Relationships of Heavy Metals in Natural Lake Waters with Physico-chemical Characteristics of Waters and Different Chemical Fractions of Metals in Sediments

The relationships between heavy metal concentrations and physico-chemical properties of natural lake waters and also with chemical fractions of these metals in lake sediments were investigated in seven natural lakes of Kumaun region of Uttarakhand Province of India during 2003–2004 and 2004–2005. The concentrations of Cr, Mn, Fe, Ni, Cu, Zn, Cd and Pb in waters of different lakes ranged from 0.29–2.39, 10.3–38.3, 431–1407, 1.0–6.6, 5.3–12.1, 12.6–166.3, 0.7–2.7 and 3.9–27.1 μg l^?1 and in sediments 14.3–21.5, 90.1–197.5, 5,265–6,428, 17.7–45.9, 13.4–32.0, 40.0–149.2, 11.1–14.6 and 88.9–167.4 μg g^?1, respectively. The concentrations of all metals except Fe in waters were found well below the notified toxic limits. The concentrations of Cr, Mn, Ni, Cu, Zn, Cd and Pb were positively correlated with pH, electrical conductivity, biological oxygen demand, chemical oxygen demand and alkalinity of waters, but negatively correlated with dissolved oxygen. The concentrations of Cr, Ni, Zn, Cd and Pb in waters were positively correlated with water soluble + exchangeable fraction of these metals in lake sediments. The concentrations of Zn, Cd and Pb in waters were positively correlated with carbonate bound fraction of these metals in lake sediments. Except for Ni, Zn and Cd, the concentrations of rest of the heavy metals in waters were positively correlated with organically bound fraction of these metals in lake sediments. The concentrations of Cr, Mn, Ni, Cu and Zn in waters were positively correlated with reducible fraction of these metals in lake sediments. Except for Cd, the concentrations of rest of the metals in waters were positively correlated with residual fraction and total content of these heavy metals in lake sediments.     

Impact of man's activities on the chemical composition of the sediments of lakes superior and Huron

The concentrations of organic matter, major elements and trace elements were determined at 15 core locations in Lake Superior and Huron. The chemical compositions of the cores are related to sediment particle size, Eh, pH, chronology and location. Concentrations of Si, Al, Ca, Mg, K, Na, and Ti, which represent the major mineral species in the sediments, are generally uniform in each core. Surface enrichments of Hg, Pb, Zn, Cu, Ni, Co, Cd, Cr, Be, V, As, Org-C, and N at many of the locations are attributed to anthropogenic inputs of these elements in recent years. Concentration profiles of Fe, Mn, P, and S are influenced by migration of these elements in the pore waters. High anthropogenic Cu loadings in Lake Superior were related to Cu mining activities in the lake basin, while high anthropogenic inputs of Ni to the Lake Huron sediments were related to Ni contamination from the Sudbury area. Sediment loading calculations show that the anthropogenic inputs of trace and nutrient elements are related to the sedimentation rate, that the inputs are dispersed over wide areas of the lakes and that inputs to Lake Superior have increased significantly since 1955. Evidence is presented that atmospheric inputs are an important source of contaminants.     

Heavy Metals in Freshly Deposited Stream Sediments of Rivers Associated with Urbanisation of the Ganga Plain,India

