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BACKGROUND: Millions of people are exposed to landscape fire smoke (LFS) globally, and inhalation of LFS particulate matter (PM) is associated with poor respiratory and cardiovascular outcomes. However, how LFS affects respiratory and cardiovascular function is less well understood. OBJECTIVE: We aimed to characterize the pathophysiologic effects of representative LFS airway exposure on respiratory and cardiac function and on asthma outcomes. METHODS: LFS was generated using a customized combustion chamber. In 8-week-old female BALB/c mice, low (25 µg/m3, 24-hour equivalent) or moderate (100 µg/m3, 24-hour equivalent) concentrations of LFS PM (10 µm and below [PM10]) were administered daily for 3 (short-term) and 14 (long-term) days in the presence and absence of experimental asthma. Lung inflammation, gene expression, structural changes, and lung function were assessed. In 8-week-old male C57BL/6 mice, low concentrations of LFS PM10 were administered for 3 days. Cardiac function and gene expression were assessed. RESULTS: Short- and long-term LFS PM10 airway exposure increased airway hyperresponsiveness and induced steroid insensitivity in experimental asthma, independent of significant changes in airway inflammation. Long-term LFS PM10 airway exposure also decreased gas diffusion. Short-term LFS PM10 airway exposure decreased cardiac function and expression of gene changes relating to oxidative stress and cardiovascular pathologies. CONCLUSIONS: We characterized significant detrimental effects of physiologically relevant concentrations and durations of LFS PM10 airway exposure on lung and heart function. Our study provides a platform for assessment of mechanisms that underpin LFS PM10 airway exposure on respiratory and cardiovascular disease outcomes.
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Asma , Camundongos Endogâmicos BALB C , Material Particulado , Fumaça , Animais , Feminino , Fumaça/efeitos adversos , Asma/fisiopatologia , Asma/etiologia , Masculino , Camundongos , Material Particulado/efeitos adversos , Camundongos Endogâmicos C57BL , Pulmão/imunologia , Pulmão/fisiopatologia , Incêndios Florestais , Modelos Animais de DoençasRESUMO
Although the presence of nanoplastics in aquatic and terrestrial ecosystems has received increasing attention, little is known about its potential effect on ecosystem processes and functions. Here, we evaluated if differentially charged polystyrene (PS) nanoplastics (PS-NH2 and PS-SO3 H) exhibit distinct influences on microbial community structure, nitrogen removal processes (denitrification and anammox), emissions of greenhouse gases (CO2 , CH4 , and N2 O), and ecosystem multifunctionality in soils with and without earthworms through a 42-day microcosm experiment. Our results indicated that nanoplastics significantly altered soil microbial community structure and potential functions, with more pronounced effects for positively charged PS-NH2 than for negatively charged PS-SO3 H. Ecologically relevant concentration (3 g kg-1 ) of nanoplastics inhibited both soil denitrification and anammox rates, while environmentally realistic concentration (0.3 g kg-1 ) of nanoplastics decreased the denitrification rate and enhanced the anammox rate. The soil N2 O flux was always inhibited 6%-51% by both types of nanoplastics, whereas emissions of CO2 and CH4 were enhanced by nanoplastics in most cases. Significantly, although N2 O emissions were decreased by nanoplastics, the global warming potential of total greenhouse gases was increased 21%-75% by nanoplastics in soils without earthworms. Moreover, ecosystem multifunctionality was increased 4%-12% by 0.3 g kg-1 of nanoplastics but decreased 4%-11% by 3 g kg-1 of nanoplastics. Our findings provide the only evidence to date that the rapid increase in nanoplastics is altering not only ecosystem structure and processes but also ecosystem multifunctionality, and it may increase the emission of CO2 and CH4 and their global warming potential to some extent.
