Antibiotic resistance genes (ARGs) are exacerbated by horizontal gene transfer. Plant growth regulators (PGRs), extensively applied in agriculture, may further accelerate the environmental dissemination of ARGs. However, research on PGR influence on environmental ARG spread remains limited. This study elucidates the impact of three PGRs—indole-3-acetic acid (IAA), ethephon (ETH), and gibberellic acid (GA3)—on ARG transfer via conjugation and transformation pathways. Key results demonstrate that IAA (800 mg/L) significantly increased conjugation frequency despite reducing recipient survival by 99

Aerosol hygroscopicity and liquid water content (ALWC) have important influences on the environmental and climate effect of aerosols. In this study, we measured the hygroscopic growth factors (GF) of particles with dry diameters of 40, 80, 150, and 200 nm during the wintertime in Nanjing. Both the GF-derived hygroscopicity parameter (κgf) and ALWC increased with particle size, but displayed differing diurnal variations, with κgf peaking around the midday, while ALWC peaking in the early morning. Nitrate, ammonium and oxygenated organic aerosols (OOA) were found as the chemical components mostly strongly correlated with ALWC. A closure study suggests that during midday photo-oxidation and nighttime high ALWC periods, the κ of organic aerosols (κorg) was underestimated when using previous parameterizations. Accordingly, we re-constructed parameterizations for κorg and the oxidation level of organics for these periods, which indicates a higher hygroscopicity of photochemically formed OOA than the aqueous OOA, yet both being much higher than the generally assumed OOA hygroscopicity. Additionally, in a typical high ALWC episode, concurrently increased ALWC, nitrate, OOA as well as aerosol surface area and mass concentrations were observed under elevated ambient RH. This strongly indicates a coupled effect that the hygroscopic secondary aerosols, in particular nitrate with strong hygroscopicity, led to large increase in ALWC, which in turn synergistically boosted nitrate and OOA formation by heterogeneous/aqueous reactions. Such interaction may represent an important mechanism contributing to enhanced formation of secondary aerosols and rapid growth of fine particulate matter under relatively high RH conditions.

Heavy metals can accelerate the dissemination of antibiotic resistance genes (ARGs) in aquatic environments by imposing environmental stresses. Signaling molecules play a role in bacterial communication and help bacteria adapt to environmental stresses. However, little is known whether the presence of signaling molecules has an effect on the spread of ARGs induced by heavy metals. In this study, we investigated how N-decanoyl-L-homoserine lactone (C10-HSL) affects copper-induced conjugative transfer of ARGs. We calculated the conjugative transfer frequency and measured reactive oxygen species (ROS) production, membrane permeability, and the expression of relevant genes. The results demonstrated that the addition of C10-HSL increased the conjugative transfer frequency of ARGs under copper ions (Cu2+) stress, showing a 7.2-fold increase under 0.5 μM Cu2+ and 0.39 μM C10-HSL treatment compared to the control. This enhancement was associated with elevated intracellular ROS production and increased membrane permeability. The reduced conjugative transfer frequency under anaerobic conditions or with thiourea treatment supported the key role of ROS in this process. Furthermore, ROS overproduction triggered the SOS response, as evidenced by a 9-fold upregulation of recA expression. C10-HSL also modulated membrane-associated gene expression by upregulating outer membrane porins and downregulating efflux pump genes under Cu2+stress. This study provides a new insight into the spread of ARGs in aquatic environments.

Antibiotic resistance poses a significant threat to the public health domain. A favorable platform for generating and disseminating antibiotic-resistant genes (ARGs) and antibiotic-resistant bacteria (ARB) is provided by landscaped fish ponds created by urbanization. This research delved into the effects exerted by different concentrations of specific antibiotics, namely tetracycline and ciprofloxacin, on the microbial community composition present in water samples obtained from a landscape pond. Additionally, we analyzed the abundance of ARGs and the class 1 integron-integrase gene (intI1), and identified potential hosts of ARGs. The results indicated that the consistent administration of antibiotics significantly influenced the microbial community structure, resulting in variations within both bacterial communities and functionalities. Furthermore, the absolute quantities of ARGs, including tetA, tetC, qnrA, and qnrS, as well as the integrase gene intI1, exhibited augmentation in response to varying types and concentrations of antibiotics. Notably, the regular input of low concentrations of antibiotics produced higher levels of abundance of ARGs than the regular input of higher concentrations of antibiotics. The use of different types of antibiotics led to diverse host bacteria structures.

