典型城市污染水体底泥中重金属形态分布和相关性

采用Tessier五步连续提取法,研究了南京市莫愁湖、玄武湖、秦淮河13个底泥样品中的重金属的形态分布情况,分析了重金属浸出量与各形态间的相关性及有机质与有机结合态的相关性,并通过红外谱图分析了有机质与重金属结合的机理.结果表明:底泥中Pb,cu,zh,Ni,Cr主要以有机结合态和残渣态俘在,两种形态的含量占总量70%以上,Zn和Cd的可交换态和碳酸盐结合态含量相列较高,Zn约占20%,Cd约占30%;Zn,Cu,Cd,Ni,Cr的浸出量均与可交换离子态呈现显著的相关性,因此可通过减小可交换离子态含量控制底泥重金属污染的风险性;研究还表明,有机质与有机结合态呈现显著的正相关,因此增加底泥中有机质含量有助于重金属向有_棚结合态转化,有机质与重金属的结合主要是由于其中-些官能团和重金属形成稳定的络合物.     

Fractionation of Heavy Metals in Surface Sediments of Taihu Lake, East China

The BCR (European Communities Bureau of Reference) three-step sequential extraction procedure was applied to fractionate heavy metals in the sediment of Taihu Lake. For the determination of total metal concentration of the sediments, sample digestion was achieved by using HF/H₂O₂/HNO₃(2/1/1) acid mixture in a microwave-irradiated closed vessel system. The concentrations of Cd, Ni, Cr, Zn, Cu and Pb in various extracts solutions were analyzed by Inductively Coupled Plasma Atomic Emission Spectrometry (ICP-AES). The results obtained from the BCR three-step sequential extraction indicated relatively high mobility of Zn, Cu, Pb and Ni in the sediments while Cd and Cr were poorly mobile. Enrichment of heavy metals was found in the sediments collected in the northern parts of Taihu Lake. In the sediments collected in the southern and western sides of the Lake, heavy metal concentrations were relatively low. The relationship between total organic carbon (TOC) and heavy metals concentrations in the sediments is discussed.     

Speciation study of trace elements in surface sediment of Winam Gulf,Lake Victoria,by sequential extraction,aqua-regia acid digestion,and ICP-OES

The speciation of trace metals in surface sediment in Kisumu Carwash area of Winam Gulf, was studied and results compared with those found at Usoma beach which was found to be several orders of magnitude less polluted. High proportions of the metals were bioavailable (fractions 1–6) with BA% ranging from 21.7% (Al) to 94.5% (Pb) at Carwash and 19.6% (Al) to ～100% (for Cd and Pb) at Usoma beach. The readily mobilizable fraction (fractions 1–4) decreased in the order: Pb > Mn > Sn > Cu > Co > Zn > Mg > Cd > Mo > Ni > Cr > Fe > Al at Carwash and Mn > Mo > Sn > Pb > Cd > Mg > Cu > Zn > Co > Ni > Fe > Cr > Al at Usoma beach. The total Zn, Cd, Cr, and Cu sediment concentrations at Carwash were higher than the threshold effect concentrations (TECs), although their bioavailable concentrations were lower than these limits. Both the total and bioavailable concentrations of Pb in surface sediment at Kisumu Carwash area were higher than the TEC threshold limit indicating significant contamination from this heavy metal. Although there was a general good agreement on data obtained by sequential extraction as compared with those obtained by direct aqua-regia digestion, there were large discrepancies for some specific metal analytes which could be accounted for in terms of analytical variations and lack of uniformity in physical and chemical composition of the sediment samples analyzed.     

Effect of lime on speciation of heavy metals during composting of water hyacinth

Composting is attractive and inexpensive method for treatment and biomass disposal of water hyacinth. However, the major disadvantage of water hyacinth composting is the high content of heavy metals in the final compost. Addition of lime sludge significantly reduced most bioavailable fractions (exchangeable and carbonate) of heavy metals. Studies were carried on composting of water hyacinth (Eichhornia crassipes) with cattle manure and sawdust (6:3:1 ratio) and effects of addition of lime (1%, 2% and 3%) on heavy metal speciation were evaluated during 30 days of composting period. The Tessier sequential extraction method was employed to investigate the changes in speciation of heavy metals such as Zinc (Zn), Copper (Cu), Manganese (Mn), Iron (Fe), Lead (Pb), Nickel (Ni), Cadmium (Cd) and Chromium (Cr) during water hyacinth composting. Effects of physicochemical parameters such as temperature, pH and organic matter on speciation of heavy metals were also studied during the process. Results showed that, the total metal content was increased during the composting process. The higher reduction in bioavailability factor (BF) of Cu, Fe, Ni, Cd and Cr was observed in lime 2 treatment about 62.1%, 64.4%, 71.9%, 62.1% and 58.9% respectively; however higher reduction in BF of Zn and Pb was observed in lime 1 treatment during the composting process. Reducible and oxidizable fractions of Ni, Pb and Cd were not observed during the process. Addition of lime was very effective for reduction of bioavailability of heavy metals during composting of water hyacinth with cattle manure and sawdust.     

