Mineralogical and geochemical patterns of urban surface soils, the example of Pforzheim, Germany

This study presents a combined geochemical and mineralogical survey of urban surface soils. Many studies on urban soils are restricted to purely chemical surveys in order to investigate soil pollution caused by anthropogenic activities such as traffic, heating, industrial processing, waste disposal and many more. In environmental studies, chemical elements are often distinguished as lithogenic and anthropogenic elements. As a novel contribution to those studies, the authors combined the analysis of a broad set of chemical elements with the analysis of the main mineralogical phases. The semi-quantification of mineralogical phases supported the assignment of groups of chemical elements to lithogenic or anthropogenic origin. Minerals are important sinks for toxic elements. Thus, knowledge about their distribution in soils is crucial for the assessment of the environmental hazards due to pollution of urban soils. In Pforzheim, surface soils (0–5 cm depth) from various land use types (forest, agriculture, urban green space, settlement areas of various site densities) overlying different geological units (clastic and chemical sediments) were investigated. Urban surface soils of Pforzheim reflect to a considerable degree the mineral and chemical composition of parent rocks. Irrespective of the parent rocks, elevated concentrations of heavy metals (Zn, Cu, Pb, Sn, Ag) were found in soils throughout the whole inner urban settlement area of Pforzheim indicating pollution. These pollutants will tend to accumulate in inner urban surface soils according to the available adsorption capacity, which is normally higher in soils overlying limestone than in soils overlying sandstone. However, inner urban surface soils overlying sandstone show elevated concentrations of carbonates, phyllo-silicates and Fe and elevated pH values compared with forest soils overlying sandstone. Thus, in comparison to forest soils overlying sandstones, inner urban soils overlying sandstone affected by pollution concurrently possess elevated concentrations of mineral phases typically providing relatively high adsorption capacities for heavy metals.     

Environment impact of heavy metals on urban soil in the vicinity of industrial area of Baoji city,P.R. China

Heavy metals in soils are of great environmental concern, in order to evaluate heavy metal contents and their relationships in the surface soil of industrial area of Baoji city, and also to investigate their influence on the soils. Soil samples were collected from 50 sites, and the concentration of Pb, Zn, Cu, Cr, Ni heavy metals and the contents of characteristics in soil from industrial area of Baoji city were determined with X-ray fluorescence method. The concentrations of Pb, Zn, Cu, Cr and Ni in the investigated soils reached the amount of 2,682.00–76,979.42, 169.30–8,288.58, 62.24–242.36, 91.96–110.54 and 36.14–179.28 mg kg⁻¹, respectively. The major element Pb contents of the topsoils were determined. to highlight the influence of ‘anthropic’ features on the heavy metal concentrations and their distributions. To compare, all values of elements were much higher than those of unpolluted soils in the middle of Shaanxi province that average 16.0–26.5, 67.1–120.0, 17.8–57.0, 46.9–65.6 and 24.7–34.6 mg kg⁻¹ for Pb, Zn, Cu, Cr and Ni, respectively. An ensemble of basic and relativity analysis was performed to reduce the precipitate of Pb in soil was extremely high and greatly relativity with other elements. Meanwhile, Pb, Zn, Cu, Cr, Ni heavy metals were typical elements of anthropic activities sources, so it was easy to infer to the tracers of anthropic pollutions from the factorial analysis, which was coming from the storage battery manufactory pollutions. The pollutant distributions were constructed for the urban area which identified storage battery manufactory soot precipitate as the main source of diffuse pollution and also showed the contribution of the topsoils of industrial area of Baoji city as the source point of pollution. Consequently, the impact of heavy metals on soil was proposed and discussed. These results highlight the need for instituting a systematic and continuous monitoring of heavy metals and other forms of pollutants in Baoji city to ensure that pollution does not become a serious problem in the future.     

