The radiation survey of the ambient environment was conducted using two gamma detectors, and the measurement results were used in the computation of the mean external radiation dose rate, mean-weighted dose rate and annual effective dose, which are 144 nGy h(-1), 0.891 mSv y(-1) and 178 μSv, respectively. A high-purity germanium detector was used to determine the activity concentrations of (232)Th, (226)Ra and (40)K in soil samples. The results of the gamma spectrometry of the soil samples show radioactivity concentration ranges from 19±1 to 405±13 Bq kg(-1) with a mean value of 137±5 Bq kg(-1) for (232)Th, from 21±2 to 268±9 Bq kg(-1)with a mean value of 78±3 Bq kg(-1) for (226)Ra and from 23±9 to 1268±58 Bq kg(-1) with a mean value of 207±13 Bq kg(-1) for (40)K. Radium equivalent activity (Raeq) and external hazard index (Hex) were 290 Bq kg(-1) and 0.784, respectively, which were safe for the population. The mean lifetime dose and lifetime cancer risk for each person living in the area with average lifetime (70 y) were 12.46 mSv and 7.25×10(-4) Sv year, respectively. The results were compared with values given in United Nations Scientific Committee on the Effects of Atomic Radiation 2000.
Concentrations of natural and fall-out radionuclides in the offshore seawater and sediment from some parts of the Bay of Bengal, Bangladesh, were determined using a coaxial germanium detector. The average activities of (238)U, (232)Th, (40)K and (137)Cs were recorded as 31.2±5.8, 51.9±9.4, 686.4±170.5 and 0.5±0.6 Bq kg(-1) dry weight, respectively, for sediment, and 4.8±1.2, 5.4±1.2 and 39.1±8.6 Bq L(-1) for (238)U, (232)Th and (40)K, respectively, in seawater. The concentration of (137)Cs in seawater was below the detection limit. The concentration of sediment (238)U was found to be positively correlated with (232)Th ([Formula: see text], p<0.05) and (40)K (r=0.96, p<0.01), while (232)Th was positively correlated with (40)K (r=0.91, p<0.05). In sediment, the concentration of (238)U was negatively correlated (r=-0.86, p<0.05) with sea depth. In the seawater sample, the only significant relationship found was between concentration of (232)Th and water depth (r=-0.86, p<0.05). One-factor analysis of variance (ANOVA) showed that the level of radioisotope concentrations of seawater and sediment was highly significant for (238)U (F=122, df=11, p=0.01), (232)Th (F=143, df=11, p=0.01) and (40)K (F=86, df=11, p=0.01). The results showed that the level of radioactivity decreased from coast to open sea. Imminent threat due to radioactivity was not observed in these parts of the Bay of Bengal.
Measurements of the environmental terrestrial gamma radiation dose rate (TGRD) in each district of Kelantan state, Malaysia, were carried out using a portable hand-held radiation survey meter and global positioning system. The measurements were done based on geology and soil types of the area. The mean TGRD was found to be 209 nGy h(-1). Few areas of relatively enhanced activity were observed in Pasir Mas, Tanah Merah and Jeli districts, which have a mean TGRD between 300 and 500 nGy h(-1). An isodose map of the area was produced using ArcGIS software version 9.3.
This study was aimed at providing the baseline data of terrestrial gamma dose rates and natural radioactivity to assess the corresponding health risk in the ambient environment of the Pahang State. Terrestrial gamma radiation (TGR) from 640 locations was measured with the mean value found to be 176 ± 5 nGy h(-1). Ninety-eight soil samples were analysed using a high-purity germanium detector (HPGe), and the mean concentrations of the radionuclides (226)Ra, (232)Th and (40)K are 110 ± 3, 151 ± 5 and 542 ± 51 Bq kg(-1), respectively.(226)Ra and (232)Th concentrations were found to be three times the world average, while that of (40)K is quite higher than the world average value. The acid-intrusive geological formation has the highest mean concentrations for (226)Ra (215 ± 6 Bq kg(-1)), (232)Th (384 ± 12 Bq kg(-1)) and (40)K (1564 ± 153 Bq kg(-1)). The radium equivalent activities (Req) and the external hazard index (Hex) for the various soil types were also calculated. Some of the soil types were found to have values exceeding the internationally recommended levels of 370 Bq kg(-1) and the unity value, respectively.
