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Persistent, aged hydrocarbons in soil hinder remediation, posing a significant environmental threat. While bioremediation offers an environmentally friendly and cost-effective approach, its efficacy for complex contaminants relies on enhancing pollutant bioavailability. This study explores the potential of immobilized bacterial consortia combined with biochar and rhamnolipids to accelerate bioremediation of aged total petroleum hydrocarbon (TPH)-contaminated soil. Previous research indicates that biochar and biosurfactants can increase bioremediation rates, while mixed consortia offer sequential degradation and higher hydrocarbon mineralization. The present investigation aimed to assess whether combining these strategies could further enhance degradation in aged, complex soil matrices. The bioaugmentation (BA) with bacterial consortium increased the TPHs degradation in aged soil (over 20% compared to natural attenuation - NA). However, co-application of BA with biochar and rhamnolipid higher did not show a statistically prominent synergistic effect. While biochar application facilitated the maintenance of hydrocarbon degrading bacterial consortium in soil, the present study did not identify a direct influence in TPHs degradation. The biochar application in contaminated soil contributed to TPHs adsorption. Rhamnolipid alone slightly increased the TPHs biodegradation with NA, while the combined bioaugmentation treatment with rhamnolipid and biochar increased the degradation between 27.5 and 29.8%. These findings encourage further exploration of combining bioaugmentation with amendment, like biochar and rhamnolipid, for remediating diverse environmental matrices contaminated with complex and aged hydrocarbons.
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Biodegradação Ambiental , Carvão Vegetal , Glicolipídeos , Hidrocarbonetos , Poluentes do Solo , Poluentes do Solo/metabolismo , Glicolipídeos/metabolismo , Carvão Vegetal/química , Hidrocarbonetos/metabolismo , Microbiologia do Solo , Petróleo/metabolismo , Solo/químicaRESUMO
As an alternative to activated carbon, biochar is a promising, environmentally friendly sorbent that can be used to remove organic groundwater pollutants, such as chlorinated ethenes (CEs). Stable isotope fractionation in biofilters is used to quantify pollutant degradation and to distinguish degradation from pollutant sorption on e.g. biochar. However, the sorption of CEs on biochar, and the potential abiotic fractionation processes remain to be tested. The sorption process of CEs and ethene on activated carbon and biochar was investigated with regard to the isotope effects for the differentiation from microbial degradation processes. Results from physical and chemical characterization of biochar indicated that biochar feedstock and pyrolysis conditions determined sorption performance depending on the surface chemistry and the pore size distribution of the coarse sorbent particles. The sorption capacity of the activated carbon was significantly higher with highly chlorinated ethenes, but similar to the biochars with low chlorination. Apparent carbon isotope fractionation factors (ε) of +0.1 to -4.4 were found above measurement uncertainties of GC/IRMS. The extent of isotope enrichment of the 13C bearing isotopologues in the residual aqueous phase (ε < 0) was characteristic for individual pairs of pollutant and sorbent material and could be related to pore-filling processes limited by the micropore size distribution of sorbent materials and the chemical properties of sorbed pollutants. Especially the large isotope fractionation during the sorption of ethene led to the assumption that diffusion processes within the pore matrix of the sorbent particles contributed to the observed isotope effects, but should still be considered a property of sorption. Concluding on the results indicated that sorption processes can have a significant contribution to carbon isotope fractionation in CEs and ethene. These should not be neglected in the evaluation of biofilters for groundwater purification, in which CEs are simultaneously degraded by microbes.
