Thermal neutron fluence from ultra low-level γ-ray spectrometry of spoons activated during the JCO criticality accident at Tokai-mura in 1999

During the JCO-accident in Tokai-mura in 1999, the surrounding village was irradiated by an uncontrolled neutron flux. At some locations in that village, the thermal neutron flux was determined retrospectively by measurement of the very low activity of ⁵¹Cr and ⁶⁰Co in stainless-steel spoons using γ-ray spectrometry in underground laboratories. Activities determined in the HADES underground facility are presented here, together with calibrations performed using a well-defined thermal neutron flux to directly estimate the fluence of thermal neutrons independent of most assumptions. The results show measurable ⁵¹Cr in three samples and ⁶⁰Co in four samples taken from locations at distances of up to 430 m from the accident location despite the elapse of 4 half-lives of ⁵¹Cr before measurement. Effects of air transport of the samples were considered and shown to be negligible.     

Measurements of 60Co in spoons activated by neutrons during the JCO criticality accident at Tokai-mura in 1999

Neutron activated items from the vicinity of the place where the JCO criticality accident occurred have been used to determine the fluence of neutrons around the facility and in nearby residential areas. By using underground laboratories for measuring the activation products, it is possible to extend the study to also cover radionuclides with very low activities from long-lived radionuclides. The present study describes gamma-ray spectrometry measurements undertaken in a range of underground laboratories for the purpose of measuring (60)Co more than 2 years after the criticality event. The measurements show that neutron fluence determined from (60)Co activity is in agreement with previous measurements using the short-lived radionuclides (51)Cr and (59)Fe. Limits on contamination of the samples with (60)Co are evaluated and shown to not greatly affect the utility of neutron fluence determinations using (60)Co activation.     

An elemental rationing technique for assessing concentration data from a complex water system

Water samples have been collected at the surface and bottom layers at 51 locations throughout Chesapeake Bay. The suspended particulate and dissolved fractions of these samples have been analyzed for Cd, Ce, Co, Cu, Fe, Mn, Mo, Ni, Pb, Sc, Sn, Th, U, and Zn using neutron activation analysis and atomic absorption spectrometry. Special chemical procedures were used to preconcentrate the elements of interest in the dissolved samples and separate them from the salt water matrix. The elemental concentrations observed in the dissolved samples were evaluated by direct comparison to those found in coastal seawater; however, the elemental concentrations in the particulate samples (mass per volume of water) were strongly influenced by the total amount of particulate material suspended in the water at time of collection. A double normalization procedure was used to calculate crustal enrichment factors for each sample, and these enrichment factors provided both a means to observe sample-to-sample variations, and also allowed a crude comparison with the natural levels occurring in the earth's crust.     

Radioactivity and elemental analysis in the Ruseifa municipal landfill, Jordan

In this study, a low background gamma-ray spectrometer based on a Hyper Pure Germanium detector was used to determine the activity concentrations of natural radionuclides in soil samples from various locations within the Ruseifa municipal landfill in Jordan. The chemical composition of the samples was also determined using a Wavelength Dispersive X-Ray Fluorescence Spectrometer. The maximum and minimum annual outdoor effective doses were found to be 103 and 36muSva(-1) in the old landfill and Abu-Sayaah village, respectively. The annual outdoor effective dose at the recent landfill site was found to be 91muSva(-1). The annual effective dose equivalents from outdoor terrestrial gamma radiation at the old landfill and the recent landfill were higher than the typical worldwide value of 70muSva(-1). Thus, some remediation of the soils on both old and recent landfills should be considered before any development for public activities. This could be achieved by mixing with clean soil from areas which are known to have lower radiation background. The concentration of heavy metals Zn, Cr, and Ba in the three sites included in this study were found to be higher than the background levels in the soil samples of the control area (Abu-Sayaah village). The enrichment factors for the above three elements were calculated and found to be: complex building site: Zn=2.52 and Ba=1.33; old landfill site: Cr=1.88, Zn=3.64, and Ba=1.26; and recent landfill site: Cr=1.57, Zn=2.19, and Ba=1.28. There was a strong negative correlation between the concentrations of the metallic elements (Mg, Al, Mn, Fe and Rb) and the concentrations of Zn, Ba, and Cr. Moreover, a strong positive correlation was found between Zn, Ba, and Cr. Thus these elements were enriched in the solid waste.     

