We present seasonal variation of four metals (Cd, Cu, Pb, and Zn) in nine pelagic and three benthic fish species from the highly polluted Cuddalore coast in Tamil Nadu, India. Metals were assessed using atomic absorption spectrometry and detected in all fish species, in at least one season, except Iniistius cyanifrons where cadmium was not detected throughout. In both benthic and pelagic fish, order of metal concentration was Zn > Cu > Pb > Cd. Multivariate statistical analysis revealed that metals may have originated from both natural and anthropogenic sources. Health risk assessment revealed that consumption of fish from Cuddalore coast does not pose health risk for now; however, hazard index values (pelagic = 0.97; benthic = 0.90) are in borderline. Even a slight increase in metal concentration in fish can prove hazardous for human consumption. Sooner or later, eating fish from Cuddalore coast may pose a considerable health risk to humans if metal pollution is not held at Bay.

This study presents the fecal contamination dynamic at the two bathing sites of Aytré Bay (Charente Maritime, France). We quantified fecal indicator bacteria (FIB) abundances (Escherichia coli and enterococci) from water and sediment samples over one-year survey. Then we measured biological (bacterial abundance, chlorophyll-a), physico-chemical (dissolved nutrients and oxygen, salinity, pH …) and climatic (temperatures, rainfall and tidal coefficient) parameters. Results showed that FIB abundances were occasionally higher than the European regulatory threshold during winter, summer and fall. The “poor quality” of the bathing water was due to high enterococci abundance. We found negative significant correlations between FIB and water temperature and salinity, and positive significant correlations between FIB and rainfall, PO₄, NO₃, NO₂, and SiO₂ mainly in water. Relationships between parameters showed that during summer and spring the main environmental drivers were temperature and salinity, while in fall and winter they were rainfall and dissolved nutrients.

The present study determined total mercury (Hg) in four ²¹⁰Pb dated sediment cores to assess the historical anthropogenic Hg accumulation in the Santos estuary, Southeastern Brazil. Background levels were identified using the deepest sections of the cores, corresponding to pre-industrial ages. Mercury distribution in the sediment cores (0.02–2.64 mg kg⁻¹) presented a large spatial and temporal variation. Contamination is highest in the upper estuary and indicates that the industrial hub, especially a chlor-alkali plant is the primary source of Hg. A contaminant trap effect is observed in this area associated with high fine sediment accumulation and Hg fluxes. The contamination pattern indicates that the regions not affected by direct inputs are influenced by reworking, resuspension, and transport of contaminated sediments by tidal flows. The Hg enrichment in the upper layers of the sediment cores demonstrates that the environmental actions fulfilled in the 1980s were insufficient to control Hg pollution in the Santos estuary.

Plastic debris degrades in the water environments due to various factors such as mechanical stress. Small-sized degradation products, including plastic monomers, are currently monitored using equipment which might be unsuitable for screening. Here, we developed a recombinant whole-cell bacterial biosensor, which could be used for this type of monitoring. The Escherichia coli pBAV1K-ACU-lucFF cells contain a luciferase-based reporter system under the control of acrylic acid specific promoter. The biosensor cells were used to detect acrylic acid monomers from both sterile water and spiked lake water samples, indicating usability with environmental samples. Furthermore, poly(acrylic acid) was incubated in salt water, and the biosensor cells could identify acrylic acid monomers originating from it. Thus, the cells could be used to observe similar processes in the environment. The results show that the bacterial biosensors could complement the current research methods of plastic monomer monitoring in water environments with a potential for higher throughputs.

This study provides an insight into the polychlorinated biphenyls (PCBs) inventories in the sediments of the northwestern Arabian/Persian Gulf. PCBs can be used as chemical markers that correlate with historical events in the region, to estimate the sedimentation rates in the northern Gulf, and to determine the sources of pollutants in the study area. The concentrations of PCBs were generally patchy in sediments. At Station 1 the ΣPCB concentrations generally fluctuated between 0.100 and 0.400 ng g⁻¹ dw throughout the depositional history measured in a sediment core. There were four peaks in the ΣPCB profile corresponding to 1969, 1979, 1983 and 1991. Station 2 showed a prominent peak at depth of 25 cm. The concentrations of the ΣPCBs and ΣICE congeners at this depth were 28 and 12 ng g⁻¹ dw respectively. Concentrations then dropped dramatically thereafter by a factor of 4. The ΣPCB concentrations at Station 3 were very low compared to the concentrations measured at Stations 1 and 2. The PCB concentration in Core 4 which was taken from open waters was 2–3 orders of magnitude lower than those in the other coastal cores. However, a 1990–91 peak was omnipresent in these cores. There is no record of PCB production within the Gulf region, and PCB releases into the Kuwait marine environment are likely to originate from their use in products. These maxima in early-1990s can be correlated to inputs from war-related activities, including the reported destruction of PCB-containing transformers and military equipment during the occupation of Kuwait. None of the recent sediment core sections at the four stations had a ΣPCB concentration near the effects range-median (ERM) concentration of 180 ng g⁻¹, or permissible exposure limits (PEL) of 189 ng g⁻¹, or were above the effect range-low (ERL) values of 22.7 ng g⁻¹.