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Abattoirs produce by-products that may become valuable resources for nutrient recycling and energy generation by including pyrolysis and biogas production in the value creation chain. This study investigated the potential of bone chars as sorbents for ammonium in order to produce a soil amendment useful for fertilizing purposes. Ammonium enriched from the digestate by membrane distillation or from pure ammonium sulphate solutions accommodated the nitrogen sorption to the bone chars. The plant availability of the sorbed nitrogen was studied by a standardized short-term plant test with rye (Secale cereale L.). The results showed that ammonium, both from biogas digestate and from pure salt solutions, could be sorbed successfully to the bone chars post-pyrolysis and increased the nitrogen concentration of the chars (1.6 ± 0.3%) by 0.2-0.4%. This additional nitrogen was desorbed easily and supported plant growth (+17 to +37%) and plant nitrogen uptake (+19-74%). The sorption of ammonium to the bone chars had a positive effect on the reversal of pure bone char phytotoxicity and on nitrogen availability. In summary, this study showed that abattoir wastes are useful pyrolysis input materials to produce bone chars and to provide ammonium source for sorption to the chars. This innovation offers the possibility to produce nitrogen-enriched bone chars as a new type of fertilizer that upgrades the known value of bone char as phosphorus fertilizer by an additional nitrogen fertilizer effect.
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Biochars from wood chips (WC) and corn cobs (CC) were prepared by slow pyrolysis and used for sorption separation of erythrosine B (EB) and thioflavin T (TT) in batch experiments. Biochar-based adsorbents were extensively characterized using FTIR, XRD, SEM-EDX, and XPS techniques. The kinetics studies revealed that adsorption on external surfaces was the rate-limiting step for the removal of TT on both WC and CC biochar, while intraparticle diffusion was the rate-limiting step for the adsorption of EB. Maximal experimental adsorption capacities Qmaxexp of TT reached 182 ± 5 (WC) and 45 ± 2 mg g-1 (CC), and EB 12.7 ± 0.9 (WC) and 1.5 ± 0.4 mg g-1 (CC), respectively, thereby indicating a higher affinity of biochars for TT. The adsorption mechanism was found to be associated with π-π interaction, hydrogen bonding, and pore filling. Application of the innovative dynamic approach based on fast-field-cycling NMR relaxometry indicates that variations in the retention of water-soluble dyes could be explained by distinct water dynamics in the porous structures of WC and CC. The obtained results suggest that studied biochars will be more effective in adsorbing of cationic than anionic dyes from contaminated effluents.
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Although the suitability of some biochars for contaminants' sorption separation has been established, not all potential feedstocks have been explored and characterized. Here, we physicochemically characterized cherry pit biochar (CPB) pyrolyzed from cherry pit biomass (CP) at 500 °C, and we assessed their As and Hg sorption efficiencies in aqueous solutions in comparison to activated carbon (AC). The basic physicochemical and material characterization of the studied adsorbents was carried out using pH, electrical conductivity (EC), cation exchange capacity (CEC), concentration of surface functional groups (Boehm titration), and surface area (SA) analysis; elemental C, H, N analysis; and Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX). AsO43- anions and Hg2+ cations were selected as model contaminants used to test the sorption properties of the sorption materials. Characterization analyses confirmed a ninefold increase in SA in the case of CPB. The total C concentration increased by 26%, while decreases in the total H and N concentrations were observed. The values of carbonate and ash contents decreased by about half due to pyrolysis processes. The concentrations of surface functional groups of the analyzed biochar obtained by Boehm titration confirmed a decrease in carboxyl and lactone groups, while an increase in phenolic functional groups was observed. Changes in the morphology and surface functionality of the pyrolyzed material were confirmed by SEM-EDX and FTIR analyses. In sorption experiments, we found that the CPB showed better results in the sorption separation of Hg2+ than in the sorption separation of AsO43-. The sorption efficiency for the model cation increased in the order CP < CPB < AC and, for the model anion, it increased in the order CPB < CP < AC.
