Natural radioactivity of bricks and brick material in the Salihli-Turgutlu area of Turkey

Some of the rocks and soil-originated materials used in building construction are the serious natural radiation sources. Soil-originated bricks and roof-tiles and their raw material in the Salihli-Turgutlu area were tested in situ for natural radiation levels using a gamma-ray spectrometer. The concentrations of the radioelements ⁴⁰K, ²³⁸U and ²³²Th and air-absorbed radiation rates were measured for soil, raw material heaps, brick and roof-tile stacks and waste brick heaps. The radium-equivalent activity Ra_eq of the raw material varied between 187.9 and 216.4 Bq kg^?1. The external radiation hazard index H_ex values ranged between 0.51 and 0.58. For building material and its products, recommended Ra_eq and H_ex levels are 370 Bq kg^-1 and 1.0, respectively. On the other hand, both Ra_eq and H_ex values for waste brick heaps, containing broken brick pieces, coal pieces and ash, were higher than the recommended levels, i.e. Ra_eq values varied from 473.8 to 651.0 Bq kg^-1 and H_ex values were within the range 1.15–1.76. The annual dose rate and radium-equivalent activity values of the brick and roof-tiles were below the level of criteria. Annual dose rate ranged between 0.42 and 0.62 mSv y^?1 and radium equivalent activity was in the range 172.9–245.2 Bq kg^?1. The external and internal radiation hazard indices were all below the value of 1.0 for the Salihli-Turgutlu area bricks and roof-tiles. Results of this study were compared with results of previous studies. Natural radiation levels of construction raw material of study area are generally higher than of those of previous studies.     

Natural radioactivity in sediment of Wei River,China

The concentrations of natural radionuclides in sediment of Wei River of China were measured using γ-ray spectrometry with the aim of estimating the radiation hazard as establishing a database for radioactivity levels of river sediment of China. The activity concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K in sediment samples ranged from 10.4 to 39.9 Bq kg⁻¹, 15.3 to 54.8 Bq kg⁻¹ and 514.8 to 1,175.5 Bq kg⁻¹, respectively. The concentrations of these radionuclides were compared with the typical world values and the average activities of Chinese soil and Shaanxi soil. Radium equivalent activity (Ra_eq), external hazard index (H _ex) and representative level index (I _γr) were calculated for the samples to assess the radiation hazards arising due to the use of these sediment samples in the construction of dwellings. All the sediment samples have Ra_eq lower than the limit of 370 Bq kg⁻¹, H _ex less than unity and I _γr close to 1 Bq kg⁻¹. The overall mean outdoor terrestrial gamma dose rate is 64.8 nGy h⁻¹ and the corresponding outdoor annual effective dose is 0.079 mSv. None of the studied location is considered a radiological risk and sediment can be safely used in construction.     

Radiological hazards of coal and ash samples collected from Xi’an coal-fired power plants of China

The natural radiological characteristics and their respective annual effective dose (AED) rates, produced by ²²⁶Ra, ²³²Th and ⁴⁰K in coal, fly ash and bottom ash from two large coal-fired power plants (CFPPs) of Xi’an were determined by means of γ-ray spectrometry. The average activity concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K in all ash samples (fly ash and bottom ash samples) from the two CFPPs were 67.6, 74.3 and 225.3 Bq kg⁻¹, respectively. The results are compared with data from other locations. To evaluate the radiological hazards of the natural radioactivity, the radium equivalent activity (Ra_eq), air absorbed dose rate (D), AED and external hazard index (H _ex) are compared with internationally accepted values. Ra_eq and H _ex of all samples except three fly ash samples were less than the limits of 370 Bq kg⁻¹ and unity, respectively. The average D and AED for ash samples were 86.8 nGy h⁻¹ and 0.11 mSv y⁻¹, respectively, which exceed the world average and Xi’an average values.     

