Assessment of lifetime cancer risk from natural radioactivity levels in Kadikoy and Uskudar District of Istanbul

The activity concentrations of ²²⁶Ra, ²³²Th, and ⁴⁰K are measured in soil samples from various locations in the Kadikoy and Uskudar district of Istanbul (Turkey). The ²²⁶Ra activity concentrations range from 19.97 Bqkg^?1 to 50.80 Bqkg^?1 and average ²²⁶Ra concentration value 31.40 Bqkg^?1 was calculated. The ²³²Th activity concentrations range from 21.38 Bqkg^?1 to 52.61 Bqkg^?1 and average ²³²Th concentration value 34.44 Bqkg^?1 was calculated. The ⁴⁰K activity concentrations range from 464.06 Bqkg^?1 to 711.27 Bqkg^?1 and average ⁴⁰K concentration value 619.59 Bqkg^?1 was calculated. In addition, radium equivalent (Ra_eq), absorbed gamma dose rate (D), annual effective dose equivalent, (AEDE), excess lifetime cancer risk (ELCR) were calculated in this study. All of the calculations have been compared with both national and international standards and similar studies. As a result of this comparison, levels of natural radioactivity and radiological effects were slightly higher than the World average and Turkey.     

Assessment of natural radioactivity,associated radiological health hazards indices and soil-to-crop transfer factors in cultivated area around a fertilizer factory in Onne,Nigeria

Concentration of natural radionuclides in three major staple food crops cultivated around a fertilizer plant in Onne, Rivers State Nigeria and the cultivated soil samples were determined using gamma spectroscopy operated on a Canberra vertical high purity 3″ × 3″ NaI(TI) detector. The average activity concentration of ²³⁸U, ²³²Th and ⁴⁰K was determined, for cassava flour (U 19.3 ± 5.0, Th 11.4 ± 3.3, K 426.9 ± 33.8) Bq kg^?1, for yam flour (U 6.3 ± 1.8, Th 8.4 ± 2.6, K 227.0.9 ± 27.3) Bq kg^?1 while for cocoyam flour (U 7.5 ± 2.7, Th 7.1 ± 2.3, K 195.8 ± 25.83) Bq kg^?1. The mean activity concentration for soil samples is 18.7 ± 3.7 Bq kg^?1, 18.0 ± 3.8 Bq kg^?1 and 308.4 ± 22.4 Bq kg^?1 for ²³⁸U, ²³²Th and ⁴⁰K, respectively. These values obtained show enhanced ⁴⁰K concentration which is attributed to the effluent discharge from a fertilizer plant and its applications to farmlands, but ²³⁸U, ²³²Th values are well within the global average and values reported in some regions and countries of the world. Radiation hazard indices obtained to estimate potential radiological health risk in both foodstuffs and soil samples are well below their permissible limit as set by UNSCEAR [Sources and effects of ionizing radiation (Report to the General Assembly), 2000]. The rate of radionuclides transfer from soil to crops was moderate with mean transfer factors of ²³²Th < ²³⁸U < ⁴⁰K.     

An analysis of naturally occurring radionuclides and <Superscript>137</Superscript>Cs in the soils of urban areas using gamma-ray spectrometry

This study of environmental radioactivity was carried out in the soils of an urban area. Naturally occurring gamma-emitting radionuclides and man-made ¹³⁷Cs were found in the soil profiles collected from four parks in the central Belgrade city area and the soil layer was examined every 10 cm and to a depth of 50 cm. Radioisotope activity concentrations (Bq kg^?1) in the samples of urban soil using the gamma-ray spectrometry method were in the range of 14–46 for ²³⁸U, 33–50 for ²²⁶Ra, 29–63 for ²¹⁰Pb, 1.2–3.4 for ²³⁵U, 28–50 for ²³²Th, 424–576 for ⁴⁰K and 0.7–35.8 for ¹³⁷Cs. Some of the basic physicochemical soil properties (pH, organic matter content, calcium-carbonate content, particle size distribution) were determined to investigate the impact on the vertical distribution of radionuclides. The results of this investigation showed that variations of activity concentration ratios of radionuclides that belong to the same (²³⁸U/²²⁶Ra) or different radioactive series (²³²Th/²²⁶Ra; ²³⁵U/²³⁸U), including ²¹⁰Pb/¹³⁷Cs ratios could well be explained by the properties of the soil. Alkaline pH reaction, the accumulation of organic matter in the uppermost and of carbonates in the deepest layers of urban soil had an effect on ²³⁸U/²²⁶Ra, and ²¹⁰Pb/¹³⁷Cs activity concentration ratio values, while ²³²Th/²²⁶Ra and partially ²³⁵U/²³⁸U ratios were associated with the particle sizes vertical distribution. A study of radionuclides in the samples of leaves of two deciduous tree species common for these parks was also conducted and ²¹⁰Pb and ⁴⁰K were found concentrated in leaves rather than other investigated radionuclides.     

