Variation of 7Be concentration in surface air at Nagano, Japan

The concentration of ⁷Be in surface air at Nagano City has been measured during the period from August 2000 to March 2005. The average monthly concentrations of ⁷Be in surface air were in the range of 3.3–14 mBq/m³ with pronounced two peaks in spring and autumn. It took 30–40 hours to recover the ⁷Be concentrations observed before, once ⁷Be was washed out by wet precipitations. For a pronounced increase in the concentrations of ⁷Be found in winter, a low-pressure trough coming close to the Japanese Islands with high concentrations of ⁷Be is responsible under the characteristic distribution of atmospheric pressure around the Japanese Islands.     

Evolution and solar modulation of 7Be during the solar cycle 23

The modulation of ⁷Be-aerosols concentration due to solar activity during the cycle 23 is studied in the present research. For that purpose, was analyzed the differences in the long-term variation of geomagnetic and solar activity to assess the physical effects over the evolution of ⁷Be during the period 1996–2010. Furthermore, exploratory data analysis was applied to understand better the behavior of ⁷Be-aerosols in the surface atmosphere. This study shows that there is an inverse relationship among ⁷Be measured in the near ground air and solar activity. The modulation of ⁷Be-aerosols during the cycle 23 was divided in two steps. In the first stage, ascending phase, 1996–2002, the solar activity played an important role in the production rate of ⁷Be, r = ?0.75. However, during the descending phase, 2002–2009, the role of the solar activity was secondary, r = ?0.30, allowing that ⁷Be-aerosols reached the maximum concentration, 9.33 mBq m^?3 in August-09 when the solar activity was zero. Moreover, the remaining solar activity after the end of the ascending phase and the last important solar storm (December-06) caused the slowdown of ⁷Be production rate from 2001 to 2004 and the rupture of the seasonal behavior of ⁷Be in 2007, respectively. Finally, this research highlight the necessity to take into account the solar cycle phase, ascending or descending, to model studies of atmospheric process with ⁷Be as tracer since the contribution of the variables studied are so different in these stages.     

Temporal variation of 7Be fallout and its inventory in purple soil in the Three Gorges Reservoir region, China

The deposition flux of ⁷Be was measured in the range from 0.4 to 5.2 Bq m^?2 d^?1, with a mean value of 2.6 Bq m^?2 d^?1, during the period of May 31, 2009?CMay 31, 2010 in the Three Gorges Reservoir region, China. The low annual deposition flux of ⁷Be was probably due to the adsorption of ⁷Be within high altitude clouds and the Qinling-Daba Mountain??s barrier and blocking effects on the cold air during winter months. There was a seasonal trend for ⁷Be deposition, showing a spring maximum and winter minimum, which may be attributed to the seasonal folding of tropopause in spring and little rainfall amount in winter. A strong positive correlation (R ² = 0.67) between ⁷Be deposition flux and rainfall was observed. The depth distribution of ⁷Be in undisturbed purple soil profiles suggested that the nuclide was mainly distributed within the top 20.0 kg m^?2 (~1.5 cm) of soil in depth and the maximum concentration occurred at a depth of 3.0 kg m^?2 (~0.2 cm), then the concentration declined quickly and exponentially with depth. The seasonal inventories of ⁷Be in soils were consistent with the values calculated from the atmospheric fluxes, which shows a great potential for using ⁷Be as a tracer to assess soil redistribution in purple soil areas of China.     

Impact of the meteorological parameters on the behaviour of 7Be at ground level in Tetouan city,Morocco from June 2015 to February 2017

For the first time, atmospheric aerosols were collected in Tetouan city (Morocco), from June 2015 to February 2017, through which ⁷Be activity was measured. We studied data variation by time series analyses and the impact of local meteorological factors on it. ⁷Be concentrations, in mBq/m³, ranged from 1.65 to 7.79 with mean value of 4.69. ⁷Be behaviour is mainly influenced by air temperature, precipitations, relative humidity and atmospheric pressure. A prediction model was suggested and validated. This study helps understanding climatic variables impact on the environmental processes as aerosols transport and deposit, and to predict ⁷Be behaviour in Mediterranean regions like Tetouan.

