2011
DOI: 10.1016/j.jenvrad.2010.12.005
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Comparative trends and seasonal variation of 7Be, 210Pb and 137Cs at two altitude sites in the central part of France

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Cited by 53 publications
(18 citation statements)
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“…Hence, we also test the hypothesis of a constant aerosol profile within the ML. Moreover, other bias between the two measurements may be due to the fact that on some occasions such as during dust episodes, high concentrations of aerosols are preferentially transported at high altitudes, as evidenced in Bourcier et al (2011). In some cases, dust or sea salt aerosols may be transported above the PUY station and hence captured by the sun photometer but not detected by the PUY in situ instrumentation.…”
Section: Cloud-free Conditionsmentioning
confidence: 99%
“…Hence, we also test the hypothesis of a constant aerosol profile within the ML. Moreover, other bias between the two measurements may be due to the fact that on some occasions such as during dust episodes, high concentrations of aerosols are preferentially transported at high altitudes, as evidenced in Bourcier et al (2011). In some cases, dust or sea salt aerosols may be transported above the PUY station and hence captured by the sun photometer but not detected by the PUY in situ instrumentation.…”
Section: Cloud-free Conditionsmentioning
confidence: 99%
“…The 137 Cs is presently found mainly in soils and vegetation, and it can get back into the atmosphere by soil resuspension (Pham et al, 2011;Povinec et al, 2012a;Sýkora et al, 2012) and by biomass burning (Bourcier et al, 2010;Hirose and Povinec, 2015). Seasonal variations of the 137 Cs concentration in the atmosphere, associated with local meteorological conditions (like winds, air temperature, pressure and precipitations) were observed in post-Chernobyl period by several authors (Rosner et al, 1996;Lee et al, 2002;Pham et al, 2011;Bourcier et al, 2011;Povinec et al, 2012a). In the ground-level air, the size distribution of 137 Cs carrying aerosols from the post-Chernobyl period was found to be 0.3e1.4 mm (Lujanien e et al, 1997).…”
Section: Introductionmentioning
confidence: 98%
“…with k a being the reload rate, t representing time (days) between the last rainfall event and sampling date, and r max being a maximum dry deposition rate, which is a step function that reflects seasonal variability in the density of aerosol particles, as shown by satellite aerosol optical depth from the wet winter season to the dry summer season (NASA, 2014), and the reported 7 Be concentration in marine air masses (Bourcier et al, 2011;Al-Azmi et al, 2001). We use an r max of 50 dpm m −2 d −1 in January and February, 100 dpm m −2 d −1 in March, April, and early May, 120 dpm m −2 d −1 in late May and June (the maximum value being half of the atmospheric production rate of 240 dpm m −2 d −1 ; Nagai et al, 2000).…”
Section: Atmospheric 7 Be Inputmentioning
confidence: 99%