The acute toxicity of titanium dioxide nanoparticles (nTiO₂) that occur concomitantly in the aquatic environment with other contaminants such as arsenic (As) is little known in crustaceans. The objective of the present study is to evaluate whether coexposure to nTiO₂ can influence the accumulation, metabolism, and oxidative stress parameters induced by arsenic exposure in the gills and hepatopancreas of the shrimp Litopenaeus vannamei. Organisms were exposed by dissolving chemicals in seawater (salinity = 30) at nominal concentrations of 10 μg/L nTiO₂ or Asᴵᴵᴵ, dosed alone and in combination. Results showed that there was not a significant accumulation of As in either tissue type, but the coexposure altered the pattern of the metabolism. In the hepatopancreas, no changes were observed in the biochemical response, while in the gills, an increase in the glutamate-cysteine-ligase (GCL) activity was observed upon exposure to As or nTiO₂ alone, an increase in the reduced glutathione (GSH) levels was observed upon exposure to As alone, and an increase in the total antioxidant capacity was observed upon exposure to nTiO₂ or nTiO₂ + As. However, these modulations were not sufficient enough to prevent the lipid damage induced by nTiO₂ exposure. Our results suggest that coexposure to nTiO₂ and As does not alter the toxicity of this metalloid in the gills and hepatopancreas of L. vannamei but does alter its metabolism, favoring its accumulation of organic As species considered moderately toxic.

The interaction between a river and the sea results in a turbidity maximum zone (TMZ) within the estuary, which has a great impact on the local ecosystem. In the Yangtze River Estuary, the magnitude and extent of the TMZ vary with water discharge. In this study, the cumulative human activity altered the water discharge regime from the river to the estuary. In the post-Three Gorges Dam (TGD) period, water discharge increased by 35.10 % at Datong in February compared with that in the pre-TGD period. The effects of water discharge variation on the characteristics of the TMZ were analyzed during spring and neap tidal periods using the three-dimensional environmental fluid dynamic code (EFDC) model. The area of the TMZ decreased by 3.11 and 17.39 % during neap and spring tides, respectively. In addition, the upper limit of the TMZ moved 11.68 km seaward during neap tide, whereas the upper limit of the TMZ in the upstream and downstream areas moved seaward 9.65 and 2.34 km, respectively, during spring tide. These findings suggest that the area and location of the TMZ are more sensitive to upstream runoff during spring tide than during neap tide. These changes in the TMZ will impact the biochemical processes in the Yangtze River Estuary. In the foreseeable future, the distribution characteristic of TMZ will inevitably change due to variations in the Yangtze River discharge resulting from new human activities (i.e., new dams), which are being constructed upstream in the Yangtze River system.

Atrazine is an herbicide widely used in crops and has drawn attention due to potential pollution present in soil, sediment, water, and food. Since conventional methods are not potentially efficient to persistent degradation of organic compounds, new technology has been developed to remove them, especially practices utilizing advanced oxidation processes (AOPs). This work aims to evaluate the use of different energies (ultraviolet (UV), microwaves (MW), and radiations (MW-UV)) to the herbicide atrazine through the process of photo-oxidation. These systems found degradation rates of around 12 % (UV), 28 % (MW), and 83 % (MW-UV), respectively, with time intervals of 120 s. After the photolytic processes, the samples were analyzed at a wavelength scanning the range of 190 to 300 nm, where the spectral analysis of the signal was used to evaluate the degradation of atrazine and the appearance of some other peaks (degradation products). The spectrum evaluation resulting from photolytic processes gave rise to a new signal which was confirmed by chromatography. This spectrum indicated the possible pathway of atrazine degradation by the process of photolytic MW-UV, generating atrazine-2-hydroxy, atrazine-desethyl-2-hidroxy, and atrazine-desisopropyl-2-hydroxy. The process indicated that in all situations, chloride was present in the analytic structure and was substituted by a hydroxyl group, which lowered the toxicity of the compound through the photolytic process MW-UV. Chromatographic analysis ascertained these preliminary assessments using spectrophotometry. It was also significantly observed that the process can be optimized by adjusting the pH of the solution, which was evident by an improvement of 10 % in the rate of degradation when subjected to a pH solution equal to 8.37.

