Despite the ubiquitous and persistent presence of microplastic (MP) in marine ecosystems, knowledge of its potential harmful ecological effects is low. In this work, we assessed the risk of floating MP (1 μm–5 mm) to marine ecosystems by comparing ambient concentrations in the global ocean with available ecotoxicity data. The integration of twenty-three species-specific effect threshold concentration data in a species sensitivity distribution yielded a median unacceptable level of 1.21 ∗ 10⁵ MP m⁻³ (95% CI: 7.99 ∗ 10³–1.49 ∗ 10⁶ MP m⁻³). We found that in 2010 for 0.17% of the surface layer (0–5 m) of the global ocean a threatening risk would occur. By 2050 and 2100, this fraction increases to 0.52% and 1.62%, respectively, according to the worst-case predicted future plastic discharge into the ocean. Our results reveal a spatial and multidecadal variability of MP-related risk at the global ocean surface. For example, we have identified the Mediterranean Sea and the Yellow Sea as hotspots of marine microplastic risks already now and even more pronounced in future decades.

Plastic pollution is among the most pervasive stressors currently influencing the marine environment and affecting even the most remote areas. To date, there are still fundamental gaps in our understanding of the major pathways and fate of plastic debris in the oceans. Here we show that oceanic insular environments are important transitory repositories of small plastic items floating in the open ocean. Monthly monitoring of seven beaches over a three-year period demonstrate that beaches of the Azores islands with particular characteristics can capture significant quantities of fragments between 2 and 5 mm in length. The beach with the highest plastic loading rates was found to occasionally accumulate densities exceeding 15,000 fragments m⁻² on part of the backshore. However, a large portion of these fragments can be rapidly washed back into the marine environment. Detailed characterization of those plastic items revealed the typology and size distribution to be similar throughout the seven beaches and through the 33 months surveyed, suggesting a same and unique source. Our results show that these oceanic islands of the North-East Atlantic are under pressure of high quantities of fragmented plastic debris that probably entered the ocean many years ago.

Microplastics are widespread across the global oceans, yet the potential risks of the ubiquitous environmental contaminant to marine organisms has been less known. Accumulation of microplastics and associated contaminants in marine fish, may pose adverse impacts to human health via seafood consumption. This study evaluated microplastic contamination in 24 fish species collected from Beibu Gulf, one of the world’s largest fishing grounds in South China Sea. Microplastics were detected in 12 fish species at an abundance of 0.027–1.000 items individual⁻¹ and found in fish stomach, intestines and gills with the count percentage of 57.7%, 34.6% and 7.7%, respectively. Transparent fibers were observed as the predominant microplastics, which might be ingested accidently by fish or transferred through other animals at lower trophic levels. Majority of microplastics were identified as polyester (44%) and nylon (38%), whereas polypropylene (6%), polyethylene (6%), and acrylics (6%) were also found. Relatively, higher microplastic abundances were found in demersal fish compared to the pelagic species. Overall, the abundance of microplastics was documented as relatively low in the commercial fish collected from the open water of Beibu Gulf, South China Sea.

The perdurability of plastics in the environment is one of the major concerns of plastic pollution and, as a consequence, oceans are accumulating large amounts of plastic. The degradation of conventional and biobased materials was evaluated through a laboratory experiment for a year simulating four different conditions in the marine environment. The water column environmental compartment was simulated under euphotic and aphotic (with and without light availability) conditions. The seafloor environmental compartment was simulated with sediment under non-polluted and polluted conditions. By combining weight loss (%), spectroscopic and thermal analyses, the degradation patterns regarding the polymer structure were assessed. The studied biobased materials were polylactic acid (PLA) based materials and showed higher degradability than conventional ones. The weight loss of conventional materials was not influenced by the water column or sediment, while in PLA-based materials, the degradation rates were ca. 5 times greater in the sediment than in the water column. The absorbance (Abs) value at 3400 cm⁻¹ for polyethylene terephthalate (PET), and carbonyl (CO) index for PET and PLA could be useful to detect early signs of degradation. The crystallization index could be a useful parameter to discriminate degradation stages. The obtained results highlight the different degradability rates of materials depending on the specific environmental marine conditions.

Rivers can receive the input of treated or untreated sewage effluents from wastewater treatment plants, urban and industrial discharges and agricultural run-off, becoming an important pathway for the transport and mobilization of pollutants to the oceans. In the present study, the occurrence of 20 PFAAs was determined in the water of Tagus River basin (Spain). PFAAs were detected in 76 out of 92 water samples collected during 5 years (2013–2018), being perfluorooctanesulfonic acid (PFOS) the predominant compound (<0.01–34 ng/L). The annual average PFOS concentrations (2.9–11 ng/L) detected in Tagus River were above the annual average environmental quality standards (AA-EQS) established in the Directive, 2013/39/EU (0.65 ng/L for inland surface waters) but below the maximum allowable concentration (MAC-EQS; 36000 ng/L). The levels of PFAAs detected in urban and industrial areas were statistically higher (p < 0.01) than those at background or remote areas. The mass flow rates amounted to <0.01–46 kg/y for PFOS and <0.01–22 kg/y for perfluorooctanoic acid (PFOA). A quantitative ecotoxicological risk assessment was conducted to evaluate the environmental potential risk related to PFAAs in the aquatic ecosystem. Risk characterization ratios (RCRwater, RCRsed and RCRoral, fish) were below 1 in all cases.

