Effects of polyethylene, polylactic acid, and tire particles on the sediment microbiome and metabolome at high and low temperatures.

Global warming has led to a high incidence of extreme heat events, and the frequent occurrence of extreme heat events has had extensive and far-reaching impacts on wetland ecosystems. The widespread distribution of plastics in the environment, including polyethylene (PE), polylactic acid (PLA), and tire particles (TPs), has caused various environmental problems. Here, high-throughput sequencing techniques and metabolomics were used for the first time to investigate the effects of three popular microplastic types: PE, PLA, and TP, on the sediment microbiome and the metabolome at both temperatures. The microplastics were incorporated into the sediment at a concentration of 3% by weight of the dry sediment (wt/wt), to reflect environmentally relevant conditions. Sediment enzymatic activity and physicochemical properties were co-regulated by both temperatures and microplastics producing significant differences compared to controls. PE and PLA particles inhibited bacterial diversity at low temperatures and promoted bacterial diversity at high temperatures, and TP particles promoted both at both temperatures. For bacterial richness, only PLA showed inhibition at low temperature; all other treatments showed promotion. PE, PLA, and TP microplastics changed the community structure of sediment bacteria, forming two clusters at low and high temperatures. Furthermore, PE, PLA, and TP changed the sediment metabolic profiles, producing differential metabolites such as lipids and molecules, organic heterocyclic compounds, and organic acids and their derivatives, especially TP had the most significant effect. These findings contribute to a more comprehensive understanding of the potential impact of microplastic contamination.IMPORTANCEIn this study, we added 3% (wt/wt) microplastic particles, including polyethylene, polylactic acid, and tire particles, to natural sediments under simulated laboratory conditions. Subsequently, we simulated the sediment microbial and ecosystem responses under different temperature conditions by incubating them for 60 days at 15°C and 35°C, respectively. After synthesizing these results, our study strongly suggests that the presence of microplastics in sediment ecosystems and exposure under different temperature conditions may have profound effects on soil microbial communities, enzyme activities, and metabolite profiles. This is important for understanding the potential hazards of microplastic contamination on terrestrial ecosystems and for developing relevant environmental management strategies.

Ongoing Laboratory Performance Study on Chemical Analysis of Hydrophobic and Hydrophilic Compounds in Three Aquatic Passive Samplers.

The quality of chemical analysis is an important aspect of passive sampling-based environmental assessments. The present study reports on a proficiency testing program for the chemical analysis of hydrophobic organic compounds in silicone and low-density polyethylene (LDPE) passive samplers and hydrophilic compounds in polar organic chemical integrative samplers. The median between-laboratory coefficients of variation (CVs) of hydrophobic compound concentrations in the polymer phase were 33% (silicone) and 38% (LDPE), similar to the CVs obtained in four earlier rounds of this program. The median CV over all rounds was 32%. Much higher variabilities were observed for hydrophilic compound concentrations in the sorbent: 50% for the untransformed data and a factor of 1.6 after log transformation. Limiting the data to the best performing laboratories did not result in less variability. Data quality for hydrophilic compounds was only weakly related to the use of structurally identical internal standards and was unrelated to the choice of extraction solvent and extraction time. Standard deviations of the aqueous concentration estimates for hydrophobic compound sampling by the best performing laboratories were 0.21 log units for silicone and 0.27 log units for LDPE (factors of 1.6 to 1.9). The implications are that proficiency testing programs may give more realistic estimates of uncertainties in chemical analysis than within-laboratory quality control programs and that these high uncertainties should be taken into account in environmental assessments.

Uptake of microplastics and impacts on plant traits of savoy cabbage.