Comparative study of the fate and mobility of metals discharged in mining and urban effluents using sequential extractions on suspended solids

The fate, bioavailability and environmental impacts of metals discharged in municipal and mining wastewater discharge will depend to a large extent on chemical speciation and distribution. Previous studies on metal bioaccumulation have shown that total metal concentrations are not a good predictor of bioavailability in the dispersion plumes of municipal effluents. The objective of this study was to determine the solid phase speciation of metals in surface waters receiving urban and mining effluents in order to assess their fate and relative mobility in the receiving environment. Suspended particulate matter was sampled using sediment traps at several sites downstream of effluent outfall plumes as well as at reference upstream sites. Particulate metal in operationally defined fractions—exchangeable/carbonates, reducible, oxidisable and residual—were determined in suspended particulate matter with a series of selective chemical extractions. Metal enrichment in suspended particles was generally observed in both mining and urban effluent discharges. When compared to its receiving environment, the mining effluent appeared to release more particulate metals (Cu, Fe, Zn) in the most reactive fractions (i.e. exchangeable/carbonates + reducible forms, 23–43%), while other released metals, such as Cd and Mn, were predominantly in the least reactive forms (i.e., oxidisable + residual, 73–97%). In contrast, the reactivity of all particulate metals, with the exception of Mn, from the urban effluent was much higher, with up to 65, 42, 30 and 43% for Cd, Cu, Fe and Zn, respectively, in the two most reactive fractions. As expected in effluent dispersion plumes, parameters such as the organic carbon, Fe oxide and carbonate contents have specific effects on the partitioning of several trace metals, particularly Cd, Cu and Zn. Our results indicated that the relative distributions of metals among geochemical fractions varied in the effluent receiving waters where organic carbon and Fe oxides appeared as the most important parameters. This could therefore decrease the exposure for aquatic organisms that are exposed to those contaminated sediments as well as the risk to human health.     

Geochemical speciation of trace metals in sediments of the northern Nile Delta Lake by sequential extraction technique

ABSTRACT

The present study was performed to investigate surface sediment samples from Lake Edku of the Nile Delta Lagoons, Egypt. The Lake is important for fishing in the region. The importance of research is to understand the mobility and bioavailability of each studied metal. The study was carried out on 10 sampling sites during 2017. The sediments were subjected to the technique of sequential extraction to examine the chemical forms of some trace metals (Fe, Mn, Zn, Cu, Pb and Ni). Five stage extractions were done as the following order: soluble and exchangeable, carbonate, iron and manganese oxides, organic matter fraction and residual fraction. Attained results from the five fractions showed variations in the concentrations of metal contents of different sites under study. The overall metal concentrations (%) in the initial four extractable fractions (exchangeable, carbonate, oxides and organic matter fractions) were assessed to configure the mobility of each studied metal. The risk assessment code (RAC) represents the summation of exchangeable and carbonate fractions, it was between low and medium risk for aquatic environment. The range percentage of RAC for the metals was in the following order: 1.8–13, 4–23.5, 15–26, 5.7–19.5, 9–25 and 4.8–18.2 for Fe, Mn, Zn, Cu, Pb and Ni, respectively. Approximately 30% of the total copper was associated to the organic fraction, which may represent a high mobility of copper in these sediments. The highest mobility of metals in the sediments could be confirmed by its bioavailability factor (BF), which was within the ranges of 0.32–0.61, 0.36–0.59, 0.64–0.83, 0.36–0.72, 0.37–0.62 and 0.52–0.78 for Fe, Mn, Zn, Cu, Pb and Ni, respectively. The BF exhibited the following order: Zn > Ni > Cu > Pb ≈ Mn?>?Fe. The high levels of BF for the studied metals may represent the potentiality for toxic metals to be easily released into the aquatic environment.     

