China is a massive mercury emitter, responsible for a quarter of the world’s mercury emissions, which transit the atmosphere and accumulate throughout its watercourses. The Changjiang (Yangtze) River is the third largest river in the world, integrating mercury emissions over its 1.8 × 10⁶ km² catchment and channelling them to the East China Sea where they can be buried. Despite its potential global significance, the importance of the East China Sea as a terminal mercury sink remains poorly known. To address this knowledge gap, total mercury and methylmercury concentrations were determined from 51 surface sediment samples revealing their spatial distribution, whilst demonstrating the overall pollution status of the East China Sea. Sedimentary mercury distributions beneath the East China Sea are spatially heterogeneous, with high mercury concentrations (> 25 ng g⁻¹) corresponding to areas of fine-grained sediment accumulation. In contrast, some sites of fine-grained sediment deposition have significantly lower values of methylmercury (< 15 ng g⁻¹), such as the Changjiang estuary and some isolated offshore areas. Fine-grained particles and organic matter availability appear to exert the dominant control over sedimentary mercury distribution in the East China Sea, whereas in situ methylation serves as an additional control governing methylmercury accumulation. Estimated annual sedimentary fluxes of mercury in the East China Sea are 51 × 10⁶ g, which accounts for 9% of China’s annual mercury emissions.

In the present study, a multistage route is proposed for the treatment of biodiesel industry wastewater (BWW) containing around 1000 mg L⁻¹ of total organic carbon (TOC), 3500 mg L⁻¹ of chemical oxygen demand (COD), and 1325 mg L⁻¹ of oil and grease. Initially, BWW aerobic biodegradability was assessed via Zhan-Wellens biodegradability test to confirm the appropriate treatment route. Then, a hybrid moving bed bioreactor (MBBR) system was chosen as the first treatment stage. The hybrid MBBR achieved 69 and 68% removal of COD and TOC removals, respectively, and provided great conditions for biomass growth. The bacterial community present in the hybrid MBBR was investigated by PCR-DGGE and potential biodegraders were identified such as: members of Desulfuromonadales, Nocardioidaceae and Pseudomonadaceae. Since biodegradation in the hybrid MBBR alone was unable to meet quality requirements, advanced oxidation processes, such as Fenton and photo-Fenton, were optimized for application as additional treatment stages. Physicochemical properties and acute toxicity of BWW were analyzed after the multistage routes: hybrid MBBR + Fenton, hybrid MBBR + photo-Fenton and hybrid MBBR + UV-C₂₅₄ₙₘ/H₂O₂. Hybrid MBBR + Fenton or photo-Fenton showed overall COD removal efficiencies greater than 95% and removed acute toxicity, thus being appropriate integrated routes for the treatment of real BWW. Graphical abstract ᅟ

In the present study, the Taguchi design (TD) and the Box-Behnken design (BBD) were used to determine the effect of surfactant concentration, flushing velocity, and dense non-aqueous-phase liquid–trichloroethylene (DNAPL TCE) mass on the time of remediation for the removal of DNAPL zones, which is one of the main persistent sources of groundwater pollution. In the Taguchi approach, the performance of the response variable is measured based on the signal-to-noise (S/N) ratio whereas estimation of the full quadratic model of the parameters is allowed in the Box-Behnken design. The mean experimental values ranged between 3.97–8.31 and 4.01–9.70 for BBD and TD, respectively. Surfactant concentration was identified as the most significant parameter contributing to remediation efficiency in both design techniques. Minimum remediation effort was determined as 5.99 at obtained optimal conditions of surfactant concentration (2.5%), flushing rate (6 cm/h), and DNAPL TCE mass (365 mg) using BBD. In the case of TD, the optimal conditions were determined at a surfactant concentration of 10%, 2 cm/h flushing rate, and 365 mg DNAPL TCE mass. Analysis of variance (ANOVA) revealed a good relationship between the predicted and experimental values with 1.96% and 0.31% of the total variation that was not explained by the model using TD and BBD, respectively. Consequently, from this comparative study, it was concluded that BBD was a more suitable alternative to TD for the evaluation of remediation of DNAPL-contaminated sites.

With increasing metal prices and declining ore grades, new mines are getting larger and mine waste disposal and management have become more difficult, particularly from an environmental perspective. While technologies keep on improving, the available space for terrestrial mine waste disposal is limited. Thus, several coastal countries still consider deep-sea tailings placement (DSTP) as a viable option. This brief review compares the environmental impacts of DSTP versus on-land disposal and suggests several factors to consider in selecting the most suitable options for mine waste disposal.

