Artificial radionuclides in sediment of the Yenisei River

Releases from the nuclear facility Mining-and-Chemical Combine (MCC) located at Zheleznogorsk have contributed to the radionuclide contamination of the Yenisei River since operations commenced in 1958. The aim of this study was to assess the activity concentrations of artificial radionuclides and the strength of their binding in Yenisei River sediments. Investigation of Yenisei River sediment samples revealed the presence of artificial radionuclides typical of the MCC radioactive discharge: namely, isotopes of europium, caesium, ⁶⁰Co and transuranium elements. The concentrations of artificial radionuclides in the sediment layers remain relatively high as far as 200 km downstream of the MCC. In sediment cores collected upstream of the MCC, γ-spectrometric measurements registered only one artificial radionuclide, ¹³⁷Cs, with a maximal activity of 8 Bq·kg^?1. Sequential extraction performed on samples of the upper layers of the sediment core showed different degrees of potential environmental availability for artificial radionuclides: the highest was recorded for ²⁴¹Am and ¹⁵²Eu (up to 85% of initial activity), followed by ⁶⁰Co (up to 32%), and finally, ¹³⁷Cs (up to 15%). In a few samples, ²⁴¹Am was present in the unextractable form, which may be accounted for by the presence of reactor fuel microparticles.     

Geochemical Associations of Sellafield-Derived Radionuclides in Saltmarsh Deposits of the Solway Firth

This paper describes a study of the geochemical associations of Sellafield waste radionuclides in saltmarsh sediments from south-west s]Scotland. The contaminant radionuclides are transported to this environment in association with particulate material and ¹³⁷Cs was found to be predominantly (80-98%) non-extractable. In the case of ^239+240Pu there was a redistribution from the oxalate extractable oxide fraction to the pyrophosphate extractable organic fraction as a consequence of on-shore transfer of contaminated sediment. The relatively aggressive nature of the chemical extractants required to remove the radionuclides from the sediments suggests that they were in a form which was unlikely to result in their being released into the aquatic environment or taken up by plants. Plutonium had a greater potential mobility or bioavailability than Cs. Values of K^D for the desorption of ¹³⁷Cs from the sediment by freshwater, groundwater and seawater were all approximately 10⁵ L kg^-1, confirming its immobility in this environment. The desorption K_D values for stable ¹³³Cs were all approximately 10⁶ L kg^-1, so the stable Cs did not have a significant influence on the radiocaesium in this sediment.     

Retention of 137cesium in acid sulphate soils of South Central Thailand

Adsorption and desorption of ¹³⁷Cs by acid sulphate soils from the Nakhon Nayok province, South Central Plain of Thailand located near the Ongkarak Nuclear Research Center (ONRC) were investigated using a batch equilibration technique. The influence of added limestone (12 and 18 tons ha^?1) on ¹³⁷Cs adsorption–desorption was studied. Based on Freundlich isotherms, both adsorption and desorption of ¹³⁷Cs were nonlinear. A large portion (98.26–99.97%) of added ¹³⁷Cs (3.7?×?10³?7.03?×?10⁵ Bq l^?1) was sorbed by the soils with or without added lime. The higher lime treatments, however, favoured stronger adsorption of ¹³⁷Cs as compared with soil with no lime, which was supported by higher K _ads values. The addition of lime, the cation exchange capacity and pH of the soil increased and hence favoured the stronger adsorption of ¹³⁷Cs. Acid sulphate soils with a high clay content, medium to high organic matter, high CEC, and predominant clay types consisting of a mixture of illite, kaolinite, and montmorillonite were the main soil factors contributing to the high ¹³⁷Cs adsorption capacity. Competing cations such as NH₄ ⁺, K⁺, Na⁺, Ca²⁺, and Mg²⁺ had little influence on ¹³⁷Cs adsorption as compared with liming, where a significant positive correlation between K _ads and soil pH was observed. The ¹³⁷Cs adsorption–desorption characteristics of the acid sulphate soils studied exhibited a very strong irreversible sorption pattern. Only a small portion (0.09–0.58%) of ¹³⁷Cs adsorbed at the highest added initial ¹³⁷Cs concentration was desorbed by four successive soil extractions. Results clearly demonstrated that Nakhon Nayok province acid sulphate soils have a high ¹³⁷Cs adsorption capacity, which limits the ¹³⁷Cs bioavailability.     

