Downward migration of radiocaesium in organic soils across a transect in Scotland

Following the accident at the Chernobyl nuclear power plant in 1986, radioactive materials including 137Cs were distributed over large parts of the former Soviet Union and Europe. Due to the relatively long physical half-life of 137Cs (30.1 y) measurable activity concentrations can still be observed...

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Published inJournal of environmental radioactivity Vol. 115; pp. 124 - 133
Main Authors Shand, C.A., Rosén, K., Thored, K., Wendler, R., Hillier, S.
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 01.01.2013
Elsevier
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Abstract Following the accident at the Chernobyl nuclear power plant in 1986, radioactive materials including 137Cs were distributed over large parts of the former Soviet Union and Europe. Due to the relatively long physical half-life of 137Cs (30.1 y) measurable activity concentrations can still be observed in the natural environment. We have determined the depth distribution of 137Cs from the testing of nuclear weapons in the atmosphere and Chernobyl, in eight highly-organic soils along an approximately east to west transect across the Central Highlands of Scotland. The 137Cs activity concentrations in the soil profiles, corrected for radioactive decay to May 1986, were between 2.8 and 14.4 kBq m−2. There were differences in the pattern of distribution of 137Cs in the soil profiles. The mean migration depth of 137Cs in the soil profiles was 12.2 cm with a range between 8.2 and 17.4 cm. Quantitative mineralogical analysis of the ash obtained after heating the soil to 400 °C indicated that clay minerals alone did not have a prime role in controlling the migration of 137Cs down the profile. ► In 1986 the Chernobyl accident contaminated soils across Europe with 137Cs. ► In 2008/2010 we measured 137Cs in 8 peaty soils from a transect across Scotland. ► The 137Cs activities were between 2.8 and 14.4 kBq m−2, decay corrected to 1986. ► The mean migration depths of 137Cs were between 8.2 and 17.4 cm. ► Clay minerals alone in the soils did not control the downward migration of 137Cs.
AbstractList Following the accident at the Chernobyl nuclear power plant in 1986, radioactive materials including 137Cs were distributed over large parts of the former Soviet Union and Europe. Due to the relatively long physical half-life of 137Cs (30.1 y) measurable activity concentrations can still be observed in the natural environment. We have determined the depth distribution of 137Cs from the testing of nuclear weapons in the atmosphere and Chernobyl, in eight highly-organic soils along an approximately east to west transect across the Central Highlands of Scotland. The 137Cs activity concentrations in the soil profiles, corrected for radioactive decay to May 1986, were between 2.8 and 14.4 kBq m−2. There were differences in the pattern of distribution of 137Cs in the soil profiles. The mean migration depth of 137Cs in the soil profiles was 12.2 cm with a range between 8.2 and 17.4 cm. Quantitative mineralogical analysis of the ash obtained after heating the soil to 400 °C indicated that clay minerals alone did not have a prime role in controlling the migration of 137Cs down the profile. ► In 1986 the Chernobyl accident contaminated soils across Europe with 137Cs. ► In 2008/2010 we measured 137Cs in 8 peaty soils from a transect across Scotland. ► The 137Cs activities were between 2.8 and 14.4 kBq m−2, decay corrected to 1986. ► The mean migration depths of 137Cs were between 8.2 and 17.4 cm. ► Clay minerals alone in the soils did not control the downward migration of 137Cs.