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Ecossistema , Gases de Efeito Estufa , Aquecimento Global , Microplásticos , Óxido Nitroso/análise , Dióxido de Carbono/análise , Metano/análise , Solo/químicaRESUMO
The long-term aging of plastic leads to weathering and biofouling that can influence the behavior and fate of plastic in the marine environment. This is the first study to fingerprint the contaminant profiles and bacterial communities present in plastic-associated inorganic and organic matter (PIOM) isolated from 10 year-aged plastic. Plastic sleeves were sampled from an oyster aquaculture farm and the PIOM was isolated from the intertidal, subtidal, and sediment-buried segments to investigate the levels of metal(loid)s, polyaromatic hydrocarbons (PAHs), per-fluoroalkyl substances (PFAS) and explore the microbial community composition. Results indicated that the PIOM present on long-term aged high-density polyethylene plastic harbored high concentrations of metal(loid)s, PAHs, and PFAS. Metagenomic analysis revealed that the bacterial composition in the PIOM differed by habitat type, which consisted of potentially pathogenic taxa including Vibrio, Shewanella, and Psychrobacter. This study provides new insights into PIOM as a potential sink for hazardous environmental contaminants and its role in enhancing the vector potential of plastic. Therefore, we recommend the inclusion of PIOM analysis in current biomonitoring regimes and that plastics be used with caution in aquaculture settings to safeguard valuable food resources, particularly in areas of point-source contamination.
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Microbiota , Poluentes Químicos da Água , Bactérias/genética , Monitoramento Ambiental , Plásticos , Polietileno , Água do Mar , Poluentes Químicos da Água/análiseRESUMO
Besides the ecotoxicological consequences of microplastics and associated chemicals, the association of microbes on plastics has greater environmental implications as microplastics may select for unique microbiome participating in environmentally significant functions. Despite this, the functional potential of the microbiome associated with different types of plastics is understudied. Here, we investigate the interaction between plastic and marine biofilm-forming microorganisms through a whole-genome sequencing approach on four types of microplastics incubated in the marine environment. Taxonomic analysis suggested that the microplastic surfaces exhibit unique microbial profiles and niche partitioning among the substrates. In particular, the abundance of Vibrio alginolyticus and Vibrio campbellii suggested that microplastic pollution may pose a potential risk to the marine food chain and negatively impact aquaculture industries. Microbial genera involved in xenobiotic compound degradation, carbon cycling, and genes associated with the type IV secretion system, conjugal transfer protein TraG, plant-pathogen interaction, CusA/CzcA family heavy metal efflux transfer proteins, and TolC family proteins were significantly enriched on all the substrates, indicating the variety of processes operated by the plastic-microbiome. The present study gives a detailed characterization of the rapidly altering microbial composition and gene pools on plastics and adds new knowledge surrounding the environmental ramifications of marine plastic pollution.
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Microbiota , Poluentes Químicos da Água , Monitoramento Ambiental , Poluição Ambiental , Microbiota/genética , Microplásticos , Plásticos , Vibrio , Poluentes Químicos da Água/análiseRESUMO
Microplastics (MPs) exposed to the natural environment provide an ideal surface for biofilm formation, which potentially acts as a reactive phase facilitating the sorption of hazardous contaminants. Until now, changes in the contaminant sorption capacity of MPs due to biofilm formation have not been quantified. This is the first study that compared the capacity of naturally aged, biofilm-covered microplastic fibers (BMFs) to adsorb perfluorooctane sulfonate (PFOS) and lead (Pb) at environmentally relevant concentrations. Changes in the surface properties and morphology of aged microplastic fibers (MF) were studied by surface area analysis, infrared spectroscopy, and scanning electron microscopy. Results revealed that aged MFs exhibited higher surface areas because of biomass accumulation compared to virgin samples and followed the order polypropylene>polyethylene>nylon>polyester. The concentrations of adsorbed Pb and PFOS were 4-25% and 20-85% higher in aged MFs and varied among the polymer types. The increased contaminant adsorption was linked with the altered surface area and the hydrophobic/hydrophilic characteristics of the samples. Overall, the present study demonstrates that biofilms play a decisive role in contaminant-plastic interactions and significantly enhance the vector potential of MFs for toxic environmental contaminants. We anticipate that knowledge generated from this study will help refine the planetary risk assessment of MPs.
