Maddenweinstein0615

The use of phytoremediation was an efficient strategy for the restoration of mine slag and the addition of modifier was favorable for improving the phytoremediation efficiency. Herein, spent mushroom compost (SMC) was added in manganese (Mn) slag to reveal the phytoremediation potential of Paulownia fortunei seedlings. The transportation, subcellular distribution and chemical forms of Mn in P. fortunei, the diurnal variation of photosynthesis and antioxidant enzyme activities in P. fortunei leaves were measured to reveal the effect of SMC (mass ratios of 10%, M+) on the phytoremediation of Mn slag. Results showed that the addition of SMC increased the accumulation content of Mn by 408.54% due to the increased biomass of P. fortunei seedlings. After SMC amendment, the maximum net photosynthetic rate (Pn) increased and the superoxide dismutase (SOD) activities decreased significantly (p  less then  0.05), which was beneficial to the tolerance of leaves to Mn stress. SMC amendment maintained the cell structural integrity of P. fortunei seedlings observed by transmission electron microscope (TEM). Additionally, SMC amendment decreased the damage level of Mn to the cell of P. fortunei seedlings by using function groups (-CH3 and -COOH) to bond Mn in the cell walls and vacuoles. SMC amendment reduced the Mn toxicity to P. fortunei seedlings and improved the phytoremediation capacity. The low nitrogen use efficiency (NUE) of fertilizers and aluminum toxicity are major limiting factors for crop development in red soil (acidic soil) of China. Biochar is a promising material for improving soil quality, alleviating aluminum and acidic toxicity. The present study was conducted on maize to evaluate the effects of biochar on NUE and soil quality under different applications of nitrogen fertilizer. Biochar was used in the following five levels in each pot; C0 (0 g), C1 (7.5 g), C2 (15 g), C3 (30 g), C4 (45 g), in combination with δ15N at two N levels N0 (0 g kg-1) and N1 (0.2 g kg-1). The biochar increased soil nutrients, exchangeable cation, and SOM. Compared with C0, the K+, Ca2+, and Mg2+ were increased by 31.58%, 95.87%, and 463.75% while total Al3+ content of C4 treatment was decreased by 91.98%-93.30% in soil, respectively. X-ray diffraction (XRD) and energy dispersive spectrometer (EDS) showed that Al2SiO5 was adsorbed on the surface of biochar in the soil due to the special physical structure of biochar. Besides, the results showed that root and shoot biomass increased by 44.5% and 89.6%, respectively under biochar treatment. The nitrogen utilization rate of the plant was increased by 11.08% after the amendment of biochar to soil. The δ15N content was increased from 11.97 to 21.32 for root and from 50.84 to 82.33 mg kg-1 for the shoot. The use of biochar with N fertilizer showed a more positive effect on improving NUE of maize and facilitating soil quality. Our results suggest that biochar could be used to improve soil available nutrients, alleviate aluminum toxicity and acidic toxicity. Therefore, biochar could also increase the NUE of maize by adjusting soil quality. On two rat cell lines, pheochromocytoma PC12 and ascites hepatoma AS-30D, and on rat liver mitochondria we studied action of paxilline (lipophilic mycotoxin from fungus Penicillium paxilli which is blocker of large-conductance potassium channels) against harmful effects of Cd(II) - one of the most dangerous toxic metals and environmental pollutants. We investigated an influence of paxilline on cell viability and mitochondrial function in the presence and in the absence of Cd2+. As found, paxilline protected partially from the Cd2+-induced cytotoxicity, namely taken in concentration of 1 μM it decreased the Cd2+-induced cell necrosis in average by 10-14 or 13-23% for AS-30D and PC12 cells, respectively. Voruciclib ic50 Nevertheless, paxilline did not affect the Cd2+-induced apoptosis of AS-30D cells. The alleviating concentration of paxilline reduced an intracellular production of reactive oxygen species (ROS) in PC12 cells intoxicated by Cd2+ and enhanced the ROS production in control AS-30D cells; however, it weakly affected mitochondrial membrane potential of the cells in the absence and in the presence of Cd2+. The ameliorative concentration of paxilline decreased the maximal respiration rates of control cells of both types after short-term (3-5 h) treatment with it while the rates reached their control levels after long-term (24-48 h) incubation with the drug. Paxilline was not protective against the Cd2+-induced membrane permeability and respiration rate changes in isolated rat liver mitochondria. As result, the mitochondrial electron transport chain was concluded to contribute in the mitigating effect of paxilline against the Cd2+-produced cell injury. Although there are numerous studies on bisphenol A (BPA) on the testis and spermatozoa, the effect of BPA on the physiological link between the testis and maturation of spermatozoa has not been studied. To provide an optimal environment (acidic pH) for sperm maturation in the epididymis, clear cells secrete protons and principal cells reabsorb bicarbonate and the secreted proton. Because of its crucial role in sperm maturation and fertility, functional changes in the epididymis following BPA exposure must be considered to fully understand the mechanisms of BPA on male fertility. Here, we identified the adverse effects of BPA exposure during puberty in male mice. CD-1 male mice were gavaged daily with vehicle (corn oil) and 50 mg BPA/kg-BW for 6 weeks. We determined the changes in epididymis, functional sperm parameters including motility, capacitation status, tyrosine phosphorylation, and fertility-related protein expression and in vitro and in vivo fertility rate following BPA exposure. Expression of vacuolar-type H + -ATPase is necessary for the secretion of protons by clear cells of the caput epididymis and was directly down-regulated following BPA exposure, while there were no changes in the other epithelial cell types in the epididymis. Also, pERK 1/2 signaling pathway was increased significantly in the caput epididymis following BPA exposure. Consequently, the luminal pH slightly increased, resulting in premature capacitation of spermatozoa. Moreover, there was a significant loss of the acrosomal membrane following an increase of protein tyrosine phosphorylation, while PKA activity decreased during sperm capacitation. Fertility-related proteins also showed aberrant expression upon BPA exposure. These modifications resulted in decreased male fertility in vitro and in vivo.