     

Beryllium-7 activity at Comprehensive Nuclear-Test-Ban Treaty stations hosted by the United Kingdom

The Comprehensive Nuclear-Test-Ban Treaty (CTBT) is supported by a global network of monitoring stations that perform high-resolution gamma-spectrometry on air filter samples for the identification of radionuclides indicative of nuclear weapons tests and reactor incidents. These daily measurements have created an invaluable resource for understanding variations in natural background radioactivity, including the contribution of ⁷Be. Statistical analysis has been performed on ⁷Be data collected by CTBT stations hosted by the United Kingdom including at British Indian Ocean Territory (RN66), St Helena (RN67) and Tristan da Cunha (RN68) during 2005–2013. The results have been found to follow a lognormal distribution which implies that the ⁷Be activity is the multiplicative product of many small independent factors, such as meteorology, elevation, local station conditions, sample acquisition and analysis. This has the potential to identify discrepant measurements not attributable to the intrinsic variability of the distribution and indicative of station malfunction. Variations in ⁷Be activity have been considered on monthly, weekly and daily timescales and characterised using the geometric mean in accordance with the properties of the lognormal probability density function. Seasonal variations have been identified, with summer maxima and winter minima that are attributable to changes in mixing within the stratosphere and troposphere. Such fluctuations have been examined using the Fast Fourier Transform which may indicate variations associated with the 27 day solar cycle.     

Investigation of7Be in the Bratislava atmosphere

Near-surface air concentrations of⁷Be and its deposition rates were measured in the atmosphere in Bratislava from 1977 to 1994. Late spring and summer maxima were observed in the near-surface air concentrations on an annual basis. Using measured deposition rates and the calculated average tropospheric content of⁷Be atoms, their mean tropospheric residence time (27–48 days) was determined. An anticorrelation between the measured⁷Be concentration and the sunspot number with correlation factor of 0.55 was observed.     

7Be and 210Pb concentrations in air in Málaga (Spain)

Measurements of ⁷Be and ²¹⁰Pb in atmospheric air (1 m above the ground) have been carried out each week over one and a half year period. The method used to determine ⁷Be and ²¹⁰Pb activities is based on the total amount of radioactive aerosols filtered from the air. The activities of ⁷Be and ²¹⁰Pb were determined by a hyper-pure germanium detector using standard gamma-spectrometry. The average weekly concentrations of ⁷Be were in the range of 1.21-12.1 mBq^.m^-3 and for ²¹⁰Pb in the range of 0.8-2.4 mBq^.m^-3. The weekly variations were discussed in relation to various meteorological factors. It can be said that our results showed a prevailing influence of weekly average temperature for ⁷Be concentration and the weight of aerosols and wind speed for ²¹⁰Pb oncentrations.     

Seasonal variation and activity size distribution of <Superscript>7</Superscript>Be in ambient air

The seasonal variation of the ⁷Be activities in air and the size distribution of the ⁷Be aerosols were studied by using a continuous air sampler and a five stage cascade impactor. The mean monthly activity level of ⁷Be at the Korea Atomic Energy Research Institute (KAERI) site varied from 0.5 to 4.8 Bq·m⁻³ and revealed a seasonal variation, in which the ⁷Be activity levels were high in winter and low in summer. The mass size distribution showed a bi-modal distribution with a higher peak around 0.49 μm and a smaller peak between 3 μm and 7.2 μm. The activity median aerodynamic diameter (AMAD) decreased with increasing ambient ⁷Be concentrations. The mean residence times by using a mean growth rate of 0.004 μm·h⁻¹ were estimated to be 2.5–6.4 days. The AMAD has an increasing tendency with higher relative humidity. It seemed that the high humidity condition facilitated the growth of the aerosol, resulting in increased deposition rates of the aerosols and the low ⁷Be content in the surface air. The AMAD of the ⁷Be aerosols increased with an increasing temperature, but the temperature dependency of AMAD should be explained with geological and meteorological conditions.     

