Climate warming promotes collateral antibiotic resistance development in cyanobacteria.

Both cyanobacterial blooms and antibiotic resistance have aggravated worldwide and posed a great threat to public health in recent years. As a significant source and reservoir of water environmental resistome, cyanobacteria exhibit confusing discrepancy between their reduced susceptibility and their chronic exposure to antibiotic mixtures at sub-inhibitory concentrations. How the increasing temperature affects the adaptive evolution of cyanobacteria-associated antibiotic resistance in response to low-level antibiotic combinations under climate change remains unclear. Here we profiled the antibiotic interaction and collateral susceptibility networks among 33 commonly detected antibiotics in 600 cyanobacterial strains isolated from 50 sites across four eutrophicated lakes in China. Cyanobacteria-associated antibiotic resistance level was found positively correlated to antibiotic heterogeneity across all sites. Among 528 antibiotic combinations, antagonism was observed for 62 % interactions and highly conserved within cyanobacterial species. Collateral resistance was detected in 78.5 % of pairwise antibiotic interaction, leading to a widened or shifted upwards mutant selection window for increased opportunity of acquiring second-step mutations. We quantified the interactive promoting effect of collateral resistance and increasing temperature on the evolution of both phenotypic and genotypic cyanobacteria-associated resistance under chronic exposure to environmental level of antibiotic combinations. With temperature increasing from 16 °C to 36 °C, the evolvability index and genotypic resistance level increased by 1.25 - 2.5 folds and 3 - 295 folds in the collateral-resistance-informed lineages, respectively. Emergence of resistance mutation pioneered by tolerance, which was jointly driven by mutation rate and persister fraction, was found to be accelerated by increased temperature and antibiotic switching rate. Our findings provided mechanic insights into the boosting effect of climate warming on the emergence and development of cyanobacteria-associated resistance against collateral antibiotic phenotypes.

The long-term release and particle fracture behaviors of nanoplastics retained in porous media: Effects of surfactants, natural organic matters, antibiotics, and bacteria.

The transport of nanoplastics (NPs) in porous media has received a lot of attention, but the studies on the long-term release of NPs retained in porous media and the particle fracture during this process are seriously lacking. For filling this deficiency, we examined the individual or synergistic effects of surfactants, natural organic matters (NOMs), antibiotics, and bacteria on the desorption, long-term release, and particle fracture behaviors of polystyrene NPs (PS-NPs) retained in porous media. It was found that the change in hydrophilicity of PS-NPs dominated the long-term release of PS-NPs retained in porous media when surfactants were present. In the single system of surfactants and the dual system of surfactants and NOMs, the release of PS-NPs were improved owing to the increasing hydrophilicity of PS-NPs, although cationic surfactants also reduced the electrostatic repulsion between PS-NPs and porous media. Increasing antibiotic concentration reduced the electrostatic repulsion between PS-NPs and porous media to inhibit the release of PS-NPs. When bacteria were present whether containing antibiotics or not, the effects on roughness of PS-NPs dominated the release of PS-NPs. The effects of surfactants and NOMs on the PS-NP desorption were similar with the long-term release, with changes in hydrophilicity dominating the process. Whereas the effects of antibiotics and bacteria on the PS-NP desorption were different with the long-term release. Surfactants and NOMs in the presence of surfactants inhibited the fracture of PS-NPs by increasing the hydrophilicity of PS-NPs brought about the coating of water molecules on PS-NPs for protection. Antibiotics had no significant effects on the fracture of PS-NPs due to unaltered vertical forces on PS-NPs and no protective effect. Bacteria in the presence or absence of antibiotics inhibited the fracture of PS-NPs by coating PS-NPs retained in porous media to protect PS-NPs from fracture.

Statuses, shortcomings, and outlooks in studying the fate of nanoplastics and engineered nanoparticles in porous media respectively and borrowable sections from engineered nanoparticles for nanoplastics.

