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The accumulation of organic pollutants in vegetables is a major global food safety issue. The concentrations of pollutants in vegetables usually differ across different tissues because of different transport and accumulation pathways. However, owing to the limitations of conventional methods, in situ localization of typical organic pollutants such as phthalate esters (PAEs) in plant tissues has not yet been studied. Here, we developed a quick and efficient method for in situ detection and imaging of the spatial distribution of PAEs in a typical root vegetable, carrot, using matrix-assisted laser desorption/ionization imaging mass spectrometry (MALDI-IMS). The use of a 2,5-dihydroxybenzoic acid matrix with a spray-sublimation coating method led to the successful identification of PAEs ion signals. The IMS results showed that a typical PAE-di-(2-ethylhexyl)phthalate (DEHP) was broadly distributed in the cortex, phloem, and metaxylem, but was barely detectable in the cambium and protoxylem. Interestingly, MALDI-IMS data also revealed for the first time the spatial distribution of sugars and β-carotene in carrots. In summary, the developed method offers a new and practical methodology for the in situ analysis of PAEs and plant metabolites in plant tissues. As a result, it could provide a more intuitive understanding of the movement and transformation of organic pollutants in soil-plant systems.

Ferrate (Fe(VI)) salts like K

Chemosphere : chemistry, biology and toxicology as related to environmental problems 232, 164-170 (2019). doi:10.1016/j.chemosphere.2019.05.038, Published by Elsevier Science, Amsterdam [u.a.]

The overuse and misuse of antibiotics in animal breeding for disease treatment and growth enhancement have been major drivers of the occurrence, diffusion, and accumulation of antibiotic resistance genes (ARGs) in wastewater. Strategies to combat ARG dissemination are pressingly needed for human and ecological safety. To achieve this goal, a biochar-based polymer, magnetic biochar/quaternary phosphonium salt (MBQ), was applied in livestock wastewater and displayed a high performance in bacterial deactivation and ARG decrease. Efficient antibacterial effects were achieved by both MBQ and quaternary phosphonium salt; however, the abundance and fold change of ARGs in the MBQ treatment indicated a more powerful ARG dissemination control than quaternary phosphonium salt. The application of MBQ evidently reduced the microbial diversity and may primarily be responsible for altering the ARG profiles in wastewater. Network, redundancy, and variation partitioning analyses were further employed to reveal that the microbial community and the presence of mobile genetic elements were two critical factors shaping the pattern of the antibiotic resistome in livestock wastewater. Considered together, these findings extend the application field of biochar and have important implications for reducing ARG dissemination risks in livestock wastewater.

The influence of an ionic functional group on the fate and behavior of chemicals in the environment has so far not been systematically investigated. This study, therefore, examines the following three substances with high structural similarity but differing charge: non-charged 4-n-dodecylphenol[phenylring

Das Umweltprogramm der Vereinten Nationen (UNEP) stellte 2019 große Lücken im Umgang mit dem weltweiten Management chemischer Substanzen fest. Um diese zu schließen, schlagen Wissenschaftler nun vor, einen Globalen Rat für Chemikalien und Abfälle ins Leben zu rufen.

The influence of an ionic functional group on the fate and behavior of chemicals in the environment has so far not been systematically investigated. This study, therefore, examines the following three substances with high structural similarity but differing charge: non-charged 4-n-dodecylphenol[phenylring-14C(U)] (14C-DP), negatively charged 4-n-dodecylbenzenesulfonicacid[phenylring-14C(U)] sodium salt (14C-DS−) and positively charged 4-n-dodecylbenzyltrimethylammonium chloride[phenylring-14C(U)] (14C-DA+). They were investigated in a soil simulation study according to the OECD 307 test guideline by measuring the distribution of the applied radioactivity (AR) among volatile, mineralized, extractable and non-extractable residues (NER) in one soil after 0, 1, 7, 14, 49, 84 and 124 days of incubation. Extractable portions of 14C were examined by means of radio-TLC and -HPLC analyses. Microbial activity of the soil incubated with and without 14C-DP, 14C-DS− and 14C-DA+ was determined measuring the reduction of dimethylsulfoxide (DMSO) over time. After 124 days of incubation highest mineralization could be observed for 14C-DS− (64.5% AR). Except CO2, no volatile residues were formed over time. Besides the parent compounds, polar (14C-DP, 14C-DS− and 14C-DA+) and nonpolar (14C-DA+) transformation products were detected. Highest amounts of 14C were extracted using methanol and were thus potentially bioavailable for soil microorganisms. Microbial activity was markedly higher in soil incubated with 14C-DP and 14C-DS− compared to 14C-DA+ or soil without any treatment. Half-lives (DT50 k2) at 18 °C were as follows: DA+ (61.8 days) > DS− (18.2 days) > DP (10.0 days). In case of the cationic compound and its transformation products we conclude that a higher sorption affinity to soil particles leads to reduced bioavailability for microorganisms and thus reduced mineralization resulting in a higher persistence compared to anionic and non-charged organic compounds in soil. The impact of our findings on the persistence assessment of chemicals when performing OECD guideline tests in soil, water-sediment and surface water is discussed.