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The study showed novel findings about changes in the fate and bioavailability of conazole fungicides (CFs) after biochar (BC) addition to soil. Two contrasting soils (low- and high-sorbing of CF; L soils, H soils) were amended by three BCs (low-, moderate-, and high-sorbing of CF; L-BC, M-BC, H-BC) at 0.2% and 2% doses. Epoxiconazole (EPC) and tebuconazole (TBC) were then added to the soil-BC mixtures, and their degradation, bioaccumulation in earthworms (Eisenia andrei), and bioconcentration in lettuce (Lactuca sativa) were studied for three months. Also, stir bar sorptive extraction (SBSE) was performed to determine CF (bio)accessibility. The EPC and TBC degradation in the soil-BC mixtures followed usually the first-order decay kinetics. The BC addition prevalently decreased the pesticides degradation in the L soil mixtures but often increased it in the H soil mixtures. In general, EPC degraded less than TBC. BC type and dose roles in the pesticides degradation were unclear. The BC addition significantly reduced pesticide uptake to the earthworms in the L soil mixtures (by 37-96%) and in the H soil mixtures (by 6-89%) with 2% BC. The BC addition reduced pesticide uptake to the lettuce roots and leaves significantly-up to two orders of magnitude, and this reduction was strong in H soil mixtures at 2% of BC. The BC addition reduced the CF (bio)accessibility measured by SBSE in all L soil mixtures and some H soil mixtures with 2% BC. Although not significant, it also seems that the pesticide bioaccumulation, bioconcentration, and (bio)accessibility were decreasing according to the BC type (L-BC > M-BC > H-BC). The pesticide concentrations in the earthworms and lettuce correlated significantly to the SBSE results, which indicates this technique as a possible predictor of biotic uptake. Our results showed that the interactions were hard to predict in the complex soil-BC-pesticide system.
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Fungicidas Industriais , Oligoquetos , Poluentes do Solo , Animais , Disponibilidade Biológica , Carvão Vegetal/metabolismo , Fungicidas Industriais/análise , Oligoquetos/metabolismo , Solo , Poluentes do Solo/análiseRESUMO
Maintaining and supporting complete biodegradation during remediation of petroleum hydrocarbon contaminated groundwater in constructed wetlands is vital for the final destruction and removal of contaminants. We aimed to compare and gain insight into biodegradation and explore possible limitations in different filter materials (sand, sand amended with biochar, expanded clay). These filters were collected from constructed wetlands after two years of operation and batch experiments were conducted using two stable isotope techniques; (i) carbon isotope labelling of hexadecane and (ii) hydrogen isotope fractionation of decane. Both hydrocarbon compounds hexadecane and decane were biodegraded. The mineralization rate of hexadecane was higher in the sandy filter material (3.6 µg CO2 g-1 day-1) than in the expanded clay (1.0 µg CO2 g-1 day-1). The microbial community of the constructed wetland microcosms was dominated by Gram negative bacteria and fungi and was specific for the different filter materials while hexadecane was primarily anabolized by bacteria. Adsorption / desorption of petroleum hydrocarbons in expanded clay was observed, which might not hinder but delay biodegradation. Very few cases of hydrogen isotope fractionation were recorded in expanded clay and sand & biochar filters during decane biodegradation. In sand filters, decane was biodegraded more slowly and hydrogen isotope fractionation was visible. Still, the range of observed apparent kinetic hydrogen isotope effects (AKIEH = 1.072-1.500) and apparent decane biodegradation rates (k = - 0.017 to - 0.067 day-1) of the sand filter were low. To conclude, low biodegradation rates, small hydrogen isotope fractionation, zero order mineralization kinetics and lack of microbial biomass growth indicated that mass transfer controlled biodegradation.
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Água Subterrânea , Petróleo , Biodegradação Ambiental , Hidrocarbonetos , Áreas AlagadasRESUMO
The individual role of biochar, compost and PGPR has been widely studied in increasing the productivity of plants by inducing resistance against phyto-pathogens. However, the knowledge on combined effect of biochar and PGPR on plant health and management of foliar pathogens is still at juvenile stage. The effect of green waste biochar (GWB) and wood biochar (WB), together with compost (Comp) and plant growth promoting rhizobacteria (PGPR; Bacillus subtilis) was examined on tomato (Solanum lycopersicum L.) physiology and Alternaria solani development both in vivo and in vitro. Tomato plants were raised in potting mixture modified with only compost (Comp) at application rate of 20% (v/v), and along with WB and GWB at application rate of 3 and 6% (v/v), each separately, in combination with or without B. subtilis. In comparison with WB amended soil substrate, percentage disease index was significantly reduced in GWB amended treatments (Comp + 6%GWB and Comp + 3%GWB; 48.21 and 35.6%, respectively). Whereas, in the presence of B. subtilis disease suppression was also maximum (up to 80%) in the substrate containing GWB. Tomato plant growth and physiological parameters were significantly higher in treatment containing GWB (6%) alone as well as in combination with PGPR. Alternaria solani mycelial growth inhibition was less than 50% in comp, WB and GWB amended growth media, whereas B. subtilis induced maximum inhibition (55.75%). Conclusively, the variable impact of WB, GWB and subsequently their concentrations in the soil substrate was evident on early blight development and plant physiology. To our knowledge, this is the first report implying biochar in synergism with PGPR to hinder the early blight development in tomatoes.
