MEASUREMENT OF URANIUM IN URINE, HAIR AND NAILS IN SUBJECTS OF NISKA BANJA TOWN, A HIGH NATURAL BACKGROUND RADIATION AREA OF SERBIA.

Urine, hair and nail samples were collected from a population of both sex aged from 40 to 87 years in Niska Banja (227 km south of Belgrade, Serbia) with a high level of natural radioactivity (HLNRA). To assess and monitor the public exposure, urine samples for each subject (24 h period) were collected and concentration of uranium (U) was analysed using alpha-particle spectrometry. Human hair and nails considered as bio-indicators of the public exposure to radionuclides over a long period of months or even years and concentration of U was determined using inductively coupled plasma-mass spectrometry. The mean concentrations of U in urine, hair and nail were 123 ng/L, 17 ng/g and 8 ng/g, respectively. There was a large variation and may be due to geological origin.

Distribution of uranium, thorium and some stable trace and toxic elements in human hair and nails in Niska Banja Town, a high natural background radiation area of Serbia (Balkan Region, South-East Europe).

Human hair and nails can be considered as bio-indicators of the public exposure to certain natural radionuclides and other toxic metals over a long period of months or even years. The level of elements in hair and nails usually reflect their levels in other tissues of body. Niska Banja, a spa town located in southern Serbia, with locally high natural background radiation was selected for the study. To assess public exposure to the trace elements, hair and nail samples were collected and analyzed. The concentrations of uranium, thorium and some trace and toxic elements (Mn, Ni, Cu, Sr, Cd, and Cs) were determined using inductively coupled plasma mass spectrometry (ICP-MS). U and Th concentrations in hair varied from 0.0002 to 0.0771 µg/g and from 0.0002 to 0.0276 µg/g, respectively. The concentrations in nails varied from 0.0025 to 0.0447 µg/g and from 0.0023 to 0.0564 µg/g for U and Th, respectively. We found significant correlations between some elements in hair and nails. Also indications of spatial clustering of high values could be found. However, this phenomenon as well as the large variations in concentrations of heavy metals in hair and nail could not be explained. As hypotheses, we propose possible exposure pathways which may explain the findings, but the current data does not allow testing them.

High variability of indoor radon concentrations in uraniferous bedrock areas in the Balkan region.

In this work the strong influence of geological factors on the variability of indoor radon is found in two of three geologically very different regions of South-Eastern Europe. A method to estimate the annual mean concentration when one seasonal measurement is missing is proposed. Large differences of radon concentrations in different rooms of the same house and significant difference in radon concentrations in one season comparing it to the others are noted in certain cases. Geological factors that can lead to such behavior are discussed.

Distribution of uranium and some selected trace metals in human scalp hair from Balkans.

The possible consequences of the use of depleted uranium (DU) used in Balkan conflicts in 1995 and 1999 for the people and the environment of this reason need attention. The heavy metal content in human hair may serve as a good indicator of dietary, environmental and occupational exposures to the metal compounds. The present work summarises the distribution of uranium and some selected trace metals such as Mn, Ni, Cu, Zn, Sr, Cd and Cs in the scalp hair of inhabitants from Balkans exposed to DU directly and indirectly, i.e. Han Pijesak, Bratoselce and Gornja Stubla areas. Except U and Cs, all other metals were compared with the worldwide reported values of occupationally unexposed persons. Uranium concentrations show a wide variation ranging from 0.9 ± 0.05 to 449 ± 12 µg kg(-1). Although hair samples were collected from Balkan conflict zones, uranium isotopic measurement ((235)U/(238)U) shows a natural origin rather than DU.

Dose effect for South Serbians due to 238U in natural drinking water.

The use of depleted uranium ammunition in South Serbia during the 1999 Kosovo conflict raised a great deal of public concern in the Balkans. Radioactivity levels of 238U in 20 wells and lake water samples were checked from the viewpoint of internal radiation exposure for South Serbian subjects. We have measured 238U concentration using inductively coupled plasma mass spectrometry, whereas thermal ionisation mass spectrometry has been used for the measurement of isotope ratios, e.g. 234U/238U and 235U/238U. The concentration of uranium in water samples varies in the range 1.37-63.18 mBq/L. 234U belongs to the 238U natural radioactive decay series, and at secular equilibrium, the abundance ratio, 234U/238U, corresponds to the ratio of their half-lives. The 234U/238U activity ratio varies in the range 0.88-2.2 and 235U/238U isotope ratio varies from 0.00698 to 0.00745. These findings indicate that uranium in water was a mixture of natural and anthropogenic origin. The annual effective dose due to 238U was estimated to be in the range 9.2 x 10(-5)-2.1 x 10(-3) mSv.

Determination of depleted uranium in environmental samples by gamma-spectroscopic techniques.

The military use of depleted uranium initiated the need for an efficient and reliable method to detect and quantify DU contamination in environmental samples. This paper presents such a method, based on the gamma spectroscopic determination of 238U and 235U. The main advantage of this method is that it allows for a direct determination of the U isotope ratio, while requiring little sample preparation and being significantly less labor intensive than methods requiring radiochemical treatment. Furthermore, the fact that the sample preparation is not destructive greatly simplifies control of the quality of measurements. Low energy photons are utilized, using Ge detectors efficient in the low energy region and applying appropriate corrections for self-absorption. Uranium-235 in particular is determined directly from its 185.72 keV photons, after analyzing the 235U-226Ra multiplet. The method presented is applied to soil samples originating from two different target sites, in Southern Yugoslavia and Montenegro. The analysis results are discussed in relation to the natural radioactivity content of the soil at the sampling sites. A mapping algorithm is applied to examine the spatial variability of the DU contamination.

Actinide analysis of a depleted uranium penetrator from a 1999 target site in southern Serbia.

Following the detection of 236U in depleted uranium (DU) ammunition used during the Balkans conflict in the 1990s, concern has been expressed about the possibility that other nuclides from the nuclear fuel cycle and, in particular, transuranium nuclides, might be present in this type of ammunition. In this paper, we report the results of uranium and plutonium analyses carried out on a depleted uranium penetrator recovered from a target site in southern Serbia. Our data show the depleted nature of the uranium and confirm the presence of trace amounts of plutonium in the penetrator. The activity concentration of (239+240)PU, at 45.4+/-0.7 Bq kg(-1), is the highest reported to date for any penetrator recovered from the Balkans. This concentration, however, is comparable to that expected to be present naturally in uranium ores and, from a radiological perspective, would only give rise to a very small increase in dose to exposed persons compared to that from the DU itself.