This review discussed the research statuses, shortcomings, and outlooks for the fate of nanoplastics (NPs) and engineered nanoparticles (ENPs) in porous media and borrowable sections from ENPs for NPs. Firstly, the most important section was that we reviewed the research statuses on the fate of NPs in porous media and the main influencing factors, and explained the influencing mechanisms. Secondly, in order to give NPs a reference of research ideas and influence mechanisms, we also reviewed the research statuses on the fate of ENPs in porous media and the factors and mechanisms influencing the fate. The main mechanisms affecting the transport of ENPs were summarized (Retention or transport modes: advection, diffusion, dispersion, deposition, adsorption, blocking, ripening, and straining; Main forces and actions: Brownian motion, gravity, electrostatic forces, van der Waals forces, hydration, filtration, bridging; Affecting elements of the forces and actions: the ENP and media grain surface functional groups, size, shape, zeta potential, density, hydrophobicity, and roughness). Instead of using the findings of ENPs, thorough study on NPs was required because NPs and ENPs differed greatly. Based on the limited existing studies on the NP transport in porous media, we found that although the conclusions of ENPs could not be applied to NPs, most of the influencing mechanisms summarized from ENPs were applicable to NPs. Combining the research thoughts of ENPs, the research statuses of NPs, and some of our experiences and reflections, we reviewed the shortcomings of the current studies on the NP fate in porous media as well as the outlooks of future research. This review is very meaningful for clarifying the research statuses and influence mechanisms for the NP fate in porous media, as well as providing a great deal of inspiration for future research directions about the NP fate in porous media.

Spatiotemporal dynamics and modeling of thiacloprid in paddy multimedia systems with the effect of wetting-drying cycles.

The widespread presence of thiacloprid (THI), a neonicotinoid, raises concerns for human health and the aquatic environment due to its persistence, toxicity, and bioaccumulation. The fate of THI in paddy multimedia systems is mainly governed by irrigation practices, but the potential impacts remain poorly documented. This study investigated the effects of water management practices on THI spatiotemporal dynamics in paddy multimedia systems by combining soil column experiments and a non-steady-state multimedia model. The results indicated the wetting-drying cycle (WDC) irrigation reduced THI occurrences in environmental phases (i.e., soil, interstitial water, and overlying water) and accelerated the THI loss through the THI aerobic degradation process. THI occurrences in the soil and water phases decreased from 18.8% for conventional flooding (CF) treatment to 9.2% for severe wetting-drying cycle (SW) treatment after 29 days, while the half-lives shortened from 11.1 days to 7.3 days, respectively. Meanwhile, the WDC decreased THI outflow from leakage water, which reduced the THI risk of leaching. There was no significant difference in THI plant uptake and volatilization between CF and WDC treatments. The mean proportions of THI fate in paddy multimedia systems followed the order: THI degradation (57.7%), outflow from leakage water (25.5%), occurrence in soil (12.4%), plant uptake (3.4%), occurrence in interstitial water (0.7%), occurrence in overlying water (0.3%), volatilization (<0.1%) after 29 days. The sensitivity analysis identified the soil organic carbon partition coefficient (KOC) as the most sensitive parameter affecting THI's fate. In addition, the topsoil layers of 0-4 cm were the main sink of THI, holding 67% of THI occurrence in the soil phase. The THI occurrence in interstitial water was distributed evenly throughout the soil profile. These findings made beneficial theoretical supplements and provided valuable empirical evidence for water management practices to reduce the THI ecological risk.

Transformation of Biofilm to Carbon Sinks after Prolonged Droughts Linked with Algal Biodiversity Change.

Global climate change significantly increased the duration of droughts in intermittent rivers, impacting benthic microbial-mediated biogeochemical processes. However, the impact of prolonged droughts on the carbon contribution of intermittent rivers remains poorly understood. In this study, we investigated the potential effects of varying drought gradients (ranging from 20 to 130 days) on benthic biofilms community structure (algae, bacteria, and fungi) and their carbon metabolism functions (ecosystem metabolism and carbon dioxide (CO2) emission fluxes) using mesocosm experiments. Our findings indicate that longer drought durations lead to reduced alpha diversity and community heterogeneity, tighter interdomain networks, and an increased role of stochastic processes in community assembly, with a discernible threshold at around 60 days. Concurrently, the biofilm transforms into a carbon sink following a drought period of 60 days, as evidenced by the transformation of CO2 emission fluxes from 633.25 ± 194.69 to -349.61 ± 277.79 mg m-2 h-1. Additionally, the partial least-squares path model revealed that the resilience of algal communities and network stability may drive biofilm's transformation into a carbon sink, primarily through the heightened resilience of autotrophic metabolism. This study underscores the significance of the carbon contribution from intermittent rivers, as the shift in carbon metabolism functions with increasing droughts could lead to skewed estimations of current riverine carbon fluxes.

