Relations between sulphate,ammonia, nitrate,acidity and trace element concentrations in tree bark in The Netherlands

Bark flakes were sampled in a biomonitoring survey throughout The Netherlands. Tree species used were oak (65 samples) and non-oak (58 samples) (poplar, elm, willow). Bark elemental analysis was carried out for As, Br, Ca, Cd, Ce, Co, Cr, Cs, Fe, Hg, K, La, Na, Ni, Pb, Rb, Sb, Sc, Se, Sm, Th, and Zn. Furthermore, bark acidity, SO₄, NH₄ and NO₃ were determined. Further variables introduced into the data-set were DIST (closest distance to sea water) and the dummy variably OAK (tree species).Straightforward multivariate correlation analysis was performed to check the effects on bark metal retention of the non-metal pollutants SO₄, NH₄ and NO₃, and of bark acidity. The OAK variable served to identify species-specific metal and non-metal pollutant behaviour. The DIST variable was used to visualize geography(source)-related variations in bark metal and non-metal pollutant concentrations, and to account for the non-random distribution of OAK and non-OAK tree species.The results indicate that the non-oak and oak bark samples may be combined to form 123 samples containing data-set for As, Br, Cd, Ce, Co, Fe, La, Na, Sc, Sm, Th, Zn, NH₄, NO₄, SO₄ and acidity, but not for Rb, Cs, Se, K, Ni, Pb and Sb (species-specific) and for Ca and Hg (H⁺-dependent). In the presented data-set, bark sulphate, ammonia and nitrate could not be shown to significantly affect bark metal retention.     

Contribution to biomonitoring of some trace metals by deciduous tree leaves in urban areas

Leaves of the deciduous tree species, horse chestnut (Aesculus hippocastanum L.) and Turkish hazel (Corylus colurna L.) were used as accumulative biomonitors of trace metal pollution in the urban area of Belgrade. Using differential pulse anodic stripping voltametry, trace metal concentrations (Pb, Cu, Zn, Cd) were determined at the single leaf level (ten leaves per species, per month), during two successive years with markedly different atmospheric level of trace metals. Increased trace metal concentrations in the leaves of A. hippocastanum reflected elevated atmospheric trace metal pollution, whereas C. colurna L. did not respond accordingly. The contents of Pb and Zn in soil over the same period also followed this trend. Anatomical analyses, in young as well as in old leaves of both species, indicated typical foliar injuries of plants exposed to stressful air conditions. Water relations that correspond to leaf age may have contributed to the considerable trace metal accumulation in leaves.     

Distribution of trace metals in marine sediments of the Bay of Palma de Mallorca (Mallorca Island, Spain)

Metals were determined in surface bottom marine sediments of the Bay of Palma de Mallorca (Spain) by microwave-assisted acid-oxidant digestion and inductively coupled plasma–optical emission spectrometry in order to assess the level and distribution of potentially metallic pollutants. Average concentrations found were 1.2?±?0.3 Al and 1.9?±?0.9 Fe (in milligrams per gram), and 8?±?2 Cr, 2?±?1 Cu, 60?±?10 Mn, 4?±?1 Ni, 6?±?4 Pb, 50?±?7 Sn and 10?±?3 Zn (in micrograms per gram). Enrichment factors using normalized values to Al were also calculated which indicated that sediments were Sn and Pb enriched. Sediments were fractionated by grain size: <63, 63–250, 250–500 and >500 (in micrometres), and the metals' affinity towards the different fractions was studied. The metals' affinity to the finer fraction was evidenced, excluding Sn and Mn that showed practically no affinity for fine grains. Latent variables were extracted from the data using principal components analysis. It allowed samples to be grouped in two clusters, and most of the metals (Al, Cr, Cu, Fe, Ni, Pb and Zn) showed a similar distribution pattern. Sn and Mn showed a distinct pattern.     

