The seasonal variations of atmospheric 134,137Cs activity and possible host particles for their resuspension in the contaminated areas of Tsushima and Yamakiya, Fukushima, Japan
Abstract:A large quantity of radionuclides was released by the Fukushima Daiichi Nuclear Power Plant accident in March 2011, and those deposited on ground and vegetation could return to the atmosphere through resuspension processes. Although the resuspension has been proposed to occur with wind blow, biomass burning, ecosystem activities, etc., the dominant process in contaminated areas of Fukushima is not fully understood. We have examined the resuspension process of radiocesium ( 134,137 Cs) based on long-term measur… Show more
“…The 134 Cs and 137 Cs concentrations around the Tsushima area in Namie town over the sample period were reported by Kinase et al (2017) (Fig. 2).…”
Section: Previous Studies On the Seasonal Change And Size Distributiomentioning
confidence: 98%
“…Sampling were collected from 8th-26th March 2013 (winter 2013), 10th-30th August 2013 (summer 2013), 24th January-9th February 2014 (winter 2014), 11th April-4th May 2014 (spring 2014), and 26th August-16th September 2014 (summer 2014). The seasons were defined as in Kajino et al (2016) and Kinase et al (2017). Size-resolved aerosol samples were also collected during several periods in 2014.…”
Section: Sampling Atmospheric Aerosolmentioning
confidence: 99%
“…Kaneyasu et al (2017) discussed that the shift in size distribution may reflect a source shift from direct emission transported as a sulfate aerosol (approximately 0.54 mm), to secondary emission from the surface area of soil particles (>2.1 mm). Kinase et al (2017) found that the back-up stage (Q7) sometimes contained coarse particles, such as pollen and soil particles, that should have been trapped in the Q1 stage. The collection efficiency would as a result then underestimate the concentrations at the Q1 stage and overestimate them at the Q7 stage.…”
Section: Previous Studies On the Seasonal Change And Size Distributiomentioning
confidence: 99%
“…Yoschenko et al (2017) estimated that, in the four years since the Fukushima accident, 74% of the radiocesium deposits were distributed in the soil and approximately 20% were distributed in the litter compartment. Kinase et al (2017) found bioaerosols on filters in the summer and autumn seasons via scanning electron microscopy (SEM), when radiocesium concentrations were high. Concentrations of water soluble organic carbon and levoglucosan were compared to the 137 Cs concentrations, but there was little correlation.…”
Section: Introductionmentioning
confidence: 99%
“…In the case of ferns, moss, fungi, and mold, it migrates to the spores. Subsequently, these become possible sources of secondary emissions (Kinase et al, 2017).…”
atmosphere. This indirect release of radionuclides is referred to as secondary emission. Secondary emissions may pose a major contamination problem and adversely affect human health over a prolonged period (Igarashi et al., 2015). Moreover, secondary emissions might extend past the contaminated area and delay the return of refugees. However, radiological emergency evaluation protocols have not included a procedure to assess the environmental impact of secondary emissions (IAEA, 2000). Potential sources of secondary emissions include the ground surface and vegetation. This arises from the aeolian transport of Japanese cedar pollen and emission of wax-like substances from plant surfaces, biomass burning (Yoschenko et al., 2006; Paatero et al., 2009), and the disposal and subsequent burning of contaminated waste from the disaster site. A number of studies (
“…The 134 Cs and 137 Cs concentrations around the Tsushima area in Namie town over the sample period were reported by Kinase et al (2017) (Fig. 2).…”
Section: Previous Studies On the Seasonal Change And Size Distributiomentioning
confidence: 98%
“…Sampling were collected from 8th-26th March 2013 (winter 2013), 10th-30th August 2013 (summer 2013), 24th January-9th February 2014 (winter 2014), 11th April-4th May 2014 (spring 2014), and 26th August-16th September 2014 (summer 2014). The seasons were defined as in Kajino et al (2016) and Kinase et al (2017). Size-resolved aerosol samples were also collected during several periods in 2014.…”
