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Progress to reduce plastic pollution has been painfully slow and the consequent damage to the natural environment and to human health is likely to increase further. This has been because the views and ways of working of four distinct stakeholder communities are not sufficiently well integrated. (1) Scientists, (2) industry, (3) society at large and (4) those making policy and legislation must in future find ways to work together.

Plastics debris in the marine environment, including resin pellets, fragments and microscopic plastic fragments, contain organic contaminants, including polychlorinated biphenyls (PCBs), polycyclic aromatic hydrocarbons, petroleum hydrocarbons, organochlorine pesticides (2,2-bis(p-chlorophenyl)-1,1,1-trichloroethane, hexachlorinated hexanes), polybrominated diphenylethers, alkylphenols and bisphenol A, at concentrations from sub ng g1 to g g1. Some of these compounds are added during plastics manufacture, while others adsorb from the surrounding seawater. Concentrations of hydrophobic contaminants adsorbed on plastics showed distinct spatial variations reflecting global pollution patterns. Model calculations and experimental observations consistently show that polyethylene accumulates more organic contaminants than other plastics such as polypropylene and polyvinyl chloride. Both a mathematical model using equilibrium partitioning and experimental data have demonstrated the transfer of contaminants from plastic to organisms. A feeding experiment indicated that PCBs could transfer from contaminated plastics to streaked shearwater chicks. Plasticizers, other plastics additives and constitutional monomers also present potential threats in terrestrial environments because they can leach from waste disposal sites into groundwater and/or surface waters. Leaching and degradation of plasticizers and polymers are complex phenomena dependent on environmental conditions in the landfill and the chemical properties of each additive. Bisphenol A concentrations in leachates from municipal waste disposal sites in tropical Asia ranged from sub g l1 to mg l1 and were correlated with the level of economic development.

Oil pollution in the marine environment is an unavoidable problem due to chronic input from local sources, particularly in urban areas and oil spills. Oil pollution not only causes immediate physical damages to surrounding wildlife but also some components, including higher molecular weight PAHs, can persist in the environment for many years and pose insidious threats to the ecosystem. Long-term and nontargeted monitoring of oil pollution is important. This paper examines the ability of International Pellet Watch (IPW) for initial identification and monitoring of oil pollution by analysing PAHs and hopanes in plastic pellet samples collected globally by volunteers. PAH concentrations with the sum of 28 parent and methyl PAHs vary geographically, ranging from 0.035 to 24.4 µg/g-pellet, in line with the presence or absence of local oil pollution sources, such as oil refineries or oil spill sites. This suggests that PAHs can be used to monitor petroleum pollution in IPW. A colour-coded categorization for PAH concentrations within IPW monitoring also is established to facilitate data presentation and understanding. PAH concentrations are generally higher in Western Europe, especially around the North Sea shorelines, moderate in East Asia and North America, and lower in South East Asia, Oceania, South America, and Africa. Hopane concentrations, with a smaller spatial variation (1.7–101 µg/g-pellet), showed no spatial pattern. This result and the poor correlation between hopanes and PAHs suggest that hopane concentrations alone are unsuited to identify petroleum pollution. However, hopane compositions can be used for fingerprinting sources of oil pollution. Thus, both PAHs and hopanes in IPW allow for low cost, remote monitoring of global oil pollution.

Polycyclic aromatic hydrocarbons (PAHs) are major air pollutants that are ubiquitously produced by the combustion of organic materials, and it is extremely important to identify their pollution sources. In this study, molecular fingerprinting and compound class-specific radiocarbon dating (CCSRA) were performed on PAHs from canal sediments and air samples collected in Kolkata, India’s third largest city (population approximately 16 million), where PAHs pollution has been a serious problem. Average PAH (Σ12-parent PAHs) concentrations in air samples were 65.1 ng m–3 in summer and 70.9 ng m–3 in winter and in canal sediments were 32.7 µg g–1, which are classified as “very high-level” pollution. Molecular fingerprinting using methyl-PAH/PAH (MPAHs/PAHs) ratios and isomer pair ratios with molecular weights of 178, 202, 228, and 276 suggested that wood and coal combustion were the dominant sources of PAHs in the sediment, and that atmospheric PAHs were influenced by oil combustion in addition to them. The fraction of contemporary carbon (ƒC) of sedimentary PAHs (0.056–0.100), together with the extremely low MPAHs/PAHs ratio results, lead to the conclusion that the major source of the high concentration of PAHs in the canals is from coal combustion. On the other hand, the ƒC of atmospheric PAHs (0.272–0.369) was close to the share of biomass fuels in India’s domestic fuel consumption in 2011 (about 35%). Furthermore, the observed ƒC-discrepancy between atmospheric and sedimentary PAHs in the same urban environment was interpreted to give an insight into the loading pathway of PAHs to canal sediments in Kolkata.