Chemical fractionation of metals in core sediments of Orogodo River,southern Nigeria

Sequential chemical extraction of metals (Cu, Ni, Mn, Fe, Pb, Cr, and Zn) from core sediments of the Orogodo River was carried out with a view of providing information on the phase distribution of these metals with respect to depths and seasons. The results indicate that copper was speciated into organic matter/sulfide, Fe–Mn oxides, and residual forms at 0–5?cm depth while at deeper sections copper was predominantly in the residual form. Nickel was speciated mainly into Fe–Mn oxides and residual forms. The average of lead in various particulate phases of the sediment are 0–100% for residual; 0–8% for carbonate; 0–16.2% for exchangeable; 0–10% for organic matter/sulfide form and 22–56% for Fe–Mn oxides bound metals. Manganese was speciated into exchangeable (10–36%) and Fe–Mn oxides bound (10–48%) at the surface layers of 0–20?cm depths and predominantly in the residual form in deeper sections implying partitioning into trioctahydral clay and/or well-defined crystalline oxides. Iron was predominantly in the Fe–Mn oxides and residual fractions, less than 8% in the organic fraction, and 24.4–37.3% in the exchangeable and carbonates fractions at the surface. The percentage contributions of iron in the exchangeable and carbonate fractions decreased to 3.2% at 55–60?cm depth. The amount of chromium in the exchangeable fraction ranged from 0% to 7% for exchangeable; 0–26.5% for organic matter/sulfide bound; 3.8–17.9% for Fe–Mn oxides; and 46.8–100% for residual fraction. The mobility factors of the metals indicated that these metals were relatively mobile at top sections as compared with deeper sections. The overall picture of metal mobility and availability indicates potential contamination risk by Fe, Zn, Mn, and Pb in the Orogodo River sediment system.     

Inorganic and methyl-mercury speciation in sediments of the Swarzędzkie Lake

Sediment samples were analysed for mercury and methylmercury content in different parts of the bottom sediment of Swarz ?dzkie Lake, which were influenced by different external pollution sources. The results of determination with two methods of mineralization using two separate media (HNO₃/H₂O₂ and HF) were compared. The accuracy of the studied methods was analysed using certified reference material IAEA 405 of river sediment. The recovery of mercury was satisfactory and ranged from 97.5 to 98.8%. Methylmercury compounds in the studied sediments were found in limited concentrations. Their concentrations ranged from 0.26 to 58.1 μg kg^?1, i.e. 1.0–7.4% of the total mercury content. The depth profile displayed high values of both total and methylmercury content at a depth of 10–20 cm, related to the heavy pollution of the lake in the 1980s. Canonical analysis displayed the relationship of both total mercury and methylmercury concentrations with organic matter and phosphorus content in bottom sediments.     

Trace metals in the coastal soils developed from estuarine floodplain sediments in the Croatian Mediterranean region

Fertile soils in the River Neretva estuary were developed by fluvial sedimentation and deposition of the eroded soil material from the karst hills within the catchment. After extensive reclamation, two reclaimed land zones (fluvial terraces and lower-laying terraces) have been delineated, both used for agriculture. The main objectives of this study were to evaluate soil chemical and geochemical properties in reclaimed zones that differ mainly in topography, soil types and agricultural land use. The origin of the trace metals in the arable soils was studied using multivariate statistics, and interpolation maps of trace metals were produced using GIS and geostatistics. Soil trace metal concentrations do not exceed a threshold value established by the Croatian Government regulation, with exception of copper. Comparative analysis of the main soil properties and trace metal concentrations in the study area showed a pronounced spatial variation and differences between two reclaimed zones in soil organic matter content, bioavailable P and total concentrations of Cd and Cu. Factor analysis in the area of the lower-laying terraces showed grouping of bioavailable P and K, organic matter content and pH (negative loading) in the component associated mostly with the land use. In the area of the fluvial terraces, bioavailable P and total Cd were grouped in the same component that may be explained by the traditional small farm agriculture and overuse of mineral fertilizers. In the whole study area, processes of secondary salinization were determined, accompanied by the raised chloride and sodium concentration measured in the saturation soil extract.     

