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A significant number of chemicals registered in national and regional chemical inventories require assessments of their potential "hazard" concerns posed to humans and ecological receptors. This warrants knowledge of their partitioning and reactivity properties, which are often predicted by quantitative structure-property relationships (QSPRs) and other semiempirical relationships. It is imperative to evaluate the applicability domain (AD) of these tools to ensure their suitability for assessment purpose. Here, we investigate the extent to which the ADs of commonly used QSPRs and semiempirical relationships cover seven partitioning and reactivity properties of a chemical "space" comprising 81,000+ organic chemicals registered in regulatory and academic chemical inventories. Our findings show that around or more than half of the chemicals studied are covered by at least one of the commonly used QSPRs. The investigated QSPRs demonstrate adequate AD coverage for organochlorides and organobromines but limited AD coverage for chemicals containing fluorine and phosphorus. These QSPRs exhibit limited AD coverage for atmospheric reactivity, biodegradation, and octanol-air partitioning, particularly for ionizable organic chemicals compared to nonionizable ones, challenging assessments of environmental persistence, bioaccumulation capability, and long-range transport potential. We also find that a predictive tool's AD coverage of chemicals depends on how the AD is defined, for example, by the distance of a predicted chemical from the centroid of the training chemicals or by the presence or absence of structural features.
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The Quantitative Structure Use Relationship (QSUR) Summit, held on November 2-4, 2022, focused on advancing the development, refinement, and use of QSURs to support chemical substance prioritization and risk assessment and mitigation. QSURs utilize chemical structures to predict the function of a chemical within a formulated product or an industrial process. This presumed function can then be used to develop chemical use categories or other information necessary to refine exposure assessments. The invited expert meeting was attended by 38 scientists from Canada, Finland, France, the UK, and the USA, representing government, business, and academia, with expertise in exposure science, chemical engineering, risk assessment, formulation chemistry, and machine learning. Workshop discussions emphasized the importance of collection and sharing of data and quantification of relative chemical quantities to progress QSUR development. Participants proposed collaborative approaches to address key challenges, including mechanisms for aggregating information while still protecting proprietary product composition and other confidential business information. Discussions also led to proposals for applications beyond exposure and risk modeling, including sustainable formulation discovery. In addition, discussions continue to construct, conduct, and circulate case studies tied to various specific problem formulations in which QSURs supply or derive information on chemical functions, concentrations, and exposures.
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Medição de Risco , Humanos , França , CanadáRESUMO
PURPOSE: Reducing chemical pressure on human and environmental health is an integral part of the global sustainability agenda. Guidelines for deriving globally applicable, life cycle based indicators are required to consistently quantify toxicity impacts from chemical emissions as well as from chemicals in consumer products. In response, we elaborate the methodological framework and present recommendations for advancing near-field/far-field exposure and toxicity characterization, and for implementing these recommendations in the scientific consensus model USEtox. METHODS: An expert taskforce was convened by the Life Cycle Initiative hosted by UN Environment to expand existing guidance for evaluating human toxicity impacts from exposure to chemical substances. This taskforce evaluated advances since the original release of USEtox. Based on these advances, the taskforce identified two major aspects that required refinement, namely integrating near-field and far-field exposure and improving human dose-response modeling. Dedicated efforts have led to a set of recommendations to address these aspects in an update of USEtox, while ensuring consistency with the boundary conditions for characterizing life cycle toxicity impacts and being aligned with recommendations from agencies that regulate chemical exposure. The proposed framework was finally tested in an illustrative rice production and consumption case study. RESULTS AND DISCUSSION: On the exposure side, a matrix system is proposed and recommended to integrate far-field exposure from environmental emissions with near-field exposure from chemicals in various consumer product types. Consumer exposure is addressed via submodels for each product type to account for product characteristics and exposure settings. Case study results illustrate that product-use related exposure dominates overall life cycle exposure. On the effect side, a probabilistic dose-response approach combined with a decision tree for identifying reliable points of departure is proposed for non-cancer effects, following recent guidance from the World Health Organization. This approach allows for explicitly considering both uncertainty and human variability in effect factors. Factors reflecting disease severity are proposed to distinguish cancer from non-cancer effects, and within the latter discriminate reproductive/developmental and other non-cancer effects. All proposed aspects have been consistently implemented into the original USEtox framework. CONCLUSIONS: The recommended methodological advancements address several key limitations in earlier approaches. Next steps are to test the new characterization framework in additional case studies and to close remaining research gaps. Our framework is applicable for evaluating chemical emissions and product-related exposure in life cycle assessment, chemical alternatives assessment and chemical substitution, consumer exposure and risk screening, and high-throughput chemical prioritization.
