Bioavailability of heavy metals bound to estuarine sediments as a function of pH and salinity values

Abstract

The role of two key-variables such as pH and salinity in chemical speciation and bioavailability of heavy metals originated by mining activities bound to sediments was evaluated under estuarine conditions. Two sediment samples collected in two estuaries in southern Spain (Ría of Huelva and Guadalquivir estuary) together with dilution of toxic mud from the Aznalcóllar mining spill (April, 1998) were used to determine their chemical speciation and bioavailability at different pH (6.5, 7.5, 8.5) and salinity (10, 20, 35) values using the estuarine clam Ruditapes philippinarum. The chemical speciation was established by means of measurements of the mobilization of heavy metals from sediments to waters and determining in it pH, salinity, alkalinity and heavy metal concentration. The geochemical model MINTEQA2 was used to establish the thermodynamic species in the assays. To assess the bioavailability of the heavy metals the concentration of metallothioneins in the clam tissues and the mortality of this organism was measured at different pH and salinity values. The influence of both salinity and pH was detected in the chemical behavior of metals and in their associated biological responses established by metallothioneins and the percentage of mortality. At low values of both variables (pH=6.5 and S=10), the biological effects were highest, and it was related to the free ion Zn²⁺.     

Factors influencing the potential mobility and bioavailability of metals in dried lake sediments

Abstract

Samples taken from polluted creek sediments were dried at temperatures between 20°C and 100°C (either in air or under a nitrogen atmosphere) and selective chemical extraction procedures were then used to examine the effect of drying temperature and oxidation on the bonding mode distribution patterns of Zn, Pb, Cd and Cu. Exposure to air during the drying stage tended to increase the fraction of total metal which was less firmly bound (i.e. ion exchangeable, weakly sorbed). Less metal was present in these categories when higher drying temperatures were used, and temperature changes had a larger effect when the samples were dried under nitrogen. The drying process appears to promote metal migration to phases having a stronger bonding power. In most of the samples studied, heating caused Pb to migrate to the carbonate phase while accumulation in the organic/sulfide phases was the dominant process for Cu and Cd. In the case of Zn, migration to the carbonate phase was favoured in some studies (e.g. using air-dried samples), in other sediments the migration end-point was the organic/sulfide phases. During storage of dried samples at room temperature for prolonged periods (e.g. months) the amount of less firmly bound metal tended to increase, and nullified the distribution changes induced by drying. The effect was most pronounced in the case of Cd. The study highlights that significant errors in metal distribution pattern analyses can arise from sample preparation procedures and it has provided information on the possible mobilisation of metal when dredged sediment is land-dumped, i.e. allowed to dry in air.     

The Effects of Drying Temperature on the Extractability of Metals from Dredged Sediments

Dredged sediments may contain considerable amounts of metallic and/or organic pollutants. The risk of metal transfer from sediment deposits to soils can be evaluated using chemical extraction procedures; however, the temperatures at which samples are dried before metal extraction vary widely from one study to another. This led us to investigate the impact of drying temperature on the extractability of metals from dredged sediments. First, water-, CaCl ₂ - and DTPA-extractions were performed on 12 dredged sediments collected in France, with analyses being carried out on both raw (i.e. not dried) samples and on samples dried at 105°C. Higher extractable Cd and Zn contents were recorded for the samples dried at 105°C than for the raw samples. In order to assess the effect of drying temperature on metal extractability, we selected one sediment and carried out CaCl ₂ -, HNO ₃ - and DTPA-extractions on the raw sample and on samples dried at three different temperatures. In general, increasing the drying temperature led to an increase in the extractability of Cr and Cu for all three extraction methods. The CaCl ₂ -extractability of Ni and Zn decreased as drying temperature increased, except for the sample dried at 105°C. The HNO ₃ - and DTPA-extractabilities of these two metals were highest when the sediments were air-dried and then decreased with increasing drying temperature. Similar behavior was observed for Cd, except in the case of HNO ₃ -extractability. As the aim of chemical analysis using selective extraction is to measure the bio-available fractions of metals in soils and sediments, we suggest that extraction should be carried out on raw samples in order to simulate plant growth conditions.     