Phosphorus (P) is an essential nutrient for aquatic organisms. However, too much P discharged into limnetic ecosystems can induce eutrophication. The concentration of P in freshwater ecosystems has escalated in Eastern China due to overuse of fertilizer and excess emission of sewage, which is the result of the development of industry and agriculture in this area. However, little is known about the P characteristics and its environmental factors in river systems. Here, we present the results of P characterization and its relationships with environmental factors in Eastern China by applying SMT and ³¹P-NMR methods. The results showed that the concentrations of P in surface sediments varied with the river system, and more than 50 % of the samples had P concentrations exceeding 500 mg kg⁻¹. HCl-Pi was the dominant Pi in surface sediments, with the highest percentage (96.5 %) in the Yellow River System. Mono-P was the dominant Po in river sediments, followed by DNA-P. The PCA approach indicated that NaOH-Pi and ortho-P clustered in one group, with a second group including mono-P, diesters-P, and HCl-Pi. Phon-P and pyro-P belonged to different groups. On a regional scale, NaOH-Pi and Po showed a negative relationship with pH in sediments. Continuous eutrophication was induced by the presence of dams, and oxygen-consuming pollutants, such as NH₃-N and CODcr, even when external P input was cut in heavily polluted rivers. The research revealed the characteristics of P in different river systems and proposed a conceptual model of P biogeochemical cycles in heavily polluted rivers. Results from this study may provide insight into P characteristics in Eastern China and would set a scientific basis for effective P management in developing countries.

Pollution of agricultural soils caused by widely employed plastic products, such as phthalic acid esters (PAEs), are becoming widespread in China, and they have become a threat to human health and the environment. However, little information is available on the influence of PAEs on vegetable crops. In this study, effects of different dimethyl phthalate (DMP) treatments (0, 30, 50, 100, and 200 mg L⁻¹) on seed germination and growth of cucumber seedlings were investigated. Although germination rate showed no significant difference compared to control, seed germination time was significantly delayed at DMP greater than 50 mg L⁻¹. Concentrations of DMP greater than 30 mg L⁻¹ reduced cucumber lateral root length and number. The measurement of five physiological indexes in cucumber leaves with increasing DMP concentration revealed a decrease in leaf chlorophyll content, while proline and H₂O₂ contents increased. Peroxidase (POD) and catalase (CAT) activities increased in cucumber plants under 30 and 50 mg L⁻¹ DMP treatments compared to control; while after a 7-day treatment, these activities were seriously reduced under 100 and 200 mg L⁻¹ DMP treatments. According to transmission electron microscopy (TEM) micrographic images, the control and 30 mg L⁻¹ DMP treatments caused no change to leaf chloroplast shape with well-structured thylakoid membrane and parallel pattern of lamellae. At concentrations higher than 30 mg L⁻¹, DMP altered the ultrastructure of chloroplast, damaged membrane structure, disordered the lamellae, and increased the number and volume of starch grains. Moreover, the envelope of starch grains began to degrade under 200 mg L⁻¹ DMP treatment.

Sintering and steel production as the main emission sources of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) may affect environment and human health. The concentrations, profiles, and distributions of PCDD/Fs in soil samples from around four typical sintering and steel production plants in Hebei Province, China, were determined. Forty-six soil samples were collected at distances from 500 to 9000 m from industrial plant chimneys. The concentrations of total 17 2,3,7,8-substituted PCDD/F congeners in the soil samples from sites A, B, C, and D were in the range 11–130, 13–284, 2.6–378, and 21–231 pg/g, respectively, and the internationally accepted toxic equivalent (I-TEQ) concentrations were 0.37–13.2, 0.31–12.1, 0.13–13.7, and 1.60–22.7 pg I-TEQ/g, respectively. Soil ingestion was estimated the major exposure pathway to PCDD/Fs. At current PCDD/F concentrations, the local population will be exposed to low amounts of PCDD/Fs in soil from around the industrial sites, and this exposure will pose potential health risks for the local population living at distances of less than 1000 m from nearest stack but will have no high health risks for people living further away. These results will be helpful when planning measures to control PCDD/F sources. The data will also benefit local environmental monitoring studies and be useful when assessing the risks posed by PCDD/Fs around the industrial sites to the environment and humans.

