Major and trace element contents in apples from a cultivated area of central Greece

Forty-two soil and apple samples from central Greece were collected and analyzed with regards to the content in major (Ca, Fe, K, Mg, Na, P, and S) and trace elements (As, B, Ba, Cd, Co, Cr, Cu, Hg, Mn, Mo, Ni, Pb, Sb, Sc, Se, Sr, Ti, and Zn). Soil samples were analyzed by inductively coupled plasma atomic emission spectrometry, while for the apples inductively coupled plasma mass spectrometry was implemented. Several elements such as As, B, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Se, Ti, and Zn, represent high concentrations in apples from the study area. These relatively high concentrations may be a consequence of the local geology, along with the excessive application of agricultural products such as fertilizers and agrochemicals.     

Spatial distribution and metal contamination in the coastal sediments of Al-Khafji area,Arabian Gulf,Saudi Arabia

To document the spatial distribution and metal contamination in the coastal sediments of the Al-Khafji area in the northern part of the Saudi Arabian Gulf, 27 samples were collected for Al, V, Cr, Mn, Cu, Zn, Cd, Pb, Hg, Sr, As, Fe, Co, and Ni analysis using inductively coupled plasma-mass spectrometer (ICP-MS). The results revealed the following descending order of the metal concentrations: Sr > Fe > Al > As > Mn > Ni > V > Zn > Cr > Cu > Pb > Co > Hg > Cd. Average levels of enrichment factor of Sr, As, Hg, Cd, Ni, V, Cu, Co, and Pb were higher than 2 (218.10, 128.50, 80.94, 41.50, 12.31, 5.66, 2.95, 2.90, and 2.85, respectively) and that means the anthropogenic sources of these metals, while Al, Zn, Cr and Mn have enrichment factor less than 2, which implies natural sources. Average values of Sr, Hg, Cd, Cr, Ni, and As in the coastal sediments of Al-Khafji area were mostly higher than the values recorded from the background shale and earth crust and from those results along coasts of the Caspian Sea and the Mediterranean Sea. The highest levels of Cu in the northern part of the studied coastline might be due to Al-Khafji desalination plant, while levels of Al, Ni, Cr, Fe, Mn, Pb, and Zn in the central part may be a result of landfilling and industrial sewage. The highest levels of As, Cd, Co, Cu, Hg, and V in the southern part seem to be due to oil pollutants from Khafji Joint Operations (KJO). The higher values of Sr in the studied sediments in general and particularly in locality 7 could relate to the hypersalinity and aragonitic composition of the scleractinian corals abundant in that area.     

Aquatic humus from an unpolluted Brazilian dark-brown stream: general characterization and size fractionation of bound heavy metals

The main pool of dissolved organic carbon in tropical aquatic environments, notably in dark-coloured streams, is concentrated in humic substances (HS). Aquatic HS are large organic molecules formed by micro-biotic degradation of biopolymers and polymerization of smaller organic molecules. From an environmental point of view, the study of metal humic interactions is often aimed at predicting the effect of aquatic HS on the bioavailability of heavy metal ions in the environment. In the present work the aquatic humic substances (HS) isolated from a dark-brown stream (located in an environmental protection area near Cubat?o city in S?o Paulo-State, Brazil) by means of the collector XAD-8 were investigated. FTIR studies showed that the carboxylic carbons are probably the most important binding sites for Hg(II) ions within humic molecules. 13C-NMR and 1H-NMR studies of aquatic HS showed the presence of constituents with a high degree of aromaticity (40% of carbons) and small substitution. A special five-stage tangential-flow ultrafiltration device (UF) was used for size fractionation of the aquatic HS under study and for their metal species in the molecular size range 1-100 kDa (six fractions). The fractionation patterns showed that metal traces remaining in aquatic HS after their XAD-8 isolation have different distributions. Generally, the major percentage of traces of Mn, Cd and Ni (determined by ICP-AES) was preferably complexed by molecules with relatively high molecular size. Cu was bound by fractions with low molecular size and Co showed no preferential binding site in the various humic fractions. Moreover, the species formed between aquatic HS and Hg(II), prepared by spiking (determined by CVAAS), appeared to be concentrated in the relatively high molecular size fraction F1 (> 100 kDa).     