Beryllium-7 in near-surface atmospheric aerosols in mid-latitude (40°N) city Beijing, China

A high-volume air sampler and a high-resolution gamma-ray spectrometer have been used to measure the activity of ⁷Be in near-surface atmospheric aerosols at sampling frequency of 3 days week for 1 year from August 2009 to July 2010 at Beijing in the mid-latitude region of East Asia monsoon. The measurements indicate that the average concentration of ⁷Be was 8.39 ± 0.49 mBq m^?3, which was significantly higher than values reported for other cities in the East Asia monsoon region and in the world during the same period. The maximum and minimum of the weekly means of ⁷Be concentration were observed in September and May, respectively. The ⁷Be concentrations varied in accordance with the monsoon phases. Low but frequent wet precipitation may have caused lower ⁷Be observed in July when southeasterly was prevailing. Higher seasonal mean of ⁷Be concentrations in autumn could be attributed to the abnormal atmospheric circulation in autumn 2009.     

Temporal evolution of radionuclides in sludge from wastewater treatment plants

22 sludge samples were analyzed from three municipal wastewater treatment plants to assess both the occurrence and the temporal behavior of radioactivity during 8 sampling campaigns carried out over the period 2007–2009. As regards natural gamma emitters radionuclides from the natural ²³⁸U series (such as ²³⁴Th, ²¹⁴Pb, ²¹⁴Bi, ²¹⁰Pb) and the ²³²Th series (such as ²²⁸Ac, ²¹²Pb, ²¹²Bi and ²⁰⁸Tl) and other natural gamma emitters such as ⁷Be, ²¹⁰Pb_u or ⁴⁰K were measured. In the case of man-made radionuclides small amounts of ¹³⁷Cs were found, while significant amounts of ¹³¹I were detected in some samples. Correlations were found between radionuclides with the same origin. No seasonal variation for the ²³⁸U and ²³²Th series was found in the studied period but ⁷Be and ²¹⁰Pb_u showed seasonal variation that was explained by the monthly rainfall. The internal and external hazard indices were calculated and the results indicate that the radiological characteristics of the sludge do not present a significant radiological risk and make them suitable for future applications.     

Radionuclide variations in the air over Monaco

Radionuclides in aerosols and precipitation have been analyzed by IAEA-MEL in Monaco since 1987 and 1999, respectively, to identify their behavior in the atmosphere and delivery into the northwestern Mediterranean Sea. While the concentration of ⁷Be in aerosols has been affected by the stratospheric-tropospheric mixing and precipitation, the concentration of ¹³⁷Cs in aerosols has been influenced by a combination of local meteorological conditions and re-suspension of ¹³⁷Cs from soil. Higher concentrations of ⁷Be, ¹³⁷Cs, ^239,240Pu and ²⁴¹Am in precipitation occurred during spring and summer. The highest deposition rates of these radionuclides were observed in spring and autumn during periods of high precipitation. A good correlation was found between the amount of precipitation and depositional flux for ⁷Be, but not for ¹³⁷Cs, ^239,240Pu and ²⁴¹Am. This indicates that the wet process as well as the dry process seem to be important factors in determining the annual deposition for transuranic radionuclides and ¹³⁷Cs.     