Following the accident at the Chernobyl nuclear power plant in 1986, radioactive materials including (137)Cs were distributed over large parts of the former Soviet Union and Europe. Due to the relatively long physical half-life of (137)Cs (30.1 y) measurable activity concentrations can still be observed in the natural environment. We have determined the depth distribution of (137)Cs from the testing of nuclear weapons in the atmosphere and Chernobyl, in eight highly-organic soils along an approximately east to west transect across the Central Highlands of Scotland. The (137)Cs activity concentrations in the soil profiles, corrected for radioactive decay to May 1986, were between 2.8 and 14.4 kBq m(-2). There were differences in the pattern of distribution of (137)Cs in the soil profiles. The mean migration depth of (137)Cs in the soil profiles was 12.2 cm with a range between 8.2 and 17.4 cm. Quantitative mineralogical analysis of the ash obtained after heating the soil to 400 °C indicated that clay minerals alone did not have a prime role in controlling the migration of (137)Cs down the profile.Following the accident at the Chernobyl nuclear power plant in 1986, radioactive materials including (137)Cs were distributed over large parts of the former Soviet Union and Europe. Due to the relatively long physical half-life of (137)Cs (30.1 y) measurable activity concentrations can still be observed in the natural environment. We have determined the depth distribution of (137)Cs from the testing of nuclear weapons in the atmosphere and Chernobyl, in eight highly-organic soils along an approximately east to west transect across the Central Highlands of Scotland. The (137)Cs activity concentrations in the soil profiles, corrected for radioactive decay to May 1986, were between 2.8 and 14.4 kBq m(-2). There were differences in the pattern of distribution of (137)Cs in the soil profiles. The mean migration depth of (137)Cs in the soil profiles was 12.2 cm with a range between 8.2 and 17.4 cm. Quantitative mineralogical analysis of the ash obtained after heating the soil to 400 °C indicated that clay minerals alone did not have a prime role in controlling the migration of (137)Cs down the profile.
Following the accident at the Chernobyl nuclear power plant in 1986, radioactive materials including ¹³⁷Cs were distributed over large parts of the former Soviet Union and Europe. Due to the relatively long physical half-life of ¹³⁷Cs (30.1 y) measurable activity concentrations can still be observed in the natural environment. We have determined the depth distribution of ¹³⁷Cs from the testing of nuclear weapons in the atmosphere and Chernobyl, in eight highly-organic soils along an approximately east to west transect across the Central Highlands of Scotland. The ¹³⁷Cs activity concentrations in the soil profiles, corrected for radioactive decay to May 1986, were between 2.8 and 14.4 kBq m⁻². There were differences in the pattern of distribution of ¹³⁷Cs in the soil profiles. The mean migration depth of ¹³⁷Cs in the soil profiles was 12.2 cm with a range between 8.2 and 17.4 cm. Quantitative mineralogical analysis of the ash obtained after heating the soil to 400 °C indicated that clay minerals alone did not have a prime role in controlling the migration of ¹³⁷Cs down the profile.
Following the accident at the Chernobyl nuclear power plant in 1986, radioactive materials including Cs-137 were distributed over large parts of the former Soviet Union and Europe. Due to the relatively long physical half-life of Cs-137 (30.1 y) measurable activity concentrations can still be observed in the natural environment. We have determined the depth distribution of Cs-137 from the testing of nuclear weapons in the atmosphere and Chernobyl, in eight highly-organic soils along an approximately east to west transect across the Central Highlands of Scotland. The Cs-137 activity concentrations in the soil profiles, corrected for radioactive decay to May 1986, were between 2.8 and 14.4 kBq m(-2). There were differences in the pattern of distribution of Cs-137 in the soil profiles. The mean migration depth of Cs-137 in the soil profiles was 12.2 cm with a range between 8.2 and 17.4 cm. Quantitative mineralogical analysis of the ash obtained after heating the soil to 400 degrees C indicated that clay minerals alone did not have a prime role in controlling the migration of Cs-137 down the profile. (C) 2012 Elsevier Ltd. All rights reserved.