In this paper, nanosized titanium dioxide as catalysts for degrading dye wastewater was in situ synthesized on the surface of cotton fabrics used tetrabutyl titanate as precursor. The morphology and structure of prepared catalysts were characterized by scanning electron microscopy, energy-dispersive spectrometer, and X-ray diffraction. The characterization results showed that anatase nanosized titanium dioxide was successfully synthesized in situ on cotton fabrics and had excellent dispersibility. Subsequently, the effects of irradiation time, catalyst dosage, dye concentration, initial pH value of dye, hydrogen peroxide dosage, and dye type on dye degradation rate were investigated one by one by a photocatalytic performance test. The test results indicated that the degradation rates of methylene blue, methyl orange, and rhodamine B were 90.4%, 81.4%, and 58.3%, separately, at catalyst dosage of 4.8 g/L, initial dye concentration of 10 mg/L, pH of 7, and hydrogen peroxide dosage of 0.24 mol/L, after 4 h of UV irradiation.

High contents of azo dyes and heavy metals enter surface waters with the wastewater from dying and dye-manufacturing industries and pose serious threat to fish. In the present study, changes in the ultra-morphological features of the scale have been evaluated as indicators of the stress of lethal and sublethal concentrations of an azo dye Acid Black-1 (AB-1, CI 20470), zinc (Zn), and their mixture AB-1 + Zn to Labeo rohita. Fish were exposed for 96 h to lethal concentration (LC) causing 0–70% mortality, i.e., LC₀, LC₂₀, LC₅₀, and LC₇₀ of AB-1 (4, 6, 8, and 10 mg/L respectively) and Zn (25, 50, 55, and 60 mg/L respectively) and LC₀, LC₅₀, and LC₇₀ of AB-1 + Zn (2 + 15, 2 + 20, and 2 + 25 mg/L respectively). Subchronic exposures of 150 days were given to 1/12, 1/6, and 1/3 of 96 h LC₅₀ values of AB-1, Zn, and AB-1 + Zn. After each exposure, the fish were kept for a recovery period of 90 days. Breakage of circuli, erosion and breakage of lepidonts, uprooting of tubercles, and disappearance of intercircular teeth were observed in all the fish, after 96 h exposure to AB-1, Zn, and AB-1 + Zn. However, damage to focus and holes were common on the scales of Zn-exposed fish. The mixture AB-1 + Zn was more toxic than either of the two as loss of circuli, lepidonts, and intercircular teeth, and sloughing of surface were observed in the scales after 96 h exposure to 2 + 25 mg/L. Damage at this concentration was more than the damage at 8/10 mg/L AB-1 and 55/60 mg/L Zn. After 150 days of exposure, damage due to sublethal concentrations was more than the damage due to all the concentrations of 96 h exposure. Irregular and sloughed circuli were common at 2 + 1.79 and 2 + 3.59 mg/L AB-1 + Zn. Cracks all over the surface (2 + 7.18 mg/L), calcium projections (2 + 3.59 and 2 + 7.18 mg/L), and holes (2 + 7.18 mg/L) hint towards synergistic toxicity of the mixture. It seems that the present dye and metal formed complexes with collagen and osteoblastic cells of the scale that caused an increase in damage during the post-exposure period. Scales of 2 + 7.18 mg/L AB-1 + Zn exposed fish were completely devoid of the normal architectural pattern on the 90th day of the recovery period. Changes in the ultra-morphology of scales at LC₀ (0% mortality) and sublethal concentrations show that these are early indicators of the stress of minute quantities of dyes and metals in water. This is a first report on the cumulative toxicity of the two most abundant components of textile industry effluents.

As transcriptomic studies are becoming more and more common, it is important to ensure that the RNA used in the analyses is of good quality. The RNA integrity may be compromised by storage temperature or freeze-thaw cycles, but these have not been well studied in poikilothermic fishes. This work studied the effects of tissue storage time and temperature, and freeze-thaw cycles of tissue and extracted RNA on RNA integrity in brown trout (Salmo trutta L.) liver. The storage time and temperature had an effect on RNA integrity, but RNA suitable for quantitative reverse transcription PCR (RT-qPCR) (RIN > 7) was still obtained from samples preserved at − 20 °C for 6 months. Freeze-thaw cycles of tissue or RNA did not compromise the integrity of RNA. RNA degradation had an effect on RT-qPCR results, and the effect depended on gene. The RT-qPCR analysis of historical samples from a bleached kraft pulp mill effluent exposure in 1984 revealed no significant cyp1a induction. Recommendations are given for the preservation and handling procedures of samples designated for transcriptomic analyses.