Factors influencing the potential mobility and bioavailability of exchangeable ammonium ion in dried lake sediments

Abstract

The effect of drying temperature and oxidation on the level of exchangeable ammonium ion found in sediments has been examined using samples collected from along a polluted creek and from shallow lake bays. The sediments were dried at temperatures between 20°C and 100°C (either in air or under a nitrogen atmosphere), and the ammonium ion content was extracted into 0.1 M KCl prior to analysis using an ion selective electrode. Exposure to air during the drying stage usually resulted in lower ammonium values, while increasing the drying temperature altered the amount of displaceable (i.e. available) ammonium ion extracted, generally in an upward direction. The amount detected (5–25 μ g^?1) varied between sites, and surface sediment values differed from the 10–50 cm core material results. The pH of the extracts varied with the drying temperature used, indicating that the heating process promoted some chemical changes in the test samples. The study has demonstrated that in nutrient level surveys, the analytical data produced can depend greatly on the sample preparation procedure selected. It also indicated the type of changes which could occur when dredged sediments are land dumped.     

Geochemical distribution of heavy metals in sediments from sewage fed fish ponds from Kolkata Wetlands,India

Abstract

Kolkata wetlands are the largest sewage fed wetlands in the world. They have been used for aquaculture since 1960. Geochemical distribution of heavy metals (Cr, Cu, Mn, Fe, Zn, Pb, Ni and Al) has been studied in surface sediments using single and sequential extractions techniques. The metal concentrations in sediments were in the following order: Fe>Al> Mn>Zn>Cu> Pb>Cr> Ni, and the average concentrations were 29 μg g^?1, 54 μg g^?1, 328 μg g^?1, 32747 μg g^?1, 169 μg g^?1, 38 μg g^?1, 25 μg g^?1 and 23371 μg g^?1 dry weights for Cr, Cu, Mn, Fe, Zn, Pb, Ni and Al, respectively. Water-soluble percentages of the trace elements are quite low (<0.01–3.75%) but in the presence of chelating agents in the sediments increase the bioavailability of trace elements (2–58%). About 40% of trace elements are in the stable form as a residual fraction of the sediment and more than 50% (nonresidual fraction) metal contamination of the Kolkata wetland sediments were from anthropogenic inputs. The contamination risks of Cr, Mn, Zn, Pb, and Ni are high as their potential availabilities are 70.96%, 58.01%, 63.13%, 55.62%, and 52.15% respectively. The mean concentration of most of the heavy metals in sediments does not exceed the recommended reference values. Zinc and lead concentrations were greater than background level and Interim Sediment Quality Guidelines but lower than Probable Effect Level. Therefore a regular program for monitoring the distribution of heavy metals in water, sediments and biota should be imposed on sewage fed fish ponds of the Kolkata wetland ecosystem.     

Distribution,Speciation and Bioaccumulation of Hg and As in Mariculture Sediments from Dongshan Bay,China

Hg and As are the major hazardous pollutants in marine sediments due to their high toxicity to benthonic organisms. Understanding the spatial distribution, speciation and bioaccumulation of these toxic elements in sediments is therefore of high environmental importance for identifying their potential risks. Sediments and bivalves Paphia undulata were collected from the mariculture area of Dongshan Bay, China, for characterizing geochemistry (by using the European Community Bureau of Reference (BCR) sequential extraction procedure) and bioaccumulation of Hg and As [by calculating the biota sediment accumulation factor (BSAF)]. Both elements in sediments were mostly associated with the residual fraction (69.52–95.06% and 88.22–91.12% of the total concentration, respectively), followed by the oxidizable (bound to sulfides and organic matter) fraction (1.25–25.32% and 3.62–6.00%, respectively). However, Hg presented a higher bioaccumulation than As. Correlation analysis indicated that As in residual fraction and Hg in oxidizable fraction exert positive contributions (R = 0.927, P < 0.01 and R = 0.869, P < 0.05, respectively) on their own bioaccumulation factor. This indicated that P. undulata could adsorb both Hg in organic fraction and As in residual fraction from the sediments. Therefore, we should pay more attention to the potential dissolution and release of metals bound to sediments in the digestive tracts of marine organisms.     

Solid-phase distribution of heavy metals as affected by single reagent extraction in dredged sediment derived surface soils

ABSTRACT

EDTA is useful to assess mobile metal pools in polluted soils and sediments. There is a need to enhance our understanding of the significance of metal fractions released. The impact of single reagent extraction with 0.05 mol L^?1 EDTA on the solid phase distribution of trace metals in surface soils sampled from confined dredged sediment disposal sites was investigated. Not extracted and EDTA extracted soils were subjected to sequential extraction to fractionate the total contents into: (1) easily exchangeable and carbonate bound fraction; (2) reducible fraction; (3) oxidisable fraction; and (4) residual fraction. With EDTA, significant portions of metals associated with the acid extractable and reducible fractions were released. The oxidisable and residual fractions remained unaffected for most of the investigated metals except for the organic matter associated metals (Cu and Pb). A decrease in the residual fraction after EDTA-extraction for Cu and Pb was attributed to artifacts of the sequential extraction procedure.     