Determination of metal-humic complexes, free metal ions and total concentrations in natural waters

A comparison of two systems for the quantitation of metal-humic complexes and free metal ions, consisting of the separation by coupled ion exchange columns followed by detection by inductively coupled plasma mass spectrometry or cold vapour atomic fluorescence spectrometry, is presented. The systems evaluated comprised the serially coupled anion and cation exchangers, Sephadex A-25/Chelex 100 and Dowex 1X8/Chelamine Metalfix. Separation and preconcentration of the species studied were accomplished with both systems, elution being carried out using 2 M HNO3. Total concentrations, metal-humic complex fractions and free metal ion fractions of Al, Ba, Cd, Co, Cu, Fe, Hg, Mn, Pb, Sr, U and Zn in nine natural waters were determined. Statistical evaluation of the data from the two cation exchange materials, including results for additional elements, showed better precision (for Al, Ba, Cr, Cu and Mo) and higher recoveries (Al, Ba, Cd, Fe, Sr and Zn) for Chelex 100 than Chelamine Metalfix for free metal ions. On the other hand, Chelamine Metalfix recovered a significantly greater amount of Ni. The amounts of metal-humic complexes were compared with modelled distributions of these species, and one advantage of the preferred Sephadex A-25/Chelex 100 system is that the elements studied are all correctly classified with respect to their binding strengths to humic substances, which is not the case with the Dowex 1X8/Chelamine Metalfix pair. With the preferred system, metal-humic complexes can be reliably determined, as indicated by the results of equilibrium speciation modelling. However, comparison with the total concentrations showed statistically significant, non-quantitative recoveries of Al, Cu, Hg, Mn, U and Zn from some samples. Thus a combination of speciation and total concentration measurements is required to obtain a complete representation of the distribution of trace elements in natural waters.     

北京灰霾天气PM10中微量元素的分布特征

采用电感耦合等离子体质谱法(ICP-MS)对北京市2008年4月和5月不同采样点采集的灰霾天PM₁₀样品中的15种微量元素进行了分析,得出了Ti、Fe、Zn、Sn、Pb为全样样品中相对含量较高元素;Ti、Mn、Ni、Cu、Zn、Pb是水溶样样品中相对含量较高元素。与晴天相比,灰霾天样品中微量元素可溶性增强,对人体危害更严重。与2002年分析数据进行对比,因2002年缺少Cr、Cd元素的测试值,全样样品中除了Co、Ni、Cu、Mo元素外,其余测试元素的浓度均有不同程度的升高,Fe和Sn元素的增幅最大。水溶样品中,参与对比元素的含量均下降。文中对含量相对较高的Cr、Mn、Fe、Cu、Zn、Cd、Sn和Pb元素进行了源解析,分析得出采样点附近的交通源及地面扬尘是这些元素的主要来源。     

Distribution and availability of trace elements in municipal solid waste composts

Trace element contamination is one of the main problems linked to the quality of compost, especially when it is produced from urban wastes, which can lead to high levels of some potentially toxic elements such as Cu, Pb or Zn. In this work, the distribution and bioavailability of five elements (Cu, Zn, Pb, Cr and Ni) were studied in five Spanish composts obtained from different feedstocks (municipal solid waste, garden trimmings, sewage sludge and mixed manure). The five composts showed high total concentrations of these elements, which in some cases limited their commercialization due to legal imperatives. First, a physical fractionation of the composts was performed, and the five elements were determined in each size fraction. Their availability was assessed by several methods of extraction (water, CaCl(2)-DTPA, the PBET extract, the TCLP extract, and sodium pyrophosphate), and their chemical distribution was assessed using the BCR sequential extraction procedure. The results showed that the finer fractions were enriched with the elements studied, and that Cu, Pb and Zn were the most potentially problematic ones, due to both their high total concentrations and availability. The partition into the BCR fractions was different for each element, but the differences between composts were scarce. Pb was evenly distributed among the four fractions defined in the BCR (soluble, oxidizable, reducible and residual); Cu was mainly found in the oxidizable fraction, linked to organic matter, and Zn was mainly associated to the reducible fraction (iron oxides), while Ni and Cr were mainly present almost exclusively in the residual fraction. It was not possible to establish a univocal relation between trace elements availability and their BCR fractionation. Given the differences existing for the availability and distribution of these elements, which not always were related to their total concentrations, we think that legal limits should consider availability, in order to achieve a more realistic assessment of the risks linked to compost use.     

