Temporal variation of 212Pb concentration in outdoor air of Milan and a comparison with 214Bi

Continuous measurement of hourly concentrations of 212Pb attached to aerosol particles was carried out during the whole year 2000 in the outdoor air of Milan (Italy). An improved experimental method based on on-line alpha spectroscopy during atmospheric particulate matter sampling allowed the contemporary determination of 212Pb and 214Bi through the deconvolution of the alpha energy spectral distribution analysis. The 212Pb hourly concentrations were about 100 times lower than 214Bi but showed a similar characteristic diurnal time trend. However, the influence of meteorological parameters such as rain and wind was more evident in 212Pb than in 214Bi concentrations. The 212Pb average annual concentration was 0.090 +/- 0.060 Bq/m3 with daily mean concentration varying from 0.013 to 0.333 Bq/m3.     

Radionuclides in hot mineral spring waters in Jordan

Hot mineral springs in Jordan are very attractive to people who seek physical healing but they are unaware of natural radioactive elements that may be contained in the hot mineral water. The activities of the natural radioactive isotopes were measured and the concentrations of the parents of their natural radioactive series were calculated. The measured radionuclides were 234Th, 226Ra, 214Pb, 214Bi, 228Ac, 228Th, 212Pb, 212Bi and 208Tl. In addition the activities of 235U and 40K were measured. The activities ranged from 0.14 to 34.8 Bq/l, while the concentrations of parent uranium and thorium isotopes ranged from 3.0 x 10(-3) to 0.59 mg/l. The results were compared with those for drinking water.     

Radon concentrations in a spa in Serbia

The paper presents the results of indoor radon concentration survey in 201 homes and offices in Niska Banja (the Spa of Nis), a well-known health resort and a spa in the South-East of Serbia. Radon indoor concentrations were determined by active charcoal method, according to standard EPA procedure. The indoor radon concentrations were in the range of up to 200 Bq/m(3) (47%), from 200-600 Bq/m(3) (26%) and over 600 Bq/m(3) (27%). Three areas of extremely high average radon concentrations were found (1,340-4,340 Bq/m(3)), with a maximum above 13,000 Bq/m(3). The content of natural radionuclides ((226)Ra, (214)Pb, (214)Bi, (235)U, (228)Ac, (212)Pb, (212)Bi, (208)Tl, (40)K) and (137)Cs, as well as the content of total uranium, thorium and potassium in mud used in peloidotherapy in the Health Institute "Niska Banja" was determined, too. The activities of the radionuclides were determined on an HPGe detector, by standard gamma spectroscopy. The results indicated considerably high amounts of total uranium and thorium (0.021 g/kg mud and 0.003 g/kg mud, respectively), due to the karsts origin of the soil.     

A combined method for evaluating radon and progeny in waters and its use at Guarani aquifer, São Paulo State, Brazil

A combined method for evaluating radon (222Rn) and progeny (214Pb and 214Bi) in water was developed by using inexpensive alpha scintillation counting and gamma ray spectrometry through NaI(Tl) scintillation detectors. A groundwater sample collected at the Po?os de Caldas alkaline massif in Brazil was submitted to the technique in order to assure its applicability by comparing the volumetric activities by different methods. Similar volumetric activity was determined for 214Pb and 214Bi in the sample analyzed that is compatible with the expected condition of radioactive equilibrium between these nuclides. The combined method was successfully used to analyze groundwater samples from Guarani aquifer in S?o Paulo State, Brazil, and the results of the measurements indicated that 214Pb and 214Bi provide useful information concerning the evaluation of the drinking water quality in terms of radiological aspects. This is because they are directly identified in the water samples, without the need of requiring the assumption of the establishment of the transient equilibrium condition with its parent 222Rn.     

