The removal and degradation of polybrominated diphenyl ethers (PBDEs) in sediments are not clear. The vertical distribution of total and dehalogenating bacteria in sediment cores collected from a typical mangrove swamp in South China and their intrinsic degradation potential were investigated. These bacterial groups had the highest abundances in surface sediments (0–5cm). A 5-months microcosm experiment also showed that surface sediments had the highest rate to remove BDE-47 than deeper sediments (5–30cm) under anaerobic condition. The deeper sediments, being more anaerobic, had lower population of dehalogenating bacteria leading to a weaker BDE-47 removal potential than surface sediments. Stepwise multiple regression analysis indicated that Dehalococcoides spp. were the most important dehalogenating bacteria affecting the anaerobic removal of BDE-47 in mangrove sediments. This is the first study reporting that mangrove sediments harbored diverse groups of dehalogenating bacteria and had intrinsic potential to remove PBDE contamination.

The effects of microplastic concentrations (10itemsl−1 and 1000itemsl−1) on the physiological responses of Atactodea striata (clearance rate, absorption efficiency, respiration rate) were investigated. The fates of ingested microplastics and the efficiency of depuration in removing ingested microplastics were also studied. A. striata ingested microplastics and the clearance rate was reduced at high concentration of microplastics. Since the respiration rate and absorption efficiency remained unchanged in exposed A. striata, reduction in the clearance rate would reduce the energy intake. Ingestion and retention of microplastics in the body were further limited by the production of pseudofaeces and faeces, and depuration in clean water, resulting in a very small amount of microplastics stored in the body of the clam.

Based on two multidisciplinary investigations conducted in summer and winter 2015, the distribution of dissolved oxygen (DO) and the associated seasonal variations off the Changjiang River Estuary (CRE) were studied. The DO content was high in winter, ranging from 6.81–10.29mg/L, and the distribution was mainly controlled by temperature and salinity. The DO concentration was 1.92–9.67mg/L in summer, and a hypoxic zone (DO<3mg/L) covered 14,800km2, which was mainly controlled by stratification and organic matter decomposition. The hypoxic zone exhibited a “dual-core” structure and the differences in the biochemical and physical processes between the southern and northern regions were compared: the northern region exhibited stronger pycnocline intensity; while larger biomass and higher TOC as well as TN contents were observed in the southern region. Hypoxia in the northern region might be mainly dominated by stratification, while that in the southern region was mainly associated with organic matter decomposition.

Marine cross-border areas are ideal for monitoring pollutants so as to increase ecosystems protection. This study was conducted at the Romanian-Ukraine border of the Black Sea to reveal evidence of contamination with toxic metals based on biomonitoring of: cadmium, lead, total chromium, nickel and copper at different water depths and prey-predator interactions, combined with environmental forensics techniques of biological sampling and separation in witnesses size groups. The species used were Mytilus galloprovincialis L. and Rapana venosa V. collected at 17.5m, 28m and 35m depth. An atomic absorption spectrometer with a high-resolution continuum source and graphite furnace was used for toxic metals quantification in various samples: sediments, soft tissue, stomach content, muscular leg, hepatopancreas. The best sample type, based on the pathology of metal location and bioaccumulation, is the hepatopancreas from R. venosa that proved a significant decrease of cadmium and lead at lower depths.

The Red Sea is a unique ecosystem with high biodiversity in one of the warmest regions of the world. In the last five decades, Red Sea coastal development has rapidly increased. Sediments from continental margins are delivered to depths by advection and diffusion-like processes which are difficult to quantify yet provide invaluable data to researchers. Beryllium-7, lead-210 and ceseium-137 were analyzed from sediment cores from the near-coast Red Sea near Jeddah, Saudi Arabia. The results of this work are the first estimates of diffusion, mixing, and sedimentation rates of the Red Sea coastal sediments. Maximum chemical diffusion and particle mixing rates range from 69.1 to 380cm−2y−1 and 2.54 to 6.80cm−2y−1, respectively. Sedimentation rate is constrained to approximately 0.6cm/yr via multiple methods. These data provide baselines for tracking changes in various environmental problems including erosion, marine benthic ecosystem silting, and particle-bound contaminant delivery to the seafloor.