Anthropogenic influences such as plastic pollution are causing serious environmental problems. While effects of microplastics on marine organisms are well studied, less is known about effects of plastic particles on terrestrial organisms such as plants. We investigated the effects of microplastic particles on different growth and metabolic traits of savoy cabbage (Brassica oleracea var. sabauda). Sections of seedlings exposed to polystyrene particles were analysed by coherent Raman scattering microscopy. These analyses revealed an uptake of particles in a size range of 0.5 µm to 2.0 µm into cells of the hypocotyl. Furthermore, plants were grown in substrate amended with polyethylene and polystyrene particles of different sizes (s1: 200-500 µm; s2: 100-200 µm; s3: 20-100 µm; s4: < 100 µm, with most particles < 20 µm; s5: < 20 µm) and in different concentrations (c1 = 0.1%, c2 = 0.01%, c3 = 0.001%). After several weeks, shoot and root biomass were harvested. Leaves were analysed for their carbon to nitrogen ratio, while amino acid and glucosinolate composition were measured using high performance liquid chromatography. Plastic type, particle size and concentration showed distinct effects on certain plant traits. Shoot biomass was interactively influenced by size and concentration of polyethylene, while root biomass was not modified by any of the plastic exposure treatments. Likewise, the composition and total concentrations of leaf amino acids were not affected, but the leucine concentration was significantly increased in several of the plastic-exposed plants. Glucosinolates were also slightly altered, depending on the particle size. Some of the observed effects may be independent of plastic uptake, as larger particles were not taken up but still could affect plant traits. For example, in the rhizosphere plastic particles may increase the water holding capacity of the soil, impacting some of the plant traits. In summary, this study shows how important the plastic type, particle size and concentration are for the uptake of microplastics and their effects on plant traits, which may have important implications for crops, but also for ecosystems.

Implications of a New Test Facility for Fragmentation Investigations on Virgin (Micro)plastics.

Littered plastics are partly introduced into water bodies, ultimately transporting this waste to the shores and oceans. At the shore, ultraviolet (UV) radiation (also present in other environmental compartments) and wave breaking cause plastics to degrade and fragment into smaller particles, called microplastics, if below 5 mm. Since these plastics' surfaces can act as vectors for hydrophobic (toxic) chemical substances (e.g., per- and polyfluoroalkyl substances (PFAS)) and leach (toxic) chemicals into the water, the increase in the surface area through the fragmentation of plastics becomes relevant. Studies investigating different effects on the fragmentation of plastics have mostly disregarded a sufficient mechanical component for fragmentation, focusing on degradation by UV radiation. Therefore, this study investigated the impact of the mechanical fragmentation drivers, wave impact, and sediment abrasion on the fragmentation of expanded polystyrene (EPS), high-density polyethylene (PE-HD), and polyethylene terephthalate (PET) particles. In a newly designed test facility called Slosh-Box, the mentioned impacts were investigated concurrently. The results reveal that the mechanical impacts alone are sufficient for plastic fragmentation, and the test facility is suitable for fragmentation investigations. Furthermore, the increase in surface area was determined via scanning electron microscopy. For EPS, the surface area increased more than 2370-fold, while for PE-HD and PET, surface areas increased between 1 and 8.6 times. Concluding from the results, the new test facility is suitable for plastic fragmentation studies. In addition, sediment was revealed to be a relevant fragmentation driver, which should be included in every experiment investigating the fragmentation of plastic in a nearshore environment independent of other drivers like UV radiation.

Abiotic Long-Term Simulation of Microplastic Weathering Pathways under Different Aqueous Conditions.