The influence of an ionic functional group on the fate of chemicals in the environment, especially the formation of non-extractable residues (NER), has not been systematically investigated. Using 4-n-dodecylphenol[phenylring

Quantification of nonextractable residues (NER) of pesticides in soil is feasible by use of radioactively labeled compounds, but structural information on these long-term stabilized residues is usually lacking. Microorganisms incorporate parts of the radiolabeled ((14)C-) carbon from contaminants into microbial biomass, which after cell death enters soil organic matter, thus forming biogenic nonextractable residues (bioNER). The formation of bioNER is not yet determinable in environmental fate studies due to a lack of methodology. This paper focuses on the development of a feasible analytical method to quantify proteinaceous carbon, since proteins make up the largest mass portion of bacterial cells. The test substance (14)C-bromoxynil after 56 days forms more than 70% of NER in soil. For further characterization of NER the amino acids were extracted, purified, and separated by two-dimensional thin-layer chromatography (TLC). Visualization of the (14)C-amino acids was performed by bioimaging, unambiguous identification by GC-MS and LC-MS/MS. Our analysis revealed that after 56 days of incubation about 14.5% of the (14)C-label of bromoxynil was incorporated in amino acids. Extrapolating this content based on the amount of proteins in the biomass (55%), in total about 26% of the NER is accounted for by bioNER and thus is not environmentally relevant.

Fish are warned about the presence of predators via an alarm cue released from the skin of injured conspecifics. The detection of this odor inherently initiates an antipredator response, which increases the chance of survival for the individual. In the present study, we assessed the effect of three commonly used pesticides on the antipredator response of zebrafish (Danio rerio). For this, we analyzed the behavioral response of zebrafish to a conspecific skin extract following 24 h of exposure to the respective contaminants. Results demonstrate that fish exposed to 20 μg/L of the organophosphate insecticide chlorpyrifos significantly reduced bottom-dwelling and freezing behavior, suggesting an impairment of the antipredator response. For the urea-herbicide linuron and the pyrethroid insecticide permethrin, no statistically significant effects could be detected. However, linuron-exposed fish appeared to respond in an altered manner to the skin extract; some individuals failed to perform the inherent behaviors such as erratic movements and instead merely increased their velocity. Furthermore, we determined whether zebrafish would avoid the pesticides in a choice maze. While fish avoided permethrin, they behaved indifferently to chlorpyrifos and linuron. The study demonstrates that pesticides may alter the olfactory-mediated antipredator response of zebrafish in distinct ways, revealing that particularly fish exposed to chlorpyrifos may be more prone to predation.

Global demand for alternative energy sources increases due to concerns regarding energy security and greenhouse gas emissions. However, little is known regarding the impacts of biofuels to the environment and human health even though the identification of such impacts is important to avoid biofuels leading to undesired effects. In this study mutagenicity and genotoxicity of the three biofuel candidates ethyl levulinate (EL), 2-methyltetrahydrofuran (2-MTHF) and 2-methylfuran (2-MF) were investigated in comparison to two petroleum-derived fuels and a biodiesel. None of the samples induced mutagenicity in the Ames fluctuation test. However, the Micronucleus assay revealed significant effects in Chinese hamster (Cricetulus griseus) V79 cells caused by the potential biofuels. 2-MF revealed the highest toxic potential with significant induction of micronuclei below 20.0 mg/L. EL and 2-MTHF induced micronuclei only at very high concentrations (>1000.0 mg/L). In regard to the genotoxic potential of 2-MF, its usage as biofuel should be critically discussed.

Many decades of research have shown that humic compounds as part of the soil organic matter (SOM) are essential for the stability and ecosystem services of soils. James P. Martin and Konrad Haider based on several pioneers in humus research improved the basis for the current knowledge of key processes in the soil environment, in particular structure and formation of humus triggered mainly by soil fungi. Other major contributions are briefly described but not in the focus of this article, such as their innovative tracer experiments with isotope-labelled xenobiotic chemicals and natural litter to study their fate. Both scientists inspired generations of younger researchers to advance their approaches and laid the cornerstone of the current understanding of soil organic matter formation. This article values the key experiments of Martin and Haider in this field and the related follow-up research finally resulting in the current view on formation mechanisms of SOM and non-extractable residues (NER) of xenobiotics. The improved understanding of these processes considering necromass with tissue residues of plants, microbes and animals challenges the traditional views of humic matter as macromolecular organic matrix, which according to the research of the last years represents only a variable part of the total organic matter besides associates of low molecular weight molecules. We discuss views on soil organic matter and humic substances that are nowadays considered not to differ in molecular diversity. We will start by demonstrating the understanding of humus characteristics and humus formation three decades ago closely related to the findings of Martin and Haider. Methodological approaches to characterize relevant structural and mechanistic pictures of SOM such as the priming effect, clay mineral catalysed reactions and the various mechanisms by which natural and xenobiotic chemicals are protected in soil are briefly illustrated by examples. Fungal activities in producing secondary metabolites like polyketides and their probably minor contributions to SOM formation are presented. Open research questions stimulated by these two soil scientists are sketched which are nowadays possible to address by new sophisticated high-resolution techniques.

