Sediment samples were collected to a depth of 60 cm along a 350-m sampling belt in a short-term-flooding riparian wetland in the Yellow River Delta of China in three sampling seasons. Contents of heavy metals were determined to investigate their spatial and temporal distributions, sources and ecotoxities. Our results showed that As contents in the top 20 cm sediments increased before decreasing along the sampling belt in summer, whereas they kept stable before increasing in fall and spring. Cd contents increased along the sampling belt in three sampling seasons, whereas Ni and Cr generally exhibited a decreasing tendency. Comparatively, Cu, Pb and Zn consistently increased at the first 50 m distance and then decreased before increasing from the distance of 150 m in summer and fall and increased to the maximum at the distance of 250 m and then showed a decrease in spring. Two “hotspots” of heavy metal accumulation in sediment cores along the belt were observed at the distance from 50 to 100 m in summer and at the distance from 200 to 300 m in spring. Most of sediment samples contained higher heavy metals in excess of threshold effect levels except for Zn and Pb in three sampling seasons and the values of toxic units in more than 30% of sediment samples exceeded 4 in summer. As, Ni and Cr had relatively higher contribution to the values of toxic units compared with other heavy metals in three sampling seasons. Multivariance analysis showed that As and Cd might originate from the same source and Cu, Zn, Cr, Pb and Ni might derive from another similar source. Cd was significantly correlated with salinity (p < 0.01) and pH (p < 0.05). Meanwhile, these heavy metals were also significantly correlated with other properties such as S, Al, TP, SOM and Silt + Clay.

Accurately predicting how marine biota are likely to respond to changing ocean conditions requires accurate simulation of interacting stressors, exposure regimes and recovery periods. Jellyfish populations have increased in some parts of the world and, despite few direct empirical tests, are hypothesised to be increasing because they are robust to a range of environmental stressors. Here, we investigated the effects of contaminated runoff on a zooxanthellate jellyfish by exposing juvenile Cassiopea sp. medusae to a photosystem II (PSII) herbicide, atrazine and reduced salinity conditions that occur following rainfall. Four levels of atrazine (0ngL⁻¹, 10ngL⁻¹, 2μgL⁻¹, 20μgL⁻¹) and three levels of salinity (35 ppt, 25 ppt, 17 ppt) were varied, mimicking the timeline of light, moderate and heavy rainfall events. Normal conditions were then slowly re-established over four days to mimic the recovery of the ecosystem post-rain and the experiment continued for a further 7 days to observe potential recovery of the medusae. Pulse-amplitude modulated (PAM) chlorophyll fluorescence, growth and bell contraction rates of medusae were measured. Medusae exposed to the combination of high atrazine and lowest salinity died. After 3 days of exposure, bell contraction rates were reduced by 88% and medusae were 16% smaller in the lowest salinity treatments. By Day 5 of the experiment, all medusae that survived the initial pulse event began to recover quickly. Although atrazine decreased YII under normal salinity conditions, YII was further reduced when medusae were exposed to both low salinity and atrazine simultaneously. Atrazine breakdown products were more concentrated in jellyfish tissues than atrazine at the end of the experiment, suggesting that although bioaccumulation occurred, atrazine was metabolised. Our results suggest that reduced salinity may increase the susceptibility of medusae to herbicide exposure during heavy rainfall events.

In the Athabasca Oil Sands Region in northeastern Alberta, Canada, oil sands operators are testing the feasibility of peatland construction on the post-mining landscape. In 2009, Syncrude Canada Ltd. began construction of the 52 ha Sandhill Fen pilot watershed, including a 15 ha, hydrologically managed fen peatland built on sand-capped soft oil sands tailings. An integral component of fen reclamation is post-construction monitoring of water quality, including salinity, fluvial carbon, and priority pollutant elements. In this study, the effects of fen reclamation and elevated sulfate levels on mercury (Hg) fate and transport in the constructed system were assessed. Total mercury (THg) and methylmercury (MeHg) concentrations in the fen sediment were lower than in two nearby natural fens, which may be due to the higher mineral content of the Sandhill Fen peat mix and/or a loss of Hg through evasion during the peat harvesting, stockpiling and placement processes. Porewater MeHg concentrations in the Sandhill Fen typically did not exceed 1.0 ng L−1. The low MeHg concentrations may be a result of elevated porewater sulfate concentrations (mean 346 mg L−1) and an increase in sulphide concentrations with depth in the peat, which are known to suppress MeHg production. Total Hg and MeHg concentrations increased during a controlled mid-summer flooding event where the water table rose above the ground surface in most of the fen. The Hg dynamics during this event showed that hydrologic fluctuations in this system exacerbate the release of THg and MeHg downstream. In addition, the elevated SO42− concentrations in the peat porewaters may become a problem with respect to downstream MeHg production once the fen is hydrologically connected to a larger wetland network that is currently being constructed.

