scholarly journals Activity size distribution of radioactive nuclide 7Be at different locations and under different meteorological conditions

2019 ◽  
Vol 212 ◽  
pp. 272-280 ◽  
Author(s):  
A. Ioannidou ◽  
K. Eleftheriadis ◽  
M. Gini ◽  
L. Gini ◽  
S. Manenti ◽  
...  
2019 ◽  
Vol 24 ◽  
pp. 97
Author(s):  
A. Ioannidou ◽  
F. Groppi ◽  
M. L. Bonardi ◽  
S. Manenti ◽  
L. Gini

The activity size distributions of the natural radionuclide tracer 7Be in different size fractions (<0.4 μm, 0.4-0.7 μm, 0.7-1.1 μm, 1.1-2.1 μm, 2.1-3.1 μm, 3.1-4.2 μm, 4.2-5.8 μm, 5.8-9.0 μm >9.0 μm) were determined at different site places in Northern Italy. Samplings were carried out during the four different seasons of the year 2011. The aim of this work was to define any differences due to the different environments and different meteorological conditions and clarify the main parameters influencing the activity size distribution of radioactive aerosols.


2015 ◽  
Vol 15 (12) ◽  
pp. 16273-16323 ◽  
Author(s):  
R. H. Mason ◽  
M. Si ◽  
J. Li ◽  
C. Chou ◽  
R. Dickie ◽  
...  

Abstract. Information on what aerosol particle types are the major sources of ice nucleating particles (INPs) in the atmosphere is needed for climate predictions. To determine which aerosol particles are the major sources of immersion-mode INPs at a coastal site in Western Canada, we investigated correlations between INP number concentrations and both concentrations of different atmospheric particles and meteorological conditions. We show that INP number concentrations are strongly correlated with the number concentrations of fluorescent bioparticles between −15 and −25 °C, and that the size distribution of INPs is most consistent with the size distribution of fluorescent bioparticles. We conclude that biological particles were likely the major source of ice nuclei at freezing temperatures between −15 and −25 °C at this site for the time period studied. At −30 °C, INP number concentrations are also well correlated with number concentrations of the total aerosol particles ≥ 0.5 μm, suggesting that non-biological particles may have an important contribution to the population of INPs active at this temperature. As we found that black carbon particles were unlikely to be a major source of ice nuclei during this study, these non-biological INPs may include mineral dust. Furthermore, correlations involving tracers of marine aerosols and marine biological activity indicate that the majority of INPs measured at the coastal site likely originated from terrestrial rather than marine sources. Finally, six existing empirical parameterizations of ice nucleation were tested to determine if they accurately predict the measured INP number concentrations. We found that none of the parameterizations selected are capable of predicting INP number concentrations with high accuracy over the entire temperature range investigated.


Chemosphere ◽  
2008 ◽  
Vol 72 (3) ◽  
pp. 496-503 ◽  
Author(s):  
St. Pateraki ◽  
Th. Maggos ◽  
J. Michopoulos ◽  
H.A. Flocas ◽  
D.N. Asimakopoulos ◽  
...  

2015 ◽  
Vol 15 (21) ◽  
pp. 12547-12566 ◽  
Author(s):  
R. H. Mason ◽  
M. Si ◽  
J. Li ◽  
C. Chou ◽  
R. Dickie ◽  
...  

Abstract. Information on what aerosol particle types are the major sources of ice nucleating particles (INPs) in the atmosphere is needed for climate predictions. To determine which aerosol particles are the major sources of immersion-mode INPs at a coastal site in Western Canada, we investigated correlations between INP number concentrations and both concentrations of different atmospheric particles and meteorological conditions. We show that INP number concentrations are strongly correlated with the number concentrations of fluorescent bioparticles between −15 and −25 °C, and that the size distribution of INPs is most consistent with the size distribution of fluorescent bioparticles. We conclude that biological particles were likely the major source of ice nuclei at freezing temperatures between −15 and −25 °C at this site for the time period studied. At −30 °C, INP number concentrations are also well correlated with number concentrations of the total aerosol particles ≥ 0.5 μm, suggesting that non-biological particles may have an important contribution to the population of INPs active at this temperature. As we found that black carbon particles were unlikely to be a major source of ice nuclei during this study, these non-biological INPs may include mineral dust. Furthermore, correlations involving chemical tracers of marine aerosols and marine biological activity, sodium and methanesulfonic acid, indicate that the majority of INPs measured at the coastal site likely originated from terrestrial rather than marine sources. Finally, six existing empirical parameterizations of ice nucleation were tested to determine if they accurately predict the measured INP number concentrations. We found that none of the parameterizations selected are capable of predicting INP number concentrations with high accuracy over the entire temperature range investigated. This finding illustrates that additional measurements are needed to improve parameterizations of INPs and their subsequent climatic impacts.


