A commonly reported challenge of using Google Search to identify studies for a systematic review is the high number of results retrieved. Thus, \'stopping rules\' are applied when screening, such as screening only the first 100 results. However, recent evidence shows that Google Search estimates a much higher number of results than the viewable number, raising the possibility of exhaustive screening. This study aimed to provide further evidence on the feasibility of screening search results from Google Search exhaustively, and to assess the desirability of this in terms of identifying studies for a systematic review. We conducted a cross-case analysis of the search results of eight Google Search searches from two systematic reviews. Feasibility of exhaustive screening was ascertained by calculating the viewable number of results. Desirability was ascertained according to: (1) the distribution of studies within the results, irrespective of relevance to a systematic review; (2) the distribution of studies which met the inclusion criteria for the two systematic reviews. The estimated number of results across the eight searches ranged from 342,000 to 72,300,000. The viewable number ranged from 272 to 364. Across the eight searches the distribution of studies was highest in the first 100 results. However, the lowest ranking relevant studies were ranked 227th and 215th for the two systematic reviews. One study per review was identified uniquely from searching Google Search, both within the first 100 results. The findings suggest it is feasible and desirable to screen Google Search results more extensively than commonly reported.

This study aimed to evaluate the radiological hazards of uranium (238U), thorium (232Th), and potassium (40K) in microgranitic rocks from the southeastern part of Wadi Baroud, a northeastern desert of Egypt. The activity concentrations of the measured radionuclides were determined by using a gamma-ray spectrometer (NaI-Tl-activated detector). The mean (238U), (232Th), and (40K) concentrations in the studied rocks were found to be 3680.3, 3635.2, and 822.76 Bq/kg, respectively. The contents in these rocks were elevated, reaching up to 6.3 wt%. This indicated the alkaline nature of these rocks. The high ratios of Th/U in the mineralized rocks could be related to late magmatic mineralization, suggesting the ascent of late magmatic fluids through weak planes such as faults and the contact of these rocks with older granites. The present data were higher than those of the United Nations Scientific Committee on the Effects of Atomic Radiation (UNSCEAR) guideline limits. All the radiological hazard results indicated high human health risks. This confirmed that this area is not radiologically safe, and care must be taken when working in this area. This study showed that the area under investigation had high U content suitable for uranium extraction that could be used in the nuclear fuel cycle.

BACKGROUND: Thorium is ubiquitous in the environment and its relationship with birth defects is still under discussion. This study aimed to investigate the associations of maternal exposure to thorium with risk of neural tube defects (NTDs) by using a case-control study, as well as the relationship between thorium exposure and the indoor air pollution from coal combustion.
METHODS: This study was conducted in 11 local healthcare hospitals during 2003-2007 in Shanxi and Hebei provinces, China. A total of 774 mothers were included as participants who delivering 263 fetuses with NTDs including 123 with anencephaly, 115 with spina bifida, 18 with encephalocele, and 7 other NTD subtypes (cases), and 511 health fetuses without NTDs (controls). Their hair samples were collected as close as to the occipital posterior scalp, of which those grew from 3 months before to 3 months after conception was cut to measure the thorium concentration by inductively coupled plasma-mass spectrometry.
RESULTS: We found a higher hair thorium concentration in the total NTD cases with 0.901 (0.588-1.382) ng/g hair [median (inter-quartile range)] than that in the controls with a value of 0.621 (0.334-1.058) ng/g hair. Similar results were found for the three concerned NTD subtypes. Maternal hair thorium concentration above its median of the controls was associated with an increased risk of the total NTDs with an adjusted odds ratio of 1.80 [95% confidence interval (CI), 1.23-2.63)] by adjusting for all confounders. There was obvious dose-response relationship between maternal hair thorium concentration and the risk of total NTDs, as well as their two subtypes (i.e. anencephaly and spina bifida). Maternal hair thorium concentration was positive associated with their exposure level to indoor air pollution from coal combustion during cooking.
CONCLUSIONS: Overall, our findings revealed that maternal periconceptional thorium exposure was associated with the risk of NTDs in North China. Reducing the coal usage in the household cooking activities may decrease maternal thorium exposure level.