Concentrations and their ratio of (222)Rn decay products in rainwater measured by gamma-ray spectrometry using a low-background Ge detector

The concentrations and the concentration ratios of individual short-lived (222)Rn decay products ((214)Pb and (214)Bi) in rainwater were measured at Kumatori village (34.39 degrees N, 135.35 degrees E, approximately 70 m above sea level) in Osaka, Japan, by gamma-ray spectrometry using a low-background Ge detector. The dependence of the time variations of the concentrations and their ratios on rainfall rate was investigated. It was observed that the concentrations were negatively correlated with the rainfall rate in some rainfall events, and that there was no clear correlation in other rainfall events. The changes in the dependence of the concentration on the rainfall rate occurred after the passage of a cold front during a single rainfall event. The concentration ratios showed a weak negative correlation with the rainfall rate for most of the observed rainfall events. A scavenging model was designed in this study in order to explain the observation results. Based on the relationship between the concentrations of (214)Pb and (214)Bi in the rainwater and the rainfall rate for an individual rainfall event, the increase in the environmental gamma-ray dose rate from (214)Pb and (214)Bi deposited on the ground was calculated, and the calculated increase agreed well with that observed by the in situ measurement on flat ground.     

Natural and anthropogenic radionuclides in airborne particulate samples collected in Barcelona (Spain)

Results for naturally occurring ⁷Be, ²¹⁰Pb, ⁴⁰K, ²¹⁴Bi, ²¹⁴Pb, ²¹²Pb, ²²⁸Ac and ²⁰⁸Tl and anthropogenic ¹³⁷Cs in airborne particulate matter in the Barcelona area during the period from January 2001 to December 2005 are presented and discussed. The ²¹²Pb and ²⁰⁸Tl, ²¹⁴Bi and ²¹⁴Pb, ⁷Be and ²¹⁰Pb radionuclide levels showed a significant correlation with each other, with correlation coefficients of 0.99, 0.78 and 0.69, respectively, suggesting similar origin/behaviour of these radionuclides in the air. Caessium-137 and Potassium-40 were transported to the air as resuspended particle from the soil. The ⁷Be and ²¹⁰Pb concentrations showed similar seasonal variations, with a tendency for maximum concentrations during the summer months. An inverse relationship was observed between the ⁷Be, ²¹⁰Pb, ⁴⁰K and ¹³⁷Cs concentrations and weekly rainfall, indicating washout of atmospheric aerosols carrying these radionuclides.     

A study on natural radiation exposure in different realistic living rooms

In the first part of the paper, the factors affecting 222Rn properties in 25 different realistic living rooms (with low ventilation rates) of different houses in El-Minia City (Upper Egypt) have been studied; they included the activity concentration of 222Rn gas (C(o)), the unattached fraction (f(p)) of 218Po and 214Pb, the unattached potential alpha energy concentration (PAEC) and the equilibrium factor (F). The activity distributions of unattached 218Po and 214Pb as well as for the PAEC were determined. With a dosimetric model calculation [ICRP, 1994b. Human Respiratory Tract Model For Radiological Protection. Pergamon Press, Oxford. ICRP Publication 66] the total deposition fraction of unattached 218Po and 214Pb in human respiratory tract was evaluated to determine the total equivalent dose. An electrostatic precipitation method and a wire screen diffusion battery technique were both employed for the determination of 222Rn gas concentration and its unattached decay products, respectively. The mean activity concentration of 222Rn gas (C(o)) was found to be 110+/-20 Bq m(-3). The mean unattached activity concentrations of 218Po and 214Pb were found to be 0.6 and 0.35 Bq m(-3), respectively. A mean unattached fraction (f(p)) of 0.09+/-0.01 was obtained at a mean aerosol particle concentration (Z) of (2.9+/-0.23) x 10(3)cm(-3). The mean equilibrium factor (F) was determined to be 0.31+/-0.02. The mean PAEC of unattached 218Po and 214Pb was found to be 8.74+/-2.1 Bq m(-3). The activity distributions of 218Po and 214Pb show mean activity median diameters (AMD) of 1.5 and 1.85 nm with mean geometric standard deviations (SD) of 1.33 and 1.45, respectively. The mean activity distribution of the PAEC shows an AMD of 1.65 nm with a geometric standard deviation of 1.25. At a total deposition fraction of about 97% the total equivalent dose to the lung was determined to be about 133 microSv. The second part of this paper deals with a study of natural radionuclide contents of samples collected from the building materials of the rooms under investigations in part one. Analyses were performed in Marinelli beakers with a gamma multichannel analyzer equipped with a NaI(Tl) detector. The samples revealed the presence of the uranium-radium and thorium radioisotopes as well as 40K. Nine gamma-lines of the natural radioisotopes corresponding to 212Pb, 214Pb, 214Bi, 228Ac, 40K and 208Tl were detected and measured. The activity concentrations of 226Ra, 232Th and 40K were determined with mean activity concentrations of 58+/-19, 31+/-11 and 143+/-62 Bq kg(-1), respectively. These activities amount to a radium equivalent (Ra(eq)) of 113 Bq kg(-1) and to a mean value of external hazard index of 0.31.     