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In the literature, there is widespread consensus that methods in plastic research need improvement. Current limitations in quality assurance and harmonization prevent progress in our understanding of the true effects of microplastic in the environment. Following the recent development of quality assessment methods for studies reporting concentrations in biota and water samples, we propose a method to assess the quality of microplastic effect studies. We reviewed 105 microplastic effect studies with aquatic biota, provided a systematic overview of their characteristics, developed 20 quality criteria in four main criteria categories (particle characterization, experimental design, applicability in risk assessment, and ecological relevance), propose a protocol for future effect studies with particles, and, finally, used all the information to define the weight of evidence with respect to demonstrated effect mechanisms. On average, studies scored 44.6% (range 20-77.5%) of the maximum score. No study scored positively on all criteria, reconfirming the urgent need for better quality assurance. Most urgent recommendations for improvement relate to avoiding and verifying background contamination, and to improving the environmental relevance of exposure conditions. The majority of the studies (86.7%) evaluated on particle characteristics properly, nonetheless it should be underlined that by failing to provide characteristics of the particles, an entire experiment can become irreproducible. Studies addressed environmentally realistic polymer types fairly well; however, there was a mismatch between sizes tested and those targeted when analyzing microplastic in environmental samples. In far too many instances, studies suggest and speculate mechanisms that are poorly supported by the design and reporting of data in the study. This represents a problem for decision-makers and needs to be minimized in future research. In their papers, authors frame 10 effects mechanisms as "suggested", whereas 7 of them are framed as "demonstrated". When accounting for the quality of the studies according to our assessment, three of these mechanisms remained. These are inhibition of food assimilation and/or decreased nutritional value of food, internal physical damage, and external physical damage. We recommend that risk assessment addresses these mechanisms with higher priority.
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Microplásticos , Plásticos , Biota , Monitoramento Ambiental , Medição de RiscoRESUMO
Biodegradability studies for the cationic surfactant cetylpyridinium chloride (CPC) are hampered by inhibitory effects on inoculum at prescribed test concentrations (10-20â¯mgâ¯organic carbon/L). In this study, we used 14C labeled CPC in the 28â¯d Headspace Test (OECD 310) and demonstrated that CPC was readily biodegradable (10->60% mineralization within a 10 day window) at test concentrations 0.006-0.3â¯mg/L with CPC as single substrate. Biodegradation efficiency was comparable over this concentration range. CPC inhibited degradation at 1â¯mg/L and completely suppressed inoculum activity at 3â¯mg/L. In an extensive sorbent modified biodegradation study we evaluated the balance between CPC bioaccessibility and toxicity. A non-inhibitory concentration of 0.1â¯mg/L CPC was readily biodegradable with 83% sorbed to SiO2, while biodegradation was slower when 96% was sorbed. SiO2 mitigated inhibitory effects of 1â¯mg/L CPC, reaching >60% biodegradation within 28â¯d; inhibitory effects were also mitigated by addition of commercial clay powder (illite) but this was primarily reflected by a reduced lag phase. At 10â¯mg/L CPC SiO2 was still able to mitigate inhibitory effects, but bioaccessibility seemed limited as only 20% biodegradation was reached. Illite limited bioaccessibility more strongly and was not able to sustain biodegradation at 10â¯mg/L CPC.