Fate of 60Co at a sludge land application site

Vertical distributions of (60)Co are determined in soil cores obtained from a 10-ha grassland, where anaerobically digested sludge was applied by surface spraying from 1986 to 1995 on the U.S. Department of Energy's Oak Ridge Reservation. These results, along with historical application records, are used to estimate vertical-migration rates and perform a mass balance. The presence of (60)Co results solely from the sludge-application process. Soil, vegetation, and surface-water samples were collected. Eleven soil cores were sectioned into 3-cm increments and analyzed by gamma-ray spectrometry. No (60)Co was detected in the vegetation or water samples. The downward migration rate of (60)Co in the upper 15cm of soil ranged from 0.50 to 0.73cm/yr. About 98%, 0.020+/-0.011Bq/cm(2), of (60)Co remained in the upper 15cm of soil, which compared favorably with the expected (60)Co activity based on historical records of 0.019+/-0.010Bq/cm(2).     

Assessment of the environmental contamination with long-lived radionuclides around an operating RBMK reactor station

The presence of man-made gamma emitting radionuclides in the region within 32km radius of the Ignalina NPP/Lithuania has been investigated during the period 2001-2004, prior to the closure of the first of the two operating RBMK 1500-type reactors. Gamma spectrometric measurements of various terrestrial and aquatic plants as well as of soil samples showed moderate environmental contamination with the fission product (137)Cs and with the neutron activation products (60)Co and (54)Mn. Traces of the activation products (65)Zn and (110m)Ag were found in the nearest vicinity of the NPP. Activity concentrations were inhomogeneously distributed in the area of interest. Moss and algae samples showed the highest uptake of radionuclides. In addition to the gamma spectrometric measurements, the levels of (14)C were determined in the same bio-indicator samples using accelerator mass spectrometry.     

Kinetics of trace element uptake and release by particles in estuarine waters: effects of pH,salinity, and particle loading

The uptake and release of 109Cd, 51Cr, 60Co, 59Fe, 54Mn, and 65Zn were studied using end-member waters and particles from Port Jackson estuary, Australia. The kinetics of adsorption and desorption were studied as a function of suspended particulate matter (SPM) loading and salinity. Batch experiments showed that the position and slope of the pH edges are dependent on the metal and on the salinity of the water (except for Mn). The general effect of salinity was to move the adsorption edge to higher pH values, with the greatest change being found for Cd. Most of the metals showed relatively simple kinetics with an increase in uptake as a function of time and suspended particle concentrations. The time dependence of Cd uptake was more complex, with an initial adsorption phase being followed by strong mobilization from the suspended sediments, explained by chlorocomplexation and competition with seawater major cations. The reversibility of the sorption decreased in the order Co>Mn>Zn>Cd>Fe>Cr. The percentage of adsorbed metal released in desorption experiments was greater in seawater than freshwater for Cd, Zn, and Co. These results are important in understanding the cycling of pollutants in response to pH, salinity, and particle concentrations in estuarine environments. In addition, they give valuable insight into the important mechanisms controlling the partitioning of heavy metals in the Port Jackson estuary.     

Preliminary evaluation of (135)Cs/(137)Cs as a forensic tool for identifying source of radioactive contamination

Ratios of the fission products (135)Cs and (137)Cs were determined in soil and sediment samples contaminated from three different sources, to assess the use of (135)Cs/(137)Cs as an indicator of source of radioactive contamination. Soil samples from the Chernobyl exclusion zone were found to have to be heavily depleted in (135)Cs ((135)Cs/(137)Cs approximately 0.45), indicative of a high thermal neutron flux at the source. Sludge samples from a nuclear waste treatment pond were found to have a (135)Cs/(137)Cs ratio of approximately 1, whereas sediment collected downstream from a nuclear reactor was highly variable in both (137)Cs activity and (135)Cs/(137)Cs ratio. Comparison of these preliminary results of variability in radiocaesium isotope ratios with reports of Pu isotope ratios suggests (135)Cs/(137)Cs similarly varies with fuel and reactor conditions, and may be used to corroborate other methods of characterizing radioactive contamination.     