The structural characterisation of actinide nanoparticles (NPs) is of primary importance and hard to achieve, especially for non-homogeneous samples with NPs less than 3 nm. By combining high-energy X-ray scattering (HEXS) and high-energy-resolution fluorescence-detected X-ray absorption near-edge structure (HERFD XANES) analysis, we have characterised for the first time both the short- and medium-range order of ThO2 NPs obtained by chemical precipitation. By using this methodology, a novel insight into the structures of NPs at different stages of their formation has been achieved. The pair distribution function revealed a high concentration of ThO2 small units similar to thorium hexamer clusters mixed with 1 nm ThO2 NPs in the initial steps of formation. Drying the precipitates at around 150 °C promoted the recrystallisation of the smallest units into more thermodynamically stable ThO2 NPs. HERFD XANES analysis at the thorium M4 edge, a direct probe for f states, showed variations that we have correlated with the breakdown of the local symmetry around the thorium atoms, which most likely concerns surface atoms. Together, HEXS and HERFD XANES are a powerful methodology for investigating actinide NPs and their formation mechanism.

The study estimated the radiological exposure levels in a mining area for miners in the Beylikova-Sivrihisar (Turkey) complex ore site containing 238U, 226Ra and 232Th. Sixty samples were collected from the study area based on a geologic map. The radionuclide activities were measured using a 78.5% efficient n-type HPGe detector. The measured mean activities were 1871 ± 38 Bq kg-1 for 238U, 1749 ± 5 Bq kg-1 for 226Ra, 3467 ± 9 Bq kg-1 for 232Th and 309 ± 2 Bq kg-1 for 40K. From the measured results, the external effective dose was calculated to be max. 3.80 ± 0.03 mSv y-1 (mean: 2.04 ± 0.03 mSv y-1) for inside gallery and max. 7.59 ± 0.05 mSv y-1 (mean: 4.08 ± 0.05 mSv y-1) for outdoor. Additionally, the external exposure index was calculated to be Hex = 33.5 ± 0.2(mean: 18.2 ± 0.3) and internal exposure index to be Hin = 45.9 ± 0.3 (mean: 22.9 ± 0.4). The results indicate that additional radiation protection measures should be taken during the mining process if an opencast mining is implemented in Beylikova complex ore deposit.

The electrophoretic mobility change of desferrioxamine B (DFO) was monitored by UV absorption spectrophotometry upon increasing the thorium(IV) concentration in the background electrolyte at two acidities ([HClO4 ]Tot = 0.0316 and 0.0100 M). These data enabled to assess the speciation model and to determine the equilibrium constant of [Th(DFO)H2 ]3+ at fixed ionic strength (I = 0.1 M (H,Na)ClO4 ). Affinity capillary electrophoresis (ACE) turned out to be most helpful in identifying the complexed species by ascertaining its charge and protonation state. The assignment of the correct stoichiometry relied on the reliable estimation of the electrophoretic mobility by assuming similar hydrodynamic radii for (DFO)H4 + and the chelate. The value of the apparent equilibrium constant (log β112 = 38.7 ± 0.4) obtained by ACE compares favorably well with those reported in the literature for thorium and a range of other metal ions, according to a linear free-energy relationship. This method is useful for studying metal-ligand binding equilibria and provides valuable information for further modelling the behavior of tetravalent actinides under environmental conditions. Structural information about the prevalent solution species in acidic conditions was gained by DFT calculations, confirming the bishydroxamato coordination mode of Th4+ by the diprotonated ligand.