Assessment of heavy metal levels in sediment samples of Kapulukaya Dam Lake (Kirikkale) and lower catchment area

In this study, the concentrations of 13 elements (Al, Fe, Mn, Cr, Ni, Zn, Co, As, Pb, Cu, Mo, Hg, and Cd) were determined in the sediments of three different sites in the Kapulukaya Dam Lake between May 2007 and November 2008. They ranged from 1.47 to 4.64 for Al, 0.92 to 3.48 for Fe (in percent), 326.60 to 1053.00 for Mn, 98.00 to 1,116.00 for Cr, 24.70 to 127.10 for Ni, 14.80 to 124.20 for Zn, 11.0 to 43.20 for Co, 5.00 to 29.30 for Cu, 9.10 to 69.70 for As, 8.60 to 34.00 for Pb, 2.50 to 5.20 for Mo, 1.00 to 1.60 for Hg, and 0.50 to1.80 for Cd in microgram per gram dry weight sediment. The contamination degree of the sediment was assessed on the basis of enrichment factor and corresponding sediment quality guideline. The calculated enrichment factors (EF, measured metal vs. background concentrations) indicated that the effect of man-made activities on the occurrence of concentrations could be accounted for the majority of heavy metals namely Mn, As, Ni, Cu, Zn, Cr, Co, Mo, and Cd, whereas such affect was not detected for Hg and Pb. The maximum values of the EF were represented by As, minimum values by Hg at all sites. Mean EF values were 36.60 and 0.70 for As and Hg, respectively. This study has clearly assessed a certain level of heavy metal pollution in the region, based particularly on the findings from sediment.     

Contamination and ecological risk assessment of toxic trace elements in the Xi River, an urban river of Shenyang city, China

The objectives of this study were to assess the enrichment, contamination, and ecological risk posed by toxic trace elements in the sediments of the Xi River in the industrialized city of Shenyang, China. Surface sediment and sediment core were collected; analyzed for toxic trace elements; and assessed with an index of geoaccumulation (Igeo), enrichment factor (EF) value, potential ecological risk factor (Er), ecological risk index (RI), and probable effect concentration quotient (PECQ). Elemental concentrations (milligram per kilogram) were 8.5–637.9 for As, 6.5–103.9 for Cd, 12.2–21.9 for Co, 90.6–516.0 for Cr, 258.1–1,791.5 for Cu, 2.6–19.0 for Hg, 70.5–174.5 for Ni, 126.9–1,405.8 for Pb, 3.7–260.0 for Sb, 38.4–100.4 for V, and 503–4,929 for Zn. The Igeo, EF, Er, and PECQ indices showed that the contamination of Cd and Hg was more serious than that of As, Cr, Cu, Ni, Pb, Sb, and Zn, whereas the presence of Co and V might be primarily from natural sources. The Igeo index for Cr and Ni might underestimate the degree of contamination, potentially as a result of high concentrations of these elements in the shale. The RI index was higher than 600, indicating a notably high ecological risk of sediment for the river. The average PECQ for As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn ranged from 1.4 to 4.1 for surface sediment and from 5.2 to 9.6 in the sediment cores, indicating a high potential for an adverse biological effect. It was concluded that the sediment in the Xi River was severely contaminated and should be remediated as a hazardous material.     