Microplastics (MPs) are one of the most abundant and widespread anthropogenic pollutants worldwide. In addition to the global spread and threats of plastic to native species by carrying toxic substances, its slow degradation rate and resulting long retention time in the environment constitute a problem that is still poorly understood. In this study, five of the most manufactured plastic types were weathered under simulated beach conditions for 18 months in freshwater, brackish water, and seawater. Those included polyethylene (PE), polypropylene (PP), polystyrene (PS), polyethylene terephthalate (PET), and polyvinyl chloride (PVC). PP was the first polymer type that fragmented after 9 months of weathering and influenced the pH of the surrounding water. Molecular surface changes were detected for all polymers, just after the first week. Hydroxyl bonds were one of the first groups incorporated into the polymers, weakening 2-3 weeks later. Carbonyl groups were also measured early, but with significantly different developments with time between the polymer types. Differences in degradation rates were proven between the water media, with the fastest degradation in seawater compared to brackish water and freshwater for PE and PP. These results are consistent with previous findings on MPs aged under environmental conditions and provide initial long-term observations of MP degradation pathways under simulated environmental conditions. These findings are valuable for assessing the fate and hazards of MPs in aquatic systems.

Plastic-Rock Complexes as Hotspots for Microplastic Generation.

Discarded plastics and microplastics (MPs) in the environment are considered emerging contaminants and indicators of the Anthropocene epoch. This study reports the discovery of a new type of plastic material in the environment─plastic-rock complexes─formed when plastic debris irreversibly sorbs onto the parent rock after historical flooding events. These complexes consist of low-density polyethylene (LDPE) or polypropylene (PP) films stuck onto quartz-dominated mineral matrices. These plastic-rock complexes serve as hotspots for MP generation, as evidenced by laboratory wet-dry cycling tests. Over 1.03 × 108 and 1.28 × 108 items·m-2 MPs were generated in a zero-order mode from the LDPE- and PP-rock complexes, respectively, following 10 wet-dry cycles. The speed of MP generation was 4-5 orders of magnitude higher than that in landfills, 2-3 orders of magnitude higher than that in seawater, and >1 order of magnitude higher than that in marine sediment as compared with previously reported data. Results from this investigation provide strong direct evidence of anthropogenic waste entering geological cycles and inducing potential ecological risks that may be exacerbated by climate change conditions such as flooding events. Future research should evaluate this phenomenon regarding ecosystem fluxes, fate, and transport and impacts of plastic pollution.

Cutting Boards: An Overlooked Source of Microplastics in Human Food?

Plastic cutting boards are a potentially significant source of microplastics in human food. Thus, we investigated the impact of chopping styles and board materials on microplastics released during chopping. As chopping progressed, the effects of chopping styles on microplastic release became evident. The mass and number of microplastics released from polypropylene chopping boards were greater than polyethylene by 5-60% and 14-71%, respectively. Chopping on polyethylene boards was associated with a greater release of microplastics with a vegetable (i.e., carrots) than chopping without carrots. Microplastics showed a broad, bottom-skewed normal distribution, dominated by <100 µm spherical-shaped microplastics. Based on our assumptions, we estimated a per-person annual exposure of 7.4-50.7 g of microplastics from a polyethylene chopping board and 49.5 g of microplastics from a polypropylene chopping board. We further estimated that a person could be exposed to 14.5 to 71.9 million polyethylene microplastics annually, compared to 79.4 million polypropylene microplastics from chopping boards. The preliminary toxicity study of the polyethylene microplastics did not show adverse effects on the viability of mouse fibroblast cells for 72 h. This study identifies plastic chopping boards as a substantial source of microplastics in human food, which requires careful attention.

A multidimensional approach for microplastics monitoring in two major tropical river basins, Malaysia.