Uranium decay products found on Mir space blanket mitt

The space blanket mitt which covered the Trek detector on Mir during four years of orbital flight has been measured for gamma radiation with HPGe and multidimensional spectrometers. Difference spectra from very-long-period spectrometer runs on the mitt and on a similar non-deployed mitt from the same manufacturer show that the mitt has acquired small but significant amounts of gamma radioactivity during orbital flight. Twelve gamma-ray peaks have been measured in the difference spectra, including peaks identified as due to 214Bi and 214Pb from the uranium-radium alpha decay series, and others possibly due to the uranium-actinium series. This implies the presence of a sparse population of uranium decay products in lower orbital space which can only have come from nuclear explosions, burned-up satellite nuclear batteries, the solar wind, or supernova fragments in the local interstellar medium.     

Assessment of natural and anthropogenic radioactivity levels in rocks and soils in the environs of Swieradow Zdroj in Sudetes, Poland, by in situ gamma-ray spectrometry

The natural radioactivity of 40K, 208Ti, 212Pb, 214Pb, 228Ac, and the fallout of 137Cs in typical rocks and soils of Swieradów Zdrój area (Sudetes Mountains, Poland) were measured in situ using a portable gamma-ray spectrometry workstation. The measurement points were chosen for different regional lithology: within hornfelses of the Szklarska Poreba schist-belt, quartz rocks, gneisses of the Swieradów Zdrój unit, leucogranites, leptinites, mica schists of the Stara Kamienica belt, and finally the zones of the southern and northern contacts of the Stara Kamienica schist-belt with leucogranites and gneisses of the Lesna unit, respectively. 40K activity varied in the range from about 320 Bq kg(-1) (quartz) to 1200 Bq kg(-1) (gneisses). The activity concentrations associated with 228Ac (232Th series) varied in the range from 25 Bq kg(-1) (quartz) to 62 Bq kg(-1) (leucogranites), whereas activity concentration of 226Ra varied in the range from about 31 Bq kg(-1) (hornfelses) to 122 Bq kg(-1) (leucogranites). Relatively low deposits of 137Cs were noted in the investigated area, where the activity concentrations ranged from 4001 (hornfelses) Bq m(-2) to less than 154 Bq m(-2) (leucogranites).     

Possible use of terrestrial mosses in detection of atmospheric deposition of 7Be over large areas

The activities of naturally occurring radionuclides (7)Be, (214)Bi and (210)Pb were measured in samples of terrestrial mosses collected in Serbia (42 degrees 26'19'N-45 degrees 23'12'N). The objective of this work was to establish if detectable amounts of (7)Be and (210)Pb can be found in mosses and investigate their possible variabilities over some area. These are the first steps in introducing mosses as a medium in possible monitoring of spatial distribution of (7)Be atmospheric deposition. The mean value of 360 Bq/kg of (7)Be activity was found in collected moss samples and some nonuniformity in spatial distribution (a 2.8-fold range in measured values) was observed.     