Earthquake-related chemical and radioactivity changes of thermal water in Kuzuluk-Adapazan,Turkey

The movements of the North Anatolian Fault Zone (NAFZ) caused two devastating earthquakes within an 87-day interval, epicentered on G?lcük-Izmit (17 August, 1999) and Düzce-Bolu (12 November, 1999). The Kuzuluk geothermal area (KGA) is located in the middle of the epicenters and the distance between the geothermal area and the fault zone is less than 5 km. Hot water samples were collected from two thermal boreholes that supply hot water to the Kuzuluk thermal complex. The water samples taken prior to and after earthquakes were analysed by Neutron Activation and Atomic Absorption Spectroscopy. Particularly, increase in total a and total beta activities, in the content of Pb, Cr, Ni, Cu and decrease in the content of Fe, Zn, Cd, Mn, and Co are significant. The highest values are 75, 35, 12 and 65 ppb for Pb, Cr, Ni and Cu, respectively. The lowest values are 45, 55, 15, 135 and 6 ppb for Fe, Zn, Cd, Mn and Co, respectively.     

Radioactivity and heavy metal composition of Nigerian phosphate rocks: possible environmental implications

Phosphate rock samples collected from the Dange Formation within the Sokoto basin were analyzed for trace element constituents using instrumental neutron activation analysis (INAA) and X-ray fluorescence analysis (XRFA) techniques, while natural activity concentrations due to 235U, 232Th, and 40K were determined by gamma-ray spectrometry. The analytical results show that the average concentrations of some toxic elements (As, Sb, Cr, and Zn) in phosphate rocks are not appreciably different from that in agricultural soils. However the U and Th contents are enriched significantly in comparison. The results were used to assess the environmental toxicity of heavy metals and radiation hazard attributable to the direct application of phosphate rock as fertilizer.     

Fate of Co at a sludge land application site

Vertical distributions of ⁶⁰Co are determined in soil cores obtained from a 10-ha grassland, where anaerobically digested sludge was applied by surface spraying from 1986 to 1995 on the U.S. Department of Energy's Oak Ridge Reservation. These results, along with historical application records, are used to estimate vertical-migration rates and perform a mass balance. The presence of ⁶⁰Co results solely from the sludge-application process. Soil, vegetation, and surface-water samples were collected. Eleven soil cores were sectioned into 3-cm increments and analyzed by gamma-ray spectrometry. No ⁶⁰Co was detected in the vegetation or water samples. The downward migration rate of ⁶⁰Co in the upper 15 cm of soil ranged from 0.50 to 0.73 cm/yr. About 98%, 0.020 ± 0.011 Bq/cm², of ⁶⁰Co remained in the upper 15 cm of soil, which compared favorably with the expected ⁶⁰Co activity based on historical records of 0.019 ± 0.010 Bq/cm².     

Transfer of 137Cs and 60Co from irrigation water to a soil-tomato plant system

An experiment has been performed at the nuclear power plant of Garigliano (Caserta, Italy), aiming at the measurement of transfer factors of 137Cs and 60Co radionuclides from the irrigation water to a soil-plant system, with particular attention to the influence on such transfers of the irrigation technique (ground or aerial). Tomato plants were irrigated weekly with water contaminated with 137Cs and 60Co (about 375 Bq/m2 week), using both irrigation techniques. After 13 weeks, fruits, leaves, stems, roots and soil were sampled, and radionuclide concentrations were measured by high-resolution gamma spectroscopy. It was found that the activity allocated to the plant organs is significantly dependent upon the irrigation technique, amounting to 2.1% and 1.6% of the activity given in the cultivation for aerial treatment and 0.4% and 0.3% for the ground treatment, for 137Cs and 60Co respectively. The activity absorbed by plants is allocated mainly in leaves (> 55%), while less then 10% is stored in the fruits, for both irrigation techniques. Transfer factors (soil-plant and irrigation water-plant) of tomato plants and of weeds have been determined for 137Cs and 60Co, as well as for natural 40K in the soil.     

Heavy metals in water, sediments, plants and fish of Kali Nadi U.P. (India)

The distribution of heavy metals viz., Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn in the water, sediments, plants and fish samples collected from the Kali Nadi (India) have been determined. The studies have shown that there was considerable variation in the concentration of heavy metals from one sampling station to the other which may be due to the variation in the quality of industrial and sewage wastes being added to the river at different places. The orders of the concentration of heavy metals in water, sediments, plants (Eicchornia crassipes) and fish (Heteropnuestes fossilis) were Fe > Zn > Cu > Mn > Cr > Ni > Pb > Co > Cd; Fe > Zn > Mn > Ni > Cr > Co > Cu > Pb > Cd; Fe > Mn > Zn > Cu > Ni > Co > Pb > Cr > Cd and Fe > Zn > Mn > Ni > Pb > Co > Cr > Cu > Cd, respectively.     

