Heavy metals are common marine and soil pollutants that are mainly the result of industrial activity, and are a threat to the environment and human health. In this study, 1H nuclear magnetic resonance (NMR)-based metabolomics was applied to adult Danio rerio to monitor the metabolic change as a response to ZnCl2 and CdCl2 exposure at different concentrations for 72?h. NMR spectroscopy was used to identify and quantify the metabolites extracted from D. rerio. The metabolite profiles of the control and heavy metal exposed group were classified by partial least squares – discriminant analysis (PLS-DA) analysis, and potential contaminant-specific biomarkers were suggested. For the ZnCl2-exposed zebrafish, the levels of ATP, aspartate and NAD+ were increased, whereas the levels of formate, inosine, hypoxanthine and succinate decreased. In addition, the CdCl2-exposed zebrafish showed an increase in the levels of ATP and formate and a decrease in the levels of glutamate, inosine and glutathione. Overall, Zn and Cd may lead to neurotoxicity, disturbances in the energy metabolism and oxidative stress. Our finding demonstrated that the application of NMR-based metabolomics might be useful for detecting the toxicity caused by sub-lethal concentrations of heavy metal contaminants in the environment. 相似文献
Time series of nanoparticle number concentration during new particle formation (NPF) events in the urban environment of Brisbane, Australia, showed that the formation of charged particles often occurred before that of neutral particles. We monitored 241 days during the calendar year 2012 over which NPF events were observed on 108 days. We studied the times at which the charged and neutral particle concentrations in the size range 1.8–3.2 nm reached their peak values and found that they were clearly different in 50 events with the peak neutral particle concentration lagging behind the charged particle concentration during 42 of these events with a mean time lag of 24±12 min. While the charged particles were more likely to form before the neutral particles, once formed, the growth rate of the particles did not depend on their charge. While ion-induced nucleation is not the dominant mechanism of NPF in the atmosphere, our observations suggest that the presence of ions in the atmosphere plays a role that cannot be ignored.
• Electrode fouling is characterized by non-destructive characterization.• Electrode fouling is highly dependent on electrochemical process.• Active chlorine can prevent the formation of polymeric fouling film. Electrode fouling is a problem that commonly occurs during electro-oxidation water purification. This study focused on identifying the fouling behavior of Pt electrode associated with the formation of polymeric layer during electro-oxidation of phenol. The in situ electrochemical measurements and non-destructive observation of the electrode morphology were reported. The results demonstrated that the electrode fouling was highly dependent on thermodynamic process of electrode that was controlled by anode potential. At anode potential lower than 1.0 V vs SHE, the direct electro-oxidation caused the electrode fouling by the formation of polymeric film. The fouling layer decreased the electrochemically active surface area from 8.38 cm2 to 1.57 cm2, indicated by the formation of polymeric film with thickness of 2.3 mm, increase in mass growing at a rate of 3.26 μg/cm2/min. The degree to which the anode was fouled was independent of anion in the electrolyte. In comparison, at anode potential higher than 2.7 V vs SHE, the anions (e.g., chloride) could exert a major influence to the behavior of electrode fouling. The presence of chloride was shown to mitigate the fouling of electrode significantly through preventing the formation of polymeric film by active chlorine (e.g., Cl• and Cl2) produced from anodic oxidation of chloride. Since chloride is the most abundant anionic species existing in both natural and engineered water system, this study not only offers a deep insight into the mechanism of electrode fouling, but also suggests strategies for anti-fouling in the presence of chloride in electro-oxidation process. 相似文献
•Direct seeding (DS) method led to more distributed Cd in aerial parts of rice.•The Cd content was significantly higher in brown rice with planting mode of DS.•Using DS lessened the Fe plaque covering the root surface in all growth stages.•Transplantation mode should be considered as a priority in Cd-contaminated areas. Global rice production practices have gradually changed from a reliance on transplanting to direct seeding. Yet how this shift may alter cadmium (Cd) accumulation in rice is poorly known. Here we conducted field experiments with two rice genotypes cultivars that were planted using three methods: via direct seeding (DS), seedling throwing (ST), and manual transplanting (MT). Rice samples were collected during four growth stages. The formation and distribution of iron plaque were analyzed using DCB (dithionite-citrate-bicarbonate) extractions and observed under micro-XRF (micro X-ray fluorescence). The results revealed that, in each growth stage, DS rice was more apt to harbor Cd distributed in the plant’s aerial parts, and the Cd concentration of brown rice from DS was 21.8%–43.3% significantly higher than those from ST and MT at maturity stage (p<0.05). During the vegetative stages, the Cd uptake percentage was higher in DS than MT rice, and those plants arising from the DS method were capable of absorbing more Cd earlier in their growth and development. Conversely, using DS decreased the amount of iron plaque covering the root surface in every growth stage, especially in the critical period of Cd accumulation, such that the roots’ middle areas were distinguished by a near-complete absence of iron plaque, thus weakening its role as an effective barrier to Cd uptake from soil. Collectively, this study demonstrated that implementing the DS mode of planting will increase Cd’s distribution in the aboveground parts of rice, and heightening the risk of Cd contamination in grain. 相似文献
