1,851 research outputs found

    Land use interacts with changes in catchment hydrology to generate chronic nitrate pollution in karst waters and strong seasonality in excess nitrate export

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    Agricultural land in karst systems can pollute water courses, with polluted waters travelling quickly to and through the sub-surface. Understanding how rapidly nitrate moves within the highly-transmissive karst critical zone (from soils to aquifers) is limited by low resolution data. To understand nitrate behavior and its controls, we deployed sensor technology at five sites to generate autonomously high-resolution time series of discharge and NO3−–N, which is the major nitrogenous component, in a farmed karst catchment in Southwestern China. The [NO3−–N] time series exhibited rapid response to rainfall-induced increases in discharge and a large magnitude in [NO3−–N], from 0.72 to 16.3 mg/L across five sites. However, the magnitude of NO3−–N response at each site was varied during rainfall events (wet season) and dry season. The highest mean [NO3−–N] and normalized annual fluvial export occurred in a headwater catchment with a developed karst aquifer system. Seasonal variation in NO3−–N export occurred in response to source availability, most notable in catchments with valley agriculture: in the wet season up to 97% of nitrate was exported from the headwater catchments in two months, but at the larger catchment scale, over the 6 month wet season, only 61% of total export occurred. At the larger catchment scale, [NO3−–N] were lower due to buffering by the karstic aquifer network. From the time series we observe little decrease in [NO3−–N] as discharge decreases in the dry season, indicating the karst aquifers are chronically-polluted with nitrate through slow flow pathways

    Global Transcriptome Profiling of Multiple Porcine Organs Reveals Toxoplasma gondii-Induced Transcriptional Landscapes

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    © 2019 He, Ma, Wang, Zhang, Li, Zhai, Wang, Elsheikha and Zhu. We characterized the porcine tissue transcriptional landscapes that follow Toxoplasma gondii infection. RNAs were isolated from liver, spleen, cerebral cortex, lung, and mesenteric lymph nodes (MLNs) of T. gondii-infected and uninfected (control) pigs at days 6 and 18 postinfection, and were analyzed using next-generation sequencing (RNA-seq). T. gondii altered the expression of 178, 476, 199, 201, and 362 transcripts at 6 dpi and 217, 223, 347, 119, and 161 at 18 dpi in the infected brain, liver, lung, MLNs and spleen, respectively. The differentially expressed transcripts (DETs) were grouped into five expression patterns and 10 sub-clusters. Gene Ontology enrichment and pathway analysis revealed that immune-related genes dominated the overall transcriptomic signature and that metabolic processes, such as steroid biosynthesis, and metabolism of lipid and carboxylic acid, were downregulated in infected tissues. Co-expression network analysis identified transcriptional modules associated with host immune response to infection. These findings not only show how T. gondii infection alters porcine transcriptome in a tissue-specific manner, but also offer a gateway for testing new hypotheses regarding human response to T. gondii infection

    iTRAQ-based quantitative proteomics analysis identifies host pathways modulated during toxoplasma gondii infection in swine

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    Toxoplasma gondii is a leading cause of foodborne illness and consumption of undercooked pig meat is a major risk factor for acquiring toxoplasmosis, which causes a substantial burden on society. Here, we used isobaric tags for relative and absolute quantification (iTRAQ) labelling coupled with liquid chromatography-tandem mass spectrometry (LC-MS/MS) to identify cellular proteins and pathways altered during T. gondii infection in pigs. We also used parallel reaction monitoring-based LC-MS/MS to verify the levels of protein expression of infected spleens and mesenteric lymph nodes (MLNs). At 6 days post-infection (dpi), 156, 391, 170, 292, and 200 differentially expressed proteins (DEPs) were detected in the brain, liver, lung, MLNs and spleen, respectively. At 18 dpi, 339, 351, 483, 388, and 303 DEPs were detected in the brain, liver, lung, MLNs and spleen, respectively. Although proteins involved in immune responses were upregulated in all infected tissues, protein expression signature in infected livers was dominated by downregulation of the metabolic processes. By weighted gene co-expression network analysis, we could further show that all proteins were clustered into 25 co-expression modules and that the pink module significantly correlated with the infection status. We also identified 163 potential anti-T. gondii proteins (PATPs) and provided evidence that two PATPs (HSP70.2 and PDIA3) can reduce T. gondii burden in porcine macrophages in vitro. This comprehensive proteomics analysis reveals new facets in the pathogenesis of T. gondii infection and identifies key proteins that may contribute to the pig’s defense against this infection

