236 research outputs found

    Evaluating two concepts for the modelling of intermediates accumulation during biological denitrification in wastewater treatment

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    The accumulation of the denitrification intermediates in wastewater treatment systems is highly undesirable, since both nitrite and nitric oxide (NO) are known to be toxic to bacteria, and nitrous oxide (N2O) is a potent greenhouse gas and an ozone depleting substance. To date, two distinct concepts for the modelling of denitrification have been proposed, which are represented by the Activated Sludge Model for Nitrogen (ASMN) and the Activated Sludge Model with Indirect Coupling of Electrons (ASM-ICE), respectively. The two models are fundamentally different in describing the electron allocation among different steps of denitrification. In this study, the two models were examined and compared in their ability to predict the accumulation of denitrification intermediates reported in four different experimental datasets in literature. The N-oxide accumulation predicted by the ASM-ICE model was in good agreement with values measured in all four cases, while the ASMN model was only able to reproduce one of the four cases. The better performance of the ASM-ICE model is due to that it adopts an “indirect coupling” modelling concept through electron carriers to link the carbon oxidation and the nitrogen reduction processes, which describes the electron competition well. The ASMN model, on the other hand, is inherently limited by its structural deficiency in assuming that carbon oxidation is always able to meet the electron demand by all denitrification steps, therefore discounting electron competition among these steps. ASM-ICE therefore offers a better tool for predicting and understanding intermediates accumulation in biological denitrification

    Edge effect removal in Fourier ptychographic microscopy via perfect Fourier transformation (PFT)

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    Edge effect may degrade the imaging precision and is caused by the aperiodic image extension of fast Fourier transform (FFT). In this letter, a perfect Fourier transform algorithm termed PFT was reported to remove the artifacts with comparable efficiency to FFT. Although we demonstrated the performance of PFT in Fourier ptychographic microscopy (FPM) only, it can be expanded in any occasion where the conventional FFT is used.Comment: 4 pages, 6 figure

    Implications of the lens redshift distribution of strong lensing systems: cosmological parameters and the global properties of early-type galaxies

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    In this paper, we assemble a well-defined sample of early-type gravitational lenses extracted from a large collection of 158 systems, and use the redshift distribution of galactic-scale lenses to test the standard cosmological model (Λ\LambdaCDM) and the modified gravity theory (DGP). Two additional sub-samples are also included to account for possible selection effect introduced by the detectability of lens galaxies. Our results show that independent measurement of the matter density parameter (Ωm\Omega_m) could be expected from such strong lensing statistics. Based on future measurements of strong lensing systems from the forthcoming LSST survey, one can expect Ωm\Omega_m to be estimated at the precision of ΔΩm0.006\Delta\Omega_m\sim 0.006, which provides a better constraint on Ωm\Omega_m than \textit{Planck} 2015 results. Moreover, use the lens redshift test is also used to constrain the characteristic velocity dispersion of the lensing galaxies, which is well consistent with that derived from the optical spectroscopic observations. A parameter fEf_E is adopted to quantify the relation between the lensing-based velocity dispersion and the corresponding stellar value. Finally, the accumulation of detectable galactic lenses from future LSST survey would lead to more stringent fits of ΔfE103\Delta f_E\sim10^{-3}, which encourages us to test the global properties of early-type galaxies at much higher accuracy.Comment: 12 pages, accepted for publication in The European Physical Journal

    Identification of subphenotypes in critically ill thrombocytopenic patients with different responses to therapeutic interventions: a retrospective study

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    IntroductionThe causes of thrombocytopenia (TP) in critically ill patients are numerous and heterogeneous. Currently, subphenotype identification is a popular approach to address this problem. Therefore, this study aimed to identify subphenotypes that respond differently to therapeutic interventions in patients with TP using routine clinical data and to improve individualized management of TP.MethodsThis retrospective study included patients with TP admitted to the intensive care unit (ICU) of Dongyang People’s Hospital during 2010–2020. Subphenotypes were identified using latent profile analysis of 15 clinical variables. The Kaplan–Meier method was used to assess the risk of 30-day mortality for different subphenotypes. Multifactorial Cox regression analysis was used to analyze the relationship between therapeutic interventions and in-hospital mortality for different subphenotypes.ResultsThis study included a total of 1,666 participants. Four subphenotypes were identified by latent profile analysis, with subphenotype 1 being the most abundant and having a low mortality rate. Subphenotype 2 was characterized by respiratory dysfunction, subphenotype 3 by renal insufficiency, and subphenotype 4 by shock-like features. Kaplan–Meier analysis revealed that the four subphenotypes had different in-30-day mortality rates. The multivariate Cox regression analysis indicated a significant interaction between platelet transfusion and subphenotype, with more platelet transfusion associated with a decreased risk of in-hospital mortality in subphenotype 3 [hazard ratio (HR): 0.66, 95% confidence interval (CI): 0.46–0.94]. In addition, there was a significant interaction between fluid intake and subphenotype, with a higher fluid intake being associated with a decreased risk of in-hospital mortality for subphenotype 3 (HR: 0.94, 95% CI: 0.89–0.99 per 1 l increase in fluid intake) and an increased risk of in-hospital mortality for high fluid intake in subphenotypes 1 (HR: 1.10, 95% CI: 1.03–1.18 per 1 l increase in fluid intake) and 2 (HR: 1.19, 95% CI: 1.08–1.32 per 1 l increase in fluid intake).ConclusionFour subphenotypes of TP in critically ill patients with different clinical characteristics and outcomes and differential responses to therapeutic interventions were identified using routine clinical data. These findings can help improve the identification of different subphenotypes in patients with TP for better individualized treatment of patients in the ICU