Freshly deposited stream sediments from six urban centres of the Ganga Plain were collected and analysed for heavy metals to obtain a general scenery of sediment quality. The concentrations of heavy metals varied within a wide range for Cr (115–817), Mn (440–1 750), Fe (28 700–61 100), Co (11.7–29.0), Ni (35–538), Cu (33–1 204), Zn (90–1 974), Pb (14–856) and Cd (0.14–114.8) in mg kg^-1. Metal enrichment factors for the stream sediments were <1.5 for Mn, Fe and Co; 1.5–4.1 for Cr, Ni, Cu, Zn and Pb; and 34 for Cd. The anthropogenic source in metals concentrations contributes to 59% Cr, 49% Cu, 52% Zn, 51% Pb and 77% Cd. High positive correlation between concentrations of Cr/Ni, Cr/Cu, Cr/Zn, Ni/Zn, Ni/Cu, Cu/Zn, Cu/Cd, Cu/Pb, Fe/Co, Mn/Co, Zn/Cd, Zn/Pb and Cd/Pb indicate either their common urban origin or their common sink in the stream sediments. The binding capacity of selected metals to sediment carbon and sulphur decreases in order of Zn > Cu > Cr > Ni and Cu > Zn > Cr > Ni, respectively. Stream sediments from Lucknow, Kanpur, Delhi and Agra urban centres have been classified by the proposed Sediment Pollution Index as highly polluted to dangerous sediments. Heavy metal analysis in the <20-μm-fraction of stream sediments appears to be an adequate method for the environmental assessment of urbanisation activities on alluvial rivers. The present study reveals that urban centres act as sources of Cr, Ni, Cu, Zn, Pb and Cd and cause metallic sediment pollution in rivers of the Ganga Plain.     

抚仙湖重金属污染强度、历史及来源的沉积记录

This study focused on the concentration change of heavy metals of sediment cores in heavily polluted north area and less polluted middle area of Fuxian Lake in Southwest China.On the basis of the analysis of Cu,Ni,Ti,V,Pb,Cd,and Zn concentration-depth profiles,the pollution history of heavy metals was studied using ¹³⁷cesium (¹³⁷Cs) dating.The sources of heavy metals were distinguished by normalization of their profiles to aluminum and analysis of heavy metal concentrations of potential source materials.Geoaccumulation index (I_geo) was used to quantify their contamination intensity.The results showed that all the heavy metals found in the Fuxian Lake sediments originated naturally before 1980s.Cu,Ni,Ti,and V were still mainly natural in the north lake after 1980s,Cu,Ni,Ti,V,and Pb were mainly natural in the middle lake at all time,but the concentrations of Pb and Zn in the north lake were influenced by industrial wastes from the phosphorus fertilizer factory and cement plants.In all the lake,the contaminations of Cd and Zn were the results of agricultural cultivation using a large amount of fertilizers and the atmospheric fallouts of dusts from cement plants.At present,the geoaccumulation indices showed that the Fuxian Lake sediments were moderately to strongly polluted by Cd in the middle lake,and unpolluted to moderately polluted by Pb and Zn and strongly polluted by Cd in the north lake.Moreover,the pollution intensities of Cd,Zn,and Pb have been increased since 1980s.     

Distribution of Trace Metals in Channel Sediment: a Case Study in South Atlantic Coast of Spain

Recently, Sancti Petri channel on the southwestern (SW) part of Iberian Peninsula has been experiencing urban, industrial, and vehicular expansion. Until recently, there have been only few published reports documenting the pattern of metal accumulation in this estuarine sediment. In the present study, trace metals such as Cu, Zn, Ni, Mn, Pb, Co, Cd, As, and Hg concentrations were analyzed from 69 sediment samples collected from 23 sampling sites of the Santi Petri channel. The magnitude of trace metal accumulation found as the following trend: Mn > Zn > Cu > Pb > Ni > Co > As > Cd > Hg. Spatial distribution pattern demonstrated overall decreasing trend of trace metal from Cadiz Bay mouth to the open ocean mouth, clearly correlative to the presence of anthropogenic inputs. Results of the principle component analysis (PCA) revealed that sediment metal chemistry of Sancti Petri channel is mainly regulated by the concentrations of Pb, Cu, Zn, and Ni; possible sources of those were from vehicular-related emissions. Pollution load index (PLI) and geo-accumulation index (I _geo ) indicated overall low values. The study will stimulate improvement of our understanding regarding the pattern of accumulation of metals in the coastal sediments, and the recorded values of metals in the present study can be used as suitable reference for future studies.     

