular for the study of aerosol physical properties, and thus strongly supports the development of a broad global network of near surface observatories to increase and homogenize the spatial coverage of the measurements, and guarantee as well data availability and quality. The results of this study also provide a valuable, freely available and easy to use support for model comparison and validation, with the ultimate goal of contributing to improvement of the representation of aerosol-cloud interactions in models, and, therefore, of the evaluation of the impact of aerosol particles on climate.


2004 ◽  
Vol 38 (20) ◽  
pp. 3341-3348 ◽  
Author(s):  
Rong Chun Yu ◽  
Hee Wen Teh ◽  
Peter A. Jaques ◽  
Constantinos Sioutas ◽  
John R. Froines

2019 ◽  
Author(s):  
Antonio Spanu ◽  
Maximilian Dollner ◽  
Josef Gasteiger ◽  
T. Paul Bui ◽  
Bernadett Weinzierl

Abstract. Aerosols and clouds affect atmospheric radiative processes and climate in many complex ways and still pose the largest uncertainty in current estimates of the Earth’s changing energy budget. Airborne in-situ sensors such as the Cloud, Aerosol, and Precipitation Spectrometer (CAPS) or other optical spectrometers and optical array probes provide detailed information about the horizontal and vertical distribution of aerosol and cloud properties. However, flow distortions occurring at the location where these instruments are mounted on the outside of an aircraft may directly produce artifacts in detected particle number concentration and also cause droplet deformation and/or break-up during the measurement process. Several studies have investigated flow-induced errors assuming that air is incompressible. However, for fast-flying aircraft, the impact of air compressibility is no longer negligible. In this study, we combine airborne data with numerical simulations to investigate the flow around wing-mounted instruments and the induced errors for different realistic flight conditions. A correction scheme for deriving particle number concentrations from in-situ aerosol and cloud probes is proposed, and a new formula is provided for deriving the droplet volume from images taken by optical array probes, reducing errors by up to one order of magnitude. Shape distortions of liquid droplets can either be caused by errors in the speed with which the images are recorded or by aerodynamic forces acting at the droplet surface caused by changes in the airflow around the instrument. These forces can lead to the dynamic breakup of droplets causing artifacts in particle number concentration and size. Furthermore, an estimation of the critical breakup diameter, as a function of flight conditions is provided. Experimental data show that flow speed at the instrument location is smaller than the ambient flow speed. Our simulations confirm the observed difference and reveal a size-dependent impact on particle speed and concentration. This leads, on average, to a 25 % overestimation of the number concentration of particles larger than ~10 μm} diameter and causes distorted images of droplets and ice crystals if the flow values recorded at the instrument are used. With the proposed correction scheme both errors are significantly reduced by a factor 10. Although the presented correction scheme is derived for the DLR Falcon research aircraft (SALTRACE campaign) and validated for the DLR Falcon (A-LIFE campaign) and the NASA DC-8 (ATom campaign), the general conclusions hold for any fast-flying research airplane.


2011 ◽  
Vol 11 (7) ◽  
pp. 3319-3332 ◽  
Author(s):  
T. Schmeissner ◽  
R. Krejci ◽  
J. Ström ◽  
W. Birmili ◽  
A. Wiedensohler ◽  
...  

Abstract. The first long-term measurements of aerosol number and size distributions in South-American tropical free troposphere (FT) were performed from March 2007 until March 2009. The measurements took place at the high altitude Atmospheric Research Station Alexander von Humboldt. The station is located on top of the Sierra Nevada mountain ridge at 4765 m a.s.l. nearby the city of Mérida, Venezuela. Aerosol size distribution and number concentration data was obtained with a custom-built Differential Mobility Particle Sizer (DMPS) system and a Condensational Particle Counter (CPC). The analysis of the annual and diurnal variability of the tropical FT aerosol focused mainly on possible links to the atmospheric general circulation in the tropics. Considerable annual and diurnal cycles of the particle number concentration were observed. Highest total particle number concentrations were measured during the dry season (January–March, 519 ± 613 cm−3), lowest during the wet season (July–September, 318 ± 194 cm−3). The more humid FT (relative humidity (RH) range 50–95 %) contained generally higher aerosol particle number concentrations (573 ± 768 cm−3 during dry season, 320 ± 195 cm−3 during wet season) than the dry FT (RH < 50 %, 454 ± 332 cm−3 during dry season, 275 ± 172 cm−3 during wet season), indicating the importance of convection for aerosol distributions in the tropical FT. The diurnal cycle in the variability of the particle number concentration was mainly driven by local orography.


2010 ◽  
Vol 10 (11) ◽  
pp. 29153-29189
Author(s):  
T. Schmeißner ◽  
R. Krejci ◽  
J. Ström ◽  
W. Birmili ◽  
A. Wiedensohler ◽  
...  

Abstract. The first long-term measurements of aerosol number and size distributions in South-American tropical free troposphere were performed from March 2007 until Mai 2009. The measurements took place at the high altitude Atmospheric Research Station Alexander von Humboldt. The station is located on top of the Sierra Nevada mountain ridge at 4765 m a.s.l. nearby the city of Mérida, Venezuela. Aerosol size distribution and number concentration data was obtained with a custom-built Differential Mobility Particle Sizer (DMPS system) and a Condensational Particle Counter (CPC). The analysis of the annual and diurnal variability of the tropical free troposphere (FT) aerosol focused mainly on possible links to the atmospheric general circulation in the tropics. Considerable annual and diurnal cycles of the particle number concentration were observed. Highest total particle number concentrations were measured during the dry season (519±613 cm−3), lowest during the wet season (318±194 cm−3). The more humid FT contained generally higher aerosol particle number concentrations (573±768 cm−3 during dry season, 320±195 cm−3 during wet season) than the dry FT (454±332 cm−3 during dry season, 275±172 cm−3 during wet season), indicating the importance of convection for aerosol distributions in the tropical FT. The diurnal cycle in the variability of the particle number concentration was mainly driven by local orography.


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