Following the accident at the Chernobyl nuclear power plant in 1986, radioactive materials including (137)Cs were distributed over large parts of the former Soviet Union and Europe. Due to the relatively long physical half-life of (137)Cs (30.1 y) measurable activity concentrations can still be observed in the natural environment. We have determined the depth distribution of (137)Cs from the testing of nuclear weapons in the atmosphere and Chernobyl, in eight highly-organic soils along an approximately east to west transect across the Central Highlands of Scotland. The (137)Cs activity concentrations in the soil profiles, corrected for radioactive decay to May 1986, were between 2.8 and 14.4 kBq m(-2). There were differences in the pattern of distribution of (137)Cs in the soil profiles. The mean migration depth of (137)Cs in the soil profiles was 12.2 cm with a range between 8.2 and 17.4 cm. Quantitative mineralogical analysis of the ash obtained after heating the soil to 400 °C indicated that clay minerals alone did not have a prime role in controlling the migration of (137)Cs down the profile.
Following the accident at the Chernobyl nuclear power plant in 1986, radioactive materials including 137Cs were distributed over large parts of the former Soviet Union and Europe. Due to the relatively long physical half-life of 137Cs (30.1 y) measurable activity concentrations can still be observed in the natural environment. We have determined the depth distribution of 137Cs from the testing of nuclear weapons in the atmosphere and Chernobyl, in eight highly-organic soils along an approximately east to west transect across the Central Highlands of Scotland. The 137Cs activity concentrations in the soil profiles, corrected for radioactive decay to May 1986, were between 2.8 and 14.4 kBq m−2. There were differences in the pattern of distribution of 137Cs in the soil profiles. The mean migration depth of 137Cs in the soil profiles was 12.2 cm with a range between 8.2 and 17.4 cm. Quantitative mineralogical analysis of the ash obtained after heating the soil to 400 °C indicated that clay minerals alone did not have a prime role in controlling the migration of 137Cs down the profile.
Author Wendler, R.
Thored, K.
Rosén, K.
Hillier, S.
Shand, C.A.
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Keywords Clay minerals
X-ray diffraction
Chernobyl
Pollution
Radioactivity
137Cs
Cesium 137
Radioactive pollution
Pollutant behavior
Migration
Radioisotope
Soil pollution
Spatial variation
X ray diffraction
Radioactivity measurement
Nuclear weapon
Transport process
Cs
Fission reactor accidents
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Snippet Following the accident at the Chernobyl nuclear power plant in 1986, radioactive materials including 137Cs were distributed over large parts of the former...
Following the accident at the Chernobyl nuclear power plant in 1986, radioactive materials including ¹³⁷Cs were distributed over large parts of the former...
Following the accident at the Chernobyl nuclear power plant in 1986, radioactive materials including (137)Cs were distributed over large parts of the former...
Following the accident at the Chernobyl nuclear power plant in 1986, radioactive materials including Cs-137 were distributed over large parts of the former...
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SubjectTerms 137Cs
Aluminum Silicates
Aluminum Silicates - analysis
analysis
Applied sciences
Cesium Radioisotopes
Cesium Radioisotopes - analysis
Chernobyl
Chernobyl Nuclear Accident
Clay minerals
Earth sciences
Earth, ocean, space
Engineering and environment geology. Geothermics
Environmental Sciences
Environmental Sciences related to Agriculture and Land-use
Exact sciences and technology
half life
highlands
Markvetenskap
Miljö- och naturvårdsvetenskap
Miljövetenskap
nuclear power
organic soils
Pollution
Pollution sources. Measurement results
Pollution, environment geology
Radiation Monitoring
Radioactivity
Scotland
Soil
Soil - analysis
Soil and sediments pollution
soil heating
Soil Pollutants, Radioactive
Soil Pollutants, Radioactive - analysis
soil profiles
Soil Science
USSR
X-ray diffraction
Title Downward migration of radiocaesium in organic soils across a transect in Scotland
URI https://dx.doi.org/10.1016/j.jenvrad.2012.08.003
https://www.ncbi.nlm.nih.gov/pubmed/22935438
https://www.proquest.com/docview/1124757302
https://www.proquest.com/docview/1663543552
https://res.slu.se/id/publ/53445
Volume 115
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