Population health risk via dietary exposure to trace elements (Cu,Zn, Pb,Cd, Hg,and As) in Qiqihar,Northeastern China

The estimated daily intakes (EDIs) of six trace elements (Cu, Zn, Pb, Cd, Hg, and As) in vegetables (leafy vegetable, i.e., bok choy, fruit vegetables, i.e., cucumber and tomato, and other categories, i.e., mushroom, kidney bean, and potato), cereals (rice and wheat flour), and meats (pork, mutton, and beef) most commonly consumed by adult inhabitants of Qiqihar, Northeastern China, were determined to assess the health status of local people. The average EDIs of Cu, Zn, Pb, Cd, Hg, and As were with 20.77 μg (kg bw)^?1 day^?1 of Cu, 288 μg (kg bw)^?1 day^?1 of Zn, 2.01 μg (kg bw)^?1 day^?1 of Pb, 0.41 μg (kg bw)^?1 day^?1 of Cd, 0.01 μg (kg bw)^?1 day^?1 of Hg, and 0.52 μg (kg bw)^?1 day^?1 of As, respectively, which are below the daily allowance recommended by FAO/WHO. However, the maximum EDIs of Pb and Cd were 4.56 μg (kg bw)^?1 day^?1 and 1.68 μg (kg bw)^?1 day^?1, respectively, which are above the recommended levels [i.e., 3.58 μg (kg bw)^?1 day^?1 for Pb and 1.0 μg (kg bw)^?1 day^?1 for Cd] by FAO/WHO. This finding indicates that the potential health risk induced by daily ingestion of Pb and Cd for the local residents should receive a significant concern. Similarly, we detected elevated Pb and Cd concentrations, i.e., with average of 13.58 and 0.60 mg kg^?1 dw, respectively, in the adult scalp hairs. Consumption of rice, potato, bok choy, and wheat flour contributed to 75 and 82% of Pb and Cd daily intake from foodstuffs. Nevertheless, human scalp hair is inappropriate biological material for determination of the nutritional status of trace elements in this region.     

Comparison of sample digestion procedures for the determination of trace elements in antarctic krill by GF‐AAS

Two independent digestion procedures for Antarctic krill samples were compared. Dry ashing (DA) and microwave (MW) acid‐assisted digestion were tested for decomposing the samples to determine essential (Cu, Fe, Cr) and toxic elements (Cd, Pb) by graphite furnace‐atomic absorption spectrometry (GF‐AAS). A mixture of HNO₃ and H₂O₂ as digesting agent was used in the microwave procedure. For the dry ashing digestion, the organic matter was oxidated at 480°C in an open system. Both digestion methods were compared in terms of accuracy and applied to the analysis of a certified reference material: MURST‐ISS‐A2 (Antarctic krill).

The detection limits for the five elements analysed ranged from 3 to 150 ng g^‐1. Both digestion procedures are suitable for the decomposition of krill samples. However, dry ashing is not recommended to determine Pb and Cd because losses can occur.     

Trace metals in fish,sediment and water from the south west coast of the Arabian sea,Pakistan

Concentrations of ten metals (As, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Zn and Hg) in the edible muscle of Arius maculatus captured from eight different near‐shore and off‐shore sites off the south west coast of the Arabian Sea, Pakistan, were determined by atomic absorption spectrophotometry. Relevant water and sediment samples from the sites were also analysed for the metals. Zinc showed the highest metal concentration (6.763 μg/g, wet weight) in the muscle of the fish, while Mn and Hg showed lowest level (0.019 μg/g, wet weight). Of all the metals investigated, largest scatter (measured as σ) was observed for Zn (σ = 2.058 /μg/g) in fish muscle, for Fe and Mn in sediment (σ = 27481 and 44.50 μg/g) and for As in water (σ = 0.270 μg/L). The metal distribution data pertaining to water, fish and sediment were examined on the basis of simple metal correlations. The statistical study revealed that Ni, Cr, Pb and Cu had significant positive correlations (r > 0.830 at ρ = 0.01). The finding substantiated a trace metal concentration gradient in the area, thereby indicating that the local marine environment is contaminated by anthropogenic sources.     