Anthropogenic 236U at Rocky Flats,Ashtabula river harbor,and Mersey estuary: three case studies by sector inductively coupled plasma mass spectrometry

236U (t(1/2)=2.3 x 10(7) y) is formed as a result of thermal neutron capture by (235)U. In naturally occurring U ores, where a high neutron flux is present from spontaneous fission of (238)U, (236)U/(238)U atom ratios are approximately 10(-4) ppm. In the natural Earth's crust, unaffected by nuclear fallout, these ratios are expected to be on the order of 10(-8) ppm. Reactor-irradiated U, however, exhibits high (236)U/(238)U atom ratios approaching 10(4) ppm. As a result, the presence of very small quantities of reactor-irradiated U will significantly enhance the "background" (236)U/(238)U atom ratio. When sufficiently elevated (236)U/(238)U ratios are present, the determination of (236)U/(238)U by rapid inductively coupled plasma mass spectrometric (ICPMS) methods is attractive. We have used sector ICPMS at medium resolving power (R=3440) to measure (236)U/(238)U atom ratios with a determination limit of 0.2 ppm. The limiting factors in the measurement are the (235)U(1)H(+) isobar and background signal at m/z 236 arising from the (238)U(+) peak tail. Based upon the analysis of replicates and considerations of possible systematic errors, uncertainties of +/-5% are found for (236)U/(238)U atom ratios of 1-100 ppm. This procedure has been demonstrated in studies of anthropogenic (236)U in the environment at three locations: (a) offsite soils from the vicinity of the Rocky Flats Environmental Technology site (Golden, Colorado, USA); (b) sediments from the Ashtabula River (Ohio, USA); and (c) sediments from the Mersey estuary (Liverpool, UK). In each of these three locations, definite plumes of elevated (236)U/(238)U are identified and characterized. Maximum (236)U/(238)U atom ratios observed in RFETS-vicinity soils, the Ashtabula River, and the Mersey Estuary are 2.8, 140, and 4.4 ppm, respectively.     

Trace elements in fish from the Savannah river near Savannah river nuclear plant

A survey of trace element residues in fish from the Savannah River near Savannah River Nuclear Plant was undertaken in 1982. Fish muscle tissue was incubated by the wet digestion method. Fifteen trace elements were determined by flame atomic absorption spectrophotometry analysi of the digests. It was found that As, Se, Mg, Hg, Ca, Zn, and Fe levels were relatively higher than Pb, Cd, Ni, Co, Cr, and Mn in all fish species. In addition, in all fish species it seems that Pb, Cd, Ni, Co, Cr, and Mn levels were relatively higher than Cs and Cu. Cs and Cu levels were negligible in all fish species analyzed. Trace element levels found in these fish species were not high enough to render them dangerous for human consumption.     

Heavy metals in organisms and sediments from Turkish Coast of the Black Sea, 1997-1998

During the period 1997-1998, macroalgae, sea snail, mussel, fish and sediment samples were collected at different stations of the Turkish Black Sea coast in order to establish the concentration of selected heavy metals. Heavy metals analyzed were Cd, Co, Cr, Ni, Zn, Fe, Mn, Pb and Cu. The results showed that the Turkish Black Sea coast is facing heavy metal pollution. The metal concentrations in macroalgae, sea snail, mussel and sediment samples are very high. However, Cd, Pb and Cu concentrations in anchovy fish decreased, while Co, Fe, Zn, Cr, Mn and Ni contents had changed when compared previous data. The metal levels in macroalgae did not follow the same pattern as concentrations in sediments at the same station. On the other hand, concentrations of Cd, Co, Cr, Zn, Fe, Mn and Cu in sea snail, mussel and fish samples were related to sediment data in the examined stations.     

