PURPOSE OF REVIEW: Mangroves are under increasing heavy metal (HM) pollution pressure from human activities because of the rapid industrialization and urbanization in coastal areas. Field and laboratory experiments showed that the tolerance of mangrove plants to HM stress is normally a mixture of metal avoidance and scavenging of reactive oxygen species (ROS). In this review, related studies during the past few decades on the accumulation and tolerance of mangrove to HMs have been synthesized. RECENT FINDINGS: In mangroves, metal accumulation mainly occurred at the root level with restricted transport to the aerial portions of the plant. The common founded HMs, such as copper, zinc, cadmium, chromium, and mercury, generally showed high bioconcentration factor in roots, while the concentration factors for these metals in leaves were usually much lower than one. The limited translocation of the toxic metals to the aerial parts renders the mangrove plants a high endurance ability to high levels of HM stress. To protect the cellular components from oxidative damage by HMs, mangroves have developed both enzymatic and nonenzymatic antioxidant mechanisms to scavenge the ROS. In some circumstances, the changes of antioxidative enzyme activity were usually in accordance with the changes of toxic metal concentrations in plant tissues. However, the responses of antioxidative enzymes in mangroves to HM stress varied with plant species, metal type, and concentration, as well as the duration of the treatment time. More toxicity tests are needed with early life stages of mangroves to determine threshold effect concentrations under more realistic conditions.

We examined hepatic concentrations of arsenic (As), cadmium (Cd), copper (Cu), lead (Pb), manganese (Mn), mercury (Hg), rubidium (Rb), selenium (Se) and zinc (Zn) in 10 breeding female common eiders (Somateria mollissima) from each of three colonies across 20° of latitude. Levels of many elements were elevated in eiders, although generally below levels of toxicological concern. We found significant differences in concentrations of As, Rb, Hg, Mn and Se among colonies, but not in a consistent pattern with latitude, and Hg:Se molar ratios did not vary among colonies. Furthermore, overlap in element concentrations from birds at different colonies meant that we could not reliably differentiate birds from different colonies based on a suite of their hepatic trace element concentrations. We encourage other researchers to assess baseline trace element levels on this important, harvested species, as a means of tracking contamination of nearshore benthic environments in the circumpolar Arctic.

The Arabian Gulf is a semi-enclosed water body that has witnessed accelerated anthropogenic activity, in terms of commissioning of nuclear power plants, desalination facilities, oil refineries and extensive coastal development. Furthermore, three wars during the past three decades is a potential worry. This study presents the first plutonium baseline in seawater from the Northern Arabian Gulf. The 239+240Pu concentrations in seawater vary, between 2.9 and 4.9mBqm−3, a range that is comparable to other water masses at this latitude. The 238Pu ranged between 0.04 and 0.05mBqm−3 and the 137Cs concentration between 1.04 and 1.18Bqm−3. The ratio of 238Pu/239+240Pu at all eight sampling stations was 0.01, while the ratio of 239+240Pu/137Cs varied between 0.01 and 0.02. The presence of 137Cs and 239+240Pu in seawater from this region can mainly be attributed to the global atmospheric deposition and fluvial transport. The seawater concentration of 239+240Pu is five order of magnitude lower than bottom sediments in the area.

Membrane photocatalytic ozonization coupled with wet absorption offers potential for elemental mercury (Hg0) removal. This study reports on a novel FeTiO2-coated polyvinylidene fluoride (PVDF) wet photocatalytic membrane reactor (WPCMR) for mercury removal in flue gas. Hg0 removal efficiency in the WPCMR reached up to 93.3%. Ozone could enhance mercury oxidation in WPCMR. Wet absorption helps to increases mercury removal efficiency. FeTiO2 catalyst was synthesized by sol-gel method and characterized by XRD, FTIR, UV–Vis, XPS and SEM. XPS analysis confirmed Hg0 oxidation to divalent mercury (Hg (II)). Elemental mercury was oxidized to mercuric oxide followed by wet absorption in the presence of OH free radical and ozone. Wet photocatalytic membrane reactor and photocatalytic membrane reactor (PCMR) of elemental mercury reaction with the FeTiO2/PVDF catalyst all follow Langmuir-Hinshelwood kinetics.

Three one-off burial treatments were designed in intertidal zone of the Yellow River estuary to determine the effects of sediment burial on decomposition and heavy metal levels of Suaeda salsa. Sediment burial showed significant effect on decomposition rate of S. salsa. With increasing burial depth, Cu, Zn, Cd and Co levels generally increased, while Cr and Mn levels decreased. Except for Zn, Mn, Cd and Co, stocks of Pb, Cr, Cu, Ni and V in S. salsa among burials were greatly different. The S. salsa in three burials was particular efficient in binding V and Co and releasing Pb, Zn and Cd, and, with increasing burial depth, stocks of Cr, Cu, Ni and Mn shifted from accumulation to release. In future, the eco-toxic risk of Pb, Cr, Cu, Zn, Ni, Mn and Cd exposure might be serious as the strong burial episodes occurred in S. salsa marsh.

