Assessment of drinking water quality using ICP-MS and microbiological methods in the Bholakpur area,Hyderabad, India

A total of 16 people died and over 500 people were hospitalized due to diarrhoeal illness in the Bholakpur area of Hyderabad, India on 6th May 2009. A study was conducted with immediate effect to evaluate the quality of municipal tap water of the Bholakpur locality. The study consists of the determination of physico-chemical properties, trace metals, heavy metals, rare earth elements and microbiological quality of drinking water. The data showed the variation of the investigated parameters in samples as follows: pH 7.14 to 8.72, EC 455 to 769 μS/cm, TDS 303.51 to 515.23 ppm and DO 1.01 to 6.83 mg/L which are within WHO guidelines for drinking water quality. The water samples were analyzed for 27 elements (Li, Be, B, Na, Mg, Al, Si, K, Ca, V, Cr, Mn, Fe, Ni, Co, Cu, Zn, As, Se, Rb, Sr, Mo, Ag, Cd, Sb, Ba and Pb) using inductively coupled plasma-mass spectrometry (ICP-MS). The concentrations of Fe (0.12 to 1.13 mg/L), Pb (0.01 to 0.07 mg/L), Cu (0.01 to 0.19 mg/L), Ni (0.01 to 0.15 mg/L), Al (0.16 to 0.49 mg/L), and Na (38.36 to 68.69 mg/L) were obtained, which exceed the permissible limits of the World Health Organization (WHO) for drinking water quality guidelines. The remaining elements were within the permissible limits. The microbiological quality of water was tested using standard plate count, membrane filtration technique, thermotolerant coliform (TTC), and most probable number (MPN) methods. The total heterotrophic bacteria ranged from 1.0 × 10⁵ to 18 × 10⁷ cfu/ml. Total viable bacteria in all the water samples were found to be too numerable to count and total number of coliform bacteria in all water samples were found to be of order of 1,100 to >2,400 MPN index/100 ml. TTC tested positive for coliform bacteria at 44.2°C. All the water samples of the study area exceeded the permissible counts of WHO and that (zero and minimal counts) of the control site (National Geophysical Research Institute) water samples. Excessively high colony numbers indicate that the water is highly contaminated with microorganisms and is hazardous for drinking purposes. Bacteriological pollution of drinking water supplies caused diarrhoeal illness in Bholakpur, which is due to the infiltration of contaminated water (sewage) through cross connection, leakage points, and back siphoning.     

Spatial distribution of major and trace elements in the water of Swarzędzkie Lake (Poland)

In order to characterize the contamination of the Swarzedzkie Lake and generate elemental distribution patterns 18 elements have been determined in samples of water, taken just above the bottom sediments. Analyses were carried out using two instrumental techniques - ICP-OES and ICP-MS. Two main sources of contamination were identified - diffuse pollution from agriculture and stormwater from the town. Three separate groups of elements were distinguished using cluster analysis and two groups using principal component analysis. These three groups are characterized as geogenic elements (Ag, As, Mg and Sb), elements supplied by the agricultural catchment (Ca, Mn, Sr, Na, K and Al) and elements originated from the urban contamination (Ni, Cr, Cu, Fe, V, Ba, Zn and Pb). PCA differentiated the above group of urban elements from the rest, originated from diffuse sources, with exception of alluminium, which was situated between two distinguished groups.     

Trace elements accumulation in edible tissues of five sturgeon species from the Caspian Sea

This study is focused on twenty trace elements (Ag, Ba, Bi, Cd, Co, Cr, Cs, Cu, Ga, In, Mn, Mo, Pb, Rb, Sb, Sn, Sr, Ti, V, Zn) accumulation in muscles of five sturgeon species (Acipenser guldenstaedti, A. persicus, A. nudiventris, A. stellatus and Huso huso) from the southern part of the Caspian Sea. Moreover the relationships between some biological characteristics and the levels of the selected elements as well as inter-elemental relationships were assessed. The samples (10 specimens for each the five species) were collected from two important sturgeon fishery zones located in the Iranian part of the Sea in 2002. Concentrations of the elements were determined using ICPMS. Only in the case of Cs could significant differences between two selected sampling areas be detected. There were significant differences in levels of Co, Ga, Rb, Sn, Ti, Pb and Bi in muscles of the species. Only in the case of Cd weight related differences among the species were found. The significant length dependent relationships were observed for Ga and Ba. Patterns of elements accumulation were assessed by statistical methods and compared to the other researches. In all the cases, the amounts of toxic trace elements (Cd, Cu, Pb and Zn) were markedly below the international guidelines for human consumption.     

