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In this study, the light absorption properties of fine organic aerosols from the burning emissions of four biomass materials were examined using UV-spectrophotometry and Aethalometer-measurements, respectively. For wood chips and palm trees, the burning experiments were carried out with different combustion temperatures (200, 250, and 300 οC) in an adjustable, electrically heated combustor. The light absorptions of water and methanol extracts of aerosols, and smoke particles showed strong spectral dependence on the burning emissions of all biomass materials. However, the burning aerosols of wood chips showed stronger absorption than those of the other biomass burning (BB) emissions. For the burning aerosols of wood chips and palm trees, organic carbon/elemental carbon (OC/EC) decreased as the combustion temperature increased from 200 to 300 °C. Absorption Ångström exponent (AAE) values tended to decrease when combustion temperature increased for smoke aerosols and methanol extracts in smoke samples. The mass absorption efficiency at 365 nm (MAE365, m2 g-1∙C-1) of water- and methanol-extractable OC fractions was highest in wood chip burning smoke samples. MAE365 values of methanol extracts for rice straw, pine needles, wood chips, and palm trees burning emission samples were 1.35, 0.92, 2.36-3.37, and 0.86-1.42, respectively. For wood chip and palm tree burning emissions, AAE320-430nm values of methanol extracts were strongly correlated with OC/EC (i.e., combustion temperature) with slopes of 0.11 (p less then 0.001) and 0.02 (p less then 0.001), and R2 values of 0.87 and 0.74, respectively. Moreover, a linear regression between MAE365 of methanol extractable OC and OC/EC showed slopes of -0.05 (p less then 0.001) and -0.004 (p less then 0.001) and R2 of 0.72 and 0.74, respectively. The results of this study clearly demonstrate that burning condition and biomass type influence the light absorption properties of organic aerosols from BB emissions.The effects and mechanisms of biochars with different silicon (Si) contents on Cadmium (Cd) uptake, translocation and accumulation in rice plants are not fully understood. SAR405 Herein, we report a pot study to disentangle the interaction mechanisms of Si-rich biochars (Sichar RH300, RH700) and Si-deficient biochars (WB300, WB700) with high-Si soil (HSS) and low-Si soil (LSS) on Cadmium (Cd) and Si accumulation in rice (including grains, straw, and roots). Sichar was found to be better than Si-deficient biochars in reducing Cd uptake and accumulation in rice, and RH300 amendment was better than the RH700 treatment. The surface complexation of Cd with carboxyl groups and Si from biochar led Cd immobilization in soil, as portrayed by Fourier transformed infrared spectroscopy and X-ray photoelectron spectroscopy. The high Si content of biochars indicates a relatively lower bioaccumulation factor and translocation factor of Cd. The Sichar (e.g., RH300) treatment significantly increases the silicon concentration in rice (including grains, straw, and roots), but the Si concentrations of rice grains and roots decrease with WB700-amended LSS. Negative correlations between the concentrations of rice Si and Cd were observed, which could be related to lower expression as observed by Si transport genes (Lsi1 and Lsi3) in rice by Sichar amendment. These findings suggest that the Si released from Sichars can reduce the gene expression of Si transport channel of rice roots and inhibit the transport channel of Si, thus thereby inhibiting the Cd uptake, probably due to the utilization of same channel for Cd and Si. Integrative mechanisms of Sichar (RH300 and RH700) reduced Cd plant accumulation can be proposed by soil immobilization, inhibition of root transport, and prevention of plant translocation.The effective mineral absorption and bioreduction were considered as two preferred processes to alleviate the bioavailability and toxicity of toxic trace metals. In this study, the bioreduction of hexavalent chromium (Cr(VI)) on goethite (FeOOH) in the presence of Pseudomonas aeruginosa (P. aeruginosa) was investigated with different environmental factors, including carbon source concentrations, pH, temperature and initial Cr(VI) concentrations. The characterization of FeOOH-P. aeruginosa indicated that P. aeruginosa was surrounded by FeOOH, which could provide the essential iron for bacterial growth and reduce Cr(VI) to Cr(III). The optimal experimental conditions for Cr(VI) (initial concentration 35 mg L-1) absorption (∼46%) and bioreduction (∼54%) involved a temperature of 45 °C and pH of 5.5. Meanwhile, extracellular polymeric substances (EPS) secreted by P. aeruginosa and its functional groups played important roles in the reduction of Cr(VI). They could reduce Cr(VI) to Cr(III) and transform to Cr(OH)3 or Fex-Cr(1-x)(OH)3 precipitation. These results of this study are of significant importance to better understand the environmental geochemical behavior of Cr(VI) with the interactions between soil minerals and microorganisms.3-Acetyldeoxynivalenol (3-Ac-DON), the acetylated derivative of deoxynivalenol (DON), has been reported to be coexisted with DON in various cereal grains. Ingestion of grain-based food products contaminated by 3-Ac-DON might exert deleterious effects on the health of both humans and animals. However, the biological toxicity of 3-Ac-DON on macrophages and the underlying mechanisms remain largely unknown. In the present study, we showed that RAW 264.7 macrophages treated with 0.75 or 1.50 μg/mL of 3-Ac-DON resulted in DNA damage and the related cell cycle arrest at G1 phase and cell death, activation of the ribotoxic stress and the endoplasmic reticulum (ER) stress responses. The 3-Ac-DON-induced cell death was accompanied by