Assessment of microplastic contamination in an eastern Pacific tuna (Katsuwonus pelamis) and evaluation of its health risk implication through molecular docking and metabolomics studies.

This work investigated microplastic (MP) pollution in a commercially-important tuna species Katsuwonus pelamis (K. pelamis) from the Eastern Pacific and health implications. 125 MPs were extracted from gills, esophagus, stomachs, intestinal tracts, and muscle of K. pelamis. MPs in the esophagus was the highest, ∼7.6 times higher than that in the gill. Polyester and polyethylene terephthalate (PET) were dominant. Molecular docking implied that PET stabilized the complex via forming 4 new hydrogen bonds that interacted with Arg83, Gln246, Thr267, and Gly268, given that PET can enter glycerol kinase protein active pocket. Metabonomic results suggested that Glycerol 3-phosphate up expressed 1.66 more times that of control groups with no MPs in the muscle. This confirmed that MPs would lie in the glycerol kinase protein active pocket, which triggered menace to K. pelamis. The results provided insights into suggested the potential influence of MPs on the sustainability of fisheries and seafood safety.

Microplastic pollution threats coastal resilience and sustainability in Xiamen City, China.

Microplastics have raised growing awareness due to their ubiquity and menaces to coastal resilience and sustainability. The abundance, distribution, and characteristics of microplastics in water and organisms in Xiamen were evaluated. Results showed that the average abundance of microplastics in the surface water of Xiamen Bay was 1.55 ± 1.94 items/m3. The dominant color, size, shape, and polymer type were white, 1.0-2.5 mm, and fragments and lines, and polyethylene and polypropylene, respectively. The average abundance of microplastics in the fish in Xiamen was 2.44 ± 1.56 items/g wet weight. They were dominated by fibers of blue polyethersulfone and polyethylene terephthalate, and sizes <2.5 mm. There was a negative correlation between the polymer type in fish and that in water, while a positive correlation between shapes of microplastics of both fish species. Results will aid in formulating management measures for preventing microplastic pollution in Xiamen, ultimately promoting coastal resilience and sustainability of coastal communities.

Transboundary microplastic pollution in Xiamen Bay and adjacent Jiulong River estuary after the outbreak of COVID-19.

Land-based transport from nearshore areas is a key pathway of microplastic (MP) pollution in the oceans. Therefore, transport, fate, and intervention on MPs necessitate an investigation of MP contamination in coastal regions. Here, MP pollution in the surface waters of Xiamen Bay and Jiulong River estuary was evaluated in 2021 after the outbreak of COVID-19. The abundance of MPs in Xiamen Bay ranged from 0.20 to 5.79 items m-3 with an average of 1.03 items m-3, whereas that in the Jiulong River estuary spanned from 0.55 to 2.11 items m-3 with a mean of 1.30 items m-3. A yearly decreasing trend in the abundance of MPs in surface waters in both regions was observed. The particle sizes of MPs were concentrated in the range of 2.50-5.00 mm, and the colors were mainly white, transparent, and green. The micro-Raman spectroscopic results showed that MP polymer types were predominantly polyethylene, polypropylene, and polystyrene. A lower abundance of MPs in Xiamen Bay with no obvious pattern was observed, while that in the Jiulong River estuary showed a wavelike distribution from upstream to downstream. Ecological risk assessment of MP pollution in surface waters of two regions was performed using the pollution load index (PLI), giving the risk level in descending order: wastewater discharge area > aquaculture area > sloughs > estuary mouth > estuarine rivers > shipping lane. The average risk level of Xiamen Bay (I) was lower than that in Jiulong River estuary (II). The MP pollution in the Jiulong River estuary appeared heavier than that in Xiamen Bay, which may be due to the combined effects of COVID-19 and marine governance. This study provided insights into the prevention and management of MP pollution in nearshore semi-enclosed bays.

Assessment of manta trawling and two newly-developed surface water microplastic monitoring techniques in the open sea.