The levels and distribution of tris-(2,3-dibromopropyl) isocyanurate (TBC) and hexabromocyclododecanes (HBCDs) of surface sediments in the Yellow River Delta wetland had been investigated. The concentrations of TBC and ∑HBCDs ranged from 0.20 to 29.03ng·g−1dw and below limits of detections (LODs) to 20.25ng·g−1dw. The average composition profile of three HBCDs isomers were 10.1%, 6.1% and 83.8% for α-, β- and γ-HBCD, respectively. Moreover, correlation analysis indicated there are similar sources among three isomers and positive correlations between total organic carbon (TOC) content and concentrations of TBC and HBCDs. The mass inventory of TBC,α-, β-, γ-HBCD, ΣHBCDs in surface sediments of Yellow River Delta wetland were estimated about 725.50, 72.76, 44.29, 548.34, 665.39kg. Therefore, further investigations on potential human health and environmental risk assessments of TBC and HBCDs were needed.

Release and microbial degradation of dissolved organic matter (DOM) and chromophoric dissolved organic matter (CDOM) from the macroalgae Ulva prolifera were studied in laboratory incubation experiments. The release of DOM and CDOM from Ulva prolifera was a rapid process, and hydrolysis played an important role in the initial leaching of the organic compounds from the algae. Bacterial activity enhanced the release of DOM and CDOM during degradation of the algae and utilization of the released organic compounds. It is calculated that 43±2% of the C and 63±3% of the N from Ulva prolifera's biomass were released during the 20-day incubation, and 65±3% of the released C and 87±4% of the released N were utilized by bacteria. In comparison, only 18±1% of the algae's C and 17±1% of its N were released when bacterial activities were inhibited. The fluorescence characteristics of the CDOM indicate that protein-like DOM was the major organic component released from Ulva prolifera that was highly labile and biodegradable. Bacteria played an important role in regulating the chemical composition and fluorescence characteristics of the DOM. Our study suggests that the release of DOM from Ulva prolifera provides not only major sources of organic C and N, but also important food sources to microbial communities in coastal waters.

Antifouling paints are widely used to avoid organisms settling on boat hulls. The active ingredients in the paints have differed over the years where lead, TBT, irgarol and diuron have been deemed too harmful to non-target organisms and subsequently been banned within the EU. Most of these compounds however are persistent in the environment and can cause problems long after they are deposited.We have examined if present-day and banned substances used in antifouling paints can be found in sediments in a national park on the Swedish west coast. Sampled locations include waterways, natural harbours and small marinas for leisure crafts to investigate if number of visiting boats affect the concentration of antifouling compounds in sediments.Few significant differences were found when comparing the different locations types, suggesting that overall boat presence is more important than specific mooring sites, however, several banned antifouling compounds were found in the surface sediments.

Bioaerosols were collected between April and November 2015 on land (Gdynia) and at sea (Southwestern Baltic), using six-step microbiological pollutant sampler. It was determined that picoplanktonic cyanobacteria of the genus Synechococcus, Synechocystis, Aphanocapsa, Aphanothece, Microcystis, Merismopedia, Woronichinia and Cyanodictyon were the most commonly found in aerosols both over land and at sea. Chlorophyta were also numerous (Chlorella vulgaris, Stichococcus bacillaris), as were Bacillariophyta and Ochrophyta (Phaeodactylum sp., Navicula cf. perminuta and Nannochloropsis cf. gaditana). As primary production and phytoplankton concentration in sea water grew, so did the diversity of the microorganisms identified in bioaerosols. Over the sea cyanobacteria and microalgae occurred more often in large aerosols (>3.3μm). Over land they were mainly the components of smaller particles. In respirable particles species both capable of producing harmful secondary metabolites and potentially toxic ones were identified. We assume that bioaerosols pose the actual threat to human health in Baltic Sea region.

The performance of a portable x-ray fluorescence spectrometer configured in a test stand and coupled to a laptop has been evaluated for the determination of various elements (including Br, Cd, Cl, Cr, Cu, Fe, Pb and Zn) in beached microplastics. Under laboratory conditions, analysis of samples that covered the 3-mm x-ray beam returned concentrations that, on average, were within 20% of concentrations determined by ICP following acid digestion. Analysis of progressively smaller offcuts (to <1mm) resulted in corresponding concentrations that were comparable to those determined in original samples but errors and detection limits that progressively increased. When the configuration was deployed in situ with two operators, up to 35 microplastics counted for 60s each could be processed per hour. Advantages of immediate measurements include the development of an iterative study strategy, rapid compliance-evaluation, and identification of specific materials for further characterisation or study in the laboratory.