Nowadays, petrochemical operations involve risks to the environment and one of the biggest is oil spills. Low molecular aromatics like benzene, toluene, and naphthalene dissolve in water, and because of their toxicological characteristics, these produce severe consequences to the environment. The oil spill cleanup strategies are mainly designed to deal with the heavy fractions accumulated on the water surface. Unfortunately, very limited information is available regarding the treatment of dissolved fractions.A commercial (Filtrasorb 400) and modified activated carbons were evaluated to remove benzene, toluene, and naphthalene from water, which are the most soluble aromatic hydrocarbons, at different ionic strengths (I) and temperatures (0–0.76 M and 4–25 °C, respectively). This allowed simulating the conditions of fresh and saline waters when assessing the performance of these adsorbents. It was found that the hydrocarbons adsorption affinity increased 12 % at a I of 0.5 M, due to the less negative charge of the adsorbent, while at a high I (≃0.76 M) in a synthetic seawater, the adsorption capacity decreased 21 % that was attributed to the adsorbent’s pores occlusion by water clusters. Approximately, 40 h were needed to reach equilibrium; however, the maximum adsorption rate occurred within the first hour in all the cases. Moreover, the hydrocarbons adsorption and desorption capacities increased when the temperature augmented from 4 to 25 °C. On the other hand, thermally and chemically modified materials showed that the interactions between adsorbent-contaminant increased with the basification degree of the adsorbent surface.

The large estuary that the River Po forms at its confluence into the Adriatic Sea comprises a multitude of transitional environments, including coastal lagoons. This complex system receives the nutrients transported by the River Po but also its load of chemical contaminants, which may pose a substantial (eco)toxicological risk. Despite the high ecological and economic importance of these vulnerable environments, there is a substantial lack of information on this risk. In light of the recent amendments of the European Water Framework Directive (2013/39/EU), the present study investigated the sediment contamination of six coastal lagoons of the Po delta and its effects on Manila clams (Ruditapes philippinarum), exposed in situ for 3 months. Sediment contamination and clam bioaccumulation of a wide range of chemicals, i.e. trace metals (Cd, Cr, Ni, Hg, Pb, As), polybrominated diphenyl ethers (PBDEs), alkylphenols (APs), organochlorine compounds (PCBs, DDTs), polycyclic aromatic hydrocarbons (PAHs) and organotins (TPhT, TBT), suggested a southward increase related to the riverine transports. Where the River Po influence was more direct, the concentrations of contaminants were higher, with nonylphenol and BDE-209 exceeding sediment quality guidelines. Biometric indicators suggested the influence of contamination on organism health; an inverse relationship between PBDEs in sediments and clam condition index has been found, as well as different biota-sediment accumulation factors (BSAFs) in the lagoons.

Food waste is the largest constituent of municipal solid waste in Hong Kong, but food waste recycling is still in its infancy. With the imminent saturation of all landfill sites by 2020, multiple technologies are needed to boost up the food waste recycling rate in Hong Kong. Conversion of food waste into animal feeds is prevalent in Japan, South Korea, and Taiwan, treating over 40 % of their recycled food waste. This direction is worth exploring in Hong Kong once concerns over food safety are resolved. Fortunately, while feeding food waste to pigs and chickens poses threats to public health, feeding it to fish is considered low risk. In order to examine the feasibility of converting food waste into fish feed in Hong Kong, this paper investigates the market demand, technical viability, feed quality, regulatory hurdles, and potential contribution. The results show that a significant amount of food waste can be recycled by converting it into fish feed due to the enormous demand from feed factories in mainland China. Two conversion technologies, heat drying and black soldier fly bioconversion, are studied extensively. Black soldier fly bioconversion is preferable because the end-product, insect powder, is anticipated to gain import approval from mainland China. The authors suggest further research efforts to speed up its application for food waste recycling in urban cities.

N-doped ZnO (N-ZnO) and N-doped ZrO₂ (N-ZrO₂) are synthesized by novel, simple thermal decomposition methods. The catalysts are evaluated for the degradation of rhodamine 6G (R6G) under visible and UV light. N-ZnO exhibits higher dye degradation under both visible and UV light compared to N-ZrO₂ due to possessing higher specific surface area, lower crystalline size, and lower band gap. However, it is less reusable than N-ZrO₂ and its photocatalytic activity is also deteriorated at low pH. At the same intensity of 3.5 W/m², UVC light is shown to be a better UV source for N-ZnO, while UVA light is more suitable for N-ZrO₂. At pH 7 with initial dye concentration of 10 mg/L, catalyst concentration of 1 g/L, and UVC light, 94.3 % of R6G is degraded by N-ZnO within 2 h. Using UVA light under identical experimental conditions, 93.5 % degradation of R6G is obtained by N-ZrO₂. Moreover, the type of light source is found to determine the reactive species produced in the R6G degradation by N-ZnO and N-ZrO₂. Less oxidative reactive species such as superoxide radical and singlet oxygen play a major role in the degradation of R6G under visible light. On the contrary, highly oxidative hydroxyl radicals are predominant under UVC light. Based on the kinetic study, the adsorption of R6G on the catalyst surface is found to be the controlling step.