Microplastics (MPs) with the size of 1 µm-5 mm are pollutants of great concern ubiquitously found in the environment. Existing efforts have found that most of the MPs present in the seas mainly originated from land via riverine inputs. Asian rivers are known to be among the top in microplastic emissions. However, field data are scarce, especially in Malaysia. This study presents the distribution and characteristics of MPs in the surface water of two major river basins of Malaysia, namely Langat River (West Coast/Straits of Malacca) and Kelantan River (East Coast/South China Sea). Water samples were collected at 21-22 locations in Kelantan and Langat rivers, covering the river, estuary and sea. MPs were physically classified based on sizes, shapes, colours and surface morphology (SEM-EDS). The average of 179.6 items/L and 1464.8 items/L of MPs had been quantified from Kelantan and Langat rivers, respectively. Fibre (91.90%) was highly recorded at Kelantan, compared to Langat whereby both fibre (59.21%) and fragment (38.87%) were prevalence. Anthropogenic activities and urbanised areas contribute to high microplastic abundance, especially in the Langat River. Micro-FTIR analysis identified 14 polymers in Kelantan River, whereas 20 polymers were found in Langat River. Polypropylene, polyethylene, polyethylene terephthalate, nylon, phenoxy resins, poly(methyl acrylate), poly(methyl methacrylate), polystyrene, polytetrafluoroethylene, polyurethane and rayon were discovered in both rivers, although only polyethylene was significant (>1 ppm) when further analysed using pyrolysis-GC/MS. Correlation analysis and multiple linear regression were used to explain the relationship between water quality and MP abundance, suggesting only turbidity was positively significant to the microplastic occurrence. This comprehensive study is first to suggest a full-scale monitoring protocol for MPs in Malaysian riverine system and is significant in understanding MPs abundance in correlation to in-situ environmental factors. Consequently, this will allow the right authorities to develop mitigation strategies to address riverine plastic pollution in major river basins in Malaysia and the South East Asia.

Microplastics in surface water from a mighty subtropical estuary: First observations on occurrence, characterization, and contamination assessment.

Estuarine contamination by Microplastics (MPs) is a mater of serious concern since these areas offer the society valuable ecosystem, economic, and recreational services such as breeding and feeding ground for fish, carbon fixation, nutrients recycling and port development. The Meghna estuary, located along the Bengal delta coast, provides livelihoods for thousands of peoples in Bangladesh, and served as breeding ground for national fish, Hilsha shad. Therefore, knowledge and understanding on any kind of pollution including MPs of this estuary is essential. In this study, the abundance, characteristics and contamination assessment of MPs from the surface water of a Meghna estuary were investigated for the first time. The results demonstrated that MPs were present in all samples and the abundance ranged from 33.33 to 316.67 item/m3 with a mean value of 128.89 ± 67.94 item/m3. Morphological analyses resulted in four types of MPs such as fibers (87%), fragments (6%), foam (4%), and films (3%) with the majority of these being colored (62%) and smaller (<0.5 mm) in size (88%). On the other hand, FTIR analysis for chemical characteristics confirmed five types of polymers, including polythene (PE), polystyrene (PS), polythene terephthalate (PET), polypropylene (PP), and polyvinyl chloride (PVC). The area was determined to be moderately to severely contaminated with MPs based on contamination factor (CF) values (6.18 ± 2.08 to 2.50 ± 1.0) and the pollutant load index (PLI) value (1.94 ± 0.33) as these values were > 3-6 for CF, and >1 for PLI. These results can be utilized to develop policy for the protection of this important environment.

The role of packaging on the flavor of fluid milk.

Few studies have addressed the effects of package material in the absence of light on contributions to fluid milk flavor. The objective of this study was to compare the sensory and chemical properties of fluid milk packaged in paperboard cartons, low-density polyethylene, high-density polyethylene (HDPE), polyethylene terephthalate (PET), linear low-density polyethylene (LLDPE), and glass. Pasteurized (high temperature short time, 77°C for 25 s) skim and whole milk were filled (280 mL ± 10 mL) into paperboard cartons, low-density polyethylene, HDPE, PET, LLDPE, and glass (control). Milks were stored at 4°C in the dark and sampled at d 0, 5, 10, and 15. Descriptive analysis was applied to document sensory profiles at each time point, and volatile compounds were extracted and identified by solid-phase microextraction with gas chromatography mass spectrometry and gas chromatography-olfactometry. Tetrad tests with consumers were conducted at d 10. Both skim and whole milks packaged in cartons had noticeable paperboard flavor by d 5 and higher levels of hexanal than skim and whole milks in other package types at d 5. Skim milks packaged in paperboard cartons and LLDPE had distinct refrigerator/stale flavor compared with milks in the other package types, concurrent with increased levels of refrigerator/package-related compounds including styrene, acetophenone and 2-ethyl-1-hexanol. Milks packaged in glass, PET and HDPE were not distinguished by consumers at d 10 post-processing. Package type influences fluid milk flavor, and these effects are greater in skim milk compared with whole milk. Paperboard cartons do not preserve milk freshness, as well as PET, HDPE, or glass, due to flavor migration and scalping. Glass remains an ideal barrier to preserve fluid milk flavor, but in the absence of light, HDPE and PET provide additional benefits while also maintaining fluid milk flavor.

