Contamination by lead in sediments at Toledo River,hydrographic basin of PARANÁ III

Due to intense agricultural and industrial activities, the environment has been affected by increasing amounts of pollutants, such as lead, a toxic heavy metal. When introduced to the environment, toxic metals are distributed and incorporated into the liquid medium, sediments, and aquatic biota; bioaccumulating. This research aimed to identify and quantify the levels of toxic metals present in the waters and sediments of Toledo River, compare the obtained results with legislation and other studies, as well as to evaluate the possible pollutant sources of the water body. Six water and sediment samples were taken at seven strategic sites. The concentrations of Cu, Zn, Fe, Mn, Cd, Pb, and Cr in water were compared to the maximum limits established by Brazilian legislation IN CONAMA No. 357/05, for class II fresh waters. The sediment samples were submitted to nitroperchloric digestion, and then the total concentrations of the metals were determined by flame atomic absorption spectrometry (FAAS). The toxicological quality of the Toledo River has been considerably affected by the activities carried out in its surroundings, such as extensive areas of agriculture, pig farming and industrial areas, causing concentrations of Cd, Fe, and mainly Pb, which is observed at concentrations higher than value allowed by the legislation.     

基于多源大数据可视化的城市居民区绿地土壤环境监测点位布设及采样研究

为科学合理的监测城市居民区绿地土壤环境状况,对居民区绿地土壤监测点位布设和采样的方法进行研究,包括代表性居民区的选取、监测点采样位置的确定、点位数量的确定等。通过多源大数据可视化手段选取某城市代表性的居民区,对其居民区内绿地土壤重金属(镉、汞、砷、铅、铜、铬、锌和镍)进行监测。结果表明:多源大数据的应用对城市土壤监测布点具有积极作用和优势;不同建筑年代的居民区土壤中重金属含量存在一定差异,为全面监测居民区土壤环境状况应选取不同建筑年代的居民区作为监测对象;不同采样位置对居民区土壤样品中重金属含量无明显影响,优先于居民区内面积占比较大的绿地采样;同一居民区内不同监测点位样品存在差异性,每个居民区内至少布设3~4个监测点位可代表该居民区土壤环境状况。     

Fractionation of Aluminum in Soil and Relation to Its Concentration in Fruits

Aluminum concentrations in the fruit samples taken from different regions were determined by atomic absorption spectrometry after dry ashing digestion. To identify the aluminum phases being most responsible for fruit-available aluminum, the soil samples near the fruit plants were also analyzed for aluminum by using various digestion and selective extraction reagents. The relation between the aluminum concentrations in fruits and in soil extracts was studied. The obtained aluminum concentrations in the fruits were in the range of 1.5 to 42.0 mg kg^-1 on dry weight basis. It was observed that the aluminum concentrations of morello cherry(R² = 0.79) and mulberry (R² = 0.99) were correlated to the aluminum concentrations in citric acid extracts of the soils. While the aluminum concentrations of the EDTA and acetic acid extracts in some soils samples include 35% and 25% of total aluminum, respectively, the other soils contain only 1–2%.     

Using public participation to sample trace metals in lake surface sediments: the OPAL Metals Survey

Members of the public in England were invited in 2010 to take part in a national metals survey, by collecting samples of littoral sediment from a standing water body for geochemical analysis. To our knowledge, this is the first national sediment metals survey using public participation and reveals a snapshot of the extent of metals contamination in ponds and lakes across England. Hg, Ni, Cu, Zn and Pb concentrations exceeding sediment quality guidelines for the health of aquatic biota are ubiquitous in ponds and lakes, not just in areas with a legacy of industrial activity. To validate the public sampling approach, a calibration exercise was conducted at ten water bodies selected to represent a range of lakes found across England. Sediment concentrations of Hg, Ni, Cu, Zn and Pb were measured in samples of soil, stream and littoral and deep water sediment to assess inputs. Significant differences between littoral sediment metal concentrations occur due to local variability, but also organic content, especially in upland, peat soil catchments. Variability of metal concentrations between littoral samples is shown to be low in small (<20 ha) lowland lakes. Larger and upland lakes with more complex inputs and variation in organic content of littoral samples have a greater variability. Collection of littoral sediments in small lakes and ponds, with or without voluntary participation, can provide a reliable sampling technique for the preliminary assessment of metal contamination in standing waters. However, the heterogeneity of geology, soils and history/extent of metal contamination in the English landscape, combined with the random nature of sample collection, shows that systematic sampling for evaluating the full extent of metal contamination in lakes is still required.     