To assess coastal ecosystem status and pollution baselines, prawns were collected from the commercial catches of eight Asia-Pacific countries (Australia, Bangladesh, Indonesia, Myanmar, Philippines, Pakistan, Sri Lanka and Thailand). Samples collected from 21 sites along regional coastlines were analysed for trace metal and stable isotopic compositions of H, C, N, O and S. A combination of simple averaging and multivariate analyses was used to evaluate the data. Sites could be assigned to easily recognise polluted and unpolluted groups based on the prawn results. Some filter-feeding clams were also collected and analysed together with the benthic-feeding prawns, and the prawns generally had lower trace metal burdens. Climate change effects were not strongly evident at this time, but altered ocean circulation and watershed run-off patterns accompanying future climate change are expected to change chemical patterns recorded by prawns along these and other coastlines. Stable isotopes, especially (15)N, can help to distinguish between relatively polluted and unpolluted sites.
Nasarawa State is located in north central Nigeria and it is known as Nigeria's home of solid minerals. It is endowed with barite, copper, zinc, tantalite and granite. Continuous releases of mining waste and tailings into the biosphere may result in a build-up of radionuclides in air, water and soil. This work therefore aims to measure the activity concentration levels of primordial radionuclides in the soil/sediment samples collected from selected mines of the mining areas of Nasarawa State. The paper also assesses the radiological and radio ecological impacts of mining activities on the residents of mining areas and their environment. The activity concentrations of primordial radionuclides ((226)Ra, (232)Th and (40)K) in the surface soils/sediment samples were determined using sodium iodide-thallium gamma spectroscopy. Seven major mines were considered with 21 samples taken from each of the mines for radiochemistry analysis. The human health hazard assessment was conducted using regulatory methodologies set by the United Nations Scientific Committee on the Effects of Atomic Radiation, while the radio ecological impact assessment was conducted using the ERICA tool v. 1.2. The result shows that the activity concentrations of (40)K in the water ways of the Akiri copper and the Azara barite mines are 60 and 67% higher than the world average value for (40)K, respectively. In all mines, the annual effective dose rates (mSv y(-1)) were less than unity, and a maximum annual gonadal dose of 0.58 mSv y(-1) is received at the Akiri copper mine, which is almost twice the world average value for gonadal dose. The external hazard indices for all the mines were less than unity. Our results also show that mollusc-gastropod, insect larvae, mollusc-bivalve and zooplankton are the freshwater biotas with the highest dose rates ranging from 5 to 7 µGy h(-1). These higher dose rates could be associated with zinc and copper mining at Abuni and Akiri, respectively. The most exposed terrestrial reference organisms are lichen and bryophytes. In all cases, the radio ecological risks are not likely to be discernible. This paper presents a pioneer data for ecological risk from ionizing contaminants due to mining activity in Nasarawa State, Nigeria. Its methodology could be adopted for future work on radioecology of mining.
The Jos Plateau has been reported to have elevated levels of natural background radiation. A few earlier studies have measured the levels of natural radioactivity for specific locations in the area. Our interest is to investigate how geology of the study area influences the activity concentrations of natural radionuclides. Thus, the activity concentrations of terrestrial radionuclides in soil samples collected across the geological formations of the Jos Plateau were determined by gamma spectrometry technique. The mean activity concentrations of 226Ra, 232Th and 40K were found to exceed their corresponding world reference values of 35, 40 and 400 Bq kg-1, respectively. Data were compared using statistical methods, analysis of variance (ANOVA) and post hoc tests. The results revealed in some instances significant influences of geological types on the activity concentrations in the area. The spatial distribution maps of activity concentrations of 226Ra, 232Th and 40K were geostatistically interpolated by ordinary Kriging method using ArcGIS software.