Heavy-metal loadings related to urban contamination in the Kooloonbung Creek catchment,Port Macquarie,New South Wales

Urbanisation and industrial development lead to contamination of estuaries and streams with dispersed loadings of heavy metals and metalloids. Contributions of these elements also occur from natural sources. This study provides baseline geochemical data on the respective natural and anthropogenic inputs of Cu, Pb, Zn, Cd, As, Sb, Cr, Ni, Mn and S to estuarine, fluvial and wetland sediments, and adjacent soils, in the Kooloonbung Creek catchment that drains the Port Macquarie urban area in north coastal New South Wales. There have been anthropogenic additions of Cu, Pb, Zn and As from dispersed urban sources at Port Macquarie, but they are restricted to the local catchment and do not impact on the adjacent Hastings River estuary. The most contaminated sediments display enrichment factors up to 20 × for Cu and Pb, 9 × for Zn and 5 × for As relative to local background values. However, only one value (for Pb) exceeds National Water Quality Management Strategy interim sediment quality guideline (high) values. On the other hand, sediments and local soils are commonly strongly enriched in Cr, Ni and Mn, reflecting adjacent ultramafic and mafic rock substrate and lateritic regolith. Concentrations of Cr and Ni are commonly well above interim sediment quality guideline (high) values for sediments, but are in mineralogical forms that are not readily bioavailable. Sediment and soil quality guideline values consequently need to recognise natural enrichments and the mineralogical siting of heavy metals. Although dissolved concentrations of heavy metals in stream waters are commonly low, there is evidence for mobility of Cu, Zn, Fe and Al. Parts of the Kooloonbung Creek wetland area lie on sulfidic estuarine sediments (potential acid sulfate soils). Experimental oxidation of uncontaminated and contaminated sulfidic sediments leads to substantial dissolution of heavy metals under acid conditions, with subsequent aquatic mobility. The results warn about disturbance and oxidation of potential acid sulfate soils that have been contaminated by urban and natural heavy-metal sources.     

Relationships between heavy metals and iron oxides,fulvic acids,particle size fractions in urban roadside soils

Urban roadside soils are the “recipients” of large amounts of heavy metals from a variety of sources including vehicle emissions, coal burning waste and other activities. The behavior of heavy metals in urban roadside soils depends on the occurrence as well as the total amount. Accordingly, knowledge of the interactions between heavy metals and other constituents in the soil is required to judge their environmental impact. In this study, correlations of heavy metal concentrations (Pb, Zn, Cu, Ag, Se, Ni, Cr and Ba) to iron extracted using dithionite–citrate–bicarbonate (DCB) buffer (Fe_DCB), fulvic acids and particle size fractions were examined from the Xuzhou urban roadside soils. Heavy metals except for Cr and fulvic acids had a positive significant correlation with Fe_DCB, indicating these metals and fulvic acids are principally associated with the surfaces of iron oxides of the soils. Significant positive correlations were also found between the contents of fulvic acids and heavy metals, showing these heavy metals (especially for Cu, Ni and Cr) form stable complexes with fulvic acids. Such finding is of importance with regard to the increased mobilization of heavy metals, e.g., into freshwater ecosystems. Ag, Se and Cr are independent of particle size fractions because of their low concentrations of Ag and Se in the studied soils. Pb, Zn, Cu, Ba and Ag are mainly enriched in the finer soil particles (especially <16 μm).     

包头市典型工业区表层土壤中重金属污染状况及其潜在生态风险研究

为了解包头市典型工业企业对其所在地土壤中重金属含量的影响及污染现状,利用相关性系数对其表层土壤中7种重金属(Cu、Zn、Pb、Cr、Cd、Mn、Ni)来源进行研究,并采用内梅罗综合污染指数法和潜在生态危害指数对其污染状况进行评价。结果表明,7种重金属含量平均值均高于内蒙古土壤背景值,其中Cd、Mn、Ni超标率已达100%,而Cu、Pb、Zn的超标率分别为97%、93%和93%,只有Cr超标率较低(53%),污染程度依次为CdPbCuNiZnMnCr,其中Pb和Cd为重度污染,Cu、Zn、Ni为中度污染,Cr、Mn为轻度污染;Cu、Zn、Cr、Mn、Ni可能同时来自工业生产和交通运输两个源,而Pb和Cd除上述来源外,燃煤烟气的排放有较大贡献。潜在生态危害依次为CdPbCuNiCrZnMn,其中Cd的潜在生态风险最大,应予以高度重视,其他金属的风险均为轻微。     

Mineralogy, geochemistry, and palynology of modern and late Tertiary mangrove deposits in the Barreiras Formation of Mosqueiro Island, northeastern Pará state, eastern Amazonia

