Previously recommended rhizosphere-based method (RHIZO) applied to moist rhizosphere soils was integrated with moist bulk soils, and termed adjusted-RHIZO method (A-RHIZO). The A-RHIZO and RHIZO methods were systematically compared with EDTA, DTPA, CaCl2 and the first step of the Community Bureau of Reference (BCR1) methods for assessing metal phytoavailability under field conditions. Results suggested that moist bulk soils are equally suited or even better than rhizosphere soils to estimate metal phytoavailability. The A-RHIZO method was preferred to other methods for predicting the phytoavailability of Ni, Cu, Zn, Cd, Pb and Mn to wheat roots with correlation coefficients of 0.730 (P < 0.001), 0.854 (P < 0.001), 0.887 (P < 0.001), 0.739 (P < 0.001), 0.725 (P < 0.001) and 0.469 (P < 0.05), respectively. When including soil properties, other extraction methods were also able to predict phytoavailability reasonably well for some metals. Soil pH, organic matter and Fe-Mn oxide contents, and cation-exchange capacity mostly influenced the extraction and phytoavailability of metals. An adjusted-RHIZO method was the most promising approach for predicting metal phytoavailability to wheat under field conditions.

Agricultural soils high in both fluoride (F) and phosphate (P) are common due to long-term accumulation of F from multi-sources and extensive application of phosphate fertilizers. Iron (Fe) and aluminum (Al) (hydro)oxides in acidic soils serve as main geochemical sinks of both P and F, influencing their transport and bioavailability. Though sorption of P and F in their single-ion system has been extensively investigated, studies on co-sorption of F and P on soils are very limited. In this study, the batch technique was used to investigate mutual effects of F and P on their co-sorption/desorption in an acidic red soil with high contents of Fe and Al (hydro)oxides. Results indicate that, in F-P coexisting system, a decrease in pH enhances the sorption of both F and P. An increase in F concentration suppresses P sorption due to competitive effect. However, F sorption can be improved in the presence of P due to surface precipitation of (Al,Fe)-F-P. Sorption of F and P follows both the Langmuir and Freundlich isotherms. Different orders of F and P addition into the soil have no appreciable effect on P sorption, but exert significant impact on F sorption. The presence of F has no measurable effect on P desorption, while the stability of F in the presence of P can be significantly diminished in comparison with that in the absence of P, which would lead to an improvement of F mobility.

This study reports on the attachment preference of a faecally derived bacterium, Escherichia coli, to soil particles of defined size fractions. In a batch sorption experiment using a clay loam soil it was found that 35% of introduced E. coli cells were associated with soil particulates >2 μm diameter. Of this 35%, most of the E. coli (14%) were found to be associated with the size fraction 15-4 μm. This was attributed to the larger number of particles within this size range and its consequently greater surface area available for attachment. When results were normalised with respect to estimates of the surface area available for bacterial cell attachment to each size fraction, it was found that E. coli preferentially attached to those soil particles within the size range 30-16 μm. For soil particles >2 μm, E. coli showed at least 3.9 times more preference to associate with the 30-16 μm than any other fraction. We report that E. coli can associate with different soil particle size fractions in varying proportions and that this is likely to impact on the hydrological transfer of cells through soil and have clear implications for our wider understanding of the attachment dynamics of faecally derived bacteria in soils of different compositions.

In 1998, the pond containing the ore wastes from a pyrite mine in Aznalcóllar (SW, Spain) broke open, spilling some 36×10⁵ m³ of acidic waters and 9 × 10⁵ m³ of tailings containing high concentrations of As and heavy metals. The affected area was around 55 km² of predominantly agricultural soils. After the clean-up of the tailings, many remediation actions were undertaken and the use of blocking agents to immobilize the As was one of the most extended measure. The first experiment performed was to determine the most important soil components in As adsorption under acidic conditions. A second experiment was conducted to neutralize the acidity caused by the solution coming from the tailings undergoing oxidation; an adequate liming material (sugar-refinery scum) was selected and the application rates were established. After the remediation measures, the zone was monitored for three years. A detailed study in four experimental plots located in the most polluted sector was carried out to test the influence of iron oxides in the As immobilization. The use of red soils of the area (rich in free-iron oxides Fed) was established as an appropriate material in the remediation of the area.