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Plásticos , Poluentes Químicos da Água , Adsorção , Biofilmes , Microplásticos , Poluentes Químicos da Água/análiseRESUMO
Microplastic pollution and climate change, the two seemingly distinct phenomena of global concern, are interconnected through various pathways. The connecting links between the two include the biological carbon pumps in the oceans, the sea ice, the plastisphere involved in biogeochemical cycling and the direct emissions of greenhouse gases from microplastics. On one hand, the presence of microplastics in the water column disrupts the balance of the natural carbon sequestration by affecting the key players in the pumping of carbon, such as the phytoplankton and zooplankton. On the other hand, the effect of microplastics on the sea ice in Polar Regions is two-way, as the ice caps are transformed into sinks and sources of microplastics and at the same time, the microplastics can enhance the melting of ice by reducing the albedo. Microplastics may have more potential than larger plastic fragments to release greenhouse gases (GHGs). Microbe-mediated emission of GHGs from soils is also now altered by the microplastics present in the soil. Plastisphere, the emerging microbiome in aquatic environments, can also contribute to climate change as it hosts complex networks of microbes, many of which are involved in greenhouse gas production. To combat a global stressor like climate change, it needs to be addressed with a holistic approach and this begins with tracing the various stressors like microplastic pollution that can aggravate the impacts of climate change.
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Micro- and nano-plastics (MNPs) are emerging contaminants found in air, water, and food. Ageing and weathering processes convert aquatic plastics into MNPs which, due to their small size, can be assimilated by organisms. The accumulation of MNPs in aquatic life (e.g., fish, oysters, and crabs) will, in turn, pose risks to the health of ecosystems and human. This study focuses on the uptake, biodistribution, and size-dependent toxicity of polystyrene nano-plastics (PS-NPs) in a commercially important food web, the Australian Bass (Macquaria novemaculeata). Fish were fed artemia containing PS-NPs of various sizes (ranging from 50 nm to 1 µm) for durations of 5 and 7 days. The findings revealed that smaller NPs (50 nm) accumulated in the brain and muscle tissues at higher concentrations, whereas larger NPs (1 µm) were primarily found in the gills and intestines. In addition, an inverse correlation was observed between the size of NPs and the rate of trophic transfer, with smaller PS-NPs resulting in a higher transfer rate from artemia to fish. Polystyrene NPs caused both activation of the enzyme superoxide dismutase and damage to the DNA of fish tissues. These effects were size dependent. Metabolomic analysis revealed that indirect exposure to different-sized PS-NPs resulted in altered metabolic profiles within fish intestines, potentially impacting lipid and energy metabolism. These results offer novel perspectives on the size-specific toxic impacts of NPs on fish and the transfer of plastics through the food chain.
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Bass , Poluentes Químicos da Água , Animais , Humanos , Poliestirenos/toxicidade , Poliestirenos/metabolismo , Microplásticos/toxicidade , Microplásticos/metabolismo , Bass/metabolismo , Ecossistema , Distribuição Tecidual , Austrália , Plásticos/metabolismo , Poluentes Químicos da Água/toxicidadeRESUMO
There are many benefits to be realized by applying a disaster risk reduction framework to the context of plastic pollution, especially in regards to operationalizing the precautionary principle that is inherent in many international treaties and conventions. We explore the implications of framing plastic pollution as a 'disaster' in light of the development of the new global instrument to end plastic pollution by aligning the objectives of the United Nations (UN) Sendai Framework for Disaster Risk Reduction 2015-2030 (SF) and the UN Sustainable Development Goals (SDGs); and thereby also complementing the many climate and non-climate mandates embedded within the UN Framework Convention on Climate Change (UNFCCC). It has been proposed that the UN global instrument to end plastic pollution could be based on the guidelines of the Paris Agreement (PA), driven by national action plans, potential to offset and mandatory reporting requirements. Adding a disaster risk reduction lens to this approach will strongly complement and enhance the environmental and human health outcomes aspired for the global and legally binding treaty to end plastic pollution. We provide an overview to reinforce the mutual benefits of cooperation and coordination, linking the SF, UNFCCC and SDGs to the future international instrument.