The ubiquitous microplastic (MP) pollution across the waterways, sediments, biota, and atmosphere has amplified concerns at a global scale. Unfortunately, harmonized MP monitoring protocols are absent for accurate evaluation on MP pollution. Few large-scale MP sampling programs involving different designs have been implemented in the open sea. In this study, a manta trawling and two newly custom-built pump filtration systems, namely, a trawl-underway pump combination system coupled in conjunction with an in-situ filtration device (Y-shaped filter, New Type I) and a stationary onboard pumping coupled to Y-shaped filter (New Type II), were evaluated for MP pollution in the mid-North Pacific Ocean. The trawling-based systems (manta trawl and New Type I) collected samples covering a large area, whereas New Type II operated at a fixed site. The new systems achieved fractionated filtration of MPs on site and prevented airborne contamination. The electronic fuel meter installed in the New Type II yielded a more accurate volume. Results showed that the average MP abundance of the aforementioned sampling techniques were 0.65, 2.56, and 7.48 items m-3, respectively. The abundances in the same particle size range (0.3-5.0 mm) from the new systems were higher. The recovered MPs from all systems were mainly white and polypropylene. Note that the MPs from the manta trawl were primarily fragments; however, they were mainly fibers from the new systems. This corroborated the capability of new systems in harvesting small items (0.1-0.3 mm) and fibers. The cost analysis showed that the new systems beat the manta trawl concerning price performance. The study results provide alternatives for future MP sampling, which will ultimately aid in the method harmonization and standardization of MP sampling.

Removal of gaseous elemental mercury by hydrogen chloride non-thermal plasma modified biochar.

Hydrogen chloride (HCl) non-thermal plasma was applied to introduce Cl active sites on biochar prepared from sorghum straw in this study. Surface modified biochar was then placed in flue gas with typical components to investigate its elemental mercury (Hg0) capture ability. To elucidate the adsorption mechanism & binding properties, samples were characterized by N2 adsorption, scanning electron microscopy with energy dispersive spectrometer (SEM-EDS) and X-ray absorption near edge structure (XANES) analysis of Hg LIII-edge, Cl K-edge and S K-edge. Experimental results showed that HCl plasma modification successfully increased Cl active sites on biochar and greatly increased its mercury removal efficiency. Both HCl treatments (w/without plasma involvement) altered biochar's surface structure and layered structure generated. XANES spectra revealed that adsorbed-Hg on HCl-treated biochars mainly in the form of Hg+. Gaseous Hg0 was believed to heterogeneously react with chlorinated sites through electron-transfer and formed Hg2Cl2 compounds. With the presence of NO or SO2 in the system, adsorbed mercury existed on biochar mainly as Hg+. SO2 competed and inhibited the adsorption of Hg0; while NO promoted Hg0 removal capacity by increasing the active sites and enhancing the adsorption kinetics of adjacent Cl-containing sites.

Study on the effects of oxygen-containing functional groups on Hg0 adsorption in simulated flue gas by XAFS and XPS analysis.

The effect of physicochemical properties of activated carbon on adsorption of elemental mercury (Hg0) was investigated on a series of modified activated carbons. Heat treatment and benzoic acid impregnation were conducted to vary the oxygen functional groups on carbon surface. Hg0 adsorption experiments were run in a fixed-bed reactor at 140 °C. Surface characteristics of carbon samples were studied by N2 adsorption, Boehm titration, X-ray photoelectron spectroscopy (XPS) and X-ray absorption fine structure (XAFS), respectively. The predominant mechanism of Hg0 removal was the formation of chemical bonds between Hg and various functional groups. Both XPS and XAFS analysis revealed that mercury bound on carbon surface was mainly in oxidation state. Under N2 atmosphere, the absorbed Hg was found as Hg2+, and coordinated to O atom. With the existence of HCl in simulated flue gas, Hg0 was bonded on Cl sites and HgCl2 was assumed to be the dominated form.