The population vulnerability of a species to pesticides is determined by the risk of its exposure to the pollutant, its sensitivity to the toxicant and the potential to sustain its populations if adversely affected (population resilience). This study uses population modelling to link the life cycle traits of a set of fish species which are highly susceptible to pesticide exposure, to their population resilience as a contribution to the needed identification of representative vulnerable species for higher-tier ecological risk assessment (ERA) of pesticides in Europe. Leslie matrix models for 21 species were parametrized using data from literature on field populations whose resilience was assessed. Phoxinus phoxinus was identified as the species with the least resilient populations for effects on fertility, Lampetra planeri for effects on juvenile survival and Esox lucius for effects on adult survival. Combining the measured effects from standard fish bio-tests with population models of these species would result in an ecologically relevant and protective risk assessment for field conditions in Europe.

In the present study we demonstrate the rhizoremediation potential of a biodiesel plant Jatropha curcas L. against lindane and discuss the field applicability of Jatropha based remediation techniques and future research prospects. Six different experimental approaches were conducted to evaluate the phytoremediation potential of Jatropha under glasshouse conditions. For this, Jatropha plants were grown in garden soil spiked with four increasing concentration of lindane (5, 10, 15 and 20 mg kg(-1)) and harvested after 45, 180 and 300 d. One set of control plants were grown in lindane free soil and another set of spiked soils were kept without Jatropha plants. At every harvesting, plant growth, lindane accumulation in plant parts, residual lindane concentration in soil as well as percentage lindane dissipation from soil were calculated. After 300 d, the accumulation of lindane in Jatropha grown in four simulated soils reached up to 5.42, 10.83, 15.95 and 20.85 mu g g(-1) plant dry matter, respectively. Correspondingly, the residual lindane soil concentrations in the above four treatments were reduced to 89, 82, 77 and 72% with respect to the applied lindane amounts, respectively. We conclude that Jatropha enhances the dissipation of lindane in simulated soil and is useful for onsite remediation. (C) 2013 Elsevier Ltd. All rights reserved.

Soils are faced with man-made chemical stress factors, such as the input of organic or metal-containing pesticides, in combination with non-chemical stressors like soil compaction and natural disturbance like drought. Although multiple stress factors are typically co-occurring in soil ecosystems, research in soil sciences on this aspect is limited and focuses mostly on single structural or functional endpoints. A mechanistic understanding of the reaction of soils to multiple stressors is currently lacking. Based on a review of resilience theory, we introduce a new concept for research on the ability of polluted soil (xenobiotics or other chemical pollutants as one stressor) to resist further natural or anthropogenic stress and to retain its functions and structure. There is strong indication that pollution as a primary stressor will change the system reaction of soil, i.e., its resilience, stability and resistance. It can be expected that pollution affects the physiological adaption of organisms and the functional redundancy of the soil to further stress. We hypothesize that the recovery of organisms and chemical-physical properties after impact of a follow-up stressor is faster in polluted soil than in non-polluted soil, i.e., polluted soil has a higher dynamical stability (dynamical stability=1/recovery time), whereas resilience of the contaminated soil is lower compared to that of not or less contaminated soil. Thus, a polluted soil might be more prone to change into another system regime after occurrence of further stress. We highlight this issue by compiling the literature exemplarily for the effects of Cu contamination and compaction on soil functions and structure. We propose to intensify research on effects of combined stresses involving a multidisciplinary team of experts and provide suggestions for corresponding experiments. Our concept offers thus a framework for system level analysis of soils paving the way to enhance ecological theory.

The demand for biofuels increases due to concerns regarding greenhouse gas emissions and depletion of fossil oil reserves. Many substances identified as potential biofuels are solvents or already used as flavors or fragrances. Although humans and the environment may be readily exposed little is known regarding their (eco)toxicological effects. In this study, the three potential biofuels ethyl levulinate (EL), 2-methyltetrahydrofuran (2-MTHF) and 2-methylfuran (2-MF) were investigated for their acute embryo toxicity and teratogenicity using the fish embryo toxicity (FET) test to identify unknown hazard potentials and to allow focusing further research on substances with low toxic potentials. In addition, two fossil fuels (diesel and gasoline) and an established biofuel (rapeseed oil methyl ester) were investigated as references. The FET test is widely accepted and used in (eco)toxicology. It was performed using the zebrafish Danio rerio, a model organism useful for the prediction of human teratogenicity. Testing revealed a higher acute toxicity for EL (LC50: 83mg/L) compared to 2-MTHF (LC50: 2980mg/L), 2-MF (LC50: 405mg/L) and water accommodated fractions of the reference fuels including gasoline (LC50: 244mg DOC/L). In addition, EL caused a statistically significant effect on head development resulting in elevated head lengths in zebrafish embryos. Results for EL reduce its likelihood of use as a biofuel since other substances with a lower toxic potential are available. The FET test applied at an early stage of development might be a useful tool to avoid further time and money requiring steps regarding research on unfavorable biofuels.