Radiological hazard assessment for building materials incorporating phosphogypsum made using Eshidiya mine rock in Jordan

The mean activity concentrations of ²²⁶Ra, ²³²Th, and ⁴⁰K in Eshidiya phosphogypsum samples were measured as 351.4 ± 23.4, 3.8 ± 0.3, and 120.7 ± 8.3 Bq kg^?1, respectively. The results show that the mean values of activity concentration of ²²⁶Ra, ²³²Th, and ⁴⁰K are in the lower range of typical values reported for phosphogypsum samples collected worldwide. Radiological hazard indices such as the radium-equivalent activity (Ra_eq), the gamma index (I _γ ) alpha index (I _α ), the absorbed gamma dose rate (D _in), and the corresponding annual effective dose (E _in) were assessed for building materials for dwellings. The results of assessment exhibit that all phosphogypsum samples are higher than the recommended safe limit for building materials for dwellings, except for the radium-equivalent activity (Ra_eq). Overall assessment, it can be concluded that the possibility of using Eshidiya phosphogypsum in building materials in proportions lower than 100 % will be safe. The mixture of phosphogypsum with normal gypsum can dilute the concentrations of natural radionuclides allowing the use of the mixed building materials to be safe from a radiological point of view.     

Evaluation of Naturally Occurring Radioactivity Materials (NORM) of Soil and Sediments in Oil and Gas Wells in Western Niger Delta Region of Nigeria

Oil mineral leases (30, 58 and 61) in Delta and River States are the major oil blocks in the oil and gas rich Niger Delta region of Nigeria that is characterized by environmental degradation from oil and gas activities. This research work presents an analytical approach on natural radioactivity assessment in soil and sediment in 15 oil fields of these OMLs. Concentrations of natural radionuclides (²²⁶Ra, ²³²Th and ⁴⁰K) were determined using gamma spectroscopy. The mean activity concentration of ²²⁶Ra, ²³²Th and ⁴⁰K for OML30 is 40.2 ± 5.1, 29.9 ± 4.2 and 361.5 ± 20.0 Bq kg^?1, respectively; the corresponding values obtained for OML58 is 20.9 ± 2.8, 19.4 ± 2.5 and 260.0 ± 14.1 Bq kg^?1, respectively. While the mean activity concentration of ²²⁶Ra, ²³²Th and ⁴⁰K for OML61 is 29.3 ± 3.5, 21.6 ± 2.6 and 262.1 ± 14.6 Bq kg^?1, respectively. These values obtained show enhanced NORMs, but are well within the world range and values reported in some regions and countries of the world, and are slightly above control values, values obtained in Southwestern region of Nigeria and some countries reported average values. The study also examined some radiation hazard indices, the mean values obtained are 86.6 ± 9.3 Bq kg^?1, 0.6 Bq kg^?1, 40.8 ηGy h^?1, 0.05 μSv y^?1, 0.2 and 0.3 for radium equivalent activity (Ra_eq), representative level index (Iγ), absorbed dose rates (D), annual effective dose rates (E _ff dose), external hazard index (H _ex) and internal hazard index (H _in), respectively. These calculated hazard indices to estimate the potential radiological health risk in soil and sediment are well below their permissible limits. The soil and sediments from the study area provide no excessive exposures for the inhabitants and can be used as construction materials without posing any radiological threat or harm to the public users. However, oil-field workers and host community residents are cautioned against excess exposure to avoid future accumulative dose of these radiations from sludge and sediment of this area.     

Gamma radiation measurements of naturally occurring radioactive samples from commercial Egyptian granites

Due to the widespread use of granites as building and ornamental materials, measurements of natural radioactivity for a total 27 selected samples of commercial granites used in Egypt were carried out by using a high pure germanium detector. The activity concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K of commercial granites ranged from 25 to 356, 5 to 161, and 100 to 1,796?(Bq?kg^?1), respectively. The concentrations of these radionuclides are compared with the international recommended values. To evaluate the radiological hazard of the natural radioactivity, the radium equivalent activity, the absorbed dose rate, the effective dose rate, and the hazard index have been calculated. The radium equivalent activity Ra_eq varied from 41 to 669?(Bq?kg^?1) which exceeds the permitted value (370?Bq?kg^?1) and the internal hazard index H _in varied from 0.2 to 2.8 which is higher than 1. The absorbed dose rate due to the natural radioactivity in the samples under investigation ranged from 19 to 310?(nGy?h^?1). The total effective dose rates per person indoors were determined to be 0.09 to 1.5?(mSv?year^?1).     