Alizarin, a dyestuff from herbs, showed effective inhibition effects on pathogenic bacteria, and thus has been frequently used in the world as the main alternative to antibiotics in the treatment of inflammations and pathogen infections. However, it was unclear whether alizarin played key a role in antibiotic-induced antibiotic-resistant gene (ARG) alterations and impacted microbial community shifts in aquatic environments. In this study, the effects of alizarin or co-exposure of alizarin with antibiotics on the fate of ARGs, class 1 integron-integrase gene (intI1), and microbial populations in lake water were investigated, and the potential hosts for ARGs were analyzed. The results showed that the absolute abundance of 16s rRNA gene, ARGs (tetA, tetC, and qnrS), and intI1 were increased during the treatment of alizarin. The combination of alizarin and antibiotics was superior to alizarin in its ability to promote population growth of bacteria and induce ARGs. Additionally, alizarin more significantly altered the community composition of microorganisms in water, which resulted in differences in bacterial communities and functions.

利用Aerodyne高分辨率飞行时间气溶胶质谱仪(HR-ToF-AMS)对南京北郊秋冬季非难熔性亚微米气溶胶(NR-PM1)的化学组分(包括有机物、硝酸盐、硫酸盐、铵盐和氯化物)和特征进行实时在线监测,并利用多元线性模型(ME-2)对其中复杂的有机物进行来源解析.观测期间,有机物、硝酸盐、硫酸盐、铵盐、氯化物对NR-PM1的贡献分别为42％,28％,15％,13％和2％.有机物解析出6类有机气溶胶:烃类有机气溶胶(HOA)、烹饪类有机气溶胶(COA)、生物质燃烧有机气溶胶(BBOA)、高氧化有机气溶胶(MO-OOA)、低氧化有机气溶胶(LO-OOA)、液相反应生成氧化有机气溶胶(aq-OOA),平均浓度分别占总有机气溶胶的18％,14％,19％,19％,11％和19％.通过不同污染事件的对比结果表明,本次观测期间二次气溶胶在污染时期占比会明显上升并且液相反应对二次组分的形成有显著的促进作用.

Tetrabromobisphenol A (TBBPA) is a new type of persistent organic pollutant, which causes environmental pollution and health problems, and has attracted the attention of the international research community. Once released into the environment, TBBPA can interact with dissolved organic matter (DOM), which affects its behavior. However, the effect of DOM on the biological toxicity of TBBPA remains unclear. The toxic effects of TBBPA on three model aquatic organisms (Chlorella pyrenoidosa, Daphnia magna, and Danio rerio), in the absence and presence of DOM were investigated. The order of acute toxicity of TBBPA to the three aquatic organisms was D. magna > D. rerio > C. pyrenoidosa. In the presence of DOM the median effect/lethal concentrations values of TBBPA to the three aquatic organisms decreased by at least 32 (C. pyrenoidosa), 52 (D. magna), and 6.6% (D. rerio), implying that DOM enhanced the acute toxicity of TBBPA to all the organisms. Moreover, the higher the concentration of DOM, the higher the acute toxicity of TBBPA. Furthermore, the presence of DOM increased total reactive oxygen species (ROS) induced by TBBPA in a concentration-dependent manner. A tracking analysis of total ROS in the three aquatic organisms also showed that the presence of DOM aggravated the accumulation of total ROS induced by TBBPA, indicating that oxidative stress is a characteristic mechanism of toxicity of TBBPA to aquatic organisms when DOM is present. In addition, the evaluated risk quotient indicated that the ecological risk of TBBPA to aquatic organisms can increase in environments rich in DOM.