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The omnipresence of microplastics (MPs) in marine and terrestrial environments as a pollutant of concern is well established and widely discussed in the literature. However, studies on MP contamination in commercial food sources like salts from the terrestrial environment are scarce. Thus, this is the first study to investigate various varieties of Australian commercial salts (both terrestrial and marine salts) as a source of MPs in the human diet, and the first to detect MPs in black salt. Using Nile red dye, the MPs were detected and counted under light microscopy, further characterised using attenuated total reflectance Fourier transformed infrared spectroscopy (ATR-FTIR) and scanning electron microscopy and energy-dispersive X-ray spectroscopy (SEM-EDS). Of all the 90 suspected particles, 78.8% were identified as MPs with a size ranging between 23.2 µm and 3.9 mm. The fibres and fragments constituted 75.78% and 24.22% respectively. Among the tested samples, Himalayan pink salt (coarse) from terrestrial sources was found to have the highest MP load, i.e. 174.04 ± 25.05 (SD) particle/kg, followed by black salt at 157.41 ± 23.13 particle/kg. The average concentration of detected MPs in Australian commercial salts is 85.19 ± 63.04 (SD) per kg. Polyamide (33.8%) and polyurethane (30.98%) were the dominant MP types. Considering the maximum recommended (World Health Organization) salt uptake by adults daily at 5 g, we interpret that an average person living in Australia may be ingesting approximately 155.47 MPs/year from salt uptake. Overall, MP contamination was higher in terrestrial salts (such as black and Himalayan salt) than the marine salt. In conclusion, we highlight those commercial salts used in our daily lives serve as sources of MPs in the diet, with unknown effects on human health.
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Microplásticos , Poluentes Químicos da Água , Humanos , Plásticos , Sais/química , Monitoramento Ambiental/métodos , Austrália , Cloreto de Sódio na Dieta/análise , Dieta , Poluentes Químicos da Água/análiseRESUMO
Wastewater treatment plants (WWTPs) efficiently eliminate over 98% of microplastics (MPs) from wastewater discharge, subsequently accumulating them in sludge. This sludge is frequently employed as fertilizer in agricultural practices or land rehabilitation. While there is significant research on biosolid application in agriculture, the discussion regarding its application in rehabilitating industrial zones and MPs contamination is limited. The current study investigates the abundance, distribution, and composition of MPs in rehabilitation land with long-term biosolid-application in Australia. Three minesite fields (designated 1-3), each with distinct biosolid application histories since 2011, 2012, and 2017, and a control field without any biosolid application history, were chosen for this study. The abundances of MPs in biosolid-applied fields 1-3 (6.04 ± 1.92 x 102 MP kg-1; 4.94 ± 0.73 x 102 MP kg-1; 2.48 ± 0.70 x 102 MP kg-1) were considerably higher compared to non-biosolid-applied field (0.70 ± 0.63 x 102 MP kg -1). This indicates that the application of biosolids significantly contributes to the presence of MPs in the soil. Moreover, the results suggest that with each successive application, the abundance of MPs increases. The abundance and size of MPs in both biosolid and non-biosolid soils decreased as the soil depth increased. Microbeads were dominant in soils where biosolids were applied (up to 61.9%), while fibres were dominant in non-biosolid soils (accounting for 85.7%). The distribution of plastic polymer types varied among fields and soil depths. Most MPs were microbeads of polyamide (PA), fragments of polyethylene (PE), foam of polystyrene (PS), and fibres of rayon. This research presents evidence that the extended utilization of biosolids results in elevated MP pollution in minesite rehabilitation land, highlighting a frequently overlooked origin of MP contamination in terrestrial settings. Additional evaluations needed to understand ecological risks of MPs in soil ecosystems affected by biosolid application.
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Microplásticos , Poluentes do Solo , Plásticos , Esgotos , Biossólidos , Ecossistema , Poluentes do Solo/análise , Solo , AustráliaRESUMO
Plastics are an intrinsic part of modern life with many beneficial uses for society. Yet, there is increasing evidence that plastic and microplastic pollution poses a risk to the environment and human health. Microplastics are increasingly grouped as a complex mix of polymers with different physicochemical and toxicological properties. This study attempts to assess the hazardous properties of common polymer types through the development of an integrated multi-criteria framework. The framework establishes a systematic approach to identify plastic polymers of concern. A semi-quantitative method was devised using twenty-one criteria. We used a case study from Victoria, Australia, to evaluate the effectiveness of the framework to characterize the environmental risk of common polymer types. A wide range of data sources were interrogated to complete an in-depth analysis across the material life cycle. We found that three polymers had the highest risk of harm: polyvinyl chloride, polypropylene, and polystyrene; with dominant sectors being: building and construction, packaging, consumer and household, and automotive sectors; and greatest leakage of plastics at the end-of-life stages. Our findings illustrate the complexity of microplastics as an emerging contaminant, and its scalability supports decision-makers globally to identify and prioritize management strategies to address the risks posed by plastics. ENVIRONMENTAL IMPLICATION: The hazardous nature of mismanaged plastics is an international concern. The negative impacts on the environment and human health are increasingly coming to light. Consequently, resource constraints limits the ability to address all problems. Our work adopts a holistic approach to evaluate the risk of harm from microplastics across the entire life cycle to allow for targeted management measures. The hazard assessment of common polymer types developed using a multi-criteria framework, presents a systematic approach to prioritize polymers at any scale. This allows for the development of optimal investments and interventions to ensure that high-risk environmental problems are addressed first.