New information on radionuclides concentration in phosphorites originating from Tunisia and Algeria

In this study we investigate the radiological hazard of naturally occurring radioactive material in Tunisian and Algerian phosphorite deposits. Eight samples of phosphorite were collected from the phosphorite mines. The Tunisian and Algerian phosphorites occur in the Late Paleocene and Lower Eocene (Ypresian-Lutetian) in age (Béji Sassi 1984 and Zaïer 1999). Activity concentrations in all the samples were measured by alpha spectrometry and gamma spectrometry. Alpha spectrometry analyses show that the specific activity values of ²³⁸U, ²³⁴U and ²³⁵U in the samples of Tunisian phosphorite were 327?±?7 (321–327), 326?±?6 (325–331) and 14.50?±?0.72 (13.90–15.57) Bq kg^?1, respectively. Specific activity measured by gamma spectrometry in the samples of the Tunisian and Algerian phosphorite shows a small difference. Specific activity levels of ⁴⁰K, ²²⁶Ra, ²³²Th, ²³⁵U and ²³⁸U in the phosphorite samples from Tunisia were, respectively, 71.10?±?3.80, 391.54?±?9.39, 60.38?±?3.74, 12.72?±?0.54 and 527.42?±?49.57 Bq kg^?1 and Algeria were 15.72?±?1.73, 989.65?±?12.52, 12.08?±?1.20, 47.50?±?1.52 and 1,148.78?±?7.30 Bq kg^?1, respectively. The measured value of specific activity of ²³²Th and ⁴⁰K in the Tunisian phosphorite samples is relatively higher than that found in the samples of Algerian phosphorite. The measured activity of uranium (²³⁸U) in the Tunisian phosphorite (527?±?49) Bq kg^?1 is lower than in Algerian phosphorite. The measured activity of ²³⁸U in the Tunisian phosphorite samples was (527–1,315?±?65) ²³⁸U Bq kg^?1 which is higher than its maximum background value of 110 Bq kg^?1 in soils of the various countries of the world (Tufail et al. Radiat Meas 41:443–451, 2006). Different geological origins of phosphorites deposits are the main reason for the large spread in worldwide specific activities. The obtained results of uranium concentrations in phosphorites of different types (Algerian and Tunisian) demonstrate that the uranium concentrations are mainly governed by the phosphatic material. The present study reveals that phosphorite deposits contain natural radioactivity higher than background level.     

Determination of radioactivity levels in Akhisar,Gördes,Gölmarmara and Sindirgi regions,Western Turkey

In this study, radioactivity measurements in the environment of Akhisar, Gölmarmara, Gördes and Sindirgi regions in Western Turkey were investigated in order to evaluate the implications of any excess radioactivity in the environment of geological formation. The radioactivity concentrations of ⁴⁰K, ²³⁸U and ²³²Th radionuclides in the soil samples were measured by a NaI(Tl) gamma spectrometer system, and the radium activity concentrations in the water samples were also analyzed by an ZnS(Ag) alpha counter by the collector chamber method. The radioactivity of ⁴⁰K, ²³⁸U and ²³²Th in soils ranged 2.80–2,347.77, 9.90–256.19 and 9.66–106.53 Bq kg^?1, respectively. The activity of ²²⁶Ra in the water samples ranged from 0.03 Bq L^?1 (0.89pCi/L) to 0.80 Bq L^?1 (21.58pCi/L). In addition, the external terrestrial gamma dose rate in air (nGy h^?1), annual effective dose rate (mSv year^?1) and radium equivalent activity (Bq kg^?1) were calculated and compared with international standard values.     