Essential and toxic elements in infant foods from Spain, UK, China and USA

Spanish gluten-free rice, cereals with gluten, and pureed baby foods were analysed for essential macro-elements (Ca and Na), essential trace elements (Fe, Cu, Zn, Mn, Se, Cr, Co and Ni) and non-essential trace elements (As, Pb, Cd and Hg) using ICP-MS and AAS. Baby cereals were an excellent source of most of the essential elements (Ca, Fe, Cu, Mn and Zn). Sodium content was high in pureed foods to improve their flavour; fish products were also rich in Se. USA pure baby rice samples had the highest contents of all studied essential elements, showing a different nutrient pattern compared to those of other countries. Mineral fortification was not always properly stated in the labelling of infant foods. Complementary infant foods may also contain significant amounts of contaminants. The contents of Hg and Cd were low enough to guarantee the safety of these infant foods. However, it will be necessary to identify the source and reduce the levels of Pb, Cr and As in Spanish foods. Pure baby rice samples contained too much: Pb in Spain; As in UK; As, Cr and Ni in USA; and Cr and Cd in China.     

Heavy metals in Yeniçağa Lake and its potential sources: soil,water, sediment,and plankton

The distribution and accumulation of heavy metals (Al, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Mo, Cd, Sn, Ba, Pb) in the water, sediments, plankton of Yeniça?a Lake, and its potential sources (creeks, sewage, artesian well, soil) were investigated during 1-year study period as monthly or seasonally. Element analyses were performed by ICP–MS. Results showed that the trace and toxic elements (Al, As, Mn, Pb, Fe) concentration in lake water and/or its feeding sources were above the recommended water standards (WHO, EC, EPA, TS-266). It was found that the maximum accumulation of the heavy metals iron, aluminum, manganese, zinc, and barium in the sediment of Yeniça?a Lake. The accumulation order of trace metals were Fe > Al > Mn > Zn > Ba > Ni > Cr > As > Cu > Pb > Co > Mo > Sn > Cd in the lake, creeks sediment, and soil samples. The similar results suggest that the accumulation of heavy metals in the sediment is a natural process. Metals accumulated in the lake are naturally mixed from the soil. However, the presence of heavy metals in the analysis of artesian well water and sewage reveals that the transportation occurs also from the groundwater to the lake. The results obtained in plankton in Yeniça?a Lake showed that aluminum, iron, manganese, zinc, and barium were most accumulated elements in the plankton. The lower averages of lead prevalent in the water and sediment during some months were seen to have a significant mean accumulation in the plankton.     

Heavy Metal Pollution Assessment in Sediments of the Izmit Bay, Turkey

Surface sediments in the fraction < 63 μm collected from eight stations along the north coastline of Izmit Bay, north-eastern Marmara Sea, Turkey, were analyzed for major (organic carbon, Al, Ba, Fe and Mg) and trace (As, Cd, Co, Cr, Cu, Mo, Ni, Pb and Zn) elements by using inductively coupled plasma atomic emission spectrometry (ICP-AES). Sediments heavily contaminated are evaluated by the Sediment Quality Guidelines (SQG) of US EPA. The results were compared with the marine sediment quality standards (SQS), as well as literature values reported to assess the pollution status of the sediments. The enrichment factors (EFs) were calculated to evaluate actual level of contamination for all the elements using the earth crust as reference matrix, based on elemental values by Mason which show a normal pattern near to unity. The analysis revealed two groups of elements: (i) Arsenic, Cd, Pb, and Zn are the most enriched elements; (ii) Barium, Co, Cr, Cu, Fe, Mg, Mo and Ni are at background levels. The results show that road traffic run-offs, paint industries and coal combustion are among the most significant sources.     

Element contents and food safety of water spinach (Ipomoea aquatica Forssk.) cultivated with wastewater in Hanoi, Vietnam

