Plastic production pellets collected from beaches of south west England contain variable concentrations of trace metals (Cr, Co, Ni, Cu, Zn, Cd and Pb) that, in some cases, exceed concentrations reported for local estuarine sediments. The rates and mechanisms by which metals associate with virgin and beached polyethylene pellets were studied by adding a cocktail of 5 μg L⁻¹ of trace metals to 10 g L⁻¹ pellet suspensions in filtered seawater. Kinetic profiles were modelled using a pseudo-first-order equation and yielded response times of less than about 100 h and equilibrium partition coefficients of up to about 225 ml g⁻¹ that were consistently higher for beached pellets than virgin pellets. Adsorption isotherms conformed to both the Langmuir and Freundlich equations and adsorption capacities were greater for beached pellets than for virgin pellets. Results suggest that plastics may represent an important vehicle for the transport of metals in the marine environment.

Sediments collected from the continental shelf of China, embracing Yellow Sea, inner shelf of the East China Sea (ECS), and the South China Sea (SCS), were analyzed for polycyclic aromatic hydrocarbons (PAHs). The concentrations of anthropogenic PAHs (Σ₁₈PAH) were 27–224 ng/g dry weight, with an average of 82 ng/g. Sedimentary PAHs in the continental shelf off China were mainly derived from mixed residues of biomass, coal, and petroleum combustion. Fluvial transport and atmospheric deposition mainly accounted for sediment PAHs in the ECS inner shelf and Yellow Sea (and the SCS), respectively. Furthermore, statistically higher levels of Σ₁₈PAH (28–224 ng/g; mean 110 ng/g) in the Yellow Sea sediment than in the SCS sediment (28–109 ng/g; mean 58 ng/g) were probably resulted from higher PAH emissions from coke industry and domestic coal combustion in North China than in South China.

The Bird’s Head Seascape located in eastern Indonesia is the global epicenter of tropical shallow water marine biodiversity with over 600 species of corals and 1,638 species of coral reef fishes. The Seascape also includes critical habitats for globally threatened marine species, including sea turtles and cetaceans. Since 2001, the region has undergone rapid development in fisheries, oil and gas extraction, mining and logging. The expansion of these sectors, combined with illegal activities and poorly planned coastal development, is accelerating deterioration of coastal and marine environments. At the same time, regency governments have expanded their marine protected area networks to cover 3,594,702ha of islands and coastal waters. Low population numbers, relatively healthy natural resources and a strong tenure system in eastern Indonesia provide an opportunity for government and local communities to collaboratively manage their resources sustainably to ensure long-term food security, while meeting their development aspirations.

Photolysis rates of phenanthrene as a function of ionic strength (salinity), oxygen levels and humic acid concentrations were measured in aqueous solution over the range of conditions found in fresh to marine waters. Photolysis followed first order kinetics, with an estimated photodegradation half-life in sunlight in pure water of 10.3±0.7h, in the mid-range of published results. Photolysis rate constants decreased by a factor of 5 in solutions with humic acid concentrations from 0 to 10mgCL⁻¹. This decrease could be modeled entirely based on competitive light absorption effects due to the added humics. No significant ionic strength or oxygen effects were observed, consistent with a direct photolysis mechanism. In the absence of significant solution medium effects, the photodegradation lifetime of phenanthrene will depend only on solar fluxes (i.e. temporal and seasonal changes in sunlight) and not vary with a freshwater to marine environment.

Cold-water coral reefs represent some of the most biodiverse and biomass rich ecosystems in the marine environment. Despite this, ecosystem functioning is still poorly understood and the susceptibility of key species to anthropogenic activities and pollutants is unknown. In European waters, cold-water corals are often found in greatest abundance on the continental margin, often in regions rich in hydrocarbon reserves. In this viewpoint paper we discuss some of the current strategies employed in predicting and minimizing exposure of cold-water coral reef ecosystems on the Norwegian margin to waste materials produced during offshore drilling operations by the oil and gas industry. In the light of recent in situ and experimental research conducted with the key reef species Lophelia pertusa, we present some possible improvements to these strategies which may be utilized by industry and managers to further reduce the likelihood of exposure. We further highlight important outstanding research questions in this field.

The Great Barrier Reef (GBR) is a World Heritage Area and contains extensive areas of coral reef, seagrass meadows and fisheries resources. From adjacent catchments, numerous rivers discharge pollutants from agricultural, urban, mining and industrial activity. Pollutant sources have been identified and include suspended sediment from erosion in cattle grazing areas; nitrate from fertiliser application on crop lands; and herbicides from various land uses. The fate and effects of these pollutants in the receiving marine environment are relatively well understood. The Australian and Queensland Governments responded to the concerns of pollution of the GBR from catchment runoff with a plan to address this issue in 2003 (Reef Plan; updated 2009), incentive-based voluntary management initiatives in 2007 (Reef Rescue) and a State regulatory approach in 2009, the Reef Protection Package. This paper reviews new research relevant to the catchment to GBR continuum and evaluates the appropriateness of current management responses.

Polycyclic aromatic hydrocarbon (PAH) levels were measured in sediments, bivalves and semi-permeable membrane devices (SPMDs) in the relatively pristine marine environment of Nelson Lagoon, Alaska. Most PAH levels in Nelson Lagoon were low, and similar to global background concentrations. Sampling media type can significantly influence conclusions of PAH contamination in the environment. Concentration of a broad size range of PAHs was observed in the tissues of blue mussels (Mytilus edulis). SPMDs collected some two- to three-ring PAHs from the dissolved water phase, while sediments collected five- to six-ring PAHs that were likely adsorbed onto particulate matter. Benzo(a)pyrene, a potent carcinogen, was found in mussels at levels similar to more industrialized harbors in Alaska.

The discharge of sewage into the Antarctic marine environments by scientific stations has resulted in local changes in these pristine sites. To assess the distribution and concentration of sewage indicators from the Brazilian Antarctic station, sediments were sampled during the 2009/10 austral summer at four points (water depth of 20 and 60m). Concentrations of faecal sterols and linear alkylbenzenes (LABs) ranged from <0.01 to 0.17μgg⁻¹ and <1.0 to 46.5ngg⁻¹ dry weight, respectively. Maximum concentration of faecal sterols was similar to the value previously calculated as the background level for this area (0.19μgg⁻¹), and it is lower than the concentration observed in previous studies (1997–2008), whereas the LABs concentrations remained practically constant (35ngg⁻¹). Despite the low concentrations of sewage markers, the permanent human activities in the region require monitoring programs to determine continuing trends and prevent the increase of anthropogenic impacts.

Sorption of anionic perfluorooctane sulfonate (PFOS) on marine sediment was investigated in detail. It was found that solution ionic composition and sediment-specific parameters played important roles in affecting the sorption of PFOS. The results indicated that sorption of PFOS in seawater to marine sediments was strong (∼10 times higher than that in freshwater) and nonlinear (Freundlich nF values of 0.77–0.96). The sorption affinity was well correlated with sediment organic carbon content, indicating the importance of hydrophobic interactions. At a PFOS aqueous concentration of 10μg/L, PFOS distribution coefficients increased with the increasing salinity in solution, with an average rate of 0.48±0.03log units per a log unit of salinity. Further studies demonstrated that among common ions contributing to the salinity in seawater, dissolved calcium and magnesium are dominantly responsible for the sorption-enhancing effect of salinity for PFOS. This work will aid in better understanding of PFOS sorption mechanisms, and be useful for fate modeling of this class of contaminants in the marine environment.