Horse mackerel is a semi-pelagic species found in abundance in the Moroccan coasts and occupies the first ranks in the catches landed by the coastal fleet. In this study, we investigated the ingestion of Polyamide, Acrylic and Polystyrene by Atlantic horse mackerel, in the Moroccan Atlantic coastal area located between Larache (35°30′N) and Boujdour (26°30′N). The objective is to map the spatial distribution of horse Mackerel containing microplastics (MPs) in their stomachs and identify hot spot areas. We also aim to verify the most ingested polymer by this fish characterized by significant daily vertical migrations. The results show that the three studied polymers were detected in the stomach contents of more than 73% of studied fishes. The hot spot areas are located more in the northern part where urbanization and fishing activity are important. Polyamide, the densest polymer, is the most abundant (86% of cases), followed by acrylic. These two polymers were found in association in 47% of cases. No correlation between the presence of MPs in the stomach contents and the size of the individual fishes was noted. Interestingly, the group of mature specimens ingested more MPs than the immature group.

Microplastics are emerging contaminants and widely distributed in the environment. They are considered as a vector of numerous organic pollutants including antibiotics in aquatic environments and thereby influence their distribution and transport behaviors. However, the effects of microplastics on the environmental behavior of antibiotics in soils remain largely unclear. In this paper, the influence of polyamide (PA) microplastics on sorption and transport of the selected antibiotic [oxytetracycline (OTC)] in a sandy loamy soil was studied by performing batch and column experiments. Results show that PA microplastics increase the pH of reaction systems, which contributes to OTC sorption onto the tested soils. However, altering pH is not the key influencing mechanism because the overall sorption capacity decreases slightly after adding PA microplastics, which can be attributed to the dilution effect. Reduction of OTC sorption by adding microplastics promotes the migration of OTC in the tested soil, which could be demonstrated by the results of column experiments that the breakthrough of OTC occurs earlier with an increasing content of PA microplastics. According to the fitting parameters of HYDRUS−1D model, PA microplastics can affect the transport of OTC by altering the soil pore structure and dispersion coefficient. These results provide new insight into the interaction between microplastics and organic pollutants in soil environments.

Rivers are viewed as major pathways of microplastic transport from terrestrial areas to marine ecosystems. However, there is paucity of knowledge on the dispersal pattern and transport of microplastics in river sediments. In this study, a three dimensional hydrodynamic and particle transport modelling framework was created to investigate the dispersal and transport processes of microplastic particles commonly present in the environment, namely, polyethylene (PE), polypropylene (PP), polyamide (PA), and polyethylene terephthalate (PET) in river sediments. The study outcomes confirmed that sedimental microplastics with lower density would have higher mobility. PE and PP are likely to be transported for a relatively longer distance, while PA and PET would likely accumulate close to source points. High water flow would transport more microplastics from source points, and high flow velocity in bottom water layer are suggested to facilitate the transport of sedimental microplastics. Considering the limited dispersal and transport, the study outcomes indicated that river sediments would act as a sink for microplastic pollutants instead of being a transport pathway. The patchiness associated with the hotspots of different plastic types is expected to provide valuable information for microplastic source tracking.

This study reports the shapes, dimensional classes, types and counts of microplastics (MPs) found in 23 individuals of N. norvegicus collected from two wild populations of the Adriatic Sea (Mediterranean basin). The focus was on three different anatomical compartments (gut, hepatopancreas and tail), which were analysed separately. MPs were found in all the investigated individuals with an average of about 17 MPs/individual. Fragments were predominant over fibers with a ratio of about 3:1. The majority of MPs were in the dimensional range 50–100 μm. The predominant polymers were polyester, polyamide 6, polyvinyl chloride and polyethylene, which together constitute about 61% of all the MPs found. Fragments were more concentrated in the hepatopancreas, with no significant difference between gut and tail, while fibers were more concentrated in the gut than in the tail with hepatopancreas somehow in between. The dimensional class of the MPs influences their anatomical distribution. There were no statistical differences among individuals from the two sampling sites. Sex of the individual did not influence the level of retained MPs, while length had a very marginal effect. The information reported here contributes to understanding of the possible risks linked to human consumption of different tissues from contaminated Norway lobsters.