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Anti-Infecciosos Locais/metabolismo , Biodegradação Ambiental , Cetilpiridínio/metabolismo , Minerais , Dióxido de Silício , TensoativosRESUMO
Chemical persistence is a key property for assessing chemical risk and chemical hazard. Current methods for evaluating persistence are based on laboratory tests. The relationship between the laboratory based estimates and persistence in the environment is often unclear, in which case the current methods for evaluating persistence can be questioned. Chemical benchmarking opens new possibilities to measure persistence in the field. In this paper we explore how the benchmarking approach can be applied in both the laboratory and the field to deepen our understanding of chemical persistence in the environment and create a firmer scientific basis for laboratory to field extrapolation of persistence test results.
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Benchmarking , Substâncias Perigosas/toxicidade , Medição de Risco , HumanosRESUMO
The Laurentian Great Lakes represent important and iconic ecosystems. Microplastic pollution has become a major problem among other anthropogenic stressors in these lakes. There is a need for policy development, however, assessing the risks of microplastics is complicated due to the uncertainty and poor quality of the data and incompatibility of exposure and effect data for microplastics with different properties. Here we provide a prospective probabilistic risk assessment for Great Lakes sediments and surface waters that corrects for the misalignment between exposure and effect data, accounts for variability due to sample volume when using trawl samples, for the random spatiotemporal variability of exposure data, for uncertainty in data quality (QA/QC), in the slope of the power law used to rescale the data, and in the HC5 threshold effect concentration obtained from Species Sensitivity Distributions (SSDs). We rank the lakes in order of the increasing likelihood of risks from microplastics, for pelagic and benthic exposures. A lake-wide risk, i.e. where each location exceeds the risk limit, is not found for any of the lakes. However, the probability of a risk from food dilution occurring in parts of the lakes is 13-15% of the benthic exposures in Lakes Erie and Huron, and 8.3-10.3% of the pelagic exposures in Lake Michigan, Lake Huron, Lake Superior, and Lake Erie, and 24% of the pelagic exposures in Lake Ontario. To reduce the identified uncertainties, we recommend that future research focuses on characterizing and quantifying environmentally relevant microplastic (ERMP) over a wider size range (ideally 1-5000 µm) so that probability density functions (PDFs) can be better calibrated for different habitats. Toxicity effect testing should use a similarly wide range of sizes and other ERMP characteristics so that complex data alignments can be minimized and assumptions regarding ecologically relevant dose metrics (ERMs) can be validated.
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Microplásticos , Poluentes Químicos da Água , Lagos , Plásticos , Ecossistema , Estudos Prospectivos , Poluentes Químicos da Água/análise , Monitoramento Ambiental , Probabilidade , Great Lakes RegionRESUMO
Persistent and mobile (PM) chemicals are considered emerging threats to the environment and drinking water because they can be transported over long distances, penetrate natural and artificial barriers, and resist removal by traditional water treatment procedures. Current chemical regulatory frameworks raise concerns over PM chemicals due to their potential to cause high human exposure through drinking water contamination. However, the criteria used to screen and identify these chemicals often rely on hazard properties related to stability and sorption, such as biodegradation half-lives and organic-carbon-normalized sorption coefficients as respective measures of P and M. Here, we conduct a model-based assessment to examine the consistency between hazard-based and exposure-based approaches in assessing PM chemicals, by evaluating whether chemicals identified as highly P and M are consistently associated with high drinking water exposure potential (DWEP). We discover that chemicals with the top DWEPs tend to be PM chemicals, but the reverse is not always true, because DWEPs are also impacted by volatilization for air-distributed chemicals and advective particle-bound transport for particle-bound chemicals. Our findings suggest that the hazard metrics are better suited for de-prioritizing, as opposed to prioritizing, chemicals that are unlikely to result in significant human exposure through drinking water, as unfavorable values of hazard metrics are a necessary but not sufficient condition for a high DWEP. We also find that distinct mechanisms determine the DWEP in different sources of drinking water: Sorption and stability are more influential on the DWEP of chemicals in groundwater and surface water, respectively, whereas both sorption and stability equally impact water undergoing riverbank filtration. Future studies should focus on optimizing the identification of persistent and mobile chemicals to ensure that exposure potential is taken into consideration.
