Although plastic is ubiquitous in marine systems, our current knowledge of transport mechanisms is limited. Much of the plastic entering the ocean sinks; this is intuitively obvious for polymers such ...as polystyrene (PS), which have a greater density than seawater, but lower density polymers like polyethylene (PE) also occur in sediments. Biofouling can cause large plastic objects to sink, but this phenomenon has not been described for microplastics <5 mm. We incubated PS and PE microplastic particles in estuarine and coastal waters to determine how biofouling changes their sinking behavior. Sinking velocities of PS increased by 16% in estuarine water (salinity 9.8) and 81% in marine water (salinity 36) after 6 weeks of incubation. Thereafter sinking velocities decreased due to lower water temperatures and reduced light availability. Biofouling did not cause PE to sink during the 14 weeks of incubation in estuarine water, but PE started to sink after six weeks in coastal water when sufficiently colonized by blue mussels Mytilus edulis, and its velocity continued to increase until the end of the incubation period. Sinking velocities of these PE pellets were similar irrespective of salinity (10 vs. 36). Biofilm composition differed between estuarine and coastal stations, presumably accounting for differences in sinking behavior. We demonstrate that biofouling enhances microplastic deposition to marine sediments, and our findings should improve microplastic transport models.
The effects of microbial colonization and biofilm formation on microplastics in the marine and coastal environments have aroused global concern recently. However, the simultaneous influences of ...exposure time and depth on biofilm formation, and subsequently on the properties variations of microplastics is less studied. In this study, polyethylene (PE) film was exposed at three depths (2 m, 6 m, and 12 m) for three time periods (30 days, 75 days, and 135 days) in the coastal seawater of Yellow Sea, China. The results show that the total amount of biofilms markedly increased with exposure time, but decreased with water depth. Typical morphologies and compositions of biofilms such as coccus-, rod-, disc-shaped bacteria and filaments, as well as a dense layer of extracellular polymeric substances were observed on the surfaces of the PE microplastics. Biofilm formation could decrease the hydrophobicity of PE microplastics, and increase the abundances of hydrophilic C−O and CO groups on the surface of PE. Alphaproteobacteria, Gammaproteobacteria and Bacteroidia were identified as the core microbiome of the PE associated biofilms, while the dominant bacteria families vary from the early to the late phases of the biofilm formation. Our results indicate that microplastics associated biofilms could affect the environmental processes and fates of microplastics in the marine and coastal environment.
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•Biofilm formation and its influences on PE properties were investigated.•The thickness of biofilms on PE increases with exposure time but decreases with depth.•Biofilms could decrease the hydrophobicity and change the functional groups of PE.•The dominant PE colonizing microbial community varies during the biofilm formation.
To follow the pathways of microplastics in aquatic environments, profound knowledge about the behaviour of microplastics is necessary. Therefore, sinking experiments were conducted with diverse ...polymer particles using fluids with different salinity. Particles ranged from 0.3 and 3.6mm with sinking rates between 6 and 91×10−3ms−1. The sinking velocity was not solely related to particle density, size and fluid density but also to the particles shape leading to considerable deviation from calculated theoretical values. Thus, experimental studies are indispensable to get basic knowledge about the sinking behaviour and to gain representative datasets for model approaches estimating the distribution of microplastics in aquatic systems. The sinking behaviour may be altered considerably by weathering and biofouling demanding further studies with aged and fouled plastic particles. Furthermore, assumptions are made about the influence of sinking fouled microplastics on the marine carbon pump by transferring organic carbon to deeper water depths.
•Sinking velocities of microplastics are determined by particle density, size and shape as well as fluid density.•Observed sinking velocities deviate distinctly from theoretical estimates.•Sinking behaviour of microplastics may be altered by weathering and biofouling.