Effect of acid rain on the fractionation of heavy metals and major elements in contaminated soils

Acid rain is a serious environmental problem worldwide. In the present study, we investigated the effect of acid rain (1:1 equivalent basis H₂SO₄:HNO₃) at pH values of 2.0, 4.0 and 7.0 on the fractionation of heavy metals (Cd, Cu, Fe, Mn, Ni, Pb and Zn) and major elements (K, Na, Ca, and Mg) in contaminated calcareous soils over a 2084 h period. Heavy metals and major elements in soil samples were fractionated before and after 2084 h kinetic release using a sequential extraction procedure. Before kinetic studies the predominant fractions of K, Na, Ca, Mg, Cd and Ni were mainly associated with carbonate fraction (CARB), whereas Fe, Mn and Zn were associated with the Fe–Mn oxide fraction (Fe–Mn oxide). The highest percentage of Pb and Cu were found in the exchangeable (EXC) and organic matter (OM) fractions, respectively. After kinetic study using different simulated acid rain solutions, the major fractions of heavy metals (expect of Cu) and Na was the same as before release. Upon the application of different acid rain solutions, K and Mg were found dominantly in Fe–Mn oxide fraction, whereas Ca was in the EXC fraction. The results provide valuable information regarding metal mobility and indicated that speciation of metals (Cu and Zn) and major elements in contaminated calcareous soils can be affected by acid rain.     

耕地土壤铜、镉、锌形态及生物有效性研究

土壤重金属总量常被用来评估土壤质量安全,但是大量事实说明单纯用土壤重金属总量并不能完全说明土壤重金属的生物有效性及其环境风险。相对于国内外常用的Tessier的五态方法,欧共体标准物质局提出的三步提取法(BCR法),中国地质调查局地质连续提取法的七态标准少见报道。本研究选取河南平原耕地样品,采用中国地质调查局地质连续提取法(DD2005-03)进行耕地中重金属元素(Cu、Cd、Zn)的形态分布,结果表明:Cu、Zn主要以残渣态存在,其残渣态分别占全量的55.80%和67.35%。Cd以离子交换态为主,占全量的27.30%。Cu、Cd、Zn各态含量占全量比例的顺序是,Cu:残渣态弱有机结合交换态铁锰氧化态碳酸盐结合态强有机结合态水溶态离子交换态。Cd:离子交换态弱有机结合交换态强有机结合态残渣态碳酸盐结合态铁锰氧化态水溶态。Zn:残渣态铁锰氧化态弱有机盐结合态离子交换态强有机结合态碳酸盐态水溶态。从生物可利用性系数k来看,Cd主要以活动性较大的状态存在,很容易被作物吸收。     

湘南某矿区菜园土中典型重金属的形态分析

分别运用Tessier连续提取法和Leleyter连续提取法研究湘南某矿区菜园土中Pb,Zn,Cu和Cd的形态分布特征.结果表明：菜园土中Pb,Zn,Cu和Cd的总浓度严重超过国家土壤环境质量标准.Pb,Zn,Cu和Cd的主要形态是残渣态,水溶态和交换态所占比例较小.重金属生物可利用性的研究表明,Pb,Zn,Cu和Cd生物可利用的含量较少;在Tessier方法中,除Cu之外,生物不可利用态是主要形态,其次是潜在生物可利用态,而在Leleyter方法中,潜在生物可利用态是主要形态,其次是生物不可利用态.     

Seasonal variations in trace metal levels,speciation and physicochemical determinants of metal availability in dumpsite soils within Akwa Ibom State,Nigeria

Physicochemical properties, total metals and metal species were investigated in surface soil samples from six urban dumpsites within Akwa Ibom State, Nigeria. Results obtained indicated that Pb, Cd and Cr levels were higher in the dry season than in wet season, whereas Ni levels were higher during the wet season. Soil pH, organic matter and cation-exchange capacity (CEC) showed higher values in wet season than in dry season, whereas sand and clay levels were higher in the dry season. Speciation analysis showed the principal fraction of the metals to be Pb (reducible), Cd (acid extractable) and Ni (residual), whereas Cr existed in the residual fraction during the dry season and in the acid-extractable fraction during the wet season. Soil pH was positively correlated at p<0.1 with all metals in both seasons, sand was negatively correlated with the metals in both seasons, and CEC was negatively correlated with all metals in both seasons, except Pb in the wet season. Organic matter showed variable relationships with metals in both seasons. Seasonal variations affected metal availability and physicochemical properties of the soil. Total metal concentrations followed the order Pb>Ni>Cd>Cr, whereas their bioavailability followed the trend Cd>Pb>Cr>Ni.     