Optimal allocation of agricultural water and land resources integrated with virtual water trade: A perspective on spatial virtual water coordination.

Agricultural production consumes the majority of global freshwater resources. The worsening water scarcity has imposed significant stress on agricultural production when regions seek food self-sufficiency. To seek optimal allocation of spatial agricultural water and land resources in each water function zone of the objective region, a multi-objective optimization model was developed to tackle the trade-offs between the water-saving objective and the economic benefit objective considering virtual water trade (VWT). The cultivated area of each crop in each water function zone was taken into account as the decision variable, while a set of strong constraints were used to restrict land resources and water availability. Then, a decomposition-simplex method aggregation algorithm (DSMA) was proposed to solve this nonlinear, bounding-constrained, and multi-objective optimization model. Based on the quantitative analysis of the spatial blue and green virtual water in each agricultural product, the proposed methodology was applied to a real-world, provincial-scale region in China (i.e., Jiangsu Province). The optimized results provided 18 Pareto solutions to reallocate the land resources in the 21 IV-level water function zones of Jiangsu Province, considering four major rainy-season crops and two dry-season crops. Compared to the actual scenario, the superior scheme increased by 7.95% (5.6 × 109 RMB) for economic trade and decreased by 1.77% (2.0 × 109 m3) for agricultural water consumption. It was mainly because the potential of spatial blue and green virtual water in Jiangsu was fully exploited by improving spatial land resource allocation. The food security of Jiangsu could be guaranteed by achieving self-sufficiency in the superior scheme, and the total VWT in the optimal scheme was 2.2 times more than the actual scenario. The results provided a systematic decision-support methodology from the perspective of spatial virtual water coordination, yet, the methodology is widely applicable.

Effects of released organic components of solid carbon sources on denitrification performance and the related mechanism.

Here, a hybrid scaffold of polyvinyl alcohol/sodium alginate (PVA/SA) was used to prepare solid carbon sources (SCSs) for treating low carbon/nitrogen wastewater. The four SCSs were divided into two groups, biodegradable polymers group (including polyvinyl alcohol-sodium alginate (PS) and PS-PHBV (PP), and blended SCSs (PS-PHBV-wood chips (PPW) and PS-PHBV-wheat straw (PPS)). After the leaching experiments, no changes occurred in elemental composition and functional groups of the SCSs, and the released dissolved organic matter showed a lower degree of humification and higher content of labile molecules in the blended SCSs groups using EEM and FT-ICR-MS. The denitrification performance of the blended SCSs was higher, with nitrate removal efficiency over 84%. High-throughput sequencing confirmed PPW had the highest alpha-diversity, and the microbial community structure significantly varied among SCSs. Results of functional enzymes and genes show the released carbon components directly affect the NADH level and electron transfer efficiency, ultimately influencing denitrification performance.

Combined effects of bacteria and antibiotics on surface properties and transport of nanoplastics in porous media.