Heavy metal phytoextraction is a soil remediation technique, which makes use of plants in removing contamination from soil. The plants must thus be tolerant to heavy metals, adaptable to soil and climate characteristics, and able to take up large amounts of heavy metals. Most of the high biomass productive plants such as, maize, oat and sunflower are plants, which do not grow in cold climates or need intensive care. In this study three “weed” plants, Borago officinalis; Sinapis alba L. and Phacelia boratus were investigated for their ability to tolerate and accumulate high amounts of Cd and Pb. Pot experiments were performed with soil containing Cd and Pb at concentrations of up to 180 mg kg⁻¹ and 2,400 mg kg⁻¹ respectively. All three plants showed high levels of tolerance. Borago officinalis; and Sinapis alba L. accumulated 109 mg kg⁻¹ and 123 mg kg⁻¹ Cd, respectively at the highest Cd spiked soil concentration. Phacelia boratus reached a Cd concentration of 42 mg kg⁻¹ at a Cd soil concentration of 100 mg kg⁻¹. In the case of Pb, B. officinalis and S. alba L. displayed Pb concentrations of 25 mg kg⁻¹ and 29 mg kg⁻¹, respectively at the highest Pb spiked soil concentration. Although the Pb uptake in P. boratus reached up to 57 mg kg⁻¹ at a Pb spiked soil concentration of 1,200 mg kg⁻¹, it is not suitable for phytoextraction because of its too low biomass.

The aim of the present study was the influence of various methods of long-term soil utilisation on the content of polycyclic aromatic hydrocarbons (PAH) in selected silty soils. Four soils were selected for the present studies, i.e.: Eutric Fluvisol originating from silty formations, Haplic Phaeozem developed from loess, Haplic Luvisol (non-uniform) developed from silt, Haplic Luvisol developed from loess. Five study sites were chosen, i.e.: apple orchards, hop gardens, fields, grasslands and natural woodland ecosystems. Samples were collected from the depth of 0-10 cm. In the samples the content of 16 PAHs was determined by means of the HPLC-UV method. The total PAHs content was at a low level. Depending on the soil and object type, the total PAHs content ranged from 72.5 to 764.0 μg·kg-¹. The pollutant level determined together with composition of individual PAHs suggested a limited anthropogenic influence relating mainly to pyrolytic processes. The total PAH content as well as the content of individual PAHs depended on agricultural land use and management. It has been shown that PAH level was influenced by environmental conditions specific for a given type of land use. In the soils in which organic carbon content differed only slightly among locations, a higher influence of the soil utilisation method on the content of individual PAHs was observed.

Plant uptake is a major pathway by which toxic metals can enter the food chain. In this laboratory study we grew spinach, radish, and perennial ryegrass on sand blends containing 50% waste foundry sand (WFS) to assess the availability of Al, B, Ba, Be, Cd, Co, Cr, Cu, Fe, Mg, Mn, Mo, Ni, Pb, V, and Zn. The WFSs utilized in this study were from aluminum, iron, and steel foundries. Although there were differences in the amounts of metals accumulated by the various plant species, excessive amounts of heavy metals were not taken up, regardless of WFS treatment. In spinach and radish, B, Cu, Fe, Mn and Zn were found to be within or close to the sufficiency range for agronomic crops. In ryegrass cuttings at 27, 57, and 87 days, Cu and Zn were within sufficiency ranges, but plants were Fe deficient and contained elevated concentrations of B, Mn, and Mo. Data from this study will be useful for state regulatory agencies interested in developing beneficial use regulations for WFSs.