Natural radioactivity measurements in building materials in Southern Lebanon

Using gamma-spectroscopy and CR-39 detector, concentration C of naturally occurring radioactive nuclides (226)Ra, (222)Rn, (214)Bi, (228)Ac, (212)Pb, (212)Bi and (40)K, has been measured in sand, cement, gravel, gypsum, and paint, which are used as building materials in Lebanon. Sand samples were collected from 10 different sandbank locations in the southern part of the country. Gravel samples of different types and forms were collected from several quarries. White and gray cement fabricated by Shaka Co. were obtained. gamma-spectroscopy measurements in sand gave Ra concentration ranging from 4.2+/-0.4 to 60.8+/-2.2 Bq kg(-1) and Ra concentration equivalents from 8.8+/-1.0 to 74.3+/-9.2 Bq kg(-1). The highest Ra concentration was in gray and white cement having the values 73.2+/-3.0 and 76.3+/-3.0 Bq kg(-1), respectively. Gravel results showed Ra concentration between 20.2+/-1.0 and 31.7+/-1.4 Bq kg(-1) with an average of 27.5+/-1.3 Bq kg(-1). Radon concentration in paint was determined by CR-39 detector. In sand, the average (222)Rn concentration ranged between 291+/-69 and 1774+/-339 Bq m(-3) among the sandbanks with a total average value of 704+/-139 Bq m(-3). For gravel, the range was found to be from 52+/-9 to 3077+/-370 Bq m(-3) with an average value of 608+/-85 Bq m(-3). Aerial and mass exhalation rates of (222)Rn were also calculated and found to be between 44+/-7 and 2226+/-267 mBq m(-2)h(-1), and between 0.40+/-0.07 and 20.0+/-0.3 mBq kg(-1)h(-1), respectively.     

Air-to-vegetation transfer rates of natural submicron aerosols

Submicron aerosol deposition to outdoor vegetation was evaluated by measuring vegetation and air concentrations of ²¹²Pb, ²¹⁴Pb, and ⁷Be attached to atmospheric aerosols. A biomass-normalized deposition velocity (V_D), with units of m³ kg^?1 s^?1, was used to compare species and isotopes with respect to air-to-vegetation transfer rates. For ²¹²Pb ($\text{t}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 10·64 h}$), higher night-time air concebtrations dominate deposition, while for ²¹⁴Pb ($\text{t}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 26·8}\text{min}$), deposition measurements over shorter time periods relative to changing atmospheric conditions were possible. Calculated V_D values were usually higher for ²¹⁴Pb, possibly reflecting wind-enhanced deposition during the afternoon period of sampling. Evergreen species, including pines, were not appreciably different from deciduous species. Most striking was the narrow range of results (factor of 6 for 34 ²¹²Pb measurements of 20 species). Beryllium-7 ($\text{t}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{= 53·3 d}$) was used to evaluate time-integrated deposition by sampling vegetation in California near the end of dry summers. Similar deposition rates were found for this isotope. The results of the study indicated that naturally radioactive atmospheric aerosols can be used to understand the dynamics of submicron aerosol deposition to ecosystems.     

Elevated concentrations of primordial radionuclides in sediments from the Reedy River and surrounding creeks in Simpsonville, South Carolina

A gamma-ray survey and analysis of 16 riverbed samples from the Reedy River watershed near Simpsonville, SC were conducted and compared with national and international studies of primordial radionuclides. The study reported here follows on a recent discovery of anomalously high uranium concentrations in several private well waters in the area. An HPGe spectrometer was used for quantification of gamma emitting radionuclides in the sediments. All sediments contained radionuclides from the uranium and thorium series as well as (40)K. Uranium-238 concentrations in sediment samples ranged from 11.1 to 74.2Bqkg(-1). The measured radionuclide concentrations were compared with data from UNSCEAR and NURE reports. The river and stream sediment data were augmented by in situ NaI(Tl) gamma-ray spectrometer measurements. Comparisons between the ex situ and in situ measurements indicate equivalently distributed uranium in the surface soils and stream sediments, the source of which is likely attributed to the monazite belts that are known to exist in the area.     