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Plásticos , Poluentes Químicos da Água , Austrália , Monitoramento Ambiental , Poluição Ambiental , Humanos , Microplásticos/toxicidade , Plásticos/análise , Polímeros , Poluentes Químicos da Água/análise , Poluentes Químicos da Água/toxicidadeRESUMO
Engineered nanomaterials (ENMs) are at the forefront of many technological breakthroughs in science and engineering. The extensive use of ENMs in several consumer products has resulted in their release to the aquatic environment. ENMs entering the aquatic ecosystem undergo a dynamic transformation as they interact with organic and inorganic constituents present in aquatic environment, specifically abiotic factors such as NOM and clay minerals, and attain an environmental identity. Thus, a greater understanding of ENM-abiotic factors interactions is required for an improved risk assessment and sustainable management of ENMs contamination in the aquatic environment. This review integrates fundamental aspects of ENMs transformation in aquatic environment as impacted by abiotic factors, and delineates the recent advances in bioavailability and ecotoxicity of ENMs in relation to risk assessment for ENMs-contaminated aquatic ecosystem. It specifically discusses the mechanism of transformation of different ENMs (metals, metal oxides and carbon based nanomaterials) following their interaction with the two most common abiotic factors NOM and clay minerals present within the aquatic ecosystem. The review critically discusses the impact of these mechanisms on the altered ecotoxicity of ENMs including the impact of such transformation at the genomic level. Finally, it identifies the gaps in our current understanding of the role of abiotic factors on the transformation of ENMs and paves the way for the future research areas.
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Ecossistema , Nanoestruturas , Metais , Nanoestruturas/toxicidadeRESUMO
Recently, hydrothermal carbonization emerges as the most viable option for the management of solid waste with high moisture content. Sludge derived hydrochar is used as an adsorbent for emerging contaminants or micro-pollutants in the domain of sustainability. Current study demonstrates the KOH activation of hydrochar produced from paper board mill sludge and evaluates its removal potential of a Non-steroidal anti-inflammatory drug, Diclofenac from aqueous solution. The activated hydrochars exhibited porous, spherical micro-structures with higher fraction of oxygenated functional groups paving way for the efficient adsorption of Diclofenac. The effect of initial Diclofenac concentration and contact time was ascertained using adsorption kinetics and isotherms. The adsorption kinetics exhibited second-order reaction for all adsorbents indicating higher coefficient of determination (R2 > 0.9). The Diclofenac adsorption on hydrochars followed Langmuir isotherm model with the post-activated hydrochar recording a highest adsorption capacity of 37.23 mg g-1 in 40 mg L-1 initial Diclofenac concentration at 15 h equilibrium time.
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Workers in the mining and construction industries are at increased risk of respiratory and other diseases as a result of being exposed to harmful levels of airborne particulate matter (PM) for extended periods of time. While clear links have been established between PM exposure and the development of occupational lung disease, the mechanisms are still poorly understood. A greater understanding of how exposures to different levels and types of PM encountered in mining and construction workplaces affect pathophysiological processes in the airways and lungs and result in different forms of occupational lung disease is urgently required. Such information is needed to inform safe exposure limits and monitoring guidelines for different types of PM and development of biomarkers for earlier disease diagnosis. Suspended particles with a 50% cut-off aerodynamic diameter of 10â µm and 2.5â µm are considered biologically active owing to their ability to bypass the upper respiratory tract's defences and penetrate deep into the lung parenchyma, where they induce potentially irreversible damage, impair lung function and reduce the quality of life. Here we review the current understanding of occupational respiratory diseases, including coal worker pneumoconiosis and silicosis, and how PM exposure may affect pathophysiological responses in the airways and lungs. We also highlight the use of experimental models for better understanding these mechanisms of pathogenesis. We outline the urgency for revised dust control strategies, and the need for evidence-based identification of safe level exposures using clinical and experimental studies to better protect workers' health.
