Muscle and liver tissues of nine fish species were analyzed to assess butyltin and phenyltin contamination. The samples were collected from three basins located in the Southern Baltic Sea coastal zone that each represent different potential for organotin pollution. Maximum total concentrations of butyltin compounds (BTs) in the fish muscles and livers were 715 and 1132ng Sn g−1 d.w., respectively, whereas triphenyltin (TPhT) was not detected. In the muscle samples, the predominant compound in the sum of butyltins was tributyltin (TBT), while in the liver samples, tributyltin degradation products were found in the majority. The results demonstrate that 6–7years after the implementation of the total ban on harmful organotin use in antifouling paints, butyltins remain present in fishes from the Polish coast of the Baltic Sea. According to the HELCOM recommendation, eight samples exceeded the good environmental status boundary for tributyltin in seafood.

Public perception research evaluating awareness and attitudes towards marine protection is limited in the United Kingdom (UK) and worldwide. Given public opinion can help drive policy and affect its successful delivery we conducted nationwide surveys in 2005, 2010 and 2015 to assess public knowledge of UK (England, Scotland and Wales) sea ‘health’ and management. Respondents from all three surveys were relatively pessimistic about sea ‘health’, perceiving this as poor-fair and largely in decline. Enthusiasm for marine conservation was high with almost two-thirds of respondents in each survey wanting >40% of UK seas highly protected from fishing and damaging activities. In 2015 there was considerable dissatisfaction with the rate of progress in Marine Conservation Zone designation and over three-quarters of respondents considered dredging and trawling to be inappropriate in protected areas, contrary to management. The UK government and devolved administrations need to better align future conservation and management with public expectations.

The impact of Hurricane Sandy (October 29, 2012) on PAH exposure was investigated in adult Atlantic menhaden (Brevoortia tyrannus) collected along the NJ coast. Collections were made in August, September and/or October of 2011, 2012 and 2013. PAHs were monitored in raw fish oil using excitation–emission matrix (EEM) spectroscopy. Results showed that raw fish oils had relatively high levels of high molecular weight, PAH-like compounds (173 to 24,421ng/mL) compared to values reported for bile in other species. EEM profiles resembled that of crude oil and excluded matrix interference by some common biological molecules that also fluoresce. Concentrations and EEM profiles varied by collection; however, collection ship, month, year and fish size did not account for the data. Replicates showed that fish from the same catch had similar PAH exposure. Overall, Hurricane Sandy did not alter body burdens of PAHs in raw fish oil of menhaden.

We provide data on regional differences in plastic ingestion for two Southern Ocean top predators: Arctocephalus fur seals and albatrosses (Diomedeidae). Fur seals breeding on Macquarie Island in the 1990s excreted small (mainly 2–5mm) plastic fragments, probably derived secondarily from myctophid fish. No plastic was found in the scats of these seals breeding on three islands in the southwest Indian and central South Atlantic Oceans, despite myctophids dominating their diets at these locations. Compared to recent reports of plastic ingestion by albatrosses off the east coast of South America, we confirm that plastic is seldom found in the stomachs of Thalassarche albatrosses off South Africa, but found no Diomedea albatrosses to contain plastic, compared to 26% off South America. The reasons for such regional differences are unclear, but emphasize the importance of reporting negative as well as positive records of plastic ingestion by marine biota.

Two primary schools and one kindergarten were selected in the city of Kozani, Greece in order to investigate the school environment, the indoor air pollutants that children are exposed to and possible health risks at school. In each school three classrooms and one outdoor position were monitored from Monday to Friday, in both non-heating (26/09/2011–14/10/2011) and heating (23/01/2012–10/02/2012) period. Temperature, relative humidity and CO2, were continuously monitored. Formaldehyde, benzene, trichloroethylene, pinene, limonene, NO2 and O3 were measured with diffusive samplers. CO was monitored every day (30 min/day). Radon was measured for four weeks with short term radon detectors. PM2.5 was gravimetrically determined while PM2.5 and PM10 fractions were measured using the optical light scattering technique. Building material emission testing for VOCs was performed using the Field and Laboratory Emission Cell (FLEC). The ventilation rate for each classroom was calculated based on the CO2 measurements.Results indicated that indoor air concentrations of the measured pollutants were within accepted limits with indicative ranges 1.5–9.4 μg/m3 for benzene, 2.3–28.5 μg/m3 for formaldehyde, 4.6–43 μg/m3 for NO2 and 0.1–15.6 μg/m3 for O3. Emissions from building materials seem to have a significant contribution to the indoor air quality. Very low ventilation rates (0.1–3.7 L/s per person) were observed, indicating inadequate ventilation and possible indoor air quality problems requiring intervention measures. The estimated average lifetime cancer risks for benzene, formaldehyde and trichloroethylene were very low.

