Perennial plant communities in the proximity of metal smelters and refineries may receive substantial inputs of base metal particulate as well as sulphate from the co-emission of sulphur dioxide. The Ni refinery at Port Colborne (Canada) operated by Inco (now Vale Canada Ltd.) emitted Ni, Co and Cu, along with sulphur dioxide, between 1918 and 1984. The objectives were to determine if vascular plant community composition, including standing litter, in twenty-one woodlots on clay or organic soil, were related to soil Ni concentration which decreased in concentration with distance from the Ni refinery. The soil Ni concentration in the clay woodlots ranged from 16 to 4130 mg Ni/kg, and in the organic woodlots, ranged from 98 to 22,700 mg Ni/kg. The concentrations of Co and Cu in the soils were also elevated, and highly correlated with soil Ni concentration. In consequence, each series of woodlots constituted a ‘fixed ratio ray’ of metal mixture exposure. For each of the woodlots, there were 16 independent measurements of ‘woodlot status’ which were correlated with elevated soil Ni concentration. Of the 32 combinations, there were eight linear correlations with soil Ni concentration, considerably more than would be expected by chance alone at a p-value of 0.05. With the exception of mean crown rating for shrubs at the clay sites, the correlations were consistent with the hypothesis that increased soil metal concentrations would be correlated with decreased diversity, plant community health or fitness, and increased accumulation of litter. Only five of the eight linear correlations were from the organic woodlots, suggesting that the observations were not confounded with soil type nor range in soil metal concentrations.

Moss is usually as an initial colonizer in alpine glacier retreated regions. We hypothesized that moss can significantly facilitate the toxic metals accumulation in alpine ecosystems based on its strong ability of absorption and the role in soil development. Hence, we investigated the trace element pool sizes and enrichment factors, especially for mercury (Hg) by using the Hg isotopic compositions to determine the source contributions in a moss-dominated ecosystem over glacial erratic in Eastern Tibetan Plateau. Results show that Hg, lead (Pb) and cadmium (Cd) are highly enriched in organic soils. Specifically, Cd concentration is 5–20 times higher than the safety limit of the acid soil (pH ≤ 5.5) in China. Atmospheric depositions dominantly contribute to the Pb and Cd sources in organic soils, and followed by the moraine particles influences. The lowering pH in organic soils increasing with glacial retreated time results in the desorption of Cd in organic soils. Atmospheric Hg⁰ uptake by moss predominantly contributes to the Hg sources in organic soils. The average Pb accumulation rate over last 125-year is about 5.6 ± 1.0 mg m⁻² yr⁻¹, and for Cd is 0.4 ± 0.1 mg m⁻² yr⁻¹, and for Hg⁰ is 27.6 ± 3.2 μg m⁻² yr⁻¹. These elevated accumulation rates are caused by the high moss biomass and elevated atmospheric Hg, Pb and Cd pollution levels in China and neighbouring regions. Our study indicates that the moss not only as the bioindicator, but also plays an important role in the hazardous metal biogeochemical cycling in alpine regions.

Amending contaminated soils with organic wastes can influence trace element mobility and toxicity. Soluble concentrations of metals and arsenic were measured in pore water and aqueous soil extracts following the amendment of a heavily contaminated mine soil with compost and biochar (10% v:v) in a pot experiment. Speciation modelling and toxicity assays (Vibrio fischeri luminescence inhibition and Lolium perenne germination) were performed to discriminate mechanisms controlling metal mobility and assess toxicity risk thereafter. Biochar reduced free metal concentrations furthest but dissolved organic carbon primarily controlled metal mobility after compost amendment. Individually, both amendments induced considerable solubilisation of arsenic to pore water (>2500 μg l−1) related to pH and soluble phosphate but combining amendments most effectively reduced toxicity due to simultaneous reductions in extractable metals and increases in soluble nutrients (P). Thus the measure–monitor-model approach taken determined that combining the amendments was most effective at mitigating attendant toxicity risk.