Currently, research on the individual effects of bacteria and antibiotics on the transport of nanoplastics (NPs) in porous media is in its infancy, while research on their combined effect is absent. It is well known that bacteria and antibiotics also interact with each other, so this synergistic transport of bacteria, antibiotics, and NPs in porous media must be very interesting. For exploring this aspect, we investigated the individual and combined effects of bacteria and antibiotics on the transport of polystyrene NPs (PS-NPs) in saturated porous media. Hydrophobicity, roughness, and the Derjaguin-Landau-Verwey-Overbeek (DLVO) interaction energy were measured and calculated. The PS-NPs' transport in porous media was fitted using a mathematical model. Enhanced roughness and size of PS-NPs with increased bacterial concentration dominated and inhibited the PS-NPs' transport in porous media, although the hydrophilicity of PS-NPs and the energy barrier between PS-NPs and porous media were also increased. An increase in antibiotic concentration reduced the energy barrier between PS-NPs and porous media, thereby decreasing the PS-NPs' transport. Combined effects of bacteria and antibiotics on the PS-NPs' transport were complex and distinct from individual effects, but the mechanisms were clear. Roughness and hydrophilicity of PS-NPs and the DLVO interaction energy between PS-NPs and porous media together influenced this process. In the presence of bacteria, antibiotics could alter the bacterial surface roughness by altering bacterial extracellular polymeric substances, and thus alter the PS-NPs' surface roughness, thereby affecting the PS-NPs' transport in porous media. When antibiotics were present, enhanced bacterial concentration increased the PS-NPs' hydrophilicity and the energy barrier between PS-NPs and porous media, thus promoting the PS-NPs' transport. The findings of this study provided a theoretical basis for clarifying the transport of NPs in porous media under complex environments, facilitating a reduction in environmental pollution of NPs.

A quaternary ammonium salt grafted tannin-based flocculant boosts the conjugative transfer of plasmid-born antibiotic resistance genes: The nonnegligible side of their flocculation-sterilization properties.

This study developed dual-function tannin-based flocculants, namely tannin-graft-acrylamide-diallyl dimethyl ammonium chloride (TGCC-A/TGCC-C), endowed with enhanced flocculation-sterilization properties. The impacts of these flocculants on proliferation and transformation of antibiotic resistance genes (ARGs) among bacteria during the flocculation-deposition process were examined. TGCC-A/TGCC-C exhibited remarkable flocculation capacities towards both Escherichia coli and Staphylococcus aureus, encompassing a logarithmic range of initial cell density (108-109 CFU/mL) and a broad pH spectrum (pH 2-11). The grafted quaternary ammonium salt groups played pivotal parts in flocculation through charge neutralization and bridging mechanisms, concurrently contributing to sterilization by disrupting cellular membranes. The correlation between flocculation and sterilization entails a sequential progression, where an excess of TGCC, initially employed for flocculation, is subsequently consumed for sterilization purposes. The frequencies of ARGs conjugative transfer were enhanced in bacterial flocs across all TGCC treatments, stemming from augmented bacterial aggregation and cell membrane permeability, elicited stress response, and up-regulated genes encoding plasmid transfer. These findings underscore the indispensable role of flocculation-sterilization effects in mediating the propagation of ARGs, consequently providing substantial support for the scientific evaluation of the environmental risks associated with flocculants in the context of ARGs dissemination during the treatment of raw water featuring high bacterial density.

Influence of humate on the degradation of chloramphenicol by sulfidated ferrihydrite under dynamic anoxic/oxic environments: A combined DFT calculation and experimental study.

Sulfidation of ferrihydrite is known to affect the degradation of contaminants, but little was known about the role of natural organic matter (NOM) in antibiotics degradation by sufidated ferrihydrite under redox-dynamic conditions. Here, a typical antibiotic (i.e., chloramphenicol (CAP)) was chosen to investigate how it redistributed when ferrihydrite reacted with reductive dissolved sulfide (S(-II)dis) in the presence of humate (HA) under dynamic anoxic/oxic environments. In anoxic environments, HA enhanced CAP reduction via dichlorination or decarboxylation by sufidated ferrihydrite in the low concentration of S(-II), while HA inhibited CAP reduction in the high concentration of S(-II) by the contribution of S(-II) and surface-bound Fe(II) (Fe(II)adsorbed). When the conditions transited from anoxic to oxic, remaining CAP molecules in solutions continued undergoing oxidative degradation to form the succinic acid, hexanedioic acid, CO2, and H2O by the attack of ·OH. Meantime, HA was adsorbed to ferrihydrite to block autocatalytic Fe(II) oxidation, which inhibited the generation of ·OH under oxic conditions. Additionally, from the density function theory (DFT) calculation and intermediate products analysis obtained from HPLC-MS/MS, two oxidative degradation pathways of CAP during the oxidation of sulfidated ferrihydrite have been proposed. Collectively, the framework elucidated different roles of HA in CAP elimination and environmental behavior of ferrihydrite when exposed to the S(-II) under the dynamic redox conditions.