Determination of Cu, Pb, Zn, Ni, Co, Cd, and Mn in road dusts of Samsun City

The dust samples from 52 different locations in central roads of Samsun City were collected in a study area of 40 km long for the purpose of determining total metal concentrations of dust samples by flame atomic absorption spectrometry. The concentrations of Cu, Pb, Co, Zn, Ni, Mn, and Cd were found in the ranges of 11.92–352.43, 5.47–223.57, 4.52–41.69, 40.85–173.10, 18.71–131.29, 133.19–179.13, and 0.02–6.16 mg/kg, respectively. The results showed that metal levels were higher around the industrial area than other locations. Principal component analysis was also carried out to ascertain the possible contributing factors towards the metal concentrations. Validation of the analytical results was tested by analysis of the BCR 032 Moroccan phosphate rock certified reference material.     

Analysis of mosses and topsoils for detecting sources of heavy metal pollution: multivariate and enrichment factor analysis

In order to assess the contribution of emission sources to the pollution of areas remote from industrial facilities, a combined approach of enrichment factor analysis and multivariate statistics was used for detecting the origin of heavy metal pollution in the Zlatibor ecosystem, in Serbia. Samples of moss (Pleurozium schreberi, Hylocomium splendens, Scleropodium purum, Hypnum cupressiforme and Thuidum delicatulum) and of topsoil (0-5 cm) were collected in 2005. The concentrations of seven heavy metals (Cd, Cr, Cu, Mn, Ni, Pb and Zn) were determined in moss and soil samples by atomic absorption spectrometry. The results obtained by enrichment factor analysis and two multivariate statistical methods, principal component analysis and cluster analysis, enabled discrimination of the lithologic and anthropogenic sources of heavy metals in the mosses. Enrichment factors, calculated to evaluate the contribution to the metal content in moss from anthropogenic sources, revealed pollution of the investigated area by Cd and Pb, originating from long-range transport and fossil fuel burning.     

Soil contamination of heavy metals in the Katedan Industrial Development Area, Hyderabad, India

Studies on quantitative soil contamination due to heavy metals were carried out in Katedan Industrial Development Area (KIDA), south of Hyderabad, Andhra Pradesh, India under the Indo-Norwegian Institutional Cooperation Programme. The study area falls under a semi-arid type of climate and consists of granites and pegmatite of igneous origin belonging to the Archaean age. There are about 300 industries dealing with dyeing, edible oil production, battery manufacturing, metal plating, chemicals, etc. Most of the industries discharge their untreated effluents either on open land or into ditches. Solid waste from industries is randomly dumped along roads and open grounds. Soil samples were collected throughout the industrial area and from downstream residential areas and were analysed by X-ray Fluorescence Spectrometer for fourteen trace metals and ten major oxides. The analytical data shows very high concentrations of lead, chromium, nickel, zinc, arsenic and cadmium through out the industrial area. The random dumping of hazardous waste in the industrial area could be the main cause of the soil contamination spreading by rainwater and wind. In the residential areas the local dumping is expected to be the main source as it is difficult to foresee that rain and wind can transport the contaminants from the industrial area. If emission to air by the smokestacks is significant, this may contribute to considerable spreading of contaminants like As, Cd and Pb throughout the area. A comparison of the results with the Canadian Soil Quality Guidelines (SQGL) show that most of the industrial area is heavily contaminated by As, Pb and Zn and local areas by Cr, Cu and Ni. The residential area is also contaminated by As and some small areas by Cr, Cu, Pb and Zn. The Cd contamination is detected over large area but it is not exceeding the SQGL value. Natural background values of As and Cr exceed the SQGL values and contribute significantly to the contamination in the residential area. However, the availability is considerably less than anthropogenic contaminants and must therefore be assessed differently. The pre- and post-monsoon sampling over two hydrological cycles in 2002 and 2003 indicate that the As, Cd and Pb contaminants are more mobile and may expect to reach the groundwater. The other contaminants seem to be much more stable. The contamination is especially serious in the industrial area as it is housing a large permanent residing population. The study not only aims at determining the natural background levels of trace elements as a guide for future pollution monitoring but also focuses on the pollution vulnerability of the watershed. A plan of action for remediation is recommended.     

