Radioactive fallout in Norway from atmospheric nuclear weapons tests

Historical data on radioactivity in air and precipitation samples have been collected and analysed from study sites in Norway. The purpose of the study was to investigate the correlation between air concentration, precipitation and deposition, and identify areas with high deposition. Areas with high precipitation have been compared with monitoring stations in other countries. The base line data contain measurements of total beta in air and precipitation on a daily basis for the period 1956-1982. Radioactive fallout correlated strongly with annual precipitation which varies from 280 to 4200mm per year in Norway. The deposition of 137Cs was calculated to be 3.23+/-1.20kBq/m2 per 1,000 mm precipitation for the period 1955-1975. Also, the relationship between total beta and 137Cs has been investigated, in order to estimate the age of fallout. The age of fallout in Norway ranges from 3 to 9 months during the test periods, which is considerably shorter than the global average, where the mean residence time for debris in the lower stratosphere is estimated to be 1.3 years. There is no evidence of local fallout from tests on Novaya Zemlya reaching Norwegian areas.     

137Cs budget during the period of 1960s in a small drainage basin on the Loess Plateau of China

A sediment profile with a thickness of 28.12 m in a failed reservoir in a small catchment of the Yuntaishan Gully in the Loess Plateau of China consisted of 44 flood couplets deposited during the period from 1960 to 1970 with total volume of 2.36 x 10(6)m(3). Specific sediment yields for a flood event varied from 300 t km(-2) to 14,400 t km(-2) and annual sediment yields varied from 2500 t km(-2) in 1966 to 40,000 t km(-2) in 1964 with a mean value of 12,700 t km(-2)a(-1) for the period. Average annual (137)Cs concentrations of the sediments increased from 0.92 Bq kg(-1) in 1960 to 4.82 Bq kg(-1) in 1963, then decreased to 1.53 Bq kg(-1) in 1970. The total (137)Cs activity in the reservoir sediments was 9.22 x 10(9) Bq, which accounted for 31.9% of the total (137)Cs fallout precipitation of 2.89 x 10(10) Bq within the catchment during the period. The proportion of the (137)Cs loss from the catchment to the (137)Cs fallout precipitation within the catchment in a year varied between 8.01% and 66.8%, and it was 20.9% for the peak (137)Cs deposition year of 1963 and 52.0% in 1964. By analysis of the (137)Cs budget in the catchment for the (137)Cs peak precipitation period from 1962 to 1964, the (137)Cs surface enrichment coefficient Gamma should be much less than 0.23. And for calculation of soil losses on the cultivated land in the inter-gully area by using the Mass Balance Model II, the value of Gamma should be 0.05-0.1.     

Temporal variation of 137Cs water column inventory in the North Pacific since the 1960s

The temporal variation of water column inventories of 137Cs in the North Pacific since the 1960s was examined based on the analysis of the 137Cs profiles in HAM database. 137Cs in seawater in the North Pacific have originated mainly from global fallout from atmospheric nuclear weapons tests, which occurred in the early 1960s. In the 1960s, both the meridional distribution of 137Cs inventory in the North Pacific and that of fallout on land stations showed mid-latitude maximum. The region with higher deposition at land stations, however, was more northern than the latitudes where the 137Cs inventory in the North Pacific showed a maximum. The difference of the latitude where maximum 137Cs deposition/inventory was observed reflects the difference of the geographical distribution of the precipitation amount in the Pacific and Atlantic Oceans followed by the different warm current systems in each ocean. A good positive relation between 137Cs inventory and annual precipitation amount was discovered in the ocean stations at the middle latitude in the North Pacific. The horizontal distribution of 137Cs inventories at the middle latitudes in the North Pacific is characterized as west-high and east-low in the early 1960s, which was basically controlled by the distribution of annual precipitation amount. Eastward advection, then, modified it to be less difference in 1966-1967 after the highest deposition periods in 1963-1965. In the 1970s and 1980s, increases of the 137Cs inventory at the lower latitude of 10-20 deg. N are found. Surface and subsurface southward transports are considered as the source of this increasing 137Cs inventory.     