Surface modification significantly changed the effects of nano-polystyrene on sediment microbial communities and nitrogen metabolism.

Nanoplastics are ubiquitous in the natural environment, and their ecological risks have received considerable attention. Surface modification is common for nanoplastics and an essential factor affecting their toxicity. However, studies on the potential effects of nanoplastics and their surface-modified forms on functional communities in aquatic systems are still scarce. This study investigated the effects of nano-polystyrene (nPS), amino-modified nPS (nPS-NH2), and carboxylated nPS (nPS-COOH) particles on sediment bacterial and fungal communities and their functions over a 60-day incubation period. The results showed that the fungal community was significantly inhibited by nPS-NH2 exposure, while the bacterial community diversity remained relatively stable in all nPS treatments. Proteobacteria and Ascomycota were the dominant phyla for the bacterial and fungal communities, respectively. Nitrification was inhibited in all nPS treatments, while denitrification was enhanced for nPS-NH2 and nPS-COOH treatments. The activity of four key denitrification enzymes (NAR, NIR, NOR, and NOS) was also significantly improved by nPS, resulting in increased nitrogen and nitrous oxide gas production, and decreased nitrate concentrations in the overlying water. This showed the total increased effect of nPS on the activity of denitrifiers. Our results suggest that surface modification significantly affects the effects of nPS on microbial communities and functions. The potential impacts of nPS on ecological functions should be elucidated with more attention.

Long-term effects of Ag NPs on denitrification in sediment: Importance of Ag NPs exposure ways in aquatic ecosystems.

The widespread use of silver nanoparticles (Ag NPs) inevitably leads to their increasing release into aquatic systems, with studies indicating that the mode of Ag NPs entry into water significantly affects their toxicity and ecological risks. However, there is a lack of research on the impact of different exposure ways of Ag NPs on functional bacteria in sediment. This study investigates the long-term influence of Ag NPs on denitrification process in sediments by comparing denitrifies responses to single (pulse injection of 10 mg/L) and repetitive (1 mg/L × 10 times) Ag NPs treatments over 60-day incubation. Results showed that a single exposure of 10 mg/L Ag NPs caused an obvious toxicity on activity and abundance of denitrifying bacteria on the first 30 days, reflecting by the decreased NADH amount, ETS activity, NIR and NOS activity, and nirK gene copy number, which resulted in a significant decline of denitrification rate in sediments (from 0.59 to 0.64 to 0.41-0.47 µmol15N L-1 h-1). While inhibition was mitigated with time and denitrification process recovered to the normal at the end of the experiment, the accumulated nitrate generated in the system showed that the recovery of microbial function did not mean the restoration of aquatic ecosystem after pollution. Differently, the repetitive exposure of 1 mg/L Ag NPs exhibited the evident inhibition on metabolism, abundance, and function of denitrifiers on Day 60, due to the accumulated amount of Ag NPs with the increased dosing number, indicating that the accumulated toxicity on functional microorganic community of repetitive exposure in less toxic concentration. Our study highlights the importance of Ag NPs entry pathways into aquatic ecosystem on their ecological risks, which affected dynamic responses of microbial function to Ag NPs.

Transport of polystyrene nanoplastics in porous media: Combined effects of two co-existing substances.