The distribution and interaction of parent and alkyl polycyclic aromatic hydrocarbons (EPA-34 PAHs) among the multiple phases were investigated in estuarine water column of Humen outlet over a 12-months period. The water column was divided into 5 vertical layers, and each layer included dissolved phase, large- and small-size suspended particular matter (SPM). Regarding to EPA-34 PAHs, alkyl homologues were abundant, especially in the dissolved phase and small-size SPM. Moreover, SPM contributed a large proportion of EPA-34 PAHs in the water column especially for the large-size SPM, which therefore play an important role for the transportation of these pollutants. The EPA-34 PAHs concentrations in water column during wet season were higher than those in the dry season due to the decreasing of KD values which were affected by TSS and salinity obviously. Generally, the EPA-34 PAHs concentrations in the water column increased with the increasing of water depth, most of the highest concentrations of EPA-34 PAHs were found in the near-bottom layer due to the rapid sinking of large-size SPM and sediment resuspension. Additionally, during the ebb-flood tide period, the EPA-34 PAHs concentrations in different phases of the water column fluctuated oppositely based on the effects of hydrodynamic conditions.

Oxytracycline (OTC) is a broad spectrum antibiotic authorized for use in European aquaculture. Its photo-degradation has been widely studied in synthetic aqueous solutions, sometimes resorting to expensive methods and without proven effectiveness in natural waters. Thus, this work studied the possibility to apply the solar photo-degradation for removal of OTC from marine aquaculture's waters. For that, water samples were collected at different locals of the water treatment circuit, from two different aquaculture companies. Water samples were firstly characterized regarding to pH, salinity, total suspended solids (TSS), organic carbon and UV–Vis spectroscopic characteristics. Then, the samples were spiked with OTC and irradiated using simulated sunlight in order to evaluate the matrix effects on OTC photo-degradation. From kinetic results, the apparent quantum yields and the outdoor half-life times, at 40°N for midsummer and midwinter days were estimated by the first time for these conditions. For a midsummer day, at sea level, the outdoor half-life time predicted for OTC in these aquaculture's waters ranged between 21 and 25 min. Additionally, the pH and salinity effects on the OTC photo-degradation were evaluated and it has been shown that high pH values and the presence of sea salt increase the OTC photo-degradation rate in aquaculture's waters, compared to results in deionised water. The results are very promising to apply this low-cost methodology using the natural sunlight in aquaculture's waters to remove OTC.

The cycling of sulfur (S), iron (Fe) and phosphorus (P) in sediments and pore water can impact the water quality of overlying water. In a heavily polluted river estuary (Yantai, China), vertical profiles of fluxes of dissolved sulfide, Fe2+ and dissolved reactive phosphorus (DRP) in sediment pore water were investigated by the Diffusive Gradients in Thin films technique (DGT). Vertical fluxes of S, Fe, P in intertidal sediment showed the availability of DRP increased while the sulfide decreased with depth in surface sediment, indicating that sulfide accumulation could enhance P release in anoxic sediment. In sites with contrasting salinity, the relative dominance of iron and sulfate reduction was different, with iron reduction dominant over sulfate reduction in the upper sediment at an intertidal site but the reverse true in a freshwater site, with the other process dominating at depth in each case. Phosphate release was largely controlled by iron reduction.

With the increasing usage of titanium dioxide nanoparticles (NPs), their release into the environment makes it important to understand their transport, fate and behaviour in natural waters. In this study, aggregation and deposition of TiO2 NPs were studied during a 3-h period by using a dynamic light scattering instrument and a UV–vis spectrophotometer, respectively. TiO2 NPs were spiked in 34 lake and 5 brackish water samples at an initial concentration of 10 mg L−1. Depending on the physicochemical properties of the natural waters, TiO2 NPs exhibited different colloidal stability. In brackish waters with high salinity, TiO2 NPs were prone to aggregate and settled rapidly. Whereas under conditions of humic and humus-poor lake waters, TiO2 NPs were suspended in water column for a longer time without remarkable change in particle size and concentration. Deposition likely occurred in nutrient-rich lakes which had high amount of nitrogen and phosphorus accompanied by high values of conductivity, alkalinity, pH and turbidity. Linear regression analysis revealed the statistically significant relationships (p ≤ 0.008) between the TiO2 NPs stability and these water properties. Our study makes a better understanding of the water properties that control the aggregation and deposition of TiO2 NPs in complex natural waters.