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Alternaria/crescimento & desenvolvimento , Bacillus subtilis/crescimento & desenvolvimento , Carvão Vegetal/farmacologia , Compostagem , Doenças das Plantas/microbiologia , Rizoma/microbiologia , Solanum lycopersicum/microbiologia , Solanum lycopersicum/crescimento & desenvolvimentoRESUMO
Biochar usage in agriculture becomes increasingly important for the improvement of soil properties. However, from the perspective of pesticides, biochar can influence exposure to pesticides of both target and non-target organisms and also pesticides' fate in soil. Our study investigated degradation and bioaccumulation (in the Eisenia andrei earthworm) of two conazole fungicides, epoxiconazole and tebuconazole, added to high- and low-sorbing soils (by means of fungicides' sorption measured beforehand) amended with low-, moderate- and high-sorbing biochars at 0.2% and 2% doses. We aimed to investigate the effects of contrasting soil and biochar properties, different doses of biochar in soil-biochar mixtures, and different compounds on the degradation and bioaccumulation. We also wanted to explore if the beforehand determined sorption of fungicides on individual soils and biochars is manifested somehow in their degradation and/or bioaccumulation in soil-biochar mixtures. The biochars' presence in the soils promoted the degradation of fungicides with a clear effect of dose and soil, but less clear effect of biochar or compound. The bioaccumulation factors were higher in low-sorbing soil variants and also decreased with increasing biochar dose. For low-sorbing soil variants, the bioaccumulation was also influenced by the type of biochar corresponding to its sorbing potential and the possible effect on the bioavailability of the fungicides. Our results show that mixing of biochars with soils changes the fate and bioaccumulation of the conazole fungicides. However, the sorption results from original materials are not straightforwardly manifested in the more complex soil-biota system.
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Fungicidas Industriais , Oligoquetos , Poluentes do Solo , Animais , Bioacumulação , Carvão Vegetal , Compostos de Epóxi , Fungicidas Industriais/análise , Solo , Poluentes do Solo/análise , TriazóisRESUMO
The application of pyrogenic materials in immobilization processes of metalloids represents a burning issue in environmental and waste applications and management. The main objective of this study was to characterize the effect of biomass pretreatment by Cu, Fe and Mg blending and pyrolysis temperature on As sorption efficiency as a model of anionic metalloids from model solutions and As immobilization in old mine soil by pyrogenic materials. The physico-chemical characterization of engineered materials produced in slow pyrolysis process at 400 and 700°C from metal-blended hard wood chips (30% w/w) showed increasing of surface areas (1.4-1.8-fold), changes in pH, and more than 50% decrease in total C content. The batch sorption processes of As ions by Cu-modified pyrogenic materials (CuPM), Fe-modified pyrogenic materials (FePM), and Mg-modified pyrogenic materials (MgPM) showed increasing uptake in order CuPM700 (Qmax 2.56 mg g-1) < CuPM400 (Qmax 3.88 mg g-1) < FePM700 (Qmax 5.90 mg g-1) < MgPM700 (Qmax 7.42 mg g-1) < MgPM400 (Qmax 9.59 mg g-1) < FePM400 (Qmax 10.55 mg g-1). Engineered pyrogenic materials produced at 400°C showed higher immobilization effect on soluble As in soil pore water of old mine site soil from Mediterranean area. FePM400 reduced mobility of arsenic > 3.2 times and MgPM400 > 5 times compared to control. Promising pyrogenic material MgPM400 showed immobilization effect also on additional heavy metals (Cd, Cu, Fe, Mn, Pb, Sr, Zn) present in studied soil.