Influence of pollution and acidification on metal concentrations in Finnish Lapland lake sediments

Fifteen Finnish Lapland lakes have been investigated to study pollution levels and possible acidification effects on nickel (Ni), copper (Cu), cobalt (Co), zinc (Zn), cadmium (Cd), lead (Pb), manganese (Mn), iron (Fe), potassium (K), sodium (Na), calcium (Ca), magnesium (Mg) and aluminium (Al) concentrations in sediments. Four lakes have average water pH lower than 6.0 and alkalinity lower than 0.050 meq/1. Contamination factor (C_f, ratio of metal concentrations in the uppermost to the deepest layers for a given lake sediment core) of Pb is high, particularly for acidic and acidifying lakes (C_f=5.2–10.4). Ni, Cu, Co, Zn and Cd concentrations increase insignificantly towards sediment surface of some lakes (with a neutral pH) with the rare exception. The influence of passible lake acidification consists of decreasing Cu, Cd, Al, Zn concentrations and organic material contents (loss on ignition) towards the sediment surface. The buffer capacity index (BCI), determined as the ratio of the sum of alkaline and alkaline-earth metals (K, Na, Ca, Mg) to Al, is lower for acidic lakes (from 0.12 to 0.36), whereas for the other lakes the BCI values are higher (from 0.42 to 1.34). Thus, BCI-values, decreased contents of Al, Cd, Zn and Cu, as well as organic matter contents (OMC in the upper lake sediment suggest acidification of freshwater environments.     

Trace metals in Valencia lake (Venezuela) sediments

An exploratory study of the trace metals Cd, Cu, Mn, Ni, Pb, and Zn in sediments of lake Valencia (Venezuela), South America, 10° 10′N, 68°68′W, gave the following results: (A) Total amounts of Cu, Ni, Pb, and Zn were within the normal range reported by the literature. (B) No consistent pattern of variation with depth was found. A and B could be taken as lack of evidence for contamination by Cu, Ni, Pb, and Zn of the studied sediments. Absence of Cu, Ni, Pb, and Zn pollution after more than 40 yr of anthropogenic discharges on this lake, was attributed mainly to the exploratory nature (limited sampling) of this work, together with some possible dilution effects due to the high CaCO₃ content of these lake sediments. (C) Manganese was above normal values in most samples, but in absence of known anthropogenic sources of this metal, the results found could not be clearly ascribed to metal pollution. (D) Cadmium showed enrichment factors of 10 to 30 indicating pollution of the lake sediments by this metal (probably by urban effluents, runoff, and electroplating industries). (E) The proportion of exchangeable metals was nil in most cases. Exceptions (Ni and Mn) had very low exchangeable fractions (<1.22%). (F) The most abundant fraction (except for Mn) was the residual one (59.7–97.8% of total metal). Other fractions (carbonates, oxides, and organic) showed intermediate values. The general pattern was that the bulk of trace metals studied were present in non-mobile, slightly or non-reactive, poorly or non-available forms.     

南海湖沉积物中生物有效态重金属含量及其空间分布

为判识湖泊沉积物中重金属的地球化学行为特征及其控制因素,以包头市南海湖为研究对象,采用连续提取法,系统开展了沉积物中生物有效态重金属的分布研究。结果表明,表层沉积物中重金属生物有效态（前4态之和）的平均比例序列为Cd〉Pb〉Zn〉Cu;Cu的生物有效态占总量的比例为23%,Pb为75%,Zn为42%,Cd为83%。总体而言,表层沉积物中Cd和Pb的潜在危害性最大。湖心区、西南和东北部湖区为表层沉积物中Cu、Pb和Zn的生物有效态含量高值区,Cd仅在西南湖区表现高值。有机物结合态为沉积物柱芯中Cu和Cd生物有效态的主导形态,铁锰氧化物结合态为Pb和Zn生物有效态的主导形态。强还原性条件下,沉积物中以铁锰氧化物结合态为主导形态的Pb、Zn、Cd有一定的潜在风险,Cu的潜在危害较小。与黄河沉积物重金属形态百分比的对比分析表明,南海湖沉积物对重金属的固定能力更强。     

Trace metals in sediments and aquatic plants from the Xiangjiang River, China

Purpose

The metal concentrations and Pb isotopic composition in sediments and plants from the Xiangjiang River, China, were investigated to understand the contamination and potential toxicity of metals in sediments; to determine the accumulation and distribution of metals in plant tissues; and to trace the possible pollution source of Pb in sediments and plants.