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.     

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.     

Multielement analysis in the fish hepatic cytosol as a screening tool in the monitoring of natural waters

The possibility of direct measurement of trace elements in hepatic cytosol of European chub (Squalius cephalus) by high-resolution inductively coupled plasma mass spectrometry (HR ICP-MS) after cytosol dilution with Milli-Q water and subsequent acidification was investigated. Due to low detection limits of this procedure, determination of 13 elements (As, Cd, Co, Cu, Fe, Mn, Mo, Pb, Sb, Sn, Sr, V and Zn) was possible in the chub hepatic cytosol, exhibiting excellent measurement repeatability in duplicates. Some of these elements were also measured by HR ICP-MS in acid digested cytosols (Cd, Co, Cu, Fe, Mn, Mo, Sr, V and Zn). Good agreement of the results obtained after sample dilution and sample digestion indicated that complex organic matrix of hepatic cytosol did not affect measurement reliability. Cytosolic concentrations of 13 trace elements in the chub liver were quantified in the following order: Fe, Zn>Cu>Mn>Mo>Sr, V, Cd>Co>As, Pb>Sn>Sb. Unlike Cd, Cu, Fe, Mn and Zn for which the cytosolic concentrations were previously reported after measurement by AAS, cytosolic concentrations of eight additional trace elements characteristic for the liver of chubs inhabiting the low contaminated river water were reported here for the first time (in nanogrammes per gramme)—Mo, 136.8–183.6; Sr, 32.7–63.0; V, 17.5–69.0; Co, 24.3–30.7; As, 9.9–29.5; Pb, 5.8–35.6; Sn, 5.5–12.4; and Sb, 0.9–2.6. The simultaneous measurement of large number of trace elements in the cytosolic fractions of fish tissues, which comprise potentially metal-sensitive sub-cellular pools, could be beneficial as a screening tool in the monitoring of natural waters, because it would enable timely recognition of increased fish exposure to metals.     

Trace element concentration in groundwater of Pesarlanka Island, Krishna Delta, India

There is a growing concern over the potential accumulation of trace element concentration in groundwater of coastal aquifer owing seawater encroachment in the last several decades. A total of 29 groundwater samples collected from Pesarlanka Island, Krishna delta, Andhra Pradesh, India were analyzed for 13 trace elements (B, V, Mn, Fe, Ni, Co, Cu, Zn, As, Sr, Cd, Ba, and Pb) using inductively coupled plasma mass spectrometry. The results reveal that B, Fe, Ni, As, Sr, and Pb vary from 11.22 to 710.2, 1.25 to 684.6, 0.02 to 37.33, 27.8 to 282.3, 164.1 to 7,009, and 1.97 to 164.4 μg/l, respectively. Ba, Cd, Co, Cu, Ni, V, and Zn are almost within permissible limits for drinking water, but As, Fe, Mn, Pb, B, and Sr are above the permissible limit. The toxic element Pb is 1.64 times more than the maximum permissible limits of drinking water. The minimum value of As is also 2.78 times more, whereas the maximum is 28.2 times the permissible limit. The spatial distributions of alkaline earths (Sr, Ba), transition metals (V, Co, Ni, Fe), metallic elements (Cu, Pb), and (As) were found in considerable variation in the entire Island. Good cross-correlations were found between As, B, Co, and Sr with total dissolved solids and among other trace elements such as B, As, Co, and Sr. The variability observed within the groundwater samples is closely connected to the sea spray input; hence, it is primarily a consequence of geographical and meteorological factors, such as distance from the ocean and time of year. The trace element levels, in particular those of heavy metals, are very low, suggesting an origin from natural sources rather than from anthropogenic contamination. A few trace elements (Sr and B) are found as sensitive parameters responding to changes in fresh to saline groundwater environment. The highly elevated trace elements in this area which may be attributed to marine sediments or death and decay of plants are presented in this paper.     