Trace Metal Concentration in Roadside Surface Soil and Tree Back: A Measurement of Local Atmospheric Pollution in Abuja, Nigeria

Cadmium, copper, lead, nickel and zinc concentrations were analysed by atomic absorption spectrophotometry in surface soil and tree bark from different districts of Abuja, Nigeria, in order to determine the atmospheric trace metal input in the area.Elevated concentrations of some of the studied metals were observed in the soil and tree bark samples from the commercial/high traffic areas of the city compared to backgroundvalues. In soil samples, the average concentration of the metals were 0.6±0.4, 18.0±4.0, 281±39, 16±4 and66±23 g g^-1 dry weight for Cd, Cu, Pb, Ni and Zn, respectively, whilst the average concentrations in tree bark were 0.3±0.2, 12±4, 133±32, 13±3 and 61±10 g g^-1 dry weight for Cd, Cu, Pb, Ni and Zn, respectively. The trend in trace metal levels suggested that automobile emissions are a major source of these metals as the highest concentrations of Pb and Zn were recorded in the commercial areas of the city known for their high traffic densities. The levels of metal in the study area were relativelylow compared to levels found in some larger and older cities in various countries worldwide.     

Evaluation of Pb, Cu, Zn, Cd, Ni and Fe levels in Rosmarinus officinalis labaiatae (Rosemary) medicinal plant and soils in selected zones in Jordan

The concentration of heavy metals including Pb, Cu, Zn, Cd, Ni and Fe in different parts of Rosmarinus officinalis medicinal plant grown in Jordan were evaluated. Medicinal plant samples and soil samples were collected from three different zones in Jordan (Irbid, Al-Mafraq and Ma’an). Samples were analyzed by atomic absorption spectrometry (AAS) after chemical treatments using acid digestion procedures. Heavy metal levels in washed and unwashed in each part of R. officinalis were analyzed and compared statistically. Results show that concentrations of investigated heavy metals were varied from plant part to another part of R. officinalis. For example, Pb, Zn, Cu and Cd in most parts of R. officinalis in the three zones were concentrated in the following order: flowers, leaves, stems, whereas Pb, Ni and Fe were concentrated in order as follows: leaves, flowers and stems. Heavy metal concentrations in soil samples was evaluated and correlated with their levels in R. officinalis. Two standard reference materials of plant (SRM 1790a; spinach leaves and CRM 281; rye grass) and one standard reference materials of soil (GBW 07406) were examined to validate the method used. Results show that high recoveries were obtained.     

Heavy metal concentrations in groundwaters and soils of Thane Region of Maharashtra, India

Thane district is one of the most industrialized districts in Maharashtra. The heavy industrialization and the increasing urbanization are responsible for the rapidly increasing stress on the water and soil environment of the area. Therefore, an attempt has been made through comprehensive study on the groundwater contamination and soil contamination due to heavy metals in Thane region of Maharashtra. The area undertaken for the study was Thane and its suburbans Kalwa, Divajunction, Dombivali, Kalyan, and Ulhasnagar. Industrialization and urbanization lead to generation of large volumes of wastewater from domestic, commercial, industrial, and other sources, which discharged in to natural water bodies like river and creek in this region. Groundwater samples and soil samples were collected from residential, commercial, agriculture, and industrial areas. Groundwater samples were analyzed for various water quality parameters. The analytical data shows very high concentration of total dissolved solids, total hardness, total alkalinity, chemical oxygen demand, chloride etc. Groundwater and soil samples were analyzed for ten heavy metals by inductively coupled plasma (ICPE-9000) atomic emission spectroscopy. The analytical data reveal that, very high concentration level of arsenic, cadmium, mercury, and nickel throughout the industrial area. The random dumping of hazardous waste in the industrial area could be the main cause of the groundwater and soil contamination spreading by rainwater and wind. In the residential areas the local dumping is expected to be the main source for heavy metals. A comparison of the results of groundwater with WHO guidelines show that most of the groundwater sampling station are heavily contaminated with organic matter and heavy metals. Groundwater samples are heavily contaminated by arsenic, cadmium, mercury, and nickel. Similarly, the results of heavy metals in soil compared with Swedish soil guideline values for polluted soil show that soil samples collected from residential, commercial and industrial areas are heavily contaminated by arsenic, cadmium, mercury, and nickel.     