Radiological risk assessment of naturally occurring radioactive materials in marine sediments and its application in industrialized coastal areas: Bay of Algeciras,Spain

Radioactivity levels in aquatic environments can be assessed through the study of superficial sediments. Anthropogenic activities may alter radioactivity levels leading to the anomalous accumulation of natural radionuclides in coastal areas. In this work, marine sediments from a significant area subjected to severe industrial development were collected in order to measure activity concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K by gamma spectrometry. Radium equivalent index (Ra_eq), absorbed gamma dose rate in air (D) and annual effective dose equivalent (H) were also calculated and used as risk assessment tools. Results showed low levels of radioactivity in marine sediments from the Bay of Algeciras, discarding any significant radiological risks. Furthermore, the obtained data set could be used as background levels for future research applications and development of environmental regulatory frameworks.     

<Superscript>226</Superscript>Ra, <Superscript>232</Superscript>Th and <Superscript>40</Superscript>K activities in soils of Cuihua Mountain National Geological Park,China

Gamma activity from the naturally occurring radionuclides namely, ²²⁶Ra, ²³²Th, the primordial radionuclide ⁴⁰K was measured in the soil of Cuihua Mountain National Geological Park, China using γ-ray spectrometry technique. The mean activity of ²²⁶Ra, ²³²Th and ⁴⁰K were found to be 27.2 ± 6.5, 43.9 ± 6.2 and 653.1 ± 127.6 Bq kg⁻¹, respectively. The concentrations of these radionuclides were compared with the typical world values and the average activities of Chinese soil. The radium equivalent activity, the air absorbed dose rate, the annual effective dose rate, and the external hazard index were evaluated and compared with the internationally approved values. All the soil samples have Ra_eq lower than the limit of 370 Bq kg⁻¹ and H _ex less than unity. The overall mean outdoor terrestrial gamma dose rate is 66.3 nGy h⁻¹ and the corresponding outdoor annual effective dose is 0.081 mSv.     

Radionuclides measurements and mineralogical studies on beach sands, East Rosetta Estuary, Egypt

Radiometric measurements were carried out for the beach sands from East Rosetta estuary to determine the activity concentrations of 238 U, 226 Ra, 232 Th, and 40 K, using a Hyper Pure Germanium spectrometer, to estimate the dose rates and radiation hazard indices. The average specific activities are 778.20 Bq/kg for 238 U; 646.89 Bq/kg for 226 Ra; 621.92 and 627.85 Bq/kg for the 222 Rn daughters 214 Pb and 214 Bi respectively. The average specific activity of 232 Th is 1510.25 Bq/kg, while the calculated specific activity for 40 K has an average of 8.41 Bq/kg. The average specific activity of 235 U is 38.61 Bq/kg. The average absorbed dose rate is 1211.36 nGy/h, 20 times higher than the estimated average global primordial radiation of 60 nGy/h and 6 times higher than that of the world range (10-200 nGy/h). The radium equivalent (Ra eq ) values are from 6 to 9 times the recommended value. The internal and external hazard indices (H int , H ex ) indicate that their values are from 6 to 11 times the permissible values of these indices. These higher values may be due to the presence of economic heavy minerals containing radionuclides as zircon and monazite as well as some trace minerals, thorite and uranothorite. The mineralogical study indicates the beach sands contain heavy minerals, zircon, monazite, rutile, ilmenite, leucoxene, magnetite and garnet. The average abundance of zircon is 0.175 wt% ranging from 0.125 wt% to 0.239 wt%, while it is 0.004wt% ranging from 0.001 wt% to 0.007 wt% for monazite. The average abundance is 0.087 wt% for rutile; 2.029 wt% for ilmenite; 1.084 wt% for magnetite; 0.384 wt% for leucoxene and 0.295 wt% for garnet.     