Seasonal variation of the concentrations of 137Cs in sediment,sea water,and some organisms collected from Izmir Bay and Didim

¹³⁷Cs in the marine environment mainly originates from fallout of atmospheric nuclear weapon tests, accidental releases from nuclear facilities, and from the Chernobyl accident. After the latter accident, many studies have been carried out in Turkey. The objective of this study is to assess the spatial distribution of ¹³⁷Cs in the coastal marine environment of the Aegean Sea.

The concentrations of ¹³⁷Cs in sediment, sea water, mussel (Mytilus galloprovincialis), and fish samples collected from the coast of the Aegean Sea at Izmir Bay and near Didim (Akbük) have been monitored for seasonal variability by the means of gamma spectroscopy: they vary between 0.10 ± 0.01 and 1.5 ± 0.3 Bq kg^?1, 1.3 ± 0.1 and 4.3 ± 0.4 Bq m^?3, <0.2 and 1.3 ± 0.3 Bq kg^?1, and 0.20 ± 0.03 and 1.8 ± 0.3 Bq kg^?1, respectively.     

Transport and redistribution of Chernobyl fallout radionuclides by fluvial processes: Some preliminary evidence

Several measurements of¹³⁷Cs concentrations in suspended sediment transported by the River Severn during the post-Chernobyl period and in recent channel and floodplain deposits along the river emphasise the potential significance of fluvial processes in the transport and concentration of fallout radionuclides.     

Sellafield waste radionuclides in Irish sea intertidal and salt marsh sediments

Low level liquid radioactive waste discharges from the Sellafield nuclear fuel reprocessing plant in north west England had generated environmental inventories of about 3 × 10¹⁶ Bq of¹³⁷Cs, 6.8 × 10¹⁴ Bq of^239,240Pu and 8.9 × 10¹⁴ Bq of²⁴¹Am by 1990. Most of the^239,240Pu and²⁴¹Am and about 10% of the¹³⁷Cs has been retained in a deposit of fine marine sediment close to the discharge point. The quantities of radionuclides discharged annually from Sellafield decreased by two orders of magnitude from the mid-1970s to 1990 but estimated critical group internal and external exposure decreased by less than one order of magnitude over this period. This indicates that during the period of reduced discharges, radionuclides already in the environment from previous releases continued to contribute to the critical group exposure and highlights the need to understand processes controlling the environmental distribution of the radionuclides. Redistribution of the contaminated marine sediment is potentially of major significance in this context, in particular if it results in transport of radionuclides to intertidal areas, where contact with the human population is relatively likely. A review is presented of published work relating to Sellafield waste radionuclides in Irish Sea sediments. Data on temporal and spatial trends in radionuclide concentrations and activity ratios are collated from a number of sources to show that the dominant mechanism of radionuclide supply to intertidal areas is by redistribution of the contaminated marine sediment. The implications of this mechanism of supply for trends in critical group radiation exposure are considered.     

Inventories and Distribution of Radiocaesium in Arctic Marine Sediments: Influence of Biological and Physical Processes

Abstract

Extensive surveys of sediment burdens of radiocaesium, specifically ¹³⁷Cs, and other radioactive contaminants in the Arctic during the 1990′s, indicate that almost all anthropogenic radionuclides buried on continental shelves adjacent to Alaska are derived from global bomb fallout. the ¹³⁷Cs (half-life: 30.2y) activities observed in surface (0–4 cm) marine sediments however, vary widely, albeit much less than the expected current inventory resulting from bomb fallout at this latitude (～100mBq cm^?2). This observed geographical variation provided the opportunity to evaluate physical and biological mechanisms that may affect caesium biogeochemistry on Arctic continental shelves. We investigated whether high biological productivity in portions of the Bering and Chukchi Seas is effective in removing dissolved radiocaesium from the water column, and whether biological production in overlying water affects total radiocaesium inventories in sediments. Based upon C/N ratios in the organic fraction of shallow sediments, we found no evidence that higher inventories or surface activities of radiocaesium are present in areas with higher deposition of particulate organic matter. Based upon stable carbon isotope ratios of organic matter in sediments, we found no evidence that terrestrial runoff contributes proportionally to higher surface activities, although terrestrial runoff may affect total inventories of the radionuclide. Radiocaesium content of surface sediments was significantly correlated with total organic carbon content of sediments and the proportion of sediments in the finest sediment fractions. Because high current flow can also be expected to influence distributions of those sedimentary parameters, we conclude that re-distribution of     