Ocean acidification increases the toxicity of contaminated sediments

Ocean acidification (OA) may alter the behaviour of sediment‐bound metals, modifying their bioavailability and thus toxicity. We provide the first experimental test of this hypothesis with the amphipod Corophium volutator. Amphipods were exposed to two test sediments, one with relatively high metals concentrations (Σ_metals 239 mg kg^?1) and a reference sediment with lower contamination (Σ_metals 82 mg kg^?1) under conditions that mimic current and projected conditions of OA (390–1140 μatm pCO₂). Survival and DNA damage was measured in the amphipods, whereas the flux of labile metals was measured in the sediment and water column (WC) using Diffusive Gradients in Thin‐films. The contaminated sediments became more acutely toxic to C. volutator under elevated pCO₂ (1140 μatm). There was also a 2.7‐fold increase in DNA damage in amphipods exposed to the contaminated sediment at 750 μatm pCO₂, as well as increased DNA damage in organisms exposed to the reference sediment, but only at 1140 μatm pCO₂. The projected pCO₂ concentrations increased the flux of nickel and zinc to labile states in the WC and pore water. However, the increase in metal flux at elevated pCO₂ was equal between the reference and contaminated sediments or, occasionally, greater from reference sediments. Hence, the toxicological interaction between OA and contaminants could not be explained by e ffects of pH on metal speciation. We propose that the additive physiological effects of OA and contaminants will be more important than changes in metal speciation in determining the responses of benthos to contaminated sediments under OA. Our data demonstrate clear potential for near‐future OA to increase the susceptibility of benthic ecosystems to contaminants. Environmental policy should consider contaminants within the context of changing environmental conditions. Specifically, sediment metals guidelines may need to be reevaluated to afford appropriate environmental protection under future conditions of OA.     

Quantitative speciation of heavy metals in soil and crops of agricultural fields of Islamabad,Pakistan

Abstract

Two root crops: carrot (Daucus carota) and spring onion (Allium fistulosum) and soil samples were selected from the agricultural fields located near Islamabad, Pakistan to determine their elemental content. Field soil speciation of the two crops was also carried out to analyse the correlation of the elements in field crop and soil. Concentrations of selected elements were evaluated in the leaf, stem, root and flowering part of the crops using flame atomic absorption spectrophotometry. The results showed that elements are mostly concentrated in soil rather than crop parts following the sequence Zn>Cu>Pb>Ni>Cr>Cd. Furthermore, soil speciation showed that Ni and Cr are more prevalent in the Fe–Mn oxide fraction, Zn and Cd as the carbonate bound fraction and Cu is found in the organic bound form. However, concentrations of Pb are similar across the carbonate, Fe–Mn oxide and organic bound fractions. The highest average concentration of Zn is found as the carbonate bound fraction (2.09 ± 0.005 mg kg^?1) and Cu as the organic bound (1.51 ± 0.029 mg kg^?1) in soil samples taken from the agricultural field of Daucus carota.     

Contrasting two methods for determining trace metal partitioning in oxidized lake sediments

A simultaneous (SIM) sediment extraction procedure for low carbonate sediments, which partitions sediment-bound trace metals (Fe, Mn, Zn, Cu, and Cd) into easily reducible (associated with Mn oxides), reducible (associated with Fe oxides) and alkaline extracted (bound to organic) metal is presented. The SIM method was compared to the sequential (SEQ) extraction procedure of Tessier et al. (1979). Both methods showed good agreement for the partitioning of Zn and Cd among the easily reducible, reducible and organic components of sediment. Both methods also showed the same general distribution of Mn, Fe and Cu among the three sediment components, however concentrations of metals recovered by the two methods differed; less Mn and Fe and more Cu was recovered from sediments by the SEQ vs. the SIM procedure. Less recovery of Mn is in part attributed to the loss of this metal in the `in between' reagent rinses required in the SEQ procedure. Greater recovery of Cu by the SEQ vs. the SIM method may be due to the pretreatment of sediment with strong reducing agents prior to the step used for liberating organically bound metals. Advantages of a SIM over the SEQ include rapid sample processing time (i.e. the treatment of 40 samples per day vs. 40 samples in three days), plus minimal sample manipulation. Hence, for partitioning metals into easily reducible, reducible and organic sediment components in sediments low in carbonate, we recommend the use of a SIM extraction over that of a SEQ procedure.     