Effects of readily dispersible colloid on adsorption and transport of Zn, Cu, and Pb in soils

Soil colloids (<0.002 mm) were extracted from three types of soils to make the colloid-bound forms of Zn, Cu, and Pb solution. The clay mineral types and composition of the colloids, the adsorption characteristics of the colloids, and the effect of readily dispersible colloid on the transport of metals and the quality of the soils and groundwater were studied. The results showed that the adsorption capacity of Cu, Zn, and Pb was greater for the Aquic Vertisols (Shajiang Black soil) as compared to the Udic Luvisols (Brown soil) and Usdic Luvisols (Cinnamon soil), due to the difference of clay content and clay mineral composition in the different soils. The adsorption capacity of Pb was much higher than that of Zn and Cu for the same soils, which would contribute to the chemical properties of metals and specific adsorption characters of the colloids. The mobility of Zn in soils was greater than that of Cu and Pb, while similar trend was found in the transportation processes for Zn and Cu. The concentration of Zn and Cu in leachates increased as the leaching solution volume increased, but the migration of Pb was negligible, and the concentration of Pb could not been detected in leachates even after 7.5 pore volume leaching solution. The influence of mobility on Zn and Cu transport was different for different type of colloids. The mobility caused by readily dispersible colloids from Aquic Vertisols was greater as compared to that of Udic Luvisols and Usdic Luvisols. Analysis of soils after column leaching indicated that Zn was distributed much deeper than Cu, but Pb was almost not migrated, and mainly accumulated in the soil surface. Therefore, Zn had greater tendency for the groundwater pollution than Cu and Pb, and Pb tends to contaminate the surface soils.     

Transfer of metals from soil to vegetables in an area near a smelter in Nanning, China

A field survey was conducted to investigate the metal contamination in soils and vegetables, and to evaluate the possible health risks to local population through foodchain transfer near a smelter in Nanning, southern China. Contamination levels in soils and vegetables with cadmium (Cd), lead (Pb), zinc (Zn) and copper (Cu) were measured, and transfer factors (TF) from soils to vegetable plants and its health risk (risk index, RI) were calculated accordingly. Results showed that both soils and vegetables from villages 1 and 2 (V1 and V2, 1500 m and 500 m from the smelter) were heavily contaminated, compared to a village 50 km from the smelter. Geometric mean of Cd and Pb concentrations in vegetables for V1 and V2, respectively, were 0.15 and 0.24 mg Cd kg(-1) and 0.45 and 0.38 mg Pb kg(-1) (on fresh weight basis). Oral intake of Cd and Pb through vegetables poses high health risk to local residents. Risk indices for V1 and V2, respectively, were 3.87 and 7.42 for Cd, and 1.44 and 13.5 for Pb. The complexity of metal contamination and their health risks are also discussed.     

Calibration of a portable HPGe detector using MCNP code for the determination of 137Cs in soils

In situ gamma spectrometry provides a fast method to determine (137)Cs inventories in soils. To improve the accuracy of the estimates, one can use not only the information on the photopeak count rates but also on the peak to forward-scatter ratios. Before applying this procedure to field measurements, a calibration including several experimental simulations must be carried out in the laboratory. In this paper it is shown that Monte Carlo methods are a valuable tool to minimize the number of experimental measurements needed for the calibration.     

Seasonal variations of aerosol residence time in the lower atmospheric boundary layer