Simulating transport of non-Chernobyl (137)Cs and (90)Sr in the North Atlantic-Arctic region

The spatial and temporal distributions of the anthropogenic radionuclides (137)Cs and (90)Sr, originating from nuclear bomb testing and the Sellafield reprocessing plants in the Irish Sea, are simulated using a global version of the Miami Isopycnic Coordinate Ocean Model (MICOM). The physical model is forced with daily atmospheric re-analysed fields for the period 1950 to present. Comparison of temporal evolution of observed and simulated concentrations of (137)Cs have been conducted for the regions east of Scotland, west of central Norway and at the entrance of the Barents Sea. It follows that the radionuclides from the Sellafield discharge reach the Barents Sea region after 4-5 years, in accordance with observations. The simulation provides a detailed distribution and evolution of the radionuclides over the integration time. For the Atlantic waters off the coast of Norway and in the southern Barents Sea, the atmospheric fallout dominates over the Sellafield release up to the mid 1960s and from the early 1990s, whereas Sellafield is the main source for the two radionuclides in the 1970s and 1980s. It is furthermore argued that model systems like the one presented here can be used for future prediction of radioactive contaminations in the Nordic Seas and the Arctic Ocean, for instance under various global warming scenarios.     

The geographic distribution of radionuclide deposition across the continental US from atmospheric nuclear testing

For the first time, calculations for the more than 3000 counties of the US have been completed that estimate the average deposition density (Bq m(-2)) of more than 40 radionuclides in fallout from atmospheric nuclear weapons tests conducted in the US (1951-1962) and 19 radionuclides from tests conducted elsewhere in the world (1952-1963). The geographic pattern of deposition across the US, as well as the amount of fallout deposited, varied significantly depending on whether the tests were conducted within or outside of the US. Fallout deposited from the Nevada Test Site (NTS) varied geographically as a result of dispersion and dilution in the atmosphere, the wind patterns following each test, and the occurrence of localized rainfall events. In general, states immediately east of the NTS received the highest deposition from tests conducted there. In contrast, the variation in deposition across the country from global fallout was less than for NTS fallout primarily reflecting variations in annual precipitation across larger regions. Hence, in the eastern and mid-western US, where rainfall is above the national average, higher levels of global fallout were deposited than in the more arid southwestern states. This paper presents a summary of the methods used and findings of our studies on fallout from NTS and global fallout, with emphasis on two of the most important radionuclides, (131)I and (137)Cs.     

Runoff variation affected by precipitation change and human activity in Hailiutu River basin,China

For recent years, runoff generation and hydrological processes in Hailiutu River basin have been greatly changed by climate change and human activity, especially water and soil conservation construction. In this study, the trends in precipitation, evapotranspiration (ET) and river runoff as well as the effects of precipitation change and human activity on runoff variation have been studied. The results showed that during 1960–2000, annual precipitation and river runoff, monthly precipitation and ET in September and October as well as monthly runoff in all months showed a significant decrease. In addition, peak flow and base flow had a large decrease. Under the joint influence of precipitation change and human activity, the mean annual runoff decreased by 35 million m³ from the baseline period (1960–1985) to the change period (1986–2000), which accounted for 60.9% and 39.1% of the total runoff decrease, respectively. Precipitation change played a primary role in the decrease of annual runoff whereas human activity, particularly water and soil conservation construction, also had remarkable impacts on runoff variation.     

Determination of radionuclide levels in rainwater using ion exchange resin and γ-spectrometry

The evaluation of radioactivity accidentally released into the atmosphere involves determining the radioactivity levels of rainwater samples. Rainwater scavenges atmospheric airborne radioactivity in such a way that surface contamination can be deduced from rainfall rate and rainwater radioactivity content. For this purpose, rainwater is usually collected in large surface collectors and then measured by γ-spectrometry after such treatments as evaporation or iron hydroxide precipitation. We found that collectors can be adapted to accept large surface (diameter 47 mm) cartridges containing a strongly acidic resin (Dowex AG 88) which is able to quantitatively extract radioactivity from rainwater, even during heavy rainfall. The resin can then be measured by γ-spectrometry. The detection limit is 0.1 Bq per sample of resin (80 g) for ¹³⁷Cs. Natural ⁷Be and ²¹⁰Pb can also be measured and the activity ratio of both radionuclides is comparable with those obtained through iron hydroxide precipitation and air filter measurements. Occasionally ²²Na has also been measured above the detection limit. A comparison between the evaporation method and the resin method demonstrated that 2/3 of ⁷Be can be lost during the evaporation process. The resin method is simple and highly efficient at extracting radioactivity. Because of these great advantages, we anticipate it could replace former rainwater determination methods. Moreover, it does not necessitate the transportation of large rainwater volumes to the laboratory.     