Shrimp aquaculture environments are a natural reservoir of multiple antibiotic resistance genes (ARGs) due to the overuse of antibiotics. Nowadays, the prevalence of these kinds of emerging contaminants in shrimp aquaculture environments is still unclear. In this study, high-throughput sequencing techniques were used to analyze the distribution of ARGs and mobile genetic elements (MGEs), bacterial communities, and their correlations in water and sediment samples in two types of typical shrimp (Procambarus clarkii and Macrobrachium rosenbergii) freshwater aquaculture environments. A total of 318 ARG subtypes within 19 ARG types were detected in all the samples. The biodiversity and relative abundance of ARGs in sediment samples showed much higher levels compared to water samples from all ponds in the study area. Bacitracin (17.44–82.82%) and multidrug (8.57–49.70%) were dominant ARG types in P. clarkii ponds, while sulfonamide (26.33–39.59%) and bacitracin (12.75–37.11%) were dominant ARG types in M. rosenbergii ponds. Network analysis underlined the complex co-occurrence patterns between bacterial communities and ARGs. Proteobacteria, Cyanobacteria, and Actinobacteria exhibited a high abundance in all samples, in which C39 (OTU25355) and Hydrogenophaga (OTU162961) played important roles in the dissemination of and variation in ARGs based on their strong connections between ARGs and bacterial communities. Furthermore, pathogens (e.g., Aeromonadaceae (OTU195200) and Microbacteriaceae (OTU16033)), which were potential hosts for various ARGs, may accelerate the propagation of ARGs and be harmful to human health via horizontal gene transfer mediated by MGEs. Variation partitioning analysis further confirmed that MGEs were the most crucial contributor (74.76%) driving the resistome alteration. This study may help us to understand the non-ignorable correlations among ARGs, bacterial diversity, and MGEs in the shrimp freshwater aquaculture environments.

A chemical ionization mass spectrometer (CIMS) was deployed to measure ambient ammonia (NH3) with a time resolution of similar to 5 min. Unexpectedly high levels of NH3, peaking at 15.5 ppbv and averaging at 2.1 +/- 1.9 ppbv, were observed near an agricultural field in Nanjing, China, during wintertime, a slack season for farming. Re partitioning from aerosols can only explain a small portion of this NH3 due to the considerably low air temperature, whereas the major source was emission from soil, as indicated by significant positive correlations of the NH3 concentration with the ground surface temperature, solar radiation intensity, and particularly the surface air temperature difference. The dissolved/adsorbed NH3 and NH4NO3 in soil likely originated from conversion of nitrogen-containing organic matter by microorganisms through ammonification and nitrification. The upward transfer of NH3 released from the soil was facilitated by convective mixing driven by solar radiation, which produced the required high soil-air temperature gradient. This winter release of NH3 from the soil is not captured by commonly used long-term, passive-sampler based methods, giving rise to an incorrect assumption that during winter, a slack season for farming, soil emits no NH3 and so this source has remained unresolved by typical emission inventory models. Our results indicate that contrary to the common assumption, agricultural background emissions are a non-negligible source of NH3 even in wintertime, which may exert a significant impact on regional air pollution formations. Hence, a refined NH3 emission inventory is critically needed to account for the haze events in wintertime northern China.

Nanocellulose is a functional material derived from natural carbon-based polymers. These nanomaterials are biodegradable and renewable in nature and hence are seen as environmentally-friendly materials in many applications. The use of such innovative materials is accelerating and inescapable there is a need to test these presumed environmentally-friendly materials with regard to their ecotoxicity. Here, the acute toxicity and the oxidative stress of nanocelluloses as induced to three aquatic organisms of different trophic levels, namely Scenedesmus obliquus, Daphnia magna, and Danio rerio, were studied in relation to the composition and morphology of the celluloses. Wood-based cellulose nanocrystals (CNCs), cotton-based CNCs, and cotton-based cellulose nanofibrils were selected as model compounds. The results clearly demonstrated a lack of impact of the different nanocellulose materials on apical endpoints like growth inhibition and mortality after short-term exposure. The nanocellulose materials did activate oxidative stress as evoked by reactive oxygen species in the three aquatic organisms. Key factors ascertained to induce the oxidative stress were the composition and morphology. The nanocellulose induced oxidative stress was observed for all the species at concentrations higher than 0.01 mg/L. This finding suggests a more general revelation of oxidative stress being a characteristic mechanism for nanocellulose toxicity to aquatic organisms.