Materials and methods

Sediments and plants were collected from 43 sampling sites in the study region. After sediments were air-dried and passed through a 63-??m sieve, they were acid-digested and DTPA-extracted for determination of total and bioavailable metals. The plants were separated into roots, leaves, and stems; dried; cut into pieces; and digested with HNO₃?CH₂O₂. Metals (As, Cd, Cr, Cu, Ni, Pb, and Zn) and Pb isotopic composition were analyzed by inductively coupled plasma-mass spectrometry.

Results and discussion

Maximum As, Cd, Cr, Cu, Ni, Pb, and Zn concentrations in sediments were 47.18, 55.81, 129.5, 161.6, 160.4, 430.7, and 1,098.8?mg?kg^?1, respectively. The bioavailable fractions of As, Cd, Cu, Pb, and Zn had significant linear relationship with their corresponding total contents in sediments while no significant relationship was observed between bioavailable and total contents of Cr and Ni. In general, plant tissues showed higher As, Cd, Cu, Pb, and Zn concentrations and lower Cr and Ni concentrations compared with sediments. The ²⁰⁶Pb/²⁰⁷Pb ratios decreased in the order of total > bioavailable > stems ?? leaves > roots. A strong linear correlation was observed between the ²⁰⁸Pb/²⁰⁶Pb and ²⁰⁶Pb/²⁰⁷Pb ratios of the plant tissues, sediments, and the possible pollution sources of Pb in the Xiangjiang River.

Conclusions

As, Cd, Cu, Pb, and Zn demonstrated higher contamination levels in sediments and plants compared with Cr and Ni. Cd had highest potential ecological risk. The Pb from anthropogenic sources with low ²⁰⁶Pb/²⁰⁷Pb ratios was preferentially associated with the bioavailable fractions in sediments and accumulated in roots. The Pb in plant tissues is mainly derived from the Pb in sediment and is taken up through the sediment-to-root pathway.     

Mobilization Potential of Heavy Metals: A Comparison Between River and Lake Sediments

Toxic metals introduced into aquatic environments by human activities accumulation in sediments. A common notion is that the association of metals with acid volatile sulfides (AVS) affords a mechanism for partitioning metals from water to solid phase, thereby reducing biological availability. However, variation in environmental conditions can mobilize the sediment-bound metal and result in adverse environmental impacts. The AVS levels and the effect of AVS on the fate of Cu, Cd, Zn, Ni in sediments in the the Changjiang River, a suboxic river with sandy bottom sediment and the Donghu Lake, a anoxic lake with muddy sediment in China, were compared through aeration, static adsorption and release experiments in laboratory. Sips isotherm equation, kinetic equation and grade ion exchange theory were used to describe the heavy metal adsorb and release process. The results showed that AVS level in the lake sediment are higher than that of the river. Heavy metals in the overlying water can transfer to sediments incessantly as long as the sediment remains undisturbed. The metal release process is mainly related to AVS oxidation in lake sediment while also related to Org-C and Fe–Mn oxyhydroxide oxidation in river sediment. The effect of sulfides on Zn and Ni is high, followed by Cd, and Cu is easy bound to Org-C. AVS plays a major role in controlling metals activity in lake sediment and its presence increase the adsorption capacity both of the lake and river sediments.     

The Impact of Biochar Addition on Nutrient Leaching and Soil Properties from Tillage Soil Amended with Pig Manure