Estimation of radiation exposure in soils and organic (animal) and inorganic (chemical) fertilizers using active technique

In this study, activity concentrations of ⁴⁰K, ²²⁶Ra and ²³²Th in fertilized soil samples and different organic and inorganic fertilizers used in agricultural soil were analysed using gamma-ray spectrometry NaI (Tl) detector in order to access the implications of extended use of fertilizers in 2–3 years. The concentrations of radionuclides in some granular fertilizer brands were discovered to be higher for ⁴⁰K, ²²⁶Ra and ²³²Th than those obtained in leafy fertilizer, animal fertilizer and fertilized soil samples. From the results, the highest overall mean concentrations of the specific activities of ⁴⁰K, ²²⁶Ra and ²³²Th were 2301.8 (granular fertilizer), 42.5 (leafy fertilizer) and 327.1 (animal fertilizer) in Bq kg^?1, while the lowest values observed in the specific activities of the same radionuclides were 357.7 (leafy fertilizer), 28.1 (animal fertilizer) and 36.5 (animal fertilizer). The radiological hazards of the radium equivalent (Ra_eq), normative value (NRN), outdoor radium equivalent (Ra_eq-out), external hazard index (H _ext), internal hazard index (H _in), dose rate, annual effective dose rate, activity utilization index and concentration accumulation index (CAI) and Ra_FZ due to the presence of these radionuclides in the investigated samples were calculated. Nevertheless, some of the fertilizer brands have higher concentration values than the recommended limit, and the values of hazard indices of fertilizer brands used in the selected teaching and research farms were within acceptable limit. Therefore, the fertilized soil samples in the studied farms are safe.     

Ra/Ra and Ra/Ba ratios to track barite formation and transport in the water column

We measured ²²⁸Ra_ex/²²⁶Ra_ex and ²²⁶Ra_ex/Ba_ex ratios in suspended and sinking particles collected at the Oceanic Flux Program (OFP) time-series site in the western Sargasso Sea and compared them to seawater ratios to provide information on the origin and transport of barite (BaSO₄) in the water column. The ²²⁸Ra_ex/²²⁶Ra_ex ratios of the suspended particles down to 2000 m are nearly identical to those of seawater at the same water depth. These ratios are much lower than expected if suspended barite was produced in surface waters and indicate that barite is produced throughout the mesopelagic layer. The ²²⁸Ra_ex/²²⁶Ra_ex activity ratios of sinking particles collected at 1500 and 3200 m varied mostly between 0.1 and 0.2, which is intermediate between the seawater ratio at these depths (<0.03) and the seawater ratios found in the upper 250 m (0.31-0.42). This suggests that excess Ba (i.e., Ba_ex = Ba_total − Ba_lithogenic), considered to be mainly barite, present in the sinking flux is a mixture of crystals formed recently in the upper water column, formed several years earlier in the upper water column, or formed recently in deeper waters. We observe a sizeable temporal variability in the ²²⁸Ra_ex/²²⁶Ra_ex ratios of sinking particles, which indicates temporal variability in the relative proportion of barite crystals originating from surface (with a high ²²⁸Ra_ex/²²⁶Ra_ex ratio) and mesopelagic (with a low ²²⁸Ra_ex/²²⁶Ra_ex ratio) sources. However, we could not discern a clear pattern that would elucidate the factors that control this variability. The ²²⁶Ra/Ba ratios measured in seawater are consistent with the value reported from the GEOSECS expeditions (2.3 dpm μmol⁻¹) below 500 m depth, but are significantly lower in the upper 500 m. High ²²⁶Ra_ex/Ba_ex ratios and elevated Sr concentrations in suspended particles from the upper water column suggest preferential uptake of ²²⁶Ra over Ba during formation of SrSO₄ skeletons by acantharians, which must contribute to barite formation in shallow waters. Deeper in the water column the ²²⁶Ra_ex/Ba_ex ratios of suspended particles are lower than those of seawater. Since ²²⁸Ra_ex/²²⁶Ra_ex ratios demonstrate that suspended barite at these depths has been produced recently and in situ, their low ²²⁶Ra_ex/Ba_ex ratios indicate preferential uptake of Ba over Ra in barite formed in mesopelagic water.     