Microplastic in the environment hides visible and invisible dangers for the ecosystems and domiciled organisms. Due to the large quantities of microplastics already distributed worldwide, comparative ...studies to investigate the associated hazards, distribution patterns, and abundances are becoming increasingly important. Due to varying efforts and budgets, there is still no homogenized detection method for microplastics in the environment, which severely compromises the comparability and reliability of results between previous studies. In this study, we compare the efficacy, degradative effect on microplastics, and microplastic recovery rates of different digestion and separation methods for isolating microplastics from mass-limited environmental samples with high biogenic content. Our results show that the most gentle and effective isolation method is an adsorption-based technique that exploits the lipophilic properties of plastic for separation. This technique achieves an average microplastic recovery rate of 98.0 ± 3.8% and a matrix removal of 96.3 ± 0.3% at low cost and minimum effort. To examine the applicability of this technique to natural environmental samples, eight sediments and two plankton net samples from the South China Sea were selected to determine microplastic abundances. In the analyzed sediment samples, 0–9 microplastic items per 10 g sediment d. w. were found, while 17–25 items per m3 were detected in net samples. Considering the respective mean plastic density, this corresponds to a calculated microplastic mass of 0–39 μg (10 g d.w.)−1 and 3.7–7.1 μg m−3 in sediment and water samples, respectively. This study represents a new way of microplastic extraction from matrix-rich mass-limited samples with high accuracy and easy feasibility at low costs, which would be useful as a worldwide homogenized method in future microplastic research projects and related data comparability.
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•New efficacy technique to separate microplastic from matrix-rich mass-limited samples.•Adsorption separation method separated small-sized microplastics with high accuracy.•Combined adsorption separation technique reaches a matrix removal of >96%.•Commonly used digestion agents degrade microplastics.•The new combined adsorption separation technique allows microplastic extraction from the particulate phase of marine samples.
Sinking experiments were conducted using irregularly shaped polyamide (PA), polymethyl methacrylate (PMMA), and polyethylene terephthalate (PET) particles sized 6 to 251 μm. Certified PS spheres were ...used to validate experiments and showed that the effect of particle size on terminal sinking velocity is well reproduced by the method. As expected sinking velocities of irregularly shaped particles were considerably lower than theoretical values for spheres of the same size range calculated via several approximations available in the literature. Despite the influence of particle shape, the dependence of terminal sinking velocity on particle size can reasonably well be described by a quadratic linear regression, with an average determination of 63%. To generalize results we present a model that predicts terminal sinking velocity as a function of particle size and particle excess density over the fluid. Improving the predictive power of this model requires further experiments with a range of particle characteristics.
•Terminal sinking velocity of sub-mm (6–251 μm) microplastic was empirically investigated.•Theoretical values overestimate measured terminal sinking velocity of sub-mm microplastic.•A multiple quadratic regression model is presented to predict sub-mm microplastic terminal sinking velocity.
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.
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•Microplastic fluxes in the deep NE Atlantic vary widely between 2003 and 2015.•Polyethylene and polyvinyl chloride are the dominant polymer type.•Detected microplastics are predominantly small fragmented (<100 μm) particles.•The lithogenic particle fluxes are correlated with the polyethylene fluxes.•A seasonal dependence was observed for polyvinyl chloride fluxes.
Record of microplastic fluxes for the period 2003–2015 in the northeast Atlantic twilight zone.
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•First comprehensive study on MPs in mangrove sediments along the coast of China.•The MPs abundance in mangrove sediments was up to 8.5 times higher than in mangrove free ...sediments.•The sandy sediments were dominated by foams, and the muddy sediments by fibers and fragments.
