Hg and 210Po in consumed fish of the Tadjoura Gulf (Djibouti): Levels and human health risk assessment.

Hg and 210Po were measured in the muscle tissue of commercially important fish species collected in the main coastal cities of the Djiboutian coast (Tadjoura Gulf) to evaluate the potential risk associated with their consumption. The levels of Hg among the different species ranged from 0.02 to 1.69 mg/kg w.w and exceeded tolerable limits as reported by the national regulation (2000-0727/PR/MAEM) and the Codex Alimentarius. The probabilistic distributions of health hazard were evaluated through Monte-Carlo simulation, which confirmed the carcinogenic risk from Hg. The levels of 210Po ranged from 4.1 to 134.5 Bq/kg w.w among muscle tissues of the eight commercially important species. The carcinogenic risk was in an unacceptable range and simulation revealed that children were the most vulnerable population. The results obtained confirms that the health impact is reduced when consuming two servings per week.

Tracing the upwelling process in the northern Benguela upwelling system (nBUS) by 129I.

New data on the presence of 129I in seawater in the Southern Hemisphere measured by Accelerator Mass Spectrometry (AMS) is presented. The samples were collected in 2014 along the Namibian coast during a cruise organised by the National Marine Information and Research Centre (NatMIRC), the national laboratories of the Ministry of Fisheries and Marine Resources (MFMR) in Namibia, and the IAEA Environment Laboratories (IAEA NAEL) in Monaco. The Benguela upwelling system is known as one of the most important marine upwelling regions in the world. Strong winds induce an offshore transport of surface seawater which is substituted by cool subsurface water inshore. As this water is nutrient-rich, which leads to high primary productivity, the Benguela upwelling system has a very important role as a fishing production area. The 129I concentrations in samples were between (0.66 ± 0.14) × 107 and (1.45 ± 0.30) × 107 atoms/kg. The highest 129I concentrations were found in the offshore surface samples. Deep-sea and inshore samples contained lower 129I concentrations, possibly as an effect of the upwelling process. A comparison with previously published studies suggests that the presence of 129I in the northern Benguela upwelling system (nBUS), is mainly due to the impact of nuclear weapons global fallout, without any evident impact of nuclear fuel reprocessing.

Presence of 236U and 237Np in a marine ecosystem: The northern Benguela Upwelling System, a case study.

The Benguela Upwelling System (BUS), off the south-western African coast, is one of the four major eastern boundary upwelling ecosystems in the oceans. However, this area has been overlooked in the field of environmental radioactivity. In this work, 236U and 237Np were collected off the coast of Namibia within the northern BUS. Surface seawater exhibited similar 236U and 237Np concentrations, ranging from 3.9·106 to 5.6·106 atoms kg-1 and from 4.6·106 to 8.5·106 atoms kg-1, respectively. The observed inventories in a water column from the continental margin, of (2.10 ± 0.11)·1012 atoms m-2 for 236U and (3.48 ± 0.13)·1012 atoms m-2 for 237Np, were in agreement with the global fallout (GF) source term in the Southern Hemisphere that was the main source of actinides to the region. A pattern was observed in the surface samples, with 237Np concentrations that decreased by 25-30% when moving from inshore to offshore stations, but such an effect could not be clearly discerned in the case of 236U within the data uncertainties. An explanation based on the larger particle reactivity of GF 237Np compared to GF 236U was proposed. Such an effect would have been important at the studied site due to the enhance presence of particles in the continental shelf triggered by the upwelling phenomenon. A value of 1.77 ± 0.20 was obtained for the 237Np/236U atom ratio for the GF source term in the marine environment.

First assessment on trace elements in sediment cores from Namibian coast and pollution sources evaluation.

Trace elements (TEs), Rare Earth Elements (REEs) and Pb isotope ratios were determined in six small cores sampled along the Namibian coast and different indices, such as Enrichment Factor, Geo-accumulation Index and Pollution load index, were calculated to evaluate possible metal contamination in the area. Concentrations of Pb, Cu, As and Cd were strongly enhanced at the upper 7 cm of core C5, which is located at Walvis Bay, at the major harbor and urban/industrial center of Namibia, indicating the impact from the recent anthropogenic activities. Principal Component Analysis was applied to the data set indicating possible common sources of the contaminants. Pb stable isotope ratios, combined with the dating of core C5 at Walvis Bay, further confirmed the anthropogenic provenance of Pb sources in the recent sediment deposits, which occurred after 1945, when the anthropogenic activities in the area began to increase. REEs profiles were also determined, showing enrichment in REEs for some of the samples, typical for the minerals present in the area. Ce anomaly was detected in one of the cores but the REEs profile did not reveal anomalies ascribable to anthropogenic influence.