Heavy Metal Pollution of Surface Soil in the Thrace Region, Turkey

Abstact Samples of surface soil were collected at 73 sites in the Thrace region, northwest part of Turkey. Two complementary analytical techniques, epithermal neutron activation analysis (ENAA) and atomic absorption spectrometry (AAS) with flame and graphite furnace atomization were used to determine 35 elements in the soil samples. Concentrations of As, Cd, Co, Cu, Mn, Ni, Pb and Zn were determined using AAS and GF AAS, and ENAA was used for the remaining 27 elements. Results for As, Ba, Br, Ca, Cd, Ce, Co, Cr, Cs, Cu Eu, Fe, Hf, I, In, K, La, Mn, Mo, Na, Nd, Ni, Pb, Rb, Sb, Sc, Sm, Sr, Ta, Tb, Th, Ti, U, V and Zn are reported for the first time for soils from this region. The results show that concentrations of most elements were little affected by the industrial and other anthropogenic activities performed in region. Except for distinctly higher levels of Pb, Cu, Cd and Zn in Istanbul district than the median values for the Thrace region, the observed distributions seem to be mainly associated with lithogenic variations. Spatial distributions of As, Cd, Cr, Cu, Ni, Pb and Zn were plotted in relation to the concentration values in soil using Geographic Information System (GIS) technology     

Age dependence of potentially toxic elements (Sb,Cd, Pb,Ag) in human liver tissue from paediatric subjects

Toxic elements are present at low concentrations in the environment. This work was undertaken to investigate the age dependence of the liver content of selected elements in paediatric populations, as an index of internal exposure. Liver samples were collected at autopsy from 157 subjects, aged < 1 day to 6 years, as part of investigations on a possible role of Sb compounds in sudden infant death syndrome (SIDS). In addition to Sb, the concentrations of Ag, Cd and Pb were also determined by inductively coupled plasma mass spectrometry on the remaining digest. Comparison of 95% confidence intervals of the median concentrations of the four elements suggested that there were no differences between the two categories of cause of death, SIDS or those who had died of an identified disease. Cadmium, lead and antimony median concentrations were lower than corresponding values observed in adult populations. Silver concentrations were significantly higher at birth and decreased with age. Cadmium levels were almost negligible in neonates and infants, but increased in older children. The finding of non-negligible concentrations of both Ag and Pb in neonatal liver provides further direct evidence that these elements cross the human placental barrier. The reported data, by far the largest collection observed in subjects less than 1 year old, are the result of exposure, during pregnancy and in early childhood, to present levels of these elements in the environment. They can serve as a reference to compare post-mortem values from individuals or groups of subjects in this age range when an exposure risk is suspected and to highlight trends in human exposure.     

Detection of metal contamination in wild asparagus near a waste disposal site

Estimating contaminant distributions in environmental media is necesary to evaluate human and ecological hazards. Because of uncertainties in release histories and transport, traditional sampling and statistical techniques applicable to the experimental sciences may not be suitable for exploratory studies at hazardous waste sites. An approach that relies on cluster analysis of principal components (PCA) was used to identify contaminated wild asparagus (Asparagus officinalis) growing in the vicinity of waste disposal sites along the Columbia River at the U.S. Department of Energy's Hanford Site in southeast Washington state. Metals in soil samples taken from the sites contained elevated levels of Ag, Al, Ba, Cd, Cr, Cu, Hg, Ni, Pb, Sb, Zn, and V. Samples of asparagus tissue were collected from the river near the waste site, from Hanford old fields abandoned 52 years ago, and from commercial fields in the neighboring communities. Dried tissues were analyzed for metals content by ICP-mass spectrometry, furnace AA, and cold vapor AA. Tissue concentrations of elements varied over 5 orders of magnitude, from K at 46 900 ppm to As and Ag at maximum concentrations below 1 ppm. PCA produced four components that accounted for 66.2% of the metals variance. Subsequent cluster analysis using Ward's minimum variance separated the data into Columbia River and old-field groups, with the River group further divided into three clusters: plants primarily upriver from the waste sites, plants primarily downriver, and plants growing in or near the waste sites. The clustering showed that the more soluble components of the discharges (Ba and Ca) showed a pattern of distribution in the asparagus plants consistent with the ground water flow pattern, in that these elements were found far downriver of the disposal sites themselves. In contrast, the less mobile elements Al, Cd, Cr, Fe, Mn, Tl, and Zn were elevated only near the most-recently used waste disposal area. Asparagus from agricultural fields, including fields abandoned 50 years ago, contained higher concentrations of Fe, Cu, Pb, K, and Ni than did the wild riverine plants.The U.S. Governments right to retain a non-exclusive royalty free licence in and to any copyright is acknowledged.     