Seasonal variation in trace metals concentrations in the Ialomita River, Romania

Sampling streams for metals is an important aspect of water-quality monitoring. Using ICP-AES the concentration of some microelements in the Ialomi?a River (Romania) were determined. In order to grasp the different phases of the river regime, samples were collected from its water-sediment interface at seven locations along the river, during three campaigns: during snow melting periods in the mountain zones (April), the period of reduced flow and high water temperature (August) and the period of high precipitations (November). HNO3 was added to the samples for fixation. Cadmium and copper appear accidentally; lead was detected only in samples collected in the vicinity of roads; the MAC (maximum admitted concentration) for surface waters is exceeded for nickel and chromium in samples collected in April and respectively in April and November; zinc concentrations were usually above the MAC; molybdenum concentration was above the set reference value, especially for samples collected in April and November. Possible explanations are given for the presence of the investigated microelements along the river.     

Determination of trace transition metals in environmental matrices by chelation ion chromatography

Trace transition metals (Fe^3?+?, Mn, Cu, Cd, Co, Zn, Ni) in environmental samples were analyzed by chelation ion chromatography using a mixed bed ion-exchange column with pyridine-2,6-dicarboxylic acid (PDCA) and oxalic acid as eluent and large volume direct injection (1,000 ??l). The two eluents, PDCA and oxalic acid, were tested, and repeatability and detection limits were compared. The total analysis time was ~15 min. The separation with PDCA was more successful than that obtained with acid oxalic. It was observed that utilizing PDCA resulted in lower detection limits, higher repeatability, and a quantitative detection of Cd and Mn, which coelute as a single peak when using the oxalic acid. At last, the PDCA calibration graphs resulted linear (r ²?>?0.999) in the range 0.4?C1,000 ??g/L. The procedure was applied to the analysis of metals in soils and in water samples. The results obtained from the analysis of natural waters have demonstrated that the method is simple and efficient, therefore, can be used for the determination of metals in natural waters using a continuous and automatic monitoring system.     

An assessment of tree health and trace element accumulation near a coal-fired generating station, Manitoba, Canada

A forest health assessment was performed in stands dominated by bur oak and trembling aspen to study the potential effects of airborne emissions from a 132 MW coal-fired station. Forty-two stands were sampled within a 16-km radius of the station for both foliar stress symptoms and trace element toxicology. The concentrations of tracer elements (As, Ba, Sr, and V) in the leaf litter were not spatially congruent with airborne emission deposition models (except Ba, which showed elevated levels immediately SE of the station), nor were they at phytotoxic levels. Elemental concentrations were significantly related to soil parameters including organic matter and texture. No patterns were found in forest health along directional or distance gradients from the generating station. Trembling aspen stands demonstrated little decline in general, but three of the 19 bur oak plots, all located on thin sandy soils developed on calcareous till, demonstrated branch dieback. In addition to poor soil conditions, two of these sites also had high water tables, and exhibited tree mortality. The bur oak decline did not appear to be related to emissions from the station, but is suspected to be a result of poor site quality, with urban development as a confounding factor.     

Monitoring trace metals in urban aerosols from Buenos Aires city. Determination by plasma-based techniques

A study was undertaken, within the framework of a 3 years national project, to assess the content of 13 elements in airborne particulate matter collected in representative zones of the metropolitan area of Buenos Aires. The sampling strategy followed consisted in collecting simultaneously 67 samples of PM10 particulate matter in 9 sampling sites covering an area of about 30 km2 during one week. The collection was performed on ash-free fibre-glass filters using high volume samplers. A combination of aqua regia and perchloric acid was used for leaching metals from filters. Key elements, namely Al, Ca, Cu, Fe, Mn, Mo, Ni, Pb, S, Sb, Sn, Zn and Zr, were determined by inductively coupled plasma-optical emission spectrometry (ICP-OES) and inductively coupled plasma-mass spectrometry (ICP-MS) at micro g g(-1) and ng g(-1) levels. Analyte concentration varied from 130 ng g(-1)(Mo) to over 30%(Ca). Multivariate statistical analysis was performed on the data set including the measured elemental compositions for the monitored period. The atmospheric concentration found for Pb confirms the decreasing levels of this element since the introduction of unleaded gasoline in 1995: 88 ng m(-3)(2001) < 220 ng m(-3)(1997) < 3900 ng m(-3)(1994). The average S concentration above 3 microg m(-3) is somehow unexpectedly high for Buenos Aires since the relatively low S content of liquid fuels and the massive usage of natural gas imply low emissions of this element from combustion activities. To the best of our knowledge, S concentrations are reported for the first time for this city.     

