Improved closed test setup for biodegradation testing of slightly volatile substances in water-sediment systems (OECD 308).

Standardized biodegradation testing methods, like the OECD 308 Aerobic and Anaerobic Transformation in Aquatic Sediment Systems, generate data on biodegradation required during environmental risk and hazard assessment of chemicals under different European and international regulations. However, difficulties arise when applying the OECD 308 guideline for testing hydrophobic volatile chemicals. Especially the use of a co-solvent (like acetone) as a measure to facilitate the application of the test chemical in combination with a closed setup to reduce losses due to volatilization tend to deplete/restrict the amount of oxygen in the test system. The result is a low oxygen or even anoxic water column in the water-sediment system. Thus, the degradation half-lives of the chemical generated from such tests are not directly comparable to the regulatory half-life values for Persistence assessment of the test chemical. The aim of this work was to further develop the closed setup to improve and maintain aerobic conditions in the water phase of the water-sediment systems for testing slightly volatile hydrophobic test chemicals. This improvement was attained by optimizing the test system geometry and agitation technique to maintain aerobic conditions in the water phase in a closed test setup, investigating appropriate co-solvent application strategy, and trialing the resulting test setup. This study shows that when using a closed test setup for OECD 308 tests, agitation of the water phase overlaying the sediment and the test item application using low co-solvent volume is critical for maintaining an aerobic water layer.

Effects of wastewater-spiked nanoparticles of silver and titanium dioxide on survival, growth, reproduction and biochemical markers of Daphnia magna.

Silver (Ag) and titanium dioxide (TiO2) nanoparticles (NPs) are released into aquatic environments through wastewater treatment plants (WWTPs). Even though these NPs are mostly retained in WWTPs, a small fraction can be found in released effluents and may exert toxic effects on aquatic biota. Currently, the available information about the sublethal effects of wastewater-borne NPs on aquatic organisms is inconclusive and the importance of exposure media remains poorly understood. Previously, we demonstrated that rainbow trout juveniles chronically exposed to wastewater-borne AgNPs or TiO2NPs caused no effects on growth, but antioxidative stress mechanisms were triggered in fish organs. Accordingly, this study aimed to: (i) assess the chronic (21-d) effects of wastewater-borne AgNPs (0.3-23.5 µg L-1 Ag) and TiO2NPs (2.7-3.9 µg L-1 Ti) on survival, growth and reproduction of Daphnia magna; (ii) determine the short-term (96-h) effects of wastewater-borne AgNPs (30.3 µg L-1 Ag) and TiO2NPs (6.3 µg L-1 Ti) at the subcellular level (biochemical markers of neurotoxicity, anaerobic metabolism and oxidative stress); and (iii) compare the effects obtained in (i) and (ii) with the corresponding ones induced by effluent-supplemented and water-dispersed NPs. Total Ag and Ti levels were analytically quantified in all treatments. It was demonstrated that both wastewater-borne NPs are considered non-toxic to daphnids at tested concentrations, considering the endpoints at the individual (survival, growth, reproduction) and subcellular (biochemical markers) levels. Contrarily, when pristine forms of NPs were supplemented to effluents or water, concentration-dependent effects were noticed, particularly on cumulative offspring of daphnids. The significant effects on anaerobic metabolism and detoxification pathways caused by the effluent indicate background toxicity. Bearing in mind the achievement of a suitable risk assessment of NPs in aquatic environments, this combined approach looking at both the individual and subcellular levels responses come up with relevant information about the ecotoxicological harmlessness of wastewater-borne NPs in complex environmental matrices like WWTP effluents.

Leaching of Titanium Dioxide Nanomaterials from Agricultural Soil Amended with Sewage Sludge Incineration Ash: Comparison of a Pilot Scale Simulation with Standard Laboratory Column Elution Experiments.