Section: Sampling Atmospheric Aerosolmentioning
confidence: 99%
“…Kaneyasu et al (2017) discussed that the shift in size distribution may reflect a source shift from direct emission transported as a sulfate aerosol (approximately 0.54 mm), to secondary emission from the surface area of soil particles (>2.1 mm). Kinase et al (2017) found that the back-up stage (Q7) sometimes contained coarse particles, such as pollen and soil particles, that should have been trapped in the Q1 stage. The collection efficiency would as a result then underestimate the concentrations at the Q1 stage and overestimate them at the Q7 stage.…”
Section: Previous Studies On the Seasonal Change And Size Distributiomentioning
confidence: 99%
“…Yoschenko et al (2017) estimated that, in the four years since the Fukushima accident, 74% of the radiocesium deposits were distributed in the soil and approximately 20% were distributed in the litter compartment. Kinase et al (2017) found bioaerosols on filters in the summer and autumn seasons via scanning electron microscopy (SEM), when radiocesium concentrations were high. Concentrations of water soluble organic carbon and levoglucosan were compared to the 137 Cs concentrations, but there was little correlation.…”
Section: Introductionmentioning
confidence: 99%
“…In the case of ferns, moss, fungi, and mold, it migrates to the spores. Subsequently, these become possible sources of secondary emissions (Kinase et al, 2017).…”
atmosphere. This indirect release of radionuclides is referred to as secondary emission. Secondary emissions may pose a major contamination problem and adversely affect human health over a prolonged period (Igarashi et al., 2015). Moreover, secondary emissions might extend past the contaminated area and delay the return of refugees. However, radiological emergency evaluation protocols have not included a procedure to assess the environmental impact of secondary emissions (IAEA, 2000). Potential sources of secondary emissions include the ground surface and vegetation. This arises from the aeolian transport of Japanese cedar pollen and emission of wax-like substances from plant surfaces, biomass burning (Yoschenko et al., 2006; Paatero et al., 2009), and the disposal and subsequent burning of contaminated waste from the disaster site. A number of studies (
We report fallout radionuclide (FRN) and major/trace element (MTE) contributions to bulk atmospheric deposition in Hanover, NH USA (43.7022°N, 72.2896°W). Deposition of 7 Be, 210 Pb and SO 4 covary [R 2 >0.4, n=461] but are discriminated by production sources, depositional mechanisms, meteorological controls, MTE associations, and seasonal biases. 7 Be is dominated by rainout (78% of total deposition), recharged by long-range transport (+23% over mean, o.m.), influenced by stratospheretroposphere-exchange (+9% o.m.) and solar activity (-2% per doubling of sunspot count). Correlation with particulate nitrogen (+9% per doubling of N) indicates 7 Be affinity for biogenic aerosols. 210 Pb is dominated by dry+washout deposition (54% of total) and convective storms (+107% o.m), is depleted in marine moisture sources (-133% o.m.), correlated with S (+9% per doubling of S) and biased to autumn with Mn, Hg, and V (+7% o.m.). Coincident long-term declines in S and 210 Pb (-14%, -4% per year) suggest co-scavenging by PbSO 4 . 7 Be: 210 Pb ratios increase asymptotically with precipitation through the dry-washoutrainout transition and recharge of 7 Be. At the global scale, 7 Be: 210 Pb increases with precipitation for North American/European sites due to recharge of 7 Be in mid-latitude storm belts [R 2 =0.64, n=31]. Conversely, 7 Be: 210 Pb is independent of precipitation for Southeast/East Asian sites where 7 Be recharge is low [R 2 =0.01, n=40]. Globally, 7 Be: 210 Pb ratios in dry deposition reflect resuspended aerosols with mean age of ca. 200 days, contributing <5% of 210 Pb deposition. Different aerosol populations contributing to FRN deposition across spatial and temporal scales should emerge as a focus in terrestrial 7 Be, 210 Pb and 10 Be tracer applications.
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