The nature of the abiotic birnessite (δ-MnO(2))-catalyzed transformation products of phenolic compounds in the presence of soil organic matter is crucial for understanding the fate and stability of ubiquitous phenolic carbon in the environment. (14)C-radioactive and (13)C-stable-isotope tracers were used to study the mineralization and transformation by δ-MnO(2) of two typical humus and lignin phenolic monomers--catechol and p-coumaric acid--in the presence and absence of agricultural and forest soil humic acids (HAs) at pH 5-8. Mineralization decreased with increasing solution pH, and catechol was markedly more mineralized than p-coumaric acid. In the presence of HAs, the mineralization was strongly reduced, and considerable amounts of phenolic residues were bound to the HAs, independent of the solution pH. The HA-bound residues were homogeneously distributed within the humic molecules, and most still contained the unchanged aromatic ring as revealed by (13)C NMR analysis, indicating that the residues were probably bound via ester or ether bonds. The study provides important information on δ-MnO(2) stimulation of phenolic carbon binding to humic substances and the molecular distribution and chemical structure of the bound residues, which is essential for understanding the environmental fates of both naturally occurring and anthropogenic phenolic compounds.

Modern societies depend on environmental sustainability and on new generations of individuals well-trained by environmental research and teaching institutions. In the past, significant contributions to the identification, assessment, and management of chemical stressors with legal consequences have been made.Within this article, we intend to elucidate the merits and the emerging challenges of chemicals-related environmental sciences. The manuscript is supported by more than 70 professors and university academics of leading institutions in Germany, Switzerland, Austria, and other countries in Europe, but addresses topics of global concern.Many environmental problems of pollutants remain to be addresses, since new chemical compounds or classes of new compounds are continuously developed and brought to the market and sooner or later "emerge" in the environment. Further issues are the inclusion of transformation products and chemical mixtures in environmental risk assessment, the long-term presence of xenobiotics bound to soils and sediments, as well as an understanding of the ecological relevance of ecotoxicological end points.We point out the need for a strong academic research and education system in chemicals-related environmental sciences to ministries, politicians, and research funding institutions and we propose to create specific units in the national funding bodies that address basic and interdisciplinary research in this field.

The long-term behavior of the herbicide atrazine and its metabolites in the environment is of continued interest in terms of risk assessment and soil quality monitoring. Aqueous desorption, detection, and quantification of atrazine and its metabolites from an agriculturally used soil were performed 22 years after the last atrazine application. A lysimeter soil containing long-term aged atrazine for20 years was subdivided into 10 and 5 cm layers (at the lysimeter bottom: soil 0-50 and 50-55 cm; fine gravel 55-60 cm depth, implemented for drainage purposes) to identify the qualitative and quantitative differences of aged (14)C-labeled atrazine residues depending on the soil profile and chemico-physical conditions of the individual soil layers. Deionized water was used for nonexhaustive cold water shaking extraction of the soil. With increasing soil depth, the amount of previously applied (14)C activity decreased significantly from 8.8% to 0.7% at 55-60 cm depth whereas the percentage of desorbed (14)C residues in each soil layer increased from 2% to 6% of the total (14)C activity in the sample. The only metabolite detectable by means of LC-MS/MS was 2-hydroxyatrazine while most of the residual (14)C activity was bound to the soil and was not desorbed. The amount of desorbed 2-hydroxyatrazine decreased with increasing soil depth from 21% to 10% of the total desorbed (14)C residue fraction. The amount of (14)C residues in the soil layers correlated well with the carbon content in the soil and in the aqueous soil extracts ( p value = 0.99 and 0.97, respectively), which may provide evidence of the binding behavior of the aged atrazine residues on soil carbon. The lowest coarse layer (55-60 cm) showed increased residual (14)C activity leading to the assumption that most (14)C residues were leached from the soil column over time.

The production of titanium parts from powder metallurgy is one of the tendencies of modern metallurgy, since it allows obtaining structures with complex geometries and controlled porosity. The purpose of this study was to produce two types of dental implant prototype, and compare them biologically. Smooth surface prototypes were obtained, by the conventional turning process and porous surface prototypes using Metal Injection Molding (MIM). The prototypes were implanted in rats that were euthanized after 3 weeks, and the bone/implant interface was analyzed. The results showed that all prototypes were clinically stable at the end of the healing period, but those produced by the MIM process presented a significantly higher percentage of osseointegration (bone/implant contact) than the milled prototypes in the same healing period. It is concluded that the bone tissue grew independent of type of implant, enabling quick, rigid fixation already in the third week of the healing process.

Natural low molecular weight organic acids (NLMWOA) have been shown to be useful in enhancing phytoextraction without a high leaching probability. Nevertheless, their efficiency has in many cases been unsatisfactory. The objective of this study was to investigate the reason for the inefficiency of three NLMWOAs (citric acid, oxalic acid and tartaric acid) in enhancing phytoextraction. In several experiments attention was directed not only to the biodegradation of the NLMWOAs, but also to the microorganisms involved, and their influence on the bioavailability of Cu. During a time period of 96 h the biodegradation of the NLMWOAs increased the natural pH-value of the soil by approximately 1 unit and decreased the bioavailability of Cu from 175 mg kg−1 to approximately 140 mg kg−1. As microorganisms were detected with polymerase chain reaction sequencing and with the aid of high performance liquid chromatography measurements, it can be deduced that the fungi, Cordyceps sp., Paecilomyces sp. and the bacteria Burkholderia sp. can degrade all three used NLMOWA. A successive application of the three NLMWOAs to increase the efficiency is therefore not feasible, because with each NLMWOA application the number of microorganisms which can degrade the NLMWOAs increases and thus the degradation is accelerated. These results combined with result from previous studies show that the NLMWOAs are unsuitable in enhancing phytoextraction of heavy metals from the soil.