Distribution of 238U, 232Th and 40K in plutonic rocks of Greece

One hundred and twenty one samples from every major plutonic body (mainly granitic) of Greece have been analyzed by γ-ray spectrometry to determine the specific activities of ²³⁸U, ²³²Th and ⁴⁰K (Bq/kg). The range of the activity concentrations of these radionuclides was 2.3–266.4, 1.8–375.5 and 55.0–1632.0 Bq/kg and their average values were 79.2, 85.3 and 881.4 Bq/kg respectively. Any possible connection between the specific activities of ²³⁸U, ²³²Th and ⁴⁰K and some characteristics of the studied samples (age, rock-type, colour, grain-size, occurrence and chemical composition) is investigated. Samples of particular colour, rock-type, occurrence and chemical composition have been identified for their distinctive levels of natural radioactivity, while age and grain-size do not affect the concentrations of ²³⁸U, ²³²Th and ⁴⁰K. The range of the Th/U ratio was 0.7–12.69. This great variation in the Th/U ratios, especially when it is found among the samples of the same pluton, is also discussed and explained by alteration and tectonic–metamorphic processes.     

Natural radioactivity distribution and gamma radiation exposure of beach sands from Sithonia Peninsula

This study aims to evaluate the activity concentrations of ²³⁸U, ²²⁶Ra, ²³²Th, ²²⁸Th and ⁴⁰K along the beaches of Sithonia Peninsula which are adjacent to the rock-types of the Sithonia Plutonic Complex. These range from 6–673, 5–767, 5–1750, 6–1760 and 185–875 Bq/kg respectively. The (% wt.) heavy magnetic (HM) fraction (epidote, allanite, hornblende, biotite and garnet), the heavy non-magnetic (HNM) fraction (monazite, zircon, titanite and apatite) and the total heavy (TH) fraction, were correlated with the concentrations of the measured radionuclides in the bulk samples. The HNM fraction seems to control the activity concentrations of ²³⁸U in all samples, while the HM fraction, at least for the heavy mineral rich samples bearing high amounts of epidote crystals with allanite cores, controls their ²³²Th content. The measured radionuclides in beach sands were normalized to the respective values measured in the granitic rocks, which are their most probable parent rocks, in order to provide data on their enrichment or depletion. The annual effective dose varies from 0.013 to 0.688 mSv y^?1 for local people working on the beach, while for tourists the annual external effective dose ranges between 0.003 and 0.165 mSv y^?1.     

Anomalous concentrations of radionuclides in the groundwater of Ede area,southwestern Nigeria: a direct impact of geology

An assessment of the groundwater in areas underlain by pegmatite in Ede, southwestern Nigeria was carried out to determine the concentration of Potassium-40 (⁴⁰K), Uranium-238 (²³⁸U) and Thorium-232 (²³²Th) radionuclides. In the earlier work, it was established that zircons in these pegmatites have suffered a high degree of metamictization that has enhanced continuous loss of some radionuclides since the time of emplacement of the pegmatite host rock to the present. The aim of this work is to determine whether or not there is corresponding increase in the concentration of radionuclides in groundwater in the study area. Fifteen groundwater samples were collected from both hand dug wells and boreholes in the area. Ten samples were from Ede town, two samples each from nearby communities of Iddo and Ekuro and one from Iwoye, where the bedrocks were not pegmatites. All the 15 samples were analyzed with the Sodium Iodide scintillator (NaI [Tl]) detector at the Centre for Energy Research and Development, Obafemi Awolowo University, Ile-Ife, Nigeria. The results showed varying concentrations of the radionuclides in the water samples. Activity concentrations of Potassium-40 (⁴⁰K) indicated an average value of 17.149 Bq/L for samples from Ede, 9.265 Bq/L for Iddo, 6.6 Bq/L for Ekuro, while Iwoye has a value of 21.21 Bq/L. The Uranium-238 (²³⁸U) series had an average value of 13.64 Bq/L for Ede, 13.49 Bq/L for Ekuro, 11.685 Bq/L for Iddo and 12.04 Bq/L for the lone sample from Iwoye. Thorium-232 (²³²Th) series had an average value of 11.182 Bq/L for Ede, while average values of 7.79 Bq/L and 9.025 Bq/L, respectively, were recorded for Iddo and Ekuro and 12.25 Bq/L for Iwoye. The annual effective dose level of ⁴⁰K is generally below the World Health Organization (WHO) recommended dosage of 0.1 mSv/y except for three locations, while those of ²³⁸U and ²³²Th are in excess of the standard values. The high radionuclides in the groundwater in the study area were not due to anthropogenic sources but directly due to geological processes which release the radioisotopes from rocks after weathering, continuous loss from metamict minerals and natural lateral mobility from regions of radionuclides’ release to other areas. There is thus the need to carry out systematic studies of the radionuclides concentrations on regional scale in the area which could lead to investigating on both short- and long-term health effects on organic species in these areas, and development of purification systems before utilizing water from the areas for domestic and industrial purposes.     