The use of uranium and to a minor extent plutonium as fuel for nuclear energy production or as components in military applications is under increasing public pressure. Uranium is weakly radioactive in its natural isotopy but its chemical toxicity, combined with its large scale industrial utilization, makes it a source of concern in terms of health impact for workers and possibly the general population. Plutonium is an artificial element that exhibits both chemical and radiological toxicities. So far, uranium (under its form uranyl, U(vi)) or plutonium (as Pu(iv)) decorporation or protecting strategies based on molecular design have been of limited efficiency to remove the actinide once incorporated after human exposure. In all cases, after human exposure, plutonium and uranium are retained in main target organs (liver, kidneys) as well as skeleton although they exhibit differences in their biodistribution. Polymers could represent an alternative strategy as their tropism for specific target organs has been reported. We recently reported on the complexation properties of methylcarboxylated polyethyleneimine (PEI-MC) with uranyl. In this report we extend our work to methylphosphonated polyethyleneimine (PEI-MP) and to the comparison between actinide oxidation states +IV (thorium) and +VI (uranyl). As a first step, thorium (Th(iv)) was used as a chemical surrogate of plutonium because of the difficulty in handling the latter in the laboratory. For both cations, U(vi) and Th(iv), the uptake curve of PEI-MP was recorded. The functionalized PEI-MP exhibits a maximum loading capacity comprised of between 0.56 and 0.80 mg of uranium (elemental) and 0.15-0.20 mg of thorium (elemental) per milligram of PEI-MP. Complexation sites of U(vi) and Th(iv) under model conditions close to physiological pH were then characterized with a combination of Fourier transform Infra Red (FT-IR) and Extended X-Ray Absorption Fine Structure (EXAFS). Although both cations exhibit different coordination modes, similar structural parameters with phosphonate functions were obtained. For example, the coordination sites are composed of fully monodentate phosphonate functions of the polymer chains. These physical chemical data represent a necessary basic chemistry approach before envisioning further biological evaluations of PEI-MP polymers towards U(vi) and Pu/Th(iv) contamination.

This study compares high resolution forward models of natural gamma-ray background with that measured by high resolution aerial gamma-ray surveys. The ability to predict variations in natural background radiation levels should prove useful for those engaged in measuring anthropogenic contributions to background radiation for the purpose of emergency response and homeland security operations. The forward models are based on geologic maps and remote sensing multi-spectral imagery combined with two different sources of data: 1) bedrock geochemical data (uranium, potassium and thorium concentrations) collected from national databases, the scientific literature and private companies, and 2) the low spatial resolution NURE (National Uranium Resource Evaluation) aerial gamma-ray survey. The study area near Cameron, Arizona, is located in an arid region with minimal vegetation and, due to the presence of abandoned uranium mines, was the subject of a previous high resolution gamma-ray survey. We found that, in general, geologic map units form a good basis for predicting the geographic distribution of the gamma-ray background. Predictions of background gamma-radiation levels based on bedrock geochemical analyses were not as successful as those based on the NURE aerial survey data sorted by geologic unit. The less successful result of the bedrock geochemical model is most likely due to a number of factors including the need to take into account the evolution of soil geochemistry during chemical weathering and the influence of aeolian addition. Refinements to the forward models were made using ASTER visualizations to create subunits of similar exposure rate within the Chinle Formation, which contains multiple lithologies and by grouping alluvial units by drainage basin rather than age.

A calculation model for determining the indoor dose due to building materials with significant concentration of radioactivity has been applied to the case study of ceramic tiles; the model allows the contribution of bearing walls and wall covering materials to be calculated. The model is implemented in FORTRAN 77 and provides a quantification of the gamma radiation field (in terms of external dose rate in air, nGyh-1) inside a room with known dimensions. Application model results have been validated both by comparison with the results obtained by other authors and by experimental measurements. Model sensitivity and performances have been analysed and lastly the case studies focused on ceramic tiles have been proposed.

Dust storms in the Middle East are common during spring. Some of these storms are massive and carry a large amount of dust from faraway regions, which pose health and pollution risks. The huge dust storm event occurred in early May, 2012 was investigated for its radioactive content using gamma ray spectroscopy. Dust samples were collected from Northern Jordan and it was found that the storm carried a large amount of both artificial and natural radioactivity. The average activity concentration of fallout (137)Cs was 17.0 Bq/kg which is larger than that found in soil (2.3 Bq/kg), and this enrichment is attributed to particle size effects. (7)Be which is of atmospheric origin and has a relatively short half-life, was detected in dust with relatively large activity concentrations, as it would be expected, with an average of 2860 Bq/kg, but it was not detected in soil. Despite the large activity concentration of (7)Be, dose assessment showed that it does not contribute significantly to the effective dose through inhalation. The concentrations of the primodial nuclides (40)K, (232)Th and (238)U were 547, 30.0 and 49.3 Bq/kg, respectively. With the exception of (40)K, these were comparable to what was found in soil.