Baseline study on trace and rare earth elements in marine sediments collected along the Namibian coast.

Namibia is a fast-growing country with extensive mineral extraction activities used in diamond, fluorspar, uranium, and metals production. To assess the impact of land based human activities on the Namibian coastal marine environment, 25 elements were analyzed in 22 surface sediments samples collected along the coast. After applying a variety of pollution assessment indices (Enrichment Factor, Igeo and Pollution Load Indexes) was concluded that As, Cd and Sb were considerably enriched in the sediments from several sites, while Cu, Pb and Zn showed very high enrichment near the Walvis Bay harbor. Pearson's correlation and Principal Component Analysis were used to investigate common metal sources. Additionally, the determination of Pb isotope ratios confirmed the contribution of land based human activities at Walvis Bay and Lüderitz as sources of pollution. The analysis of REEs did not reveal any important enrichment due to anthropogenic activities, but provides a needed baseline for further investigations.

Investigation of key factors in preparation of alpha sources by electrodeposition.

The electrodeposition for alpha source preparation, using several electrolyte solution-cathode material combinations, is investigated and evaluated. The investigated factors focused on the electrodeposition time, the applied current, electrolyte volume and anode-cathode distances for the conventional electrodeposition cell (with no external stirring or cooling system). The conditions (temperature and the solution pH) during the electrodeposition process were also studied and discussed. The optimized parameters for each system are provided, and evaluated for the usage in determination of actinides (uranium, plutonium, americium and curium radioisotopes) in various samples.

RADIONUCLIDE AND MAJOR ELEMENT ANALYSIS OF THERMAL AND MINERAL WATERS IN CROATIA WITH A RELATED DOSE ASSESSMENT.

Major elements concentrations (Na, K, Ca, Mg) and the activity concentrations of 226,228Ra, 234,238U, 210Po, 210Pb, 40K and 137Cs in northern and eastern Croatian thermal and mineral waters, collected directly from springs (or wells), are presented herein with total effective doses assessed for those waters that are considered as drinking 'cures' and are available for consumption. The methods used for radionuclide determination included alpha-particle spectrometry, gas-proportional counting and gamma-ray spectrometry, while the major element composition was determined by ICP-MS. The activity concentrations of all of the radionuclides were found to be below the guidance levels set by the WHO and EC Directive, with the exception of one water sample that measured 0.26 Bq L-1 of 228Ra. The effective ingestion dose assessment for the consumption of the so-called water 'cures' during 1, 2 or 4 weeks' time period throughout 1 year was well below the recommended 0.1 mSv for drinking water.

Evaluation of several electrolyte mixture-cathode material combinations in electrodeposition of americium radioisotopes for alpha-spectrometric measurements.

Three different types of electrolytes, subsequently modified and adjusted, in combination with three cathode materials used as source backings were analysed for electrodeposition of americium isotopes for alpha-spectrometric measurements. The obtained results are discussed in terms of electrodeposition yield and source quality (source homogeneity and spectral resolution, FWHM). The optimal conditions for source preparation are provided.

Mussels (Mytilus galloprovincialis) as a bio-indicator species in radioactivity monitoring of Eastern Adriatic coastal waters.

Croatian Adriatic coastal waters are systematically monitored within the Mediterranean Mussel Watch Project using mussels (Mytilus galloprovincialis) as a bio-indicator species. The study includes determination of naturally occurring ((7)Be, (40)K, (232)Th, (226)Ra and (238)U), as well as anthropogenic (137)Cs radionuclides. Activity concentrations in dry weight of mussels' soft tissue along the Croatian Adriatic coast are presented, with spatial and seasonal variations given and discussed. Samples were collected in spring and autumn for the period between 2009 and 2013. Radionuclides were determined by gamma-ray spectrometry. Activity concentrations of (7)Be were the highest in spring periods, especially in the areas with significant fresh water discharges. Activity concentrations of (40)K did not vary significantly with season or location. (137)Cs activities were low, while (232)Th, (226)Ra and (238)U activities were mostly below the detection limit of performed gamma-spectrometric measurement.