Nanoscale titanium dioxide (nTiO2 (Hombikat UV 100 WP)) was applied to sewage sludge that was incinerated in a large-scale waste treatment plant. The incineration ash produced was applied to soil as fertilizer at a realistic rate of 5% and investigated in pilot plant simulations regarding its leaching behavior for nTiO2. In parallel, the applied soil material was subject to standard column leaching (DIN 19528) in order to test the suitability of the standard to predict the leaching of nanoscale contaminants from treated soil material. Relative to the reference material (similar composition but without nTiO2 application before incineration) the test material had a total TiO2 concentration, increased by a factor of two or 3.8 g/kg, respectively. In contrast, the TiO2 concentration in the respective leachates of the simulation experiment differed by a factor of around 25 (maximum 91.24 mg), indicating that the added nTiO2 might be significantly mobilisable. Nanoparticle specific analysis of the leachates (spICP-MS) confirmed this finding. In the standard column elution experiment the released amount of TiO2 in the percolates between test and reference material differed by a factor of 4 to 6. This was also confirmed for the nTiO2 concentrations in the percolates. Results demonstrate that the standard column leaching, developed and validated for leaching prediction of dissolved contaminants, might be also capable to indicate increased mobility of nTiO2 in soil materials. However, experiments with further soils are needed to verify those findings.

Chronic effects of wastewater-borne silver and titanium dioxide nanoparticles on the rainbow trout (Oncorhynchus mykiss).

Even though nanoparticles (NPs) are mostly removed by wastewater treatment plants, wastewater-borne NPs may show an altered toxicity to aquatic organisms. The main objectives of this work were: i) to assess the chronic (28 days) effects of wastewater-borne NPs of silver (AgNPs, 1.4-36.2 µg L-1) and titanium dioxide (TiO2NPs, 3.1-50.2 µg L-1) at the individual (growth) and biochemical (biomarkers of neurotoxicity, oxidative stress and energy metabolism) levels in rainbow trout Oncorhynchus mykiss; and ii) to compare them with their effluent-supplemented and water-dispersed counterparts. The total Ag and Ti levels were determined in several fish organs. The growth of O. mykiss was not affected by the NPs in any treatment, except a 29% increase at 5.5 µg L-1 of total Ag supplemented to effluents. The Ag level in organs of O. mykiss was significantly higher after exposure to water-dispersed AgNPs than their wastewater-borne or effluent-supplemented counterparts. No significant Ti uptake could be observed. Effluent-supplemented TiO2NPs (50.1 µg L-1 Ti) potentially induced neurotoxic effects, indicated by a 24% increase in acetylcholinesterase activity comparatively to controls. Energy reserves were unaffected by TiO2 treatments, while nearly all AgNP-containing treatments caused a depletion of total lipids, proteins and carbohydrates in the muscle, suggesting an increased energy demand for detoxification processes to cope with AgNPs. Besides NPs, the effluent matrix and dispersing agent (for AgNPs) induced significant effects on energetic reserves and oxidative stress, indicating background toxicity of both treatments at the biochemical level. Our study is the first to assess chronic effects of wastewater-borne NPs on rainbow trout. While no effects were found at the individual level, several biochemical markers were changed by the NPs exposure. Our results highlight the importance of using complex matrices for a reliable risk assessment of NPs in the aquatic environment.

Biodegradation testing of volatile hydrophobic chemicals in water-sediment systems - Experimental developments and challenges.