Characterization and source identification of airborne trace metals in Singapore

Airborne particulate trace metals have important health implications. As a consequence, their concentrations are increasingly monitored in many urban locations worldwide. In this study, fine atmospheric particles (PM(2.5)) were collected in Singapore over a period of 83 consecutive days during 2000, and analysed to determine the concentration of trace elements using ICP-MS. Altogether, eighteen airborne trace metals were quantified: Al, Ag, Ba, Cd, Cr, Co, Cu, Fe, Ga, Li, Mn, Ni, Pb, Sr, Zn, V, Si, and Ti. While Li was the least abundant trace metal with a mean concentration of 0.2 ng m(-3), Zn showed the maximum mean concentration of 279.1 ng m(-3). Calculation of enrichment factors indicated that the elements Pb, Zn, Cd, V, Ni, Cr, and Cu were enriched by factors of 30 to 5000 relative to their natural abundance in crustal soil. The extent of metal pollution in the study area was assessed by comparing the measured concentrations to those reported in the literature for a selected number of urban sites in other parts of the world. Factor analysis was used to identify the major sources affecting particulate air pollution in Singapore. The sources that contribute to the loading of trace metal-bearing aerosols in the Singapore urban atmosphere include fuel oil-fired power plants, metal processing industry, land reclamation and construction activities, municipal solid waste incinerators, and traffic emissions.     

Assessment of Groundwater Quality in a Structurally Deformed Granitic Terrain in Hyderabad, India

Geochemical study of groundwater from a structurally deformed granitic terrain near Hyderabad (India) was carried out to understand and evaluate the hydrogeochemical processes and quality of groundwater. Several trace elements (Fe, Mn, Be, Al, V, Cr, Co, Ni, Cu, Zn, As, Sr, Mo, Cd, Sb, Ba, Pb, U) along with major ions and minor elements were precisely estimated in shallow and drilled wells to know the suitability of water for drinking and irrigation purposes. Analytical data shows that pH and major ion chemistry in dug wells and bore wells do not vary significantly, while some trace elements (Fe, Mn, Al, Be, Co, Pb, U and Zn) vary in dug wells and bore wells, which can be attributed to differential mineral weathering and dissolution/precipitation reactions along fractures/joints. Although the water is not potable, it was found to be suitable for irrigation with little danger in the development of harmful level of exchangeable sodium. It is inferred that the chemical composition of the groundwater in this region is likely to have its origin from silicate weathering reactions and dissolution/precipitation processes supported by rainfall and groundwater flow.     

Examination of honeys and flowers as soil element indicators

Detection of soil element deficiencies is time consuming, requiring a major commitment for field work and analysis. Bees concentrate some elements in their honey which could allow soil element concentrations to be predicted without having to take large numbers of soil samples. We measured 14 element concentrations in soil, sunflower, acacia flower and honey samples from two different regions of Hungary. Across sites, the elements with significant correlation coefficients between honey and soil concentrations, in descending order of probability, were Cu > Ba >Sr = Ni > Zn > Mn = Pb >As. Bioconcentration from soil to honey was similar for areas with acacia and sunflower flowers. In the macroelements, it was the greatest for K, S and P and least for Mg and Na, and in the microelements, greatest for B, then Zn, then Cu, then As, Mo and Sr and least for Fe, Ba, Mn and Pb. It is concluded that in acacia and sunflower-growing regions, honey can give an accurate estimate of soil element concentrations for Cu and Ba and provides relevant information for Sr, Ni, Zn, Mn, Pb and As.     