CO₂, SO₂, and NO are the main components of flue gas and can cause serious environmental issues. Utilization of these compounds in oleaginous microalgae cultivation not only could reduce air pollution but could also produce feedstock for biodiesel production. However, the continuous input of SO₂ and NO inhibits microalgal growth. In this study, the toxicity of simulated flue gas (15% CO₂, 0.03% SO₂, and 0.03% NO, balanced with N₂) was reduced through automatic pH feedback control. Integrated lipid production and CO₂ fixation with the removal of SO₂ and NO was achieved. Using this technique, a lipid content of 38.0% DW was achieved in Chlorella pyrenoidosa XQ-20044. The lipid composition and fatty acid profile indicated that lipid production by C. pyrenoidosa XQ-20044 cultured with flue gas is suitable as a biodiesel feedstock; 81.2% of the total lipids were neutral lipids and 99.5% of the total fatty acids were C16 and C18. The ratio of saturated fatty acids to monounsaturated fatty acids in the microalgal lipid content was 74.5%. In addition, CO₂, SO₂, and NO from the simulated flue gas were fixed and converted to biomass and lipids with a removal efficiency of 95.9%, 100%, and 84.2%, respectively. Furthermore, the utilization efficiencies of CO₂, SO₂, and NO were equal to or very close to their removal efficiencies. These results provide a novel strategy for combining biodiesel production with biofixation of flue gas.

The unique geographic location of Mt. Yulong in the Tibetan Plateau (TP) makes it a favorable site for mercury (Hg) study. Various snow samples, such as surface snow, snow pit, and snowmelt water were collected from Mt. Yulong in the southeastern TP. The average concentration of Hg was found to be 37 ± 26 ng L⁻¹ (mean ± SD), comparable to Hg concentration from other parts of TP in the same year, though it was comparatively higher than those from previous years, suggesting a possible increase of Hg concentration over the TP. The concentration of Hg was higher in the lower elevation of the glaciers possibly due to the surface melting concentration of particulates. Higher concentration of Hg was observed in the fresh snow, suggesting the possibility of long-range transportation. The average concentration of Hg from the snow pit was 1.49 ± 0.78 ng L⁻¹, and the concentration of Hg in the vertical profile of the snow pit co-varied with calcium ion (Ca²⁺) supporting the fact that the portion of Hg is from the crustal origin. In addition, the principal component analysis (PCA) confirmed that the source of Hg is from the crustal origin; however, the presence of anthropogenic source in the Mt. Yulong was also observed. In surface water around Mt. Yulong, the concentration of HgT was found in the order of Lashihai Lake > Reservoirs > Rivers > Swamps > Luguhu Lake. In lake water, the concentration of HgT showed an increasing trend with depth. Overall, the increased concentration of Hg in recent years from the TP can be of concern and may have an adverse impact on the downstream ecosystem, wildlife, and human health.

Mass transport and residence time of saline water from road salt applications in soil columns composed of Toyoura sand and weathered granite sand were investigated by simulations and in laboratory experiments. Both are sands found in Japan, especially the weathered granite sand. The Toyoura sand has a fairly uniform particle size of 0.1 to 0.4 mm diameter, and a saturated hydraulic conductivity Kₛ = 0.0296 cm/s, while the weathered granite sand used consisted of 13% fine materials (silt and clay) and 87% coarse materials (sand and gravel) with a saturated hydraulic conductivity Kₛ = 0.00393 cm/s. A model was developed to simulate rinsing of brine from a soil column. Assuming a steady, homogeneous flow induced by rainwater infiltration into the soil column, the model was found to match the experimental results for Toyoura sand very well. The normalized salt concentration in the effluent from the 40 cm tall soil column remained constant until about t = 500 s; the concentration then decreased with time quickly and, finally, approached zero. For the weathered granite sand, however, the salt concentrations in the effluent simulated by the model with assumption of homogeneous flow are inconsistent with the experimental data collected. A substantial delay occurs in mass transport of salt from the column, which is different from the Toyoura sand. The delay is attributed to shifts in “active” and “inactive pores” created in the soil due to fine particles such as silt and clay. The proportion of “active pores” and “inactive pores” is not constant but variable with time due to physical and/or electrochemical processes such as pore-size distributions and salt depletion in the soil. A modified model presented, using a time-variable active pore parameter k(t), can reproduce the experimental results for salt mass left in the soil better.