Ra/Ra and Ra/Ba ratios in the Western Mediterranean Sea: Barite formation and transport in the water column

²²⁶Ra, ²²⁸Ra and Ba distributions as well as ²²⁸Ra/²²⁶Ra and ²²⁶Ra/Ba ratios were measured in seawater, suspended and sinking particles at the DYFAMED station in the Western Mediterranean Sea at different seasons of year 2003 in order to track the build-up and fate of barite through time. The study of the ²²⁸Ra_ex/²²⁶Ra_ex ratios (Ra_ex = Ra activities corrected for the lithogenic Ra) of suspended particles suggests that Ba_ex (Ba_ex = Ba concentrations corrected for the lithogenic Ba, mostly barite) formation takes place not only in the upper 500 m of the water column but also deeper (i.e. throughout the mesopelagic layer). Temporal changes in the ²²⁸Ra_ex/²²⁶Ra_ex ratios of sinking particles collected at 1000 m depth likely reflect changes in the relative proportion of barite originating from the upper water column (with a high ²²⁸Ra/²²⁶Ra ratio) and formed in the mesopelagic layer (with a low ²²⁸Ra/²²⁶Ra ratio). ²²⁸Ra_ex/²²⁶Ra_ex ratios measured in sinking particles collected in the 1000 m-trap in April and May suggest that barite predominantly formed in the upper water column during that period, while barite found outside the phytoplankton bloom period (February and June) appears to form deeper in the water column. Combining ratios of both the suspended and sinking particles provides information on aggregation/disaggregation processes. High ²²⁶Ra_ex/Ba_ex ratios were also found in suspended particles collected in the upper 500 m of the water column. Because celestite is expected to be enriched in Ra [Bernstein R. E., Byrne R. H. and Schijf J. (1998) Acantharians: a missing link in the oceanic biogeochemistry of barium. Deep-Sea Res. II45, 491-505], acantharian skeletons may contribute to these high ratios in shallow waters. The formation of both acantharian skeletons and barite enriched in ²²⁶Ra may thus contribute to the decrease in the dissolved ²²⁶Ra activity and ²²⁶Ra/Ba ratios of surface waters observed between February and June 2003 at the DYFAMED station.     

Assessment of natural radioactivity in aquifer medium bearing uranium ores in Koprubasi,Turkey

Koprubasi, located within Manisa Province near the Izmir, is the biggest uranium mine where uranium ores originate from Neogene aged altered sandstone and conglomerate layers. The main objective of this study is to determine the radiation hazard associated with radioactivity levels of uranium ores, and the rocks and sediments around Koprubasi. In this regard, measured activity levels of ²²⁶Ra, ²³²Th and ⁴⁰K were compared with world averages. The average activity levels of ²²⁶ Ra, ²³²Th and ⁴⁰K were measured to be 5369.75, 124.78 and 10.0 Bq/kg in uranium ores, 24.32, 52.94 and 623.38 Bq/kg in gneiss, 46.24, 45.13 and 762.26 Bq/kg in sandstone and conglomerate, 73.11, 43.15 and 810.65 Bq/kg in sediments, respectively. All samples have high ²²⁶Ra and ⁴⁰K levels according to world average level. As these sediments are used as construction materials and in agricultural activities within the study area, the radiation hazard are calculated by using dose rate (D), annual effective dose rate (He), radium equivalent activity (Ra_eq) and radiation hazard index (I_yr). All the samples have Ra_eq levels that are lower than the world average limit of 370 Bq/kg. On the other hand, D, He and I_yr values are higher than world average values. These results indicate that the uranium ores in the Koprubasi is the most important contributor to the natural radiation level. The radioactivity levels of sediments and rocks make them unsuitable for use as agricultural soil and as construction materials. Moreover, it is determined that shallow groundwater in sediments and deep groundwater in conglomerate rocks and also surface water sources in the Koprubasi have high ²²⁶Ra content. According to environmental radioactive baseline, some environmental protection study must be taken in Koprubasi uranium site and the environment.     