A coastal environment has been interpreted from 110 cm thick mudstone deposits found at the base of a 10 m immature laterite profile, which forms the modern coastal cliff on Mosqueiro Island in northeastern Pará state, northern Brazil. The late Tertiary sediment deposits of the Barreiras Formation are studied by multi-element geochemistry and pollen analyses. The mineralogical and geochemical results show that the gray, organic-rich deposits are composed of kaolinite, quartz, and illite/muscovite, as well as pyrite and anatase. They are rich in SiO₂, Al₂O₃, and some FeO. The composition is homogenous, indicating that the detritus source area is formed of lateritic soils derived from acid rock composition. Their chemical composition, including trace elements, is somewhat comparable to continental shale, and the values are below the upper continental Earth crust composition. The pollen analytical data document that the mudstone deposits were formed by an ancient mangrove ecosystem. Mineralogical, geochemical, and pollen analytical data obtained from late Tertiary mangrove deposits are compared with modern mangrove deposits from the Bragança Peninsula of the northeastern coast of Pará state. Although the pollen composition of the deposits is very similar to the modern one, the geochemical and mineralogical composition is different. Smectite was only found in the modern deposit; illite/mica occurs in the ancient deposit, along with Mg, K, and Na. The pollen signature and detrital minerals (kaolinite, quartz and anatase) found in both mangrove deposits show that during the Miocene, a humid tropical climate condition prevailed, similar to modern conditions.     

A national-scale geochemical and mineralogical survey of soils of the conterminous United States

In 2007, the US Geological Survey initiated a low-density (1 site per 1600 km², c. 4800 sites) geochemical and mineralogical survey of soils of the conterminous USA. The ideal sampling protocol at each site includes a sample from 0–5 cm depth, a composite of the soil A horizon, and a sample from the soil C horizon. The <2-mm fraction of each sample is analyzed for Al, Ca, Fe, K, Mg, Na, S, Ti, Ag, Ba, Be, Bi, Cd, Ce, Co, Cr, Cs, Cu, Ga, In, La, Li, Mn, Mo, Nb, Ni, P, Pb, Rb, Sb, Sc, Sn, Sr, Te, Th, Tl, U, V, W, Y and Zn by inductively coupled plasma-mass spectrometry and inductively coupled plasma-atomic emission spectrometry following a near-total digestion in a mixture of HCl, HNO₃, HClO₄ and HF. Separate methods are used for As, Hg, Se and total C on this same size fraction. The major mineralogical components are determined by a quantitative X-ray diffraction method. Sampling was completed in 2010 with chemical and mineralogical analysis currently underway. Preliminary results for a swath from the central USA to Florida clearly show the effects of soil parent material and climate on the chemical and mineralogical composition of soils. A sample archive will be established and made available for future investigations.     

Selenium and heavy metals content in some Mediterranean soils

The study of metal contents in industrial, agricultural or/and polluted soils compared with natural or unpolluted soils is currently necessary to obtain reference values and to assess soil contamination. Nonetheless, very few works published appear in international journals on elements like Se, Li and Sr in Spanish soils. This study determines the total levels of Se, Li, Sr, As, Cd, Co, Cr, Cu, Ni, Pb, V, Zn, Fe, Mn and Ba in 14 natural (unpolluted) soils (Gypsisols, Leptosols, Arenosols and Acrisols), 14 agricultural soils (Anthrosols, Fluvisols and Luvisols), and 4 industrial–urban affected-surface soil horizons (Anthrosols and Fluvisols) of Eastern Spain. The geochemical baseline concentrations (GBC) and reference values (RV) have been established, and the relationships among elements and also between soil properties and elemental concentrations have been analysed. The RV obtained in this study were (mg kg⁻¹): Se 2.68, Li 115, Sr 298, Cd 0.97, Co 35, Cr 217, Cu 46, Ni 50, Pb 137, V 120, Zn 246, Fe 124,472, Mn 2691, and Ba 743. The RV for Se and Li were used as a preliminary approach to assess soil contamination in Spanish soils. The results confirm human impact on Sr, As, Cd, Cr, Cu, Ni, Pb and Zn soil concentrations, but evidence no deviation from natural Se, Li, Co, V, Fe, Mn and Ba concentrations. The results obtained from the statistical analysis reveal significant correlations between some elements and clay and soil organic matter (SOM) contents, indicating that metal concentrations are controlled by soil composition. One particularly interesting finding is the high correlation coefficients obtained between SOM and Se, Cd, Cr, V, Fe, and Mn, and between clay and Cd, Zn, V, Fe and Mn. Once again, these facts confirm the role of SOM and clay minerals in soil functions and that soil is an ecosystem element responsible for maintaining environmental quality.     