Both surfactants and natural organic matters (NOMs) are substances commonly found in aqueous environments, and their effects on the transport of nanoplastics that is gradually gaining widespread attention in porous media are currently in their infancy, while their combined effects are absent. We investigated innovatively the combined effect of surfactants and NOMs on the transport of polystyrene nanoplastics (PS-NPs) in saturated porous media. Adsorption tests of surfactants and NOMs onto PS-NPs, adsorption tests of PS-NPs onto quartz sand, and transport tests of PS-NPs in saturated quartz sand were conducted. Hydrophobicity and Derjaguin-Landau-Verwey-Overbeek (DLVO) interaction energy were measured and calculated. A mathematical model was employed to fit the transport of PS-NPs in porous media. It was found that the effects and action mechanisms of cationic cetyl trimethylammonium bromide (CTAB) and anionic sodium dodecylbenzene sulfonate (SDBS) on the transport of PS-NPs in porous media were distinct. In the presence of CTAB, 1 mg/L humic acid (HA) and 10 mg/L sodium alginate (SA) could promote aggregation of PS-NPs by decreasing the absolute zeta potential of PS-NPs, and reducing the energy barrier between PS-NPs and porous media and increasing the blocking and straining, thus inhibiting the transport of PS-NPs. In the presence of SDBS, SA and HA could improve the adsorption of SDBS onto PS-NPs by bridging and increasing adsorption sites, thus increasing the hydrophilicity of PS-NPs and improving the transport of PS-NPs. Whether or not NOMs were present, the transport of PS-NPs in porous media was mainly governed by the DLVO interaction energy in the presence of cationic surfactants and by hydrophobicity in the presence of anionic surfactants. This innovative observation has led to an understanding on the environmental behaviour of nanoplastics in porous media under complex environments.

Influence of natural organic matters on fate of polystyrene nanoplastics in porous media.

Natural organic matters (NOMs) are widely present in aqueous environments. The effect of NOMs on the fate of nanoplastics that are gradually receiving widespread attention in porous media needs to be noticed, but relevant research is lacking. To fill this gap, the present study focused on elucidating the influence of NOMs and metal cations with varying concentrations upon the transport, long-term release, and particle fracture of polystyrene nanoplastics (PS-NPs) in saturated porous media. The adsorption, transport, long-term release, and particle fracture tests were conducted. A mathematical model and the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory were used in this research. NOMs could adsorb onto PS-NPs leading to a reduction in the PS-NPs' zeta potential and an increase in the energy barrier and steric hindrance between PS-NPs and quartz sand, ultimately facilitating the transport of PS-NPs through porous media. On the other hand, an increase in concentration and valence of metal ions enhanced the PS-NPs' zeta potential, resulting in PS-NPs' aggregation and increased size when NOMs were present. This reduced the energy barrier between porous media and PS-NPs, resulting in increased blocking and straining, allowing decreased PS-NPs' transport. Long-term release tests demonstrated release ability and mobilities of PS-NPs decreased as the enhanced NOM concentration, addition of metal cations, and decreased valence of metal ions, in agreement with the transport test findings. In the research about particle fracture, NOMs were found to inhibit the fracture of PS-NPs by adsorbing on their surface to protect them from fracture. Metal cations and increased metal cation valence promoted the fracture of released PS-NPs when NOMs were present by promoting NOM aggregation and thus hindering the protection of NOMs for the nanoplastics.

Effects of input concentration, media particle size, and flow rate on fate of polystyrene nanoplastics in saturated porous media.

Nanoplastics have gradually attracted widespread attention, but the studies in this area are still very scarce. In this research, the adsorption, transport, long-term release, and particle fracture of polystyrene nanoplastics (PS-NPs) in saturated porous media were investigated at different media particle sizes, input concentrations, and flow rates. The increased PS-NPs concentration and sand grain size promoted the adsorption of PS-NPs onto quartz sand. In transport tests, the peak breakthrough amounts of PS-NPs ranged from 0.5761 to 0.8497, demonstrating their high mobility in saturated quartz sand. Transport of PS-NPs in saturated porous media increased with decreasing input concentration and increasing media particle sizes. The effect of input concentration could be predicted by the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory, in which adsorption played a dominant role. The effect of media particle size was mainly dominated by filtration rather than adsorption. As a result of higher shear force, increasing flow rate might boost transport of PS-NPs. With increasing media particle size and flow rate, more retained PS-NPs were released, which was in line with the findings of the transport tests on the mobility of PS-NPs. Notably, PS-NPs could be broken down into smaller PS-NPs during long-term release and the percentage of released PS-NPs (<100 nm) was gradually increased from 1st to 3rd PV effluent in all media particle sizes and flow rates. The fracture of released PS-NPs from medium quartz sand was the most in relation to fine and coarse and showed a decreased trend with increasing flow rate, which was likely to be governed by the force perpendicular to the contact surface with the media particle. This study showed that PS-NPs have strong mobility in porous media and are easily broken into smaller particles during long-term release. The findings of this research provided fundamental information for clarifying transport laws of nanoplastics in porous media.

