scholarly journals On the sub-micron aerosol size distribution in a coastal-rural site at El Arenosillo Station (SW – Spain)

2011 ◽  
Vol 11 (21) ◽  
pp. 11185-11206 ◽  
Author(s):  
M. Sorribas ◽  
B. A. de la Morena ◽  
B. Wehner ◽  
J. F. López ◽  
N. Prats ◽  
...  
Keyword(s):  
Size Distribution ◽  
Particle Formation ◽  
Rural Site ◽  
Aerosol Size Distribution ◽  
Land Breeze ◽  
Air Masses ◽  
Desert Dust ◽  
Median Size ◽  
The Mean ◽  
Marine Air

Abstract. This study focuses on the analysis of the sub-micron aerosol characteristics at El Arenosillo Station, a rural and coastal environment in South-western Spain between 1 August 2004 and 31 July 2006 (594 days). The mean total concentration (NT) was 8660 cm−3 and the mean concentrations in the nucleation (NNUC), Aitken (NAIT) and accumulation (NACC) particle size ranges were 2830 cm−3, 4110 cm−3 and 1720 cm−3, respectively. Median size distribution was characterised by a single-modal fit, with a geometric diameter, median number concentration and geometric standard deviation of 60 nm, 5390 cm−3 and 2.31, respectively. Characterisation of primary emissions, secondary particle formation, changes to meteorology and long-term transport has been necessary to understand the seasonal and annual variability of the total and modal particle concentration. Number concentrations exhibited a diurnal pattern with maximum concentrations around noon. This was governed by the concentrations of the nucleation and Aitken modes during the warm seasons and only by the nucleation mode during the cold seasons. Similar monthly mean total concentrations were observed throughout the year due to a clear inverse variation between the monthly mean NNUC and NACC. It was related to the impact of desert dust and continental air masses on the monthly mean particle levels. These air masses were associated with high values of NACC which suppressed the new particle formation (decreasing NNUC). Each day was classified according to a land breeze flow or a synoptic pattern influence. The median size distribution for desert dust and continental aerosol was dominated by the Aitken and accumulation modes, and marine air masses were dominated by the nucleation and Aitken modes. Particles moved offshore due to the land breeze and had an impact on the particle burden at noon, especially when the wind was blowing from the NW sector in the morning during summer time. This increased NNUC and NAIT by factors of 3.1 and 2.4, respectively. Nucleation events with the typical "banana" shape were characterised by a mean particle nucleation rate of 0.74 cm−3 s−1, a mean growth rate of 1.96 nm h−1 and a mean total duration of 9.25 h (starting at 10:55 GMT and ending at 20:10 GMT). They were observed for 48 days. Other nucleation events were identified as those produced by the emissions from the industrial areas located at a distance of 35 km. They were observed for 42 days. Both nucleation events were strongly linked to the marine air mass origin.

scholarly journals Analysis of particle size distribution changes between three measurement sites in Northern Scandinavia

2013 ◽  
Vol 13 (4) ◽  
pp. 9401-9442 ◽  
Author(s):  
R. Väänänen ◽  
E.-M. Kyrö ◽  
T. Nieminen ◽  
N. Kivekäs ◽  
H. Junninen ◽  
...  
Keyword(s):  
Particle Size ◽  
Size Distribution ◽  
Aerosol Particle ◽  
Particle Growth ◽  
Particle Formation ◽  
Aerosol Size Distribution ◽  
New Particle Formation ◽  
Air Masses ◽  
Aerosol Dynamics ◽  
Particle Sizer

Abstract. We investigated atmospheric aerosol particle dynamics in a boreal forest zone in Northern Scandinavia. We used aerosol size distribution data measured with either a Differential Mobility Particle Sizer (DMPS) or Scanning Mobility Particle Sizer (SMPS) at three stations (Värriö, Pallas and Abisko), and combined these data with the HYSPLIT air mass trajectory analysis. We compared three approaches: analysis of new particle formation events, investigation of air masses transport from the ocean to individual stations with different over-land transport times, and analysis of changes in aerosol particle size distributions during the air masses transport from one measurement station to another. Aitken mode particles were found to have an apparent average growth rate of 0.6–0.7 nm h−1 when the air masses travelled over land. Particle growth rates during the NPF events were 3–6 times higher than the apparent particle growth. When comparing aerosol dynamics between the different stations for different over-land transport times, no major differences were found except that in Abisko the new particle formation events were observed to take place in air masses having shorter over-land times than at the other stations. We speculate that this is related to the meteorological differences along the paths of air masses caused by the land surface topology. When comparing between air masses travelling the east-to-west direction to those traveling the west-to-east directions, clear differences in the aerosol dynamics were seen. Our results suggest that the condensation growth has an important role in aerosol dynamics also when new particle formation is not evident.