Clay minerals in soils control the sorption and mobility of nitroaromatics in munitions contaminated soils. Therefore, effect of exchangeable cations (NH4+ , K+, Ca2+, and Al3+) on sorption-desorption of trinitrotoluene (TNT) was studied in two reference soils viz sandy loam and silty clay. Compared to control soils, K+ ion saturation significantly increased TNT sorption in both the soils, while other cations decreased TNT sorption. Effect of K+ saturation on sorption of TNT was more pronounced in organic matter poor sandy loam soil (seven times) then silty clay (two times). Desorption followed the reverse trend and greater amounts of sorbed TNT were retained in the K+ saturated soils.

There has been increasing interest in enhancing natural attenuation of munitions-contaminated soils. Present study reports the effect of increasing soil organic matter content on fate and mobility of trinitrotoluene (TNT) and metabolites in soil columns. This study was performed using 30-cm-long columns containing a top 5 cm of contaminated soil as a source layer and an uncontaminated soil (25 cm) adjusted to 0.5, 1.0, 1.5 and 3.0% organic carbon (OC) content using compost. Contaminated soil layer was fortified with uniformly ring-labeled (14)C-trinitrotoluene (TNT) or 2,4-dinitrotoluene (DNT); in total there were 8 treatments. Columns were leached with synthetic rain water under unsaturated flow conditions in downside up direction. There was significant increase in the retention of both (14)C-TNT and (14)C-DNT in soils with increasing soil OC content and in 3.0% soil OC content column1% TNT/DNT was recovered in the leachate. Further, degradation of TNT and metabolites from contaminated soil was significantly increased and resulted in greater soil-bound residues. Formation of monoamino-dinitrotoluene (ADNTs), diamino-mononitrotoluene (DANTs) and monoamino-mononitrotoluene (ANTs) metabolites was greatly enhanced with increase in OC content of soils. Study suggests that increasing OC content of contaminated soil to 3.0% significantly enhanced the reduction of nitroaromatics to more polar amine metabolites and the formation of soil-bound residues.

The low-cost, plant-based phytoextraction technique has often been described as a promising technique to remediate heavy metal contaminated agricultural land. The application of chelating agents has shown positive effects in increasing the solubility of heavy metals in soil and therefore in enhancing phytoextraction. This paper gives an overview of the chelating agents applied in recent studies. Various synthetic aminopolycarboxylic acids, such as ethylene diamine tetraacetic acid, and natural ones such as, ethylene diamine disuccinate and nitrilotriacetic acid, are described. Additionally, results of the application of natural low molecular weight organic acids, such as citric and tartaric acid are given. The effectiveness of these different chelating agents varies according to the plant and the heavy metals used. Furthermore, a focus is laid on the chelating agents fate after application and on its toxicity to plants and soil microorganisms, as well as it degradation. The rate of degradation is of great importance for the future of chelate assisted phytoextraction as it has a direct impact on the leaching probability. An effective prevention of leaching will be crucial for the acceptance and the economic breakthrough of enhanced phytoextraction, but a satisfactory solution to this key issue has so far not been found. Possibly further experiments in the field of enhanced phytoextraction will be able to solve this major problem, but over decades various greenhouse experiments and recently field experiments have resulted in different observations. Therefore, it is questionable if further research in this direction will lead to a promising solution. Phytoextraction has possibly reached a turning point in which it should distance itself from chelate assisted phytoextraction and focus on alternative options.

Phytoextraction, the use of plants to extract contaminants from soils and groundwater, is a promising approach for cleaning up soils contaminated with heavy metals. In order to enhance phytoextraction the use of chelating agents has been proposed. This study aims to assess whether ethylene diamine disuccinate (EDDS), a biodegradable chelator, can be used for enhanced phytoextraction purposed, as an alternative to ethylene diamine tetraacetate (EDTA). EDDS revealed a higher toxicity to tobacco ( Nicotiana tabacum ) in comparison to EDTA, but no toxicity to microorganisms. The uptake of Cu was increased by the addition of EDTA and EDDS, while no increase was observed in the uptake of Cd. Both chelating agents showed a very low root to shoot translocation capability and the translocation factor was lower than the one of the control. Heavy metals where significantly more phytoavailable than in the control, even after harvesting, resulting in a high heavy metal leaching possibility, probably owing to a low biodegradation rate of EDDS. New seedlings which were transplanted into the EDDS treated pots 7 d after the phytoextraction experiment, showed signs of necrosis and chlorosis, which resulted in a significantly lower biomass in comparison to the control. The seedlings on the EDTA treated pots showed no toxicity signs. Contrary to previous opinions the results of this study revealed the chelating agents EDTA and EDDS as unsuitable for enhanced phytoextraction using tobacco.