Estimation of excess lifetime cancer risk and radiation hazard indices in southern Iraq

Relatively high activity concentrations of some radionuclides (²²⁶Ra, ²³⁸U, ²³²Th, and ⁴⁰K) have been measured in surface and subsurface soils in areas (southern Iraq) where many warfare actions have taken place during the Iran–Iraq and Gulf wars. Such high activity concentrations might be related to the increase in cancerous injuries and birth defects recently reported. The study was aimed to estimate the activity concentrations of some nuclides and a comparison of results with international health hazard indices. In addition, the excess lifetime cancer risk (ELCR) was assessed. Soil samples were collected at three depths (0, 30, and 60 cm) in three locations in Abu Al Khasib and Ad Dayr in Basrah governorates. The average activity concentrations were estimated employing hyper-pure germanium HPGe gamma-ray detection technology. The values obtained in Abu Al Khasib were: 58.44 Bq/kg (²²⁶Ra), 43.56 Bq/kg (²³⁸U), 19.38 Bq/kg (²³²Th), and 321.76 Bq/kg (⁴⁰K) whereas in Ad Dayr 45.71 Bq/kg (²²⁶Ra), 35.53 Bq/kg (²³⁸U), 20.33 Bq/kg (²³²Th), and 337.02 Bq/kg (⁴⁰K). According to UNSCEAR (Sources and effects of ionizing radiations: a report on the effects of atomic radiation to the general assembly with scientific annexes, Annex B, United Nations, New York, 2000) report, higher levels of ²²⁶Ra, ²³⁸U concentrations than the world’s average values (35 Bq/kg) were observed in both locations. In addition, some radiation hazard indices were determined for both locations: average outdoor external dose (D _out), average indoor external dose (D _in), total average value of the external dose (D _tot), average annual outdoor effective dose (E _out), average annual indoor effective dose (E _in), and averaged total annual effective dose (E _tot). Values for D _tot and E _tot were higher than the worldwide median (143 nGy/h and 0.48 mSv/y, respectively) in both regions. The measured values of activity concentrations were also used to estimate the outdoor, indoor, and total ELCR. The ELCR values were higher than the worldwide averages. Further analyses and studies need to assess the real risks for human health and possible soil remediation.     

Investigation of natural background radiation of sediments in Rameswaram Island,Tamil Nadu,India

The aim of the study is to assess the natural background radiation in and around Rameswaram Island. In this context, samples were collected to measure the gamma radiations of ²³⁸U, ²³²Th, and ⁴⁰K using NaI(Tl) detector-based gamma ray spectrometer. The average activity concentrations of ²³⁸U, ²³²Th, and ⁴⁰K are noted to be well below the world average values. The calculated absorbed dose rate, radium equivalent activity, and hazard index values were below the prescribed limit. The grain size of the sediment was analyzed following Trefethen’s nomenclature, and its correlation with the natural background radioactivity was studied. The sample that contained clay show elevated activity of ⁴⁰K. The percentage of heavy minerals shows concomitant variation in natural radioactivity, especially in the activity of ²³⁸U and ²³²Th.     