Sediment accumulation and bio-diffusion mixing rates derived from excess <Superscript>210</Superscript>Pb and <Superscript>137</Superscript>Cs profiles in sediment cores of Mumbai Harbor Bay

Bio-diffusion mixing rates (D_b) were estimated from depth profiles of excess ²¹⁰Pb and ¹³⁷Cs in three sediment cores collected from Mumbai Harbour Bay (MHB) using a steady state vertical advection - diffusion model. The mean of ²¹⁰Pb and ¹³⁷Cs derived D_b values along the studied area were obtained to be about 23 and 36 cm²y^?1 respectively. These derived values were within the range of literature values reported for other equivalent environment internationally. The relatively higher D_b values for ¹³⁷Cs profiles demonstrated that particles have diffused more intensely within the surface layer of sediments over 1 year. Conversely, low D_b values for ²¹⁰Pb indicate slow mixing rates in the sediment profile which might be resulted from low ²¹⁰Pb flux and diffusion of ²²²Rn to the seafloor. The significant differences between ²¹⁰Pb and ¹³⁷Cs derived D_b values among cores indicate that there appeared to be as regional differences in sediment properties and local variability in the intensity of seafloor mixing. Furthermore, D_b values also depend on differences in characteristic time and depth scales of radionuclides in cores, benthic fauna abundances, organic carbon flux to the sediments and primary production in overlying surface waters. Comparison of ²¹⁰Pb derived D_b values with those calculated from ¹³⁷Cs distributions reveals better agreement for core 2 than core 1 and 3. The agreement may be fortuitous because ¹³⁷Cs appears significantly deeper than ²¹⁰Pb in all cores. It was also observed that D_b values increases as sediment accumulation rate increases for both radionuclide.     

Comparison of heavy metal concentrations in fish samples from three fish farms (Eastern Mediterranean) utilizing antifouling paints

Although aquaculture is considered the fastest growing food production industry, nevertheless there is little information regarding pollutant levels in cultured fish. Samples of cultured sea bass – Dicentrarchus labrax (Linnaeus, 1758), sea bream – Sparus aurata (Linnaeus, 1758), and sharpsnout sea bream – Diplodus puntazzo (Walbaum, 1792) from three fish farms located in the Eastern Mediterranean which utilized antifouling paints on the nets were analyzed for quantitative determination of zinc (Zn), chrome (Cr), and copper (Cu) in the gills, the liver, and the muscle separately for each tissue and fish. The results show that the highest levels of zinc (up to 29.6 mg kg^?1 dry wt) were found in the gills of all samples of sea bream and sharpsnout sea bream while in the samples of sea bass, the highest levels of zinc and chrome were found in the liver (up to 39.3 and 13.8 mg kg^?1 dry wt, respectively). Insofar, as copper is concerned the highest exposure was found in the liver of sharpsnout sea bream (up to 5.49 mg kg^?1 dry wt). The results indicate that the use of antifouling paints in aquaculture practices are a significant source of chemical pollution in cultured fish and poses a risk to the exposed organisms.     

Etude de la décontamination d'Arenicola marina (annélide,polychète) après contamination expérimentale par le caesium 137 ou le cobalt 60

From a nuclear protection standpoint, problems of decontamination are of great interest. In Arenicola marina L. a comparative study has been made on the elimination of two radionuclides, the metabolic functions of which are very different: ¹³⁷Cs and ⁶⁰Co. After experimental contamination with ¹³⁷Cs, significant decontamination is possible; however, elimination of ¹³⁷Cs accumulated in muscles is very slow. The elimination of ⁶⁰Co is very slow; its biological half-life in A. marina is about 3 months.     

Essential and nonessential elements in the red-crowned crane Grus japonensis of Zhalong Wetland,northeastern China

The concentrations of four essential (Ca, Mg, Zn, and Cu) and two nonessential elements (Pb and Cd) in feathers and kidneys, livers, gut walls, and muscles of eight carcasses of migratory red-crowned cranes (Grus japonensis) from Zhalong Wetland, northeastern China, were examined. The concentrations of Cd in the feathers were between 0.4 mg kg^?1 dry weight (dw) and 3.1 mg kg^?1 dw, in the livers between 0.4 and 4.4 mg kg^?1 dw, the maximum of which exceeded a level considered to be environmental exposure risk (i.e., 3 mg kg^?1 dw in the liver or kidney). High Pb levels (0.4–3.2 mg kg^?1 dw, with an average of 1.8 mg kg^?1) were also detected in livers, which exceeded a level considered toxicosis in birds (1.7 mg kg^?1 dw). Pb and Cd had the highest scores in principal component analysis. Relatively high Pb and Cd concentrations in the migratory cranes were thought to be associated with their habitat and prey.     