Degradation data are crucial for the persistence assessment of chemicals and they are generated using standard OECD guidelines. The OECD 308 describes a simulation biodegradation test of chemicals in water-sediment systems. This guideline is not applicable for testing highly volatile chemicals and recommends a closed biometer test setup for testing slightly volatile chemicals. However, proper details on system geometries, construction and monitoring of aerobic conditions are not provided. The choice of system geometry and sediment:water ratio influences the partitioning of test chemicals between different compartments (water, sediment and headspace) and can therefore affect their degradation. The guideline recommends the addition of test chemical via aqueous solutions, which however is not possible for hydrophobic volatile chemicals due to their volatilization losses and low solubility. Thus, the use of a co-solvent is necessary for the application of such chemicals but its effects in a closed setup has not been studied. We recently developed an improved closed test setup for testing volatile chemicals in soil. The objective was to adapt this improved test setup to conduct OECD 308 tests using 14C labelled chemicals with different volatilities. Using the adapted test setup it was possible to obtain a complete mass balance even for n-decane and tetralin having the highest Henry's constants of the tested chemicals. However, the use of co-solvent affected the oxygen levels, which in turn affected microbial activity and likely also the degradation of test chemicals. Therefore, the adapted test setup needs further developments for the testing of volatile hydrophobic chemicals.

Biodegradation of Volatile Chemicals in Soil: Separating Volatilization and Degradation in an Improved Test Setup (OECD 307).

During environmental risk assessments of chemicals, higher-tier biodegradation tests in soil, sediment, and surface-water systems are required using OECD standards 307, 308, and 309 guidelines, respectively. These guidelines are not suitable for testing highly volatile chemicals, and a biometer closed-incubation setup is recommended for testing slightly volatile chemicals. In this setup, the degradation kinetics of highly volatile chemicals can largely be influenced by volatilization. Additionally, guidelines lack sufficient information on test-system geometry and guidance on how to measure and maintain aerobic conditions during the test. Our objectives were (1) to design a closed test setup for biodegradation tests in soil in which the maintaining and measuring of aerobic conditions was possible without the loss of volatile test chemicals and (2) to suggest data-treatment measures for evaluating the degradation kinetics of volatile test chemicals. With the new setup, full-scale OECD 307 tests were performed using the volatile 14C-labeled chemicals decane and tetralin. For both test chemicals, reproducible complete mass balances were observed, and the new setup ensured that the volatilization losses were kept below the mineralized fraction. Based on the obtained data, an extended model was developed that enabled consideration of the volatilization in the modeling of degradation kinetics.

Silver nanoparticles in sewage treatment plant effluents: chronic effects and accumulation of silver in the freshwater amphipod Hyalella azteca.

BACKGROUND: Increasing amounts of engineered nanoparticles (NPs) in wastewater can reach the aquatic environment by passing through the sewage treatment plant (STP). NPs can induce ecotoxicological effects due to their specific chemical properties. However, their bioavailability and toxicity are potentially influenced by transformation processes caused by substances present in the STP, e.g., humic acids or sulfides. Due to the lack of a test system allowing to test NPs under realistic environmental conditions, we coupled two existing test systems, the activated sludge simulation test (OECD TG 303A 2001) and the chronic exposure test with the freshwater amphipod Hyalella azteca (Environment Canada 2013), to gain a test scenario that allows to consider the altered behavior and fate of NPs induced by the STP process. This should improve the environmental realism of the chronic exposure test with Hyalella. In the first study, we tested the STP effluent containing AgNPs. In the second and third study, tap water and control STP effluent were spiked with AgNPs and used as test media. RESULTS: The chronic exposure studies with the freshwater amphipod H. azteca showed that the investigated AgNPs lose most of their toxicity while passing through the STP. Over all studies with total Ag concentrations ranging from 0.85 to 68.70 µg/L, significant effects of the AgNPs were only observed in the survival of test animals exposed to tap water containing the highest Ag concentration (62.59 µg/L). Accumulation of silver in the body of test animals was clearly dependent on the pretreatment of the AgNPs. Silver ions (Ag+) released from AgNPs are supposed to be the major pathway leading to body burden following exposure to test media containing AgNPs. CONCLUSION: The coupled test system is suitable for testing substances that can reach the environment via the STP effluent. The investigated AgNPs lose most of their toxicity while passing through the STP. Accumulation of silver in the animals exposed to the different treatments was apparent, whereby silver ions (Ag+) released from AgNPs were supposed to be the major pathway leading to body burden.