Assessment of metals in soil extracts and their uptake and movement within Tamarix nilotica at Lake Nasser banks,Egypt

This study aims to determine heavy-metal levels in soil from the banks of Lake Nasser, the ability of Tamarix nilotica to accumulate such metals from soil and hence its potential for phytoextraction. Soil and Tamarix samples were collected from the banks of four bights around Lake Nasser and analysed for Fe, Mn, Ca, Mg, Cr, Cu, Ni, Zn, Cd and Pb by atomic absorption spectrometry, whereas Na and K were measured by atomic emission spectrophotometry. Three different methods of extraction were used for the soil samples. Lead, copper and zinc were equally distributed between the exchangeable phase and Fe/Mn oxide-bound form, while other measured metals were mainly present in the Fe/Mn oxide fraction. With the exception of iron, all metals studied showed total concentrations within the geochemical background values. T. nilotica exhibited elevated concentrations of Na (36.2–48.5?mg?g^?1) and K (2.74–4.33?mg?g^?1) in stems, and relatively high concentrations of Pb, Cd and Co (0.39–1.03?µg?g^?1, 0.24–1.3?µg?g^?1 and 1.94–5.3?µg?g^?1, respectively) are found in plant leaves. Bioaccumulation factors of Na and K (9.3 and 12.63, respectively) were high in T. nilotica stems. While the bioaccumulation of Pb, Cd, Co and Ni (2870.1, 2035.4, 10.5 and 5313.2, respectively) was high in plant leaves, Fe, Mn, Ca and Mg were accumulated relatively equally in plant stems and leaves. T. nilotica was found to secrete high amounts of Na, Ca and K, in addition to small amounts of all accumulated metals except Cd and Cu. These secreted metals appeared as salt crystals (67.5% Na; 25.8% Ca; 5% Mg; 1.5% K and 0.16% trace and minor elements) on the plant surface. The concentrations of all the metals studied in T. nilotica were higher than in the salt crystals. Statistical analysis of the database suggests bioaccumulation of these metals from soil to T. nilotica. This reflects the importance of using T. nilotica as a model in the phytoremediation process as an established environmental clean-up technology.     

Determination of cadmium in water and herbal medicine by Penicillium chrysogenum immobilized on silica gel for flame atomic absorption spectroscopy

Penicillium chrysogenum was immobilized on silica to develop a simple and cost effective method for solid phase extraction of Cd(II) and determination using flame atomic absorption spectrometry (FAAS). The sorbent was characterized by Fourier transform infrared spectroscopy and packed into a column. The conditions for quantitative sorption and desorption of Cd(II) were optimized. The preconcentration factor was 100 while detection limit was 0.61 µg L^?1 with a relative standard deviation of 1.0%. The method was applied for determination of Cd in herbal medicine and tap water.     

Body burden of chromium,copper, cadmium and lead in the neustonic copepod Anomalocera patersoni (pontellidae) collected from the Mediterranean sea

The amounts of Cr, Cu, Cd and Pb in the copepod Anomalocera patersoni were determined for 47 individuals by flameless atomic absorption spectrophotometry. The following mean body burdens of these elements were obtained: Cr 0.6, Cu 13, Cd 0.5, Pb 1.5 ng individual^-1, or Cr 2.1, Cu 42, Cd 1.5 and Pb 4.8 ng mg^-1 (dry weight). Cr, Cu and Cd contents did not differ significantly between males and females, however Pb did, with males having more. The data indicate that while the Cr, Cu and Pb body Hurden in these copepods follows the logarithmic normal distribution, Cd follows a normal distribution. Thus, the arithmetic means and the modes of Cd body burden are almost the same, while for the other elements the arithmetic means differ from the geometric means. This indicates that measurements of a few individuals suffice for estimating the mean body burden of Cd. On the other hand, many measurements are necessary for the body burden estimation of other elements, especially Cu.     

Heavy metals in the Sea-Skater Halobates robustus from the Galápagos Islands: Concentrations in nature and uptake experiments,with special reference to cadmium

Samples of Halobates robustus Barber (Heteroptera: Gerridae) from the Galápagos Islands were analysed by optical emission spectrometry. The levels (in g g^-1 dry weight) of Zn (134), Cu (155), Pb (< 1), Cd (7), and Cr (3) were not significantly different among insects of different sexes or developmental stages. The low natural levels of Cd in H. robustus from the relatively unpolluted environment of the Galápagos Islands are compared to the high concentrations of Cd in Halobates spp. from relatively polluted regions. Since the measured levels of Cd in their natural zooplankton food rarely exceed 10 g g^-1, and very little of the Cd is found in the soft tissues, the high Cd concentrations (100 to 200 g g^–1) in some seaskater species have evidently been derived by drinking from the surface microlayer of the seawater.     