Joint biomarker responses, oxidative stress and membrane systems, were determined for nano-metal-oxides (nMeO, i.e., nCeO2, nMgO, and nFe3O4) and sulfadiazine (SDZ) exposed at relevant low concentrations to two freshwater microalgae Scenedesmus obliquus and Chlorella pyrenoidosa. The impacts of dissolved organic matter (DOM) on the joint biomarker responses were also investigated. Results indicated that the presence of SDZ significantly decreased the level of intercellular reactive oxygen species (ROS) in the algal cells exposed to each nMeO. Reduction of cell membrane permeability (CMP) and mitochondrial membrane potential (MMP) in the algal cells was observed when the algae were exposed to the mixture of SDZ and the nMeO. The degree of reduction of the ROS level, CMP, and MMP significantly went down with the addition of DOM to a certain extent. Changes in cellular oxidative stress and membrane function depended on the types of both nMeO and algal species. This contribution provides an insight into the hazard assessment of a mixture consisting of emerging contaminants and DOM, as they can coexist in the aquatic environment.

The importance of attention to unravel the interaction of nano-plastic particles (NPs) with natural acidic organic polymer (NAOP) in freshwater environment should not be neglected. However, toxicological data available for the interaction between NPs and NAOP remain limited. Here, we investigate the toxicological effects of three model polystyrene (PS) NPs with different functional groups (unmodified, amino- and carboxyl-modified PS NPs) on two freshwater organisms of different trophic levels (Scenedesmus obliquus and Danio rerio) in the absence and presence of two classes of NAOP, namely fulvic acid and humic acid. The NAOP interaction with the NPs is shown to alter oxidative stress and disturb membrane function in S. obliquus cells to a certain extent. Combined oxidative stress responses to the NPs and NAOP in D. rerio as a function of their mixture levels showed inhibition, alleviation, and reinforce. Changes in cellular oxidative stress and membrane function depended on the concentration and types of both NPs and NAOP. Furthermore, the characterization parameters of the NPs were important for the explanation of the ecotoxicological mechanism of the NPs in the presence of NAOP. Our findings emphasized the critical role of NAOP in the fate and toxicity of plastic particles in freshwater environment.

Concomitant releases of various engineered nanoparticles (NPs) into the environment have resulted in concerns regarding their combined toxicity to aquatic organisms. It is however, still elusive to distinguish the contribution to toxicity of components in NP mixtures. In the present study, we quantitatively evaluated the relative contribution of NPs in their particulate form (NP(particle)) and of dissolved ions released from NPs (NP(ion)) to the combined toxicity of binary mixtures of ZnO NPs and graphene oxide nanoplatelets (GO NPs) to three aquatic organisms of different trophic levels, including an alga species (Scenedesmus obliquus), a cladoceran species (Daphnia magna), and a freshwater fish larva (Danio rerio). Our results revealed that the effects of ZnO NPs and GO NPs were additive to S. obliquus and D. magna but antagonistic to D. rerio. The relative contribution to toxicity (RCT) of the mixture components to S. obliquus decreased in the order of RCTGO NP(particle) >RCTZnO NP(particle)>RCTZnO NP(ion), while the RCT of the mixture components to D. magna and D. rerio decreased in the order of RCTZnO NP(particle)>RCTGO NP(particle)>RCTZnO NP(ion). This finding also implies that the suspended particles rather than the dissolved Zn-ions dictated the combined toxicity of binary mixtures of ZnO NPs and GO NPs to the aquatic organisms of different trophic level. The alleviation of the contribution to toxicity of the ionic form of ZnO NPs was caused by the adsorption of the dissolved ions on GO NPs. Furthermore, the ZnO NP(particle) and GO NP(particle) displayed a different contribution to the observed mixture toxicity, dependent on the trophic level of the aquatic organisms tested. The difference of the contributions between the two particulate forms was mainly associated with differences in the intracellular accumulation of reactive oxygen species. Our findings highlight the important role of particles in the ecological impact of multi-nanomaterial systems.

