The pH change and the release of organic matter and metals from sediment, due to the potential CO₂ acidified seawater leakages from a CCS (Carbon Capture and Storage) site are presented. Column leaching test is used to simulate a scenario where a flow of acidified seawater is in contact with recent contaminated sediment. The behavior of pH, dissolved organic carbon (DOC) and metals As, Cd, Cr, Cu, Ni, Pb, Zn, with liquid to solid (L/S) ratio and pH is analyzed. A stepwise strategy using empirical expressions and a geochemical model was conducted to fit experimental release concentrations. Despite the neutralization capacity of the seawater-carbonate rich sediment system, important acidification and releases are expected at local scale at lower pH. The obtained results would be relevant as a line of evidence input of CCS risk assessment, in an International context where strategies to mitigate the climate change would be applied.

Mercury loads in tropical estuaries are largely controlled by the rainfall regime that may cause biodilution due to increased amounts of organic matter (both live and non-living) in the system. Top predators, as Trichiurus lepturus, reflect the changing mercury bioavailability situations in their muscle tissues. In this work two variables [fish weight (g) and monthly total rainfall (mm)] are presented as being important predictors of total mercury concentration (T-Hg) in fish muscle. These important explanatory variables were identified by a Weibull Regression model, which best fit the dataset. A predictive model using readily available variables as rainfall is important, and can be applied for human and ecological health assessments and decisions. The main contribution will be to further protect vulnerable groups as pregnant women and children. Nature conservation directives could also improve by considering monitoring sample designs that include this hypothesis, helping to establish complete and detailed mercury contamination scenarios.

The bivalve Scrobicularia plana, an important species for the structure and functioning of estuarine and coastal mudflats, was studied in thirteen sites from NW France differing by their degree of contamination to document the presence of reproduction impairments (intersex, sex ratio, gonadosomatic indices) in relation to the condition revealed by using hepatosomatic and condition indices. In agreement with recent studies in other European estuaries, intersex was revealed in all the studied estuaries, including sites the chemical and ecological status of which is considered “good” according to the criteria of the European Water Framework Directive. The presence of endocrine disrupting chemicals (EDCs) could result in such disturbances. Our results re-inforce the concern linked to the subtle effects of EDCs, which are active at very low doses, often in the absence of any major sign of toxicity. However at this stage, no clear link may be established between intersex and population effects.

Polyethylene passive samplers (PE) were deployed in Narragansett Bay, RI, to examine freely dissolved concentrations of polybrominated diphenyl ethers (PBDEs) in surface, bottom, and sediment porewater. PBDE congeners in the water column and porewater were below 3 pg L⁻¹. In the surface water, only PBDE congeners containing up to 5 bromines were detected, while in the deeper water congeners 153 and 154 (6 bromines) were also detected. Activity ratios of surface-bottom water and porewater-bottom water suggested that lower brominated (di-tetra) congeners reached Narragansett Bay from surface waters and sediments. PBDEs in the surface water probably originated from a combination of air–water exchange, freshwater runoff, rivers, and wastewater treatment plants. It is suggested that deep water was the source of higher brominated PBDEs to the Bay implying that the more hydrophobic PBDEs reached depth on particles and/or that these congeners were degraded in sediments. On-going sources supply PBDEs to Narragansett Bay.

In natural environments fish are exposed to endocrine disrupting compounds (EDCs) present at low concentrations and with different modes of actions. Here, adult zebrafish of both sexes were exposed for 21 days to an estrogenic mixture (Mix) of eleven EDCs previously quantified in Douro River estuary (Portugal) and to 100 ng/L 17α-ethinylestradiol (EE2) as positive control. Vitellogenin mRNA and HSI in males confirmed both exposure regimes as physiologically active. Potential candidates for estrogenic disturbance of steroidogenesis were identified (StAR, 17β-HSD1, cyp19a1), but Mix only affected cyp19a1 in females. Significant differences in the response of FSHβ, cypa19a2, 20β-HSD were observed between EE2 and Mix. Mtf-1 and tfap2c transcription factor binding sites were discovered in the putative promoter regions and corresponding transcription factors were found to be differentially expressed in response to Mix and EE2. The results suggest that “non-classical effects” of estrogenic EDC in fish are mediated via transcription factors.

