Marine Protected Areas (MPAs) are designated to enable the management of damaging activities within a discrete spatial area, and can be effective at reducing the associated impacts, including habitat loss and over-exploitation. Such sites, however, may be exposed to the potential impacts from broader scale pressures, such as anthropogenic litter, due to its diffuse nature and lack of constraint by legislative and/or political boundaries. Plastic, a large component of litter, is of particular concern, due to increasing evidence of its potential to cause ecological and socio-economic damage. The presence of sensitive marine features may mean that some MPAs are at greater potential risk from the impacts of plastic pollution than some non-protected sites. Understanding the abundance, distribution and composition of litter along coastlines is important for designing and implementing effective management strategies. Gathering such data, however, can be expensive and time-consuming but litter survey programmes that enlist citizen scientists are often able to resolve many of the logistical or financial constraints. Here, we examine data collected over 25-years (1994–2018), by Marine Conservation Society volunteers, for spatial patterns in relation to the English MPA network, with the aim of highlighting key sources of litter and identifying management priority areas. We found that MPAs in southeast (Kent) and southwest (Cornwall and Devon) England have the highest densities of shore-based litter. Plastic is the main material constituent and public littering the most common identifiable source. Items attributed to fishing activities were most prevalent in southwest MPAs and sewage related debris was highest in MPAs near large rivers and estuaries, indicating localised accumulation. When comparing inside and outside of MPAs, we found no difference in litter density, demonstrating the need for wider policy intervention at local, national and international scales to reduce the amount of litter.

Polycyclic aromatic hydrocarbons (PAHs) are a byproduct of combustion processes. They are common pollutants in oil-producing countries because fossil fuel processing generates PAHs that associate with dust. Airborne particles containing PAHs are transported into houses during dust storms, which are common in the arid oil-producing countries, and consequently the children and adults in the household are exposed to PAHs in indoor house dust. The goal of this study was to present a systematic survey of PAHs in indoor house dust in Kuwait. The PAHs concentrations and composition of indoor house dust was determined, along with their probable source and the potential carcinogenic risks. Total PAHs concentrations (ƩPAH) were, on average (±standard deviation) 1112 ± 347 μg/kg and ranged from 450 to 2242 μg/kg. Heavier congeners (4–6 ring PAHs) represented 61% of the ƩPAH. Petroleum combustion and traffic emissions were the major source of PAHs, based on the isomeric ratios of PAHs in indoor house dust. The incremental lifetime cancer risks (ILCRs) of exposure to PAHs in indoor house dust was 2.23 × 10⁻³ (95% CI: 1.99 × 10⁻³ – 2.48 × 10⁻³) for children and 2.15 × 10⁻³ (95% CI: 1.94 × 10⁻³ – 2.37 × 10⁻³) for adults, exceeding the US EPA safe limit of 1 × 10⁻⁶. Therefore, exposure to PAHs present in indoor house dust increases the cancer risk for children and adults in Kuwait.

Total concentrations of hydrophobic organic contaminants (HOCs) in sediment present a poor quality assessment parameter for aquatic organism exposure and environmental risk because they do not reflect contaminant bioavailability. The bioavailability issue of HOCs in sediments can be addressed by application of multi-ratio equilibrium passive sampling (EPS). In this study, riverbed sediment samples were collected during the Joint Danube Survey at 9 locations along the Danube River in 2013. Samples were ex-situ equilibrated with silicone passive samplers. Desorption isotherms were constructed, yielding two endpoints: pore water (CW:₀) and accessible (CAS:₀) concentration of polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), polycyclic aromatic hydrocarbons (PAHs) and polybrominated diphenyl ethers in sediment. CW:₀ concentrations of DDT and its breakdown products exhibited elevated levels in the low Danube, with the maximum in the river delta. Other investigated HOCs did not show any clear spatial trends along the river, and only a moderate CW:₀ variability. CAS:₀ in sediment ranged from 10 to 90% of the total concentration in sediment. CW:₀ was compared with freely dissolved concentration in the overlaying surface water, measured likewise by passive sampling. The comparison indicated potential compound release from sediment to the water phase for PAHs with less than four aromatic rings, and for remaining HOCs either equilibrium between sediment and water, or potential compound deposition in sediment. Sorption partition coefficients of HOC to organic carbon correlated well with octanol-water partition coefficients (KOW), showing stronger sorption of PAHs to sediment than that of PCBs and OCPs having equal logKOW. Comparison of CW:₀ values with European environmental quality standards indicated potential exceedance for hexachlorobenzene, fluoranthene and benzo[a]pyrene at several sites. The study demonstrates the utility of passive sampling as an innovative approach for risk-oriented monitoring of HOCs in river catchments.