Mangroves are a unique and important type of coastal wetlands in the tropical and subtropical zones worldwide. The abundance and spatial distribution of microplastics in the mangrove sediments however are still poorly understood. The present study aimed to illustrate the characteristics, abundance and spatial distribution of microplastics in different mangrove sediments along the south-eastern coastal zones of China. Microplastic samples (roughly 10–20 kg fresh sediments at each site) taken from 21 sampling sites showed various shapes, colors, composition, sizes, surface morphology, abundance and strong spatial heterogeneity. Five different shapes of microplastics with a variety of colors were detected in the mangrove sediments, among which foams (74.6%) and fibers (14.0%) were the dominant types. The polymer composition of the microplastics identified based on the FT-IR and μ-FTIR covered polystyrene (75.2%), polypropylene (11.7%), rayon (4.6%), polyester (3.4%), polyethylene (2.8%) and acrylic (2.4%). The observed microplastics with a size range of less than 2 mm made up 58.6% of the total microplastic particles. The microplastics had various surface morphologies, exhibiting complicated weathered surfaces. The abundance of microplastics showed a substantial variation among the sampling sites, ranging from 8.3 to 5738.3 items kg−1 (dry sediment). Altogether, our study provides a better understanding of microplastic pollution status and prevention policy-making of mangrove habitats in China.
Salinity is a major factor controlling the distribution of biota in aquatic systems, and most aquatic multicellular organisms are either adapted to life in saltwater or freshwater conditions. ...Consequently, the saltwater-freshwater mixing zones in coastal or estuarine areas are characterized by limited faunal and floral diversity. Although changes in diversity and decline in species richness in brackish waters is well documented in aquatic ecology, it is unknown to what extent this applies to bacterial communities. Here, we report a first detailed bacterial inventory from vertical profiles of 60 sampling stations distributed along the salinity gradient of the Baltic Sea, one of world's largest brackish water environments, generated using 454 pyrosequencing of partial (400 bp) 16S rRNA genes. Within the salinity gradient, bacterial community composition altered at broad and finer-scale phylogenetic levels. Analogous to faunal communities within brackish conditions, we identified a bacterial brackish water community comprising a diverse combination of freshwater and marine groups, along with populations unique to this environment. As water residence times in the Baltic Sea exceed 3 years, the observed bacterial community cannot be the result of mixing of fresh water and saltwater, but our study represents the first detailed description of an autochthonous brackish microbiome. In contrast to the decline in the diversity of multicellular organisms, reduced bacterial diversity at brackish conditions could not be established. It is possible that the rapid adaptation rate of bacteria has enabled a variety of lineages to fill what for higher organisms remains a challenging and relatively unoccupied ecological niche.
Using shells collected from a sediment trap series in the Madeira Basin, we investigate the effects of seasonal variation of temperature, productivity, and optimum growth conditions on calcification ...in three species of planktonic Foraminifera. The series covers an entire seasonal cycle and reflects conditions at the edge of the distribution of the studied species, manifesting more suitable growth conditions during different parts of the year. The seasonal variation in seawater carbonate saturation at the studied site is negligible compared to other oceanic regions, allowing us to assess the effect of parameters other than carbonate saturation. Shell calcification is quantified using weight and size of individual shells. The size-weight scaling within each species is robust against changes in environmental parameters, but differs among species. An analysis of the variation in calcification intensity (size-normalized weight) reveals species-specific response patterns. In Globigerinoides ruber (white) and Globigerinoides elongatus, calcification intensity is correlated with temperature (positive) and productivity (negative), whilst in Globigerina bulloides no environmental forcing is observed. The size-weight scaling, calcification intensity, and response of calcification intensity to environmental change differed between G. ruber (white) and G. elongatus, implying that patterns extracted from pooled analyses of these species may reflect their changing proportions in the samples. Using shell flux as a measure of optimum growth conditions, we observe significant positive correlation with calcification intensity in G. elongatus, but negative correlation in G. bulloides. The lack of a consistent response of calcification intensity to optimum growth conditions is mirrored by the results of shell size analyses. We conclude that calcification intensity in planktonic Foraminifera is affected by factors other than carbonate saturation. These factors include temperature, productivity, and optimum growth conditions, but the strength and sign of the relationships differ among species, potentially complicating interpretations of calcification data from the fossil record.
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.
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