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Arsênio/química , Recuperação e Remediação Ambiental/métodos , Mineração , Pirogênios/química , Poluentes do Solo/química , Adsorção , Biomassa , Região do Mediterrâneo , Metais Pesados/química , Pirogênios/síntese química , PiróliseRESUMO
Biochar, a carbonaceous material, is increasingly used in the remediation of the anthropogenically polluted soils and the restoration of their ecological functions. However, the interaction mechanisms among biochar, inorganic and organic soil properties and soil biota are still not very clear. The effect of biochar on soil microorganisms is very diverse. Several mechanisms of these interactions were suggested. However, a well acceptable mechanism of biochar effect on soil microorganisms is still missing. Therefore, efforts were made to examine and proposed a mechanism of the interactions between biochar and microorganisms, as well as existing problems of biochar impacts on main groups of soil enzymes, the composition of the microbiota and the detoxification (heavy metals) and degradation (polycyclic aromatic hydrocarbons) of soil pollutants. The data on the process of biochar colonization by microorganisms and the effect of volatile pyrolysis products released by biochar on the soil microbiota were analysed in detail. The effects of biochar on the physico-chemical properties of soils, the content of mineral nutrients and the response of microbial communities to these changes are also discussed. The information provided here may contribute to the solution of the feasibility, effectiveness and safety of the biochar questions to enhance the soil fertility and to detoxify pollutants in soils.
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Carvão Vegetal , Microbiologia do Solo , Poluentes do Solo/metabolismo , Biodegradação Ambiental , Concentração de Íons de Hidrogênio , Metais Pesados/metabolismo , Microbiota , Hidrocarbonetos Policíclicos Aromáticos/análise , Hidrocarbonetos Policíclicos Aromáticos/metabolismo , Solo/químicaRESUMO
Copper-based fungicides have been used for a long time in viticulture and have accumulated in many vineyard soils. In this study, incrementing Cu(OH)2-based fungicide application from 0.05 to 5 g Cu kg-1 on two agricultural soils (an acidic sandy loam (L, pH 4.95) and an alkaline silt loam (D, pH 7.45)) resulted in 5 times more mobile Cu in the acidic soil. The most sensitive parameters of alfalfa (Medicago sativa) growing in these soils were the root nodule number, decreasing to 34% and 15% of the control at 0.1 g Cu kg-1 in soil L and at 1.5 g Cu kg-1 in soil D, respectively, as well as the nodule biomass, decreasing to 25% and 27% at 0.5 g Cu kg-1 in soil L and at 1.5 g Cu kg-1 in soil D, respectively. However, the enzymatic N2-fixation was not directly affected by Cu in spite of the presence of Cu in the meristem and the zone of effective N2-fixation, as illustrated by chemical imaging. The strongly different responses observed in the two tested soils reflect the higher buffering capacity of the alkaline silt loam and showed that Cu mitigation and remediation strategies should especially target vineyards with acidic, sandy soils.
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Cobre/metabolismo , Fungicidas Industriais/efeitos adversos , Medicago sativa/efeitos dos fármacos , Fixação de Nitrogênio/efeitos dos fármacos , Nodulação/efeitos dos fármacos , Disponibilidade Biológica , Hidróxidos/metabolismo , Medicago sativa/crescimento & desenvolvimento , Medicago sativa/microbiologiaRESUMO
Biochar (BC) is increasingly tested as a soil amendment for immobilization of heavy metals (HMs) and other pollutants. In our study, an acidic soil amended with wood chip-derived BC showed strongly enhanced Cu and Cd sorption after 15 months of aging under greenhouse conditions. X-ray absorption near edge structure suggested formation of Cu(OH)2 and CuCO3 and upon aging increasingly Cu sorption to the BC organic phase (from 9.2% to 40.7%) as main binding mechanisms of Cu on the BCs. In contrast, Cd was predominantly bound as CdCO3 on the BCs even after 15 months (82.7%). We found indications by mid-infrared spectroscopy that the formation of organic functional groups plays a role for increased HM sorption on aged BCs. Yet, our data suggest that the accessibility of BC's pore network and reactive surfaces is likely to be the overriding factor responsible for aging-related changes in HM sorption capacity, rather than direct interactions of HMs with oxidized functional groups. We observed highly weathered BC surface structures with scanning electron microscopy along with strongly increased wettability of the BCs after 15 months of soil aging as indicated by a decrease of water contact angles (from 62.4° to 4.2°).