Extensive aquatic or semi-aquatic production of water spinach (Ipomoea aquatica Forssk.) for human consumption takes place in Southeast Asia. The aim of this study was to assess the concentrations of 38 elements in soil and water spinach cultivated under different degrees of wastewater exposure in Hanoi, Vietnam. The results showed no effect of wastewater use on the overall element concentrations in soil and water spinach. Mean soil concentrations for selected potentially toxic elements at the studied field sites had the following ranges 9.11–18.7 As, 0.333–0.667 Cd, 10.8–14.5 Co, 68–122 Cr, 34.0–62.1 Cu, 29.9–52.8 Ni, 32.5–67.4 Pb, 0.578–0.765 Tl and 99–189 Zn mg kg⁻¹ dry weight (d.w.). In all samples Cd, Pb and Zn soil concentrations were below the Vietnamese Guideline Values (TCVN 7209-2002) for agricultural soils whereas As and Cu exceeded the guideline values. Maximum site element concentrations in water spinach were 0.139 As, 0.032 Cd, 0.135 Cr, 2.01 Cu, 39.1 Fe, 57.3 Mn, 0.16 Ni, 0.189 Pb and 6.01 Zn mg kg⁻¹ fresh weight (f.w.). The site and soil content of organic carbon were found to have high influence on the water spinach element concentrations whereas soil pH and the total soil element concentrations were of less importance. The estimated average daily intake of As, Cd, Cu, Fe, Pb and Zn for adult Vietnamese consumers amounts to <11% of the maximum tolerable intake proposed by FAO/WHO for each element. It is assessed that the occurrence of the investigated elements in water spinach will pose low health risk for the consumers.     

Assessment of the effects of municipal sewage,immersed idols and boating on the heavy metal and other elemental pollution of surface water of the eutrophic Hussainsagar Lake (Hyderabad,India)

The surface water qualities of Hussainsagar, an eutrophic urban lake in the midst of twin cities of Hyderabad and Secunderabad (India) receiving large quantities of external inputs—both untreated municipal sewage containing industrial effluents, and treated sewage, a large number of annually immersed idols of God and Goddess, and intense boating activities were assessed in relation to the concentration of elements including heavy metals of the water along the necklace road of the lake. Elemental analyses of water using ICP-MS revealed 26 elements including heavy metals—As, Cd, Cr, Ni, Pb, Cu, Fe, Mn, Se, Ba, Zn, Mo, V, Co, Ag, Sr, Rb, Mg, K, Ca, Al, Si, Sb, Na, Li, and B, in the surface water of the lake. Of these, the first 15 elements were found in elevated concentrations in the water at the outfall point of the untreated municipal sewage (site 3), which was the main dominating source of contamination of the lake water while Cu and Sb were recorded in higher concentrations at the outfall of treated effluent from Sewage Treatment Plant, and three elements (Ba, Si, and B) were in higher concentration at the sites of outfall of sewage flowing from an oxygenated pond (site 4), Ca, Zn, and Sr, at the site immersed with idols (site 1), and Pb, Ag, and Al at the center of the lake (site 5) with intense boating activities. Concentrations of most of these elements exceeded the maximum permissible limits of national (Indian Council Medical Research) standards for drinking water. The concentrations of most of the elemental contaminants showed significant positive correlations between them.     

Seasonal Variability of Heavy Metals in Surface Sediment of Lake Sapanca, Turkey

Lake Sapanca is exposed to heavy urbanization and industrialization because of its natural beauty and its proximity to the metropolitan İstanbul, Turkey. In this study, it was aimed to investigate seasonal changes of some heavy metals (Pb, Cr, Cu, Mn, Ni, Zn and Cd) concentration of surface sediment. Nine different stations were chosen as sampling points. Samples were taken every three months and the seasonal and annual average concentration of the elements were determined. Seasonal highest values of heavy metals were observed as follows; Cr, Cu, Mn, Ni and Zn in Summer, Cd in Autumn. There was no seasonal difference for Pb, Cr and Cd. It seems that Lake Sapanca has not been polluted yet. However, it was found that Cu and Ni concentrations in surface sediment exceed lowest effect level.     