Soil Contribution to the Elemental Composition of Epiphytic Lichens (Tuscany, Central Italy)

Total concentrations of Al, Ba, Cd, Co, Cr, Cu, Fe, Mn, Mo, Pb, Sr, Ti, V and Zn in the epiphytic lichen Parmelia sulcata and superficial soils from 60 remote sampling sites in Tuscany (central Italy) were determined to evaluate the contribution of soil to the elemental composition of the lichen. The results showed that in the Mediterranean environment, the trace element content of unwashed lichen samples is greatly affected by soil contamination. However, despite the strong correlations between the concentrations of lithogene elements such as Al, Fe and Ti in P. sulcata, lichen levels of these elements were not at all linearly correlated with their concentrations in the soil, suggesting that dust contamination is highly variable and probably dependent on local site characteristics. All methods evaluated to minimize soil contamination indicated Cu, Pb and Zn as elements of atmospheric origin. However, while levels of Pb were similar to those reported for background areas, moderate pollution by Cu and Zn, probably from fertilizers used in agriculture, was revealed. For elements such as Cd and Mo, identified as atmophile, some uncertainty exists due to the fact that they are essential for lichen metabolism and accumulate intracellularly in lichens; they may therefore occur in soluble form in the lichen thallus.     

Assessment of heavy metal enrichment in the offshore fine-grained sediments of the Caspian Sea

Sampling of the offshore seabed sediments of southwestern part of the Caspian Sea was carried out by gravity corer in order to study heavy metal concentration and the physicochemical factors controlling their distribution in the fine-grained fraction. The grain size distribution, amount, and type of clay minerals, total organic carbon (TOC) content, and Eh–pH of the sediments were determined. The average concentrations of the heavy metals in ppm are Mn (563), Cu (207.5), Sr (187), Zn (94), Pb (26.3), Ni (14.5), Co (11.5), Cd (2.56), and Ag (1.04) in their order of abundances. Co and Zn mostly indicate increase in silt-size fraction of the sediments suggesting their probable detrital provenance but the Mn, Ni, Cu, Sr, Pb, Cd, and Ag concentrations show a similar trend to distribution of the clay-size fraction. The concentrations of Mn, Co, and Cd increase with increase in the TOC content but the Cu, Pb, Ni, Ag, and Sr concentrations decrease with increase of the TOC content. The amounts of Zn, Cu, Sr, Pb, Cd, and Ag increase with increase in the CaCO₃ content. The calculated enrichment factor indicates that the sediments are very strong to extremely enriched in Ag, significantly enriched in Cu and Cd, and depleted to mineral for Pb, Sr, Co, Ni, and Zn. Variations of the Cu, Sr, Cd, Ag, and Pb concentrations are similar to the clay and CaCO₃ distributions.     

Geochemical patterns in soils in and around Siddipet, Medak District, Andhra Pradesh, India

This paper reports the first results of geochemical survey carried out in and around Siddipet, taking soil (topsoil 0–25 cm and subsoil 70–95 cm) as the sampling media. The data were obtained in a consistent way from 61 sites. The samples were analyzed for 29 elements (As, Ba, Cd, Co, Cr, Cu, F, Mo, Ni, Pb, Rb, Se, Sr, Th, U, V, Y, Zn, Zr, Si, Al, Fe, Mn, Mg, Ca, Na, K, Ti, and P) by X-ray fluorescence spectrometer, and baseline levels for these elements are presented. Results reveal that the correlation between the geochemical patterns in the soils developed on different litho-variants is not straight forward, but some general trends can be observed. Regional parent materials and pedogenesis are the primary factors influencing the concentrations of trace elements while anthropogenic activities have secondary influence.     

微波消解-电感耦合等离子体质谱法同时测定废水中20种元素

采用微波消解-电感耦合等离子体质谱法,同时测定了废水中Be、V、Cr、Mn、Co、Ni、Cu、Zn、As、Se、Mo、Ag、Cd、Sb、Ba、Hg、Tl、Pb、Th、U等20种元素,比较了5种不同消解体系对废水样品的加标回收结果,确定采用硝酸+过氧化氢消解体系。Hg在0.050μg/L～2.00μg/L、其他元素在5.00μg/L～500μg/L范围内线性良好,检出限为0.01μg/L～0.2μg/L,国家有证标准物质的测定结果符合要求,废水样品平行测定的RSD为2.6%～6.5%,加标回收率为84%～110%。     

Assessment of trace elements in the shell layers and soft tissues of the pearl oyster Pinctada radiata using multivariate analyses: a potential proxy for temporal and spatial variations of trace elements