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Concern regarding the human health implications that exposure to nano- and microplastic particles (NMPs) potentially represents is increasing. While there have been several years of research reporting on the ecotoxicological effects of NMPs, human health toxicology studies have only recently emerged. The available human health hazard data are thus limited, with potential concern regarding the relevance and reliability for understanding the potential human health implications. In this study we develop and apply a NMP toxicity screening assessment tool (NMP-TSAT) for evaluating human health effects studies against a suite of quality assurance and quality control (QA/QC) criteria for both in vivo and in vitro studies. A total of 74 studies representing either inhalation or oral exposure pathways were identified and evaluated. Assessment categories include particle characterization, experimental design, and applicability for risk assessment; with critical and non-critical criteria organized to allow screening and prioritization. It is observed that the majority of studies evaluated using the NMP-TSAT have been performed on monodisperse particles, predominately spheres (≈60%), consisting of polystyrene (≈46%). The majority of studies have tested particles < 5 µm, with a minimal particle size of 10 nm and a maximum particle size of about 200 µm. The total assessment score (TAS) possible for in vivo studies is 52, whereas for in vitro studies it is 46, which is based on receiving a maximum score of 2 against 26 and 23 criteria, respectively. The evaluated TAS ranged from between 12 and 44 and 16-34, for in vivo and in vitro studies, respectively. Given the challenges associated with prioritizing studies based on ranking them according to their TAS we propose a Tiered approach, whereby studies are initially screened based on how they score against various critical criteria, which have been defined for their relevance for assessing the hazards and risks for human health. In this instance, studies that score a minimum of '1' against each of the critical criteria, regardless of how they rank according to their TAS, are prioritized as part of a Tier 1 screening and prioritization phase, which would then be followed by an expert evaluation, representing a Tier 2 level of assessment. Using this approach we identify 10 oral ingestion and 2 inhalation studies that score at least 1 against all critical criteria. Lastly, several key observations for strengthening future effects studies are identified, these include a need for the generation and access to standard reference materials representative of human exposure to NMPs for use in toxicity test systems and/or the improved characterization and verification of test particle characteristics, and the adoption of study design guidance, such as recommended by OECD, when conducting either in vivo inhalation or oral ingestion toxicity tests. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s43591-021-00023-x.
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Microplastics have been documented in drinking water, but their effects on human health from ingestion, or the concentrations at which those effects begin to manifest, are not established. Here, we report on the outcome of a virtual expert workshop conducted between October 2020 and October 2021 in which a comprehensive review of mammalian hazard studies was conducted. A key objective of this assessment was to evaluate the feasibility and confidence in deriving a human health-based threshold value to inform development of the State of California's monitoring and management strategy for microplastics in drinking water. A tiered approach was adopted to evaluate the quality and reliability of studies identified from a review of the peer-reviewed scientific literature. A total of 41 in vitro and 31 in vivo studies using mammals were identified and subjected to a Tier 1 screening and prioritization exercise, which was based on an evaluation of how each of the studies addressed various quality criteria. Prioritized studies were identified largely based on their application and reporting of dose-response relationships. Given that methods for extrapolating between in vitro and in vivo systems are currently lacking, only oral exposure in vivo studies were identified as fit-for-purpose within the context of this workshop. Twelve mammalian toxicity studies were prioritized and subjected to a Tier 2 qualitative evaluation by external experts. Of the 12 studies, 7 report adverse effects on male and female reproductive systems, while 5 reported effects on various other physiological endpoints. It is notable that the majority of studies (83%) subjected to Tier 2 evaluation report results from exposure to a single polymer type (polystyrene spheres), representing a size range of 0.040 to 20 µm. No single study met all desired quality criteria, but collectively toxicological effects with respect to biomarkers of inflammation and oxidative stress represented a consistent trend. While it was possible to derive a conservative screening level to inform monitoring activities, it was not possible to extrapolate a human-health-based threshold value for microplastics, which is largely due to concerns regarding the relative quality and reliability of current data, but also due to the inability to extrapolate data from studies using monodisperse plastic particles, such as polystyrene spheres to an environmentally relevant exposure of microplastics. Nevertheless, a conservative screening level value was used to estimate a volume of drinking water (1000 L) that could be used to support monitoring activities and improve our overall understanding of exposure in California's drinking water. In order to increase confidence in our ability to derive a human-health-based threshold value in the future, several research recommendations are provided, with an emphasis towards strengthening how toxicity studies should be conducted in the future and an improved understanding of human exposure to microplastics, insights critically important to better inform future risk assessments. Supplementary Information: The online version contains supplementary material available at 10.1186/s43591-022-00030-6.