Rock composition and origin of the Duwi Formation calcareous rocks, Upper Egypt

Upper Cretaceous phosphorite beds of the Duwi Formation, Upper Egypt, are intercalated with limestone, sandy limestone, marl, calcareous shales, and calcareous sandstone. Calcareous intercalations were subjected to field and detailed petrographic, mineralogical and geochemical investigations in order to constrain their rock composition and origin. Mineralogically, dolomite, calcite, quartz, francolite and feldspars are the non-clay minerals. Smectite, kaolinite and illite represent the clay minerals. Major and trace elements can be classified as the detrital and carbonate fractions based on their sources. The detrital fraction includes the elements that are derived from detrital sources, mainly clay minerals and quartz, such as Si, Al, Fe, Ti, K, Ba, V, Ni, Co, Cr, Zn, Cu, Zr, and Mo. The carbonate fraction includes the elements that are derived from carbonates, maily calcite and dolomite, such as Ca, Mg and Sr. Dolomite occurs as being dense, uniform, mosaic, very fine-to-fine, non-ferroan, and non-stoichiometrical, suggesting its early diagenetic formation in a near-shore oxidizing shallow marine environment. The close association and positive correlation between dolomite and smectite indicates the role of clay minerals in the formation of dolomite as a source of Mg^2＋ -rich solutions. Calcareous rocks were deposited in marine, oxidizing and weakly alkaline conditions, marking a semi-arid climatic period. The calcareous/argillaceous alternations are due to oscillations in clay/carbonate ratio.     

宁沪高速公路句容段两侧土壤磁化率异常与重金属元素的关系研究

高速公路两侧土壤的磁化率从路中央向两侧具有逐渐降低的特征,相对应的样品中的重金属Cu、Pb、Zn、N i、Cr、Fe等元素的含量也具有从路中心向两侧逐渐降低的现象。相关分析表明,土壤磁化率与土壤中的Cu、Pb、Zn、N i、Cr、Fe的相关性显著,因而可以利用磁化率异常来指示高速公路两侧土壤的重金属污染状况。元素的赋存形态分析表明铁锰氧化物态与残渣态是Cu、Pb、Zn、N i、Cr、Fe的主要赋存形式;各元素的形态分析结果与土壤磁化率的相关统计分析表明,高速公路两侧土壤的磁化率与可交换态中的Cu、Pb、Zn、铁锰氧化物态中的Fe、Pb、Zn、有机还原态中的Cu、Cr、Fe、Zn和残渣态中的Cu、Pb、Zn、Cr、Co、N i具有明显的相关性。     

Chromium and nickel distribution in soils, active river, overbank sediments and dust around the Burrel chromium smelter (Albania)

Chromium ore was treated to produce ferrochromium from 1979 until 2000 in a smelter in Burrel, 35 km NE of Tirana (Albania). As a consequence, large amounts of solid waste, i.e. slags (about 9.10⁶ m³) have been disposed next to the smelter, disfiguring the landscape. In an attempt to define contaminated sites, heavy metal content of the different sampling media have been compared with respective background samples.In the study area, the determination of background values in soil samples is complicated due to the different geological substrates. Cr and Ni background concentrations in serpentinite-derived soils, west of the smelting plant, are markedly higher than in the Pliocene gravel/sandy soils, where the smelter is situated (Cr 2147 and 193 mg/kg, respectively; Ni 2356 and 264 mg/kg). These values are clearly lower than those encountered around the smelter. Average total Cr and Ni concentrations in soils around the smelter are 3117 and 1243 mg/kg, respectively. The highest concentrations of Cr (up to 2.3 wt.%), were recorded in samples taken near the smelting compartment within the industrial plant and next to the slags clearly indicating that the smelter forms a point source of Cr contamination. The Cr / Fe ratio is the best indicator to differentiate non-polluted (Cr / Fe Serpentinite soil: 130–390; Pliocene soils: < 130) from polluted areas (> 390 smelting nearby of the slags).Cr and Ni values for local backgrounds in stream and overbank sediments were taken in the Mat river 6 km upstream and to the east of the smelter (268 and 430 mg/kg for Cr, and 306 and 604 mg/kg for Ni, respectively). Equivalent sediments taken from the Zalli i Germanit river, which drains the smelter area are respectively 816 and 1126 mg/kg for Cr and 1115 and 1185 mg/kg for Ni.Dust samples, taken from the lofts of houses up to 2 km from the smelter, display high concentrations of Cr, Ni and Zn (average contents of 2899, 436 and 902 mg/kg, respectively). The later concentrations in the dust samples have been confirmed by mineralogical analysis where Cr-bearing mineral phases such as ferrochromium and chromium oxides, clearly relate to the activity of the smelter. Consequently, atmospheric deposition of dust particles forms a serious problem and can also be responsible for the elevated contents encountered in soil samples around the smelter.All these data show that the degree of contamination caused by industrial activity of the Burrel Cr-smelter is severe, although no Cr(VI) was detected in soil water extractions nor in the surface or groundwater where concentrations were < 0.01 mg/kg.     