太湖流域漕桥河沉积物重金属污染特征分布

研究了太湖流域漕桥河沉积物的重金属含量特征,结果显示,漕桥河沉积物的Cu、Pb、Zn、Ni、Cd的平均含量分别为46.5、40.6、149.9、58.7、0.54 mg·kg-1,不同的重金属之间存在显著相关关系(P<0.05),说明漕桥河沉积物重金属之间存在一定的同源性.除Cd外,其它重金属有效态比例均在15%以下.有效态随着总量的增加而增加,两者之间达到显著相关关系(P<0.05).沉积物中的不同重金属均呈现富集的趋势.生物毒性效应评价显示,Ni是可能造成生物负面影响的主要因子,其次是Cu、Zn;ERMQ评价说明漕桥河部分区域的沉积物已经存在生物毒性的风险.     

外源铅铜镉在长三角和珠三角农业土壤中的转化

选择了我国经济发达地区的长江三角洲和珠江三角洲10个代表性农业土壤，采用室内培养和化学分级方法研究了加入外源铅、铜、镉在土壤中的动态变化及转化趋势，探讨了碳酸钙、粉煤灰、猪粪和钢渣等土壤改良剂对土壤重金属形态的影响。结果表明，随着土壤重金属负荷的提高，土壤中交换态重金属的比例增大，残余态比例下降，有效性提高，对环境威胁增大。当重金属加入最较低时，重金属优先向氧化物结合态、有机质结合态转化；而当加入最较高时，向交换态和碳酸盐结合态转化的比例明皿增加。pH和土壤组分对重金属在土壤中的转化有显著的影响，土壤pH下降可使交换态Cd、Cu、Pb的比例递增。加入碳酸钙、粉煤灰、猪粪和钢渣等改良剂可显著地降低土壤中交换态重金属比例，增加其它形态的重金属比例。     

镉对北京城郊土壤潜在硝化速率的影响

采集北京城郊5个区县的3种土壤褐土、潮土和山地棕壤,通过急性毒性实验,研究了外源添加镉(Cd)对土壤潜在硝化速率(PNR)的影响。结果表明,5个采样点土壤的PNR分别随土壤中总Cd和有效态Cd含量呈先增后减的趋势。所有处理土壤的有效态Cd含量与PNR的相关关系(R2=0.42,p0.001)优于土壤总Cd含量与PNR的相关关系(R2=0.27,p=0.001)。在土壤总Cd含量和PNR的逐步回归分析中,引入土壤有机质和阳离子交换量(CEC)2个变量可提高其相关性。基于土壤总Cd的EC50(PNR降低至对照50%时的土壤Cd浓度)和有效态Cd的EC50的最大值与最小值之间分别相差2.3倍和3.3倍,而EC10(PNR降低至对照10%的土壤Cd浓度)的最大值与最小值之间分别相差8.5倍和10.8倍。基于总Cd的EC50最低值出现在CEC最小的丰台土壤,而最高值出现在有机质含量最多的灵山土壤,但这2个EC50值未达到显著性差异,表明5个采样点的土壤有机质和CEC虽然在一定程度上影响Cd对PNR的毒性,但不足以引起EC50的显著变化。     

Annual production and molecular weight as an influential factor for environmental distribution of chemicals — a case study in Japan

The changes promoted by treatment of a highly polluted soil with sulphuric acid or calcium hydroxide for changing its pH value are studied by controlling physical properties (particle size, TGA and DTA curves), evolution of metal species (exchangeable, as carbonates, related to Fe‐Mn oxides, linked to organic matter and residual) and metal uptake by plant cultures. Metal contents were determined, after wet digestion with HF—HNO₃—HC1O₄ when necessary, by AAS (Ca, Mg, Cu, Pb, Mn, Fe, Zn) or emission (Na, K). The treatment of soil with successive amounts of sulphuric leads to changes in particle size, hydration properties and exothermic peak for organic matter combustion. Very small changes were, however, detected in the alkaline treatment of soil. Soil treatments do not have practical influence on speciation of some metals (Na, K, Mg, Pb, Mn, Fe), but the intensity of the acid treatment leads to both an increase in the Cu extraction and a decrease in the Ca solubilization, probably through gypsum formation. In the case of zinc a maximum solubility in the middle of the range of acid treatment was observed. The comparison among extractants shows solubilities high for two pollutants (Pb, Cu), associated mainly to Fe—Mn oxides and organic matter, and low for two macrocomponents (Fe, K). The rest of metals, basically present in soil as carbonates or oxides, have intermediate extractions. Pot cultures weights depended mainly on both the treatment of soil (poor development in the more acid sample and drainage difficulties in the rest of acid treatments) and the situation (very low weights in laboratory runs as compared with outside), but the irrigation with water or a diluted sulphuric acid solution (at pH = 4.0) did not produce significant weight changes. Tendencies to increase plant pollution were observed for smaller soil pH, acid irrigation and probably for outside cultures, due to uptake by leaves.     

