No anthropogenic pollutant is more widespread in the aquatic and terrestrial environment than microplastic; however, there are large knowledge gaps regarding its origin, fate, or temporal variations in the oceans. In this study, we analyzed sediment trap material from the deep subtropical Northeast Atlantic (2000 m) in a long-term record (2003–2015) to assess the role of the deep ocean as a potential sink of microplastics. Microplastic particles were identified in all 110 analyzed samples with flux rates of 1.13–3146.81 items d⁻¹ m⁻². Calculated microplastic mass fluxes ranged between 0.10 and 1977.96 μg d⁻¹ m⁻², representing up to 8% of the particle flux. Between years, the composition of the different polymers changed significantly, dominated by polyethylene, whose amount was correlated with the lithogenic input. The correlation between polyethylene and the lithogenic fraction was attributed to an air transport pathway from northeast Africa and surrounding regions. The second most abundant polymer detected in our study was polyvinyl chloride, which is not correlated with lithogenic or biogenic particle flux fractions. Instead, we observed seasonality for polyvinyl chloride with recurring high fluxes in winter before the plankton bloom and significantly lower amounts in summer. Other polymers identified were polypropylene, polyethylene terephthalate, and lower numbers of polystyrene and polymethyl methacrylate. The average microplastic particle size for all samples and polymers was 88.44 ± 113.46 μm, with polyethylene and polyvinyl chloride having the highest proportion of small particles (<100 μm). Our findings provide first insights into temporal variations of sinking microplastics, which are crucial for understanding the fate of plastic in the oceans.

Using simple models, coupled with parameters extracted from published studies, the annual inputs of macro and micro plastics to the Scottish Atlantic Coast and the Scottish North Sea Coast regions are estimated. Two estimates of land-based sources are used, scaled by catchment area population size. The oceanic supply of floating plastic is estimated for wind-driven and general circulation sources. Minimum, typical and maximum values are computed to examine the magnitude of uncertainties. Direct inputs from fishing and the flux of macroplastic onto the seabed are also included. The modelled estimates reveal the importance of local litter sources to Scottish coastal regions, and hence local management actions can be effective. Estimates provide a scale against which removal efforts may be compared, and provide input data for future more complex modelling. Recommendations for research to improve the preliminary estimates are provided. Methods presented here may be useful elsewhere.

This study reports plastic ingestion in various fish found from coastal and offshore sites in Scottish marine waters. Coastal samples consisted of three demersal flatfish species (n=128) collected from the East and West coasts of Scotland. Offshore samples consisted of 5 pelagic species and 4 demersal species (n=84) collected from the Northeast Atlantic. From the coastal fish sampled, 47.7% of the gastrointestinal tracts contained macroplastic and microplastic. Of the 84 pelagic and demersal offshore fish, only 2 (2.4%) individuals from different species had ingested plastic identified as a clear polystyrene fibre and a black polyamide fibre. The average number of plastic items found per fish from all locations that had ingested plastic was 1.8 (±1.7) with polyamide (65.3%), polyethylene terephthalate (14.4%) and acrylic (14.4%) being the three most commonly found plastics. This study adds to the existing data on macroplastic and microplastic ingestion in fish species.

Particle flux material collected in 2000 m depth in the Northeast Atlantic at 33°N and 22°W was analyzed for trace metals and persistent organic pollutants. Element enrichment factors relative to lithogenic Al were elevated indicating possible anthropogenic contributions for all trace metals except V. Polycyclic aromatic hydrocarbons, polychlorinated biphenyls and the pesticide DDT exhibited median fluxes of 10.40 μg m⁻²d⁻¹,0.29 μg m⁻² d⁻¹, and 0.90 μg m⁻² d⁻¹, respectively. Flux composition reflected long range transport, with low molecular weight and low-chlorinated compounds dominating ∑₁₅PAH and ∑₂₃PCB. PAH isomer ratios identified fossil fuel combustion as the main ∑₁₅PAH source. The composition of ∑₄DDT suggested inputs of the fresh technical pesticide during high dust intensity periods. Pollutant fluxes showed seasonality linked to export production in the region, as well as a dependence on annual and sub-annual dust input events.