Eukaryotes contribute more than bacteria to the recovery of freshwater ecosystem functions under different drought durations.

Global climate change mostly impacts river ecosystems by affecting microbial biodiversity and ecological functions. Considering the high functional redundancy of microorganisms, the unknown relationship between biodiversity and ecosystem functions obstructs river ecological research, especially under the influence of increasing weather extremes, such as in intermittent rivers and ephemeral streams (IRES). Herein, dry-wet alternation experiments were conducted in artificial stream channels for 25 and 90 days of drought, both followed by 20 days of rewetting. The dynamic recovery of microbial biodiversity and ecosystem functions (represented by ecosystem metabolism and denitrification rate) were determined to analyse biodiversity-ecosystem-function (BEF) relationships after different drought durations. There was a significant difference between bacterial and eukaryotic biodiversity recovery after drought. Eukaryotic biodiversity was more sensitive to drought duration than bacterial, and the eukaryotic network was more stable under dry-wet alternations. Based on the establishment of partial least squares path models, we found that eukaryotic biodiversity has a stronger effect on ecosystem functions than bacteria after long-term drought. Indeed, this work represents a significant step forward for further research on the ecosystem functions of IRES, especially emphasizing the importance of eukaryotic biodiversity in the BEF relationship.

Fabrication of an intimately coupled photocatalysis and biofilm system for removing sulfamethoxazole from wastewater: Effectiveness, degradation pathway and microbial community analysis.

Sulfamethoxazole (SMX) is an extensively applied antibiotic frequently detected in municipal wastewater, which cannot be efficiently removed by conventional biological wastewater processes. In this work, an intimately coupled photocatalysis and biodegradation (ICPB) system consisting of Fe3+-doped graphitic carbon nitride photocatalyst and biofilm carriers was fabricated to remove SMX. The results of wastewater treatment experiments showed that 81.2 ± 2.1% of SMX was removed in the ICPB system during the 12 h, while only 23.7 ± 4.0% was removed in the biofilm system within the same time. In the ICPB system, photocatalysis played a key role in removing SMX by producing hydroxyl radicals and superoxide radicals. Besides, the synergism between photocatalysis and biodegradation enhanced the mineralization of SMX. To understand the degradation process of SMX, nine degradation products and possible degradation pathways of SMX were analyzed. The results of high throughput sequencing showed that the diversity, abundance, and structure of the biofilm microbial community remained stable in the ICPB system at the end of the experiments, which suggested that microorganisms had accommodated to the environment of the ICPB system. This study could provide insights into the application of the ICPB system in treating antibiotic-contaminated wastewater.

Performance Enhancement of Biogenetic Sulfidated Zero-Valent Iron for Trichloroethylene Degradation: Role of Extracellular Polymeric Substances.

Chemical sulfidation has been considered as an effective strategy to improve the reactivity of zero-valent iron (S-ZVI). However, sulfidation is a widespread biogeochemical process in nature, which inspired us to explore the biogenetic sulfidation of ZVI (BS-ZVI) with sulfate-reducing bacteria (SRB). BS-ZVI could degrade 96.3% of trichloroethylene (TCE) to acetylene, ethene, ethane, and dichloroethene, comparable to S-ZVI (97.0%) with the same S/Fe ratio (i.e., 0.1). However, S-ZVI (0.21 d-1) exhibited a faster degradation rate than BS-ZVI (0.17 d-1) based on pseudo-first-order kinetic fitting due to extracellular polymeric substances (EPSs) excreted from SRB. Organic components of EPSs, including polysaccharides, humic acid-like substances, and proteins in BS-ZVI, were detected with 3D-EEM spectroscopy and FT-IR analysis. The hemiacetal groups and redox-activated protein in EPS did not affect TCE degradation, while the acetylation degree of EPS increased with the concentration of ZVI and S/Fe, thus inhibiting the TCE degradation. A low concentration of HA-like substances attached to BS-ZVI materials promoted electron transport. However, EPS formed a protective layer on the surface of BS-ZVI materials, reducing its TCE reaction rate. Overall, this study showed a comparable performance enhancement of ZVI toward TCE degradation through biogenetic sulfidation and provided a new alternative method for the sulfidation of ZVI.