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The environmental distribution and fate of microplastic in the marine environment represents a potential cause of concern. One aspect is the influence that microplastic may have on enhancing the transport and bioavailability of persistent, bioaccumulative, and toxic substances (PBT). In this study we assess these potential risks using a thermodynamic approach, aiming to prioritize the physicochemical properties of chemicals that are most likely absorbed by microplastic and therefore ingested by biota. Using a multimedia modeling approach, we define a chemical space aimed at improving our understanding of how chemicals partition in the marine environment with varying volume ratios of air/water/organic carbon/polyethylene, where polyethylene represents a main group of microplastic. Results suggest that chemicals with log KOW > 5 have the potential to partition >1% to polyethylene. Food-web model results suggest that reductions in body burden concentrations for nonpolar organic chemicals are likely to occur for chemicals with log KOW between 5.5 and 6.5. Thus the relative importance of microplastic as a vector of PBT substances to biological organisms is likely of limited importance, relative to other exposure pathways. Nevertheless, a number of data-gaps are identified, largely associated with improving our understanding of the physical fate of microplastic in the environment.
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Modelos Teóricos , Nanoestruturas/química , Compostos Orgânicos/química , Plásticos/química , Absorção , Exposição Ambiental , Cadeia Alimentar , Água do Mar , TermodinâmicaRESUMO
As part of the Global Atmospheric Passive Sampling (GAPS) study, XAD-resin based passive samplers are being deployed for consecutive one-year periods at numerous sites on all seven continents to determine annually averaged concentrations of persistent organic pollutants. Concentrations of banned organochlorine pesticides as well as a number of current-use pesticides in samples from the first four years, roughly coinciding with 2005, 2006, 2007 and 2008, show distinct spatial and temporal patterns. Whereas organochlorine pesticides such as alpha- and gamma-hexachlorocyclohexane, endosulfans, DDT and its metabolites, and chlordane-related compounds tend to be more prevalent in developing countries, especially in Asia, concentrations of current use pesticides such as trifluralin and chlorothalonil are often higher in Europe and North America. Based on 15 stations with four years of data, levels of hexachlorobenzene, hexachlorocyclohexanes and chlordanes decline in most world regions, which may reflect decreased usage in response to global restrictions. Levels of organochlorine pesticides in India, however, remain exceptionally high. Concentrations of alpha-endosulfan, chlorothalonil and trifluralin decrease in the European atmosphere during the sampling periods, indicating reduced usage. Consistently high alpha/gamma-HCH ratios in air samples from high Northern latitudes confirm that re-volatilization from the Arctic Ocean is a significant source of alpha-HCH. The highest levels of alpha-HCH, however, occur in conjunction with high gamma-HCH levels, suggesting that lindane use is now the major source of alpha-HCH to the global atmosphere. Although a wide variety of sampling site types aids in characterizing the entire global concentration variability of a pesticide, it also increases greatly the number of sites required for a robust regional differentiation.