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Cádmio/química , Carvão Vegetal/química , Cobre/química , Metais Pesados/química , Poluentes do Solo/química , Solo/química , Metais Pesados/análise , Poluentes do Solo/análiseRESUMO
Methylated analogues of polycyclic aromatic hydrocarbons (PAHs) represent important environmental contaminants produced often at process of feedstock thermochemical conversion. In the present study, we determined and compared levels of 1-methylnaphtalene and 2-methylnaphtalene in municipal sewage sludge (MSS), sludge-derived pyrogenic carbonaceous materials produced at 350⯰C (PCM350) and 500⯰C (PCM500) in process of slow pyrolysis. The highest extraction efficiency of both aromatic structures from MSS, PCM350 and PCM500 for toluene as extraction agent and 36â¯h of extraction time was revealed. The total concentrations of 1-methylnaphtalene reached values 8.7â¯mg/kg for MSS, 14.6â¯mg/kg for PCM350 and 18.1â¯mg/kg for PCM500.2-methylnaphtalene was quantified in concentrations 12.5â¯mg/kg for MSS, 19.3â¯mg/kg for PCM350 and 23â¯mg/kg for PCM500. Available levels of 1-methylnaphtalene and 2-methylnaphtalene determined by Tenax resin desorption test during 36 days showed decreasing trend in order PCM500â¯>â¯PCM350â¯>â¯MSS. In summary, pyrolysis treatment of sewage sludge can increase total amount of methylated PAHs in produced carbonaceous materials but decrease their available forms. This fact can contribute to global ecotoxicological assessment of organic pollutants in biochars and pyrogenic carbonaceous materials applied in agronomy as soil amendments.
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Naftalenos/química , Hidrocarbonetos Policíclicos Aromáticos/química , Esgotos/química , Poluentes do Solo/química , Hidrocarbonetos Policíclicos Aromáticos/análise , Pirólise , Poluentes do Solo/análiseRESUMO
Metal-blending of biomass prior to pyrolysis is investigated in this work as a tool to modify biochar physico-chemical properties and its behavior as adsorbent. Six different compounds were used for metal-blending: AlCl3, Cu(OH)2, FeSO4, KCl, MgCl2 and Mg(OH)2. Pyrolysis experiments were performed at 400 and 700⯰C and the characterization of biochar properties included: elemental composition, thermal stability, surface area and pore size distribution, Zeta potential, redox potential, chemical structure (with nuclear magnetic resonance) and adsorption behavior of arsenate, phosphate and nitrate. Metalblending strongly affected biochars' surface charge and redox potential. Moreover, it increased biochars' microporosity (per mass of organic carbon). For most biochars, mesoporosity was also increased. The adsorption behavior was enhanced for all metal-blended biochars, although with significant differences across species: Mg(OH)2-blended biochar produced at 400 °C showed the highest phosphate adsorption capacity (Langmuir Qmax approx. 250â¯mgâ¯g-1), while AlCl3-blended biochar produced also at 400 °C showed the highest arsenate adsorption (Langmuir Qmax approx. 14â¯mgâ¯g-1). Significant differences were present, even for the same biochar, with respect to the investigated oxyanions. This indicates that biochar properties need to be optimized for each application, but also that this optimization can be achieved with tools such as metal-blending. These results constitute a significant contribution towards the production of designer biochars.
