Rivers are the key conduits for land-to-sea debris transport. We present in situ monitoring data of macro debris and microplastic along the supercritical Citarum River in Indonesia We identified the dams as concentrated areas of microplastic. Plastics accounted for 85% of the riverine debris (5369 ± 2320 items or 0.92 ± 0.40 tons daily). We estimated macrodebris releases of 6043 ± 567 items or 1.01 ± 0.19 tons daily with a microplastic concentration of 3.35 ± 0.54 particles per m³ from Citarum River to sea. It has been suggested that population density and urbanization rate are major factors determining the spatiotemporal variability of macrodebris and microplastic abundances in the Citarum River. Our research highlights the importance of long-term monitoring to estimate debris and microplastics inflows along the Indonesian river to the world ocean as a benchmark for the reduction of macro and microdebris into the environment.

The main objective of the present study is to estimate the heavy metal concentrations and ecological risk index (ERI) in the seawater of Kakinada Bay. Turbidity, suspended particulate matter (SPM), pH, salinity, dissolved oxygen, along with heavy metals were recorded from twelve locations of the Bay to understand its hydrographical conditions. The distribution of environmental variables and heavy metal concentrations was noticed mostly from the south to north gradient. Significant positive correlations were detected in some pairs of metals such as Cu with Zn (R² = 0.515; p < 0.05), Pb with both Cr (R² = 0.810; p < 0.01) and Cd (R² = 0.511; p < 0.05), and Cr with Ni (R² = 0.573; p < 0.05) indicating their common origin. The ERI values (7.93–35.2) of seawater of Kakinada Bay in the present study were in the ecologically high-risk category. Industrial operations, domestic sewage, and natural processes are the major contaminant sources of Kakinada Bay leading its environment to a potential ecological concern.

The dinoflagellate genus Alexandrium comprises most of the toxic bloom-forming species producing paralytic shellfish toxins (PSTs) in the sea. Recently, repeated paralytic shellfish poisoning episodes have been recorded in Qinhuangdao located at the west coast of the Bohai Sea. To elucidate the relationship between toxic Alexandrium blooms and the poisoning episodes, a year-round investigation was carried out in this region from July 2020 to July 2021. Two qPCR assays were used to detect A. catenella and A. pacificum, and LC-MS/MS was applied to analyze PSTs in phytoplankton and shellfish samples. The blooms of A. catenella and A. pacificum were found in April and July, respectively, and PST content in three bivalves exhibited notable increase following the bloom of A. catenella. The results revealed bloom dynamics of the two toxic Alexandrium species in the Bohai Sea for the first time, and further confirmed A. catenella as the causative agent of poisoning episodes.

Different extraction methods have been proposed to study the ingestion of microplastics by marine organisms, including enzymatic digestion. While mussels have been the focus of research, crustaceans' enzymatic digestion has received little attention. An overlooked source of information for microplastic research is analysis of long-term time-series biotic samples. These collections are invaluable for the detection and monitoring of changes in ecosystems, especially those caused by anthropogenic factors. Here, crustacean larvae collected in two periods, 1985 and 2020, in the central North Sea were used to develop and optimise an effective and gentle enzymatic digestion method suitable for microplastic research. Sequential breakdown of these chitinaceous samples via a mechanical and surfactant (Sodium Dodecyl Sulphate 1% v/v) pre-treatment, followed by proteinase K (100 mU/mL) and chitinase (50 mU/mL) digestion, efficiently removed >96% of biomass of 1985 and 2020 samples. The optimised method was effective without interfering with the identification of naturally weathered microplastics via FTIR Spectroscopy.

The major sources and sinks of total mercury (THg) and methylmercury (MeHg) in Kongsfjorden were estimated based on spreadsheet-based ecological risk assessment for the fate of mercury (SERAFM). SERAFM was parameterized and calibrated to fit Kongsfjorden using the physical properties of the fjord, runoff coefficients of Hg, transformation rate constants of Hg, partition coefficients of Hg, Hg loadings from freshwater, and solid balance parameters. The modeled Hg concentrations in the seawater matched with the measured concentrations, with a mean bias of 12% and a calibration error of 0.035. The mass budget showed that the major THg sources were tidal inflow and glacial runoff, while the major MeHg sources were tidal inflow and in situ methylation in shallow halocline water, which agreed with the distributions of THg and MeHg in seawater. The coupling of observation and fate modeling in Kongsfjorden provides a basic understanding of Hg cycles in the Arctic fjords.