Cassiterite LA-MC-ICP-MS U/Pb and muscovite 40Ar/39Ar dating of tin deposits in the Tengchong-Lianghe tin district,NW Yunnan,China

The Tengchong-Lianghe tin district in northwestern Yunnan, China, is an important tin mineralization area in the Sanjiang Tethyan Metallogenic Domain. There are three N–S trending granite belts in the Tengchong-Lianghe area, with emplacement ages ranging from Early Cretaceous to Late Cretaceous and Early Cenozoic. Tin mineralization is spatially associated with these granitic rocks. However, the petrogenetic link between the tin deposits and the host granites is not clear because of the lack of age data for the tin mineralization. We investigate the possibility of direct dating of cassiterite from three typical tin deposits in the Tengchong-Lianghe tin district, using laser ablation multicollector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS). In situ LA-MC-ICP-MS dating of seven cassiterite samples from the Lailishan (LLS-1 and LLS-2), Xiaolonghe (XLH, WDS, DSP, and HJS), and Tieyaoshan (TYS) tin deposits yielded well-defined ²⁰⁶Pb/²⁰⁷Pb–²³⁸U/²⁰⁷Pb isochron ages. To assess the accuracy of the in situ U/Pb dating of cassiterite, ⁴⁰Ar/³⁹Ar dating of coexisting muscovite (in samples LLS-1, DSP, and TYS) was also performed. The cassiterite in situ U/Pb ages (47.4?±?2.0, 71.9?±?2.3, and 119.3?±?1.7 Ma, respectively) are in excellent agreement with the coexisting muscovite ⁴⁰Ar/³⁹Ar ages (48.4?±?0.3, 71.9?±?1.4, and 122.4?±?0.7 Ma, respectively). The U/Pb ages of cassiterite combined with the ⁴⁰Ar/³⁹Ar ages of muscovite indicate that there are three tin mineralization events in this district: the Lailishan tin deposit at 47.4?±?2.0 to 52?±?2.7 Ma, the Xiaolonghe tin deposit at 71.6?±?2.4 to 3.9?±?2.0 Ma, and the Tieyaoshan tin deposit at 119.3?±?1.7 to 122.5?±?0.7 Ma. These ages are highly consistent with the zircon U/Pb ages of the host granites. It is su.ggested that the Cretaceous tin mineralization might have taken place in a subduction environment, while the Early Tertiary tin metallogenesis was in a postcollisional geodynamic setting.     

Natural radioactivity levels and evaluation of radiological hazards from Beni Haroun dam sediment samples,northeast Algeria

Levels of naturally occurring radioactivity in sediment samples of Beni Haroun dam have been investigated. The activity concentrations of ²³⁸U and ²³²Th decay chains and ⁴⁰K primordial radionuclide have been measured using high-resolution HPGe detector. Activity concentrations of ²²⁶Ra, ²³²Th, and ⁴⁰K radionuclides were found in the ranges 9–66, 14–37, and 177–288 Bq/kg with the mean values 24.67, 25.98, and 208.10 Bq/kg, respectively. Radiological hazard parameters were estimated based on the activity concentrations for ²²⁶Ra, ²³²Th, and ⁴⁰K to find out any radiation hazard associated with the sediments. Correlation studies between pairs of radionuclides were performed and discussed, and the obtained results are compared with international recommended values.     

A comparative study of aquifer systems occurring at the Paraná sedimentary basin, Brazil: U-isotopes contribution

The radioactivity due to ²³⁸U and ²³⁴U in three aquifer systems occurring within the Paraná sedimentary basin, South America, has been investigated. Uranium is much less dissolved from fractured igneous rocks than from the porous sedimentary rocks as indicated by the U-mobility coefficients between 7.6 × 10^?6 and 1.2 × 10^?3 g cm^?3. These values are also compatible with the U preference ratios relative to Na, K, Ca, Mg and SiO₂, which showed that U is never preferentially mobilized in the liquid phase during the flow occurring in cracks, fissures, fractures and faults of the igneous basaltic rocks. Experimental dissolution of diabase grains on a time-scale laboratory has demonstrated that the U dissolution appeared to be a two-stage process characterized by linear and second-order kinetics. The U dissolution rate was 8 × 10^?16 mol m^?2 s^?1 that is within the range of 4 × 10^?16–3 × 10^?14 mol m^?2 s^?1 estimated for other rock types. The ²³⁴U/²³⁸U activity ratio of dissolved U in solutions was higher than unity, a typical result expected during the water–rock interactions when preferential ²³⁴U-leach from the rock surfaces takes place. Some U-isotopes data allowed estimating 320 ka for the groundwater residence time in a sector of a transect in São Paulo State. A modeling has been also realized considering all U-isotopes data obtained in Bauru (35 samples), Serra Geral (16 samples) and Guarani (29 samples) aquifers. The results indicated that the Bauru aquifer waters may result from the admixture of waters from Guarani (1.5 %) and Serra Geral (98.5 %) aquifers.     