scholarly journals On the sub-micron aerosol size distribution in a coastal-rural site at El Arenosillo Station (SW-Spain)

2011 ◽  
Vol 11 (2) ◽  
pp. 3813-3856 ◽  
Author(s):  
M. Sorribas ◽  
B. A. de la Morena ◽  
B. Wehner ◽  
J. F. López ◽  
N. Prats ◽  
...  
Keyword(s):  
Size Distribution ◽  
Particle Concentration ◽  
Total Concentration ◽  
Total Surface Area ◽  
Rural Site ◽  
Aerosol Size Distribution ◽  
Land Breeze ◽  
Scanning Mobility Particle Sizer ◽  
Accumulation Mode ◽  
Total Particle

Abstract. This study is focused on the analysis of the sub-micron aerosol characteristics at rural and coastal environment in Southwestern Spain. Particle number size distributions were measured in the size range (14–673) nm using a Scanning Mobility Particle Sizer (SMPS, Model 3936-TSI), from 15 July 2004 to 31 July 2006 at El Arenosillo Station. Mean total concentration was 8660 cm−3 and mean concentrations for the nucleation, Aitken and accumulation modes particles were 2830 cm−3, 4110 cm−3 and 1720 cm−3, respectively. Mean geometric diameters of the four modes particles, which characterized the mean size distribution per month, were about 16 nm, 42 nm, 103 nm and 237 nm. Two kinds of episodes produced a maximum of the total concentration around noon: the new particle formation and the regional recirculation such as the sea-land breeze. Two types of nucleation events (called N$1 and N2) were observed. Events N1 were an example of the influence of regional sources and Events N2 showed the weight of local industries over the rural and coastal background levels. The 60% of nucleation events were related to NE and NW wind sectors (N1 and N2 respectively), a ΔT higher than 12 °C, a wind speed higher than 2.3 m s−1 and a total surface area for the accumulation mode particles below of 11 190 μ m2 cm−3. The influence of the sea-land breeze processes has been analyzed, observing increases of up to 50%, 110% and 90% of the particle concentration for the nucleation, Aitken and accumulation modes. Annual evolution of monthly averages allowed to conclude that the increase or decrease of 1 cm−3 of the concentration for nucleation mode particles was related to opposite trend of 0.5 cm−3 of the concentration for accumulation mode. This anti-correlation produced a weak seasonal evolution of the total particle concentration.

scholarly journals Modeling particle nucleation and growth over northern California during the 2010 CARES campaign

2015 ◽  
Vol 15 (21) ◽  
pp. 12283-12313 ◽  
Author(s):  
A. Lupascu ◽  
R. Easter ◽  
R. Zaveri ◽  
M. Shrivastava ◽  
M. Pekour ◽  
...  
Keyword(s):  
Size Distribution ◽  
Particle Number ◽  
Particle Formation ◽  
Number Concentration ◽  
Aerosol Size Distribution ◽  
Particle Nucleation ◽  
Particle Number Concentration ◽  
New Particle Formation ◽  
Organic Vapors ◽  
Diurnal Variability