田湾核电站周边土壤及植物中137Cs含量调查及人群内辐射风险评价

为了调查田湾核电站运行后土壤环境中核素137Cs放射性水平的变化及评估其对当地居民的健康风险,采用现场采样测定的方法,分析了田湾核电站装料2年后周边土壤及植物中137Cs的放射性水平,并与运行前的本底调查结果进行了比较,同时利用放射性核素对人群内辐射风险评价模型结合田湾地区居民饮食情况对人群辐射风险进行了评估.结果表明,核电站运行2年后周边土壤中137Cs的放射性水平与运行前相比总体上没有明显变化,但个别村镇点位的137Cs放射性水平升高;核电站周边植物中137Cs的放射性水平均远低于我国相关国家标准(GB14882-1994)和运行前的本底值;田湾地区高公岛居民核素137Cs的年总摄入量为18.62Bq·a-1,远低于我国国标成人限值(GB14882-1994).通过摄入137Cs引起的人群内辐射总致癌风险较低,为1.51×10-7a-1,其中超过50%的风险来源于摄入鱼类海产品.     

Release,deposition and elimination of radiocesium (137Cs) in the terrestrial environment

Radionuclide contamination in terrestrial ecosystems has reached a dangerous level. The major artificial radionuclide present in the environment is ¹³⁷Cs, which is released as a result of weapon production related to atomic projects, accidental explosions of nuclear power plants and other sources, such as reactors, evaporation ponds, liquid storage tanks, and burial grounds. The release of potentially hazardous radionuclides (radiocesium) in recent years has provided the opportunity to conduct multidisciplinary studies on their fate and transport. Radiocesium’s high fission yield and ease of detection made it a prime candidate for early radio-ecological investigations. The facility setting provides a diverse background for the improved understanding of various factors that contribute toward the fate and transfer of radionuclides in the terrestrial ecosystem. In this review, we summarize the significant environmental radiocesium transfer factors to determine the damaging effects of radiocesium on terrestrial ecosystem. It has been found that ¹³⁷Cs can trace the transport of other radionuclides that have a high affinity for binding to soil particles (silts and clays). Possible remedial methods are also discussed for contaminated terrestrial systems. This review will serve as a guideline for future studies of the fate and transport of ¹³⁷Cs in terrestrial environments in the wake of the Fukushima Nuclear Power Plant disaster in 2011.     

137 Cs在我国滨海核电周边海洋生物的富集及生态风险研究

铯-137(~(137)Cs)是滨海核电站液态流出物中主要人工放射性核素和重要监控指标之一,易被水生生物累积,有关核电周边海域内海洋生物的核素富集状况备受关注。通过分析海洋生物富集放射性~(137)Cs的方式、生物富集系数的种群特征、人工放射性核素在生物体内的辐射剂量率状况,结果显示:1)滨海核电周边海域内~(137)Cs的放射性水平较低; 2)海洋生物对于~(137)Cs的富集未呈现显著的种群规律; 3)目前对放射性铯的富集能力较高的生物主要是底栖生物; 4)核电厂周边海域内海洋生物通常未达到可导致电离辐射损伤的辐射剂量率水平。随着滨海核电在我国的大力发展,对能够快速反映环境放射性状况的指示生物的筛选、生物放射性质量安全及其生态健康风险需进一步关注。     

Temperature effects on accumulation and retention of radionuclides in the sea star,Asterias forbesi: implications for contaminated northern waters