Monazite and xenotime U–Th–Pb geochronology by ion microprobe: dating highly fractionated granites at Xihuashan tungsten mine, SE China

Zircon, monazite, and xenotime have proven to be valuable chronometers for various geological processes due to their commonly high-U–Th and low common Pb contents. However, zircons that have crystallized in highly fractionated granites often have such high-U contents that radiation damage can lead to scattered U–Pb ages when measured with secondary ion mass spectrometry (SIMS). In this study, monazite and xenotime were separated from a number of highly fractionated granites at the Xihuashan tungsten mine, Southeast China, for alternative dating methods by SIMS. For monazite analysis, obvious excess ²⁰⁴Pb signal (mainly from interference of ²³²Th¹⁴⁴Nd¹⁶O₂ ⁺⁺) was observed in high-Th (>2 wt%) monazite, which hinders ²⁰⁴Pb-based common Pb corrections. A ²⁰⁷Pb-based common Pb correction method was used instead. By employing power law relationships between Pb⁺/U⁺ versus UO₂ ⁺/U⁺, Pb⁺/Th⁺ versus ThO₂ ⁺/Th⁺ and suitable exponentials, monazites with ThO₂ contents in the range of ~3–19 % do not exhibit this matrix effect. Independent SIMS U–Pb ages and Th–Pb ages of three phases of Xihuashan granite samples were consistent with each other and yielded dates of 158.7 ± 0.7, 158.0 ± 0.7, and 156.9 ± 0.7 Ma, respectively. Xenotime does show marked matrix effects due to variations of U, Th, and Y [or total rare earth element (REE), referred as ΣREE hereafter] contents. Suitable correction factors require end-member standards with extremely high or low U, Th, and Y (or ΣREE) contents. No excess ²⁰⁴Pb was observed, indicating that the ²⁰⁴Pb-based common Pb correction method is feasible. Independent ²⁰⁷Pb/²⁰⁶Pb ages can be obtained, although multi-collector mode is necessary to improve precision. The main difficulties with dating xenotime are when high-Th (U) mineral inclusions are ablated. We can identify when this occurs, however, by comparing the measured UO₂ ⁺/U⁺ and ThO₂ ⁺/Th⁺ with those in xenotime standards. Three xenotime samples from the first phase of Xihuashan granite yielded a weighted mean ²⁰⁷Pb/²⁰⁶Pb date of 159.5 ± 4.4 Ma (MSWD = 1.0) and a ²⁰⁶Pb/²³⁸U date of 159.4 ± 0.9 Ma (MSWD = 1.6), which are consistent with monazite U–Pb and Th–Pb ages from the same granites. This study demonstrates that monazite and xenotime are better SIMS chronometers for highly fractionated granites than zircon, which can yield doubtful ages due to high-U contents.     

Natural and artificial radioactivity levels and hazards of soils in the Kücük Menderes Basin,Turkey

In this study, natural and artificial radionuclide activity concentrations in surface soils of Kücük Menderes Basin have been measured using gamma spectroscopy. The soil samples were collected from agricultural lands in the Kücük Menderes Basin in Turkey. The activity concentrations of ²²⁶Ra, ²³²Th, ⁴⁰K and ¹³⁷Cs in the soils were found to be range of 12.63 ± 2.28–72.51 ± 11.23, 11.45 ± 2.4–58.12 ± 4.76, 234.8 ± 14.85–1058.52 ± 24 Bq kg^?1 dw and 2.31 ± 0.18–7.75 ± 1.14 Bq kg^?1, respectively. The natural gamma radioactivity of the terrestrial radionuclides in soil samples and the gamma absorbed dose rate, the annual effective dose equivalent, the radium equivalent activity, the external hazard index, were calculated and compared with the international recommended values.     