Aliphatic hydrocarbons (AHs), biomarker and polycyclic aromatic hydrocarbons (PAHs) concentrations of surface water and sediment samples collected from Yellow River Estuary and adjacent coastal area in China were measured to determine their spatial distributions, analyze their sources and evaluate the ecological risk of PAHs in the water–sediment system. The spatial distributions of n-alkane in sediments are mainly controlled by the mixing inputs of terrigenous and marine components. In comparison with AHs, the total concentrations of Σ16PAHs in surface sediments from a transect of the offshore area were noticeably higher than that of the riverine and estuary areas. Additionally, the AHs and total PAHs concentrations all indicated an overall pattern of a seaward decrease. The PAHs concentrations during the dry season (mainly in the form of dissolved phase) were higher than that of PAHs (mainly dissolved phase and particulate phase form) in the flooding season. In comparison with global concentration levels of PAHs, the level of PAHs in suspended particulate matter and sediments from the Yellow River Estuary was lower than those from other countries, while the concentration of PAHs in the dissolved phase were in the middle range. Petroleum contamination, mainly from oil exploration and discharge of pollutants from rivers, was the main source of n-alkanes. The PAHs in the river were mostly of petrogenic origin, while those in the estuarial and marine areas originated mainly from pyrogenic sources. The results of the toxicology assessment suggested that the PAHs in sediments from Yellow River Estuary and adjacent coastal area exhibited a low potential eco-toxicological contamination level.

The present study aimed to use primary liver cell culture derived from the orange-spotted grouper, Epinephelus coioides, to assess the toxic effects of nonylphenol (NP) on the hepatocyte viability and the liver antioxidant system. E. coioides was selected due to its commercial importance. NP was used in this study because of its high potential of producing oxidative stress due to increased reactive oxygen species (ROS). A liver of E. coioides was digested with PBS containing 0.1% collagenase IV. The digested cells were moved to Leibovitz L-15 culture medium with 20% fetal bovine serum (FBS), 100IUmL−1 penicillin, 100μgmL−1 streptomycin. Aliquots of cell suspension were seeded as a monolayer into sterile 25cm2 tissue culture flasks and incubated at 30°C for 14days. The medium, containing non-attached cells, was removed after 24 to 48h and a new medium was added. The IC50 of 10−4molL−1 was determined for nonylphenol using MTT assay. Cells were then incubated with L-15 medium containing 10−5, 2×10−5, 3×10−5molL−1 of NP and samples were taken after 6, 12 and 24h of incubation for analysis of LPO, SOD, CAT, GPx, LDH, AST, ALT, and ALP. Based on the results, the lowest concentration of NP was not markedly cytotoxic to primary hepatocytes and the cell sensitivity to NP increased dose-dependently. The activities of SOD, CAT and GPx decreased significantly, while activities of LPO, LDH, AST, ALT and ALP, increased significantly in a dose-related pattern in NP-treated cells. In conclusion, this study revealed that NP could induce the oxidative stress in cultivated hepatocytes of E. coioides during a short-term exposure. NP toxicity is mainly due to the induction of the reactive oxygen species (ROS), which lead to cell membrane disruption, damage of cellular metabolism, and interference with cellular macromolecules.

Chlorine dioxide (ClO2) is seen as an effective alternative to chlorine, which is widely used as an antifouling biocide. However, data on its efficacy against marine macrofoulants is scanty. In this study, acute toxicity of ClO2 to larval forms of the fouling barnacle Amphibalanus reticulatus was investigated. ClO2 treatment at 0.1mg/L for 20min elicited 45–63% reduction in naupliar metamorphosis, 70% inhibition of cyprid settlement and 80% inhibition of metamorphosis to juveniles. Increase in concentration to 0.2mg/L did not result in any significant difference in the settlement inhibition or metamorphosis. Treatment with 0.2mg/L of ClO2 elicited substantial reduction in the settlement of barnacle larvae compared to control. The study indicates the possibility of using ClO2 as an alternative antifouling biocide in power plant cooling water systems. However, more work needs to be done on the environmental effects of such switchover, which we are currently undertaking.

In this article, we investigated the effect of low intensity pulsed ultrasound (US), temperature and salinity on cleaning efficacy of fine bubbles with diameter <50μm for diesel contaminated sands. About 47% and 76% diesel removal was achieved from 10% (w/w) diesel contaminated fine and medium sands respectively, after 30min treatment with 40kHz low intensity intermittent pulsed US together with MBs in contrast to 41% and 68% diesel removal while treatment with MBs alone. The effect of high temperature was found to be prominent during the initial stages of cleaning. In addition, MBs generated in 599mM saline water efficiently removed 85% diesel from fine sand within 30min in contrast to only 41% diesel removal with MBs in fresh water. This study provides evidence for developing highly efficient MBs based chemical free technology for diesel contaminated sediments.

The size and settling velocity of oil-mineral aggregates (OMAs) derived from diluted bitumen are primary constituents in predictive models for evaluating the potential fate of oil spilled in the aquatic environment. A series of low sediment concentration (15mg·L−1), colder water (<10°C) wave tank experiments designed to measure variability in these parameters in naturally-formed OMAs in response the presence or absence of chemical dispersant are discussed. Corresponding lab experiments revealed settling velocities of artificially formed OMAs on the order of 0.1–0.4mm·s−1. High-resolution imagery of settling particles were analyzed for particle size, density and settling velocity. In situ formation of OMAs in the wave tank was unsuccessful. Possible effects of chemical dispersant on natural sediment flocculation, the size of suspended oil droplets and clearance rates of suspended particles are discussed.