ACCUMULATION OF HEAVY METALS IN KIDNEY AND HEART TISSUES OF Epinephelus Microdon FISH FROM THE ARABIAN GULF

Levels of Pb, Co, Cu, Ni, Zn, Mn and Cd in the kidney and heart tissues of Epinephelus Microdon collected from the Arabian Gulf, Eastern province of Saudi Arabia, were determined by wet digestion-based atomic absorption method. The results indicated that accumulation pattern of analyzed metals in the kidney tissues followed the order; Zn > Cu > Pb > Ni > Co > Mn > Cd, with Zn at 47.73 ± 13.26 ppm and Cd at 0.41 ± 0.16 ppm. Cu, Mn, Co and Ni levels in the kidney tissues were significantly lower or within the ranges reported previously. In the heart tissue the analyzed metals followed almost the same pattern of metal accumulation; Zn > Cu > Pb > Co > Ni > Mn > Cd. The average lead (3.19 ± 2.03 ppm), nickel (1.69 ± 0.52 ppm), cobalt (1.75 ± 0.44 ppm), copper (3.96 ± 0.98 ppm) and cadmium (0.34 ± 0.23 ppm) concentrations were found high in the heart tissues whereas zinc and manganese levels were found high in kidney tissues. In general, the data indicated that marine {fish from the sampling site of Arabian Gulf are comparatively clean and unpolluted.     

Analysis of selected biomonitors to evaluate the suitability for their complementary use in monitoring trace element atmospheric deposition

The biomonitoring properties of oak tree bark compared with the epiphytic moss Hypnum cupressiforme and the influence of the tree bark, as its growth substrate, on the content of heavy metals in moss were investigated. Samples of the epiphytic moss H. cupressiforme and oak tree bark (Quercus spp.) were collected in Eastern Romania at a total of 44 sampling sites. Parallel moss and bark samples were collected from the same sides of the trunk circumference. V, Cr, Ni, Cu, Zn, As, Mo, Cd, In, Tl, Sn, Pb, and Bi were determined by ICP-MS. Principal component analysis was used to identify possible sources of metals in bark and moss. Six factors explaining 87 % of the total variance in the data set were chosen. The main factors represent long-range atmospheric transport of elements (Zn, Cd, (Pb), Bi, (Mo), (Tl)), local emissions from industrial sources (As, Cr, Ni, V), road traffic (Pb, Zn) and agricultural activities (Cu, (Zn)). The element concentrations in moss and bark samples are of the same order of magnitude. For almost all the elements, higher concentrations were obtained in moss. Significant correlations between concentrations in moss and bark samples were obtained for 7 of the 13 elements: V, Ni, Cu, Zn, Cd, In, and Bi, all typical anthropogenic pollutants. The use of tree bark for monitoring purposes might be an alternative in areas where there is a scarcity of mosses.     

Interseasonal distribution and partitioning of heavy metals in subtidal sediment of Qua Iboe Estuary and associated Creeks, Niger Delta (Nigeria)

An analysis of the distribution and chemical forms of selected metals: cadmium (Cd), chromium (Cr), copper (Cu), nickel (Ni) and lead (Pb) in subtidal sediments of Qua Iboe Estuary and adjourning creeks, collected between June 2000 and January 2001, were studied using a sequential chemical extraction method. The concentration of metals in each extracted fraction was determined using inductively coupled plasma spectrometer (ICP-AES). Pb, Cd and Cu appear to be the most abundant metal in the sediments of the systems, and are predominantly associated with the residual, organic and oxidisable phases. Results indicate that there are also insignificant components that are bound to both the exchangeable and carbonates fractions. Ni is largely associated with bioavailable phases with insignificant bound to organic matter and residual fractions. In general, an insignificant component of Cd and Pb are bound to organic matter phase. Moreover, speciation results indicate that metal contamination in the ecosystems investigated primarily comes from human-mediated sources. Thus, based on index of geoaccumulation calculated, sediments of these ecosystems have been classified as uncontaminated by Cr, Cu and Ni, strongly contaminated by Pb and extremely contaminated by Cd.     