Poses dam in the Seine River estuary acts as receptacle of water drain-offs from highly urbanized and industrialized catchment area; therefore, this water is highly contaminated by trace metals. Most trace elements are mainly bound to particulate matter and are incorporated rapidly into the sediments. Scavenging of these metals in the sediments can be reversible due to several perturbations so as sediments also act as a source of pollutants for the overlying water. For instance, natural events (tide, flood, storm) and anthropogenic processes (water management actions) can cause disturbance of sediments and subsequent remobilization of pollutants to the water column, thereby posing a potential threat for aquatic organisms. The purpose of this study was to evaluate the mobility of trace metals by different methods in the Seine estuary sediments. The surface sediment sampled at Poses dam was characterized by high pollution level of Cd, Cu, Zn, and Pb. The estimation of metal bioavailability through ratio ΣSEM/AVS (simultaneously extracted metals/acid volatile sulfides) indicates a potential bioavailability of trace metals. The chemical partitioning using the European Community of Bureau of Reference sequential extraction method revealed that over 85, 82, and 80 % of the total Cd, Zn, and Pb, respectively, were found to be associated with the exchangeable and reducible fractions of the sediment. Another approach used consists in the quantification of dissolved metals released by sediment resuspension experiments in laboratory under controlled conditions. The results indicated that metals are released rapidly from sediment with a sharp peak at the beginning of the experiment, followed by a fast coprecipitation and/or adsorption processes on the suspended particles. Also, the Cd, Pb, and Ni mobility is higher compared to that of the other metals.     

Distribution of Trace Elements in Meromictic Pit Lake

Studies were conducted at the deepest location of the meromictic Piaseczno pit lake, southern Poland, which was created in abandoned sulphur opencast. Pearson correlation and PCA were used to established the relationship between the elements and physico-chemical parameters of the water, whereas discriminant test to study vertical and time differentiation of Cd, Pb, Sr, Cu, Zn, Mn, and Fe concentrations. The results indicated both vertical (except Cu and Zn) and time differentiations of studied elements in the lake water. The highest concentrations of Cd, Pb, and Sr were found in the monimolimnion, that of Mn and Fe in the anoxic water. Depth profiles of Cu and Zn did not show any pronounced trend. Pb and Sr distributions in the water were related to alkalinity, Cl^? and COD, Cd to alkalinity and Cl^?, Mn and Fe to the redox conditions, Mn to water pH, and Fe to the alkalinity. The upper (0–15 cm) layer of the sediment consisted mainly of S (24.2 Atom%), Fe (21.62%), Ca (18.4%), Si (14.3%), and (Al 6.3%) and reflected mainly processes proceeded in the anoxic water-sediment interface. Calculated accumulation coefficients (K _d) of the elements in the sediment are discussed.     

Trace elements and polycyclic aromatic hydrocarbons in road gully sediments from different land uses,Hong Kong

Purpose

This study investigated the concentrations of cadmium (Cd), chromium (Cr), copper (Cu), lead (Pb), nickel (Ni), zinc (Zn), and polycyclic aromatic hydrocarbons (PAHs) in sediments collected from gully pots for road drainage in Hong Kong. The presence and intensity of anthropogenic contamination of road gully sediments were assessed. Identifications of potential sources of trace elements and PAHs were performed to help understand the situation for future control of pollution to the land and aquatic environments.

Materials and methods

Gully sediment samples were collected from gully pots of 18 roads that are potentially exposed to different pollution sources in Hong Kong. The selection of roads considered different road features, adjacent land uses, and traffic volumes. Composite samples were collected for the analysis of trace elements (Cd, Cr, Cu, Pb, Ni, and Zn) and PAHs by an accredited environmental testing laboratory. Geo-accumulation index (I_geo), contamination factor (C_f), modified degree of contamination (mC_d), ecological risk factor (Er), and pollution load index (PLI) were used to assess the level of ecological risk of trace element contamination. Positive matrix factorization (PMF) and PAH diagnostic ratios were applied to identify the sources of trace elements and PAHs.

Results and discussion

Elevated trace element concentrations were commonly found in gully sediments. The concentrations of Zn (267–3700 mg kg^?1) were the highest compared to the other trace elements. Noticeable high concentrations of Cu (27–1020 mg kg^?1), Pb (21–332 mg kg^?1), and Cr (14–439 mg kg^?1) were found in all samples. The PAH contents were moderate to high (0.6 to 24.7 mg kg^?1). Commercial/industrial emissions and road features that cause frequent acceleration-deceleration and turning events showed important influences on the contaminant levels. Strong correlations between the concentrations of Cd, Cr, Pb, and Zn were identified, implying that these trace elements are likely from common sources. The contamination assessment indices reflect significant sediment pollution. The ecological risk ranges from the considerable/moderate-risk class to over the high-risk class.