Atmospheric concentrations of 7Be and 210Pb in Granada, Spain

Aerosols samples in near-surface air of Granada (Spain) were collected on a weekly basis. The seasonal ²¹⁰Pb and ⁷Be concentrations were determined during the five-year period, from October 1993 to September 1997. The elements, despite their different origin and their different distribution throughout the atmosphere, present the same seasonal variation. There was a tendency for a maximum during the summer season and a minimum during fall and/or winter. In this work, the concentration of ⁷Be and ²¹⁰Pb and meteorological data have been used in order to determine the periods of the potential radioactive pollution. This study, also, shows that the deposition of ⁷Be occurs primarily by precipitation except during the investigation periods where precipitation was scarce and irregular.This revised version was published online in November 2005 with corrections to the Cover Date.     

Beryllium-7 activity concentration in maize during the growth period

Beryllium-7 (⁷Be) activity in maize was measured in Yangling County, Shaanxi Province, on the Loess Plateau Region of China in 2007. The ⁷Be mass activity concentration in maize leaf samples was significantly greater than in maize stem, maize root and maize grain samples. The ⁷Be activity in maize leaves accounted for 78% of the total maize ⁷Be activity. The ⁷Be mass activity concentration in maize varied from 25.4 to 122.4 Bq kg⁻¹ and areal activity concentration held by maize from 1.2 to 111.5 Bq m⁻² during the growth period. The percentage of ⁷Be areal activity concentration held by maize relative to the ⁷Be areal activity concentration measured in reference soils ranged from 0.4 to 24.2% with a mean of 13.7%.     

<Superscript>7</Superscript>Be in the lower atmosphere at a mid-latitude (40°N) during the year 2009 of a particular minimum of solar activity

⁷Be activity concentrations were measured in the lower atmosphere at Thessaloniki, Northern Greece (40°38′N, 22°58′E) over the year 2009, a year of a particular minimum of solar activity. The mean annual activity concentration of ⁷Be at that year was 6.01 mBq m⁻³. The variability of ⁷Be surface concentrations related to the solar cycle appeared to be deviated about 40% between the maximum and the minimum values. A positive correlation (R = 0.97) was revealed between the activity concentrations of ⁷Be and the temperature, confirming that the increased rates of vertical transport within the troposphere, especially during the warmer months, resulted in carrying down to the surface layer air masses enriched in ⁷Be. Relatively high values of ⁷Be activity concentrations were observed by increasing of the tropopause height. A negative correlation (R = −0.65) between the ⁷Be activity concentrations and the relative humidity was due to the condensation process in the lower atmosphere which resulted in increased aerosol particle sizes with higher scavenging rates of aerosols and low activity concentrations of ⁷Be in the atmosphere. Influence of precipitation on the changes of ⁷Be activity concentrations was also observed.     

Atmospheric concentration of 210Pb and 7Be at Sarufutsu, Hokkaido, Japan

The atmospheric concentration of ²¹⁰Pb and ⁷Be was observed at Sarufutsu on the coast of the Sea of Okhotsuk in Hokkaido, Japan. Measurements were carried out during the period from February to August, 2001. The atmospheric concentrations of ²¹⁰Pb and ⁷Be ranged from 0.2 to 2.5 mBq/m³ and from 0.0 to 4.2 mBq/m³, respectively. The seasonal variation pattern of the atmospheric concentration of ²¹⁰Pb indicated that the air mass from Chinese Continent reached the coast of the Sea of Okhotsuk.     

Spatial distribution of 7Be in soils of Lower Austria after heavy rains

The ⁷Be approach in estimating the erosion rates is based on the assumption that the deposition of ⁷Be fallout associated with the erosive event is spatially uniform. The objective of the present work was to verify this assumption by assessing the influence of heavy rainfalls on the ⁷Be spatial distribution in Seibersdorf soils, Austria. Incremental and bulk soil depth profiles were collected from a flat site, undisturbed for the last 9 months prior sampling and with no evidence of erosion or deposition after the occurrence of heavy rains (>30 mm day^?1). The mean value of the ⁷Be areal activities (Bq m^?2) measured at 10 different points from the selected area was 312 Bq m^?2. This value corresponded to a total rainfall of 295 mm within the last 5 months prior sampling, considering that the highest mass activity of ⁷Be at soil surface will decay below the minimum detectable activity after 5 months’ time. The resulted coefficient of variation had a value of 19 % showing acceptable spatial variability of ⁷Be fallout connected with individual storm events on a local scale.     