Radioactive waste disposal and nuclear testing concentrated in high latitudes in the northern hemisphere have resulted in the accumulation of radionuclides in Arctic marine ecosystems, but little is known of the consequences for marine biota in these waters. Under controlled laboratory conditions in May through September 1994, we examined the bioaccumulation in sea stars, Asterias forbesi (Desor), or the radionuclides ²⁴¹Am, ⁵⁷Co and ¹³⁷Cs, all of which are important components of disposed radioactive wastes. Experiments at 2 and 12°C determined the relative importance of food (the bivalve, Macoma balthica) and water as sources of radionuclides and assessed the influence of temperature on radionuclide influx and efflux rates. The lower temperature greatly increased the retention of radionuclides ingested with food; for instance, the biological half-life (tb _1/2) of ²⁴¹Am in the sea stars was 31 d at 12°C, but was virtually infinite at 2°C. Retention of ingested ⁵⁷Co was also increased at 2°C (tb _1/2=41 d). ¹³⁷Cs was not accumulated from food. Low temperature significantly reduced net influx rates of ¹³⁷Cs from water, but did not affect net uptake of ²⁴¹Am or ⁵⁷Co. Temperature had little effect on the retention of all three isotopes obtained from the dissolved phase. These experiments suggest that extrapolation of results of previous radioecological studies, conducted at warmer temperatures, to polar or temperate winter environments may be problematic, and that nuclear waste isotopes obtained through trophic transfer may be retained far more efficiently in high latitude marine biota than by fauna from warmer ecosystems.     

The potential of Berkheya coddii for phytoextraction of nickel,platinum, and palladium contaminated sites

The study involved assessing the potential of the native plant species (Berkheya coddii) for the phytoextraction of nickel, palladium, and platinum contaminated sites. Plant and soil samples were randomly collected from Barberton area, near Agnes mine, Mpumalanga Province, South Africa. Samples were analysed for total nickel, palladium, and platinum concentrations together with other elements found in the soil and in the plants' roots, and leaves. Soil versus leaves and soil versus roots uptake of these metals by the plant were compared. The mean concentration of nickel in the leaves/canopy was found to be 13,980?±?10,780?mg?kg^?1?dry mass, in the roots it was 2046?±?789?mg?kg^?1 dry mass, and in the soil it was 1040?±?686?mg?kg^?1?dry mass. This resulted in a mean concentration ratio in the leaves to soil of 13.44. The platinum mean concentration in the leaves was 0.22?±?0.15?mg?kg^?1?dry mass, in the roots it was 0.14?±?0.04?mg?kg^?1?dry mass, and in the soil it was 0.04?±?0.03?mg?kg^?1?dry mass. This resulted in a mean concentration ratio in the leaves to soil of 5.5. Palladium was found to have a mean soil concentration of 0.07?±?0.045?mg?kg^?1?dry mass. The mean concentrations in the roots and in the leaves were 0.18?±?0.07 dry mass and 0.71?±?0.52?mg?kg^?1?dry mass, respectively. This gave a mean concentration ratio in the leaves to soil of 10.1 for palladium. Other elements that were found to have a mean concentration ratio in the leaves to soil of around 2.5 or above are sodium, potassium, magnesium, calcium, and sulfur. Berkheya coddii was found to be most efficient in accumulating nickel, palladium, and platinum from the soil. The results for the first time revealed that the plant may have the potential to uptake platinum and palladium; both metals are in the same group of the periodic table as nickel.     

Heavy Metal Concentrations in Sea Urchin Tissues From Egypt,Ireland and United Kingdom

Abstract

Sea urchins (Paracentrotus lividus) were collected from the Mediterranean coast off Alexandria, Egypt and the Atlantic coast of Ireland to the west of Galway. Samples of another urchin species, Psammechinus miliaris, were collected from the entrance to Southampton Water, U.K. Both the Alexandria coast and Southampton Water receive domestic and industrial waste water inputs whilst the western Irish coast is relatively unpolluted.

Sampled animals were dissected to separate coelomic fluids, Aristotle's lantern, gonads and tissue (digestive tract plus connective tissue). the concentrations of heavy metals (cadmium, copper, lead, nickel and zinc) in the different parts were measured using flame atomic absorption spectroscopy.

Many levels of heavy metals in the different parts were similar in specimens taken across the wide range of sites and the two species. A notable exception was the high level of copper (33 μg g^?1 dry wt.) and zinc 328 μg g^?1? dry wt.) in urchin tissue from Southampton Water.

The metal concentrations in the gonads of Paracentrotus lividus are of particular interest because of human consumption of this species. the highest levels of copper (3.3–5.2 g^?1? dry wt.) and zinc (74–181 μ g^?1? dry wt.) dry wt.) in gonads were found in the samples from Egypt. Data from this study are compared with other results reported from the Mediterranean.