During a one year period, from Jan. 2002 up to Dec. 2002, approximately 130 air samples were analyzed to determine the atmospheric air activity concentrations of short- and long-lived (222Rn) decay products 214Pb and 210Pb. The samples were taken by using a single-filter technique and gamma-spectrometry was applied to determine the activity concentrations. A seasonal fluctuation in the concentration of 214Pb and 210Pb in surface air was observed. The activity concentrations of both radionuclides were observed to be relatively higher during the winter/autumn season than in spring/summer season. The mean activity concentration of 214Pb and 210Pb within the whole year was found to be 1.4+/-0.27 Bq m(-3) and 1.2+/-0.15 mBq m(-3), respectively. Different 210Pb:214Pb activity ratios during the year varied between 1.78 x 10(-4) and 1.6 x 10(-3) with a mean value of 8.9 x 10(-4) +/- 7.6 x 10(-5). From the ratio between the activity concentrations of the radon decay products 214Pb and 210Pb a mean residence time (MRT) of aerosol particles in the atmosphere of about 10.5+/-0.91 d could be estimated. The seasonal variation pattern shows relatively higher values of MRT in spring/summer season than in winter/autumn season. The MRT data together with relative humidity (RH), air temperature (T) and wind speed (WS), were used for a comprehensive regression analysis of its seasonal variation in the atmospheric air.     

Pre-concentration of naturally occurring radionuclides and the determination of (212)Pb from fresh waters

A novel technique has been developed for determining the ²¹²Pb activity of fresh waters. This is of interest to environmental monitoring programmes that utilise gross α-activity methods to screen for anthropogenic radionuclides. The contribution from ²¹²Pb varies, and is difficult to experimentally measure due to its relatively short half-life (t_½ = 10.6 h) and low environmental activity (<0.1 Bq l⁻¹). The use of a three-stage technique that encompasses a unique form of pre-concentration, separation and analysis by liquid scintillation counting allows a lower detection limit of 0.006 Bq l⁻¹ with a chemical yield of 92.5 ± 5.6%. The measurement can be obtained within 7 h of sample collection, and is calculated using the radioactive decay of ²¹²Bi. Other naturally occurring radionuclides may also be extracted using the pre-concentration stage of the technique, with efficiencies above 90% at a range of pH values.     

Seasonal variation of 210Pb activity concentration in outdoor air of Milan (Italy)

Weekly measurements of 210Pb activity concentration on aerosol particles were performed at ground level in outdoor air in Milan (Italy) during the years 2000-2001. The experimental method was based on the delayed alpha spectrometry of in-grown 210Po activity detected on airborne particles collected on a filter support. On the same filter the 214Pb activity concentration was also measured during the sampling. 210Pb weekly concentration values showed a great variability and the average monthly values exhibited a seasonal pattern characterised by maxima in winter and minima in spring-summer. The same seasonal trend was also observed in 214Pb concentration values. 210Pb average yearly values were 0.70 and 0.82 mBq/m3 in 2000 and 2001, respectively, in good agreement with literature data registered at continental sites of similar latitude and longitude. The activity ratio 210Pb/214Pb was used to evaluate the residence time of fine aerosols in the urban air of Milan, which was 1-2 days.     

Inventories of fallout 210Pb and 137Cs radionuclides in moorland and woodland soils around Edinburgh urban area (UK)

Inventories of fallout (210)Pb and (137)Cs have been measured in moorland and woodland soils around the Edinburgh urban area, using a high purity germanium detector. The (210)Pb inventories in moorland soils were relatively uniform, with a mean value of 2520+/-270Bqm(-2). The mean (137)Cs inventory in moorland soils varied greatly from 1310 to 2100Bqm(-2), with a mean value of 1580+/-310Bqm(-2). The variability was ascribed mainly to the non-uniform distribution of fallout Chernobyl (137)Cs. The mean (210)Pb and (137)Cs inventories in woodland canopy soils were found to be 3630+/-380Bqm(-2) and 2510+/-510Bqm(-2), respectively. At sites for which both moorland and woodland data were available, the mean inventories provided fairly similar average enhancements of (47+/-7)% and (46+/-18)% of (210)Pb and (137)Cs under woodland canopy soils relative to open grassland soils, respectively. The enhancement factors are broadly in line with other independent findings in literature. Enhancement of both (210)Pb and (137)Cs in woodland soils relative to moorland soils is, in part, due to deposition by impaction during air turbulence, wash-off, gravitational settling and deposition during leaf senescence. Results of this study suggest that these processes affect both (210)Pb and (137)Cs carrier aerosols in a similar way.