矿区复合污染土壤真菌多样性及其对稀土-重金属离子的吸附特征

大量的稀土-重金属通过尾矿坝的浮尘、地表径流和渗滤液排放到周边土壤中,影响了土壤中的微生物群落结构。【目的】分析稀土和重金属复合污染土壤真菌群落结构并分离具有同时吸附稀土和重金属的菌株。【方法】本研究基于ITS基因,采用Illumina-Hiseq测序技术分析了包头稀土尾矿坝周边5份稀土-重金属污染土壤样品和距尾矿区20 km的1份相对未受污染的土壤样品的真菌群落特征,同时采用富集培养法从污染样品中筛选出金属耐性真菌,并对其进行吸附稀土-重金属的特性分析。【结果】群落结构为:在门水平,除了未分类门真菌(unclassified Fungi)外,子囊菌门(Ascomycota)真菌在所有土壤中占比较大(13.5%–90.5%);在纲水平上,除了未分类纲真菌外,粪壳菌纲(Sordariomycetes)真菌在B2 (73.1%)、B3 (28.4%)和B4 (20.8%)的丰度显著高于对照样点C (7.4%),而座囊菌纲(Dothideomycetes)在B5 (11.8%)的丰度明显高于B1 (3.5%);在属水平,除了未分类属,足孢子虫属(Podospora)是C(0.9%)和B3(23.6%)样点的优势种。曲霉属(Aspergillus)、未分类的格孢腔菌目(unclassified Pleosporales)和未分类的戴维迪科(unclassified Davidiellaceae)分别为B1 (3.0%)、B4 (10.5%)和B5(5.8%)的优势种,而蜡蚧属(Lecanicillium)真菌只在B2样点土壤存在且占优(51.6%)。Zn污染对真菌群落结构的影响大于稀土元素污染,且其浓度与优势的未分类真菌相对丰度呈负相关。从污染样品中共分离出6株真菌,它们分属于曲霉属(Aspergillus)(5株)和镰刀霉菌属(Fusarium)(1株)。所有分离菌株对镧(La~(3+))的吸附率均显著高于锌(Zn~(2+)),其中Aspergillus sp. B6-3对La~(3+)和锌Zn~(2+)的吸附率最高,分别为19.7%和3.9%。【结论】该研究为利用真菌去除稀土和重金属以优化生物吸附过程导向的环境生物修复和保护策略提供了机制基础。     

Sequential extraction and speciation of Ba,Cu, Ni,Pb and Zn in soil contaminated with automotive industry waste

Abstract

Sequential extraction or fractionation of heavy metals in the solid phase and their speciation in soil solution are important tools for assessing changes resulting from land use and/or pollution. The distribution of the various forms of Ba, Cu, Ni, Pb and Zn was evaluated in soil samples taken from a polluted area, and the speciation of cations and anions in a soil solution contaminated with automotive industry waste. We evaluated the sequential extraction and speciation of Ba, Cu, Ni, Pb and Zn in a Leptosol associated with a Cambisol and contaminated with automotive industry waste. Soil samples were collected at 0-0.2 m (a mix of soil and waste); 0.2-0.4 m (waste only), and 0.4-0.6 m (soil only) both in the polluted area and in two contiguous unpolluted areas: a sugarcane plantation and a forest fragment. Total concentrations of metals in the polluted area were above limits for intervention established by European Community regulations. Cu was mostly distributed in the residual and in the oxide-bonded fractions, except for the waste-only sample, in which the carbonate-bonded fraction was significant. Zn was concentrated in the residual and carbonate-bonded fractions, while Ba, Ni and Pb predominated in the residual fraction of the contaminated samples. Metals in the soil solution were predominantly in the hydroxyl forms, except for Ba, which was mostly in the ionic form (Ba²⁺).     