新兴纳米材料石墨烯的环境行为与效应研究备受关注.环境中普遍存在的腐殖酸(HA)可与石墨烯发生相互作用,而有关这种相互作用对石墨烯环境行为的影响研究仍十分有限.该文研究了一种HA类似物对本征石墨烯(G)和氧化石墨烯(GO)在绿藻毒性测试介质中的物理化学性质(表面电荷、电泳流动性及水动力学粒径)的影响.实验结果表明,随着HA浓度的升高,G和GO的表面电荷值越负、电泳流动性值越负、水动力学粒径越小,说明HA显著提高了G和GO在水相中的分散稳定性,且HA浓度越高,稳定性提升的幅度越大,同时该影响规律并不依赖于时间的延长.相比GO言,HA对G的水相稳定性影响更大.HA影响G和GO水相稳定性的机理为静电作用和空间位阻效应.研究结果对于研究和规避石墨烯材料的环境风险有着重要意义.

Metal-based nanoparticles (NPs) are the most widely used engineered nanomaterials. The individual toxicities of metal-based NPs have been plentifully studied. However, the mixture toxicity of multiple NP systems (n ≥ 3) remains much less understood. Herein, the toxicity of titanium dioxide (TiO2) nanoparticles (NPs), silicon dioxide (SiO2) NPs and zirconium dioxide (ZrO2) NPs to unicellular freshwater algae Scenedesmus obliquus was investigated individually and in binary and ternary combination. Results show that the ternary combination systems of TiO2, SiO2 and ZrO2 NPs at a mixture concentration of 1 mg/L significantly enhanced mitochondrial membrane potential and intracellular reactive oxygen species level in the algae. Moreover, the ternary NP systems remarkably increased the activity of the antioxidant defense enzymes superoxide dismutase and catalase, together with an increase in lipid peroxidation products and small molecule metabolites. Furthermore, the observation of superficial structures of S. obliquus revealed obvious oxidative damage induced by the ternary mixtures. Taken together, the ternary NP systems exerted more severe oxidative stress in the algae than the individual and the binary NP systems. Thus, our findings highlight the importance of the assessment of the synergistic toxicity of multi-nanomaterial systems.

The present study investigated the impacts of dissolved organic matters (DOM) on joint toxicity involved in zinc oxide nanoparticles (ZnO NPs) and tetrabromobisphenol A (TBBPA) at relevant low-exposure concentrations (< 1 mg/L). It was found that ZnO NPs in single and combined systems exhibited severe inhibition effects on a freshwater microalgae Scenedesmus obliques. However, the presence of DOM slightly alleviated the growth inhibition toxicity induced by the binary mixtures of ZnO NPs and TBBPA. Ultrastructure analysis revealed that ZnO NPs caused structural damage to cells, including plasmolysis, membrane destruction, and the disruption of thylakoid in the chloroplast, regardless of the presence of coexisting substances. Oxidative stress biomarker quantitative analysis and in situ observations indicated that the massive accumulation of reactive oxygen species in the binary mixtures of ZnO NPs and TBBPA caused severe oxidative damage, but the presence of DOM significantly mitigated the damage.

