Human activities introduce significant contamination into aquatic systems that impact biodiversity and ecosystem function. Many contaminants accumulate, and remediation options are now required worldwide. One method for bioremediation involves the application of macrofauna to stimulate microbial ecosystem processes including contaminant removal. However, if we are to confidently apply such a technique, we need clarity on the effect of bioturbators on different contaminants and how these vary under different environmental scenarios. Here we used a systematic review and meta-analysis to analyse current knowledge on the activities of bioturbating macrofauna in contaminated sediments and quantify how bioturbation-bioremediation changes depend on the taxonomic group, the aquatic ecosystem and important environmental variables. Three common contaminant classes were reviewed and analysed: metals, nutrients (i.e. ammonia and phosphorous) and polycyclic aromatic hydrocarbons (PAH). In addition, meta-regressions were calculated to estimate the effect of environmental and experimental design variables on effect sizes. Meta-analytic results revealed that deeper burrowing and more active sediment surface animals (e.g. polychaetes) increased metal release from sediments, nutrients and oxygen uptake by microbial fractions in comparison to bioturbators that inhabit shallower depths in sediments. In addition, there was a different effect of bioturbators on response variables in different aquatic systems. Finally, bioturbator effects on nutrient and metal release appeared modulated by context-specific variables such as temperature, pH, sediment grain size, animal density and experimental duration. Our findings highlight critical knowledge gaps such as field applications, less studied macrobenthic fauna and the incorporation of molecular approaches. Our results provide the first quantitative synthesis of the effects of bioturbators on contaminant fate and the variables that need to be considered for the optimization of this method as a viable approach for sediment remediation and contaminant management in aquatic systems.

Microplastics (MPs) are an emerging concern and potential risk to marine and terrestrial environments. Surface soils are reported to act as a sink. However, MP vertical mobility in the subsurface remains uncertain due to a lack of scientific data. This study focused on MP penetration in sand soil column experiments. Here we report the mobility of five different MPs, which consisted of polyethylene (PE) and polypropylene (PP) particles of various sizes and densities. We observed that the smallest sized PE MPs (21 μm) had the greatest movement potential. Moreover, it was found that when these MPs were subjected to greater numbers of wet-dry cycles, the penetration depth significantly increased, with an apparent linear relationship between depth and wet-dry cycle number (r2 = 0.817). In comparison, increasing the volume of infiltration liquid or the surface MP concentration had only negligible or weak effects on migration depth (r2 = 0.169 and 0.312, respectively). Based on the observed wet-dry cycle trend, we forecast 100-year penetration depths using weather data for 347 cities across China. The average penetration depth was calculated as 5.24 m (95% CI = 2.78–7.70 m), with Beijing Municipality and Hebei, Henan and Hubei provinces being the most vulnerable to MP vertical dispersion. Our results suggest that soils may not only represent a sink for MPs, but also a feasible entryway to subsurface receptors, such as subterranean fauna or aquifers. Finally, research gaps are identified and suggested research directions are put forward to garner a better understanding MP vertical migration in soil.

In this study, reactive pyrite (FeS2) particles were prepared through a modified hydrothermal method and tested for immobilization of Cr(VI) in contaminated soil and synthetic groundwater. The addition of a NaAc buffer in the synthetic process resulted in pyrite particles of greater specific surface area, more uniform size, and more crystalline structure. The particles can effectively immobilize Cr(VI) in both water and a model Chinese loess soil. Over 99.9% of Cr(VI) was rapidly removed from water at pH 6.0 (Initial Cr(VI) = 25 mg/L, FeS2 dosage = 0.48 g/L), and the removal remained high (>82%) even at pH 9.5. Both adsorption and reductive precipitation were found operative in the Cr(VI) immobilization, with ∼66% of Cr immobilized due to reduction. Fe(II) ions associated on the FeS2 surface played a key role in the reduction of Cr(VI) to Cr(III), and S22− also facilitated the reductive removal of Cr(VI). The presence of humic acid enhanced Cr(VI) removal at pH 4.0, but the effect was negligible at pH 6.0. Batch kinetic tests showed that treating a Cr(VI)-laden soil with 0.48 g/L (as Fe) of FeS2 decreased the equilibrium water-leachable Cr(VI) by >99.0% at pH 6.0 and by >70.0% at pH 9.0. The distribution coefficient (Kd) value of the pyrite-amended soil was 1477.8 at pH 6.0, which is 306 times higher than for the untreated soil. Column elution tests showed that installation of a 3-cm reactive layer of FeS2 in a soil column was able to capture the leachable Cr(VI) from the soil, and the retardation factor (Rd) for the 3-cm FeS2 layer sample was 381 times higher than that for the plain soil. The synthetic pyrite particles may serve as an reactive material for effective removal or immobilization of Cr(VI) in contaminated water or soil.