Perfluorinated surfactants (PFSs) in Asian freshwater fish species were analyzed to investigate tissue distribution, temporal trends, extent of pollution, and level of PFS exposure through food intake. Freshwater fish species, namely carp, snakehead, and catfish, were collected in Japan, Vietnam, India, Malaysia, and Thailand, and 10 PFSs, including perfluorooctanesulfonate (PFOS) and perfluorooctanoate, were analyzed by liquid chromatography–tandem mass spectrometry. PFSs in carp in Tokyo were more concentrated in kidneys (Σ10 PFSs = 257 ± 95 ng/g wet weight [ww]) and livers (119 ± 36 ng/g ww) than in ovaries (43 ± 2 ng/g ww) and muscles (24 ± 17 ng/g ww). Concentrations of PFOS and its precursor, perfluorooctane sulfonamide, in livers of carp and in waters in Tokyo showed a dramatic decrease during the last decade, probably because of 3 M’s phasing-out of the manufacture of perfluorooctanesulfonyl-fluoride-based products in 2000. In contrast, continuing contamination by long-chain perfluorocarboxylates (PFCAs) with ≥ 9 fluorinated carbons was seen in multiple media, suggesting that these compounds continue to be emitted. PFS concentrations in freshwater fish species in tropical Asian countries were generally lower than those in developed countries, such as Japan, e.g., for PFOS in muscle, Vietnam < 0.05–0.3 ng/g ww; India < 0.05–0.2 ng/g ww; Malaysia < 0.05–0.2 ng/g ww; Thailand < 0.05 ng/g ww; and Japan (Tokyo) = 5.1–22 ng/g ww. Daily intake of short-chain PFCAs with ≤ 8 fluorinated carbons from freshwater fish species in Japan was approximately one order of magnitude lower than that from drinking water, whereas daily intake of PFOS and long-chain PFCAs with ≥ 9 fluorinated carbons from freshwater fish species was comparable with or greater than that from drinking water. Because the risk posed by exposure to these compounds through intake of fish species is a matter of concern, we recommend the continued monitoring of PFS levels in Asian developing countries.

The environmental impacts of microplastics (MPs) and nanoplastics (NPs), and their occurrence in aquatic, terrestrial, and aerial biomes have engrossed global attention. Most impact assessment studies have majorly linked the ecological hazards of MPs with the leaching of their additives, and the sorption and transport of co-contaminants due to prolonged environmental exposure. However, it is unclear whether the fresh (unaged) polymers themselves could significantly impact the biota. In this study, we have reported the impacts of virgin polypropylene (PP), polyvinyl chloride (PVC), and polylactic acid (PLA) MPs (0%, 0.05%, 0.1%, and 0.5% w/w dry soil) on the germination of an agricultural herb, coriander (Coriandrum sativum L.), under outdoor (field pots) and indoor (greenhouse) conditions. We observed that all three polymeric MPs in the soil delayed the germination (60–100% inhibition up to day 7) and impacted the seedling length within the 30-day exposure. The inhibitory effect was higher in the field than in the greenhouse. PVC showed the highest inhibition of germination under both conditions, followed by PP and PLA. PLA impaired the root length of the seedlings more than PP and PVC. At 0.5% (w/w), all polymers showed significantly elevated levels of reactive oxygen species in the root tips than control, suggesting MP-induced oxidative stress as a potential mechanism behind the impaired germination and seedling growth. These results clearly indicated a potential decline in crop survival and productivity caused by virgin MPs. The findings proposed that the soil MPs could be a global threat to the plants and ecosystem succession.

Polybrominated diphenyl ethers (PBDEs) are extensively used as flame retardants in many consumer products, and leachates from landfills have been identified as one of the possible sources of PBDEs in the environment. Meanwhile, the unprecedented economic and population growths of some Asian countries over the last decade have led to significant increases in the amount of waste containing PBDEs in that region. This study investigates the status of PBDEs in leachates from municipal solid waste dumping sites (MSWDS) in tropical Asian countries. A total of 46 PBDE congeners were measured, both in the adsorbed ( n  = 24) and dissolved ( n  = 16) phases, in leachate samples collected, from 2002 to 2010, from ten MSWDS distributed among the eight countries of Lao PDR, Cambodia, Vietnam, India, Indonesia, Thailand, the Philippines, and Malaysia. PBDEs were predominantly found in the adsorbed phase. Partitioning of PBDEs in the dissolved phase was associated with the presence of dissolved organic matter; the apparent organic carbon-normalized partition coefficients ( K ′ oc ) of the BDE congeners were lower by two to four orders of magnitude than the K oc predicted from the octanol–water partition coefficients ( K ow ). The total PBDE concentrations from mono- to deca-BDEs ranged from 3.7 to 133,000 ng/L, and showed a trend toward higher concentrations in the more populous and industrialized Asian countries. The congener profiles in the leachates basically reflected the composition of PBDE technical mixtures. The occurrence of congeners not contained, or in trace concentrations, in technical products (e.g., BDEs 208, 207, 206, 202, 188, 179, 49, 17/25, 8, 1) was observed in most of the leachate samples, suggesting the debromination of technical mixtures, including BDE-209, in the MSWDS of tropical Asian countries. Moreover, the temporal trend indicated the reduction of BDE-209 over time, with a corresponding increase in and/or emergence of lower brominated PBDE congeners. The results indicated that MSWDS of tropical Asian countries are potential sources of environmental PBDEs, which may be transported to the aquatic environment via dissolution with dissolved organic matter. MSWDS could be amplifiers of PBDE toxicity in the environment, possibly through debromination.