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Biomassa , Carvão Vegetal/química , Metais/química , AdsorçãoRESUMO
Biochar is a promising immobilization tool for various contaminants in liquid wastes, aqueous solutions and soils. To further improve the sorption characteristics, a biochar/montmorillonite composite was produced and synthesized in an experimental pyrolysis reactor, using bamboo as biomass feedstock. The composite was characterized by physico-chemical and structural methods (FTIR, SEM, SEM/EDX, SSA, Low temperature nitrogen adsorption method). Based on these methods, the successful preparation of a bamboo based biochar/montmorillonite composite preparation has been demonstrated. The particles of montmorillonite were distributed across the biochar surface. The adsorption studies for removal nitrates from aqueous solutions were investigated by a batch method at laboratory temperatures. The experimental data were fitted by three adsorption models (Langmuir, Freundlich and DR; R2â¯>â¯0.93). The maximum adsorption capacity achieved by biochar at pH 4, was about 5â¯mgâ¯g-1 and by biochar/montmorillonite composite 9â¯mgâ¯g-1. The results suggest that the bamboo-based biochar/montmorillonite composite can be used effectively in the treatment of industrial effluents or waste water containing anionic pollutants such as nitrates.
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Nitratos , Poluentes Químicos da Água , Adsorção , Bentonita , Carvão VegetalRESUMO
In soil, mixed contamination with potentially toxic trace elements and polycyclic aromatic hydrocarbons (PAHs) may persist for a long time due to strong adsorption to the soil matrix and to its toxicity to microorganism. We conducted an incubation batch experiment to test the effect of soil amendments (biochar, gravel sludge, iron oxides) on the immobilisation of trace elements. To monitor microbial degradation, a 13C-PHE (phenanthrene) label was introduced to soil for 13C-PLFA (phospholipid fatty acid) analysis. Soil amendments increased soil pH, reduced mobility of NH4NO3-extractable trace elements Cd and Zn, and increased mobile Cu. A small consortium of PHE degraders was identified mainly in the microbial groups of gram-negative bacteria and actinomycetes. The degradation process of PHE peaked 9days after incubation start. PAH concentrations remained constant in the soil within the 30-day incubation, except for the easily available 13C-PHE in the amended treatment. In order to test the effect of plants and soil amendments under more realistic conditions, we also conducted an outdoor pot experiment with black locust (Robinia pseudoacacia Nyirsegi). Furthermore, soil amendments increased the mobility of soil Cu and As and decreased the mobility of Cd, Pb and Sb. The uptake of trace elements to leaves was low. Σ 16 U.S. EPA PAHs were significantly reduced only in the combined treatment of black locust and soil amendments after 12months of plant growth. Soil amendment-assisted phytoremediation showed a high efficiency in PAH dissipation and may be a useful remediation technique for mixed contaminated soils.
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Copper (Cu)-based fungicides have been used in viticulture to prevent downy mildew since the end of the 19th century, and are still used today to reduce fungal diseases. Consequently, Cu has built up in many vineyard soils, and it is still unclear how this affects soil functioning. The present study aimed to assess the short and medium-term effects of Cu contamination on the soil fungal community. Two contrasting agricultural soils, an acidic sandy loam and an alkaline silt loam, were used for an eco-toxicological greenhouse pot experiment. The soils were spiked with a Cu-based fungicide in seven concentrations (0-5000 mg Cu kg-1 soil) and alfalfa was grown in the pots for 3 months. Sampling was conducted at the beginning and at the end of the study period to test Cu toxicity effects on total microbial biomass, basal respiration and enzyme activities. Fungal abundance was analysed by ergosterol at both samplings, and for the second sampling, fungal community structure was evaluated via ITS amplicon sequences. Soil microbial biomass C as well as microbial respiration rate decreased with increasing Cu concentrations, with EC50 ranging from 76 to 187 mg EDTA-extractable Cu kg-1 soil. Oxidative enzymes showed a trend of increasing activity at the first sampling, but a decline in peroxidase activity was observed for the second sampling. We found remarkable Cu-induced changes in fungal community abundance (EC50 ranging from 9.2 to 94 mg EDTA-extractable Cu kg-1 soil) and composition, but not in diversity. A large number of diverse fungi were able to thrive under elevated Cu concentrations, though within the order of Hypocreales several species declined. A remarkable Cu-induced change in the community composition was found, which depended on the soil properties and, hence, on Cu availability.