Little information exists on interaction effects between air pollution and influenza vaccination on allergic respiratory diseases. We conducted a large population-based study to evaluate the interaction effects between influenza vaccination and long-term exposure to ambient air pollution on allergic respiratory diseases in children and adolescents.A cross-sectional study was investigated during 2012–2013 in 94 schools from Seven Northeastern Cities (SNEC) in China. Questionnaires surveys were obtained from 56 137 children and adolescents aged 2–17 years. Influenza vaccination was defined as receipt of the influenza vaccine. We estimated air pollutants exposure [nitrogen dioxide (NO2) and particulate matter with aerodynamic diameters ≤1 μm (PM1), ≤2.5 μm (PM2.5) and ≤10 μm (PM10)] using machine learning methods. We employed two-level generalized linear mix effects model to examine interactive effects between influenza vaccination and air pollution exposure on allergic respiratory diseases (asthma, asthma-related symptoms and allergic rhinitis), after controlling for important covariates.We found statistically significant interactions between influenza vaccination and air pollutants on allergic respiratory diseases and related symptoms (doctor-diagnosed asthma, current wheeze, wheeze, persistent phlegm and allergic rhinitis). The adjusted ORs for doctor-diagnosed asthma, current wheeze and allergic rhinitis among the unvaccinated group per interquartile range (IQR) increase in PM1 and PM2.5 were significantly higher than the corresponding ORs among the vaccinated group [For PM1, doctor-diagnosed asthma: OR: 1.89 (95%CI: 1.57–2.27) vs 1.65 (95%CI: 1.36–2.00); current wheeze: OR: 1.50 (95%CI: 1.22–1.85) vs 1.10 (95%CI: 0.89–1.37); allergic rhinitis: OR: 1.38 (95%CI: 1.15–1.66) vs 1.21 (95%CI: 1.00–1.46). For PM2.5, doctor-diagnosed asthma: OR: 1.81 (95%CI: 1.52–2.14) vs 1.57 (95%CI: 1.32–1.88); current wheeze: OR: 1.46 (95%CI: 1.21–1.76) vs 1.11 (95%CI: 0.91–1.35); allergic rhinitis: OR: 1.35 (95%CI: 1.14–1.60) vs 1.19 (95%CI: 1.00–1.42)]. The similar patterns were observed for wheeze and persistent phlegm. The corresponding p values for interactions were less than 0.05, respectively. We assessed the risks of PM1-related and PM2.5-related current wheeze were decreased by 26.67% (95%CI: 1.04%–45.66%) and 23.97% (95%CI: 0.21%–42.08%) respectively, which was attributable to influenza vaccination (both p for efficiency <0.05).Influenza vaccination may play an important role in mitigating the detrimental effects of long-term exposure to ambient air pollution on childhood allergic respiratory diseases. Policy targeted at increasing influenza vaccination may yield co-benefits in terms of reduced allergic respiratory diseases.

A multinational demersal longline survey was conducted on the Gulf of Mexico continental shelf over the years 2015 and 2016 to generate a Gulf-wide baseline of polycyclic aromatic hydrocarbon (PAH) concentrations in demersal fishes. Tilefish (Lopholatilus chamaeleonticeps) were sampled in all regions of the Gulf of Mexico for biometrics, bile, and liver. Tilefish liver was also obtained from surveys in the northwest Atlantic Ocean for comparison. Liver tissues (n = 305) were analyzed for PAHs and select alkylated homologs using QuEChERS extractions and gas chromatography tandem mass spectrometry. Bile samples (n = 225) were analyzed for biliary PAH metabolites using high-performance liquid chromatography with fluorescence detection. Spatial comparisons indicate the highest levels of PAH exposure and hepatic accumulation in the north central Gulf of Mexico, with decreasing concentrations moving from the north central Gulf counterclockwise, and an increase on the Yucatán Shelf. Hepatic PAH concentrations were similar between the Gulf of Mexico and the northwest Atlantic, however, Tilefish from the northwest Atlantic had higher concentrations and more frequent detection of carcinogenic high molecular weight PAHs. Overall, results demonstrate that PAH pollution was ubiquitous within the study regions, with recent exposure and hepatic accumulation observed in Tilefish from both the Gulf of Mexico and northwest Atlantic.

The Bohai Sea is a shallow-water, semi-enclosed marginal sea of the Northwest Pacific. Since the late 1990s, it has suffered from nutrient over-enrichment. To better understand the eutrophication characteristics of this important coastal sea, we examined four survey datasets from summer (June 2011), late autumn (November 2011), winter (January 2016), and early spring (April 2018). Nutrient conditions in the Bohai Sea were subject to seasonal and regional variations. Survey-averaged N/P ratios in estuarine and nearshore areas were 20–133. In contrast, the central Bohai Sea had mean N/P ratios of 16.9 ± 3.4 in late autumn, 16.1 ± 3.0 in winter and 13.5 ± 5.8 in early spring, which are close to the traditional N:P Redfield ratio of 16. In summer, both dissolved inorganic nitrogen (DIN) and dissolved inorganic phosphate (DIP) were used up in the surface waters of the central Bohai Sea, suggesting that the biological consumption of DIN and DIP may also follow the Redfield ratio. Wintertime nutrient budgets of the central Bohai Sea water were then established based on a mass balance study. Our results suggest that the adjacent North Yellow Sea supplied additional DIP to the central Bohai Sea via wintertime water intrusion, balancing terrigenous excess DIN that was introduced in summer. A water-mixing simulation combining these two nutrient sources with atmospheric nitrogen deposition suggests that eutrophication in the central Bohai Sea will likely be enhanced by the large-scale accumulation of anthropogenic nitrogen in adjacent open oceans. Such changes in nutrients may have fundamentally contributed to the recent development of algal blooms and seasonal hypoxia in the central Bohai Sea.