Zero valent iron (ZVI) has been widely tested and used in remediation of both contaminated soils and groundwater, and in general, the in situ amendment of the contaminated media is used as remediation approach. However, concerns remain as to the potential detrimental effects of both the immobilized ZVI and the adsorbed pollutants as the treated system could undergo transformations over time. Accordingly, plans for soil remediation by in situ immobilization of sorbents should include a long-term monitoring of the treated systems. Here, we report on a comparative study in which artificially Cu-contaminated sandy and organic soils characterized by different metal binding capacities were treated by either (i) in situ immobilization of ZVI in the soils, or (ii) by a ZVI amendment followed by magnetic retrieval of formed ZVI-Cu complexes prior to plant growth studies. The latter relies on the combination of the high metal adsorption capacity and magnetism of ZVI. Two plant species, Lactuca sativa (lettuce) and Brassica juncea (Indian mustard) were used to assess the efficiency of the two treatment methods in eliminating the bioavailable fraction of Cu. Overall, the results showed that, if soil remediation by in situ immobilization reduces the bio-accessible fraction of Cu, treatment using ZVI amendment followed by magnetic separation performs better. The latter resulted in less Cu accumulated in the shoots and roots of plants. In parallel to the plant growth study, we used MetPLATE™, a short-term bioassay based on the inhibition of the β-galactosidase enzyme by the bioavailable fraction of heavy metal cations, to predict the efficiency of the two treatment methods with regard to the elimination of Cu phyto-toxicity. The results of the bioassay confirmed the trends of phyto-toxicity results, suggesting that MetPLATE™ could be an adequate alternative to the more expensive, labor intensive, and time consuming plant growth studies.

Co-contaminated soils by organic pollutants (OPs), antibiotics and antibiotic resistance genes (ARGs) have been becoming an emerging problem. However, it is unclear if an interaction exists between mixed pollutants and ARG abundance. Therefore, the potential relationship between OP contents and ARG and class 1 integron-integrase gene (intI1) abundance was investigated from seven dairy farms in Nanjing, Eastern China. Phenanthrene, pentachlorophenol, sulfadiazine, roxithromycin, associated ARG genes, and intI1 had the highest detection frequencies. Correlation analysis suggested a stronger positive relationship between the ARG abundance and the bioaccessible OP content than the total OP content. Additionally, the significant correlation between the bioaccessible mixed pollutant contents and ARG/intI1 abundance suggested a direct/indirect impact of the bioaccessible mixed pollutants on soil ARG dissemination. This study provided a preliminary understanding of the interaction between mixed pollutants and ARGs in co-contaminated soils.

Terrestrial export of dissolved organic carbon (DOC) to watercourses has increased in boreal zone. Effect of decomposing material and soil food webs on the release rate and quality of DOC are poorly known. We quantified carbon (C) release in CO₂, and DOC in different molecular weights from the most common organic soils in boreal zone; and explored the effect of soil type and enchytraeid worms on the release rates. Two types of mor and four types of peat were incubated in laboratory with and without enchytraeid worms for 154 days at + 15 °C. Carbon was mostly released as CO₂; DOC contributed to 2–9% of C release. The share of DOC was higher in peat than in mor. The release rate of CO₂ was three times higher in mor than in highly decomposed peat. Enchytraeids enhanced the release of CO₂ by 31–43% and of DOC by 46–77% in mor. High molecular weight fraction dominated the DOC release. Upscaling the laboratory results into catchment level allowed us to conclude that peatlands are the main source of DOC, low molecular weight DOC originates close to watercourse, and that enchytraeids substantially influence DOC leaching to watercourse and ultimately to aquatic CO₂ emissions.

Sorption is commonly agreed to be the major process underlying the transport and fate of polycyclic aromatic hydrocarbons (PAHs) in soils. However, there is still a scarcity of studies focusing on spatial variability at the field scale in particular. In order to investigate the variation in the field of phenanthrene sorption, bulk topsoil samples were taken in a 15 × 15-m grid from the plough layer in two sandy loam fields with different texture and organic carbon (OC) contents (140 samples in total). Batch experiments were performed using the adsorption method. Values for the partition coefficient Kd(L kg⁻¹) and the organic carbon partition coefficient KOC(L kg⁻¹) agreed with the most frequently used models for PAH partitioning, as OC revealed a higher affinity for sorption. More complex models using different OC compartments, such as non-complexed organic carbon (NCOC) and complexed organic carbon (COC) separately, performed better than single KOCmodels, particularly for a subset including samples with Dexter n < 10 and OC <0.04 kg kg⁻¹. The selected threshold revealed that KOC-based models proved to be applicable for more organic fields, while two-component models proved to be more accurate for the prediction of Kdand retardation factor (R) for less organic soils. Moreover, OC did not fully reflect the changes in phenanthrene retardation in the field with lower OC content (Faardrup). Bulk density and available water content influenced the phenanthrene transport mechanism phenomenon.