To develop the extraction media for Cd and Ni from aqueous solutions, magnetic beads containing IDA group with strong attraction to heavy metals were produced using the activating agents Epichlorhydrin (Ep) and 1,4-Butanedioldiglycidylether (Bu), respectively. Then the beads were agitated at a pH of 6 after being added to Cd and Ni aqueous solutions of various concentrations. It was confirmed that the heavy metals combined with the magnetic beads within a short time through the process. After the process, the magnetic beads were collected with a magnet, and then dissolved in acid for the analysis of heavy metal concentration. The analysis of heavy metals in the acid solution could be analyzed with an AAS (atomic absorption spectrometer). The results showed that the heavy metal extraction efficiency of Bu was relatively higher than that of the Ep. It supported the hypothesis that the relatively longer length of Bu’s spacer made more free positioning possible when the IDA group combined with the heavy metal.

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.

It was examined in this study that magnetic beads, which are assumed to be environmentally functional, could be effective in processing heavy metals that are water pollutants. For the purpose, magnetic beads containing carboxyl groups, which has strong binding force with heavy metals, are mixed with each Cd, Pb, Ni, Cu and Cr(III) solution, then stirred in pH 6. As a results of the process, it was proven that heavy metals bind quickly with magnetic beads through the reaction. In order to analyze heavy metal concentration, magnetic beads bind with heavy metal were collected by external magnetic force and dissolved in acid. The graphite furnace AAS was used to get heavy metal concentration melted in the acid solution. The results showed that heavy metal extractions by magnetic beads were influenced by the type and the concentration of a heavy metal, and over 90% of a heavy metal can be extracted in ppm level save for Cr(III). It was also examined in the study whether heavy metal extraction is influenced when other ions exist in each heavy metal solution. According to experiment, adding other heavy metals to a solution did have little influence on extracting an intended heavy metal. But in case salt or heavy metal chelate was added, Ni extraction changed sensitively although extracting other heavy metals were influenced only when the concentration of an added substance is high. In conclusion, it was shown that magnetic beads could be used to treat wastewater with relatively high heavy metal concentration.

Phytoremediation, the use of plants to extract contaminants from soils and groundwater, is a promising approach for cleaning up soils contaminated with heavy metals. However its use is limited by the time required for plant growth, the nutrient supply and, moreover, by the limited metal uptake capacity. Synthetic chelators have shown positive effects in enhancing heavy metal extraction, but they have also revealed several negative side-effects. The objective of this study was to investigate the use of three natural low molecular weight organic acids (NLMWOA) (citric, oxalic, and tartaric acid) as an alternative to synthetic chelators. Slurry-, column-, toxicity- and phytoextraction experiments were performed. For the phytoextraction experiment the three NLMWOA were applied to a copper- and a lead-contaminated soil respectively. A significant increase in copper uptake was visible only in the citric acid treatment (67 mg kg-1) in comparison to the EDTA treatment (42 mg kg-1). The NLMWOA application showed no enhanced effect concerning the lead phytoextraction. A possible explanation for this lack of significance could be the rate of the degradation of NLMWOA. This rate might well be too high for these heavy metals with low mobility and bioavailability such as lead. The amounts of NLMWOA applied to the soil were very high (62.5 mmol kg-1 of soil) and the effect was too little. In this respect EDTA, which was applied in very small amounts (0.125 mmol kg-1) was more efficient. Thus making NLMWOA unsuitable to enhance phytoextraction of heavy metals from soil.

The analytic possibility of mobile lead contained in soil has been studied using carboxylated magnetic beads. Extraction of heavy metal was performed to contaminated soil that has been collected and supplied for tests. As experiment materials, soil sample, distilled water and magnetic beads were only used. It means that the lead was extracted under neutral condition. In this condition, only the mobile fraction of lead could be extracted by magnetic beads. The mobile lead in the soil was quickly combined with magnetic beads in the mixture process. Then, the magnetic beads were dissolved into acids after collection by external magnetic force, and the lead combined with the beads was eluted and analyzed by Graphite Furnace Atomic Absorption Spectroscopy (GFAAS). In the results of extraction experiments for 3 sandy soils, the efficiency using beads was similar to or higher than that of EDTA (Ethylendiamintetraacetic acid), which is normally used for analyzing mobile heavy metal concentration in soil. With this, it was shown that this method is a more accurate and simple method to analyze mobile lead when analyzing mobile heavy metal concentration in sandy soil, rather than conventional method using EDTA.

14C-labelled simazine was composted together with biowaste on a pilot (m3) scale. The herbicide was quickly bound to the compost matrix. By aqueous extraction of 29 and 200 days old compost (equivalent to thermophilic and mesophilic phase of composting) only 4.2% and 3.1% respectively of the radioactivity in the compost samples could be extracted with water. Analysis of the extracts using high-performance size exclusion chromatography (HPSEC) revealed that the dissolved organic matter (DOM) had molecular weights ranging between 2 and 28 kDa. The amount of DOM-associated radioactivity increased from 53% (day 29) to 65% (day 200) of total extractable radioactivity. The type of binding of the 14C-labelled residues and the DOM was elucidated by silylation of humic matter and subsequent HPSEC. The data demonstrated that besides polar metabolites also intact simazine was bound to the DOM. A distinct shift from rather weak interactions to strong covalent linkages of simazine and its metabolites with increasing age of the compost was observed. The results showed that only low amounts of free simazine and its degradates can be extracted with water. We concluded that the shift towards stable covalent linkages is equivalent to a detoxification of the contaminant in aged compost. Consequently, the use of the analysed compost in its mature stage should not pose an environmental risk to the groundwater or the subsoil.