Influences of input concentration, media particle size, metal cation valence, and ionic concentration on the transport, long-term release, and particle breakage of polyvinyl chloride nanoplastics in saturated porous media.

The environmental impact of nanoplastics has gradually attracted widespread attention; however, nanoplastics of polyvinyl chloride, one of the most commonly used plastics, have not yet been studied. In this study, we investigated the transport, long-term release behavior, and particle fracture of polyvinyl chloride nanoplastics (PVC NPs) in saturated quartz sand with different metal cations, ionic concentrations, input concentrations, and sand grain sizes by determining breakthrough, long-term release, and particle size distribution curves. The breakthrough curves and retention profiles were simulated by a mathematical model. The transport of PVC NPs increased with increased input concentration and sand grain size, which could be predicted by the Derjaguin-Landau-Verwey-Overbeek (DLVO) and colloid filtration theories. Increased ionic concentration and metal cation valence could restrain the transport of PVC NPs in saturated quartz sand owing to the decreased energy barrier between PVC NPs and sand grains. The total released amount of PVC NPs in the long-term release tests with different experimental conditions ranged from 3.91 to 21.95%. Increased sand grain size and decreased metal cation valence and ionic concentration resulted in an increased released amount of retained PVC NPs in saturated quartz sand, indicating increased release ability and mobility. The particle fracture results indicated that the PVC NPs were not broken down during long-term release under the experimental conditions of this research. This opens up a completely new and meaningful study of whether nanoplastics are broken down into smaller nanoplastics during their long-term release under various conditions.

Dynamic responses of carbon metabolism of sediment microbial communities to Ag nanoparticles: Effects of the single and repeated exposure scenarios.

The widespread use of nanosilver will inevitably lead to their release into aquatic environment, threating the health of freshwater ecosystem. The toxic effects of silver nanoparticles (AgNPs) on sediment microbial diversity, community composition, and functional enzyme activity are well established, while little is known about how sediment microbes dynamically respond to the stress of different AgNPs exposure scenarios. Herein, microcosm experiments were performed to investigate the impacts of repeated (1 mg/L, applied every 6 days for 10 times) and single (10 mg/L) exposure scenarios of AgNPs on the specific functions of sediment microbes (5-60 days). The carbon metabolism of sediment microbial communities was measured using BIOLOG ECO microplates, and carbon metabolic rate and functional diversity indices were calculated. Compared to control group, the maximum carbon source utilization capacity of the microbial community increased by 6.6 and 15.4 % in the single and repeated exposure group, respectively. And the metabolic rates of sediment microorganisms were significant increased by 6.1 % in the repeated exposure group, which suggested that repetitive low-dosing of AgNPs induce a larger alteration of both capacity and rate of microbial carbon metabolism. Notably, different AgNPs exposure scenarios resulted in a shift in the carbon source preference of the microorganisms. After exposure for 60 days, compared with the controls, the ability to utilize polymers was significantly increased by 51.5 and 21.7 % in the single and repeated exposure groups, respectively, and decreased by 33.7 and 10.5 % in the utilization of miscellaneous, both exhibiting significant differences (P < 0.05), implying that AgNPs exposure scenarios affected the microbial-mediated carbon cycling processes in sediment. These results highlight that different exposure scenarios of AgNPs have different effects on the carbon metabolism capacity of microbial communities, thus affecting the carbon cycling processes in which microorganisms are involved.