Levels of major and trace elements, including rare earth elements, and ²³8U in Croatian tap waters.

Concentrations of 46 elements, including major, trace, and rare earth elements, and (238)U in Croatian tap waters were investigated. Selected sampling locations include tap waters from various hydrogeological regions, i.e., different types of aquifers, providing insight into the range of concentrations of studied elements and (238)U activity concentrations in Croatian tap waters. Obtained concentrations were compared with the Croatian maximum contaminant levels for trace elements in water intended for human consumption, as well as WHO and EPA drinking water standards. Concentrations in all analyzed tap waters were found in accordance with Croatian regulations, except tap water from Sibenik in which manganese in concentration above maximum permissible concentration (MPC) was measured. Furthermore, in tap water from Osijek, levels of arsenic exceeded the WHO guidelines and EPA regulations. In general, investigated tap waters were found to vary considerably in concentrations of studied elements, including (238)U activity concentrations. Causes of variability were further explored using statistical methods. Composition of studied tap waters was found to be predominately influenced by hydrogeological characteristics of the aquifer, at regional and local level, the existing redox conditions, and the household plumbing system. Rare earth element data, including abundances and fractionation patterns, complemented the characterization and facilitated the interpretation of factors affecting the composition of the analyzed tap waters.

Radiological characterization of tap waters in Croatia and the age dependent dose assessment.

Activity concentrations of (234)U, (238)U, (226)Ra, (228)Ra, (210)Po and (210)Pb in tap waters, originating from various geological regions of Croatia, were determined. Activity concentrations of measured radionuclides are in general decreasing in this order: (238)U≈(234)U>(228)Ra≈(210)Pb>(226)Ra≈(210)Po. Based on the radionuclide activity concentrations average total annual internal doses for infants, children and adults, as well as contribution of each particular radionuclide to total dose, were assessed and discussed. The highest doses were calculated for infants, which makes them the most critical group of population. All values for each population group were well below the recommended reference dose level (RDL) of 0.1mSv from one year's consumption of drinking water according to European Commission recommendations from 1998. Contribution of each particular radionuclide to total doses varied among different age groups but for each group the lowest contribution was found for (226)Ra and the highest for (228)Ra.

Seasonal and spatial variations of 210Po and 210Pb activity concentrations in Mytilus galloprovincialis from Croatian coast of the Adriatic Sea.

Results of 2 years monitoring of (210)Po and (210)Pb activity concentrations in soft tissue of the species Mytilus galloprovincialis from Croatian part of the Adriatic coast are presented. The samples were collected at thirteen coastal stations (some of which are also a part of the Mediterranean Mussel Watch Project) in spring and autumn of 2010 and 2011. The collected mussels were ranging between 4 cm and 6 cm in shell length. After sample pre-treatment lead and polonium were radiochemically separated on Sr resin. (210)Po was determined by alpha-particle spectrometry and (210)Pb was determined, via (210)Bi, by a low-level gas proportional counter. The results of (210)Po activity concentrations were found to vary between (104±11) and (1421±81) Bq kg(-1) dry weight while (210)Pb activity concentrations were much lower and in range (8.2±5.3)-(94.1±29.8) Bq kg(-1) dry weight. Higher (210)Po and (210)Pb activity concentrations were determined in spring period. The inter-site differences seen in their activity concentrations can be due to natural background levels of sites. The (210)Po/(210)Pb activity concentration ratios in all cases exceeded unity for all mussel samples and ranged between 4.0 and 47.9.

Sequential separation of Fe and Sr from liquid samples by using Sr resin and rapid determination of 55Fe and (89,9°)Sr.

The obtained results showed that the Sr resin can be used for the chromatographic separation of Fe (III) and Sr (II) ions by using a mixture of HCl and HNO3. It was shown that the binding strength of Fe (III) decreases with increasing concentration of HNO3 while the binding strength of Sr (II) increases. It was found that the optimal bonding strength is achieved in 6 mol/L HCl:3 mol/L HNO3 and varying concentrations of acid in the mixture allow their selective separation. On basis of these results, a method for the separation of (55)Fe and (89,90)Sr from liquid samples which consists of binding of Fe and Sr on Sr resin and separation from a number of elements by 6 mol/L HCl:3 mol/L HNO3 and their mutual separation by eluting of Sr with 4 mol/L HCl is established. The method enables efficient simultaneous separation (with high recovery) of (89,90)Sr and (55)Fe and in combination with Cerenkov counting rapid determination of (89,90)Sr.