Assessment of background levels of trace metals in water and soil from a remote region of Himalaya

Selected trace metals were estimated by atomic absorption spectrometry in the water and soil samples collected from the remote region of Himalaya. The soil samples were analysed for soluble and acid extractable fraction of trace metals. In water samples, Ca, Na, Mg and K emerged as dominant contributors, whereas, Ca, Na, K, Mg, Fe and Pb were estimated at comparatively higher levels in the water extract of the soil. In case of acid extract of the soil samples, Ca, K, Fe, Mg, Mn and Na were found at elevated concentrations. Based on mean levels of the metals, following decreasing concentration order was observed in water samples: Ca > Na > Mg > K > Pb > Co > Cu > Zn > Mn > Cr > Fe > Cd > Li, however, in the acid extract of the soil, following order was noted: Ca > K > Fe > Mg > Mn > Na > Pb > Zn > Cr > Li > Cu > Co > Cd. The correlation study revealed appreciably diverse mutual relationships of trace metals in the water and soil samples. The multivariate cluster analyses exhibited divergent apportionment of trace metals in water and soil samples. Among the trace metals, Cd, Pb, Li, Zn, Cr, Cu, Mn and Co exhibited extreme to significant anthropogenic enrichment in the soil samples, while the rest of the metals were mostly contributed by the natural processes.     

Investigation of trace elements in agricultural soils by BCR sequential extraction method and its transfer to wheat plants

In this study, soil samples were collected from Edirne, Turkey in both summer and winter seasons and subjected to the modified Community Bureau of Reference (BCR) sequential extraction procedure in order to investigate the chemical partitioning of metals in soils and to predict heavy metals uptake by wheat grains which grown at the same soils. The samples were subjected to a three stage extraction procedure proposed by the BCR. The three phases that were separated out in the following order: (1) carbonate, exchangeable, (2) Fe?CMn oxides, and (3) organic matter. Metal concentrations of soil fractions and grain samples were determined by inductively coupled plasma atomic emission spectroscopy. The wheat samples were prepared to analysis using microwave acid digestion procedure. The pseudo-total concentrations of metals were determined after aqua regia digestion. The analytical accuracy of the method was evaluated by using the Standard Reference Materials (BCR 142R Light Sandy Soil, NIST 2711 Montana Soil, and NIST 2704 Buffalo River Sediment). The sum of the metal contents obtained from the modified BCR sequential extraction procedure and pseudo-total metal contents for soil samples were used to calculate recovery values. In order to evaluate the bioavailability of metals, the relationships between the wheat-metal and soil-extractable metal concentrations were compared.     

Determination of Pb and Cd in road dusts over the period in which Pb was removed from petrol in the UK