Graphene-family nanomaterials (GFNs) exhibit universal applications and consequently will inevitably enter aquatic systems. However, both the fate and behavior of GFNs in aquatic environments have not been completely explored at field relevant conditions. Herein, we have systematically investigated the aqueous aggregation and stability of graphene nanoplatelets (GNPs), graphene oxide (GO), and reduced graphene oxide (RGO) under varied solution chemistry parameters (pH, divalent cations, and dissolved organic carbon (DOC)) during 21 days of incubation in simulated natural environmental conditions. Results indicate that pH values from 6 to 9 had a notable impact on the aqueous behaviors of the three GFNs. Divalent cations (Ca2+ and Mg2+) at the concentrations of 2.5 and 10 mM remarkably increased the extent of aggregation of the three GFNs and resulted in severe sedimentation, independently of surface chemical functionalization. The presence of only DOC ranging from 0.5 to 2 mg C/L significantly elevated the dispersion stability of GNPs and RGO in a dose-dependent manner, whereas no effects were observed on GO. Furthermore, DOC at the studied concentrations and surface functionality were insufficient to counterbalance the impact of the divalent cations. Direct visual and in situ observations further supported the conclusions on the effects of divalent cations or/and DOC. These findings further underline that the environmental behaviors of GFNs are controlled by the complex interplay between water chemistry parameters and GFN surface properties.

This study investigated the impact of dissolved organic matters (DOM) on the ecological toxicity of aluminum oxide nanoparticles (Al2O3NPs) at a relatively low exposure concentration (1 mg L-1). The unicellular green alga Scenedesmus obliquus was exposed to Al2O3NP suspensions in the presence of DOM (fulvic acid) at various concentrations (1, 10, and 40 mg L-1). The results show that the presence of DOM elevated the growth inhibition toxicity of Al2O3NPs towards S. obliquus in a dose-dependent manner. Moreover, the combination of DOM at 40 mg L-1 and Al2O3NPs resulted in a synergistic effect. The relative contribution of Al-ions released from Al2O3NPs to toxicity was lower than 5%, indicating that the presence of the particles instead of the dissolved ions in the suspensions was the major toxicity sources, regardless of the presence of DOM. Furthermore, DOM at 10 and 40 mg L-1 and Al2O3NPs synergistically induced the upregulation of intercellular reactive oxygen species levels and superoxide dismutase activities. Analysis of the plasma malondialdehyde concentrations and the observation of superficial structures of S. obliquus indicated that the mixtures of DOM and Al2O3NPs showed no significant effect on membrane lipid peroxidation damage. In addition, the presence of both DOM and Al2O3NPs contributed to an enhancement in both the mitochondrial membrane potential and the cell membrane permeability (CMP) in S. obliquus. In particular, Al2O3NPs in the presence of 10 and 40 mg L-1 DOM caused a greater increase in CMP compared to Al2O3NPs and DOM alone treatments. In conclusion, these findings suggest that DOM at high concentrations and Al2O3NPs synergistically interrupted cell membrane functions and triggered subsequent growth inhibition toxicity.

A combined ecotoxicity study was carried out with nano-zinc oxide (nZnO) and nano-copper oxide (nCuO) to freshwater algae Scenedesmus obliquus. Concentration-response analysis indicated that the dissolved metal fraction was not the major source of individual and combined toxicity of the metal-oxide nanoparticles (MONPs). Moreover, the contribution of the nCuO (based on metallic mass) to the combined toxicity was greater than that of the nZnO. The observed combined toxicity can be predicted by the pharmacological concepts of concentration addition (CA) and independent action (IA). Combined toxicity prediction (in terms of median effect concentration) based on both concepts tends to overestimate the overall observed toxicity of the MONP mixtures. CA was more accurate for predicting the combined toxicity than IA. It may be concluded that CA gives a valid estimation of the overall ecotoxicity for mixtures comprising of similar acting MONPs.

A combined ecotoxicity study was carried out with nano-zinc oxide (nZnO) and nano-copper oxide (nCuO) to freshwater algae Scenedesmus obliquus . Concentration–response analysis indicated that the dissolved metal fraction was not the major source of individual and combined toxicity of the metal-oxide nanoparticles (MONPs). Moreover, the contribution of the nCuO (based on metallic mass) to the combined toxicity was greater than that of the nZnO. The observed combined toxicity can be predicted by the pharmacological concepts of concentration addition (CA) and independent action (IA). Combined toxicity prediction (in terms of median effect concentration) based on both concepts tends to overestimate the overall observed toxicity of the MONP mixtures. CA was more accurate for predicting the combined toxicity than IA. It may be concluded that CA gives a valid estimation of the overall ecotoxicity for mixtures comprising of similar acting MONPs.