Current contamination by 137Cs and 90Sr of the inhabited part of the Techa river basin in the Urals

Previous discharges of radioactivity from the Mayak Production Association plant in the Urals have resulted in considerable radionuclide contamination of the Techa River, and consequent high radiation doses during the late 1940s and 1950s to residents of villages along the Techa river. The most contaminated villages close to the site were evacuated in the period 1954-1962. The objective of this recent study was to conduct a preliminary assessment of the current radioactive contamination of soil, vegetation and foodstuffs in the two remaining villages closest to the Mayak site, Muslyumovo and Brodokalmak. The highest contamination levels in soil were found in the floodplain at 5.5 MBq m(-2) for 137Cs and 1.0 MBq m(-2) for 90Sr. Radionuclide contamination in soil of the villages was much lower, but exceeded that expected from global fallout. Data from 1207 measurements of 137Cs in milk and 1180 for 90Sr in milk for the period 1992-1999 were collated. There was no change with time in the 90Sr or 137Cs activity concentration in milk over the measured period. There were significantly higher 137Cs activity concentrations in milk sampled during the housed winter period in Muslyumovo compared with the grazing summer period, but compared to that for Brodokalmak or for either settlement for 90Sr. The highest measured activity concentrations in food products of 137Cs and 90Sr were found in river fish, waterfowl, poultry and milk. The measured activity concentrations of 137Cs and 90Sr in some animal products were higher than that expected from soil and vegetation from fields and pasture in the villages (not including the floodplain) confirming that the highly contaminated floodplains are contributing to contamination of some animal products.     

Effects of environmental factors on the seasonal growth of <Emphasis Type="Italic">Picea abies</Emphasis> L. (Karst.) in northern Karelia

The seasonal growth of shoots, needles, and the trunk in the Norway spruce has been studied in a bilberry spruce forest in the middle taiga subzone of Karelia. The results show that the growth of vegetative organs in this tree species depends mainly on the air temperature regime, whereas the effect of variations in factors such as the period of sunshine, precipitation, and air humidity is relatively weak.     

A simple approach for collective dose estimation in assessing the consequences of atmospheric releases of radioactive material

A method is described that allows rapid and easy calculation of collective dose. Doses for inhalation of ¹³¹I and its ingestion with milk for the Windscale accident of 1957 are calculated as an example. They show good agreement with values obtained in a more detailed analysis. The method should provide reliable estimates when activity is evenly dispersed or when population and land use are fairly evenly distributed. In other circumstances, useful upper and lower limits of collective dose can be readily estimated.     

Influence of spruce and pine on the acidity and composition of atmospheric fallout in north taiga forests of an industrially developed region

The ideas concerning the spatial and temporal variation of acidity and composition of atmospheric fallout in forests of the boreal zone are discussed. The role played by the atmospheric component in the functioning of these forests depends on the acidity and composition of fallout and the extent of their transformation by the biocenosis. The most profound transformation of fallout occurs during the growing season. In spaces between crowns, the corresponding changes are atmogenic; in undercrown areas, they are obviously biogenic (autogenic). Spruce transforms the fallout more intensively than pine. Under conditions of industrial pollution, the atmobiogenic character of fallout is supplemented with a technogenic component, as its acidity and concentration of pollutants and other elements sharply increase. Concentrations of principal cations reach high values because of their leaching from the crown by acid precipitation. The traditional concept of atmospheric load on boreal forests should be reconsidered taking into account their spatial structure.     

Increased environmental gamma-ray dose rate during precipitation: a strong correlation with contributing air mass

It has long been observed that the environmental gamma-ray dose rate increases noticeably during precipitation intervals. This increase, due to the presence of radon progeny in the rain droplets (or snow flakes), can affect the reliability of the monitoring of artificial radioactivity and long term estimates of exposure to ambient natural radionuclides in surveillance network. Predicting the amplitude of the dose increase has been shown to be surprisingly challenging. In this work, standard air mass back trajectory analysis is used to show that the amplitude of the increase can be quantitatively linked to the history of the air mass where the precipitation is occurring. Furthermore, we show how back trajectory analysis, environmental gamma and rain data can be used to obtain estimations of relative radon emanation rates for locations far from the actual point of detection.     

Monitoring of radiation and radioactivity in the environment

This report lists the programs for monitoring radiation and radioactivity in the environment that are known to be in operation or to have been in operation recently. It is intended as a guide to be used when seeking information on the programs of other institutions. Sources of the data have been the literature and personal correspondence and discussions.The programs are divided into the categories of weapons test fallout, natural activity and environmental monitoring of releases from specific facilities. Where possible, the types of measurements being made are also listed. While the data are as up to date as possible the field is changing rapidly and there may be ommissions.     