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Poluentes Atmosféricos/análise , Atmosfera/química , Monitoramento Ambiental/métodos , Praguicidas/análise , Clordano/análise , Endossulfano/análise , Hexaclorobenzeno/análise , Hexaclorocicloexano/análiseRESUMO
Microplastic particles have been observed in the environment and routinely detected in the stomachs and intestines of aquatic organisms over the last 50 yr. In the present review, information on the ingestion of plastic debris of varying sizes is collated, including data for >800 species representing approximately 87 000 individual organisms, for which plastic debris and microplastic particles have been observed in approximately 17 500, or 20%. The average reported number of microplastic particles/individual across all studies is estimated to be 4, with studies typically reporting averages ranging from 0 to 10 particles/individual. A general observation is that although strong evidence exists for the biological ingestion of microplastic particles, they do not bioaccumulate and do not appear to be subject to biomagnification as a result of trophic transfer through food webs, with >99% of observations from field-based studies reporting that microplastic particles are located within the gastrointestinal tract. Overall, there is substantial heterogeneity in how samples are collected, processed, analyzed, and reported, causing significant challenges in attempting to assess temporal and spatial trends or helping to inform a mechanistic understanding. Nevertheless, several studies suggest that the characteristics of microplastic particles ingested by organisms are generally representative of plastic debris in the vicinity where individuals are collected. Monitoring of spatial and temporal trends of ingested microplastic particles could thus potentially be useful in assessing mitigation efforts aimed at reducing the emission of plastic and microplastic particles to the environment. The development and application of standardized analytical methods are urgently needed to better understand spatial and temporal trends. Environ Toxicol Chem 2020;39:1119-1137. © 2020 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.
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Organismos Aquáticos/metabolismo , Monitoramento Ambiental/métodos , Microplásticos/metabolismo , Poluentes Químicos da Água/metabolismo , Animais , Bioacumulação , Ingestão de Alimentos , Cadeia Alimentar , Microplásticos/análise , Poluentes Químicos da Água/análiseRESUMO
The cationic surfactants cetyltrimethylammonium bromide (CTAB) and cetylpyridinium chloride (CPC) can exert inhibitory effects on micro-organisms responsible for their biodegradation. However, under environmentally relevant exposure scenarios the presence of and sorption to organic and inorganic matter can lead to significant reduction of inhibitory effects. In our studies we investigated silica gel and seven clays as inert sorbents to mitigate these inhibitory effects in a 28 day manometric respirometry biodegradation test. CTAB was not inhibitory to the used inoculum, but we did observe that seven out of eight sorbents increased maximum attainable biodegradation, and four out of eight decreased the lag phase. The strongly inhibitory effect of CPC was successfully mitigated by most sorbents, with five out of eight allowing >50% biodegradation within 28 days. Results further indicate that bioaccessibility of the sorbed fractions in the stirred manometric test systems was higher than in calmly shaken headspace test systems. Bioaccessibility might also be limited depending on characteristics of test chemical and sorbent type, with montmorillonite and bentonite apparently providing the lowest level of bioaccessibility with CPC. Clay sorbents can thus be used as environmentally relevant sorbents to mitigate potential inhibitory effects of test chemicals, but factors that impede bioaccessibility should be considered. In addition to apparently increased bioaccessibility due to stirring, the automated manometric respirometry test systems give valuable and highly cost-effective insights into lag phase and biodegradation kinetics; information that is especially relevant for test chemicals of gradual biodegradability.
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Biodegradação Ambiental , Argila/química , Desinfetantes/química , Adsorção , Silicatos de Alumínio/química , Bentonita/química , Cátions , Cetilpiridínio , Tensoativos/químicaRESUMO
Biodegradation potential of cationic surfactants may be hampered by inhibition of inoculum at concentrations required to accurately measure inorganic carbon. At >0.3â¯mg/L cetyltrimethylammonium bromide (CTAB) negatively impacted degradation of the reference compound aniline. We used silicon dioxide (SiO2) and illite as inorganic sorbents to mitigate toxicity of CTAB by lowering freely dissolved concentrations. In an OECD Headspace Test we tested whether 16.8â¯mg/L CTAB was readily biodegradable in presence of two concentrations of SiO2 and illite. SiO2 adsorbed 85% and 98% CTAB, resulting in concentrations of 2.5 and 0.34â¯mg/L, mineralized to CO2 >60% within 16 and 23â¯d, respectively. With 89% and 99% sorbed to illite, 60% mineralization was reached within 9 and 23â¯d, respectively. However, higher sorbent concentrations increased time needed to reach >60% mineralization. Thus, desorption kinetics likely decreased bioaccessibility. It is therefore essential to determine appropriate concentrations of mitigating sorbents to render a Headspace Test based on carbon analysis suitable to determine ready biodegradability of compounds which might inhibit inoculum. This would avoid use of expensive radiolabeled compounds. However, high sorbent concentrations can reduce bioaccessibility and limit degradation kinetics, particularly for relatively toxic substances that require strong mitigation.