Angola is one of the countries with a high rate of waterborne diseases, due to the scarcity and poor quality of water for human consumption. The watercourses are receptors of many effluents, mainly domestic sewage, due to a precarious or inexistent sanitation system and a small number of wastewater treatment plants. Therefore, this study aims: (i) to evaluate the water quality (physicochemical and microbiological parameters) of three Angolan rivers (Kwanza, Bengo and Dande) in locations where water is used as drinking water or abstracted for human consumption; (ii) to develop a new water quality index able to quantitatively express the water quality in those sites; and (iii) to assess the spatial distribution of water pollution through principal component analysis (PCA).Water quality assessment was performed by conducting four field surveys (campaigns I to IV); the first two campaigns took place in the dry season, while the last two ones took place in the rainy season. In the first two campaigns, the water quality was suitable to be treated for the production of drinking water, while in the last two campaigns, the water was unsuitable for that purpose (high levels of faecal coliforms were detected). The water quality index allowed to classify the water as generally excellent (campaigns I and II) and poor (campaigns III and IV). The rudimentary disinfection usually performed by individual water suppliers may improve the water quality, but it was not enough to achieve the parametric values required for human consumption in the rainy season (campaigns III and IV) except for Bengo sites. PCA identified sampling sites with the same water quality patterns, grouping into four groups (Kwanza sites) and two groups (Dande and Bengo sites). Therefore, the results of this study may support decision-makers as regards water supply management in the river stretches under study.The new developed Water Quality Index can support decision-makers in terms of water supply management, especially in countries with a high rate of waterborne diseases (e.g. Angola).

The urban nitrogen (N) and carbon (C) cycles are substantially influenced by human activity. Alterations to these cycles include increased inputs from fossil fuel combustion and fertilizer use. The leaf chemistry of urban trees can be used to distinguish between these different N and C sources. Here, we evaluated relationships between urban vegetation and different N and C sources in street and residential trees in the Salt Lake Valley, Utah. We tested three hypotheses: 1) unfertilized street trees on high traffic density roads will have higher leaf %N, more enriched δ¹⁵N and more depleted δ¹³C than unfertilized street trees on low traffic density roads; 2) trees in high income residential neighborhoods will have higher leaf %N, more depleted δ¹⁵N and more enriched δ¹³C than trees in lower income neighborhoods; and 3) unfertilized street trees will have lower leaf %N, more enriched δ¹⁵N and more depleted δ¹³C than fertilized residential trees. Leaf δ¹⁵N was more enriched near high traffic density roads for one study species. However, street tree δ¹⁵N and δ¹³C were largely influenced by vehicle emissions from primary and secondary roads within 1000 m radius rather than the immediately adjacent road. Leaf δ¹³C was correlated with neighborhood income, although this relationship may be the result of variations in irrigation practices rather than variations in C sources. Finally, unfertilized trees in downtown Salt Lake had lower leaf %N, more enriched δ¹⁵N and more depleted δ¹³C than fertilized trees. These results highlight that urban trees can serve as biomonitors of the environment. Moreover, they emphasize that roads can have large spatial footprints and that the leaf chemistry of urban vegetation may be influenced by the spatial patterns in roads and road densities at the landscape scale.

In this study, comparative effects of foliar application of ceria nanoparticles (NPs) and Ce3+ ions on common bean plants were investigated. Soil grown bean seedlings were exposed to ceria NPs and Ce3+ ions at 0, 40, 80, and 160 mg Ce·L−1 every other day at the vegetative growth stage for 17 d. The plants were harvested 47 d after the last treatment. Performed analyses involved growth, physiological and biochemical parameters of the plants and nutritional quality of the pods. Ceria NPs at 40 mg Ce·L−1 increased dry weight of the plants by 51.8% over the control. Neither ceria NPs nor Ce3+ ions significantly affected other vegetative growth parameters. Pod yields and nutrient contents except for several mineral elements were also not significantly different among groups. Compared to control, pods from ceria NPs at 80 mg Ce·L−1 had significantly less S and Mn. At 40 and 80 mg Ce·L−1, ceria NPs reduced pod Mo by 27% and 21%, while Ce3+ ions elevated Mo contents by 20% and 18%, respectively, compared with control. Ce3+ ions at 80 and 160 mg Ce·L−1 significantly increased pod Zn by 25% and 120%, respectively, compared with control. At the end of the experiment, Ce3+ ions at 40, 80, and 160 mg Ce·L−1 increased contents of malondialdehyde (MDA) by 46%, 65%, and 82% respectively as compared with control. While ceria NPs led to a significant increase of MDA level only at the highest concentration. X-ray absorption near edge structure (XANES) analysis of the leaf samples revealed that both ceria NPs and Ce3+ ions kept their original chemical species after foliar applications, suggesting the observed effects of ceria NPs and Ce3+ ions on the plants were probably due to their nano-specific properties and ionic properties respectively.