Geochemical factors controlling accumulation of major and trace elements in Greenland coastal and fjord sediments

 The major (Al, Ti, Ca, Mg, Fe, Mn, Si) and trace element (Cd, Cr, Cu, Hg, Li, Ni, Pb, V, Zn) concentrations in surficial (<20 cm) sediments from fjords and open coastal waters around Greenland have been determined. Regionally, high concentrations of Fe, Ti, Mg, Cr, Cu, Ni, and V occur in some west and east coast sediments, but they appear to be natural in origin, as there is no indication of anthropogenic influence. Chemical partition indicates that most of the heavy metals are structurally bound in various silicate, oxide, and sulfide minerals. These host minerals occur more or less equally in the coarse and fine sediment fractions (material >63 μm and <63 μm) and have accumulated at the same rate as other detrital clastic material. Provenance and glaciomarine deposition are the main factors controlling the abundance and distribution of the major and trace elements. The chemical composition reflects the mineralogical differences in the provenance of glacial marine material deposited by water and ice adjacent to Greenland. The main source of the sediments enriched in Ti, Fe, Mg, Cr, Cu, Ni, and V appears to be material derived from the volcanic rocks of the Mesozoic-Tertiary Provinces of Greenland by glacial erosion. Received: 26 June 1995 · Accepted: 11 August 1995     

Distribution of heavy metals in Gaborone urban soils (Botswana) and its relationship to soil pollution and bedrock composition

The capital city of Botswana, Gaborone, has seen unprecedented population, economic, and industrial growth in recent years. In order to assess how this rapid urbanisation process impacts the environment, 106 silt and clay (particle size <0.053 mm) samples, separated from Gaborone surface soil samples representing urban, agricultural and rural sites, were investigated. The concentrations of nine heavy metals (Sc, Cr, Co, Ni, Cu, Zn, Nb, Cd, and Pb) were measured using ICP–MS and GFAAS, and the resulting patterns were correlated to the bedrock composition and anthropogenic activities. As expected, we found that samples from soils on top of dolerites show higher levels of Cr, Ni, and Cu than those on top of granites and rhyolites. However, our studies also show that Gaborone city centre soils are moderately polluted by Pb (up to 222 mg/kg, i.e. 5.7-fold the concentration in comparable rural soils), as a result of heavy traffic. Furthermore, Cr and Ni pollution originating from agrochemicals were shown to be accumulating in Gaborone crop soils. Our studies also showed moderate levels of Zn pollution and low level, dot-shaped pollution of Cr, Co, Ni, Cu detected in Gaborone residential and industrial soils that are correlated to waste disposal. Interestingly, the highest levels of Sc, Cr, Co, Ni and Zn pollution are found near two abandoned sewage works. The results of sequential extraction indicate that the polluting Co and Ni exist in all speciations; the polluting Cu mainly exists in the residue of the sequential extraction, whereas the polluting Pb is mostly bound to organic matters and Fe- and Mn-oxides. These results highlight the need for instituting a systematic and continuous monitoring of heavy metals and other forms of pollutants in Gaborone to ensure that pollution does not become a serious problem in the future.     

