Mangroves provide vital climate change mitigation and adaptation (CCMA) ecosystem services (ES), yet have suffered extensive tropics-wide declines. To mitigate losses, rehabilitation is high on the conservation agenda. However, the relative functionality and ES delivery of rehabilitated mangroves in different intertidal locations is rarely assessed. In a case study from Panay Island, Philippines, using field- and satellite-derived methods, we assess carbon stocks and coastal protection potential of rehabilitated low-intertidal seafront and mid- to upper-intertidal abandoned (leased) fishpond areas, against reference natural mangroves. Due to large sizes and appropriate site conditions, targeted abandoned fishpond reversion to former mangrove was found to be favourable for enhancing CCMA in the coastal zone. In a municipality-specific case study, 96.7% of abandoned fishponds with high potential for effective greenbelt rehabilitation had favourable tenure status for reversion. These findings have implications for coastal zone management in Asia in the face of climate change.

Mercury (Hg) and methylmercury (MeHg) are highly toxic and poorly studied in mangroves. Burrowing Uca crabs change sediment topography and biogeochemistry and thus may affect Hg distribution and MeHg formation. We studied added 203Hg distribution, Me203Hg formation and sulfate reduction rates (SRR) in sediment aquariums containing Uca leptodactyla; and analyzed profiles of Me203Hg formation and SRR in sediment cores from two mangroves with distinct environmental impacts. MeHg formation and SRR were higher in the top (≤6cm) sediment and there was no significant difference in Hg methylation in more or less impacted mangroves. In aquariums, crab bioturbation favored Hg retention in the sediment. In the treatment without crabs, Hg volatilization and water Hg concentrations were higher. Hg methylation was higher in bioturbated aquariums but SRR were similar in both treatments. These findings suggest that bioturbating activity favors Hg retention in sediment but also promotes MeHg formation near the surface.

The goal of this study was to investigate co-selection of antibiotic resistance in gram-negative epiphytic bacteria. Halimione portulacoides samples were collected from metal(loid)-contaminated and non-contaminated salt marshes. Bacterial isolates (n=137) affiliated with Vibrio, Pseudomonas, Shewanella, Comamonas, Aeromonas and with Enterobacteriaceae. Vibrio isolates were more frequent in control site while Pseudomonas was common in contaminated sites. Metal(loid) and antibiotic resistance phenotypes varied significantly according to site contamination, and multiresistance was more frequent in contaminated sites. However, differences among sites were not observed in terms of prevalence or diversity of acquired antibiotic resistance genes, integrons and plasmids. Gene merA, encoding mercury resistance, was only detected in isolates from contaminated sites, most of which were multiresistant to antibiotics. Results indicate that metal(loid) contamination selects for antibiotic resistance in plant surfaces. In salt marshes, antibiotic resistance may be subsequently transferred to other environmental compartments, such as estuarine water or animals, with potential human health risks.

This study was carried out to evaluate the present-day chemical properties of methylmercury in surface sediment in Minamata Bay where a dredging project was completed 28years ago. Present-day sediment from Minamata Bay consists of sandy silt, and the average loss-on-ignition in surface sediment was 7.0±2.3%. The average methylmercury concentrations in the upper sediment layers were significantly higher than those in the lower sediment layers. Currently, the concentrations in sediments in Minamata Bay do not exceed the Japanese regulatory standard value for mercury. The average concentration of methylmercury in Minamata Bay surface sediment was 1.74±1.0ng/g on a dry weight basis (n=107). The methylmercury concentration in Minamata Bay surface sediment was almost 16 times higher than that in surface sediment from Isahaya Bay surface sediment, which was 0.11±0.045ng/g on a dry weight basis (n=5).

Khuzestan, Iran is heavily industrialised with petrochemical and refinery companies. Herein, sediment and soil samples were collected from Hendijan coast, Khore Mosa and Arvandroud River. The CHEMSIC (CHEmometric analysis of Selected Ion Chromatograms) method was used to assign the main sources of polycyclic aromatic hydrocarbon (PAH) pollution. A four-component principal component analysis (PCA) model was obtained. While principal component 1 (PC1) was related to the total concentration of PAHs, the remaining PCs described three distinct sources: PC2 and PC3 collectively differentiate between weathered petrogenic and pyrogenic, and PC4 is indicative for a diagenetic input. The sources of PAHs in the Arvandroud River were mainly relatively fresh oil with some samples corresponding to a weathered oil input. Further, perylene (indicator for diagenetic source) was identified. Samples from Khore Mosa revealed a mixture with high proportions of high-molecular-weight PAHs, indicating a pyrogenic/weathered petrogenic source. Samples from Hendijan coast contained low relative concentrations of PAHs, thus only little information on pollution sources.