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Cetrimônio/farmacocinética , Tensoativos/farmacocinética , Adsorção , Compostos de Anilina/farmacocinética , Biodegradação Ambiental , Disponibilidade Biológica , Radioisótopos de Carbono/análise , Cátions , Cetrimônio/toxicidade , Poluentes Ambientais/farmacocinética , Poluentes Ambientais/toxicidade , Cinética , Minerais/química , Dióxido de Silício/químicaRESUMO
Emissions of plastic waste to the environment and the subsequent degradation into microplastic particles that have the potential to interact with biological organisms represent a concern for global society. Current understanding of the potential impacts on aquatic and terrestrial population stability and ecosystem structure and function associated with emissions of microplastic particles is limited and insufficient to fully assess environmental risks. Multistakeholder discussions can provide an important element in helping to identify and prioritize key knowledge gaps in assessing potential risks. In the present review, we summarize multistakeholder discussions from a 1-d International Council of Chemical Associations-sponsored symposium, which involved 39 scientists from 8 countries with representatives from academia, industry, and government. Participants were asked to consider the following: discuss the scientific merits and limitations of applying a proposed conceptual environmental risk assessment (ERA) framework for microplastic particles and identify and prioritize major research needs in applying ERA tools for microplastic particles. Multistakeholder consensus was obtained with respect to the interpretation of the current state of the science related to effects and exposure to microplastic particles, which implies that it is unlikely that the presence of microplastic in the environment currently represents a risk. However, the quality and quantity of existing data require substantial improvement before conclusions regarding the potential risks and impacts of microplastic particles can be fully assessed. Research that directly addresses the development and application of methods that strengthen the quality of data should thus be given the highest priority. Activities aimed at supporting the development of and access to standardized reference material were identified as a key research need. Environ Toxicol Chem 2019;38:2087-2100. © 2019 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals, Inc. on behalf of SETAC.
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Microplásticos/toxicidade , Bioacumulação , Monitoramento Ambiental , Recuperação e Remediação Ambiental , Microplásticos/química , Microplásticos/metabolismo , Tamanho da Partícula , Medição de RiscoRESUMO
Environmental fate and exposure models are a powerful means to integrate information on chemicals, their partitioning and degradation behaviour, the environmental scenario and the emissions in order to compile a picture of chemical distribution and fluxes in the multimedia environment. A 1995 pioneering book, resulting from a series of workshops among model developers and users, reported the main advantages and identified needs for research in the field of multimedia fate models. Considerable efforts were devoted to their improvement in the past 25 years and many aspects were refined; notably the inclusion of nanomaterials among the modelled substances, the development of models at different spatial and temporal scales, the estimation of chemical properties and emission data, the incorporation of additional environmental media and processes, the integration of sensitivity and uncertainty analysis in the simulations. However, some challenging issues remain and require research efforts and attention: the need of methods to estimate partition coefficients for polar and ionizable chemical in the environment, a better description of bioavailability in different environments as well as the requirement of injecting more ecological realism in exposure predictions to account for the diversity of ecosystem structures and functions in risk assessment. Finally, to transfer new scientific developments into the realm of regulatory risk assessment, we propose the formation of expert groups that compare, discuss and recommend model modifications and updates and help develop practical tools for risk assessment.