Evaluation of radiation dose due to naturally occurring radionuclides in rock samples of different origins collected from Azad Kashmir

The state of Azad Kashmir is rich in three types of rocks, namely, sedimentary, metamorphic, and igneous rocks. These rocks contain extensive deposits of graphite, marble, limestone, quartzite, granite, dolerite, and sandstone, which are widely used for the construction of dwellings in Azad Kashmir and Pakistan. Therefore, knowledge about the presence of natural radioactivity in these materials is desirable to assess the radiological hazards associated with it. In this context, 30 rock samples were collected from different geologic formations of the Muzaffarabad Division, Azad Kashmir. After processing the samples, the specific activities of ²²⁶Ra, ²³²Th, and ⁴⁰ K in them were measured using a P-type coaxial high-purity germanium detector. The observed highest dose rate values for sedimentary, metamorphic, and igneous rocks have been found to be 83.16 ± 1.08, 135.87 ± 1.18, and 115.98 ± 1 nGy ⋅ h^–1, respectively. The radium equivalent activity (Ra_eq) varied from 23.76 ± 1.15 for dolerite sample (igneous rock) to 293.69 ± 2.60 Bq ⋅ kg^–1 for marble (metamorphic rock). The Ra_eq values of all rock samples are lower than the limit mentioned in the Organization for Economic Cooperation and Development (OECD, 1979) report (370 Bq ⋅ kg^–1, equivalent to γ-dose of 1.5 mSv ⋅ y^–1). The values of external (H_ex) and internal hazard indices (H_in) are less than unity. The mean outdoor and indoor annual effective dose equivalents are 0.073 mSv ⋅ y^–1 and 0.29 mSv ⋅ y^–1, respectively. The mean (over all types of rock samples) annual effective dose equivalent is reported as 0.36 mSv ⋅ y^–1.     

Raexcess/Ba growth rates and U-Th-Ra-Ba systematic of Baltic Mn/Fe crusts

We analyzed ²³⁸U, ²³⁴U, ²³²Th, ²³⁰Th, and ²²⁶Ra by thermal ionization mass spectrometry (TIMS) and Ba by inductively coupled plasma optical emission spectrometry (ICP-OES) on eight Mn/Fe crusts from the Mecklenburg Bay (SW Baltic) and on one from the Bothnian Bay (N Baltic) to test the ²²⁶Ra_ex/Ba ratio as potential geochronometer. ²²⁶Ra_ex/Ba ratios decrease as a function of depth within the concretions in all analyzed profiles. Calculated diffusion coefficients are relatively low (∼9 · 10⁻⁷ cm²/yr for Ra and 5 · 10⁻⁷ cm²/yr for Ba) and suggest that diffusion is negligible for the Ra and Ba record. In addition, ²²⁶Ra_ex/Ba ages are consistent and independent from the growth rate and growth direction within a crust. Thus, the decline in ²²⁶Ra_ex/Ba ratio is most likely due to radioactive decay of ²²⁶Ra_ex, although the influence of varying oxic conditions has still to be evaluated. ²²⁶Ra_ex/Ba growth rates range from 0.021 to 0.0017 mm/yr and tend to be lower than those calculated and based on stratigraphic methods (1 to 0.013 mm/yr). ²²⁶Ra_ex/Ba ages of concretions from shallow water environment (20 m depth, Mecklenburg Bay/SW Baltic) cover a time interval from 990 ± 140 yr to 4310 ± 310 yr BP corresponding to the stabilization of the sea level close to the present position about 5500 to 4500 yr ago. One sample from greater depth (70 m, Bothnian Bay-/N Baltic) showed a higher ²²⁶Ra_ex/Ba age of 6460 ± 520 yr BP.     