Heavy-metal accumulation trends in Yixing,China: an area of rapid economic development

Geochemistry of soils encapsulated by urban development and dendrochemistry were evaluated to reconstruct heavy-metal accumulation trends in an area of rapid economic development in China. The urban-covered soil spans a time period of 56 years from 1950 to 2006, and the tree cores cover the period from 1977 to 2006. Results from the six heavy-metal elements (Cd, Cr, Cu, Ni, Pb, and Zn) analyzed in this study indicate that heavy-metal concentrations increase significantly in urban-covered soils dating from 1980, which is corroborated by data from corresponding tree cores. The accumulation rates of Cd, Cr, Cu, Ni, Pb and Zn (1980–2006) were estimated at 0.91, 0.84, 1.42, 1.39, 1.34 and 1.86% per year, respectively. These high rates of accumulation suggest that anthropogenic sources resulting from rapid economic development led to the magnitude and rates of heavy-metal accumulation. Although reconstruction of heavy-metal accumulation trends using the urban-covered soils (substitutes space for time) introduces some uncertainty when compared with long-term experiments, this study demonstrates that urban-covered soils can provide a vehicle by which historical rates of heavy-metal accumulation can be approximated.     

Discrimination of lithogenic and anthropogenic sources of metals and sulphur in soils of the central-northern part of the Zambian Copperbelt Mining District: A topsoil vs. subsurface soil concept

Samples of topsoil together with reference samples of subsurface soil from a depth of 80–90 cm were collected in the central-northern part of the Zambian Copperbelt to distinguish lithogenic sources of metals from anthropogenic contamination of soils caused by fallout of dust from mining operations, flotation ore treatment plants, tailings dams, smelters and slag dumping grounds. The total sulphur, Cu and Co contents were found to be significantly higher in topsoil relative to subsurface soil over a large part of the surveyed area, and Zn, Pb, As and Hg contents showed a definite increase in the close neighbourhood of smelters and in the direction of prevailing winds. This indicates that the increase of these elements in the topsoil is due to anthropogenic activities. The areal extent and degree of anthropogenic contamination of topsoil can be expressed by an enrichment index (EI) based on the average ratio of the actual and median concentrations of the given contaminants. Although the contamination of soil by dust fallout decreases progressively with depth in the soil profile, in areas strongly affected by mining and mineral processing the anthropogenic contamination by sulphur and copper can be traced to a depth of 80–90 cm. In contrast, the concentration of elements such as Cr, Ni, and V, that show a direct correlation with the content of iron in the soils, increases in the subsurface soil relative to the topsoil. This is particularly evident in areas underlain by rocks of the Katanga Supergroup.     

Abundance, Sources and Speciation of Trace Elements in Humus-Rich Streams Affected by Acid Sulphate Soils

The behaviour of trace elements (Al, As, Cd, Co, Cr,Cu, Fe, Mn, Ni, V, Zn) was studied in five humus-richstreams (dissolved organic carbon = 14–40 mg/L)impacted by acid sulphate soils developed in marinesulphide-bearing fine-grained sediments. During heavyrainfalls in autumn, on which the study focusses, themetals Al, Cd, Co, Cu, Mn, Ni and Zn are extensivelyleached from these acidic soils (pH = 2.5–4.5), whileAs, Cr, Fe and V are not leached more strongly fromthis soil type than from areas of till and peat. Aspeciation experiment, based on anion and cationexchange of the stream waters in the field, showedthat (1) the metals Al, Cd, Co, Mn, Ni and Zn aretransported in the streams mainly as inorganiccations, (2) Cu exists mainly in cationic form but isalso to a significant extent associated with dissolvedhumic substances, (3) Fe occurs mainly in the anionicfraction explained by organic coating on colloidal Feoxyhydoxides and (4) the hydrochemistry of As, Cr andV is complex as these elements may exist in severalunquantified anionic fractions and to a minor extentin cationic species/forms. Whereas the proportion ofacid sulphate soils in the catchments had a largeimpact on concentrations levels of several elements inthe stream waters, these soils did not have a largeaffect on the speciation of elements in water.     