Heavy Metal Levels in Biota and Sediments in the Northern Coast of the Marmara Sea

Concentration of Cd, Co, Cr, Ni, Zn, Fe, Mn, Pb and Cu were determinedin biota and sediment samples collected from the Marmara Sea in Turkey. The levels of Zn, Fe, Mn, Pb and Cu in the macroalgae are higher than previous studies in the Marmara Sea. Moreover, Cu and Zn concentrations at the present study are significantly high than Bosphorus and Black Sea algae. The order heavy metal concentrations in the mussel samples was: Fe > Zn > Ni > Mn > Cu > Pb > Cr > Cd > Co. The metal concentrations are generally lower when compared with the Black Sea mussels except Pb. At the same time, concentrations of Pb, Cu and Zn in the mussel species are lower when compared with the results in the Aegean Sea. The ranges of Mn and Cu in the tested fish samples are higher than Black Sea fish. On the other hand, Cd, Co, Cr, Zn and Pb concentrations are lower. The northern coast of the Marmara Sea having the highest metal concentrations in sediments as follows: Co, Cr, Ni, Fe at ?arköy ; Pb, Cu at M. Ere?li; Cd, Zn, Mn at Menek?e. The heavy metal levels in the sediment samples are lower than other areas in the Marmara Sea.     

Heavy metal concentrations in two barb, Barbus xanthopterus and Barbus rajanorum mystaceus from Atatürk Dam Lake, Turkey

Concentration of some heavy metals (Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb and Zn) were determined in muscle, liver, kidney and gill of two barb, Barbus xanthopterus and Barbus rajanorum mystaceus, which have great economic values, in the Atatürk Dam Lake (Turkey). Heavy metal levels in fish samples were analyzed by inductively coupled plasma spectroscopy (ICP/OES). Heavy metal concentrations vary significantly, depending on the type of the tissue in fish species. The metal accumulation in the liver, kidney and gill of Barbus xanthopterus and Barbus rajanorum mystaceus was found to be quite high in comparison with that in the muscle. The mean concentrations of heavy metals in muscle tissues of Barbus xanthopterus were as follows: Co, 0.09; Cr, 0.12; Cu, 0.27; Fe, 5.26; Mn, 0.20; Ni, 0.08; Pb, 0.68; Zn, 1.39, whereas in muscle tissues of Barbus rajanorum mystaceus were as follows: Co, 0.11; Cr, 0.10; Cu, 1.07; Fe, 3.97; Mn, 019; Ni, 0.04; Pb, 0.66; Zn, 1.70 microg/g wet weight. Cd levels in gill and muscle tissues were below detection limits. All metal levels detected in tissues were safe for human consumption and within the limits for fish proposed by FAO/ WHO, EU and Turkish Food Codes.     

Concentrations, enrichment and predominant sources of Sb and other trace elements in size classified airborne particulate matter collected in Tokyo from 1995 to 2004

APM was collected and trace elements existing in the particles were monitored since May 1995 in this study. APM sample was collected separately by size (d < 2 microm, 2-11 microm and >11 microm) on the roof of the university building (45 m above ground) in the campus of Faculty of Science and Engineering, Chuo University, Tokyo, Japan, using an Anderson low volume air sampler. The collected sample was digested by HNO3, H2O2 and HF using a microwave oven, and major elements (Na, Mg, Al, K, Ca and Fe) were measured by ICP-AES, and trace elements (Li, Be, Ti, V, Cr, Mn, Co, Ni, Cu, Zn, As, Se, Mo, Cd, Sb, Ba and Pb) were measured by ICP-MS. It was observed that the APM concentration was higher between the winter and the spring, compared to during the summer. The enrichment factor was calculated for each element in each set of APM (d < 2 microm, 2-11 microm and >11 microm). Seasonal trends of enrichment factors were examined, and the elements were classified into 3 groups according to the common seasonal behavior. It is likely that the elements in the same group have common origins. Toxic pollutant elements (Sb, Se, Cd, Pb and As) were found in small particles with d of <2 microm in concentrated levels. Antimony (Sb) had the highest enrichment factor, and the results suggested that Sb level in APM was extremely high. The origins of Sb were sought, and wastes from plastic incineration and brake pad wears of automobiles were suspected. Each set of APM (d < 2 microm, 2-11 microm and >11 microm) was classified by the shape, and the shape-dependent constituents of a single APM particle were quantitatively measured by SEM-EDX. High concentration of Sb was found in APM <2 microm and square particles. Particles less than 2 microm and square shaped particles were major particles produced by actual car braking experiments. From these experimental results it was concluded that the source of Sb in squared APM <2 microm is considered to be from brake pad wear.