Limited attention has been given to the presence of MPs in the atmospheric environment, particularly in indoor environments where people spend about 90% of their time. This study quantitatively assesses the prevalence, source and type of MPs in Australian homes with the goal of evaluating human health exposure potential. Thirty-two airborne indoor deposited dust samples were collected in glass Petri dishes from Sydney (Australia) homes, over a one-month period in 2019. Participants completed a questionnaire on their household characteristics. Samples were analysed using a stereomicroscope, a fluorescent microscope and micro-Fourier transform infrared (FTIR) spectroscopy for their colour, size, shape and composition. Inhalation and ingestion rates were modelled using US EPA exposure factors. Microplastic fibre deposition rates ranged from 22 to 6169 fibres/m²/day. Deposited dust comprised 99% fibres. The highest proportion of fibres (19%) were 200–400 μm in length. The majority were natural (42%); 18% were transformed natural-based fibres; and 39% were petrochemical based. A significant difference was observed between the deposition rate and the main floor covering (p-value <0.05). Polyethylene, polyester, polyamide, polyacrylic, and polystyrene fibres were found in higher abundance in homes with carpet as the main floor covering. Where carpet was absent, polyvinyl fibres were the most dominant petrochemical fibre type, indicating the role of flooring materials (e.g. wood varnishes) in determining MP composition. Vacuum cleaner use was significantly related to MP deposition rates (p-value <0.05). MP ingestion rates peaked at 6.1 mg/kg-Bw/year for ages 1–6, falling to a minimum of 0.5 mg/kg-Bw/year in >20 years age group. Mean inhaled MP weight and count was determined to be 0.2±0.07 mg/kg-Bw/year and 12891±4472 fibres/year. Greatest inhalation intake rates were for the <0.5-yr age group, at 0.31 mg/kg-Bw/year. The study data reveal that MPs are prevalent in Australian homes and that the greatest risk of exposure resides with young children. Notwithstanding the limited number of global studies and the different methods used to measure MPs, this study indicates Australian deposition and inhalation rates are at the lower end of the exposure spectrum.

Polycyclic aromatic hydrocarbons are widespread and environmentally persistent chemicals that readily bind to particles in air, soil and sediment. Plastic particles, which are also an ubiquitous global contamination problem, may thus modulate their environmental fate and ecotoxicity. First, the acute aqueous toxicity of phenanthrene in adult Gammarus roeseli was determined with a LC₅₀ of 471 μg/L after 24 h and 441 μg/L after 48 h. Second, considering lethal and sublethal endpoints, effects of phenanthrene concentration on G. roeseli were assessed in relation to the presence of anthropogenic and natural particles. The exposure of gammarids in presence of either particle type with phenanthrene resulted after 24 and 48 h in reduced effect size. Particle exposure alone did not result in any effects. The observed reduction of phenanthrene toxicity by polyamide contradicts the discussion of microplastics acting as a vector or synergistically. Especially, no difference in modulation by plastic particles and naturally occurring sediment particles was measured. These findings can most likely be explained by the similar adsorption of phenanthrene to both particle types resulting in reduced bioavailability.

The microplastic particles with 29 pyrolyzate compounds of marine water samples from the seashore locations in Cape Town, South Africa were analysed using Pyrolysis- GC-TOF-MS. The mass spectra data documented the presence of various chemical groups that include alkanes, alkenes, dienes, fatty acids and esters, biphenyl and benzene (along with derivatives). Out of 16 identified polymers in the study area, polythene (PE) was the dominant in six out of seven locations with 87.5% followed by polyethylene terephthalate (PET) and polyvinylchloride (PVC) in five (71.4%) and four (57.1%) out of seven locations respectively. The other constituent polymers of microplastics identified through pyrolyzates were polystyrene (PS), polyamide 12 (PA-12) polyacrylic acid (PAA) and ethyl vinyl acetate (EVA) copolymer. The microplastic samples contained six additives predominantly in the family of fatty acid esters and nine plasticizers from alcohols, carboxylic esters and acids. The base peaks of m/z 41, 43, 55, 57, 69, 73, 91, 102, 105, 127 and 154 were characterized respectively with the fragmented species of C₃H₅⁺, C₃H₇⁺, C₄H₇⁺, C₄H₉⁺, C₅H₉⁺, C₃H₅O₂⁺, C₇H₇⁺, C₃H₁₀O₂⁺(McLafferty ion), C₈H₉⁺, C₈H₁₅O⁺ and C₁₂H₁₀⁺. Accordingly to Globally Harmonized System (GHS) of hazard classification, about 27.4% of pyrolyzates are Irritants, 31.4% of pyrolyzates found to be Irritants along with other hazards such as Flammable, Compressed Gas, Environmental Hazard, Corrosive, Health Hazard, Acute Toxicity and Allergy. About 41.2% of the pyrolyzates are not classified under the Irritant category. Characterizations of the plastic microparticles from the seven seashore locations such as FTIR, SEM with EDX and TGA were also done and discussed to understand the functional groups, surface morphology with elemental composition and stability respectively of the polymeric microparticles.