Conclusions

The collected gully sediments are identified as highly contaminated and need to be isolated from the environment upon final disposal. Through the comprehensive analysis of the collected data, this study provides a detailed insight into the contaminant levels of road gully sediments and potential sources of contamination. Disposal of gully sediments and potential impacts due to release of contaminants into the downstream aquatic environment during rainstorm events should receive attention and need further investigation.

     

Impact of man's activities on the chemical composition in the sediments of Lakes Ontario,Erie and Huron

The concentrations of organic matter, major elements and trace elements were determined at 14 core locations in Lakes Ontario, Erie and Huron. The chemical composition of the cores was related to the sediment particle size, Eh, pH, chronology and location of sampling site. Concentrations of Si, Al, Fe, Mg, Ti, K and Na, which represent the major mineral species in the sediments, are generally uniform in each core. Surface enrichments of Hg, Pb, Zn, Cd, Cu, Be, V, Org-C, N and P are observed at most locations, with their concentrations, usually much greater above the Ambrosia horizon (≈ 120 yr BP), irrespective of the depth of the horizon. The enrichment of these elements is attributed to anthropogenic inputs in recent years. Concentration profiles for Mn and S are related to the migration of these elements in the pore waters. Anthropogenic loadings of the trace metals and nutrients parallel the population and degree of industrialization of each lake drainage basin. Natural loadings parallel the sedimentation rates. Although it is not possible to evaluate the contributions of the trace metals from various sources, evidence is presented that atmospheric inputs are important.     

Aspects of trace metal contamination in the coastal rivers of Israel

Nine trace elements of biological concern: Cr, Co, Cu, Cd, Ni, Pb, Hg, Zn and Ag were investigated in the sediments of the most important coastal steams in Israel. All of these are subjected to some degree of domestic and/or industrial sewage input with the consequent liability of contamination by trace metals. The Ayyalon, Gadura, Qishon and locally the Hadera rivers contain sediments exhibiting severe pollution effects. There is a danger of infiltration through the soils into the groundwaters as well as exposing nearshore fauna to sediments contaminated by possibly toxic trace metals. The other rivers bear smaller levels of trace metals; however, an increase of the Pb and the Zn levels occurs near major highways.     

Sediment toxicity and heavy metals in eleven lime reference lakes of Sweden

Sediments from an eutrophic reference lake (L. HjÄlmaren) and eleven oligotrophic Swedish lakes were analyzed for heavy metals (Cd, Cr, Cu, Hg, Ni, Pb, and Zn) and tested for whole sediment toxicity to Daphnia magna. Whole sediment toxicity, expressed as 48-hr EC50 on a wet weight basis in reconstituted dilution water, ranged from 2.8% (most toxic) to >32% (least toxic). Correlations between bulk sediment heavy metal concentrations and toxicity were significant (P≤0.05) for Hg, Pb, and Zn. However, a causal connection between the concentrations of these metals and toxicity was not supported by the results from metal-spiked sediment toxicity tests. In addition sediment toxicity was not affected by the addition of EDTA, which is a strong chelator known to reduce metal toxicity. After storage for several months test sediments either remained nontoxic, toxic, or increased in toxicity. These results illustrate some of the difficulties in the interpretation of bulk sediment chemistry data and the release of toxic chemicals from sediment samples, highlighting the effect of sediment storage on toxicity.     