青岛城区土壤重金属环境地球化学研究

为研究青岛城区土壤的环境地球化学特征,对青岛市南区、市北区、四方区、李沧区、崂山区5区进行了广泛的土壤地质调查。在每1km2一个样品的取样密度下取得表层土样(0～10cm深度)319个,经前期处理后,利用多种仪器如X射线荧光光谱(XRF)、等离子体发射光谱(ICP-OES)和等离子体质谱(ICP-MS)等分析测得所有样品的72种元素的含量,本文探讨了重金属元素Cd、Cr、Cu、Ni、Pb和Zn及类金属元素As的含量分布。结果表明,人类活动导致表层土壤中元素Cd、Cu、Pb和Zn含量的增加,而元素As、Cr和Ni主要是地质起源,但也会受到人类活动的影响。其中Zn的含量值变化较大,Zn元素含量值增高的地区是工业、交通密集处等人类活动频繁的地区。     

An assessment of soil contamination due to heavy metals around a coal-fired thermal power plant in India

Combustion of coals in thermal power plants is one of the major sources of environmental pollution due to generation of huge amounts of ashes, which are disposed off in large ponds in the vicinity of the thermal power plants. This problem is of particular significance in India, which utilizes coals of very high ash content (∼55 wt%). Since the thermal power plants and the ash ponds are located in densely populated areas, there is potential chance for contamination of soil and groundwater of the surrounding areas from the toxic trace elements in the ash. An attempt has been made to study the extent of soil contamination around one of the largest thermal power plants of India located at Kolaghat, West Bengal India. Chemical analysis of the top soils and the soils collected from the different depth profiles surrounding the ash ponds, show that the top soils are enriched in the trace elements Mo, As, Cr, Mn, Cu, Ni, Co, Pb, Be, V, Zn, which show maximum enrichment (2–5) in the top soils collected from all the soil profiles. These elements are also enriched in the pond ash. Since there are no other sources of industrial effluents, it can be said that the enrichment of the trace elements (Mn, Co, Mo, Cr, Cu, Pb, Zn, As, Ni, Be, V) is attributed to their input from ash from the disposal pond. The study has been further strengthened by log-normal distribution pattern of the elements.     

济南市土壤元素地球化学特征及环境质量

以济南市土壤为研究对象,采用R-2.6.1程序、半方差函数模型和因子分析法对区内土壤元素含量统计特征、结构特征和分布特征进行了分析研究,并对土壤环境质量进行评价。结果表明:研究区土壤中多数元素含量总体受自然空间格局控制,但人类活动对市区土壤Cd、Hg、Pb、Se、As、p H值等元素(指标)含量有明显影响,表层土壤p H值呈现从外围向市区中心增加的碱化趋势;盛行风向对表层土壤重金属的分布叠加也产生影响,沿顺风向产生漂移。受人类活动(主要为工业污染)历史长短及强度的不同,济南市区、历城区和章丘市总体为轻度污染,局部存在Hg、Cu、Cr、Cd等中度或重度污染,污染区分布与各类工业空间布局相吻合,而长清、济阳土壤环境质量较好,总体属警戒限级。按土壤综合污染指数排序,土壤综合环境质量从优到劣为济阳长清章丘历城市区。     

Assessment of heavy metal contamination in soils around Balanagar industrial area,Hyderabad, India

The concentration of heavy metals such as Ba, Co, Cr, Cu, Ni, Pb, Rb, Sr, V, Y, Zn, Zr were studied in soils of Balanagar industrial area, Hyderabad to understand heavy metal contamination due to industrialization and urbanization. This area is affected by the industrial activities like steel, petrochemicals, automobiles, refineries, and battery manufacturing generating hazardous wastes. The assessment of the contamination of the soils was based on the geoaccumulation index, enrichment factor (EF), contamination factor, and degree of contamination. Soil samples were collected from Balanagar industrial area from top 10–50 cm layer of soil. The samples were analyzed using X-ray fluorescence spectrometer for heavy metals. The data revealed that the soils in the study area are significantly contaminated, showing high level of toxic elements than normal distribution. The ranges of concentration of Cr (82.2–2,264 mg/kg), Cu (31.3–1,040 mg/kg), Ni (34.3–289.4 mg/kg), Pb (57.5–1,274 mg/kg), Zn (67.5–5819.5 mg/kg), Co (8.6–54.8 mg/kg), and V (66.6–297 mg/kg). The concentration of above-mentioned other elements was similar to the levels in the earth’s crust pointed to metal depletion in the soil as the EF was <1. Some heavy metals showed high EF in the soil samples indicating that there is a considerable heavy metal pollution, which could be correlated with the industries in the area. A contamination site poses significant environmental hazards for terrestrial and aquatic ecosystems. They are important sources of pollution and may results in ecotoxicological effects on terrestrial, groundwater and aquatic ecosystems.