Dielectrophoresis (DEP) process could enhance the removal the Cd2+ and Pb2+ with less absorbent.The removal rates of both Cd2+ and Pb2+ increased with the increase of voltage.The overall removal rate of Cd2+ and Pb2+ in the binary system is higher than that of Cd2+ or Pb2+ in the single system.DEP could cause considerable changes of the bentonite particles in both surface morphology and microstructure. Dielectrophoresis (DEP) was combined with adsorption (ADS) to simultaneously and effectively remove Cd2+ and Pb2+ species from aqueous solution. To implement the process, bentonite particles of submicro-meter size were used to first adsorb the heavy metal ions. These particles were subsequently trapped and removed by DEP. The effects of the adsorbent dosage, DEP cell voltage and the capture pool numbers on the removal rate were investigated in batch processes, which allowed us to determine the optimal experimental conditions. The high removal efficiency, 97.3% and 99.9% for Cd2+ and Pb2+, respectively, were achieved when the ions are coexisting in the system. The microstructure of bentonite particles before and after ADS/DEP was examined by scanning electron microscopy. Our results suggest that the dielectrophoresis-assisted adsorption method has a high capability to remove the heavy metals from wastewater. 相似文献
Heavy metals can act as co-selecting agents and promote antibiotic resistance.Most frequent resistances to heavy metals are observed for zinc and cadmium.P. aeruginosa and E. coli are commonly resistant to heavy metals and antibiotics.Heavy metals proliferate antibiotic resistance through co- and cross-resistance.Heavy metal and antibiotic resistances are common near anthropogenic activities. Antibiotic resistance in human pathogens can proliferate under selective pressures. Heavy metals in environmental reservoirs may contribute to selecting antibiotic-resistant strains. To determine the associations between heavy metals and antibiotic resistance, a literature review was conducted to systematically collect and categorize evidence for co-occurrence of resistance to heavy metals and antibiotics within human pathogenic bacteria in water, wastewater, and soil. In total, 42 publications adhered to inclusion criteria. Across the reservoirs, zinc and cadmium were the most commonly observed heavy metals associated with resistance to antibiotics. Pseudomonas aeruginosa and Escherichia coli were the most commonly studied bacteria with reported co-occurrence of resistance to several heavy metals and antibiotic classes. As co-selecting agents, prevalence of heavy metals in the environment can proliferate resistance to heavy metals and antibiotics through co-resistance and cross-resistance mechanisms. In comparing different reservoirs, soils and sediments harbor higher heavy metal and antibiotic resistances compared to water environments. Additionally, abiotic factors such as pH can affect the solubility and hence, the availability of heavy metals to bacterial pathogens. Overall, our review demonstrates heavy metals act as co-selecting agents in the proliferation of antibiotic resistance in human pathogens in multiple environmental reservoirs. More studies that include statistical data are needed to further describe the exposure-response relationships between heavy metals and antibiotic resistance in different environmental media. Moreover, integration of culture-based and molecular-based methods in future studies are recommended to better inform our understanding of bacterial co- and cross-resistance mechanisms to heavy metals and antibiotics. 相似文献
This long‐term inhalation study was designed to describe the toxicity and the carcinogenic risk from Cd compounds because it had been shown from former long‐term inhalation studies that cadmium choloride induced primary lung tumors in Wistar rats. It was therefore logical to examine whether other cadmium compounds to which human beings are more frequently exposed have also carcinogenic potency. In a long‐term inhalation study cadmium aerosols consisting of cadmium chloride (CdCl2), cadmium oxide (CdO) as dusts and fumes, cadmium sulfate (CdSO4), cadmium sulfide (CdS) and a combination of cadmium oxide/zinc oxide were used. Wistar rats were continuously exposed in inhalation chambers for 18 months 22 hrs a day or for 40 hrs a week. The studies will be terminated at the mean survival life time of the species. The aerosols were generated by several different systems. The particles of the cadmium aerosols have the average mass medium diameters in the range from 0.2 to 0.5 μm. 相似文献