Environmental change and the chemical record in Loch Lomond sediments

The chemical record in Loch Lomond sediments deposited since the end of the last Ice Age provides evidence of the Flandrian marine transgression some 5500–7000 ¹⁴C years B.P., sedimentation rates and the influence of man's local activities, environmental pollution and its sources since the onset of the Industrial Revolution, and of elemental mobility linked with the reduction-diffusion-oxidation cycle of early sedimentary diagenesis. Information derived from vertical profiles of halogen elements bromine and iodine, radionuclides ¹⁴C and ²¹⁰Pb, heavy metals lead, zinc, and cadmium, stable lead isotopes ²⁰⁶Pb and ²⁰⁷Pb, and redox-sensitive elements manganese, iron and arsenic is reviewed and assessed.     

Distribution of heavy metals in surface sediments of the Bacochibampo Bay,Sonora, Mexico

Abstract

The aim of this study was to determine the levels of heavy metals (Al, Cd, Cr, Cu, Fe, Mn and Pb) in the geochemical fractions of the coastal surface sediments from the Bacochibampo Bay in Sonora, Mexico. Two surveys were conducted (March and September) during 2004, at eight sampling stations inside the bay, and in three natural effluents discharged into this bay. The extraction of metals was carried out using a microwave oven method and the quantification was done by atomic absorption spectro-photometry. The highest detected concentration of total heavy metals in sediments was: Fe>Al>Mn>Pb>Cr>Cu>Cd, with the following concentration values: Fe (1.72%), Al (1.03%), Mn (416.31 mg kg^?1), Pb (11.73 mg kg^?1), Cr (11.41 mg kg^–1), Cu (6.78 mg kg^–1) and Cd (1.33 mg kg^–1). The levels of total heavy metals (Al, Cr, Cu, Fe, Mn and Pb) were much less than the lowest observable effect level (LEL) which indicates that the sediments were not from polluted areas and that the origin of the metals was due to natural conditions. However, concentrations of Cd were much higher than the low effect level (LEL), over 40% of metal was detected in the exchangeable fraction and carbonates. The normalisation study showed a high degree of enrichment of Cd in all the sampling stations in the Bacochibampo Bay (samples EF 34–87) and in the natural flows that discharge into this bay (samples EF 22–35%), which exceeds by several orders of magnitude the value of sample EF 1, which indicates that Cd is anthropogenically induced. Based on these results, it is important that precautionary measures are established, since the deposited Cd in these fractions may be potentially toxic, due to the physicochemical changes that occur in the environment. Thus, future studies will focus on identifying problems involved with Cd bioaccumulation in different trophic levels.     

Sequential extraction of trace metals and particle size distribution studies of Kainji Lake sediment,Nigeria

Abstract

Sequential extraction was carried out to determine the concentrations of some trace metals (Mn, Cu, Fe, Pb and Cd) in the Kainji lake sediments from seven different locations in four fractions: exchangeable, bound to iron and manganese oxide, bound to organic matters and residual. This was to undertaken to assess the environmental fate of these trace metals. The BCR technique, a modified form of the Tessier method of sequential extraction was used.

The proportion of the mean metal concentrations of the bioavailable metals follows the order Fe>Cu>Pb>Mn>Cd. Generally, Fe was most abundant metal in the sediment and about 40% was found in its bioavailable form. Although Cd contributed least to the bioavailable content, a greater percentage (~60%) was found in the bioavailable fraction. This suggests that Cd is highly mobile and, since it is known to be toxic, its concentration in the bioavailable form constitutes an environmental threat.

The contribution of metals bound to organic matter was found to be high and of the same magnitude as those bound to oxides and constitutes about 70% of the non-bioavailable metal contents. The petrological analysis of the sediments revealed that the sediments were predominantly quartz and rock clays with percussion marks and indentations.     

Operationally determined chemical speciation of barium and chromium in drilling fluid wastes by sequential extraction

ABSTRACT

A study has been conducted to determine the influence of pH on the speciation and distribution of barium and chromium in drilling mud. Samples in equilibrium under controlled conditions were subjected to sequential extraction procedure to fractionate the heavy metals into the designated forms of exchangeable, adsorbed, organically bound, carbonate and residual phases. This provides an insight into the potential availability of the heavy metals for possible release into groundwaters and/or surface waters. The major portion of both the metals studied was found in the carbonate and residual forms with the relative distribution depending on the pH. Generally, decreasing pH caused a shift from the residual form towards the carbonate or organic forms of metals. The occurrence of metals in more stable organic, carbonate and residual forms in drilling mud, coupled with no significant release to the aqueous phase upon varying the pH indicates the resistance of these metals to remobilisation from drilling mud.     