Fish farming in coastal areas has become an important source of food to support the world’s increasing population. However, intensive and unregulated mariculture activities have contributed to changing seawater carbonate chemistry through the production of high levels of respiratory CO₂. This additional CO₂, i.e. in addition to atmospheric inputs, intensifies the effects of global ocean acidification resulting in localized extreme low pH levels. Marine calcifying macroalgae are susceptible to such changes due to their CaCO₃ skeleton. Their physiological response to CO₂-driven acidification is dependent on their carbon physiology. In this study, we used the pH drift experiment to determine the capability of 9 calcifying macroalgae to use one or more inorganic carbon (Cᵢ) species. From the 9 species, we selected the rhodolith Sporolithon sp. as a model organism to investigate the long-term effects of extreme low pH on the physiology and biochemistry of calcifying macroalgae. Samples were incubated under two pH treatments (pH 7.9 = ambient and pH 7.5 = extreme acidification) in a temperature-controlled (26 ± 0.02 °C) room provided with saturating light intensity (98.3 ± 2.50 μmol photons m⁻² s⁻¹). After the experimental treatment period (40 d), growth rate, calcification rate, nutrient uptake rate, organic content, skeletal CO₃⁻², pigments, and tissue C, N and P of Sporolithon samples were compared. The pH drift experiment revealed species-specific Cᵢ use mechanisms, even between congenerics, among tropical calcifying macroalgae. Furthermore, long-term extreme low pH significantly reduced the growth rate, calcification rate and skeletal CO₃⁻² content by 79%, 66% and 18%, respectively. On the other hand, nutrient uptake rates, organic matter, pigments and tissue C, N and P were not affected by the low pH treatments. Our results suggest that the rhodolith Sporolithon sp. is susceptible to the negative effects of extreme low pH resulting from intensive mariculture-driven coastal acidification.

Plastics are crucial for our modern lifestyle and yet pose a major threat to our environment. Rising levels of microplastics (MP) in rivers and oceans are a big challenge for our economy and regulatory institutions as well as from a scientific point of view. Smaller microplastic particles, in particular, are especially hard to identify and even harder to quantify in environmental samples. Hence, we present a novel and inexpensive approach to quantify microplastics (MP) on a weight basis, relying on a thermoanalytical method. The Elemental Analysis combined with Overdetermined Equation Method (EA-OEM) was originally developed for determining the plastic content of refuse-derived fuels. It makes use of the distinct differences in the organic elemental composition (C, H, N, S, O) of plastics, biogenic and inorganic materials to calculate the (micro)plastic content on a detailed weight base. The study presented provides the first experimental results yielded from the application of the EA-OEM and two different laboratory approaches to the analysis of polyethylene (PE) and polypropylene (PP) MP content in industrial effluent samples from one source. In this way, it was possible to ensure that the polymer composition was known and the MP content therein (10–29%) could be derived. Further, the study reveals good MP recovery rates when applying the methodology to PE/PP-spiked samples.

The residence times of plastics in the oceans are unknown, largely because of the durability of the material and the relatively short (decadal) period of time over which plastic products have been manufactured. In this study, classic LEGO bricks constructed of acrylonitrile butadiene styrene (ABS) and washed up on beaches of southwest England have been subjected to X-ray fluorescence (XRF) analysis and the spectra and any other identifiers matched with unweathered blocks stored in collections or sets of known history. Relative to unweathered equivalents, weathered blocks exhibit varying degrees of yellowing, fracturing and fouling, and are of lower mass, average stud height and mechanical strength. These effects are attributed to photo-oxidative degradation and the actions of physical stress and abrasion while exposed to the marine environment. Infrared spectra indicate that the polymer remains largely intact on weathering but with photo-degradation of the polybutadiene phase of ABS, while quantification of XRF spectra reveals that pigments like cadmium sulphoselenide become more heterogeneously distributed in the matrix when in the environment. Using measured mass loss of paired (weathered versus unweathered) equivalents and the age of blocks obtained from storage we estimate residence times of between about 100 and 1300 years for this type and thickness of plastic, with variations reflecting differences in precise additive composition and modes of weathering.

We utilized volcanic CO₂ vents at Castello Aragonese off Ischia Island as a natural laboratory to investigate the effect of lowered pH/elevated CO₂ on the bioactivities of extracts from fleshy brown algae Sargassum vulgare C. Agardh. We analysed the carbohydrate levels, antioxidant capacity, antibacterial, antifungal, antiprotozoal, anticancer properties and antimutagenic potential of the algae growing at the acidified site (pH ∼ 6.7) and those of algae growing at the nearby control site Lacco Ameno (pH∼8.1). The results of the present study show that the levels of polysaccharides fucoidan and alginate were higher in the algal population at acidified site. In general, extracts for the algal population from the acidified site showed a higher antioxidant capacity, antilipidperoxidation, antibacterial, antifungal, antiprotozoal, anticancer activities and antimutagenic potential compared to the control population. The increased bioactivity in acidified population could be due to elevated levels of bioactive compounds of algae and/or associated microbial communities. In this snapshot study, we performed bioactivity assays but did not characterize the chemistry and source of presumptive bioactive compounds. Nevertheless, the observed improvement in the medicinal properties of S. vulgare in the acidified oceans provides a promising basis for future marine drug discovery.