The concentrations of 23 polycyclic aromatic hydrocarbons (PAHs; 16 parent PAHs and 7 alkyl-PAHs) were determined in 45 surface sediment and 7 basal sediment box core samples retrieved from the Estuary and Gulf of St. Lawrence in eastern Canada. The concentration sums of 16 priority PAHs (Σ₁₆PAHs) in the surface sediments (representing modern times or at least younger than the last decade) ranged from 71 to 5672 ng g⁻¹. Σ₁₆PAHs in the basal sediments ranged from 93 to 172 ng g⁻¹ among the pre-industrial samples (pre-1900 common era or CE) and from 1216 to 1621 ng g⁻¹ among the early post-industrial samples (~1930s and ~1940s CE). The highest Σ₁₆PAH values occurred in samples retrieved from the Baie-Comeau-Matane area, an area affected by intense industrial anthropogenic activities. Source-diagnostic PAH ratios suggest a predominance of pyrogenic sources via atmospheric deposition, with a minor contribution of petrogenic seabed pockmark sources. The PAH concentrations in the sediments from the study areas reveal low ecological risks to benthic or other organisms living near the water-sediment interface.

Plastic bags are among the most discarded waste items as they are generally only used once and are often improperly eliminated and transported by rivers and estuaries to the ocean. We developed an experimental design to mimic the effect of plastic bag deposition in a tropical estuary and investigated its short-term impact on benthic community structure. We observed a significant influence of the presence of plastic bags on the abundance, richness and diversity of benthic fauna after an eight-week exposure period. Plastic bags acted as a barrier and interfered in processes that occur at the water-sediment interface, such as organic matter and silt-clay deposition. Our results indicate that plastic bags, in addition to directly affecting benthic fauna, may alter processes such as carbon burying, known as “blue carbon”, thus making its storage in the sediment more difficult.

In recent decades shipping traffic has increased, leading to elevated underwater ambient noise levels. Research has been conducted on the noise generated by ships underway, however little is known about potential noise from ships at anchor. In coastal regions, commercial vessels can seek anchorages prior to entering port, leading to concern regarding the impacts on the soundscape and marine ecosystems. Cowichan Bay, British Columbia, a coastal region (800 Ha) 70 km away from the Port of Vancouver, was examined as a case study to understand the possible soundscape contribution from anchored bulk carriers. When a carrier anchored, sound pressure levels (SPL: 20–24,000 Hz) were elevated 2–8 dB re: 1 μPa throughout the bay. These results demonstrate the change anchored carriers can have on underwater soundscapes and is an important step in understanding the potential impact these vessels may have on marine organisms and important ecosystems.

The present study was carried out to quantify microplastic prevalence among 20 sandy beaches on the Gujarat coast. Beaches were categorised into three different classes, viz. low-impacted sites, moderately impacted sites, and highly impacted sites based on anthropogenic pressure. Microplastic (MP) (≤ 5 mm) contamination on the beaches varied with an average of 1.4 MPs/kg to 26 MPs/kg sediment. Sutrapada site-1 and Porbandar showed the highest and lowest mean abundance of microplastics, respectively, among 20 selected beaches. Out of the total assessed microplastics, threads were the maximum (89.98%), followed by the films (4.75%), fragments (3.36%) and foam (1.89%). In terms of colour and size, different microplastics were recorded in this study. The chemical composition of microplastics was identified by ATR-FTIR as polypropylene (47.5%), polyethylene (26%), and polystyrene (25%). Tourism and fishing activities are the possible sources of higher microplastic contamination at highly impacted sites.

The study on the concentration of trace elements in Antarctic krill and in water in the deep areas of the Atlantic sector of the Antarctic was performed. Concentrations of 22 trace elements were studied to determine their spatial distribution in krill, and to assess the accumulation ability of the krill against 8 of them. The trace elements concentration in krill diminished in the following order: Fe > Cu > Zn > Bа > B > Se > As > Cr > Ni > Ag > Li > Mn > V > Mo > Cd > Co > Hg > Be. Concentrations of Pb, Ti, Tl, Sb were below their detection limits. Concentration factors of trace elements by krill varied from n × 10² to n × 10⁴. The Cu and As concentrations in dry krill exceeded their MPC. Concentrations of all trace elements in wet mass of krill were not exceeded established regulative values.