Late Cretaceous granitoids in Karakorum,northwest Tibet: petrogenesis and tectonic implications

New zircon LA-ICP-MS U–Pb age, zircon Hf isotope, and whole-rock major and trace elemental data of the Late Cretaceous Ageledaban complex in the Karakorum Terrane (KKT), northwest Tibet, provide new constraints on the tectonic processes of the collision and thickening of the terrane between the Lhasa and Qiangtang terranes. The granitoids from the Ageledaban complex have a variable SiO₂ content, from 62.83 to 73.35 wt.% and A/CNK<1.1 (except for YM61-2). They have rare earth element and trace element patterns that are enriched in light rare earth elements, Rb, Pb, Th, and U, and are depleted in Ba, P, Sr, Ti, and Nb, indicative of weakly peraluminous-metaluminous I-type affinity. Zircon U–Pb dating reveals that the Ageledaban complex was emplaced at ca. 80 Ma. Zircons from the monzogranite and monzonite samples with concordant ²⁰⁶Pb/²³⁸U ages about 80 Ma have a zircon ε_Hf(t) of ?6.6 to ?1.1, corresponding to the Mesoproterozoic Hf crustal model ages (T_DM^C = 1.2–1.6 Ga); the remaining inherited zircons from the monzonite with concordant ²⁰⁶Pb/²³⁸U ages of about 108.1 Ma have ε_Hf(t) values that range from ?8.3 to ?5.0, corresponding to the Mesoproterozoic Hf crustal model ages with an average of 1.6 Ga. These signatures indicate that the Ageledaban granitoids may have been derived from the partial melting of a mixed mantle-crust source. Together with the age and geochemical data in the literature, we propose that the collisional event in the KKT in northwestern Tibet would postdate the northern Lhasa–southern Qiangtang collision, which occurred first in the Amdo in the east and later in the Shiquanhe in central Tibet. Our results support the previous view that the collision of the Bangong–Nujiang suture zone (BNSZ) may be diachronous.     

Natural radionuclide concentrations in thermal springs of east Algeria

The variation of the natural radionuclide concentrations depends on the chemical composition of each site. In this work, two thermal springs in the east of Algeria have been chosen to assess the activity concentration of natural radionuclide, mainly the three natural radioactive series ²³⁸U, ²³⁵U and ²³²Th, and ⁴⁰K. The high-resolution gamma ray spectroscopy was used to determine these concentrations. In these water samples, ²³⁵U, ²³⁴Th, ²¹⁰Pb, ²²⁶Ra radionuclides are less than the minimum detectable activity. The activity of ²³⁸U is dominant. The ²³⁸U activity was determined by taking the mean activity of two separate photo-peaks of daughter nuclides ²¹⁴Pb at 351.92 (37.2%) keV and ²¹⁴Bi at 609.31 (45%) keV. The measured activity concentrations of ²³⁸U in water samples obtained from the concentrations of ²¹⁴Bi and ²¹⁴Pb ranged from 0.56 ± 0.20 to 1.13 ± 0.20 Bq/L. The annual effective dose value due to the ingestion of the measured radionuclide ²³⁸U in 1 L of water, for an adult, ranged from 9.20 to 18.56 µSv.     

Assessment of soil radon potential in Hong Kong, China, using a 10-point evaluation system

Radon and its progenies have been ranked second of being responsible for lung cancer in humans. Hong Kong has four major groups of uranium-rich plutonic and volcanic rocks and is suffering from radon emanated therefrom. However, there is a lack of radon potential maps in Hong Kong to resolve the spatial distribution of radon-prone areas. A ten-point radon potential system was developed in Germany (2005) to predict radon potential using both the in situ geogenic and geographic parameters under hierarchical ranking. Primarily, the ten-point system requires the desk study of the geological environment of sampling sites, which has an advantage of saving resources and manpower in extensive radon potential mapping over the traditional soil radon concentration sampling method. This paper presents a trial of radon potential mapping in Hong Kong to further verify the system. Despite some slight departures, the system demonstrates an acceptable correlation with soil radon concentrations (R ² = 0.62–0.66) from 768 samples of mainly intermediate radon potential. Hong Kong has a mean soil radon concentrations of 58.9 kBqm^?3, while the radon potential from the ten-point system achieves an average of 4.93 out of 10 over the territory. The vicinity of fault zone showed high soil radon concentrations and potentials, which were conducive to uranium enrichment and rapid soil-gas diffusion near faults. High uranium-238 content in soil was found to cause high soil radon concentration with a large R ², 0.84. The Jurassic granite and volcanic crystal tuff cover more than 85 % of the whole Hong Kong area, and they show relatively high radon concentrations (Geometric mean 83 and 49 kBqm^?3, respectively) which are associated with their high uranium contents (Geometric mean 234 and 197 Bqkg^?1, respectively). While indoor radon concentration is an important factor for radon risk assessment, this study has not considered the correlation between indoor radon concentration and radon potential. The reason is that almost all buildings in Hong Kong are high-rise buildings where indoor radon concentrations are governed only by the radium content in the building materials and the ventilation conditions.     