The impact of a salinity barrier on the partitioning of heavy metals in sediments of a tropical backwater system

Abstract

Concentrations of heavy metals (Cd, Co, Cr, Cu and Fe) in surface sediments and their partitioning behaviour between exchangeable, reducible (Fe-Mn oxide bound) and organic/residual phases of the sediments in a typical backwater system of Kerala, viz. the southern upstream part of Cochin Estuarine System (South India), have been studied. Spatial and temporal variations of trace metals are discussed with special reference to pH, dissolved oxygen, salinity, organic carbon and texture of sediment. Metal concentrations in the tide gated part of the estuary were found to be significantly higher when compared to metal concentrations reported from the unrestricted part of the Cochin estuarine system and also those from many of the unpolluted estuaries worldwide. The higher levels of heavy metals in the study area and their characteristic distribution and partitioning behaviour in the surficial sediments were attributed to the presence of a salinity barrier across the backwater system and also by the massive use of pesticides and chemical fertilizers in the vast area of agricultural land near the backwater system.     

Distribution,speciation, and ecological risk assessment of heavy metals in surface sediments of Jiaozhou Bay,China

This paper analyzed the distribution and speciation of seven heavy metals in sediments in Jiaozhou Bay. The ecological risk was assessed using three index approaches (i.e., risk assessment code (RAC), contamination factor (CF), and potential ecological risk index (PERI)) and by a comparison with sediment quality guidelines (Chinese Marine Sediment Quality Standards (CMSQS), and threshold effect level (TEL) and probable effect level (PEL) from the USEPA). Pb, Cr, As, Cu, Zn, and Hg contents at most sites were above the corresponding TEL and Class I criteria (CMSQS) value. Particularly, high contents of Cu, detected at sites S₇ (124.5 mg kg^?1) and S₈ (118.3 mg kg^?1), exceeded the respective PEL value, indicating that harmful biological effects might occur. Speciation analysis, individual CF, and RAC calculations suggested that Cd had the highest bioavailable fraction and thus posed a very high risk to aquatic ecosystem; Cu and Zn showed a medium–high risk. Both global CF and PERI analysis indicated a high pollution risk at sites S₇, S₁, S₃, and S₂, but the assessments of specific sites were different. The incomplete consistency suggested that it is necessary to consider both total contents and chemical speciation for providing a more realistic appraisal for the risk of heavy metals in sediments.     

Speciation of trace element compounds in samples of biota from marine ecosystems

Abstract

The toxicity, mobility, bioavailability and bioaccumulation of metals are dependent on the particular physico-chemical form in which the element occurs in the environment. Special attention has been paid to metals which are essential for the proper functioning of organisms if present in appropriate amounts but are toxic if in excess (i.e. Se, Cr), and also to non-essential elements (i.e. Hg, Pb, Cd, Sn and As). To assess the potential hazard to the health of marine organisms, qualitative and quantitative analyses of metal species accumulating along the food chain needs to be carried out. This paper reviews the available information on the speciation of trace elements in the food chain in marine ecosystems and the analytical tools used for acquiring reliable information in this field. Advantages and limitations of commonly used techniques indicate that all metal species in different samples need diverse extraction, separation and detection conditions. Although not recommending which procedure is the most suitable to determine a given compound, speciation analysis has the potential to be a powerful tool for the identification of trace element species in biological samples.     

Distribution and mobility of scandium and yttrium in selected types of soils in Poland

Abstract

This study was conducted to investigate the chemical speciation of yttrium and scandium in selected types of soils and also determined the total content and profile distribution of those elements. The research was performed on soil samples from forest areas in Puszcza Borecka (Poland) known as a non-contaminated site. Soil samples were collected from natural brown, lessive and rusty soil profiles.

The sequential extraction procedure was applied to separate fractions of scandium and yttrium according to the Tessier method. The range of total content of scandium and yttrium was respectively: 0.63-6.48 mg kg^-1 and 2.25 to 27.93 mg kg^-1. Scandium and yttrium occurred predominantly in residual fraction (F5) in each genetic horizon. Also both elements occurred mainly in fraction bound to organic matter (F4). The mean percentage content of scandium measured in mobile fractions (∑F1-F2) reached about 3% (in Bbr, Bt horizons) to 14% (in Bv horizons) in relation to the total content of the element in the analysed soils. The percentage content of yttrium measured in mobile fractions reached about 4% (in A, Bv horizons) to 28% in Bt horizons in relation to the total content of the element in forest soils of Puszcza Borecka.