Assessment of barium diffusion from therapeutic mud wrapped in micro-perforated polyethylene bags towards the human organism.

Barium is present within the clay-derived therapeutic mud packs deposed on the patient's skin for treating some rheumatologic conditions. We studied in twenty-four young healthy volunteers the diffusion of Ba from mud wrapped in micro-perforated polyethylene bags and soaked in mineral water. No significant systematic increase in plasma or urine Ba levels was evidenced when comparing pre- and post-treatment samples using inductively-coupled plasma mass spectrometry. These levels were markedly inferior to the recommended thresholds in nearly all the participants. Noticeably variability in blood and especially urine Ba concentrations was large and mainly explained by environmental exposure (alimentation). Interestingly, we evidenced an intense Ba accumulation within the therapeutic mud at the end of the regimen. Because we chose a clay with one of the highest Ba content available in France for medical therapy and participants with an optimal transcutaneous diffusion capacity (young individuals with low-fat mass), we conclude unambiguously that there is no risk of Ba overexposure in patients receiving pelotherapy according to the procedure used in French medical spas.

Preliminary Study on the Role of Mangroves in Entrapping Microplastics in Tuticorin Coast of Gulf of Mannar, Southeast Coast of India.

Mangroves constitute a unique and important type of coastal wetlands in tropical and subtropical zones worldwide. The abundance of microplastics (MPs) in the mangrove sediments is poorly understood. This study aimed to quantify the role of mangrove root systems in effectively entrapping MPs in the mangrove areas of Tuticorin and Punnakayal Estuary. It investigated the abundance, characteristics, and weathering patterns of MPs in different mangrove sediments. Sediment samples were collected from ten mangrove sites and two control sites without mangroves. Microplastics were extracted from mangrove sediments by density separation method, and then counted and categorized according to their shape, size, and colour. Microplastics were identified in all ten sampling sites. Punnakayal Estuary has a greater MPs concentration (27 ± 2.65 items/kg dw) than Tuticorin (9.33 ± 2.52 items/kg dw). Also, microplastic concentrations are higher in the mangrove sites than in the control sites. Most MPs are fibres with size ranges of 1-2 mm and 2-3 mm dominating. Blue and transparent are the predominant colours. Four polymers were identified, namely polyethylene (PE), polypropylene (PP), polymethyl methaacrylate (PMMA), and polyurethane (PUR). The degree of weathering was confirmed by carbonyl index and the values vary between 0.28 and 1.25 for PE and 0.6 and 1.05 for PP.

Identification of microplastics from urban informal solid waste landfill soil; MP associations with COD and chloride.