荣成天鹅湖沉积物中重金属的分布特征研究

通过对表层沉积物中重金属及粒度的分析,研究了荣成天鹅湖重金属的含量水平及分布特征,并对沉积物的环境质量进行了初步评价。结果表明,天鹅湖重金属的总体水平较低,Cd、Cr、Pb、Cu、Zn的平均含量均低于国家海洋沉积物I类质量标准,其中Cr和Pb存在轻度污染。Cd、Cr、Ni、Pb、Cu、Zn的含量范围分别为0～0.84、1.75～116.11、1.50～29.06、17.36～27.25、2.00～34.98mg.kg-1和11.48～92.61mg.kg-1,平均含量排序为Zn〉Cr〉Pb〉Cu、Ni〉Cd。天鹅湖重金属的富集状况与沉积物的粒度以及人类活动密切相关,大部分元素的高值区出现在颗粒较细的湖中央以及污染严重的西北部,东南部含量较低。相关分析表明,各重金属之间的相关性较好,其中Cd、Cu、Mn、Zn、Fe间呈高度的正相关,空间分布规律相似;重金属与有机质、粘粒含量呈极显著正相关,而与砂粒呈极显著负相关。根据加拿大制定的沉积物评价标准,天鹅湖沉积物中Cr具有较大的生态危害性。     

Chronology of anthropogenic trace element input to four Utah lakes reconstructed using sediment cores

Trace element deposition chronologies are presented for radionuclide dated sediment cores collected from four Utah lakes. A core collected from Mirror Lake, a remote lake located in northern Utah, records a century long period of atmospheric deposition of anthropogenic Pb, Zn, Cu, Cd and Sn. Trace element concentration profiles in a core collected from Panguitch Lake, a remote lake located in southern Utah, give no indication of enhanced atmospheric deposition of trace elements in that part of the state. Sediment cores collected from Echo Reservoir and Deer Creek Reservoir, located near Salt Lake City, record releases of Pb, Zn, Cu, Cd, As, Sb, and Tl rich mine wastes into watershed streams from the now defunct Park City mining complex.     

Quality Evaluation of Sediments from 24 Tributaries of the Po River, Italy

Sediment samples from 24 tributaries of the Po River (Italy) were screened for selected trace elements (Cd, Cu, Hg, Pb, and Zn) and extractable organic compounds; a proxy for contamination by organic microcontaminants. The toxicity of sediment extracts was evaluated using a battery of biotests (Dugesia gonocephala, Paracentrotus lividus, and Tamnocephalus platyurus). Contamination by trace elements (including very high Hg pollution – 4 to 16ppm total Hg – in one sub-basin) reached potentially harmful levels only in the sediments of four tributaries; while contamination by organic microcontaminants was present in most sub-basins. Sediments from most study sites did actually show signs of anthropogenic stress and were able to elicit a toxic response. A more detailed evaluation of sediment quality in the Po River tributaries seems to be urgently needed for developing the necessary remediation strategies. Research priorities should include more thorough testing of sediment toxicity, determination of metal background levels in the various sub-basins and a more detailed identification of the organic micropollutants of possible concern.     

Controlled experimental acidification of lake sediments and resulting trace metal behavior

Severe stream water acidification occurs at higher altitudes (> 600 m a.s.l.) in the Western Harz mountains in Northern Germany. Since 1986 an interdisciplinary research team has followed the fate of pollutants in the 50 km² catchment of an important drinking water reservoir (Lake Söse). An acidification experiment has estimated the role of the remobilization of selected elements from the lake sediments via acidification. Aquaria were used to monitor the effects of a stepwise acidification (from the natural pH of 6.5 to 5.0, 4.0 and 3.0) of the water column over a reconstituted sediment layer. The sediment chemistry has been analyzed before and after the acidification by XRF. The water chemistry was sampled at time intervals and analyzed by ICP-MS. With a pH drop from 6.5 to 3.0, many elements increase in concentration in the water of the acidified basins. Enrichment factors were: Al (5000), Ba (10), Cd (220), Co (800), Cu (170), Ni (90), Pb (5000), and Zn (400). This corresponds fairly well with the field data. Al, Cd, Fe, Mn, and Pb exceed German drinking water limits at pH 4.0. The combined high concentrations (μg L^?1) of Al (1000–2600), Cd (2–4), Cu (4–7), Pb (30–60), and Zn (100–300) in the water column of the acidified streams are not only toxic for fish but also for many other aquatic organisms. Chemical changes in the sediment are not significant within the experimental setup.