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Exposição Ambiental/análise , Poluentes Ambientais/análise , Modelos Teóricos , Monitoramento Ambiental/métodos , Medição de Risco , IncertezaRESUMO
To support the goals articulated in the vision for exposure and risk assessment in the twenty-first century, we highlight the application of a thermodynamic chemical activity approach for the exposure and risk assessment of chemicals in the environment. The present article describes the chemical activity approach, its strengths and limitations, and provides examples of how this concept may be applied to the management of single chemicals and chemical mixtures. The examples demonstrate that the chemical activity approach provides a useful framework for 1) compiling and evaluating exposure and toxicity information obtained from many different sources, 2) expressing the toxicity of single and multiple chemicals, 3) conducting hazard and risk assessments of single and multiple chemicals, 4) identifying environmental exposure pathways, and 5) reducing error and characterizing uncertainty in risk assessment. The article further illustrates that the chemical activity approach can support an adaptive management strategy for environmental stewardship of chemicals where "safe" chemical activities are established based on toxicological studies and presented as guidelines for environmental quality in various environmental media that can be monitored by passive sampling and other techniques. Environ Toxicol Chem 2018;37:1235-1251. © 2018 The Authors. Published by Wiley Periodicals, Inc. on behalf of SETAC.
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Exposição Ambiental/análise , Poluentes Ambientais/toxicidade , Medição de Risco , Guias como Assunto , Probabilidade , SolubilidadeRESUMO
Polyurethane foam (PUF) disks were deployed at global background sites, to test logistical issues associated with a global monitoring network for persistent organic pollutants (POPs). alpha-HCH, exhibited relatively high and uniform concentrations (17-150 pg/m3) at temperate and arctic sites with elevated concentrations associated with trans-Pacific inflow. Concentrations were much lower (<5 pg/m3) in Bermuda, Chile and Cape Grim. Concentrations for gamma-HCH, the main component of lindane, were spatially similar to the alpha-HCH pattern but lower in magnitude (typically, <10 pg/m3). Chlordane concentrations (sum of cis-chlordane, trans-chlordane and trans-nonachlor) were also low (<10 pg/m3). Dieldrin concentrations were in the range 2-25 pg/m3 at most sites but elevated in Bermuda. Back trajectories suggest that advection from Africa and the US may contribute. Endosulfan, a popular current-use pesticide, exhibited highest concentrations ranging from tens to hundreds of pg/m3. There was good agreement between duplicate samplers at each site and PUF disk-derived air concentrations agreed with high volume data. Few logistical/analytical problems were encountered in this pilot study.
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Poluentes Atmosféricos/análise , Poluição do Ar/análise , Monitoramento Ambiental/métodos , Hidrocarbonetos Clorados/análise , Resíduos de Praguicidas/análise , Movimentos do Ar , Clordano/análise , Dieldrin/análise , Endossulfano/análise , Monitoramento Ambiental/instrumentação , Desenho de Equipamento , Geografia , Hexaclorocicloexano/análise , Poliuretanos , Reprodutibilidade dos Testes , Estações do AnoRESUMO
The present study investigated the route and degree of uptake of 2 ionizable pharmaceuticals (diclofenac and fluoxetine) and 1 ionizable compound used in personal care products (triclosan) into the sediment-dwelling worm Lumbriculus variegatus. Studies were done on complete worms ("feeding") and worms where the head was absent ("nonfeeding") using (14) C-labeled ingredients. Biota sediment accumulation factors (BSAF), based on uptake of (14) C, for feeding worms increased in the order fluoxetine (0.3) < diclofenac (0.5) < triclosan (9), which is correlated with a corresponding increase in log octanol-water partition coefficient. Biota sediment accumulation factor estimates are representative of maximum values because the degree of biotransformation in the worms was not quantified. Although no significant differences were seen between the uptake of diclofenac and that of fluoxetine in feeding and nonfeeding worms, uptake of the more hydrophobic antimicrobial, triclosan, into the feeding worms was significantly greater than that in the nonfeeding worms, with the 48-h BSAF for feeding worms being 36% higher than that for the nonfeeding worms. The results imply that dietary uptake contributes to the uptake of triclosan, which may be a result of the high hydrophobicity of the compound. Models that estimate exposure of ionizable substances may need to consider uptake from both the water column and food, particularly when assessing risks from dynamic exposures to organic contaminants.