Feammox, i.e., Fe(III) reduction coupled to anaerobic ammonium oxidation, is a potential alternative to ammonium removal in natural and artificial ecosystems. However, the efficiency of Feammox is quite low to restrain its practical application in wastewater/solid disposal. In this study, three batch experiments, including control (Fe₂O₃/AQDS-free), Fe₂O₃ group (25 mM Fe₂O₃ only) and AQDS-Fe₂O₃ group (25 mM Fe₂O₃ and 0.6 mM AQDS), were conducted in 200 mL serum vials to explore whether AQDS can promote Feammox. Results showed that the nitrogen removal efficiency of the AQDS-Fe₂O₃ group was 82.6%, compared with 64.3% of the Fe₂O₃ group and 46.0% in the control. AH₂QDS, the reduced state of AQDS, was detected in the AQDS-Fe₂O₃ group. Another experiment indicated that AH₂QDS was oxidized back to AQDS by Fe₂O₃. These results suggested that AQDS/AH₂QDS had been serving as electron shuttles between ammonium and Fe₂O₃ to successively forward the oxidation of NH₄⁺. X-ray diffraction analysis showed that new Fe(III) species were found in the systems, implying that a Fe(II)/Fe(III) cycle also occurred. In agreement, both iron-reducing and oxidizing bacteria were detected in the systems.

Microplastics pose a great threat to entire marine ecosystems, but little is known about their impacts on phytoplankton, especially for the harmful dinoflagellates. In this study, effects of micro polyvinyl chloride (mPVC) on the growth, chlorophyll content and photosynthetic efficiency of the dinoflagellate Karenia mikimotoi at different periods (0, 24, 48, 72 and 96 h) were assessed using gradient concentrations (0, 5, 25, 50 and 100 mg L⁻¹) of mPVC with a size of 1 μm. PVC microplastics had dose-dependent adverse effects on K. mikimotoi growth, chlorophyll content and photosynthetic efficiency. The density of algal cell decreased with increasing mPVC concentrations and the highest inhibitory rate (IR) was 45.8% at 24 h under 100 mg L⁻¹ of mPVC. The total chlorophyll content and chlorophyll content in a single algal cell decreased at 96 h and the ФPSⅡ and Fv/Fm decreased 25.3% and 17.1%, respectively. The SEM images provided an intuitive visual method to observe the behaviors and interactions between microplastics and microalgae. It was found from the SEM images that microalgae was wrapped by microplastic beads. The physical blockage and aggregation were also responsible for the cytotoxicity of K. mikimotoi. Our study clarified that PVC microplastics can reduce algal growth, chlorophyll content and photosynthetic efficiency, and it is beneficial to evaluate the possible impact of plastics on aquatic ecosystems.

Control of organic matter, nutrients and disinfection byproduct formation is a major challenge for the drinking water treatment plants on Matsu Islands, Taiwan, receiving source water from the eutrophic reservoirs. A pilot entrapped biomass reactor (EBR) system was installed as the pretreatment process to reduce organic and nitrogen contents into the drinking water treatment plant. The effects of hydraulic retention time (HRT) and combination of preceding physical treatment (ultraviolet and ultrasound) on the treatment performance were further evaluated. The results showed that the EBR system achieved higher than 81%, 35%, 12% and 46% of reduction in chlorophyll a (Chl a), total COD (TCOD), dissolved organic carbon (DOC) and total nitrogen (TN), respectively under varied influent concentrations. The treatment performance was not significantly influenced by HRT and presence/absence of physical pretreatment and the effluent water quality was stable; however, removal efficiencies and removal rates of Chl a, TCOD and DOC showed strong correlation with their influent concentrations. Excitation–emission matrix (EEM) fluorescence spectroscopy identified fulvic-like and humic-like substances as the two major components of dissolved organic matter (DOM) in the reservoir, and decreased intensity of the major peaks in effluent EEM fluorescence spectra suggested the effective removal of DOM without production of additional amount of soluble microbial products in the EBR. Through the treatment by EBR, about 10% of reduction of total trihalomethane formation potential for the effluent could also be achieved. Therefore, the overall results of this study demonstrate that EBR can be a potential pretreatment process for drinking water treatment plants receiving eutrophic source water.

The humic-like substances were the main organic components in most wastewater (e.g. domestic sewage, toilet wastewater and landfill leachate). Two types of actual humic-like substances (fulvic acid (FA) and biologically treated landfill leachate (BTLL)) were selected to describe the changes in the properties of humic-like substances (complexation ability, aromaticity and mobility) during electrochemical oxidation. Meanwhile, the acute cytotoxicity of FA and BTLL was also tested by acute toxicological test of luminescent bacteria. The results showed that the consumption of coordinating groups such as phenolic groups and hydrogen bonds reduced the complexation ability of FA and BTLL. The functional groups were degraded with the removal order of quinone group, phenolic group and aromatic group, and finally realized the molecular saturation and aromaticity decrease for humic-like substances. The mobility of FA and BTLL was decreased because of the enhancement of hydrophobicity during electrolysis process. Furthermore, the available chlorine produced during electrochemical oxidation was the main acute cytotoxicity substance, therefore, it is necessary to remove it before discharge in order to reduce ecological risks. This study provides a basis for understanding and evaluating the electrochemical degradation process of humic-like substances in detail.