Spatial, temporal, and speciation variations of heavy metals in sediments of Nan'ao Island, a representative mariculture base in Guangdong coast, China

Heavy metals in sediments from Baisha Bay, Nan'ao Island, one of Guangdong Province's largest mariculture bases in Southern China, were investigated. The results display that the concentrations of 6 heavy metals from surface sediments were 0.040-0.220 (Cd), 24.22-39.61 (Pb), 25.30-42.66 (Cr), 10.83-19.54 (Ni), 15.06-39.24 (Cu) and 55.12-141.73 mg kg(-1) (Zn), respectively. The highest concentrations and the greatest increasing rates of heavy metals were found in a sediment core in a fish cage culture area due to receiving sewage discharge, uneaten fish bait, and boat gasoline combustion. Cd was preferentially associated with the acid-soluble fraction and Pb mainly with the reducible fraction in surface sediments. Meanwhile, Cd and Pb displayed greatest labile fractions, indicating anthropogenic origin. A principal component analysis (PCA) revealed three groupings (Cd; Cr, Ni and Cu; Pb and Zn) that mainly result from different distributions of the metals in the various fractions. The ecological risk of the polluted sediments stemmed mainly from Cd, and from Pb and Cu to a lesser degree. It is suggested that the density of fish-stocking be controlled, periodic movement of rafts (cages) be introduced, and the total numbers of net-cages and human activities in the mariculture zones be restricted. in order to facilitate the recovery of the polluted sediment.     

An assessment of contamination of the Fusaro Lagoon (Campania Province,southern Italy) by trace metals

The Fusaro Lagoon is a shallow lagoon, located in SW Italy, largely influenced in the last decades by several anthropic impacts. The study examined the pollution status of the lagoon, during year 2011–2012 at nine sampling stations with the aim to find out proper measurements of water lagoon restoration. Concentrations of heavy metals (HMs) (aluminium [Al], barium [Ba], cadmium [Cd], copper [Cu], iron [Fe], manganese [Mn], vanadium [V] and zinc [Zn]) were examined in water, sediments and specimens of the ascidian Ciona intestinalis sp. A. Low levels of dissolved oxygen concentration were detected at many stations, with mean values of 5.2–6.4 mg L^?1. The redox potential of surface waters was also low, ?2.7 to 50.7 mV. Sediments possessed high organic matter content, 17.7–29.4 %. In sediments, the mean Zn level, 251.4 mg kg^?1, was about sixfold higher than that recorded in year 2000 (38.5 mg kg^?1) and considerably higher than that recorded in 2007 (191 mg kg^?1). The mean levels of Cd were outstandingly high, with a mean value of 70.5 mg kg^?1, about 30- and 50-fold higher than those determined in 2000 and 2007, respectively. Cadmium (Cd), Cu and nickel (Ni) appeared in excess with respect to most current guidelines, reaching significant pollution levels. C. intestinalis sp. A was detected only at few stations, with metals accumulated preferentially in the body in respect to the tunic, from 1.2 times for Zn (178 mg kg^?1) to 4.0 times for V (304 mg kg^?1). Data suggests the necessity of an immediate action of eco-compatible interventions for environmental restoration.     