It is commonly agreed that automobile exhaust has been the most important source of Pb pollution in urban areas, and that Cd may come from wear and tear of tyres. This study evaluates the fall in Pb concentrations in road dusts in Manchester as a consequence of the removal of Pb from petrol in January 2000. In the work presented here a slurry graphite furnace atomic absorption methodology for the determination of Pb and Cd in road dusts has been developed and is compared with an acid digestion method in terms of efficiency. The reproducibility and accuracy of the results obtained by acid digestion and the slurry method have been studied and a certified reference material CRM 038 was analysed to confirm the reliability of the proposed methods. Different factors were evaluated throughout this work including: (i) the effect of traffic density on Pb and Cd levels in road dust samples collected weekly during the period of May 1999 until September 2000; (ii) comparison between the Pb and Cd levels in a busy road and a residential street; (iii) the effect of distance from the source on Pb and Cd levels; The results of these experiments show a reduction in Pb levels over the sampling period. The relationship between road dust particle size and Pb and Cd concentration was also investigated in the 4-250 microns size range using the slurry method, showing that there is a relationship between metal concentration and particle size; the highest concentrations being for the smallest particle size.     

Total petroleum hydrocarbons and trace heavy metals in roadside soils along the Lagos–Badagry expressway, Nigeria

This study reports the level of total petroleum hydrocarbons (TPH) and trace heavy metals (lead, copper, and cadmium) in soil samples collected randomly from Iyana–Iba garage, Lagos State University bus stop, Adeniran Ogunsanya College of Education bus stop, and a control site off Lusada–Atan road, near Crawford University, Igbesa, Ogun state. TPH was estimated gravimetrically after Soxhlet extraction and column clean up, while soil metals were determined by atomic absorption spectrometry using mineral acid digestion. For TPH, the sites have mean values of 19.43 ± 1.27, 16.11 ± 1.85, and 11.43 ± 4.33 mg/g with a control mean value of 0.33 ± 0.16 mg/g. For trace heavy metals, cadmium was not detected. However, the mean levels of lead are 4.24 ± 3.10, 3.72 ± 0.60, and 3.70 ± 1.32 μg/g, respectively, whereas mean copper concentrations are 20.63 ± 9.02, 19.35 ± 3.61, and 16.76 ± 3.02 μg/g in all sites, respectively, compared to the control mean of 0.25 ± 0.13 and 5.99 ± 1.23 μg/g for lead and copper, respectively. Sites studied have higher levels of TPH and metals compared to the control soil samples. This is indicated by a statistically significant difference found between the concentration of analyzed elements in soils collected along Lagos–Badagry expressway and the control site.     

Trace metal (Cd,Cu, Pb,Zn) fractionation in urban-industrial soils of Ust-Kamenogorsk (Oskemen), Kazakhstan—implications for the assessment of environmental quality

Ust-Kamenogorsk is one of the largest cities and industrial centers in Kazakhstan. Non-ferrous metallurgy (Zn–Pb smelter) has acted as a predominating industrial branch in the city since late 1940s. The industrial plants are situated directly adjacent to the residential area of the city which creates grievous ecotoxicological hazard. In the present paper, we aimed at assessing the trace metal pollution of top soils in Ust-Kamenogorsk and its potential threats to the local population. The top soils were sampled at 10 sites throughout the city center. We determined the physical and chemical properties of soils as well as the contents of Cd, Cu, Pb, and Zn. In addition, the soil samples were subjected to a five-step sequential extraction to ascertain the fractionation of trace metals. On this basis, we calculated the geoaccumulation index (I_geo) and pollution load index (PLI) and assessed bioavailability of the elements. From our data, it emerged that the soils displayed a strong polymetallic pollution. PLI was as high as 33.4. Throughout the city, the trace metal contents exceeded the geochemical background and allowable values for residential, recreational, and institutional areas. The I_geo obtained were 3.7–6.5 for Cd, 1.5–4.7 for Cu, 2.8–5.7 for Pb, and 2.6–4.6 for Zn. The soils in Ust-Kamenogorsk displayed extremely high contamination with Cd, moderate to strong contamination with Pb and Zn, and low to moderate contamination with Cu. Cd and Pb were found to be the most bioavailable elements. The mobility of trace metals in the soils changed in the order Cd > Pb > Zn > Cu.     