In this study, the abundance of microplastics (MPs) in the Uppanar and Gadilam estuaries in Cuddalore, on the southeast coast of India, is reported. In the estuarine sediments, MP abundance ranged from 36.3 ± 3.39 to 51.6 ± 2.05 particles/Kg dw. Different types of MP shapes, such as fibers (41.7–47.9%), films (21.2–27.2%), and fragments (18.3–25.5%) were observed in the size range of 100–1000 µm. Diverse colours of MPs were observed, among which red (30.1–34.5%) was predominantly noticed in the estuarine sediments. Six polymers were identified by µ-FTIR, among which LDPE (39%) and PP (35%) were dominant. MPs pollution in these estuaries is composed of domestic, industrial, and fishing wastes. Risk assessments show that the area falls under hazard categories I to III, indicating low to high risk. This study improves knowledge on MPs contamination in Uppanar and Gadilam estuaries and provides impetus for further research to identify the actual sources and impacts of MPs on aquatic systems along the east coast of India.

Microplastic pellets (MPPs) are one of the significant sources of plastic pollution on shorelines worldwide. In this study, for the first time, we have examined the occurrence of MPPs and their spatial and seasonal distributions, adsorbed contaminants, polymer composition, and ecological risks at eight renowned beaches of Andhra Pradesh, central east coast of India. A total of 3950 MPPs were collected from eight beaches along the central east coast of India during October 2020, representing pre-northeast monsoon (pNEM), and during January 2021, representing the northeast monsoon (NEM). The abundance of MPPs was higher during the NEM than those found in the pNEM. ATR-FTIR and SEM analyses were conducted to characterize the polymer types and weathering patterns of MPPs. Energy-Dispersive X-ray spectrometer (EDS) results show the MPP adsorbance of heavy metals such as Ni, Cr, Cu, Pb, and Zn. The degree of contamination and polymer hazard risks of MPPs were assessed using the pollution load index (PLI) and polymer hazard index (PHI). The conducive wind and currents during the NEM lead to higher MPP abundance than during the pNEM. However, the spatial variations of MPPs showed significant differences among the beaches. This study revealed that the presence of MPPs on the beaches along the central east coast of India might pose a considerable polymer hazard risk to the ecosystem. The substantial surface weathering features of MPPs would lead to more toxic nanoplastics in the future.

Microplastic (MP) content in the gastropod, Telescopium telescopium, collected from the mangrove forest of Versova Creek, Mumbai was investigated. In total, 60 specimens were collected and pooled into six groups of 10 animals, each according to their weight and size. The concentration of extracted MP was expressed as the number of MP particles g-1 soft tissue (wet weight) and Ind.-1 (individual). MP was detected in all six groups and ranged from ~1 to 4 MP/g soft tissue and -4 to 23 MP/individual. The minimum number of MP both in soft tissue and in each individual were 1.12 MP/g and 3.6 MP/Ind, respectively, and were found to be present in the lowest wet weight group (3.21±0.33 g). The size of the longest dimension of MP varied from 21-435 pm, most of which were smaller than 100 pm. The majority of the MP found in each weight group were colorless and transparent fragments were the most prevalent shape (55.20%). FTIR analysis showed polyethylene, polypropylene, and polyurethane were the major polymer types. The study reports the microplastic content in a gastropod, Telescopium inhabiting the mangroves of Mumbai, India. As an algal feeder/detritivore, the presence of MP in its soft tissue suggests molluscans are prone to consuming MP, relative to the environmental availability. They had a higher proportion of MP than body weight, indicating the potential transfer of MP into higher trophic levels of the mangrove ecosystem. Irregular fragment MP dominance indicates Telescopium graze on weathered plastic items covered by fouling algae and contributes to MP formation.