PM2.5 and PM10 samples were collected in a rural area from December 2014 to August 2015 near a coal-fired power plant on the southeast coast of China. The total mercury concentrations in PM2.5 ranged from 116.2 to 1070.9 pg/m3 and in PM10 from 173.4 to 1456.8 pg/m3, with averages of 309.5 ± 94.9 and 387.5 ± 133.5 pg/m3, respectively. These were much higher than those found in many foreign cities. The concentrations of mercury in PM2.5 and PM10 varied seasonally, with the highest average concentration in winter. This was probably due to the seasonal variation of meteorological conditions and concentration of particulates. The highest mass-based concentration of mercury in PM2.5 and PM10 was observed in spring. This result might be related to the prevailing sea winds in spring. The spatial variation of particulate mercury conformed to the concentration distribution characteristics of pollutant discharged from coal-fired power plant elevated source at the downwind area. The seasonal variation in the concentrations of the four mercury species (including exchangeable particulate mercury: EXPM, HCl-soluble particulate mercury: HPM, elemental particulate mercury: EPM, and residual particulate mercury: RPM) were all identical to the seasonal variation of total particulate mercury (TPM) in PM2.5 and PM10 (winter > spring > summer). Owing to the variation of meteorological conditions, the proportion of different mercury species in TPM followed different seasonal trends. In contrast to RPM, the percentage of both HPM and EPM in PM2.5 was higher than in PM10.

The present study evaluates the PCB-dehalorespiring capabilities and dynamics of indigenous Dehalococcoides mccartyi population in a PCB contaminated marine sediment. Specialized PCB-dechlorinase genes pcbA1, pcbA4 and pcbA5 previously characterized in pure cultures of D. mccartyi, were here found for the first time in environmental samples. Reductive dechlorination was stimulated by spiking Aroclor1254 to the sediment and by imposing strictly anaerobic conditions both with and without bioaugmentation with a Dehalococcoides mccartyi enrichment culture. In line with the contaminant dechlorination kinetics, Dehalococcoides population increased during the entire incubation period showing growth yields of 4.94E+07 Dehalococcoides per μmolCl−1 and 7.30E+05 Dehalococcoides per μmolCl−1 in the marine sediment with and without bioaugmentation respectively. The pcbA4 and pcbA5 dechlorinase genes, and to a lesser extent pcbA1 gene, were enriched during the anaerobic incubation suggesting their role in Aroclor1254 dechlorination under salinity conditions.

Qualitative inferences and sparse bay-wide measurements suggest that shoreline erosion increased after the 2010 BP Deepwater Horizon (DWH) disaster, but quantifying the impacts has been elusive at the landscape scale. We quantified the shoreline erosion of 46 islands for before and after the DWH oil spill to determine how much shoreline was lost, if the losses were temporary, and if recovery/restoration occurred. The erosion rates at the oiled islands increased to 275% in the first six months after the oiling, were 200% of that of the unoiled islands for the first 2.5years after the oiling, and twelve times the average land loss in the deltaic plain of 0.4%y−1 from 1988 to 2011. These results support the hypothesis that oiling compromised the belowground biomass of the emergent vegetation. The islands are, in effect, sentinels of marsh stability already in decline before the oil spill.

Nitrogen (N) supply by atmospheric deposition, wastewater, and fertilizers controls estuarine eutrophication. In New England, atmospheric N loads recently decreased by 50% and land-derived contributions rose about 80%, owing to national-scale emission controls and local urban development. The decrease in atmospheric deposition was large enough to balance increases in land-derived N loads, so total N loads to Waquoit Bay estuaries in Cape Cod did not change significantly between 1990 and 2014. Unchanged N regimes were corroborated by finding no differences in estuarine nutrient concentrations and macrophyte biomass between pre-2005 and in 2015. Coastal zones, subject to reasonably rapid changes in global and local driver variables, will require that assessment and management of eutrophication include adaptive strategies that capture effects of changing baselines. Management initiatives will be constrained by spatial scale of driver variables: local efforts may address wastewater and fertilizer N sources, but atmospheric sources require national or international attention.

Resident mussels are effective indicators of ecosystem health and have been utilized in national assessment and monitoring studies for over two decades. Mussels were chosen because contaminant concentrations in their tissues respond to changes in ambient environmental levels, accumulation occurs with little metabolic transformation and a substantial amount of historic data were available. Mussels were collected from 10 previously studied locations approximately a year after Hurricane Sandy. Regionally, concentrations of polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) decreased significantly, while concentrations of organochlorine pesticides (OCPs) remained unchanged, and polybrominated diphenyl ethers (PBDEs) increased compared to historic concentrations. Although concentrations of PCBs, OCPs and PAHs were at or near record low concentrations, long-term trends did not change after Hurricane Sandy. To effectively measure storm-induced impacts it is necessary to understand the factors influencing changes in mussel body burdens and have a long-term monitoring network and an ability to mobilize post event.