Summer distribution of trace metals in the western sector of the Ross Sea, Antarctica

The more important water masses generated by the interaction of Circumpolar Deep Water and the shelf waters in the western sector of the Ross Sea are characterized for trace element contents. The distribution of cadmium, lead, copper, zinc, iron, manganese and chromium during the austral summer is analysed and discussed according to the physical, chemical and biological processes which affect the composition of the water masses. The Cd concentration is found to have a relative high variability that can be related to biological activity and the water mass age, MCDW presents a mean dissolved concentration (SD) of 0.77 (0.07) nmol kg(-1), while the HSSW and AASW have a mean concentration of 0.63 (0.06) and 0.61 (0.16) nmol kg(-1), respectively. Lead features the typical distribution of a scavenged element with a surface maximum ranging between 22 and 130 pmol kg(-1) decreasing to 11 pmol kg(-1) in deep waters. However, the vertical distribution in the shelf area features a maximum concentration in intermediate/deep waters and we can hypothesize that the distribution may be influenced by more than one source. The surface dissolved concentration of zinc and copper were un-homogeneously distributed, the mean (SD) values were 5.25 (2.92) and 1.99 (1.49) nmol kg(-1) for zinc and copper, respectively and increased with depth for both the elements. We may therefore hypothesize enrichment in the dissolved phase deriving from recycling in deep waters. 95% of the chromium was in dissolved form and showed a superficial depletion; the mean concentrations were 1.6 +/- 0.2 and 2.6 +/- 0.8 nmol kg(-1) for surface and deep waters respectively. The vertical distribution of dissolved manganese was quite homogeneous with a mean concentration 0.96 +/- 0.7 nmol kg(-1). The particulate iron and manganese concentration trends are similar and feature a significant bottom increase implying a significant input from resuspension; the mean concentration of particulate ranged between 1.4 and 7.4 nmol kg(-1) for iron and ranged between 0.072 and 0.29 nmol kg(-1) for manganese.     

Source identification and assessment of sediment contamination of trace metals in Kogarah Bay,NSW, Australia

The distribution of trace metals (spatial and temporal) and sedimentary fractions were investigated to identify the concentrations and sources of trace metals within Kogarah Bay, NSW, Australia. A total of 59 surface sediments and six subsurface samples from core of the sediment were collected. The contamination factor and pollution load index indices used to evaluate environmental effects of trace metals. The study area was found to be uncontaminated with Cr and Ni, moderately contaminated with As and considerably contaminated with Cu, Zn and Pb. The concentrations of Cr and Ni were below both effect range low and effect range median, while As, Cu, Zn and Pb were slightly above effect range low. The highest concentrations of these trace metals such as Cu, Zn and Pb were found in the north, northwest and southeast of the bay, close to discharge points, stormwater outlets and around boatyards and watercrafts. The spatial distributions of metals were strongly related to muddy particles and organic matter. The temporal sediments of metals declined with increased sediment depth, which reflects accumulation of trace metals since European settlement in this area. Furthermore, the source of the trace metals was found to be stormwater outlets, gasoline fumes, boatyards and other human activities.     

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.     

Contribution of a municipal solid waste incinerator to the trace metals in the surrounding soil

This study analyses the pedological environment of the area near a municipal waste incinerator that has been operating in the south-east district of Pisa for approximately 20?years. There are many other industrial activities in the area besides the incinerator, which represent possible sources of pollution, as well as heavy road traffic. The study area was defined by a 0-4-km zone around the site with a population of approximately 12,000 residents. The study included the physical and chemical characterisation of 100 samples of soil and an analysis of trace metals such as Cr, Ni, Pb, Zn, Hg, As and Cd. The samples were grouped into soil use categories. The results showed Zn, Pb and Hg correlated with their potentially mobile fractions, and suggested an anthropic contribution to their presence in the soil. Ni, Cr and As showed values attributable to a lithological origin. This was consistent with the PCA results. The aim was to define the environmental state of the soil of the area in order to create a reference for future research and to verify the possible presence of pollution from other sources (local industrial activities and traffic).     