    A data-driven model to quantify the impact of river discharge on tide-river dynamics in the Yangtze River estuary

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    Understanding the role of river discharge on tide-river dynamics is of essential importance for sustainable water management (flood control, salt intrusion, and navigation) in estuarine environments. It is well known that river discharge impacts fundamental tide-river dynamics, especially in terms of subtidal (residual water levels) and tidal properties (amplitudes and phases for different tidal constituents). However, the quantification of the impact of river discharge on tide-river dynamics is challenging due to the complex interactions of barotropic tides with channel geometry, bottom friction, and river discharge. In this study, we propose a data-driven model to quantify the impact of river discharge on tide-river dynamics, using water level time series data collected through long-term observations along an estuary with substantial variations in river discharge. The proposed model has a physically-based structure representing the tide-river interaction, and can be used to predict water level using river discharge as the sole predictor. The satisfactory correspondence of the model outputs with measurements at six gauging stations along the Yangtze River estuary suggest that the proposed model can serve as a powerful instrument to quantify the impacts of river discharge on tide-river dynamics (including time-varying tidal properties and tidal distortion), and separate the contribution made by riverine and tidal forcing on water level. The proposed approach is very efficient and can be applied to other estuaries showing considerable impacts of river discharge on tide-river dynamics.info:eu-repo/semantics/publishedVersio

    Unravelling the spatial variation of nitrous oxide emissions from a step-feed plug-flow full scale wastewater treatment plant

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    This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/Plug-flow activated sludge reactors (ASR) that are step-feed with wastewater are widely adopted in wastewater treatment plants (WWTPs) due to their ability to maximise the use of the organic carbon in wastewater for denitrification. Nitrous oxide (N2O) emissions are expected to vary along these reactors due to pronounced spatial variations in both biomass and substrate concentrations. However, to date, no detailed studies have characterised the impact of the step-feed configuration on emission variability. Here we report on the results from a comprehensive online N2O monitoring campaign, which used multiple gas collection hoods to simultaneously measure emission along the length of a full-scale, stepfed, plug-flow ASR in Australia. The measured N2O fluxes exhibited strong spatial-temporal variation along the reactor path. The step-feed configuration had a substantial influence on the N2O emissions, where the N2O emission factors in sections following the first and second step feed were 0.68% ± 0.09% and 3.5% ± 0.49% of the nitrogen load applied to each section. The relatively high biomass-specific nitrogen loading rate in the second section of the reactor was most likely cause of the high emissions from this section

    The SIK1/CRTC2/CREB1 and TWIST1/PI3K/Akt/GSK3β signaling pathways mediated by microRNA-25-3p are altered in the schizophrenic rat brain

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    Schizophrenia is a group of severe mental disorders. MiR-25-3p was shown to be involved in various neuropsychiatric diseases and can regulate SIK1 and TWIST1. The CRTC2/CREB1 and PI3K/Akt/GSK3β signaling pathways are downstream pathways of SIK1 and TWIST1, respectively. This study investigated whether miR-25-3p-mediated SIK1/CRTC2/CREB1 and TWIST1/PI3K/Akt/GSK3β signaling pathways are present in an animal model relevant to schizophrenia. A schizophrenic rat model was established by using sub-chronic MK-801 administration. An RNA-seq test was performed to examine the differentially expressed genes (DEGs) in the rat prefrontal cortex (PFC). The mRNA levels of miR-25-3p, SIK1, and TWIST in the PFC and caudate putamen (CPu) were assessed by qRT-PCR. Phosphorylation of the SIK1/CRTC2/CREB1 and TWIST1/PI3K/Akt/GSK3β pathways in the two brain regions was examined by Western blots. The RNA-seq data revealed down-regulated miR-25-3p expression and up-regulated SIK1 and TWIST1 mRNA expression induced by MK-801. Additionally, SIK1 and TWIST1 were shown to be possible downstream responders of miR-25-3p in previous studies. qRT-PCR confirmed the changes of miR-25-3p, SIK1, and TWIST1 induced by MK-801 in both brain regions, which, however, was reversed by risperidone. Furthermore, the phosphorylation of the SIK1/CRTC2/CREB1 pathway was repressed by MK-801, whereas the phosphorylation of the TWIST1/PI3K/Akt/GSK3β pathway was increased by MK-801 in either of the two brain regions. Moreover, the altered phosphorylation of these two signaling pathways induced by MK-801 can be restored by risperidone. In conclusion, this study suggests that altered SIK1/CRTC2/CREB1 and TWIST1/PI3K/Akt/GSK3β signaling pathways mediated by miR-25-3p is very likely to be associated with schizophrenia, revealing potential targets for the treatment and clinical diagnosis of schizophrenia
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