Bioconcentration and transformation of the potent and persistent xeno-estrogen 17α-ethinylestradiol (EE2) by organisms at the basis of the food web have received only little research attention. In this study, uptake, elimination, and biotransformation of radiolabeled EE2 ((14)C-EE2) by the freshwater green alga Desmodesmus subspicatus were investigated. The alga highly incorporated radioactivity following (14)C-EE2 exposure. Up to 68% of the test compound was removed from the medium by D. subspicatus within a rather short time period (72 h C(algae)/C(water): 2200 L/kg wet weight). When the algae were transported to clear medium, a two-stage release pattern was observed with an initially quick elimination phase following slower clearance afterward. Interestingly, D. subspicatus brominated EE2 when bromide was available in the medium, a transformation process demonstrated to occur abiotically but not by algae. The consequence of the presence of more hydrophobic mono- and dibrominated EE2 in the environment remains to be further investigated, as these products were shown to have a lower estrogenic potency but are expected to have a higher bioaccumulation potential and to be more toxic than the mother compound.

Increased use of nanomaterials in everyday products leads to their environmental release and therefore, the information need on their fate and behaviour. Nanomaterials have to be suspended with high repeatability and comparability for studies on environmental effects. They also have to be well characterised with a focus on the state of agglomeration and particle size distribution. Dynamic light-scattering (DLS) is a common technique used for these measurements. If suspensions are prepared in different laboratories, then concern has risen about the comparability of the measured results, especially when different DLS instruments are used. Therefore, for quality assurance, a round-robin test was conducted to assess the comparability of different DLS instruments and a dispersion protocol in ten independent laboratories. Polystyrene and TiO2 were chosen as test (nano)materials. For the comparability of the DLS instruments, the average sizes of the PSL and a stabilised TiO2 suspension were measured. The measured average hydrodynamic diameter shows an overall good inter-laboratory comparability. For the PSL suspension, an average hydrodynamic diameter of 201 ± 13 nm and for the TiO2 suspension an average diameter of 224 ± 24 nm were detected. For the TiO2 suspension that was prepared at each laboratory following an established suspension preparation protocol, an average hydrodynamic diameter of 211 ± 11 nm was detected. The measured average particle size (mode) increased up to 284 nm with a high standard deviation of 119 nm if the preparation protocol could not established and different procedures or different equipment were employed. This study shows that no significant differences between the employed DLS instrument types were determined. It was also shown that comparable measurements and suspension preparation could be achieved if well-defined suspension preparation protocols and comparable equipment can be used.

The fate assessment of nanomaterials in municipal sewage treatment plants (STP) is a crucial step for their environmental risk assessment and may be assessed by monitoring full scale STP, dosage to medium scale pilot STP or by laboratory testing. For regulatory purposes preferably standardised test protocols such as the OECD guidelines for testing of chemicals should be used. However, these test protocols have not yet been specifically designed for nanoparticles. Therefore, the fate and behavior of a TiO2 nanomaterial (P25, average hydrodynamic diameter250 nm) was investigated in laboratory sewage treatment plants according to the OECD Guideline for the Testing of Chemicals 303 A. It is concluded that this guideline is applicable for the testing of nanomaterials if modifications regarding the dosage, nitrifying conditions, and a characterisation of the nanoparticles in the effluent are applied. A compilation of the cumulative mass balance by comparison of the total dosage added with the amount in the outflow and in the activated sludge is recommended. In this study, the majority of the TiO2 nanomaterial (95%) was retained in the sewage sludge and only 3-4% was found in the effluent. No effect of the TiO2 nanomaterials on the biodegradation or nitrification was observed.

The sorption of organic contaminants in soil is mainly attributed to the soil organic matter (SOM) content. However, recent studies have highlighted the fact that it is not the total carbon content of the organic matter, but its chemical structure which have a profound effect on the sorption of organic contaminants. In the present study sorption of two nitroaromatic contaminants viz. trinitrotoluene (TNT) and 2,4-dinitrotoluene (2,4-DNT) was studied in different SOM fractions viz. a commercial humic acid, commercial lignin and humic acid and humin extracted from a compost. 13C-DP/MAS NMR studies indicated that the structural composition of the organic carbon in different SOM fractions was different. The order of sorption of the nitroaromatics in the different sorbents was: humic acid-commercial > humic acidcompost > humin about lignin. Among the aliphatic and aromatic carbon fractions (representing bulk of SOM matrix), adsorption parameter Kf(1/n) for nitroaromatics sorption correlated well with the aliphatic carbon (r = 0.791 for TNT and 0.829 for 2,4-DNT) than the aromatic carbon (r = 0.634 for TNT and r = 0.616 for 2,4-DNT). However, among carbon containing functional groups, carbonyl carbon showed strong positive correlation with sorption of TNT (r = 0.991) and 2,4-DNT (r = 0.967) while O-alkyl carbon showed negative correlation (r = 0.832 for TNT and r = 0.828 for 2,4-DNT). The study indicates that aliphatic domains in the SOM significantly affect the non-specific sorption of both the nitroaromatic contaminants.