南昌市街道灰尘重金属时空分布特征及健康风险评估

分析了南昌市夏季和冬季街道104个灰尘样品中的V、Cr、Co、Ni、Cu、Zn、As、Cd和Pb含量，并利用地积累指数（Igeo）计算其污染程度，并参考美国国家环保局(US EPA)推荐的健康风险模型评价灰尘重金属暴露的人体致癌和非致癌风险，通过主成分和相关分析识别南昌市灰尘重金属的可能来源。结果表明：南昌市街道灰尘中重金属Cr、Ni、Cu、Zn、Cd和Pb含量均显著高于江西省土壤背景值，而V、Co和As含量与江西省土壤背景值含量相近。重金属V、Co和As含量无显著季节差异，但冬夏季节含量的空间异质性较高，而Cu在季节和空间分布上均表现出显著的季节差异，其它重金属的高值区均分布在南昌市中心及老工业园附近；Igeo结果表明Cd、Cu、Zn和Cr的污染程度相对较高，而V、As和Co污染程度较轻；重金属3种暴露途径的风险排序为手-口暴露>皮肤接触暴露>呼吸暴露，其中儿童会遭受更大的非致癌风险。除了灰尘As和Cr对儿童的暴露在局部区域HQ和HI值大于1，其它重金属对不同人群的HQ和HI值均小于1。总体而言，南昌市灰尘重金属的致癌风险CR均在安全阈值范围内，大小排序为Cr > As > Co > Ni > Cd。南昌市灰尘重金属的来源广泛，其中As、Co和V主要来源于岩石风化，其它重金属元素主要来源于交通和工业等人类活动。 关键词： 街道灰尘；重金属；时空分布；健康风险；南昌市     

Radioecological investigations in shallow bays of the Novaya Zemlya Archipelago in 2002-2005

The results of a survey of underwater disposal sites of potentially hazardous objects in the Kara Sea and Oga, Tsivolky, Stepovoy and Abrosimov Bays are presented. Radionuclide levels were determined, using gamma-spectrometric and radiochemical methods, in zones near to and remote from buried solid radioactive waste in the outer and inner parts of the Bays. At the repository of the solid radioactive waste containers in the inner part of the Stepovoy Bay and Abrosimov Bay, higher than background concentrations of (137)Cs were determined in samples of bottom sediments. At one of the sites located in the Stepovoy Bay (137)Cs and (60)Co were detected.     

Exposure to heavy metals and PCDD/Fs by the population living in the vicinity of a hazardous waste landfill in Catalonia, Spain: Health risk assessment

Most fly ashes produced in municipal waste incinerators of Catalonia (Spain) are deposited in a hazardous waste landfill (HWL) placed in Castellolí (Barcelona). This facility means a concern for the population living nearby. In response to this, we performed a probabilistic study focused on assessing human health risks derived from environmental exposure to heavy metals and polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) around the HWL. Concentrations of various metals and PCDD/Fs were determined in soil and air samples collected at the HWL, and in 4 locations around it. Health risks were evaluated according to the distance from the sampling locations to the HWL (near and far-sites). In general terms, metal and PCCD/F levels were relatively low in air and soil samples. However, concentrations of PCDD/Fs, as well as those of some metals, were found to be relatively higher in the HWL and Castellolí (the nearest village) samples than in those collected far away, resulting in a slight increase of exposure to those pollutants. Anyhow, the current concentrations of metals and PCDD/Fs suggest that it is highly unlikely that there are any additional non-carcinogenic and carcinogenic risks for the population living near the HWL.     

Environmental geochemistry and pollution studies of Aliaga metal industry district

The Aliaga metal industry district located 50 km northwest of Izmir City, in Turkey, includes many metal factories. The geology of the area is represented by Mesozoic flysch deposits and Cenozoic volcano sedimentary rocks. Tectonic elements are NE-SW and NW-SE trending faults and a W-NW trending fault direction that is important for water supply. Rock, soil, stream sediment, and water samples taken at various distances from the industrial area were analyzed for Fe, Ti, Mn, Cr, Pb, Cu, Ni, Zn, and Mo. According to the results, the elements in rocks are reasonable for the range of "Clarke" values, but in the soils and stream sediment, they comprise higher values than are acceptable for agricultural activities. Toxicity analyses were carried out in the drinking artesian water of Cakmakli village and wastewater samples of the factories and river water both of which are used for irrigation of the agricultural areas in and around the investigated area. The people should, however be made aware that this waste and river water is unacceptable for agriculture. Additionally, the contamination of seawater in Nemrut Bay is probably caused by contaminated river and underground water running to the sea. The chemical and toxicity analysis of drinking water samples show that they are above accepted standards and harmful. Previous air pollution studies (funnel gas emission analyses) also show that gas emission contains high amount of dust particles with high Fe, Zn, Pb, and Cu concentrations. As a result, all elements analyzed are of great importance relative to problems concerning contamination of the soil, stream sediment, ground surface water, and air by individual metals from uncontrolled processing of some metal factories.