The Tibet Plateau, the so-called Third Pole of the world, is home to the headstreams of many great rivers. The levels of microplastic pollution in those rivers, however, are unknown. In this study, surface water and sediment samples were collected from six sampling sites along five different rivers. The surface water and sediment samples were collected with a large flow sampler and a stainless steel shovel, respectively. The abundance of microplastics ranged from 483 to 967 items/m3 in the surface water and from 50 to 195 items/kg in the sediment. A large amount of small, fibrous, transparent microplastics were found in this study. Five types of microplastics with different chemical compositions were identified using micro-Raman spectroscopy: polyethylene terephthalate (PET), polyethylene (PE), polypropylene (PP), polystyrene (PS), and polyamide (PA). These results demonstrate that rivers in the Tibet Plateau have been contaminated by microplastics, not only in developed areas with intense human activity but also in remote areas, where microplastic pollution requires further attention.

Although evidence suggests the ubiquity of microplastics in the marine environment, our knowledge of its occurrence within remote habitats, such as the deep sea, is scarce. Furthermore, long term investigations of microplastic abundances are even more limited. Here we present a long-term study of the ingestion of microplastics by two deep-sea benthic invertebrates (Ophiomusium lymani and Hymenaster pellucidus) sampled over four decades. Specimens were collected between the years 1976–2015 from a repeat monitoring site >2000 m deep in the Rockall Trough, North East Atlantic. Microplastics were identified at a relatively consistent level throughout and therefore may have been present at this locality prior to 1976. Considering the mass production of plastics began in the 1940s - 50s our data suggest the relatively rapid occurrence of microplastics within the deep sea. Of the individuals examined (n = 153), 45% had ingested microplastics, of which fibres were most prevalent (95%). A total of eight different polymer types were isolated; polyamide and polyester were found in the highest concentrations and in the majority of years, while low-density polystyrene was only identified in 2015. This study provides an assessment of the historic occurrence of microplastics on the deep seafloor and presents a detailed quantification and characterisation of microplastics ingested by benthic species. Furthermore these data advance our knowledge on the long-term fate of microplastic in marine systems.

Although the hazards of microplastics (MPs) have been quite well explored, the aberrant metabolism and the involvement of the autophagy pathway as an adverse response to environmental MPs in benthic organisms are still unclear. The present work aims to assess the impact of different environmental MPs collected from the south coast of the Mediterranean Sea, composed by polyethylene (PE), polyethylene vinyl acetate (PEVA), low-density polyethylene (LDPE), high-density polyethylene (HDPE), polypropylene (PP) and polyamide (PA) on the metabolome and proteome of the marine polychaete Hediste diversicolor. As a result, all the microplastic types were detected with Raman microspectroscopy in polychaetes tissues, causing cytoskeleton damage and induced autophagy pathway manifested by immunohistochemical labeling of specific targeted proteins, through Tubulin (Tub), Microtubule-associated protein light chain 3 (LC3), and p62 (also named Sequestosome 1). Metabolomics was conducted to further investigate the metabolic alterations induced by the environmental MPs-mixture in polychaetes. A total of 28 metabolites were differentially expressed between control and MPs-treated polychaetes, which showed elevated levels of amino acids, glucose, ATP/ADP, osmolytes, glutathione, choline and phosphocholine, and reduced concentration of aspartate. These novel findings extend our understanding given the toxicity of environmental microplastics and unravel their underlying mechanisms.