Distinguishing lower and upper crustal processes in magmas erupted during the buildup to the 7.7 ka climactic eruption of Mount Mazama, Crater Lake, Oregon, using 238U–230Th disequilibria

Uranium-series isotope ratios determined for 35 volcanic rocks and 4 glass separates erupted from ~36 to 4.8 ka at Mt. Mazama, Crater Lake, Oregon, identify both ²³⁰Th-excess and ²³⁸U-excess components. U–Th isotope compositions cover a wide range, exceeding those previously measured for the Cascade arc. Age-corrected (²³⁰Th/²³²Th) and (²³⁸U/²³²Th) activity ratios range from 1.113 to 1.464 and from 0.878 to 1.572 (44.4 % ²³⁰Th-excess to 8.8 % ²³⁸U-excess), respectively. The most distinctive aspect of the data set is the contrast in U–Th isotope ratios between low and high Sr (LSr, HSr) components that have been previously identified in products of the 7.7 ka caldera-forming climactic eruption and preclimactic rhyodacite lavas. The LSr component exclusively contains ²³⁸U-excess, but the HSr component, as well as more primitive lavas, are marked by ²³⁰Th-excess. ²³⁰Th-excesses such as those recorded at Mt. Mazama are commonly observed in the Cascades. Melting models suggest that high ²³⁰Th-excesses observed in the more primitive lavas evolved through mixing of a mantle melt with a partial melt of a mafic lower crustal composition that contained garnet in the residuum that was produced through dehydration melting of amphibolite that was initially garnet free. Dehydration melting in the lower crust offers a solution to the “hot-slab paradox” of the Cascades, where low volatile contents are predicted due to high slab temperatures, yet higher water contents than expected have been documented in erupted lavas. The ²³⁸U-excess observed at Mt. Mazama is rare in Cascade lavas, but occurs in more than half of the samples analyzed in this study. Traditionally, ²³⁸U-excess in arc magmas is interpreted to reflect slab fluid fluxing. Indeed, ²³⁸U-excess in arcs is common and likely masks ²³⁰Th-excess resulting from lower crustal interaction. Isotopic and trace element data, however, suggest a relatively minor role for slab fluid fluxing in the Cascades. We propose that ²³⁸U-excess reflects melting and assimilation of young, hydrothermally altered upper crust. The processes related to generating ²³⁸U-excess are likely important features at Mt. Mazama that accompanied development of a large-scale silicic magma chamber that led to the caldera-forming eruption.     

Potential effect of natural radionuclides in riverbed sediments: a statistical approach based on granulometric and magnetic mineral differences

South India is one of the regions in the world that has the highest background radiation levels. In this region, river sediments are used in large quantities as building material. Therefore, the knowledge of the radionuclides distribution in such sediments is important for assessing their potential adverse effects on humans residing in buildings made of sediment material. For this goal, we focus on the determination of the natural radioactivity levels and magnetic properties in sediment samples collected from 33 locations along the southwestern Bharathapuzha river originating from the Anamalai hills. The sediment samples were subdivided into two categories according to particle size. It is observed that the average activity concentrations of ²²⁶Ra, ²³²Th, and ⁴⁰K in sediment samples varied greatly with granulometric and geological differences. The average values of ²²⁶Ra, ²³²Th, and ⁴⁰K and its associated radiological hazard parameters for category II samples (particle size between 149 μm and 2 mm) were lower than category I sediment samples (bulk samples). Moreover, the average radionuclide activity concentrations (except for ⁴⁰K) and the calculated radiation hazard parameters are higher in the lowland region compared to the highland and the midland regions. The mass-specific magnetic susceptibility values ranged widely along the river, as well as between physiographic regions, e.g., average values for category I sediment samples were 950.2 × 10^?8, 351.1 × 10^?8 and 131.8 × 10^?8 m³ kg^?1 (for high-, mid- and lowland regions, respectively). Differences between physiographic regions and sediment fractions from both radioactivity determinations and magnetic parameters were analyzed with statistical tests and multivariate analysis, which showed the advantages of using both independent techniques.