Neutron activation and atomic absorption analysis of Ulva Lactuca and Gracilaria Verrucosa from Thermaikos Gulf,Greece

NAA and AAS have been applied to determine the content of As, Br, Ca, Cd, Co, Cr, Cu, Fe, K, La, Mn, Na, Ni, Pb, Sb, Sc, Sm and Zn in Ulva lactuca and Gracilaria verrucosa from Thermaikos Gulf, Greece. The analytical data has been subjected to cluster and stepwise discriminant analysis. Thus the influence of some industrial sources on the pollution of water in the Gulf is detected and correlation between Zn‐Co‐Cr‐La; Br‐K; Cu‐Ni; Cd‐Sb‐Mn in the investigated algae is established.     

Levels of heavy metals in blue whiting caught from the eastern Black Sea area of Turkey

This paper presents data on the concentrations of 5 metals, copper (Cu), cadmium (Cd), iron (Fe), zinc (Zn) and lead (Pb) in Blue Whiting sampled from the Eastern Black Sea coast of Turkey. The highest metal concentrations of Cu, Cd, Fe, Zn and Pb were recorded in Blue Whiting with the values of 2.71, 0.601, 14.137, 15.322 and 1.078 μg g^‐1 dry weight, respectively. On average the metal concentrations in Blue Whiting followed the order of Zn > Fe > Cu > Pb > Cd. Temporal differences of concentrations of these metals were significant (p < 0.05). Spatial fluctuations of Cu, Cd, Fe, Zn and Pb concentrations in Blue Whiting were also significant (p < 0.01). It was found that the concentrations of Cu, Cd, Fe, Zn and Pb in the muscle in Blue Whiting were below the limit of Public Health Regulation in Turkey.     

Electrochemical hydride generation of tin(II) and its determination by electrothermal atomic absorption spectrometry with in situ trapping in the graphite tube atomizer

An electrolytic hydride generation system for the determination of tin(II) by means of batch electrochemical hydride generation-electrothermal atomic absorption spectrometry (EcHG-ETAAS) with in situ trapping in a graphite tube atomizer is described. The effects of four permanent chemical modifiers – palladium, tungsten, iridium, and platinum – for graphite tube treatment on analyte absorbance and the effects of four cathode materials, i.e., Pb, Sn, Pb–Sn alloy, and glassy carbon, are checked. Three electrolytes, i.e., nitric acid, sulfuric acid, and hydrochloric acid, are examined as catholyte solutions. The influence of several parameters on EcHG is investigated using multivariate and univariate methods. Interferences of some concomitant ions are evaluated. The calibration curve is linear from 1 to 200?µg?L^?1, with a detection limit of 0.8?µg?L^?1 and a relative standard deviation of 6.2% (n?=?3) for 100?µg?L^?1 Sn(II). The proposed method was successfully applied in the analysis of real environmental water samples and reference materials, and good spiked recoveries over the range of 93.1–115% were obtained. The proposed technique provides a means for developing hydride generation of other elements.     

Trace metal levels of fish from the marmara and black sea

Concentration of Ag, As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Pb, Se and Zn were determined in various fish species from the Marmara and Black Sea during 1987 and 1988. Neutron activation analysis, atomic absorption spectrophotometry and X‐ray fluorescence methods were used for analysis. No significant differences between metal values in fish collected in 1987 and 1988 were noted except As and Pb. The As and Pb concentrations in the same species of fish were higher in the eastern Black Sea compared with the other locations. The Hg concentration in Thunnus thynnus muscle ranged from 1.05–3.05 μg/g dry weight. On the other hand, the Hg levels in the other species were found below the detection limit. Comparison of the results obtained with data reported for the Mediterranean Sea shows an agreement in general for most of the metal levels.     