Seasonal variation of 7Be deposition in Japan

Seasonal variations of ⁷Be deposition in regions throughout Japan (26°18'N-43°05'N, 127°54'E-141°27'E) were observed during the period of 1989-1995. The observation indicated that ⁷Be deposition peaked in spring all over Japan except in the inland central basin. However, spring peak was not always the annual maximum. Along the coastal side of the Japan Sea, especially around Hokuriku region, ⁷Be deposition was at its maximum in winter. In addition, September peak also was observed in some regions, which was presumably caused by high precipitation or blowing in of northern air stream. Variations were classified into 4 types according to meteorological factors and local geographical conditions: winter peak, double peaks (spring and September peaks), spring peak and non-peak. A correlation between ⁷Be deposition and precipitation was observed in winter.     

Cosmogenic 22Na, 7Be and terrestrial 137Cs, 40K radionuclides in ground level air samples collected weekly in Kraków (Poland) over years 2003–2006

A low background gamma spectrometer with an Etruscan, 2500 years old lead shield and a muon veto detector were applied to study ²²Na and ⁷Be activity concentration in ground level air aerosol samples collected weekly over the years 2003–2006 in Kraków. Each sample was formed with ca 100 000 m³ of passed air, collected with two parallel ASS-500 high volume air samplers. The results for ⁴⁰K and ¹³⁷Cs are also presented for reference and comparison. Presented frequency distributions for activity concentration and correlation between the obtained results are discussed. The activity concentration results confirmed seasonal variation of activity to be different for all the investigated radionuclides. Moreover, the seasonal variation in nucleus activity ratio was also noticed for ²²Na and ⁷Be. Cosmogenic radionuclides being mainly of stratospheric origin, are subsequently attached to fine aerosols, via which they are transported to the ground level air. The mean aerosol transport time within the troposphere was estimated as equal to 7.5 days on average, reaching even 50 days in warm seasons. Limitations of the applied model were identified.     

An improved method for determination of 7Be in mosses

We have measured ⁷Be activity in moss samples collected from in and around Mumbai, India. The use of heavily shielded Compton suppressor system is more efficient than the conventional gamma spectroscopic system for detection of ⁷Be. The ⁷Be accumulation capacities of mosses are more than other plant samples. Therefore monitoring of young moss samples by Compton suppressor system is an excellent tool for determination of atmospheric fallout of ⁷Be. A positive bias in the high altitude samples has been observed which might be due to any of the two reasons (i) higher cosmic ray flux in the high altitude or (ii) high pollution in the lower altitude area ultimately inhibits uptake of ⁷Be.     

Airborne gamma-ray emitters from Fukushima detected in New York State

An air-sampling network that operates continuously as part of New York State’s environmental surveillance program collected radionuclides emitted as a result of the Fukushima nuclear accident. Samples were collected, typically for 7 days each, by drawing ~600 m³ of air through a particulate-collecting filter followed in series by a canister containing activated charcoal. Additional air sampling was implemented at ~3-day intervals at two locations. Gamma-ray spectroscopy was used to confirm the detection of ¹³¹I, ¹³⁷Cs, ¹³⁴Cs, and ⁷Be in the particulate phase at all sites, with maximum concentrations near 1,260, 160, 160, and 5,200 μBq/m³, respectively. Gas-phase ¹³¹I, collected on activated charcoal, exhibited a maximum concentration of 3,400 μBq/m³ at the sites. Assessment of radionuclide levels in the air samples suggests that there were minimal health impacts from the airborne radionuclides as the activities contributed an insignificant amount to the annual human dose.