A simple, short term, elevated water column copper uptake experiment was undertaken with Paracentrotus lividus which showed an increase in gonad concentrations of this element.     

Selenium improves physiological responses and nutrient absorption in wheat (Triticum aestivum L.) grown under salinity

Abstract

Salinity is a serious limiting factor for crop growth and production. The present study was conducted to investigate the response of wheat grown at salinities of 0.12, 0.30 and 0.60?S?m^?1 on soil supplemented with 0, 0.5, 1 and 4?mg?kg^?1 Se as selenite. Chlorophyll a and b, carotenoid contents, Fe, Zn and Se in shoots as well as shoot dry weight were negatively affected by increased salinity. Se had a dual effect: at 0.5?mg?kg^?1, chlorophyll b, proline, and shoot Fe content were increased, catalase activity was stimulated; there was no effect on Zn content and shoot dry weight. At the two higher concentrations, Se led to decreases in chlorophyll content, nutrient concentration, and shoot dry weight. Thus, moderate addition of Se to soil could be a strategy to improve physiological responses and micronutrient status in wheat under salinity stress.     

Arsenic speciation in polychaetes (Annelida) and sediments from the intertidal mudflat of Sundarban mangrove wetland, India

This paper documents the concentration of total arsenic and individual arsenic species in four soft-bottom benthic polychaetes (Perenereis cultifera, Ganganereis sootai, Lumbrinereis notocirrata and Dendronereis arborifera) along with host sediments from Sundarban mangrove wetland, India. An additional six sites were considered exclusively for surface sediments for this purpose. Polychaetes were collected along with the host sediments and measured for their total arsenic content using inductively coupled plasma mass spectrometry. Arsenic concentrations in polychaete body tissues varied greatly, suggesting species-specific characteristics and inherent peculiarities in arsenic metabolism. Arsenic was generally present in polychaetes as arsenate (As^V ranges from 0.16 to 0.50 mg kg^?1) or arsenite (As^III ranges from 0.10 to 0.41 mg kg^?1) (30–53 % as inorganic As) and dimethylarsinic acid (DMA^V <1–25 %). Arsenobetaine (AB < 16 %), and PO₄-arsenoriboside (8–48 %) were also detected as minor constituents, whilst monomethylarsonic acid (MA^V) was not detected in any of the polychaetes. The highest total As (14.7 mg kg^?1 dry wt) was observed in the polychaete D. arborifera collected from the vicinity of a sewage outfall in which the majority of As was present as an uncharacterised compound (10.3 mg kg^?1 dry wt) eluted prior to AB. Host sediments ranged from 2.5 to 10.4 mg kg^?1 of total As. This work supports the importance of speciation analysis of As, because of the ubiquitous occurrence of this metalloid in the environment, and its variable toxicity depending on chemical form. It is also the first work to report the composition of As species in polychaetes from the Indian Sundarban wetlands.     

Contamination and source assessment of metals,polychlorinated biphenyls,and polycyclic aromatic hydrocarbons in urban soils from Addis Ababa,Ethiopia

Urban areas in developing countries are facing vast environmental problems as a result of rapid urbanization and industrialization. Of major concern is the contamination of soils which are increasingly becoming sinks for environmental pollutants. However, to date only little is known about the pollution in the megalopolises of developing countries. The aim of this study was to assess the contamination and potential sources of metals, polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) in the urban environment of Addis Ababa, the capital of Ethiopia. The investigation revealed the presence of most of the analyzed pollutants in soil and sediment samples with total concentrations (dry wt) of PAHs ranging from 186 to 3150?µg?kg^?1, PCBs from 0.4 to 19?µg?kg^?1, Cu from 14 to 173?mg?kg^?1, Zn from 36 to 440?mg?kg^?1, Pb from 9 to 700?mg?kg^?1, and Ni from 16 to 72?mg?kg^?1. In addition, polyaromatic sulfur heterocycles, typical for oil and petrol residues, were detected in several soil samples. Source identification approaches revealed that Pb, Zn, and Cu are most likely derived from pyrolytic sources, with elevated values in samples related to waste combustion and traffic emissions. Ni is most probably of geogenic origin. For PCBs it is indicated that they are derived from a single source. However, correlations with technical PCB mixtures were inconsistent. PAHs originate from the combustion of biomass, vehicular exhausts, and petrogenic sources.