After 22 years of aging under natural conditions in an outdoor lysimeter the bioaccessibility of C-14-labeled atrazine soil residues to bacteria was tested. Entire soil samples as well as sand-sized, silt-sized, and clay-sized aggregates (> 20, 20-2, and < 2 mu m aggregate size, respectively) were investigated under slurried conditions. The mineralization of residual radioactivity in the outdoor lysimeter soil reached up to 4.5% of the total C-14-activity after 16 days, inoculated with Pseudomonas sp. strain ADP. The control samples without inoculated bacteria showed a mineralization maximum of only about 1% after 44 days of incubation. Mineralization increased in the clay-sized aggregates up to 6.2% of the total residual 14C-activity within 23 days. With decreasing soil aggregate sizes, residual C-14-activity increased per unit of weight, but only minor differences of the mineralization in the soil and soil size aggregates using mineral-media for incubation was observed. Using additional Na-citrate in the incubation,the extent of mineralization increased to 6.7% in soil after 23 days following incubation with Pseudomonas sp. strain ADP. These results show that long-term aged IT-atrazine residues are still partly accessible to the atrazine degrading microorganism Pseudomonas sp. strain ADP.

Phytoextraction has revealed great potential, however it is limited by the fact that plants need time and nutrient supply and have a limited metal uptake capacity. Although the use of synthetic chelators, such as EDTA, enhances heavy metal extraction, it also produces the negative side effects of high phytotoxicity, as well as leaching of essential metals. The aim of this research was to investigate the application of wool, in mobilising metals and in improving the phytoextraction of metals-contaminated soil. We performed column experiments with 14 d and 7 d partially hydrolysed wool as chelating agent on a silty-loamy sand agricultural soil. In the column experiment the 14 d wool hydrolysate mobilised 68% of Cu in soil, whereas in the case of Cd it mobilised 5.5%. The model plant selected for the phytoextraction experiments was tobacco (Nicotiana tabacum). The plant uptake of Cd and Cu, assisted by the application of 6.6 g kg(-1) wool hydrolysate was increased by 30% in comparison to the control plants. The application of 13.3 g kg(-1) wool hydrolysate enhanced the Cu uptake by up to 850%. Moreover, high leaching probability frequently observed when applying chelating agents, such as EDTA or ethylene diamine disuccinate (EDDS), were not detected. The use of hydrolysed wool therefore merits further investigation.

Although cyanide is highly toxic, it is economically attractive for extracting gold from ore bodies containing only a few grams per 1000 kg. Most of the cyanide used in industrial mining is handled without observable devastating consequences, but in informal, small-scale mining, the use is poorly regulated and the waste treatment is insufficient. Cyanide in the effluents from the latter mines could possibly be removed by the water hyacinth Eichhornia crassipes because of its high biomass production, wide distribution, and tolerance to cyanide (CN) and metals. We determined the sodium cyanide phytotoxicity and removal capacity of E . crassipes . Toxicity to 5–50 mg CN L −1 was quantified by measuring the mean relative transpiration over 96 h. At 5 mg CN L −1 , only a slight reduction in transpiration but no morphological changes were observed. The EC 50 value was calculated by probit analysis to be 13 mg CN L −1 . Spectrophotometric analysis indicated that cyanide at 5.8 and 10 mg L −1 was completely eliminated after 23–32 h. Metabolism of K 14 CN was measured in batch systems with leaf and root cuttings. Leaf cuttings removed about 40% of the radioactivity from solution after 28 h and 10% was converted to 14 CO 2 ; root cuttings converted 25% into 14 CO 2 after 48 h but only absorbed 12% in their tissues. The calculated K m of the leaf cuttings was 12 mg CN L −1 , and the V max was 35 mg CN (kg fresh weight) −1 h −1 . Our results indicate that E . crassipes could be useful in treating cyanide effluents from small-scale gold mines.

Use of municipal biowaste for composting instead of its disposal has become a major source of concern as regards contamination by hazardous substances. To elucidate the hazard potential of compost application, municipal biowaste was amended with 14C-labelled model substances (pyrene, simazine) and incubated in a pilot-scale composting simulation system. A mass balance incorporating the mineralization, metabolism and sorption of the two model substances was established over a period of 370 days. The results are quite different for the two chemicals, reflecting their intrinsic properties: more than 60% of the applied 14C-simazine resulted in non-extractable residues (NER). Silylation experiments indicated that the formation of NER from simazine and its metabolites was due to both physical entrapment in the matrix and chemical binding. The mineralization and formation of NER represented the major pathways of disappearance for pyrene during one year of composting, accounting for 60 and 26% of initially applied 14C-activity, respectively. Mineralization occurred delayed after the thermophilic phase. As regards remobilization, release of pyrene from NER during composting could be excluded, whereas simazine, data were inconclusive in this respect.

Proteases in preparations of carboxypeptidase A progressively inactivate solutions of the apoenzyme but not the metal-containing enzyme. Free amino acids generated by proteolysis interfere with spectral studies after reconstituting the apoenzyme with cobalt. Purification by affinity chromatography eliminates this effect. Affinity-purified apoenzyme is susceptible to digestion with chymotrypsin but the metalloenzyme is not.