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Cobre/toxicidade , Monitoramento Ambiental , Fungos/efeitos dos fármacos , Microbiologia do Solo , Poluentes do Solo/toxicidade , Agricultura/métodos , Biomassa , Fungicidas Industriais , Solo/químicaRESUMO
Co-contaminations of soils with organic and inorganic pollutants are a frequent environmental problem. Due to their toxicity and recalcitrance, the heterogeneous pollutants may persist in soil. The hypothesis of this study was that degradation of polycyclic aromatic hydrocarbons (PAHs) is enhanced if heavy metals in soil are immobilized and their bioavailability reduced. For metal immobilization and enhanced biodegradation, distinct mineral and organic soil amendments (iron oxides, gravel sludge, biochar) were deployed in an incubation batch experiment. The second part of the experiment consisted of a greenhouse pot experiment applying fast-growing and pollution-tolerant woody plants (willow and black locust). Soil amendments initially immobilized NH4NO3-extractable zinc, cadmium, and lead; after 100 days of incubation, soil amendments showed reductions only for cadmium and a tendency to enhance arsenic mobility. In order to monitor the remediation success, a 13C-phenanthrene (PHE) label was applied. 13C-phospholipid fatty acid analysis (13C-PLFA) further enabled the identification of PHE-degrading soil microorganisms. Both experiments exhibited a similar PLFA profile. Gram-negative bacteria (esp. cy17:0, 16:1ω7 + 6, 18:1ω7c) were the most significant microbial group taking up 13C-PHE. Plants effectively increased the label uptake by gram-positive bacteria and increased the biomass of the fungal biomarker, although their contribution to the degradation process was minor. Plants tended to prolong PAH dissipation in soil; at the end of the experiment, however, all treatments showed equally low total PAH concentrations in soil. While black locust plants tended not to take up potentially toxic trace elements, willows accumulated them in their leaves. The results of this study show that the chosen treatments did not enhance the remediation of the experimental soil.
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Hidrocarbonetos Policíclicos Aromáticos/análise , Robinia/crescimento & desenvolvimento , Salix/crescimento & desenvolvimento , Microbiologia do Solo , Poluentes do Solo/análise , Oligoelementos/análise , Áustria , Biodegradação Ambiental , Isótopos de Carbono/análise , Metais Pesados/análise , Modelos Teóricos , Fenantrenos/análise , SoloRESUMO
Besides carbon sequestration and improvement of soil properties, biochar (BC) has increasingly been studied as an amendment to immobilise heavy metals in contaminated soils. In a 2-year experiment, we analysed the effects of poplar BC (P-BC, mixed with compost) and gravel sludge with siderite-bearing material (GSFe) on a Cd-, Pb- and Zn-contaminated soil and on metal concentration in Miscanthus × giganteus shoots under greenhouse and field conditions. In the greenhouse, 1% (m/m) P-BC addition reduced NH4NO3-extractable Cd, Pb and Zn concentrations by 75, 86 and 92%, respectively, at the end of the study. In the leachates, P-BC (1%) could significantly reduce Cd and Zn in both years. In the field, P-BC (3%) induced a reduction of extractable Cd by 87% whereas a combination of P-BC + GSFe reduced Pb by 82% and Zn by 98% in the first year and by 83 and 96% in the second year. In contrast, the metal immobilisation in the soil was hardly reflected in the shoots of Miscanthus × giganteus which generally showed metal concentrations close to control. While Cd was not influenced in both years, Pb and Zn were slightly reduced. Our study confirmed that Miscanthus is an efficient metal excluder, corroborating its suitability for the production of renewable biomass on metal-contaminated soils.