We studied the uptake of microplastics under field conditions. At six locations along the French–Belgian–Dutch coastline we collected two species of marine invertebrates representing different feeding strategies: the blue mussel Mytilus edulis (filter feeder) and the lugworm Arenicola marina (deposit feeder). Additional laboratory experiments were performed to assess possible (adverse) effects of ingestion and translocation of microplastics on the energy metabolism (cellular energy allocation) of these species. Microplastics were present in all organisms collected in the field: on average 0.2 ± 0.3 microplastics g−1 (M. edulis) and 1.2 ± 2.8 particles g−1 (A. marina). In a proof of principle laboratory experiment, mussels and lugworms exposed to high concentrations of polystyrene microspheres (110 particles mL−1 seawater and 110 particles g−1 sediment, respectively) showed no significant adverse effect on the organisms' overall energy budget. The results are discussed in the context of possible risks as a result of the possible transfer of adsorbed contaminants.

An on-site active solid-phase microextraction (SPME) sampling technique coupled with gas chromatography-mass spectrometry (GC–MS) for sampling and monitoring 16 polycyclic aromatic hydrocarbons (PAHs) and 8 organochlorine pesticides (OCPs) in seawater was developed. Laboratory experiments demonstrated that the sampling-rate calibration method was practical and could be used for the quantification of on-site sampling. The proposed method was employed for field tests which covered large amounts of water samples in the Pearl River Estuary in rainy and dry seasons. The on-site SPME sampling method can avoid the contamination of sample, the losses of analytes during sample transportation, as well as the usage of solvent and time-consuming sample preparation process. Results indicated that the technique with the designed device can address the requirement of modern environment water analysis. In addition, the sources, bioaccumulation and potential risk to human of the PAHs and OCPs in seawater of the Pearl River Estuary were discussed.

The distribution and fate of perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA) were investigated in the water and sediment of Bohai Bay, China, during 2011–2013. A total of 360 water samples and 60 sediment samples were collected from 20 locations. The median concentrations of PFOS and PFOA were 4.8 and 12.15 ng/L in the water, and 2.65 and 0.62 ng/g-dry in the sediment, respectively. Significant enrichment were observed for PFOS and PFOA in water of sea surface microlayer. The concentrations of these two compounds showed an apparent gradient from nearshore to offshore stations. The correlation analysis and the distribution tendencies indicated that freshwater inflowing to the bay was the main source of PFOS and PFOA. The salinity of seawater and the total organic carbon (TOC) content of sediment heavily affected the spatial distribution and the partitioning of PFOS and PFOA in the sediment-water system.

To control algae bloom and eutrophication in the tropical semi-closed harbor of the Hongsha Bay in Sanya, China, polyculture systems with macroalgae Eucheuma gelatinae and bivalves Gafrarium tumidum were studied. First, nine polyculture combinations with E. gelatinae and G. tumidum were selected in a pool. Two combinations were then chosen by response surface analysis and used for further study to validate their effect on controlling the microalgae density and reducing the nutrition concentration in the pool. Subsequently, the two selected combinations were used to study the effect on the purification of eutrophic seawater and control of algae bloom in a sea mesocosm. The results indicated that polyculture with E. gelatinae and G. tumidum enhanced the purification of eutrophic seawater and control of algae bloom. These two polyculture combinations are considered suitable for the Hongsha Bay of Sanya in China. The two combinations present an excellent effect on controlling the microalgae density and reducing the nutrition concentration.

A fine-scale survey of δ15N, δ13C, tissue-N in seaweeds was conducted using samples from 17 sampling points at two sites (Grandcamp-Maisy (GM), Courseulles/Mer (COU)) along the French coast of the English Channel in 2012 and 2013. Partial triadic analysis was performed on the parameter data sets and revealed the functioning of three areas: one estuary (EstA) and two rocky areas (GM∗, COU∗). In contrast to oceanic and anthropogenic reference points similar temporal dynamics characterized δ15N signatures and N contents at GM∗ and COU∗. Nutrient dynamics were similar: the N-concentrations in seawater originated from the River Seine and local coastal rivers while P-concentrations mainly from these local rivers. δ15N at GM∗ were linked to turbidity suggesting inputs of autochthonous organic matter from large-scale summer seaweed beachings made up of a mixture of Rhodophyta, Phaeophyta and Chlorophyta species. This study highlights the coupling between seaweed beachings and nitrogen sources of intertidal macroalgae.