    The Adsorption Potential of Cr from Water by ZnO Nanoparticles Synthesized by Azolla pinnata

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    Aqueous solutions containing toxic elements (TEs) (such as hexavalent chromium (Cr (VI)) can be toxic to humans even at trace levels. Thus, removing TEs from the aqueous environment is essential for the protection of biodiversity, hydrosphere ecosystems, and humans. For plant fabrication of zinc oxide nanoparticles (PF-ZnONPs), Azolla pinnata plants were used, and X-ray diffraction (XRD), energy dispersive spectroscopy (EDS), SEM, and FTIR techniques were used for the identification of PF-ZnONPs and ZnONPs, which were used to remove Cr (VI) from aqueous solution. A number of adsorption parameters were studied, including pH, dose, concentration of metal ions, and contact time. The removal efficiency of PF-ZnONPs for Cr (VI) has been found to be 96% at a time (60 min), 69.02% at pH 4, and 70.43% at a dose (10 mg·L-1). It was found that the pseudo-second-order model best described the adsorption of Cr (VI) onto PF-ZnONPs, indicating a fast initial adsorption via diffusion. The experimental data were also highly consistent with the Langmuir isotherm model calculations

    Laser-assisted collision effect on nonsequential double ionization of helium in a few-cycle laser pulse

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    Nonsequential double ionization (NSDI) of helium in an intense few-cycle laser pulse is investigated by applying the three-dimensional semi-classical re-scattering method. It is found that the momentum distribution of He2+^{2+} shows a single-double-single peak structure as the pulse intensity increases. According to the different mechanisms dominating the NSDI process, the laser intensity can be classified into three regimes where the momentum distribution of He2+^{2+} exhibits different characteristics. In the relatively high intensity regime, an NSDI mechanism named the "laser-assisted collision ionization" is found to be dominating the NSDI process and causing the single peak structure. This result can shed light on the study of non-sequential ionization of a highly charged ion in a relatively intense laser pulse

    Observation of a near-threshold enhancement in th p pbar mass spectrum from radiative J/psi-->gamma p pbar decays

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    We observe a narrow enhancement near 2mp in the invariant mass spectrum of ppbar pairs from radiative J/psi-->gamma ppbar decays. The enhancement can be fit with either an S- or P-wave Breit Wigner fuction. In the case of the S-wave fit, the peak mass is below the 2mp threshold and the full width is less than 30 MeV. These mass and width values are not consistent with the properties of any known meson resonance.Comment: 5 pages, 4 figures, submitted to Phys. Rev. Let

    Measurements of the Mass and Full-Width of the ηc\eta_c Meson

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    In a sample of 58 million J/ψJ/\psi events collected with the BES II detector, the process J/ψ→γηc\psi\to\gamma\eta_c is observed in five different decay channels: γK+K−π+π−\gamma K^+K^-\pi^+\pi^-, γπ+π−π+π−\gamma\pi^+\pi^-\pi^+\pi^-, γK±KS0π∓\gamma K^\pm K^0_S \pi^\mp (with KS0→π+π−K^0_S\to\pi^+\pi^-), γϕϕ\gamma \phi\phi (with ϕ→K+K−\phi\to K^+K^-) and γppˉ\gamma p\bar{p}. From a combined fit of all five channels, we determine the mass and full-width of ηc\eta_c to be mηc=2977.5±1.0(stat.)±1.2(syst.)m_{\eta_c}=2977.5\pm1.0 ({stat.})\pm1.2 ({syst.}) MeV/c2c^2 and Γηc=17.0±3.7(stat.)±7.4(syst.)\Gamma_{\eta_c} = 17.0\pm3.7 ({stat.})\pm7.4 ({syst.}) MeV/c2c^2.Comment: 9 pages, 2 figures and 4 table. Submitted to Phys. Lett.
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