Histology of Sculpin spp. in East Greenland. II. Histopathology and trace element concentrations

Abstract

For many years, the sculpin has been utilized as a sentinel monitoring species for anthropogenic impacts on the marine environment. To further develop its potential as a screening model body burden of several trace elements, including cadmium (Cd), copper (Cu), mercury (Hg), lead (Pb) and selenium (Se), were investigated. In addition, histopathology in shorthorn sculpins (Myoxocephalus scorpius; n?=?20) and fourhorn sculpins (Myoxocephalus quadricornis; n?=?10) were examined at three sites around the Scoresby Sound settlement in Central East Greenland. Fourhorn sculpins caught at the most distant site from the settlement, contained significantly higher hepatic Cu and Cd concentrations as well as significantly elevated gill Pb levels compared to the shorthorn sculpins collected at two other sites closer to the settlement. Histological examinations showed that fish with significantly higher concentrations of hepatic Cd and Se exhibited greater nuclear alterations, interstitial hyperplasia/hypertrophy, interstitial mononuclear infiltrations and granulomas. Further, fish with higher Cd and Cu gill tissue levels displayed a significantly higher number of cytoplasmic alterations and lamellar epithelium lifting, hypertrophic and hyperplastic epithelium along with mucus cell hyperplasia. While the presence of liver lesions were not species or sex-specific, the presence of gill lesions decreased in the order female fourhorn sculpins?>?female shorthorn sculpins?>?male fourhorn sculpins?>?male shorthorn sculpins. Hepatic Hg concentrations exceeded known lowest observable effect doses (LOED) for fish (0.1–0.5?μg g^?1 ww) in 27% of fish, while liver Cd residues in 80% exceeded LOED (0.42–1.8?μg g^?1 ww). Based upon these results, data suggest that using the sculpin as a valuable sentinel fish species histopathology may serve as a reliable tool for assessing marine ecosystem exposure to trace metals. However, confounding physiological and ecological factors also need to be considered.     

Assessment of potentially toxic elements in Swiss chard and sediments of Akaki River,Ethiopia

For the determination of 15 potentially toxic elements (V, Cr, Fe, Mn, Co, Ni, Cu, Zn, As, Se, Ag, Cd, Sn, Hg, and Pb) in plant and sediment samples of the Akaki River, Ethiopia, inductively coupled plasma–mass spectrometry, inductively coupled plasma–optical emission spectrometry, and a RA-915+ mercury analyzer were applied. Sediment and plant samples were mineralized using a closed-vessel microwave-assisted digestion system. The elemental concentrations varied considerably in plant and sediment samples. The minimum concentration was observed for known toxic elements (As, Hg, and Cd) while the highest concentration was observed for the elements of relatively low toxicity Zn, Mn, and Fe. The concentration of Cr, Fe, Pb, Zn, and As in Swiss chard surpassed the maximum permissible levels at specific sites. At some of the sites, the sediment quality guidelines are surpassed for Cu, Zn, and Pb.     

Ultrasound-assisted emulsification/microextraction based on solidification of trace amounts of thallium prior to graphite furnace atomic absorption spectrometry determination

In the present work, determination of ultratrace amounts of thallium in water samples was performed by ultrasound-assisted emulsification microextraction based on solidification of a floating organic drop as sample preparation method prior to furnace atomic absorption spectrometry. 1-(2-Pyridylazo)-2-naphthol was used as chelating agent. The factors influencing the complex formation and extraction, such as pH of the aqueous solution, the type and the volume of extraction solvent, the volume of chelating agent solution, and the extraction time were investigated. Under optimized conditions, the enrichment factor was 200. The calibration graph was linear from 0.2 to 10.0 μg L^?1 with a correlation coefficient of 0.9966, the detection limit was 0.03 μg L^?1 and reproducibility was ±3.3% (C = 5.0 μg L^?1, n = 8). The method was successfully applied for the determination of thallium in water samples.     

Heavy metals in soils and crops in Southeast Asia

In a reconnaissance soil geochemical and plant survey undertaken to study the heavy metal uptake by major food crops in Malaysia, 241 soils were analysed for cation exchange capacity (CEC), organic carbon (C), pH, electrical conductivity (EC) and available phosphorus (P) using appropriate procedures. These soils were also analysed for arsenic (As), cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), mercury (Hg), nickel (Ni), lead (Pb) and zinc (Zn) using aqua regia digestion, together with 180 plant samples using nitric acid digestion. Regression analysis between the edible plant part and aqua regia soluble soil As, Cd, Cr, Cu, Hg, Ni, Pb and Zn concentrations sampled throughout Peninsular Malaysia, indicated a positive relationship for Pb in all the plants sampled in the survey (R ² = 0.195, p < 0.001), for Ni in corn (R ² = 0.649, p < 0.005), for Cu in chilli (R ² = 0.344, p < 0.010) and for Zn in chilli (R ² = 0.501, p < 0.001). Principal component analysis of the soil data suggested that concentrations of Co, Ni, Pb and Zn were strongly correlated with concentrations of Al and Fe, which is suggestive of evidence of background variations due to changes in soil mineralogy. Thus the evidence for widespread contamination of soils by these elements through agricultural activities is not strong. Chromium was correlated with soil pH and EC, Na, S, and Ca while Hg was not correlated with any of these components, suggesting diffuse pollution by aerial deposition. However As, Cd, Cu were strongly associated with organic matter and available and aqua regia soluble soil P, which we attribute to inputs in agricultural fertilisers and soil organic amendments (e.g. manures, composts).     