2012 ◽  
Vol 12 (11) ◽  
pp. 29967-30019 ◽  
Author(s):  
P. Tunved ◽  
J. Ström ◽  
R. Krejci

Abstract. In this study we present a qualitative and quantitative assessment of more the 10 yr of aerosol number size distribution data observed in the Arctic environment (Mt Zeppelin (78°56' N, 11°53' E, 474 m a.s.l.), Ny Ålesund, Svalbard). We provide statistics on both seasonal and diurnal characteristics of the aerosol observations and conclude that the Arctic aerosol number size distribution and auxiliary parameters such as integral mass and surface have a very pronounced seasonal variation. This seasonal variation seems to be controlled by both dominating source as well as meteorological conditions in general. In principle, three distinctly different periods can be identified during the Arctic year: the haze period characterized by a dominating accumulation mode aerosol (March–May) followed by the sunlit summer period with low abundance of accumulation mode particles but high concentration of small particles which likely are recently and locally formed (June–August). The rest of the year is characterized by comparably low concentration of accumulation mode particles and negligible abundance of ultra fine particles (September–February). Minimum aerosol mass and number concentration is usually observed during September/October. We further show that the transition between the different regimes is fast, suggesting rapid change in conditions defining their appearance. A source climatology based on trajectory analysis is provided and it is shown that there is a strong seasonality of dominating source areas, with dominance of Eurasia during the autumn-winter period and dominance of North Atlantic air during the summer months. We also show that new particle formation events seem to be a rather common phenomenon during the Arctic summer, and this is the result of both photochemical production of nucleating/condensing species and low condensation sink. It is also suggested that wet removal play a key role in defining the Arctic aerosol year, and plays a crucial role for removal of accumulation mode size particles as well as it may play a pivotal role for facilitating the conditions favoring new particle formation events. In summary the aerosol Arctic year seems to be at least qualitatively predictable based on knowledge of seasonality of transport paths and associated source areas, meteorological conditions and removal processes.


2013 ◽  
Vol 13 (7) ◽  
pp. 3643-3660 ◽  
Author(s):  
P. Tunved ◽  
J. Ström ◽  
R. Krejci

Abstract. In this study we present a qualitative and quantitative assessment of more than 10 yr of aerosol number size distribution data observed in the Arctic environment (Mt. Zeppelin (78°56' N, 11°53' E, 474 m a.s.l.), Ny Ålesund, Svalbard). We provide statistics on both seasonal and diurnal characteristics of the aerosol observations and conclude that the Arctic aerosol number size distribution and related parameters such as integral mass and surface area exhibit a very pronounced seasonal variation. This seasonal variation seems to be controlled by both dominating source as well as meteorological conditions. Three distinctly different periods can be identified during the Arctic year: the haze period characterized by a dominating accumulation mode aerosol (March–May), followed by the sunlit summer period with low abundance of accumulation mode particles but high concentration of small particles which are likely to be recently and locally formed (June–August). The rest of the year is characterized by a comparably low concentration of accumulation mode particles and negligible abundance of ultrafine particles (September–February). A minimum in aerosol mass and number concentration is usually observed during September/October. We further show that the transition between the different regimes is fast, suggesting rapid change in the conditions defining their appearance. A source climatology based on trajectory analysis is provided, and it is shown that there is a strong seasonality of dominating source areas, with Eurasia dominating during the Autumn–Winter period and dominance of North Atlantic air during the summer months. We also show that new-particle formation events are rather common phenomena in the Arctic during summer, and this is the result of photochemical production of nucleating/condensing species in combination with low condensation sink. It is also suggested that wet removal may play a key role in defining the Arctic aerosol year, via the removal of accumulation mode size particles, which in turn have a pivotal role in facilitating the conditions favorable for new-particle formation events. In summary the aerosol Arctic year seems to be at least qualitatively predictable based on the knowledge of seasonality of transport paths and associated source areas, meteorological conditions and removal processes.


2018 ◽  
Vol 18 (12) ◽  
pp. 8667-8688 ◽  
Author(s):  
Ayodeji Akingunola ◽  
Paul A. Makar ◽  
Junhua Zhang ◽  
Andrea Darlington ◽  
Shao-Meng Li ◽  
...  

Abstract. We evaluate four high-resolution model simulations of pollutant emissions, chemical transformation, and downwind transport for the Athabasca oil sands using the Global Environmental Multiscale – Modelling Air-quality and Chemistry (GEM-MACH) model, and compare model results with surface monitoring network and aircraft observations of multiple pollutants, for simulations spanning a time period corresponding to an aircraft measurement campaign in the summer of 2013. We have focussed here on the impact of different representations of the model's aerosol size distribution and plume-rise parameterization on model results. The use of a more finely resolved representation of the aerosol size distribution was found to have a significant impact on model performance, reducing the magnitude of the original surface PM2.5 negative biases 32 %, from −2.62 to −1.72 µg m−3. We compared model predictions of SO2, NO2, and speciated particulate matter concentrations from simulations employing the commonly used Briggs (1984) plume-rise algorithms to redistribute emissions from large stacks, with stack plume observations. As in our companion paper (Gordon et al., 2017), we found that Briggs algorithms based on estimates of atmospheric stability at the stack height resulted in under-predictions of plume rise, with 116 out of 176 test cases falling below the model : observation 1 : 2 line, 59 cases falling within a factor of 2 of the observed plume heights, and an average model plume height of 289 m compared to an average observed plume height of 822 m. We used a high-resolution meteorological model to confirm the presence of significant horizontal heterogeneity in the local meteorological conditions driving plume rise. Using these simulated meteorological conditions at the stack locations, we found that a layered buoyancy approach for estimating plume rise in stable to neutral atmospheres, coupled with the assumption of free rise in convectively unstable atmospheres, resulted in much better model performance relative to observations (124 out of 176 cases falling within a factor of 2 of the observed plume height, with 69 of these cases above and 55 of these cases below the 1 : 1 line and within a factor of 2 of observed values). This is in contrast to our companion paper, wherein this layered approach (driven by meteorological observations not co-located with the stacks) showed a relatively modest impact on predicted plume heights. Persistent issues with over-fumigation of plumes in the model were linked to a more rapid decrease in simulated temperature with increasing height than was observed. This in turn may have led to overestimates of near-surface diffusivity, resulting in excessive fumigation.


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