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Pneumopatias , Doenças Profissionais , Exposição Ocupacional , Carvão Mineral/efeitos adversos , Poeira/análise , Humanos , Pulmão , Pneumopatias/induzido quimicamente , Pneumopatias/etiologia , Doenças Profissionais/induzido quimicamente , Doenças Profissionais/etiologia , Exposição Ocupacional/efeitos adversos , Qualidade de Vida , Dióxido de Silício/efeitos adversosRESUMO
Conditioning films (CFs) are surface coatings formed by the adsorption of biomolecules from the surrounding environment that can modify the material-specific surface properties and precedes the attachment of microorganisms. Hence, CFs are a biologically relevant identity that could govern the behavior and fate of microplastics in the aquatic environment. In the present study, polyethylene terephthalate (PET) and polylactic acid (PLA) plastic cards were immersed in natural seawater to allow the formation of CFs. The changes in the surface roughness after 24 h were investigated by atomic force microscopy (AFM), and the surface changes were visualized by scanning electron microscopy (SEM). The global elemental composition of the conditioned surface was investigated by energy dispersive spectroscopy (EDS). Results indicated that marine conditioning of PET and PLA samples for 24 h resulted in an increase of â¼11 and 31% in the average surface roughness, respectively. SEM images revealed the attachment of coccoid-shaped bacterial cells on the conditioned surfaces, and the accumulation of salts of sodium and phosphate-containing precipitates was revealed through the EDS analysis. The results indicate that the increase in surface roughness due to conditioning is linked to a material's hydrophilicity leading to a rapid attachment of bacteria on the surfaces. Further investigations into the CFs can unfold crucial knowledge surrounding the plastic-microbe interaction that has implications for medical, industrial, and environmental research.
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The ubiquitous presence of microplastics in the food web has been established. However, the mass of microplastics exposure to humans is not defined, impeding the human health risk assessment. Our objectives were to extract the data from the available evidence on the number and mass of microplastics from various sources, to determine the uncertainties in the existing data, to set future research directions, and derive a global average rate of microplastic ingestion to assist in the development of human health risk assessments and effective management and policy options. To enable the comparison of microplastics exposure across a range of sources, data extraction and standardization was coupled with the adoption of conservative assumptions. Following the analysis of data from fifty-nine publications, an average mass for individual microplastics in the 0-1â¯mm size range was calculated. Subsequently, we estimated that globally on average, humans may ingest 0.1-5â¯g of microplastics weekly through various exposure pathways. This was the first attempt to transform microplastic counts into a mass value relevant to human toxicology. The determination of an ingestion rate is fundamental to assess the human health risks of microplastic ingestion. These findings will contribute to future human health risk assessment frameworks.
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Microplásticos , Poluentes Químicos da Água , Monitoramento Ambiental , Cadeia Alimentar , Humanos , Plásticos/toxicidade , Medição de Risco , Poluentes Químicos da Água/análise , Poluentes Químicos da Água/toxicidadeRESUMO
Particulate matter (PM) is a complex mixture of solid particles and liquid droplets suspended in the air with varying size, shape, and chemical composition which intensifies significant concern due to severe health effects. Based on the well-established human health effects of outdoor PM, health-based standards for outdoor air have been promoted (e.g., the National Ambient Air Quality Standards formulated by the U.S.). Due to the exchange of indoor and outdoor air, the chemical composition of indoor particulate matter is related to the sources and components of outdoor PM. However, PM in the indoor environment has the potential to exceed outdoor PM levels. Indoor PM includes particles of outdoor origin that drift indoors and particles that originate from indoor activities, which include cooking, fireplaces, smoking, fuel combustion for heating, human activities, and burning incense. Indoor PM can be enriched with inorganic and organic contaminants, including toxic heavy metals and carcinogenic volatile organic compounds. As a potential health hazard, indoor exposure to PM has received increased attention in recent years because people spend most of their time indoors. In addition, as the quantity, quality, and scope of the research have expanded, it is necessary to conduct a systematic review of indoor PM. This review discusses the sources, pathways, characteristics, health effects, and exposure mitigation of indoor PM. Practical solutions and steps to reduce exposure to indoor PM are also discussed.