Monitoring iodine-129 in air and milk samples collected near the Hanford Site: an investigation of historical iodine monitoring data

While other research has reported on the concentrations of (129)I in the environment surrounding active nuclear fuel reprocessing facilities, there is a shortage of information regarding how the concentrations change once facilities close. At the Hanford Site, the Plutonium-Uranium Extraction (PUREX) chemical separation plant was operating between 1983 and 1990, during which time (129)I concentrations in air and milk were measured. After the cessation of chemical processing, plant emissions decreased 2.5 orders of magnitude over an 8-year period. An evaluation of (129)I and (127)I concentration data in air and milk spanning the PUREX operation and post-closure period was conducted to compare the changes in environmental levels. Measured concentrations over the monitoring period were below the levels that could result in a potential annual human dose greater than 1 mSv. There was a measurable difference in the measured air concentrations of (129)I at different distances from the source, indicating a distinct Hanford fingerprint. Correlations between stack emissions of (129)I and concentrations in air and milk indicate that atmospheric emissions were the major source of (129)I measured in environmental samples. The measured concentrations during PUREX operations were similar to observations made around a fuel reprocessing plant in Germany. After the PUREX Plant stopped operating, (129)I concentration measurements made upwind of Hanford were similar to the results from Seville, Spain.     

Distribution of some natural gamma-emitting radionuclides in the soils of the coastal areas of Nigeria

Studies on the radiation level and the radionuclide distribution of some naturally occurring radioactive materials (NORM) in the soils of the coastal areas of Southern Nigeria were undertaken. The purpose of this study is to provide baseline data for the effective monitoring of unforeseeable radioactive fallout in these areas where a lot of oil exploration activities are going on. The radioactivity concentrations of these naturally occurring radionuclides (specifically (40)K, (238)U and (232)Th) in the soil samples were analyzed using a high-resolution, low-background, hyper-pure coaxial gamma-ray detector (EG&G ORTEC HPGe) coupled to an amplifier and multi-channel analyzer. The activity of (40)K ranges between 111.9 and 444.7 kBq kg(-1) with a median value of 283.28 kBq kg(-1); the activity of (226)Ra (a daughter of (238)U) varies from 23.24 to 43.66 kBq kg(-1) with a median value of 34.54 kBq kg(-1); and that of (232)Th ranges from 6.45 to 12.79 kBq kg(-1) with a median value of 9.17 kBq kg(-1). The mean absorbed dose rate in air due to these NORM is found to be (33.655+/-3.409) nGy h(-1). The correlation analyses showed a positive relationship between the three radionuclides in all the five coastal states.     

Comparative assessment of natural radioactivity in fallout samples from Patras and Megalopolis, Greece

Bulk deposition samples were collected simultaneously from two Greek cities, Patras and Megalopolis, with different emission sources of natural radioactivity, on a monthly basis, during a whole year. Gross beta-activity and 238U- and 232Th-activities were determined in a total of 95 samples of deposited dust. The results were statistically analyzed in order to determine the natural radioactivity levels and their variations in the above cities. No significant difference was found in deposited dust amount between the two cities, while the values of gross beta-, 238U- and 232Th-activities were about 3, 71 and 4 times higher in Megalopolis than in Patras, respectively. This was attributed to the operation of lignite power plants A and B in the vicinity of the city of Megalopolis, while natural radioactivity concentrations in Patras' fallout samples were of natural sources.     

Tritium concentrations in the atmospheric environment at Rokkasho, Japan before the final testing of the spent nuclear fuel reprocessing plant

This study aimed at obtaining background tritium concentrations in precipitation and air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Tritium concentration in monthly precipitation during fiscal years 2001-2005 had a seasonal variation pattern which was high in spring and low in summer. The tritium concentration was higher than that observed at Chiba City as a whole. The seasonal peak concentration at Rokkasho was generally higher than that at Chiba City, while the baseline concentrations of both were similar. The reason for the difference may be the effect of air mass from the Asian continent which is considered to have high tritium concentration. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH₃T) fractions, and the samples collected every 3 d-14 d during fiscal year 2005 were analyzed for these fractions. The HTO concentration as radioactivity in water correlated well with that in the precipitation samples. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH₃T concentrations. The HT and CH₃T concentrations did not have clear seasonal variation patterns. The HT concentration followed the decline previously reported by Mason and Östlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH₃T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH₄ to estimate global warming in its 2007 report. The longer environmental half-life of CH₃T suggested its supply from other sources than past nuclear weapon testing in the atmosphere.     