Factors affecting metal concentrations in the upper sediment layer of intertidal reedbeds along the river Scheldt

Factors that play a role in determining metal accumulation in sediments of 26 intertidal marshes which are mainly vegetated by reed plants (Phragmites australis) were assessed along the Scheldt estuary (Belgium and The Netherlands). In the upper 20 cm sediment layer, several physico-chemical properties (clay, silt and sand content, organic matter, carbonate and chloride content, pH and conductivity) and aqua regia extractable metals (Cd, Cr, Cu, Ni, Pb, Zn) were determined. The sediments were significantly contaminated with trace metals. The Cd concentrations often exceeded the Flemish soil remediation thresholds for nature areas, whereas Cr, Cu and Zn levels indicated moderate contamination. Pb concentrations occasionally were high, whereas Ni concentrations leaned towards background values. Organic matter was the single most important predictor variable for total metal contents in regression models, except for Cr. Additional significant predictor variables were clay or chloride content, depending on the metal. Observed metal concentrations at sites within a range of a few km from specific point-sources of metals (e.g. shipyards, industrial areas with metallurgic activities, affluents, major motorways) were somewhat higher than predicted by the models, whereas they were lower than predicted at sites which are regularly subjected to flooding by water of high salinity. The ratio between observed and predicted concentrations seems to be a valuable tool for the identification of areas which are specifically impacted by point sources.     

Evaluation of trace element contents of some herbal plants and spices retailed in Kayseri,Turkey

The trace element contents of seven kinds of herbal plants and spice samples retailed in local markets in Kayseri-Turkey were determined by flame atomic absorption spectrometry after digestion with HNO₃/H₂O₂ mixture. The concentration ranges for the studied elements were found as 6.0–15.2, 0–32.2, 80.0–324.8, 8.1–386.3, and 13.1–36.2 μg/g for copper, nickel, iron, manganese, and zinc, respectively. The levels of cobalt, lead, and chromium ions in all the investigated samples were found to be below the detection limit of flame atomic absorption spectrometry. The results found in the present work were compared with values in the literature.     

全自动石墨消解-原子荧光法测定土壤总汞

采用全自动石墨消解-原子荧光光度法对土壤总汞进行测定,确定最佳消解时间为1 h,消解液最佳用量为8.0 m L。方法在总汞质量浓度为0.2~2.0μg/L范围内具有良好的线性,相关系数为0.999 9,当取样量为0.500 0 g时,检出限为0.002 mg/kg;测定不同标准土壤样品总汞的结果均在保证值范围内,精密度为4.0%~7.0%,加标回收率为95.0%~108.5%;对甘肃省实际土壤及沉积物样品测定进一步验证了方法的适用性。该法适合大批量样品分析,对于提高工作效率有重要意义。     

微波消解—原子吸收/原子荧光光度法测定活性污泥中的Cd、Pb、Ni、Cu、Zn、Cr、K、As、Hg

通过实验,建立了活性污泥中金属和重金属的测定方法。活性污泥样品经硝酸—氢氟酸或硝酸—高氯酸微波消解处理后,Pb、Ni、Cu、Zn、Cr、K选用火焰原子吸收分光光度法测定,Cd用石墨炉原子吸收分光光度法测定,As、Hg用原子荧光光度法测定。该方法操作简单,结果准确,重现性好。样品加标回收率为93%-108%,相对标准偏差〈5%。     

Total and Leachable Heavy Metals in Muddy and Sandy Sediments of Egyptian Coast Along Mediterranean Sea

The assessment of marine pollution due to metals was made for surficial sediments sampled from 20 sites along Mediterranean coast of Egypt. The samples were dried, acid digested and analyzed for leachable and total heavy metal contents (Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, and Zn) by flame atomic absorption spectrophotometer (air–acetylene) with deuterium background correction. Evaluation of the heavy metals pollution status was carried out using enrichment factors (EFs), the effect range-low (ERL) and the effect range-median (ERM). The study showed high concentrations of Cd, Co, Pb, Ni and moderate concentrations of Cr, Cu and Mn were contaminated in the sediments of studied sites. The results of Spearman correlation, factor and cluster analysis of the heavy metals analyzed in the collected sediment were discussed. The main source of contamination is the offshore oil field and industrial wastes, which arise due to the ineffective and inefficient operation equipments, illegal discharge and lack of supervision and prosecution of offenders.