Determination of trace heavy metals in harvested rainwater used for drinking in Hebron (south West Bank,Palestine) by ICP-MS

Rainwater samples harvested for drinking from the west part of Hebron (south of West Bank in Palestine), the largest city in the West Bank, were analyzed for the content of different trace heavy metals (Cr, Mn, Co, Ni, Cu, Zn, Mo, Ag, Cd, Bi, and Pb) by inductively coupled plasma mass spectrometry (ICP-MS). This study was conducted to determine the water quality of harvested rainwater used for drinking of south West Bank (case study, Hebron area). A total of 44 water samples were collected in November 2012 from 44 house cisterns used to collect rainwater from the roofs of houses. The samples were analyzed for their pH, temperature, electrical conductivity, total dissolved solids, and different heavy metal contents. The pH of all water samples was within the US Environmental Protection Agency limits (6.5–8.5), while some water samples were found to exceed the allowed WHO limit for total dissolved solids (TDSs) in drinking water. Results showed that concentrations of the heavy metals vary significantly between the 44 samples. Results also showed that the concentration of five heavy metals (Cr, Mn, Ni, Ag, and Pb) is higher than the WHO limits for these heavy metals in drinking water. Overall, our findings revealed that harvested rainwater used for drinking of this part of south West Bank is contaminated with heavy metals that might affect human health.     

Assessment of trace metals using lichen transplant from automobile mechanic workshop in Ile-Ife metropolis,Nigeria

The level of air pollution around the automobile mechanic workshops has been generally overlooked. This study, examined the level of trace metals in automobile mechanic workshops and the suitability of using transplanted lichen thalli of Lepraria incana for measuring air pollution in such areas. Samples of the lichen thalli were transplanted into seven different sites and were attached to the bark of trees at each site. The samples were harvested from the sites after 3-month exposure. Concentrations of Pb, Cu, Cd, Fe, Zn, and S content were determined using an atomic absorption spectrophotometer. Results showed that there was a significant difference in the trace metals concentrations across the sites (p?<?0.05). The analyzed lichen samples showed a range of 91.26–119.35 ppm for Fe, 30.23–61.32 ppm for Zn, 1.25–2.45 ppm for Cu, 0.017–0.043 ppm for Cd, 0.018–0.051 ppm, and 0.37–0.42 ppm for S. From the study, sites 6 and 7 presented higher concentrations of Cd, Pb, and Zn than other sites. The enrichment factor calculated showed that Zn, Cd, and Pb were greatly enriched from the workshops. The trend in the concentration of these heavy metals suggests that activities in these workshops might become a major source of certain heavy metals in the environment and if the pollution activities persist, it might become worrisome over time.     

Distribution of mercury and other trace metals in the sediments of Cochin estuary (a Ramsar site), Kerala, India

Sediment quality data provide essential information for evaluating ambient environmental quality conditions. Sediments are important carriers of trace metals in the environment and reflect the current quality of the system. In the present study, distribution of mercury, lead, cadmium, copper, zinc, chromium and manganese in Cochin estuary were studied. The distribution of oxides of metals and textural quality were also studied in detail. It was found that the concentration of metals in the sediments near the industrial belt was extremely high. Correlation of different metals and metal oxides were analysed. It was found that all the alloys were correlated significantly (α?<?0.01) but in case of metals, correlation was only among certain metals.     

Recent trends of plutonium fallout observed in Japan: plutonium as a proxy for desertification

Plutonium in monthly deposition samples collected in Tsukuba (the Meteorological Research Institute), Japan from 1990 to end of 2001 is reported, together with monthly plutonium deposition in Nagasaki and Yonaguni in 2000. The annual deposition of (239,240)Pu during the period from 1990 to 2001 shows no systematic interannual variation. However, monthly (239,240)Pu depositions show a typical seasonal variation with a maximum in spring season (March to April), which corresponds to seasonal cycle of soil dusts originating from the East Asian arid area. Plutonium isotopic ratios in the deposition samples suggest that significant amounts of the recent (239,240)Pu deposition observed in Japan are attributed to the resuspension of plutonium-bearing surface soil particles; resuspended plutonium originates from the East Asian arid areas. The recent increased tendency of (239,240)Pu content in residues in deposition samples may reflect desertification in the East Asian continent.     

