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Sasa argenteostriata and Indocalamus decorus consistently maintained higher antioxidant enzyme activities and free proline levels than the other species under Pb treatment, and the total biomass per pot of the new bamboo decreased the least compared to that in the Pb-free treatment for these two species. Therefore, these bamboo species may be used in the long-term continuous remediation of Pb-contaminated soil.Aluminum (Al) is a ubiquitous environmental metal toxicant that causes osteoblast (OB) damage which leads to Al-related bone diseases. Mitochondrial damage plays a key role in Al-related bone diseases, and while mitophagy can clear damaged mitochondria and improve OB function, the relationship between mitophagy and Al-induced OB dysfunction is unknown. To explore the role of mitophagy in Al-induced OB dysfunction in vitro, we used 2 μM carbonyl cyanide m-chlorophenylhydrazone (CCCP) and 0.4 μM Cyclosporin A (CsA) to activate and inhibit mitophagy, respectively. MC3T3-E1 cells were treated with 0 mM AlCl3 (control group); 2 mM AlCl3 (Al group); 2 μM CCCP (CCCP group); 2 μM CCCP and 2 mM AlCl3 (CCCP + Al group); 0.4 μM CsA (CsA group); 0.4 μM CsA and 2 mM AlCl3 (CsA + Al group). The results showed that Al induced ultrastructural and functional impairment of MC3T3-E1 cells. Compared to the Al group, mitophagy activation caused mitochondrial membrane potentials to collapse, up-regulated PINK1, Parkin, and LC3 expression, down-regulated p62 expression, and increased mitophagosome numbers. Mitophagy activation also reduced Al-induced oxidative stress and MC3T3-E1 cell functional damage, as seen in improvement in cell viability, cellular calcium and phosphorus contents, and collagen I, osteocalcin, and bone alkaline phosphatase gene expression. Mitophagy inhibition had the opposite effects on activation. Overall, these results show that mitophagy can protect against Al-induced OB dysfunction.The release of untreated wastewater containing biotoxic substances in the form of heavy metals is one of the most crucial environmental and health challenges faced by our community. The recent advances in microbes derived removal has propelled bioremediation as a better and effective alternative to conventional techniques. Present study investigates the detoxification mechanisms evolved by the nickel (Ni(II)) resistant fungal strains, isolated from the industrial drain sites. The molecular detailing of the isolated fungal isolates confirms their identity as Neurospora crassa and Aspergillus flavus. Laboratory-scale experiments have established influence of different ranges of dose, pH, time, and metal concentration on the removal and uptake trends. Further, the variations in the carbon and nitrogen sources and agitation conditions has revealed the best substratum for achieving optimum results for the industrial exploitation of these microbes. SEM micrographs and FTIR spectra elucidates the superficial alterations on the mycelium of the fungal isolates and the involvement of active functional groups in the bioremediation of Ni(II) respectively. Biosorption of Ni(II) on living biomass has followed the Langmuir adsorption model. [https://www.selleckchem.com/products/adenosine-disodium-triphosphate.html Adenosine disodium triphosphate in vivo] The findings of the study have provided a promising insight in the simultaneous action of different mechanistic removal approaches to explore a large scale removal of Ni(II) from the waste generating industries.4-Carboxyphenylboronic acid was used as the single precursor to facilely prepare fluorescent carbon quantum dots by one-step solvothermal method. The as-obtained carbon dots (CDs) exhibited highly selective and sensitive for benzo[a]pyrene (BaP), and may be a splendid sensor for sensing BaP. The principle was that the as-prepared CDs could form a complex with BaP through hydrophobic interaction which causes the decrease of fluorescence intensity of CDs by static quenching principle. The constructed ﬂuorescent sensor exhibited excellent linearity ranged from 0.002 to 0.06 μg mL-1 and provided a low limit of detection of 0.16 ng mL-1. The experimental results showed that this ﬂuorescent sensor resulted in simplicity, rapidness, low cost, short analytical time, and high sensitivity and stability. Validation with real water samples endowed the sensor high reliability and feasibility for BaP determination in practical application in various samples.Europium(III), i.e., Eu(III), is chemically analogous to the trivalent lanthanides (Ln) and actinides (An). A good understanding of the adsorption behaviour of Eu(III) on mica group minerals is critical to the safety evaluation of the radioactive contamination. Nevertheless, the structural complexity of micaceous minerals makes it difficult to draw a consistent conclusion in the study of Eu(III) migration. In this work, we contrastively studied Eu(III) adsorption on dioctahedral muscovite and trioctahedral phlogopite as functions of pH, ionic strength, background electrolytes, interaction sequence, and fulvic acid (FA). Batch experiments showed that Eu(III) adsorption on both micas was strongly dependent on pH but quite independent on ionic strength that is determined by Na+. Planar sites are available on both muscovite and phlogopite while interlayer sites only on phlogopite under Na+ and Ca2+ electrolytes (not for K+ and Cs+). An interlayer expansion of phlogopite, as indicated by a newly appeared diffraction peak at ~6° 2-theta, occurred along with Eu(III) adsorption, which was also confirmed by transmission electron microscopy. Furthermore, the initial Eu(III) concentrations, the concentration ratios between Eu(III) and Cs+, and the reaction sequences of Eu(III)-electrolytes-FA affected both the adsorption behaviour of Eu(III) and reversely the structural alteration of phlogopite. The sequential extraction showed that the adsorbed Eu(III) was mainly in the ion-exchangeable form while the addition of FA could increase the portion of coordinative species. The currently proposed Eu(III) adsorption mechanism can shed new light on predicting the migration of Ln/An(III) at the mica-rich solid-liquid interface on a molecular scale.Nanoscale zero-valent iron (nZVI) based (nano)composites supported by clay mineral substrates are a promising technology for the in-situ remediation of groundwater and (sub)soils contaminated with chlorinated hydrocarbons, such as trichloroethene (TCE). However, the physicochemical processes and interaction mechanisms between nZVI particles, clay minerals and TCE are poorly understood, yet. We immobilized nZVI particles on a commercial bentonite substrate to prepare a novel nZVI-B nanocomposite and tested its performance for TCE removal from solution against pure nZVI in batch reactors. The nZVI-B exhibited a higher reactivity (2.2·10-3 L h-1·m-2) and efficiency (94%) for TCE removal than nZVI (2.2·10-4 L h-1·m-2; 45%). Sorption of TCE onto the clay surfaces and reductive de-chlorination in "micro-reactors" developing within the nZVI-B controlled the kinetics and the magnitude of TCE loss from solution. Contrary to pure nZVI, no signs of nZVI particle agglomeration or inactivation due to oxide shell formation were found in nZVI-B.