Microplastics (MPs) are an issue of prime environmental concern globally. The abundance of MP particles in the informal open solid waste landfill soil was evaluated showing 180-1120 MP particles per kg of soil. Moisture content (MC), electrical conductivity (EC) and pH of the MP-contaminated soil compared to the baseline showed 2.96% MC, 187-441 µS/cm EC and 6.94 pH. Morphology of extracted MPs in SEM showed particle fragmentation as film fragments (13.7%), fragments (56.1%), fibres (26.4%) and foam (3.8%). EDS results showed Carbon 71.8% and 24.5% oxygen with traces of Na, Al, Si and Cl-. FTIR of field obtained MPs identified were polyethylene and polypropylene. The association of MP particles with COD and chloride was discovered. MP particles of Low-density Polyethylene of size of 1 mm × 1 mm and thickness 25 µm up to 20 numbers showed no effect adding to the COD values. The COD values increased with increase in MP particle numbers. Similarly, chloride associations with MP particles showed an increase in MP particles reducing chloride values by 31% in landfill runoff water. It is interpreted that MP particle disintegration into nano-sized plastics (NPs) in the soil/runoff water can greatly increase the COD values and impair the salt mass balance.

Investigating biodegradation of polyethylene and polypropylene microplastics in Tehran DWTPs.

Microplastic (MP) pollution is a growing concern and various methods are being sought to alleviate the level of pollution worldwide. This study investigates the biodegradation capacity of MPs by indigenous microorganisms of raw water from Tehran drinking water treatment plants. By exposing polypropylene (PP) and polyethylene (PE) MPs to selected microbial colonies, structural, morphological, and chemical changes were detected by scanning electron microscope (SEM), cell weight measurement, Fourier transform infrared (FTIR), Raman spectroscopy test, and thermal gravimetric analysis (TGA). Selected bacterial strains include Pseudomonas protegens strain (A), Bacillus cereus strain (B), and Pseudomonas protegens strain (C). SEM analysis showed roughness and cracks on PP MPs exposed to strains A and C. However, PE MPs exposed to strain B faced limited degradation. In samples related to strain A, the Raman spectrum was completely changed, and a new chemical structure was created. Both TGA and FTIR analysis confirmed changes detected by Raman analysis of PP and PE MPs in chemical changes in this study. The results of cell dry weight loss for microbial strains A, B, and C were 13.5, 38.6, and 25.6%, respectively. Moreover, MPs weight loss was recorded at 32.6% for PP MPs with strain A, 13.3% for PE MPs with strain B, and 25.6% for PP MPs with strain C.

Plastic waste in sandy beaches and surface water in Thanh Hoa, Vietnam: abundance, characterization, and sources.

The occurrence and characterization of marine debris on beaches bring opportunities to track back the anthropogenic activities around shorelines as well as aid in waste management and control. In this study, the three largest beaches in Thanh Hoa (Vietnam) were examined for plastic waste, including macroplastics (≥ 5 mm) on sandy beaches and microplastics (MPs) (< 5 mm) in surface water. Among 3803 items collected on the beaches, plastic waste accounted for more than 98%. The majority of the plastic wastes found on these beaches were derived from fishing boats and food preservation foam packaging. The FT-IR data indicated that the macroplastics comprised 77% polystyrene, 17% polypropylene, and 6% high-density polyethylene, while MPs discovered in surface water included other forms of plastics such as polyethylene- acrylate, styrene/butadiene rubber gasket, ethylene/propylene copolymer, and zein purified. FT-IR data demonstrated that MPs might also be originated from automobile tire wear, the air, and skincare products, besides being degraded from macroplastics. The highest abundance of MPs was 44.1 items/m3 at Hai Tien beach, while the lowest was 15.5 items/m3 at Sam Son beach. The results showed that fragment form was the most frequent MP shape, accounting for 61.4 ± 14.3% of total MPs. MPs with a diameter smaller than 500 µm accounted for 70.2 ± 7.6% of all MPs. According to our research, MPs were transformed, transported, and accumulated due to anthropogenic activities and environmental processes. This study provided a comprehensive knowledge of plastic waste, essential in devising long-term development strategies in these locations.

Toxicity assessment of polyethylene microplastics in combination with a mix of emerging pollutants on Physalaemus cuvieri tadpoles.