Silver and gold nanoparticle separation using asymmetrical flow-field flow fractionation: Influence of run conditions and of particle and membrane charges.

Flow-Field Flow Fractionation (Flow-FFF), coupled with online detection systems is one of the most promising tools available for the separation and quantification of engineered nanoparticles (ENPs) in complex matrices. To correctly relate the retention of nanoparticles in the Flow-FFF-channel to the particle size, ideal separation conditions must be met. This requires optimization of the parameters that influence the separation behavior. The aim of this study was therefore to systematically investigate and evaluate the influence of parameters such as the carrier liquid, the cross flow, and the membrane material, on the separation behavior of two metallic ENPs. For this purpose the retention, recovery, and separation efficiency of sterically stabilized silver nanoparticles (AgNPs) and electrostatically stabilized gold nanoparticles (AuNPs), which represent two materials widely used in investigations on environmental fate and ecotoxicology, were investigated against a parameter matrix of three different cross-flow densities, four representative carrier solutions, and two membrane materials. The use of a complex mixture of buffers, ionic and non-ionic surfactants (FL-70 solution) together with a medium cross-flow density provided an acceptable compromise in peak quality and recovery for both types of ENPs. However, these separation conditions do not represent a perfect match for both particle types at the same time (maximized recovery at maximized retention). It could be shown that the behavior of particles within Flow-FFF channels cannot be predicted or explained purely in terms of electrostatic interactions. Particles were irreversibly lost under conditions where the measured zeta potentials suggested that there should have been sufficient electrostatic repulsion to ensure stabilization of the particles in the Flow-FFF channel resulting in good recoveries. The wide variations that we observed in ENP behavior under different conditions, together with the different behavior that has been reported in published literature for the same NPs under similar conditions, indicate a need for improvement in the membrane materials used for Flow-FFF analysis of NPs. This research has shown that careful adjustment of separation conditions can result in acceptable, but not ideal, separation conditions for two fundamentally different stabilized materials, and that it may not be possible to separate a set of different particles under ideal conditions for each particle type. This therefore needs to be taking into account in method development and when interpreting FFF results from complex samples.

Asymmetrical Flow-Field-Flow Fractionation coupled with inductively coupled plasma mass spectrometry for the analysis of gold nanoparticles in the presence of natural nanoparticles.

Flow-Field-Flow Fractionation (Flow-FFF), coupled with online detection systems, is one of the most promising tools available for the analysis and characterization of engineered nanoparticles (ENPs) in complex matrices. In order to demonstrate the applicability of Flow-FFF for the detection, quantification, and characterization of engineered gold nanoparticles (AuNPs), model dispersions were prepared containing AuNPs with diameters of 30 or 100nm, natural nanoparticles (NNPs) extracted from a soil sample, and different concentrations of natural organic matter (NOM), which were then used to investigate interactions between the AuNPs and the NNPs. It could be shown that light scattering detection can be used to evaluate the fractionation performance of the pure NNPs, but not the fractionation performance of the mixed samples that also contained AuNPs because of specific interactions between the AuNPs and the laser light. A combination of detectors (i.e. light absorbance and inductively coupled plasma mass spectrometry (ICP-MS)) was found to be useful for differentiating between heteroaggregation and homoaggregation of the nanoparticles (NPs). The addition of NOM to samples containing 30nm AuNPs stabilized the AuNPs without affecting the NP size distribution. However, fractograms for samples with no added NOM showed a change in the size distribution, suggesting interactions between the AuNPs and NNPs. This interpretation was supported by unchanged light absorption wavelengths for the AuNPs. In contrast, results for samples containing 100nm AuNPs were inconclusive with respect to recovery and size distributions because of problems with the separation system that probably related to the size and high density of these nanoparticles, highlighting the need for extensive method optimization strategies, even for nanoparticles of the same material but different sizes.