Abstract. Accurate representation of the aerosol lifecycle requires adequate modeling of the particle number concentration and size distribution in addition to their mass, which is often the focus of aerosol modeling studies. This paper compares particle number concentrations and size distributions as predicted by three empirical nucleation parameterizations in the Weather Research and Forecast coupled with chemistry (WRF-Chem) regional model using 20 discrete size bins ranging from 1 nm to 10 μm. Two of the parameterizations are based on H2SO4, while one is based on both H2SO4 and organic vapors. Budget diagnostic terms for transport, dry deposition, emissions, condensational growth, nucleation, and coagulation of aerosol particles have been added to the model and are used to analyze the differences in how the new particle formation parameterizations influence the evolving aerosol size distribution. The simulations are evaluated using measurements collected at surface sites and from a research aircraft during the Carbonaceous Aerosol and Radiative Effects Study (CARES) conducted in the vicinity of Sacramento, California. While all three parameterizations captured the temporal variation of the size distribution during observed nucleation events as well as the spatial variability in aerosol number, all overestimated by up to a factor of 2.5 the total particle number concentration for particle diameters greater than 10 nm. Using the budget diagnostic terms, we demonstrate that the combined H2SO4 and low-volatility organic vapor parameterization leads to a different diurnal variability of new particle formation and growth to larger sizes compared to the parameterizations based on only H2SO4. At the CARES urban ground site, peak nucleation rates are predicted to occur around 12:00 Pacific (local) standard time (PST) for the H2SO4 parameterizations, whereas the highest rates were predicted at 08:00 and 16:00 PST when low-volatility organic gases are included in the parameterization. This can be explained by higher anthropogenic emissions of organic vapors at these times as well as lower boundary-layer heights that reduce vertical mixing. The higher nucleation rates in the H2SO4-organic parameterization at these times were largely offset by losses due to coagulation. Despite the different budget terms for ultrafine particles, the 10–40 nm diameter particle number concentrations from all three parameterizations increased from 10:00 to 14:00 PST and then decreased later in the afternoon, consistent with changes in the observed size and number distribution. We found that newly formed particles could explain up to 20–30 % of predicted cloud condensation nuclei at 0.5 % supersaturation, depending on location and the specific nucleation parameterization. A sensitivity simulation using 12 discrete size bins ranging from 1 nm to 10 μm diameter gave a reasonable estimate of particle number and size distribution compared to the 20 size bin simulation, while reducing the associated computational cost by ~ 36 %.

scholarly journals Quantifying aerosol size distributions and their temporal variability in the Southern Great Plains, USA

2019 ◽  
Vol 19 (18) ◽  
pp. 11985-12006 ◽  
Author(s):  
Peter J. Marinescu ◽  
Ezra J. T. Levin ◽  
Don Collins ◽  
Sonia M. Kreidenweis ◽  
Susan C. van den Heever
Keyword(s):  
Size Distribution ◽  
Great Plains ◽  
Diurnal Cycle ◽  
Particle Formation ◽  
Aerosol Size Distribution ◽  
Size Distributions ◽  
New Particle Formation ◽  
Scanning Mobility Particle Sizer ◽  
Southern Great Plains ◽  
Particle Sizer

Abstract. A quality-controlled, 5-year dataset of aerosol number size distributions (particles with diameters (Dp) from 7 nm through 14 µm) was developed using observations from a scanning mobility particle sizer, aerodynamic particle sizer, and a condensation particle counter at the Department of Energy's Southern Great Plains (SGP) site. This dataset was used for two purposes. First, typical characteristics of the aerosol size distribution (number, surface area, and volume) were calculated for the SGP site, both for the entire dataset and on a seasonal basis, and size distribution lognormal fit parameters are provided. While the median size distributions generally had similar shapes (four lognormal modes) in all the seasons, there were some significant differences between seasons. These differences were most significant in the smallest particles (Dp<30 nm) and largest particles (Dp>800 nm). Second, power spectral analysis was conducted on this long-term dataset to determine key temporal cycles of total aerosol concentrations, as well as aerosol concentrations in specified size ranges. The strongest cyclic signal was associated with a diurnal cycle in total aerosol number concentrations that was driven by the number concentrations of the smallest particles (Dp<30 nm). This diurnal cycle in the smallest particles occurred in all seasons in ∼50 % of the observations, suggesting a persistent influence of new particle formation events on the number concentrations observed at the SGP site. This finding is in contrast with earlier studies that suggest new particle formation is observed primarily in the springtime at this site. The timing of peak concentrations associated with this diurnal cycle was shifted by several hours depending on the season, which was consistent with seasonal differences in insolation and boundary layer processes. Significant diurnal cycles in number concentrations were also found for particles with Dp between 140 and 800 nm, with peak concentrations occurring in the overnight hours, which were primarily associated with both nitrate and organic aerosol cycles. Weaker cyclic signals were observed for longer timescales (days to weeks) and are hypothesized to be related to the timescales of synoptic weather variability. The strongest periodic signals (3.5–5 and 7 d cycles) for these longer timescales varied depending on the season, with no cyclic signals and the lowest variability in the summer.

scholarly journals On the Tropospheric Ozone Variations in a Coastal Area of Southwestern Europe under a Mesoscale Circulation

2010 ◽  
Vol 49 (4) ◽  
pp. 748-759 ◽  
Author(s):  
J. A. Adame ◽  
E. Serrano ◽  
J. P. Bolívar ◽  
B. A. de la Morena
Keyword(s):  
Solar Radiation ◽  
Coastal Area ◽  
Surface Ozone ◽  
Land Breeze ◽  
Industrial Complex ◽  
Atmospheric Conditions ◽  
Air Masses ◽  
Solar Radiation Intensity ◽  
Synoptic Forcing ◽  
The Mean