Mineralogy,geochemistry, radioactivity and environmental impacts of Gabal Marwa granites,southeastern Sinai,Egypt

The Gabal Marwa area is located in the southeastern part of Sinai,Egypt.It comprises gneisses and migmatites,granodiorites and monzogranites.Field,petrographic,mineralogic and chemical investigations indicated that the Gabal Marwa granites are classified as granodiorites and monzogranites.The monzogranites constitute the most predominant rock unit exposed in the study area.They have been subjected to hydrothermal alterations,especially along the shear zones.Sericitization,desilicification,nametasomatism and development of spotty or dendritic manganese oxides are the most pronounced alteration features.These alterations resulted in the increase of TiO2,Al2O3,FeOt,MnO,CaO,MgO,Na2O,K2O and Cr,Zr,Rb,Y and Sr and the decrease of SiO2,P2O5,Ni,Zn,Ba and Nb.Radiometric studies indicated that the altered granites belong to high thorium,high uranium granites.The U,Th,U and Th,Th/U,Th and U-K variation diagrams suggested that magmatic processes controlled the distribution of these elements but the effect of hydrothermal alteration processes were clearly distinct.The Scanning Electron Microscope and X-ray Diffraction analyses indicated that the most important radioactive minerals include uranothorite,thorite,zircon,monazite and samarskite.Cinnabar and Mn minerals were also found.From the U,Th,Ra and K activity concentrations obtained for all the studied granitic samples,radium equivalent activity(Raeq),external hazard index(Hex),and internal hazard index(Hin),were calculated to assess the radiation hazard to human beings living in dwellings made of the studied granites.Altered monzogranites have radioactivity above the proposed acceptable level and,therefore,caution must be taken when these granites are used as building materials.     

Determination of natural radioactivity levels in soil and travertine of the region of Tokat and Sivas,Turkey

In this study, the environmental radioactivity measurements for Tokat and Sivas provinces in the northeast of Turkey were performed. Using gamma ray spectrometry, the activity concentrations of natural radionuclides in soil and travertine samples (²³²Th, ²²⁶Ra, and ⁴⁰K) were determined. The annual effective dose equivalent, the absorbed doses rate in air, the radium equivalent, and the external hazard index were obtained from these activities. The activity concentrations vary from 9.09 to 17.04 Bq kg^?1 for ²³²Th, from 36.53 to 76.95 Bq kg^?1 for ²²⁶Ra, and from 216.56 to 576.59 Bq kg^?1 for ⁴⁰K in soil samples. The activity concentrations in travertines vary from 15.99 to 21.01 Bq kg^?1 for ²³²Th, from 19.89 to 67.71 Bq kg^?1 for ²²⁶Ra, and from 179.89 to 314.43 Bq kg^?1 for ⁴⁰K. The average dose rate in air for soil and travertine samples was 43.41 and 41.05 nGy h^?1 respectively. The obtained results are presented and compared with other studies, and the results of this study are lower than the international recommended value (55 nGy h^?1) given by UNSCEAR ( 2000). The results show that the region has a background radiation level within the natural limits.     

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.     

Coupling between Pbex and organic matter in sediments of a nutrient-enriched lake: An example from Lake Chenghai, China