Rieselfelder

Soils of the large sewage farm area south of Berlin are contaminated with heavy metals such as Cd, Cr, Cu, Hg, Ni, Pb, Zn. Based on earlier studies the total amount and the bioavailable proportions of heavy metals in soil samples were analysed. In some samples very high levels of total heavy metal concentrations were detected. For Pb, Cd, Cu and Hg the maximum values were 1360, 29.7, 817 and 40.8 mg/kg soil dry matter, respectively. The biovailable fractions of heavy metals which were found primarily in the acetate and EDTA fractions and to a lesser degree in the water extract account for about 50 % (Pb, Ni), 70 % (Cd) or 90% (Zn) of their total amount and may therefore pose a considerable environmental risk.     

Physicochemical characterization of sediments from Tajan river basin in the northern Iran

Abstract

Continuous monitoring of water quality of freshwater bodies may prevent outbreak of diseases and occurrence of hazards through employment of effective protection measures. The aim of the current investigation was to determine occurrence of water and sediment pollution in Tajan River North Iran which ultimately may be a threat to recreational beaches of Caspian Sea. Water samples were analyzed for various physicochemical parameters including pH, electrical conductivity (EC), total dissolved solids (TDS), bicarbonates, sulfates, cations, chlorides and heavy metals. The concentrations of zinc (Zn), cadmium (Cd), chromium (Cr) and lead (Pb) were determined using atomic absorption spectroscopy. Similarly, sediment samples were assessed for physicochemical characteristics including pH, EC, saturation percentage, organic matter, organic carbon, texture and cations. Overall, pH, EC, organic matter, and cation values were within acceptable limits according to USEPA water quality guidelines. However, phosphorus (P) concentration up to 5.6?mg/L was considered as “unsafe” which might result in undesirable eutrophication and increased accumulation of sediment organic content leading to excessive growth of algal species in riverine ecosystem. Heavy metal concentrations of Cd (0.08?ppm) and Pb (3?ppm) were above USEPA threshold limits which may consequently affect sustainability of Tajan River. The unacceptable levels of Cd, Pb and P may produce eutrophication of Caspian Sea coasts and damage the ecosystem.     

Evaluation of tests to assess the quality of mine-contaminated soils

An acid metal-contaminated soil from the Aljustrel mining area (a pyrite mine located in SW Portugal in the Iberian Pyrite Belt) was subjected to chemical characterisation and total metal quantification (Cd, Cr, Cu, Ni, Pb and Zn). Water-soluble metals were determined and a sequential extraction procedure was used to investigate metal speciation. Two bioavailable metal fractions were determined: a mobile fraction and a mobilisable fraction. Soil ecotoxicity was studied using a battery of bioassays: plant growth test and seed germination with cress (Lepidium sativum L.), earthworm (Eisenia fetida) mortality, E. fetida avoidance behaviour, luminescent inhibition of Vibrio fischeri and Daphnia magna immobilisation. Although the total content of Cu, Zn and Pb in the soil was large (362, 245 and 1,250 mg/kg dry matter, respectively), these metals were mostly structurally bound (87% for Cu, 81% for Zn and 89% for Pb) and, therefore, scarcely bioavailable. Nonetheless, the D. magna immobilization test using soil leachate showed an EC₅₀ (48 h) of 36.3% (v/v), and the luminescent inhibition of V. fischeri presented an EC₂₀ (15 min) of 45.2% and an EC₂₀ (30 min) of 10.7% (v/v), suggesting a considerable toxic effect. In the direct exposure bioassays, E. fetida avoided the mine soil at the highest concentrations (50%, 75% and 100% v/v). At the same soil concentrations, cress showed negligible growth. The results suggest the need to use a battery of toxicity tests, in conjunction with chemical methods, in order to assess the quality of mine-contaminated soils correctly.