We analyzed per- and polyfluoroalkyl substances (PFAS) in aqueous film-forming foams (AFFFs) used to extinguish a major fire in a petrochemical terminal from the Port of Santos (Brazil). Eight AFFFs from seven known commercial brands and one unknown sample (AFFF-1 to AFFF-8) were evaluated. 17 PFAS were identified and quantified using high performance liquid chromatography (LC/MS). The concentrations of Σ17 PFAS in the AFFFs ranged from 500 to 9000 ng/g, with prevalence of short chain PFAS (~85 %), followed by long chain PFAS. Perfluorooctane sulfonic acid (PFOS) and perfluorooctanoic acid (PFOA), included in the global treaty of the Stockholm Convention, were also detected. We estimated that at least 635.96 g of PFAS were introduced in the estuary, representing a massive input of these substances. This investigation reports the PFAS composition of AFFFs used in firefighting in the GRULAC Region (Group of Latin American and Caribbean countries).

PURPOSE OF REVIEW: Increasing environmental problems demand mitigation solutions to fulfill sustainability development goals. Microalgae offer possibility of valorizing the CO₂ and wastewater-derived nutrients to produce numerous industrial bioproducts. However, developing self-sustained systems for the complete valorization of algal biomass into valuable biobased products is challenging. Currently, sustainable algal processing faces several challenges including costly cultivation, difficult harvesting, and incomplete biomass valorization. This review assessed the prospects of emerging technologies focusing on the integrated approaches for sustainable algal biorefinery development ensuring the sustainability of environment-water-energy nexus. RECENT FINDINGS: Evaluation of various upstream, midstream, and downstream processing technologies provided insights into the processing issues. In upstream processing, high-rate algal ponds and integrated carbon capture and transformation technologies offer waste valorization into eco-friendly algal production. A brief comparison of harvesting technologies mainly focusing on chemical and biological flocculation has shown that integrating physical and biological harvesting methods are more reliable and efficient. Overview of downstream processing has indicated that biomass processing in a cascading manner offers the complete biomass valorization in a zero-waste paradigm. Assessment of cultivation-to-production technologies highlighted that “zero-waste” algal biorefinery has the potential to become reality by integrating the industry 4.0 and phenomics approaches with eco-friendly cultivation, harvesting, and processing technologies. Hybrid methods based on integrated cascading processing offer complete biomass valorization in a circular bioeconomy paradigm.

Discarded plastic bag is a main component of marine debris, posing potential threats to marine biota. This study was conducted to assess the potential effects of microplastics on juvenile Lates calcarifer. Fish were exposed via diet to two microplastic types from conventional polyethylene (PE) and biodegradable (Bio) plastic bags for 21 days. Antioxidative enzymes activity, intestinal microbiome and proteome were determined. PE and Bio microplastics were found to accumulate in gastrointestinal tracts, and no mortality was observed. Microplastics exposure did not induce significant antioxidant response except for the glutathione reductase (GR) modulation. Intestinal microbiome diversity decreased significantly in PE group based on Simpson index. Both types of microplastics induced proteome modulation by down-regulating proteins associated with immune homeostasis. Bio microplastics maintained higher intestinal microbial diversity and induced more proteins alteration than PE microplastics. This study provides toxicological insights into the impacts of conventional and biodegradable microplastics on juvenile L. calcarifer.

This study collected 100–1000 L of surface water from 70 to 74 sites in the Inner Gulf of Thailand in both dry and wet seasons to investigate the relationship between the spatiotemporal distribution of microplastics and environmental variables. The quantity of microplastics in the wet season (34.59 ± 46.02 pieces/L) was significantly higher than the dry season (8.70 ± 15.34 pieces/L). Spatial distribution revealed an abundance of microplastics in river estuaries and seasonal current circulations. Polymeric characterization results showed that the plastic samples primarily consisted of polypropylene and polyethylene. New functional groups, including carbonyl, hydroxyl, and vinyl groups, were found in the chemical structures of the microplastic samples. The amount of freshwater runoff and the negative relationship with salinity confirmed that the river is the key factor in the transportation of microplastics to the coastal sea.

Concentrations of 13 phase-partitioned polycyclic aromatic hydrocarbons (PAHs) in seawater were monitored monthly off Oki Island, Japan, during 2015–2019 to elucidate seasonal variations, main source, and transport pathways of PAHs in the southwestern Sea of Japan. Total PAH (dissolved plus particulate) concentrations in surface seawater at 36°09.0′N, 133°17.3′E (site OK) were in the range 0.49–9.36 ng L⁻¹ (mean 2.77, SD 2.05 ng L⁻¹) with higher levels in summer–autumn, an order of magnitude lower than those in the East China Sea during 2005 and 2009–2011 and about one-third of those recorded in the Sea of Japan in 2008 and 2010. The main sources of dissolved and particulate PAHs were combustion products. Increasing dissolved PAH levels during July–October indicate that the area around southern Oki Island is impacted by PAH-rich summer continental-shelf water transported by the Tsushima Warm Current flowing from the East China Sea.