Spatial distribution and human contamination quantification of trace metals and phosphorus in the sediments of Chaohu Lake,a eutrophic shallow lake,China

Distinguishing and quantifying anthropogenic trace metals and phosphorus accumulated in sediment is important for the protection of our aquatic ecosystems. Here, anthropogenic proportion and potential sources of trace metals and phosphorus in surface sediments of Chaohu Lake were evaluated based on the exhaustive geochemical data. The analysis shows that concentrations of major and trace metals, and phosphorus, displayed significant spatial diversity and almost all elements were over the pre-industrial background value, which should be related to the variations of sediment composition partially. Therefore, conservative element normalization was introduced and calculated enrichment factors (EFs) of the elements were referenced highlighting the human contamination. EFs of the major and trace metals, except Zn, Pb, and Cu, were all nearly 1.0, indicating the detrital origin. The EFs of Zn, Pb, Cu and phosphorus were 1.0–10.4, 1.0–3.8, 1.0–4.9, and 1.0–7.6, respectively, showing moderate to significant contamination. Higher EFs of Zn, Pb and Cu occurred in the mouth areas of Nanfei River and Zhegao River, and they decreased to the lake center in the northwest and northeast lake areas, respectively. We deduced that anthropogenic Zn, Pb, and Cu were mainly from urban and industrial point sources and the non-point sources of atmospheric deposition contributed little to their contamination. The EFs of phosphorus showed similar spatial degradation with that of Zn, Pb, and Cu. Moreover, higher EFs (>1) of phosphorus also occurred in other areas adjacent to the river mouths besides Nanfei River and Zhegao River. This indicated that the non-point agricultural source may also be responsible for the contamination of phosphorus in Chaohu Lake in addition to the urban sewage sources. Anthropogenic phosphorus was mainly concentrated in the speciation of NaOH-P, which had higher potential biological effects than the detrital proportion. Concentrations of Zn, Pb and Cu surpassed the threshold effect concentrations (TEC) of consensus-based sediment quality guidelines of freshwater ecosystems, especially in the contaminated northwest area of Chaohu Lake. This highlighted the contributions of anthropogenic contamination to the elevated potential biological effects of trace metals. Though there had been no obvious human contamination of Cr and Ni in Chaohu Lake, concentrations were all over the TECs, which may be due to higher background levels in the parent materials of soils and bedrocks in Chaohu Lake catchment.     

Mobility and ecological risk assessment of trace metals in polluted estuarine sediments using a sequential extraction scheme

The three-stage sequential extraction procedure for the fractionation of Cd, Cr, Cu, Ni, Pb, and Zn, proposed by the Commission of the European Communities Bureau of Reference, was applied to sediment five samples collected from the Sal estuary, Sergipe State, northeast Brazil, in September 2009. The method showed satisfactory recoveries, detection limits, and standard deviations for determinations of trace metals in the sediments. Cd and Pb were the metals most prevalent in the bioavailable fractions (carbonates, Fe and Mn oxides, organic matter, and sulfides), while Ni, Zn, Cu, and Cr showed higher percentages in the inert fraction. The order of mobility of the metals was Cd (66 %) > Pb (65 %) > Zn (59 %) > Ni (57 %) = Cr (57 %) > Cu (56 %). Possible toxicity related to these metals was examined using the risk assessment code, and by comparing the chemical data with sediment quality guideline ERL-ERM values. Results obtained using the two methods were in agreement, and showed low to medium risk for all metals, indicating that adverse effects on aquatic biota should rarely occur.