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Poluentes Atmosféricos , Poluição do Ar em Ambientes Fechados , Poluição do Ar , Poluentes Atmosféricos/análise , Poluição do Ar em Ambientes Fechados/análise , Culinária , Monitoramento Ambiental , Humanos , Tamanho da Partícula , Material Particulado/análiseRESUMO
Microplastics are an emerging contaminant in aquatic environments. Information on the occurrence and characteristics of microplastics in Australia is limited and their interactions with chemical contaminants have not been addressed. Therefore, the aim of this study was to generate baseline information on the physical and chemical characteristics of microplastics on Australian shorelines to facilitate further detailed risk assessment. Field collected microplastics were categorised by colour, shape and polymer type. Plastic particles were primarily clear, blue, white and green and consisted mainly of fragments (57.80%) and pellets (30.68%). Polymer characterisation revealed that shoreline microplastics were polyethylene (53.17%), polypropylene (35.17%), polystyrene (6.61%) and polyethylene terephthalate (1.85%). Analysis of metal(loid)s found that concentrations of Mn, Cr, Cu, As, Zn and Pb were significantly higher on microplastics associated with industrial locations compared with other land uses, indicating that aged microplastics have the potential to adsorb toxic metals and that metals levels may be location-dependent.
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Plásticos , Poluentes Químicos da Água/análise , Austrália , Ciência do Cidadão , Monitoramento Ambiental , Metais/análise , MicroplásticosRESUMO
Plastics pollution is ubiquitous. Microplastics (<5 mm in diameter) and mesoplastics (5-20 mm in diameter) are emerging as the most common plastic particulates found in the marine environment. In this study, the occurrence of microplastics and mesoplastics in the gastrointestinal tract (GI) of some commercially important fish collected from Chennai and Nagapattinam of Tamil Nadu, Southeast coast of Bay of Bengal was assessed. A new and improved alkaline digestion method, using alcoholic potassium hydroxide (KOH) was carried out to destroy the organic matter. Following this method, twenty plastic particulates were isolated from the GI tract of 17 individual fish. Fourier Transform Infrared Radiation analysis (FTIR) showed that polymers found in GI tracts were of Polyethylene, Polyamide and Polyester types. Given the dry fish is India's biggest market and popular delicacy, the presence of microplastics in the fish gut is a potential serious human health concern, as they are directly consumed.
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Monitoramento Ambiental , Peixes , Conteúdo Gastrointestinal/química , Microplásticos/análise , Poluentes Químicos da Água/análise , Animais , Baías , Índia , Plásticos , Inquéritos e QuestionáriosRESUMO
Wastewater treatment plants are a significant pathway of microplastics (MPs) to aquatic environments. To develop suitable management options and reduce microplastic emissions in treated effluent and sludge, we must first develop a reliable method to understand their transport and fate throughout the treatment process. An improved methodology was applied to determine the size, shape, polymer type and partitioning behaviour of MPs using a combination of oxidation treatment, fluorescent staining and Attenuated Total Reflectance Fourier Transform Infrared Spectroscopy (ATR-FTIR) to detect small MPs ≤20 µm in wastewater. The mean number of MPs (<5 mm) detected using this methodology was 11.80 ± 1.10 MP/L in raw sewage, 5.23 ± 0.25 MP/L in degritted wastewater, 7.91 ± 0.44 MP/L in waste activated sludge and 2.76 ± 0.11 MP/L in the final treated effluent. An increase in MPs following primary screening suggests that WAS is a sink for several stealth microplastics, including glitter, which is returned to the effluent during the treatment process. The estimated MP removal efficiency for the studied WWTP is relatively poor compared with global data for secondary WWTPs, which is likely due to the release of partially treated effluent into the Pacific Ocean via a second discharge point. The information generated through this study can be useful to; firstly, inform on-site wastewater management practices, and secondly, reduce MP concentrations in final treated effluents discharged to the marine environment.