Although oil and gas explorations contribute to atmospheric methane (CH₄) emissions, their impact and influence along the shelf seas of China remain poorly understood. From 2012 to 2017, we conducted four ship-based surveys of CH₄ in the seawater column and boundary layer of the Bohai Sea, China, and further measured CO₂ and several meteorological parameters. The average observed CH₄ mixing ratios in the boundary layer and its concentrations in seawater column were 1950 ± 46 ppb in November 2012 (dissolved CH₄ was not observed in this survey), 2222 ± 109 ppb and 13.0 ± 5.9 nmol/L in August 2014, 2014 ± 20 ppb and 5.4 ± 1.4 nmol/L in February 2017, and 1958 ± 25 ppb and 5.3 ± 3.8 nmol/L in May 2017, respectively. The results demonstrated that the CH₄ emissions from the oil and gas platforms accounted for approximately 72.5 ± 27.0% of the increase in the background atmospheric CH₄ in the local area. The remaining emissions were attributed to land–sea air mass transportation. Conversely, the influence of the air–sea exchange was negligible, measuring within the 10⁻³ ppb range. For carbon balance calibration, the mean flaring efficiency of the oil-associated gas based on the enhancement of CO₂ (ΔCO₂) and enhancement sum of CO₂ and CH₄ (ΔCO₂ + ΔCH₄) was 98.5 ± 0.5%. Furthermore, the CH₄ emission rate from the oil and gas platforms was 0.026 ± 0.017 Tg/year, which was approximately 7.2 times greater than the sea-to-air CH₄ flux over the entire Bohai Sea area. Thus, oil and gas platforms must be recognized as important artificial hotspot sources of atmospheric CH₄ in the Bohai Sea.

Pollution of coastal and marine environments by mismanaged anthropogenic debris is a global threat requiring complex, multilateral solutions and mitigation strategies. International efforts to catalogue and quantify the density, extent and nature of mismanaged waste have not yet assessed the heterogeneity of debris between nearby areas. Better understanding of how debris types and density can be used as a proxy between regions and between land and seafloor habitats at a global scale can aid in developing cost effective and representative debris monitoring systems. Using volunteer collected clean-up and survey data, we compared the proportion and density of both total debris and specific items across 19,428 coastal land and seafloor sites from International Coastal Cleanups and Dive Against Debris surveys, from 86 countries between 2011 and 2018. We show that although some items common on land are also common on the seafloor, there is an overall global mismatch between debris types and densities on land and the seafloor from nearby areas. Correlations in land/seafloor debris type/density occurred primarily for items which entangle and/or sink, including fishing line, plastic bags, glass and polyethylene terephthalate (PET) bottles. Minimal similarity between land and seafloor surveys occurs for items which float or degrade. We suggest that to accurately evaluate local debris density, land and seafloor surveys are required to gain a holistic understanding. When detailed information on debris type, relative concentration, and likely source and transport are assessed, more cost effective and efficient policy interventions can be designed and implemented from local through to global scales.

In parts of developing countries, the over-exploitation of sands from inland waters has led to serious environmental concerns. However, understanding of the impacts of commercial sand dredging on inland water ecosystem functions remains limited. Herein, we assess the effects of this activity on the functional structure of the macroinvertebrate community and its recovery processes based on a 4-year survey, in the South Dongting Lake in China. Our result showed a simplified macroinvertebrate functional structures within the dredged area, as evidenced by a loss of certain trait categories (e.g., oval and conical body form) and a significant reduction in trait values due to the direct removal of macroinvertebrates and indirect alternations to physical environmental conditions (e.g., water depth and %Medium sand). Moreover, clear increases were observed in certain trait categories (e.g., small body size and swimmer) resulting from the dredging-related disturbance (e.g., increased turbidity) within the adjacent area. Furthermore, one year after the cessation of dredging, a marked recovery in the taxonomic and functional structure of macroinvertebrate assemblages was observed with most lost trait categories returning and an increase in the trait values of eight categories (e.g., body size 1.00–3.00 cm and oval body form) within the dredged and adjacent area. In addition, dispersal processes and sediment composition were the main driver for the structuring of the macroinvertebrate taxonomic and functional assemblages during the dredging stages, whilst water environmental conditions dominated the taxonomic structure and dispersal processes determined the functional structure during the recovery stage. Implications of our results for monitoring and management of this activity in inland waters are discussed.