A comprehensive, weight-of-evidence based ecological risk assessment approach integrating laboratory and in situ bioaccumulation and toxicity testing, passive sampler devices, hydrological characterization tools, continuous water quality sensing, and multi-phase chemical analyses was evaluated. The test site used to demonstrate the approach was a shallow estuarine wetland where groundwater seepage and elevated organic and inorganic contaminants were of potential concern. Although groundwater was discharging into the surficial sediments, little to no chemical contamination was associated with the infiltrating groundwater. Results from bulk chemistry analysis, toxicity testing, and bioaccumulation, however, suggested possible PAH toxicity at one station, which might have been enhanced by UV photoactivation, explaining the differences between in situ and laboratory amphipod survival. Concurrently deployed PAH bioaccumulation on solid-phase micro-extraction fibers positively correlated (r² ≥ 0.977) with in situ PAH bioaccumulation in amphipods, attesting to their utility as biomimetics, and contributing to the overall improved linkage between exposure and effects demonstrated by this approach.

Ecological assessments over large spatial scales require that anthropogenic impacts be distinguishable above natural variation, and that monitoring tools are implemented to maximise impact detection and minimise cost. For three heavily modified and four relatively ‘pristine’ estuaries (disturbance category), chemical indicators (metals and PAHs) of anthropogenic stress were measured in benthic sediments, suspended sediments and deployed oysters, together with other environmental variables. These were compared with infaunal and hard-substrate invertebrate communities. Univariate analyses were useful for comparing contaminant loads between different monitoring tools and identified the strongest relationships between benthic and suspended sediments. However, multivariate analyses were necessary to distinguish ecological response to anthropogenic stressors from environmental “noise” over a large spatial scale and to identify sites that were being impacted by contaminants. These analyses provide evidence that suspended sediments are a useful alternative monitoring tool to detect potential anthropogenic impacts on benthic (infaunal and hard-substrate) communities.

A large portion of polychlorinated biphenyls (PCBs) from e-waste released into the coastal areas may be the potential source of PCBs to the global oceans. The paper presents data of PCBs concentrations in fifty surface sediment samples and a dated sediment core in Yangtze River Delta (YRE) and adjacent East China Sea (ECS). The total PCBs levels varied from 5.08 to 19.64 ng/g dry weight, with the highest concentrations situate within the river-sea boundary zone which is so-called “marginal filter”. Concurrent with the operation of e-waste recycling over the last two decades, PCB fluxes started to rise again after 1980s and reached a maximum in this century. The full data set was used to estimate the burden of PCBs in YRE and adjacent ECS. A total sediment burdens were 192.8 tons, with the spatial density of 364 ng/cm² which accounts for 1.9% of all the PCBs in China.

Polybrominated diphenyl ethers (PBDEs) of sixty-three sediment samples from the coastal East China Sea (ECS), extending ∼1000 km from the Yangtze River Estuary to the south, were measured. The levels of BDE-209 and ∑PBDE₇ (sum of BDE-28, 47, 99, 100, 153, 154, 183) were 0.3–44.6 ng/g (dry weight) and nd-8.0 ng/g, respectively. BDE-209 was the predominant congener, followed by BDE-99/100. This was consistent with the historical and current usage of PBDE mixtures in China. The compositions and distribution of PBDEs suggest that the PBDEs in this area could be mainly from the coastal electronic waste dismantling/recycling and Yangtze River input. The poor correlations between TOC, grain size of sediments with PBDEs imply that the PBDE distribution is more related to their land-based inputs rather than the sediment characters in the area. The coastal ECS is an important sink of PBDEs (7.5 t/yr) in the world.

Spatial distribution and source apportionment of polycyclic aromatic hydrocarbons (PAHs) in the surface sediments of the Yangtze Estuary, especially the North Branch, have been fully investigated. PAH concentrations increased with the descending distance from the inner estuary to the adjacent sea, and varied significantly in various estuarine regions. Water currents (e.g., river runoff and ocean current) greatly affected the distribution pattern. In addition, ambient sewage and traffic also contributed to the PAH pollution in the estuary. In the adjacent sea, PAH values along the −20m isobath were higher than those along the −10m isobath due to the “marginal filter” phenomenon formed by different water currents. In most sites, PAHs had poor correlations with sediment size, but had positive correlations with total organic carbon. Based on the qualitative and quantitative analysis results, PAH sources were proved to be mainly from a mixture of petroleum combustion, biomass, and coal combustion.