Concentrations of trace elements (Cd, Cu, Ni, Pb, V, and Zn) were determined in the soft tissues (adductor muscle and gills) of the pearl oyster Pinctada radiata and surficial sediments from two sampling sites located in the northern part of the Persian Gulf by Graphite Furnace Atomic Absorption Spectrophotometer (GFAAS). Moreover, the levels of Li, Mg, Al, Mn, Fe, Cu, Sr, Ba, Pb, and Zn were measured in two shell layers (prismatic and nacreous) using Laser Ablation Inductively Coupled Plasma Mass Spectrometer (LA-ICP-MS). There were significant differences between the sampling sites with regard to mean concentrations of Cu, Mn, and Al in the prismatic layers of the shells. But in terms of the soft tissues, only in the case of Ni accumulation in the muscle significant differences between the sites could be observed. No significant differences could be found between the sites from the elements concentrations in the sediments point of view. The levels of Cd, Cu, Ni, and Zn in the gills were markedly higher than those in the muscle. Concentrations of Mn, Mg, Li, and Cu in the prismatic layer were significantly higher than in the nacreous but the reverse case could be found for Sr. The patterns of metal occurrence in the selected tissues, shell layers, and sediments exhibited the following descending order: Zn, Ni?>?Cd, Cu?>?V, and Pb and Zn, Ni, Cd?>?Cu, V, and Pb for muscle and gills, respectively; Zn?>?Cu, Ni, Pb, Cd, and V for sediments; Mg?>?Sr, Mn, Li, Al, Fe, Ba, Cu, Pb, and Zn for the prismatic layer; and Sr, Mg?>?Mn, Al, Fe, Li, Ba, Cu, Pb, and Zn for the nacreous layer. In most cases, the temporal variations of the elements levels in the prismatic layer were clearer than those in the nacreous layer (especially for Li, Mg, Mn, Pb, and Fe). Comparison of the gained data from this study with the other relevant researches shows that in most cases the levels of the elements in this investigation either fell within the range for other world areas or were lower. Generally, it can be concluded that the shell (especially prismatic layer) of P. radiata can be considered as a suitable proxy for temporal and spatial variations of the trace elements (and probably some environmental parameters) in the study area.     

Levels of synthetic musk compounds in municipal wastewater for potential estimation of biota exposure in receiving waters

We analyzed water samples from the confluence of three municipal sewage treatment effluent streams, surface water, and whole carp (Cyprinus carpio) for synthetic musks for a period of 7-12 months. The lipid content of each fish was determined and compared with the concentration of musks in the whole fish tissue. Enhanced methods were used for water sampling and musk extraction. The data presented here provide insight as to the relationship between concentrations of synthetic musks in the municipal effluent and associated biota. This study confirmed the presence of polycyclic and nitro musk compounds in sewage effluent, Lake Mead water, and carp. The concentrations were found to be considerably lower than previous studies conducted in other countries. This study also provides data for polycyclic and nitro musk compounds, as well as some of the nitro musk metabolites in sewage treatment plant effluent, lake water, and carp.     

Atmospheric heavy metals in tropical South America during the past 22,000 years recorded in a high altitude ice core from Sajama, Bolivia

V, Co, Cu, Zn, As, Rb, Sr, Ag, Cd, Ba, Pb, Bi and U have been analysed by inductively coupled plasma sector field mass spectrometry in various sections of a dated snow/ice core drilled at an altitude of 6542 m on the Sajama ice cap in Bolivia. The analysed sections were dated from the Last Glacial Stage ( approximately 22,000 years ago), the Mid-Holocene and the last centuries. The observed variations of crustal enrichment factors (EFc) for the various metals show contrasting situations. For V, Co, Rb, Sr and U, EFc values close to unity are observed for all sections, then showing that these elements are mainly derived from rock and soil dust. For the other metals, clear time trends are observed, with a pronounced increase of EFc values during the 19th and 20th centuries. This increase shows evidence of metal pollution associated with human activity in South America. For Pb an important contribution was from gasoline additives. For metals such as Cu, Zn, Ag and Cd an important contribution was from metal production activities, with a continuous increase of production during the 20th century in countries such as Peru, Chile and Bolivia.