Phenolic endocrine disrupting chemicals (EDCs) in an estuarine water column in a depth profile of five water layers (0.05 D, 0.20 D, 0.60 D, 0.80 D and 0.90 D, D = Depth, 10.7 ± 0.7 m) and their corresponding environmental parameters (tide, salinity and particle size) were investigated over a year. Water sample from each layer was further separated into three fractions, which were dissolved, coarse (SPM-D, Φ ≥ 2.7 μm) and fine (SPM-F, 2.7 μm > Φ ≥ 0.7 μm) suspended particulate matters. Most of EDCs in the water column were presented in the dissolved fraction. Vertical profiles of salinity fluctuations showed that the upper water layer was most influenced by upstream flow. Estriol (E3), mestranol (Mes) and 17α-ethynylestradiol (EE2) concentrations were significantly higher in ebb tide than in flood tide, indicating that EDCs mainly came from terrestrial source, the upstream flow. Dissolved EDCs also exhibited high levels in the surface layer (0.05 D) due to the upstream source and atmosphere deposition, followed by the bottom layer (0.90 D) owing to the re-suspension of EDCs-containing sediment. Compared to the dissolved phase, the contents of BPA, Mes and EE2 in the solid phase were affected by particle size and exhibited a trend of SPM-F > SPM-D > sediment. On the other hand, the concentrations of octylphenol (OP) and t-nonylphenol (NP), the degradation products from common nonionic surfactants, in sediment were higher than those in suspended particles, and NP concentration was higher in flood tide than that in ebb tide. For both SPM-D and SPM-F, their corresponding EDCs concentrations were negatively related to SPM concentrations due to particle concentration effect (PCE). Owing to the “salting-out effect”, salinity pushed EDCs from dissolved fraction to particulate or sedimentary phase.

Increasing use of carbon nanotubes (CNTs) has led to their introduction into the environment where they can interact with dissolved organic matter (DOM). This study focuses on solution chemistry effects on DOM adsorption/desorption processes by single-walled CNTs (SWCNTs). Our data show that DOM adsorption is controlled by the attachment of DOM molecules to the SWCNTs, and that the initial adsorption rate is dependent on solution parameters. Adsorbed amount of DOM at high ionic strength was limited, possibly due to alterations in SWCNT bundling. Desorption of DOM performed at low pH resulted in additional DOM adsorption, whereas at high pH, adsorbed DOM amount decreased. The extent of desorption conducted at increased ionic strength was dependent on pre-adsorbed DOM concentration: low DOM loading stimulated additional adsorption of DOM, whereas high DOM loading facilitated release of adsorbed DOM. Elevated ionic strength and increased adsorbed amount of DOM reduced the oxidation temperature of the SWCNTs, suggesting that changes in the assembly of the SWCNTs had occurred. Moreover, DOM-coated SWCNTs at increased ionic strength provided fewer sites for atrazine adsorption. This study enhances our understanding of DOM–SWCNT interactions in aqueous systems influenced by rapid changes in salinity, and facilitates potential use of SWCNTs in water-purification technologies.

More than 35 million people in coastal Bangladesh are vulnerable to increasing freshwater salinization. This will continue to affect more people and to a greater extent as climate change projections are realised in this area in the future. However the evidence for health effects of consuming high salinity water is limited. This research examined the association between drinking water salinity and blood pressure in young adults in coastal Bangladesh. We conducted a cross-sectional study during May-June 2014 in a rural coastal sub-district of Bangladesh. Data on blood pressure (BP) and salinity of potable water sources was collected from 253 participants aged 19–25 years. A linear regression method was used to examine the association between water salinity exposure categories and systolic BP (SBP) and diastolic BP (DBP) level. Sixty five percent of the study population were exposed to highly saline drinking water above the Bangladesh standard (600 mg/L and above). Multivariable linear regression analyses identified that compared to the low water salinity exposure category (<600 mg/L), those in the high water salinity category (>600 mg/L), had statistically significantly higher SBP (B 3.46, 95% CI 0.75, 6.17; p = 0.01) and DBP (B 2.77, 95% CI 0.31, 5.24; p = 0.03). Our research shows that elevated salinity in drinking water is associated with higher BP in young coastal populations. Blood pressure is an important risk factor of hypertension and cardiovascular diseases. Given the extent of salinization of freshwater in many low-lying countries including in Bangladesh, and the likely exacerbation related to climate change-induced sea level rise, implementation of preventative strategies through dietary interventions along with promotion of low saline drinking water must be a priority in these settings.