Studies in recent years have shown that aquatic pollution by microplastics (MPs) can be considered to pose additional stress to amphibian populations. However, our knowledge of how MPs affect amphibians is very rudimentary, and even more limited is our understanding of their effects in combination with other emerging pollutants. Thus, we aimed to evaluate the possible toxicity of polyethylene MPs (PE-MPs) (alone or in combination with a mix of pollutants) on the health of Physalaemus cuvieri tadpoles. After 30 days of exposure, multiple biomarkers were measured, including morphological, biometric, and developmental indices, behavioral parameters, mutagenicity, cytotoxicity, antioxidant and cholinesterase responses, as well as the uptake and accumulation of PE-MPs in animals. Based on the results, there was no significant change in any of the parameters measured in tadpoles exposed to treatments, but induced stress was observed in tadpoles exposed to PE-MPs combined with the mixture of pollutants, reflecting significant changes in physiological and biochemical responses. Through principal component analysis (PCA) and integrated biomarker response (IBR) assessment, effects induced by pollutants in each test group were distinguished, confirming that the exposure of P. cuvieri tadpoles to the PE-MPs in combination with a mix of emerging pollutants induces an enhanced stress response, although the uptake and accumulation of PE-MPs in these animals was reduced. Thus, our study provides new insight into the danger to amphibians of MPs coexisting with other pollutants in aquatic environments.

Identification and Quantification of Nanoplastics in Surface Water and Groundwater by Pyrolysis Gas Chromatography-Mass Spectrometry.

Nanoplastics (NPs) are currently considered an environmental pollutant of concern, but the actual extent of NP pollution in environmental water bodies remains unclear and there is not enough quantitative data to conduct proper risk assessments. In this study, a pretreatment method combining ultrafiltration (UF, 100 kDa) with hydrogen peroxide digestion and subsequent detection with pyrolysis gas chromatography-mass spectrometry (Py-GC/MS) was developed and used to identify and quantify six selected NPs in surface water (SW) and groundwater (GW), including poly(vinylchloride) (PVC), poly(methyl methacrylate) (PMMA), polypropylene (PP), polystyrene (PS), polyethylene (PE), and poly(ethylene terephthalate) (PET). The results show that the proposed method could detect NPs in environmental water samples. Nearly all selected NPs could be detected in the surface water at all locations, while PVC, PMMA, PS, and PET NPs were frequently below the detection limit in the groundwater. PP (32.9-69.9%) and PE (21.3-44.3%) NPs were the dominant components in both surface water and groundwater, although there were significant differences in the pollution levels attributed to the filtration efficiency of riverbank, with total mass concentrations of 0.283-0.793 µg/L (SW) and 0.021-0.203 µg/L (GW). Overall, this study quantified the NPs in complex aquatic environments for the first time, filling in gaps in our knowledge about NP pollution levels and providing a useful methodology and important reference data for future research.

Identification and Quantification of Microplastics in the Marine Environment Using the Laser Direct Infrared (LDIR) Technique.

Here, we evaluate for the first time the performances of the newly developed laser direct infrared (LDIR) technique and propose an optimization of the initial protocol for marine microplastics (MPs) analysis. Our results show that an 8 µm porosity polycarbonate filter placed on a Kevley slide enables preconcentration and efficient quantification of MPs, as well as polymer and size determination of reference plastic pellets of polypropylene (PP), polyethylene (PE), polystyrene (PS), polyvinyl chloride (PVC), and polyethylene terephthalate (PET), with recoveries ranging from 80-100% and negligible blank values for particle sizes ranging from 200 to 500 µm. A spiked experiment using seawater, sediment, mussels, and fish stomach samples showed that the method responded linearly with significant slopes (R2 ranging from 0.93-1.0; p < 0.001, p < 0.01). Overall, 11 polymer types were identified with limited handling and an analysis time of ca. 3 h for most samples and 6 h for complex samples. Application of this technique to Mediterranean marine samples (seawater, sediment, fish stomachs and mussels) indicated MP concentrations and size distribution consistent with the literature. A high predominance of PVC (sediment, fish stomachs) and PE and PP (seawater, mussels) was observed in the analyzed samples.