The Cananéia–Iguape system is located in a Southeastern Brazilian coastal region, acknowledged by UNESCO as Biosphere Reserve of the Atlantic Rainforest. This system underwent important environmental changes due to the opening of the artificial channel of Valo Grande and by past intensive Pb ore mining activities. In view of this scenario, this study evaluated Cu, Pb and Zn availability in sediments from Cananéia–Iguape system, based on the content associated with the main components of the sediments. Moreover, in order to assess local contamination, the metals' contents were compared to Canadian quality guidelines, the past levels of metals preceding the mining activities and background sediment values. Concerning Cu and Zn in a state of chemical remobilization, both elements would possibly present no harm to the local communities. However, Pb available content exceeded the comparison values in various sampling sites, suggesting the need of monitoring regarding its bioavailability.

A bacterial consortium was selected in the presence of Cu from sediment samples taken from Sepetiba Bay, Brazil, which is a site historically contaminated by metals. Bacteria were exposed to 0, 1, 6, 12.5, 25 and 50μg·mL−1 Cu, Pb and Cu+Pb for 11days of bioassay. Results showed Alcanivorax dominance (81%) and cell counts of 108cells·mL−1. However, a reduction in dehydrogenase activity was observed from the fifth day of exposure for all Cu, Pb, and Cu+Pb concentrations tested. Esterase activity tended to increase, indicating higher energy demand to complete the bacterial lifecycle. Pb concentrations in the filtered culture medium (0.2μm) were below the detection limit, indicating biosorption, whereas concentrations of Cu were close to the tested concentrations, indicative of efflux. Results suggest the need for biomarkers, such as esterase and dehydrogenase enzymatic activity, in the assessment of resistance and tolerance of communities previously exposed to stressors.

The amounts and sources of polycyclic aromatic hydrocarbons (PAHs) and their bioaccumulation factors (BAFs) in the zooplankton community of Chabahar Bay were investigated. The highest amounts of total PAHs (tPAHs) in the water and zooplankton samples were 62.2ngL−1 and 1478.6ngg−1 dry weights, in near the Shahid Beheshti Port and desalination, respectively. The greatest amount of BAF (51,780) was obtained in the entry of Bay, and it was related to the phenanthrene accumulation. Using molecular ratio, the results showed that the major input source of PAH compounds in zooplankton of Chabahar Bay was pyrolytic (fuel) source.

New International Maritime Organization regulations require shippers to classify all solid bulk cargo to indicate whether they are Harmful to the Marine Environment (HME). The objective of this work was to adapt the freshwater Transformation/Dissolution Protocol (T/DP) to marine water to provide a method to determine, when compared with marine Ecotoxicity Reference Values (ERVs), whether a metal-bearing substance is HME. The substances examined were: Cu2O powder; Ni metal powder; Co3O4 powder; and a Ni–Co–Fe alloy, as wire cuttings, which were the same substances examined in the freshwater T/D validation study and afforded comparisons of the reactivity, or measure of the rate and extent of metal release from the metal-bearing substances in freshwater versus marine conditions. The marine T/D method is suitable for conducting examinations of metal-bearing substances with a wide range of reactivities, from the relatively reactive Cu2O powder and the alloy to the Co3O4 powder, which was the least reactive.

Cadmium concentrations were determined in the tissues of muscle and liver of Carcharhinus falciformis (silky shark) sampled in Todos Santos, Baja California South, Mexico. This is one of the main shark species for human consumption in Mexico. Results indicate that accumulation of Cd varied in both sexes, based on its metabolism, sex, maturity and other biological characteristics. High Cd values were observed in the liver of adults of male (529.61μgg−1) and female (457.43μgg−1), whereas, in muscular tissues it was low (0.37μgg−1) than the prescribed permissible limits for seafood (0.5μgg−1). Substantial correlations were observed between body length and Cd values in adults except young male due to faster growth rate and its metabolism. The study indicated the impact of environmental conditions in the accumulation of Cd and its risk to the food web structure in the marine environment and health hazard for humans.