a protective autophagy, because gene silencing of Atg5 using the small interfering RNA enhanced cell death. Results of further experiments revealed a role for lysosomal membrane permeabilization in the 3-Ac-DON triggered inhibition of autophagic flux. Additional work also showed that increased lysosomal biogenesis and leakage of cathepsin B (CTSB) from lysosomes to cytosol was critical for the 3-Ac-DON-induced cell death. Importantly, 3-Ac-DON-induced DNA damage and cell death were rescued by CA-074-me, a CTSB inhibitor. Collectively, these results indicated a critical role of lysosomal membrane permeabilization in the 3-Ac-DON-induced apoptosis of RAW 264.7 macrophages.Background Child abuse and neglect (CAN) cost United States society $136 billion to $428 billion annually. Preventive interventions that reduce CAN may improve people's lives and generate economic benefits to society, but their magnitude is likely to vary greatly with assumptions about victim costs avoided through intervention. Objective We examined the implications of different assumptions about avoided victim costs in a benefit-cost analysis of Promoting First Relationships® (PFR), a 10-session attachment and strengths-based home visiting intervention. Participants and setting Participants were 247 child protection-involved but intact families in Washington State randomized to receive PFR (n = 124) or resource and referral (n = 123). Methods We monetized intervention effects on out-of-home placements and implicit effects on CAN and calculated net present values under three scenarios (1) benefits from avoided system costs, (2) additional benefits from avoided tangible victim costs, and (3) additional benefits from avoided tangible and intangible quality-of-life victim costs. For scenarios 2 and 3, we varied the CAN effect size and estimated the effect size at which PFR was reliably cost beneficial. Results PFR's societal net benefit ranged from $1 (scenario 1) to $5514 - $25,562 (scenario 2) and $7004 - $32,072 (scenario 3) (2014 USD). In scenarios 2 and 3, PFR was reliably cost beneficial at a CAN effect size of approximately -0.25. Conclusions PFR is cost beneficial assuming tangible victim costs are avoided by PFR. Research into the long-term health and economic consequences of reducing CAN in at-risk populations would contribute to comprehensive, accurate benefits models.Atmospheric fine particulate matter exposure (PM2.5) can increase the incidence and mortality of heart disease, and raise the risk of fetal congenital heart defect, which have recently drawn much attention. In this study, C57BL/6 mice were exposed to PM2.5 (approximately equivalent to 174 μg/m3) by intratracheal instillation during the gestation. After birth, 10 weeks old offspring mice were divided into four groups male exposed group (ME), female exposed group (FE), male control group (MC), female control group (FC). The pathological injury, pro-inflammatory cytokines, histone acetylation levels, and expressions of GATA-binding protein 4 (GATA4) and downstream genes were investigated. The results showed that exposure to PM2.5 in utero increased pathological damage and TNF-α and IL-6 levels in hearts of offspring mice, and effects in ME were more serious than FE. Notably, GATA4 protein levels in hearts in ME were significantly lower than that of MC, accompanied by down-regulation of histone acetyltransferase (HAT)-p300 and up-regulation of histone deacetylase-SIRT3. As GATA4 downstream genes, ratios of β-MHC gene expression to α-MHC significantly raised in ME relative to the MC. Results of chromatin immunoprecipitation (ChIP)-qPCR assay found that binding levels of acetylated histone 3 lysine 9 (H3K9ac) in GATA4 promoter region in the hearts of ME or FE were markedly decreased compared with their corresponding control groups. It suggested that maternal exposure to PM2.5 may cause cardiac injury in the offspring, heart damage of male mice was worse than female mice, in which process HAT-p300, H3K9ac, transcription factor GATA4 may play an important regulation role.The present study focuses on the determination of the occurrence and levels of per- and polyfluoroalkyl substances (PFASs) in the drinking and source water from the Philippines and Thailand. A total of 46 samples (18 commercial bottled waters, 5 drinking water from vending machine (re-fill stations) and 23 source water) were analyzed using liquid chromatography with tandem high-resolution mass spectrometry. Using the targeted method, 12 different PFASs were detected in the drinking water samples with total quantifiable PFASs (∑PFASs) levels ranging from 7.16 to 59.49 ng/L; 15 PFASs were detected in source water with ∑PFASs ranging from 15.55 to 65.65 ng/L. A 100% detection frequency was observed for perfluoroheptanoic acid (PFHpA), perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), and perfluorosulfonic acid (PFOS) in all water samples. Six other PFASs, not included in the targeted analysis, were detected using the suspect screening approach. For the first time, the presence of 2-(N-methylperfluorooctanesulfonamido) acetic acid (N-MeFOSAA) in drinking water is reported, and 3 novel PFASs (C5H5OF8, C6H4O2F6, and C9H2O2F16) were detected using suspect screening in source water. Combined results from target and suspect screening analysis showed that PFASs detected were predominantly (52%) short-chain (with fluorinated alkyl chain of ≤6) which could be explained by their high mobility in the environment. The detected PFASs levels in drinking water will not likely pose immediate health risk to consumers according to US EPA health advisory for PFOS and PFOA of 70 ng/L, but inclusion of bottled and drinking water from re-fill stations in monitoring programs is warranted.
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