Abstract It is well established that surface ozone levels are greatly affected by orography, solar radiation intensity, meteorological conditions, and the levels of their precursors. In this work, the authors study the sea–land breeze circulation in its relation with the behavior of ozone in a coastal area, located in southwestern Europe, with high levels of solar radiation and an important industrial complex emitting air pollutants. Hourly mean data over a 7-yr period (1999–2005) have been used in the study. Two patterns of sea–land breeze have been identified after analyzing 2298 days of measurements: a “pure” breeze (179 cases) and another one, called a “nonpure” breeze (284 cases), which is the resulting flow of the former and northwesterlies synoptic forcing. Among other results, the highest levels of surface ozone were observed under pure sea–land breeze, with hourly values up to 100 μg m−3 in the mean daily evolution. In contrast, for a nonpure breeze, the 24-h average daily value was lower than the corresponding one under a pure breeze by a factor of 1.16 and could reach 1.60 in representative real cases. These findings give evidence that the formation and accumulation of ozone are favored by the conditions under a pure sea–land breeze: that is, perpendicular wind directions toward the coastline, effective recirculation of air masses, and formation of ozone residual layers above the sea. Because these atmospheric conditions occur in other coastal regions in the world, the conclusions of this study could be extended to them.

scholarly journals Optical Properties of the Urban Aerosol Particles Obtained from Ground Based Measurements and Satellite-Based Modelling Studies

2015 ◽  
Vol 2015 ◽  
pp. 1-12 ◽  
Author(s):  
Genrik Mordas ◽  
Nina Prokopciuk ◽  
Steigvilė Byčenkienė ◽  
Jelena Andriejauskienė ◽  
Vidmantas Ulevicius
Keyword(s):  
Optical Properties ◽  
Light Scattering ◽  
Urban Environment ◽  
Size Distribution ◽  
Number Concentration ◽  
Scattering Coefficient ◽  
Dust Particles ◽  
Aerosol Size Distribution ◽  
Air Masses ◽  
The Impact

Applications of satellite remote sensing data combined with ground measurements and model simulation were applied to study aerosol optical properties as well as aerosol long-range transport under the impact of large scale circulation in the urban environment in Lithuania (Vilnius). Measurements included the light scattering coefficients at 3 wavelengths (450, 550, and 700 nm) measured with an integrating nephelometer and aerosol particle size distribution (0.5–12 μm) and number concentration (Dpa> 0.5 μm) registered by aerodynamic particle sizer. Particle number concentration and mean light scattering coefficient varied from relatively low values of 6.0 cm−3and 12.8 Mm−1associated with air masses passed over Atlantic Ocean to relatively high value of 119 cm−3and 276 Mm−1associated with South-Western air masses. Analysis shows such increase in the aerosol light scattering coefficient (276 Mm−1) during the 3rd of July 2012 was attributed to a major Sahara dust storm. Aerosol size distribution with pronounced coarse particles dominance was attributed to the presence of dust particles, while resuspended dust within the urban environment was not observed.

scholarly journals Application of absolute principal component analysis to size distribution data: identification of particle origins

2007 ◽  
Vol 7 (3) ◽  
pp. 887-897 ◽  
Author(s):  
T. W. Chan ◽  
M. Mozurkewich
Keyword(s):  
Principal Component Analysis ◽  
Size Distribution ◽  
Aerosol Particles ◽  
Principal Component ◽  
Component Analysis ◽  
Trace Gas ◽  
Rural Site ◽  
Aerosol Size Distribution ◽  
Urban Site ◽  
Distribution Data

Abstract. Absolute principal component analysis can be applied, with suitable modifications, to atmospheric aerosol size distribution measurements. This method quickly and conveniently reduces the dimensionality of a data set. The resulting representation of the data is much simpler, but preserves virtually all the information present in the original measurements. Here we demonstrate how to combine the simplified size distribution data with trace gas measurements and meteorological data to determine the origins of the measured particulate matter using absolute principal component analysis. We have applied the analysis to four different sets of field measurements that were conducted at three sites in southern Ontario. Several common factors were observed at all the sites; these were identified as photochemically produced secondary aerosol particles, regional pollutants (including accumulation mode aerosol particles), and trace gas variations associated with boundary layer dynamics. Each site also exhibited a factor associated specifically with that site: local industrial emissions in Hamilton (urban site), processed nucleation mode particles at Simcoe (polluted rural site), and transported fine particles at Egbert (downwind from Toronto).

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