A quantitative and qualitative assessment of microplastics collected at two public beaches along the east and south-east coast of Mauritius.

Microplastics had been collected at two sites namely Trou d'eau Douce (TD) and La Cambuse (LC) public beaches, lying in the east coast and south-east coast of Mauritius, respectively, over 6 months from September 2019 to February 2020. The sizes of the latter varied from 180 µm to 4 mm. A higher amount of microplastics collected/6-kg sand sample was recorded at LC. Two-way ANOVA revealed that (1) there was a considerable gap in the variability regarding quantity and size distribution of microplastics on the two beaches. The post-hoc analysis showed that the majority of the microplastics at LC were > 1.40 mm, whereas the smaller plastic fragments < 1.40 mm were more dominant at TD. (2) There was a significant interaction between location and event (p value = 0.025). The post-hoc analysis showed that the torrential rain hitting the island prior to sampling week 7 had decreased the microplastic counts at both TD and LC, but not significantly. Interestingly, the two hurricanes, prior to weeks 8 and 9, had appreciably reduced the microplastic counts at TD and, on the other hand, there was an increase in the amount of microplastics at LC, but not to a significant effect. The chemical nature (qualitative analysis) of microplastics was determined by density flotation and FTIR spectroscopy. Microplastics at TD were exclusively high-density polyethylene (HDPE) in origin, whereas, at LC, microplastics were both HDPE and polypropylene (PP) in origin.

Spatial, seasonal and ecological risk assessment of microplastics in sediment and surface water along the Thoothukudi, south Tamil Nadu, south east India.

Microplastics are a widespread environmental contaminant that raises serious concern for aquatic organisms. Hence, the present study was conducted to investigate the spatial and seasonal variation of microplastics, their characteristics, polymer types and the risk assessment caused by the microplastics in six sampling sites along the Thoothukudi region. The average microplastic abundance ranged from 32 ± 26 to 232 ± 229 items/kg and 54 ± 41 to 619 ± 377 items/l in sediment and surface water, respectively, and they exhibited a significant spatial difference among the sampling sites. The microplastic abundance also showed a significant difference among the seasons with the monsoon significantly recording the highest mean microplastic abundance in sediment (160 ± 130 items/kg) and surface water (454 ± 374 items/l). In sediment and surface water, fragment (sediment: 52.72%, surface water: 40.89%), 0.5-1 mm (sediment: 43.96%, surface water: 31.11%) and blue-coloured (sediment: 52.33%, surface water: 41.85%) microplastics were dominant with no significant difference both spatially and seasonally. Polyethylene, the dominant polymer, was observed in both the sediment and surface water, accounting for about 47.58% and 49.83%, respectively, and it showed no significant difference among the selected sites. This signifies that they are homogenously distributed along the coast and further suggests that these particles persisted in the sediment and surface water for a longer period of time. The results of the polymer hazard index show that the sediment (PHI = 1181.63) and surface water (PHI = 1018.66) were severely contaminated (hazard level V) with microplastic polymers such as PE, PP, PS, PET and PA. It was also found that the degree of the microplastic contamination in sediment (PLI = 3.57) and surface water (PLI = 3.84) was lower (hazard level I). The overall risk index (RI) for sediment (253.48) and surface water (444.74) falls under the higher risk category. From the correlation analysis, a significantly positive relationship was observed between microplastics in sediment and surface water based on each classification (abundance, shape, size, colour and polymer). This suggests that microplastics rejoin the water column from the sediment through resuspension, which occurs due to the circulation, tides and sedimentation rate. This might be the reason for the higher microplastic abundance in the surface water than in the sediment. As a result, proper management measures to reduce plastic waste disposal in the marine environment should be implemented to lessen the effects of microplastics on marine biota and on public health.