Spatial and temporal distributions of 14 polycyclic aromatic hydrocarbons (PAHs) were investigated in surface waters of Haikou Bay, China from October 2013 to September 2014. The total PAHs concentrations ranged from 420.2 to 2539.1ngL−1 with the average value of 1016.3±455.8ngL−1, which were predominated by low molecular weight PAHs (2- and 3-ring PAHs). Moreover, PAHs displayed spatial and temporal variations in the concentration and composition pattern. Source analysis based on isomer ratios indicated that the PAHs mostly originated from petroleum and combustion processes. An eco-toxicological risk assessment showed that the potential risk of individual PAHs had reached moderate to high levels and the total concentrations of PAHs had also reached a relatively high level compared with previous studies. This study offers important information on the pollution levels of 14 PAHs in the surface waters of Haikou Bay and recommends that prevention and control of PAHs pollution should be implemented in the region.

A high selective pre-treatment method for the extraction and analysis of mebendazole in environmental water samples was developed based on molecularly imprinted solid-phase extraction (MISPE). The mebendazole imprinted polymers were synthesized in acetonitrile using methacrylic acid and ethylene glycol dimethacrylate as functional monomer and cross-linker respectively. The imprinted materials showed high adsorption ability for mebendazole and were applied as special solid-phase extraction sorbents for selective separation of mebendazole. An off-line MISPE procedure was developed for the purification and enrichment of mebendazole from natural seawater samples prior to high-performance liquid chromatography analysis. The recoveries of spiked seawater on the MISPE cartridges were from 83.0% to 90.6%, and the values of the relative standard deviation were in the range of 2.78–4.13% (n=3). The satisfied results showed that this pre-treatment methodology for extracting mebendazole in seawater was simple and effective.

The successful management of sustainable coastal environments that are beneficial to both humans and marine ecosystems requires knowledge about factors that are harmful to such environments. Here, we investigated seawater nutrient and carbon parameters between 2010 and 2012 in Kwangyang Bay, Korea, a coastal environment that has been exposed to intensive anthropogenic activities. The data were analyzed using cluster and factor analysis. We found that the biogeochemical cycles of nutrients and carbon were determined by river discharge into the bay and biological activity. However, the impacts of these factors varied both spatially and seasonally. During the past 10years, nutrient loads from the river and industrial complexes to the bay have decreased. The impacts of this decrease are visible in the phosphate concentration, which has fallen to a third of its initial value. We also examined the potential role of atmospheric nitrogen deposition in nitrogen cycling in the study area.

The occurrence of 14 polycyclic aromatic hydrocarbons (PAHs) listed by the United States Environmental Protection Agency was investigated in surface seawater of Yangpu Bay, China in November 2013 (winter) and May 2014 (summer). Seventy-two samples were collected from 12 sampling sites. The total concentrations of PAHs in Yangpu Bay showed obvious variations in different seasons, which varied from 582.8 to 2208.3ngL−1 in winter and 952.4 to 1201.7ngL−1 in summer, respectively. Two-ring PAHs accounted for more than 91.6% of total PAHs in winter, and three-ring PAHs were dominant with 81.6% of total PAHs in summer. Molecular indices analyses indicated that the main source of PAHs in Yangpu Bay could be petrogenic contamination. The ecological risk assessment by Risk quotients (RQNCs and RQMPCs) showed a potential ecological risk of PAHs in Yangpu Bay, indicating a close attention should be paid to pollution of PAHs in the coastal area of Yangpu.