Contamination from tank installations in the Arctic is an important issue, since tanks are a necessary feature of all communities, and may be a source of local pollution. Soil samples from below and around three tank installations and one reference site in the Northwest Greenlandic village of Tasiusaq were analysed for the total content of hydrocarbons (THC), lead, cadmium and organic content in the soil. Concentrations up to 77,000 mg/kg DW THC were found, mainly as weathered oil products. Elevated levels of lead and cadmium were also found in many of the samples, with concentrations up to 300 and 2 mg/kg DW, respectively. The tank installation areas were contaminated by THC, lead and cadmium compared to the reference site, and parts of the areas were highly contaminated, exceeding the Danish environmental quality criteria. The correlation between lead and cadmium concentrations was significant (p < 0.01), while no correlation existed between THC and organic matter. Small spills from daily use of the tank installations are suggested to be the source of the THC contamination, whereas the lead and cadmium contamination is suggested to originate primarily from the plume of smoke from waste incineration.

Highly organic soils, and in particular ombrotrophic bogs, have been often used to reconstruct climate changes and heavy metal contaminations. Ombrotrophic peat bogs, in fact, are domed peatlands in which the surface layers are hydrologically isolated from the influence of local groundwaters and surface waters, and are supplied only by atmospheric depositions. In the present work, the attention of Authors has been focused on Pb, Cu, and Zn, coming mainly from anthropogenic activities, and ¹³⁷Cs, released mostly during the Chernobyl disaster. Practically, an undisturbed peat profile was cored in 2005 from a Swiss ombrotrophic bog and analysed using energy-dispersive miniprobe multielement analyzer X-ray fluorescence and Low Background γ-ray spectrometry in order to investigate and quantify the impact of human activities (e.g., industry, traffic, combustion of fossil fuels, “environmental disasters”) in causing Pb, Cu, Zn, and ¹³⁷Cs contaminations during the centuries. Obtained data show that highly organic soils in general, and ombrotrophic bogs in particular, reflect the anthropogenic inputs in heavy metal and radionuclide contaminations. In fact, these environments allowed to follow the depositional history of Pb, Cu, and Zn, both underlining a general increasing of their production since the Industrial Revolution, and remarking past single impacting events such as the introduction of leaded gasoline and of particular agricultural practices. Further, although ¹³⁷Cs showed a main peak corresponding to the Chernobyl disaster, confirming the role of bogs as archive of human activity, data revealed a certain mobility of this radionuclide along the profile. Thus, highly organic soils can be considered as both “witness” of the impact of human activity during centuries and indicator of the health of our planet.

A critical appraisal of single-step extraction procedures of chromium species from soil was done in terms of their selectivity towards Cr(III) and Cr(VI) species. Samples of natural mineral and organic soil and samples of soil enriched with different chromium compounds of various solubility (in liquid or solid form) were used to simulate contamination of soil by liquid and solid wastes. The efficiency of extraction of Cr(III) and Cr(VI) species with various reagents, e.g. acetic acid, chelating agents (EDTA, DTPA) or inorganic salts (phosphates and carbonates), was evaluated on the basis of recovery results obtained for enriched samples. None of used reagents allow for quantitative extraction of added Cr(III) form. Procedures based on extraction of soil with Na₂CO₃ at room and elevated temperature (90–95 °C) were suitable for extraction of Cr(VI) species from mineral soil, whereas for organic soil, the procedure based on extraction with Na₂CO₃ at room temperature was recommended. The developed extraction procedures were validated using certified reference material (CRM 041 soil) and applied for analysis of contaminated soil samples. The studies showed that the physical state of waste, initial form and oxidation state of chromium and soil properties influenced the final chromium species and their mobility in soil, which have an impact on contamination of environment. The analysis of contaminated soil samples from a tannery area showed that the share of Cr(VI) was very low (only 0.8–4.5%) despite the high total content of chromium, which confirmed that chromium was present in immobile forms.