Source identification of particulate matter and associated intake of elements through inhalation in an industrial area of Odisha,India

Particulate matter concentrations were measured in an industrial region in the Ganjam district of Odisha. The average levels of suspended particulate matter (SPM) were measured to be 142 ± 8 and PM₁₀ of particulate matter with a size of less than 10 micrometers (PM₁₀) to be 50 ± 15 μg m^?3. Out of the 14 elements determined, Ca, Na, Mg, Fe, and K contributed more than 95% of the total weight. In enrichment factors, the trace elements, i.e., Zn, Pb, Cd, and Hg were observed to be highly enriched in the SPM and PM₁₀. Factor analysis indicates that more than 75% of the variance was due to five component factors, which have eigenvalues greater than 1. Intake of elements through inhalation route to adults has been estimated.     

PIXE characterization of PM10 and PM2.5 particulates sizes collected in Ikoyi Lagos,Nigeria

Ambient concentrations of PM₁₀ (x?≤?10?µm) and PM_2.5 (x?≤?2.5?µm) particulate fractions collected from Ikoyi Lagos, Nigeria, as well as their elemental compositions are presented in this study. Both size-segregated fractions were collected using a double staged ‘Gent’ stack filter unit sampler. Elemental characterizations of dust laden filters were carried out using proton-induced X-ray emission (PIXE) technique. Twenty-two elements (Si, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Pb, Br, Rb, Sr, Zr, Ag, Cd, and Ta) were detected as well as their concentrations and correlations were determined for both particulate size fractions. Their correlation matrix result indicates that some of the trace elements detected could have common source origins or similar chemical properties. The results were similar to the levels observed in moderately polluted urban areas and there is need for source identification and apportionment using receptor models in future studies.     

Levels of selected heavy metals in commercial fish from five freshwater lakes,Pakistan

The levels of As, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Zn and Hg are estimated by atomic absorption in the muscle of six commercial species of fish belonging to five freshwater lakes of Pakistan. The species included Mastacembelus armatus, Tor putitura, Mystus seenghala, Wallago attu, Catla catla and Labeo rohita. The fish were procured in comparable weight ranges so that a viable comparison of trace metal content could be effected. As, Fe, Pb, Zn and Hg showed elevated levels of 0.006–6.967, 0.933–6.133, 0.060–4.108, 0.978–5.363 and 0.030–3.211 μg/g, wet weight. The relevant statistical parameters, such as standard deviation, standard error, skewness and its t‐value are also reported for establishing the randomness of the distribution in relation to the corresponding data of freshwater lakes of the world and examined in view of species‐specificity and origin.     

Potentially toxic elements in some fresh water bodies in Ethiopia

A total of thirty three water samples were collected from Tinishu Akaki River, Lake Awassa, and Lake Ziway, Ethiopia. Multi-element determination of trace elements (V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Se, Ag, Cd, Sn, Hg, and Pb) in water samples was carried out by inductively coupled plasma-mass spectrometry after acidification with 1% HNO₃. The concentration (in µg?L^?1) of the elements were in the range of 1.0–19, <0.42–83, 1.1–1580, <45–1760, <0.11–2.0, 0.43–13, 0.77–13, 6–300, <0.94–2.0, <0.3–1.5, <0.012–0.63, 0.13–4.8, <0.29, and 0.2–7.2 for V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Se, Ag, Cd, Sn, Hg, and Pb, respectively. The concentrations of all the quantified elements, with the exception of Mn, were in the range of the permissible limits of the Ethiopian, European Community, and World Health Organization for both drinking water quality guidelines and irrigation water guidelines. The accuracy of the method was validated by analyzing trace elements in water standard reference material (SRM 1643e). The measured values of trace elements in the SRM agreed well with the certified values at the 95% confidence level.