Sediment cores were collected from deep-water areas of Lake Chenghai, China in June 1997. The vertical profile of ¹³⁷Cs activity gives reliable geochronological results. The results also indicate that sediment accumulation rates in deep-water areas of Lake Chenghai were relatively constant in recent decades, averaging 0.43 g cm^− 2 y^− 1, despite a variable organic carbon influx. ²¹⁰Pb_eq (= ²²⁶Ra) activity was relatively constant also, with an average value of 54.3 ± 3.2 Bq kg^− 1. Vertical profiles of ²¹⁰Pb_ex (= ²¹⁰Pb_total − ²²⁶Ra) decreased exponentially, resulting in somewhat lower sediment accumulation rates (0.3 g cm^− 2 y^− 1). These lower rates are likely less reliable, as the relatively large fluctuations in ²¹⁰Pb_ex activities correlate closely to the organic carbon (C_org) content of the sediments. For example, the vertical profile of ²¹⁰Pb_ex activity displays peaks at mass depths of 3.7-4.7 g cm^− 2 (10-12 cm) and 10-11 g cm^− 2(25-28 cm), similar to the maxima in the vertical profile of C_org. This phenomenon must be related to the delivery of particulate organic matter (POM) from the water to the sediments, or to watershed soil erosion. Since the mean atomic ratios of H_org / C_org and C_org / N_org in Lake Chenghai sediments are 5.5 and 7.0, respectively, indicating that POM was predominantly derived from the remains of authigenic algae, this eliminates watershed erosion rates as a primary control on lake sedimentation rates as resolved by ²¹⁰Pb_ex. Sedimentation fluxes (F(C_org)) of particulate organic carbon since 1970 varied between 60 to 160 g m^− 2 y^− 1, and appeared to closely influence variations in ²¹⁰Pb_ex concentrations. For example, sedimentation fluxes of ²¹⁰Pb_ex (F(²¹⁰Pb_ex)) showed maxima in the years 1972-1974 and 1986-1989, likely reflecting historical variations of lake biological productivity or carbon preservation.     

Precise two chronometer dating of Pleistocene travertine: The Th/U and Raex/Ra(0) approach

In order to determine the geochemical evolution of a freshwater limestone cave system located in central Switzerland (Hell Grottoes at Baar/Zug,) young postglacial tufaceous limestone and travertine precipitates were investigated using the ²³⁰Th/²³⁴U ingrowth system. Additional analyses of further radionuclides within the ²³⁸U decay chain, i.e. ²²⁶Ra and ²¹⁰Pb, showed that the Th/U chronometer started with insignificant inherited ²³⁰Th over the entire formation period of the travertine setting (i.e. ²³⁰Th(0)=0). A contribution from detrital impurities with ²³⁰Th/²³⁴U in secular equilibrium could be precisely subtracted by applying isochron dating of cogenetic phases and recently formed travertine. The resulting precise ²³⁰Th/²³⁴U formation ages were found to be consistent with the geological stratigraphy and were furthermore used to demonstrate the applicability of the next geologically important chronometer in the ²³⁸U-decay series, based on decay of excess ²²⁶Ra normalized to the initial, i.e.²²⁶Ra_ex/²²⁶Ra(0). This system is suitable for dating phases younger than 7000 yr when the correction of a detritus component increasingly limits the precision of the ²³⁰Th/²³⁴U chronometer. Analytical solutions of the coupled ²³⁴U/²³⁰Th/²²⁶Ra radionuclide system predicted that the ²²⁶Ra_ex/²²⁶Ra(0) chronometer is independent of the actual ²³⁰Th activity build up from decay of ²³⁴U, if the systems starts with zero inherited ²³⁰Th(0). The data set confirmed this hypothesis and showed furthermore that the initially incorporated ²²⁶Ra excess must have remained almost uniform in all limestone over a period of at least 7000 yr, i.e. 4–5 half-lives of ²²⁶Ra. This is concluded because (i) the ²²⁶Ra_ex/²²⁶Ra(0) ages agreed well with those derived from ²³⁰Th/²³⁴U, (ii) all data plot within uncertainty on the ²²⁶Ra_ex/²²⁶Ra(0) decay curve and (iii) the atomic Ba/Ca ratio was found to be constant in the travertine material independent of the sample ages. Provided that such boundary conditions hold, ²²⁶Ra_ex/²²⁶Ra(0) should be applicable to materials which are suitable for ²³⁰Th/²³⁴U dating in sedimentology and oceanography, i.e. travertine, corals, phosphorites, etc., and should strongly support ²³⁰Th/²³⁴U for samples that have been formed a few thousand years ago.