This study entails the measurement of the specific activity of natural radionuclides (226Ra, 40K and 232Th) in 18 tooth samples obtained from the clinic of the Universiti Sains Malaysia (USM), Penang, by using an HPGe detector. The specific activity of 226Ra, 40K and 232Th was measured to estimate the hazard index of the radionuclides, radium equivalent activities (Raeq), external, internal hazard indices (Hex, Hin), and absorbed dose (Dout, Din). The maximum values of concentration of 226Ra, 232Th and 40K in the tooth samples were found to be 60.82, 60.29 and 594.22 Bq kg-1, respectively. Maximum values of Raeq, Hex, Hin, Dout and Din were found to be 192.78 Bq kg-1, 0.520, 0.685, 89.29 and 169.81 nGy h-1, Iγ and Iα as 0.702 and 0.304, respectively. The results were lower than the average world value (UNSCEAR). In addition, a strong correlation was found between the concentrations of 226Ra and Raeq, between energy and net area, as well as between radionuclides (226Ra, 40K and 232Th) in tooth samples and age of volunteers. This study showed that the concentrations and hazard indices of tooth samples are below the recommended safe levels; therefore, the study area is considered safe in terms of radiological health hazards.
An extensive study was conducted to determine the activity concentrations of natural and artificial radionuclides 226Ra, 232Th, 40K, and 137Cs in soil samples of each governate of Jordan. A total of 370 samples have been measured using a high-purity germanium detector. The activity concentration for 226Ra, 232Th, 40K, and 137Cs has mean values of 42 ± 3, 23 ± 3, 309 ± 21, and 3.7 ± 0.9 Bq kg-1, respectively. The highest mean activity concentration for 226Ra was found to be 138 ± 4 Bq kg-1 in the Alkarak governate. In the Ajloun and Jarash governates, the highest mean activity concentration was 35 ± 3 Bq kg-1 for 232Th, and 14.2 ± 1.9 Bq kg-1 for 137Cs, respectively. Geological influence on the activity concentrations was investigated using the one-way analysis of variance (ANOVA) and independent samples. The ANOVA results indicate that there are strong significant differences between the activity concentrations of 232Th, 40K, and 137Cs based on geological formations the radionuclides occur. The main contribution to gamma dose rate was due to 226Ra activity concentration. Radium equivalent and external hazard index are associated with a mean value of 98 Bq kg-1, and 0.266, respectively.
Terrestrial gamma radiation dose (TGRD) rates were measured in situ from different locations in Katsina State, Nigeria, using a portable radiation survey metre based on geological formations and soil types. The measured TGRD rates ranged from 45 to 271 nGyh-1 with an average value of 116 ± 1 nGyh-1. Geological formation (silicified sheared rock) and soil type (lithosols and ferruginous crusts and ferruginous tropical soils) appeared to have the highest mean TGRD values of 163 and 134 nGyh-1 with sandstone geological formation and alluvial and hydromorphic soils having the lowest TGRD with values of 80 and 61 nGyh-1, respectively. One way ANOVA results shows that the tested null hypothesis was rejected. Thus, indicating that there exists a strong relationship between the various geological formations, soil types with the measured TGRD values based on the alternate hypothesis. Human health hazard indices like annual effective dose equivalent (AEDE), lifetime outdoor annual equivalent dose, and relative excess lifetime outdoor cancer risk associated with the mean TGRD of the study area were also calculated and found to be 0.711, 9.955 mSv, and 5.79 × 10-4, respectively. These values were higher than the world average values but favourable compared with the safety limits recommended by ICRP.