Natural radionuclides in bottled drinking waters produced in Croatia and their contribution to radiation dose.

Activity concentrations of (234)U, (238)U, (226)Ra, (228)Ra, (210)Po and (210)Pb in all Croatian bottled drinking natural spring and natural mineral water products, commercially available on the market, were determined. The samples originated from various geological regions of Croatia. Activity concentrations of measured radionuclides are in general decreasing in this order: (234)U>(238)U>(226)Ra>(228)Ra>(210)Pb>(210)Po and (226)Ra>(228)Ra>(234)U>(238)U>(210)Pb>(210)Po for natural spring and mineral waters, respectively. Based on the radionuclide activity concentrations average total annual effective ingestion doses for infants, children and adults, as well as contribution of each particular radionuclide to total dose, were assessed and discussed. The highest doses were calculated for children from 7 to 12 years of age, which makes them the most critical group of population. All values for each type of water, as well as for each population group, were well below the recommended reference dose level (RDL) of 0.1 mSv from one year's consumption of drinking water according to the European Commission recommendations from 1998. Contribution of each particular radionuclide to total doses varied among different water types and within each water type, as well as between different age groups, where the lowest contribution was found for uranium isotopes and the highest for (228)Ra.

(210)Po and (210)Pb activity concentrations in Mytilus galloprovincialis from Croatian Adriatic coast with the related dose assessment to the coastal population.

Activity concentrations of (210)Po and (210)Pb in the species Mytilus galloprovincialis from Croatian Adriatic coast were determined. The samples were collected in thirteen sampling places which are also a part of Croatian Mediterranean mussel watch project. The results of (210)Po and (210)Pb activity concentrations were found to vary between (22.1±2.5)-(207±21) Bq kg(-1) fresh weight and (2.8±1.4)-(9.3±0.7) Bq kg(-1) fresh weight, respectively. (210)Po/(210)Pb ratio ranged between 6.2 and 30.7. The highest measured activities were found in the enclosed basins of the Neretva channel, where the majority of Croatian mussel cultivation is taking place. The estimated consequent average total annual effective ingestion dose due to (210)Po and (210)Pb from mussel consumption in Croatian coastal region is 202±99 µSv with 96% contribution of (210)Po to the total effective dose.

Determination of uranium and thorium in complex samples using chromatographic separation, ICP-MS and spectrophotometric detection.

The paper describes a research of possible application of UTEVA and TRU resins and anion exchanger AMBERLITE CG-400 in nitrate form for the isolation of uranium and thorium from natural samples. The results of determination of distribution coefficient have shown that uranium and thorium bind on TRU and UTEVA resins from the solutions of nitric and hydrochloric acids, and binding strength increases proportionally to increase the concentration of acids. Uranium and thorium bind rather strongly to TRU resin from the nitric acid in concentration ranging from 0.5 to 5 mol L(-1), while large quantities of other ions present in the sample do not influence on the binding strength. Due to the difference in binding strength in HCl and HNO(3) respectively, uranium and thorium can be easily separated from each other on the columns filled with TRU resin. Furthermore, thorium binds to anion exchanger in nitrate form from alcohol solutions of nitric acid very strongly, while uranium does not, so they can be easily separated. Based on these results, we have created the procedures of preconcentration and separation of uranium and thorium from the soil, drinking water and seawater samples by using TRU and UTEVA resins and strong base anion exchangers in nitrate form. In one of the procedures, uranium and thorium bind directly from the samples of drinking water and seawater on the column filled with TRU resin from 0.5 mol L(-1) HNO(3) in a water sample. After binding, thorium is separated from uranium with 0.5 mol L(-1) HCl, and uranium is eluted with deionised water. By applying the described procedure, it is possible to achieve the concentration factor of over 1000 for the column filled with 1g of resin and splashed with 2L of the sample. Spectrophotometric determination with Arsenazo III, with this concentration factor results in detection limits below 1 microg L(-1) for uranium and thorium. In the second procedure, uranium and thorium are isolated from the soil samples with TRU resin, while they are separated from each other on the column filled with anion exchanger in alcohol solutions. Anion exchanger combined with alcohol solutions enables isolation of thorium from soil samples and its separation from a wide range of elements, as well as spectrophotometric determination, ICP-MS determination, and other determination techniques.