In order to achieve remediation of contaminated substrates, phyto-extraction in pot experiments utilizing lettuce seedlings as universal accumulator plants was investigated. As test substrates, mine tailings from Shiheung and Okdong mines in Korea (particularly high in Pb, Zn, Cu, and Cd), as well as samples from historic mining site at Oberzeiring in Austria (particularly high in Pb, Sb and As) were used, and compared with adjacent farmland soils. After 21 days of growth in the test substrate, the lettuce plants were harvested, and the adjacent soils parted in bulk and root soils. Special soil bacteria, adapted to high Cd levels (Exiguobacter sp.) and capable of adsorbing large amounts of cadmium from solution, as well as perlite (Samson Perlite Inc.) were added to the test substrates before plant growth. Speciation changes in the solids were investigated by sequential leaching, utilizing neutral MgCl₂ (exchangeable), 0.16 M acetic acid, hydroxylamine pH 2, oxalate pH 3, H₂O₂ oxidation, and reflux with aqua regia. Plant growth induced differentiation between root and bulk soils, the differences were more pronounced for the non-contaminated controls. The iron-hydroxide phase increased about 30%, and also the amount of iron-hydroxide bound Be, Cd, Co, Cu, Mg, Mo, Sb and V concentrations, coming mainly from less mobile fractions. The Mn hydroxide phase, however (hydroxylamine), remained rather constant. After plant growth, the root soils were significantly lower in available P, and significantly higher in available Ca, Mn, and Na than the corresponding bulk soils. Addition of Cd-adapted soil bacteria led to a severe decrease of plant yield, but metal uptake changed in both directions. Exchangeable P in both root and bulk soil decreased, and Be, Co, Cr, Fe, K, Li, Mg, Mn, Ni, and Sr in the residual organic fraction increased. This can be interpreted as competition for nutrients, dissolution of residuals by bacterial action, and adsorption to a tightly bound biomass. Addition of perlite hardly affected the plant yield, and again metal uptake changed in both directions, but led to a decrease of siderophilic elements in the Fe- and Mn hydroxides of the bulk soil. In the root soil, perlite addition above all decreased available K, P and As, with respect to the untreated samples. Bacteria addition to perlite treated soils shifted some elements from weak acid mobile towards less available fractions.

Surface water is frequently contaminated by the trace metals, in particular lead and zinc, produced by mining activities. The infiltration of this water is likely to pollute surface soils and ground water. The study of the transfer of trace elements, especially lead, under real conditions is difficult to carry out due to the physicochemical and hydrodynamic complexity of real soil (preferential flows, conditions of unsaturation...), of the presence of colloids and of many candidate elements. The objective of the present study was to gain a better understanding of the parameters influencing the migration processes of trace elements in simplified systems; it was based on the study of Pb transfer in laboratory columns filled with soil. The results showed that retention of lead in soil is strongly dependent on feed flow rate, particulate bed tortuosity, bed height, water-soil surface contact and volume of water. Increase in bed height, water-soil surface contact and particulate bed tortuosity leads to higher contact time thus higher lead retention by soil, whereas increase in feed flow rate and volume of water leads to lower contact time thus lower lead retention by soil.

Lowland heath is an internationally important habitat type that has greatly declined in abundance throughout Western Europe. In recent years this has led to a growing interest in the restoration of heathland on agricultural land. This generally requires the use of chemical treatments to return soil chemical conditions to those appropriate for the support of heathland ecosystems. However, the potential for negative impacts on the environment due to the potential of these treatments to increase the availability of trace metals via raised soil acidity requires investigation. A large-scale field study investigated the effect of two chemical treatments used in heathland restoration, elemental sulphur and ferrous sulphate, on soil acidity and whether it is possible to predict the effect of the treatments on availability of two potentially toxic cations (Al and Cd) in the soil along with their subsequent accumulation in the shoots of the grass Agrostis capillaris. Results showed that both treatments decreased soil pH, but that only elemental sulphur produced a pH similar to heathland soil. The availability of Al, measured by extraction with 1 M ammonium nitrate, could not be predicted by soil pH, depth in the soil and total Al concentration in the soil. By contrast, availability of Cd could be predicted from these three variables. Concentrations of both Al and Cd in the shoots of A. capillaris showed no significant relationship with the extractable concentration in the soil. Results are discussed in light of the possible environmental impacts of the chemical restoration techniques.