Precipitation scavenging of 7Be and 137Cs radionuclides in air

Atmospheric depositional fluxes of the naturally occurring 7Be of cosmogenic origin and 137Cs from fallout of the Chernobyl accident were measured over a 6-year period (January 1987-December 1992) at Thessaloniki, Greece (40 degrees 38'N, 22 degrees 58'E). Total precipitation accumulation during 1987-1992 varied between 33.7 cm and 65.2 cm, reflecting a relatively dry (precipitation-free) climate. The activity concentrations of 7Be and 137Cs in rainwater depended on the precipitation rate, being higher for low precipitation rates and lesser for high precipitation rates. 137Cs was removed by rain and snow more efficiently than 7Be. Snowfall was more efficient than rainfall in removing the radionuclides from the atmosphere. The annual bulk depositional fluxes of 7Be varied between 477 and 1133 Bq m(-2) y(-1) and this variability was attributed to the amount of precipitation and the variations of the atmospheric concentrations of 7Be. The annual bulk depositional fluxes of 137Cs showed a significant decrease over time from 1987 to 1992, resulting in a removal half-life of 1.33 years. The presence of 137Cs in air, and therefore in rainwater and snow, long after the Chernobyl accident (26 April 1986) was mainly due to the resuspension process. The normalized depositional fluxes of both radionuclides showed maximal values during the spring season where the maximum amount of precipitation occurred. The relatively high positive correlation between 7Be and 137Cs normalized depositional fluxes indicates that the scavenging process of local precipitation controlled the fluxes of both radionuclides. The dry depositional flux of 7Be was less than 9.37% of total (wet and dry) depositional flux. The fraction of dry-to-total depositional flux of 137Cs was much higher than that of 7Be, due to the resuspended soil.     

Spatial and temporal distribution of Pu in the Northwest Pacific Ocean using modern coral archives

Historical ²³⁹Pu activity concentrations and ²⁴⁰Pu/²³⁹Pu atom ratios were determined in skeletons of dated modern corals collected from three locations (Chuuk Lagoon, Ishigaki Island and Iki Island) to identify spatial and temporal variations in Pu inputs to the Northwest Pacific Ocean. The main Pu source in the Northwest Pacific is fallout from atmospheric nuclear weapons testing which consists of global fallout and close-in fallout from the former US Pacific Proving Grounds (PPG) in the Marshall Islands. PPG close-in fallout dominated the Pu input in the 1950s, as was observed with higher ²⁴⁰Pu/²³⁹Pu atom ratios (> 0.30) at the Ishigaki site. Specific fallout Pu contamination from the Nagasaki atomic bomb and the Ivy Mike thermonuclear detonation at the PPG were identified at Ishigaki Island from the ²⁴⁰Pu/²³⁹Pu atom ratios of 0.07 and 0.46, respectively. During the 1960s and 1970s, global fallout was the major Pu source to the Northwest Pacific with over 60% contribution to the total Pu. After the cessation of the atmospheric nuclear tests, the PPG again dominated the Pu input due to the continuous transport of remobilised Pu from the Marshall Islands along the North Equatorial Current and the subsequent Kuroshio Current. The Pu contributions from the PPG in recent coral bands (1984 onwards) varied over time with average estimated PPG contributions between 54% and 72% depending on location.     

Dynamic model for radionuclide uptake in lichen

Samples of atmospheric particulate material and terrestrial plants, including lichens, were collected in New Brunswick, Canada between 1980 and 1983 and analyzed for a wide range of artificial and naturally-occuring radionuclides, including fission products (¹⁴¹Ce, ¹⁴⁴Ce, ¹⁰³Ru, ¹⁰⁶Ru, ⁹⁵Zr and ¹³⁷Cs) derived from the 16 October 1980 Chinese nuclear test. Activity ratios of some of the short-lived fission products in air particulates and lichens are in reasonable agreement with those predicted from fission product yields for nuclear weapons tests, indicating that only minor fractionation occurred for these radionuclides during their transport through air particulate and lichen environmental phases. The ⁷Be inventories measured in a suite of lichen (Cladonia rangiferina) samples were used to calibrate each lichen plant for its collection efficiency for atmospheric particulates and fallout radioactivity.A lichen model has been developed to predict lichen inventories of radioactivity for different lichen growth functions and bio-elimination rates. Assuming that lichen growth results in a linear increase in surface area with time, the experimental results yield biological residence times of 1–2 years for ²¹⁰Pb and Pu and 5–8 years for ¹³⁷Cs. The more efficient retention of ¹³⁷Cs is probably due to its physiological uptake in lichen plants as a proxy for potassium, as evidenced by an observed, inverse relationship between ¹³⁷Cs and ⁴⁰K activities in lichen.