339 research outputs found

    Deep Learning-Based Rapid Flood Inundation Modeling for Flat Floodplains With Complex Flow Paths

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    Flood inundation emulation models based on deep neural networks have been developed to overcome the computational burden of two-dimensional (2D) hydrodynamic models. Challenges remain for flat and complex floodplains where many anabranches form during flood events. In this study, we propose a new approach to simulate the temporal and spatial variation of flood inundation for a floodplain with complex flow paths. A U-Net-based spatial reduction and reconstruction method (USRR) is used to find representative locations on the floodplain with complex flow paths. The water depths at these locations are simulated using one-dimensional convolutional neural network (1D-CNN) models, which are well-suited to handling multivariate timeseries inputs. The flood surface is then reconstructed using the USRR method and the simulated flood depths at the representative locations. The combined 1D-CNN and USRR method is compared with a previously developed approach based on the long short-term memory recurrent neural network (LSTM) models and a 2D linear interpolation-based SRR method. Compared to the LSTM model, the 1D-CNN model is not only more accurate, but also takes less time to develop. Although both surface reconstruction methods take <1 s to produce an inundation map for a specific point in time, the USRR method is more accurate than the SRR method, leading to an increase of 5.6% in the proportion of correctly detected inundation area. The combination of 1D-CNN and USRR can detect over 95% of the inundated area simulated using a 2D hydrodynamic model but is 98 times faster.Yuerong Zhou, Wenyan Wu, Rory Nathan, and Q. J. Wan

    Development of a Fast and Accurate Hybrid Model for Floodplain Inundation Simulations

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    High computational cost is often the most limiting factor when running high-resolution hydrodynamic models to simulate spatial-temporal flood inundation behavior. To address this issue, a recent study introduced the hybrid Low-fidelity, Spatial analysis, and Gaussian Process learning (LSG) model. The LSG model simulates the dynamic behavior of flood inundation extent by upskilling simulations from a low-resolution hydrodynamic model through Empirical Orthogonal Function (EOF) analysis and Sparse Gaussian Process learning. However, information on flood extent alone is often not sufficient to provide accurate flood risk assessments. In addition, the LSG model has only been tested on hydrodynamic models with structured grids, while modern hydrodynamic models tend to use unstructured grids. This study therefore further develops the LSG model to simulate water depth as well as flood extent and demonstrates its efficacy as a surrogate for a high-resolution hydrodynamic model with an unstructured grid. The further developed LSG model is evaluated on the flat and complex Chowilla floodplain of the Murray River in Australia and accurately predicts both depth and extent of the flood inundation, while being 12 times more computationally efficient than a high-resolution hydrodynamic model. In addition, it has been found that weighting before the EOF analysis can compensate for the varying grid cell sizes in an unstructured grid and the inundation extent should be predicted from an extent-based LSG model rather than deriving it from water depth predictions.Niels Fraehr, Quan J. Wang, Wenyan Wu, and Rory Natha

    Alternative splicing and genetic diversity of the white collar-1 (wc-1) gene in cereal Phaeosphaeria pathogens

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    The white collar-1 (wc-1) gene encodes an important light-responsive protein (wc-1) that maintains circadian clocks and controls numerous light-dependent reactions including sporulation in ascomycete fungi. The structure and expression of the wc-1 gene in wheat-biotype Phaeosphaeria nodorum (PN-w) was studied. It was shown that the full-size (3,353 bp in length) wc-1 gene in PN-w contained 4 introns in which introns 1 and 2 were flanked by GC-AG splice borders and were spliced constitutively. However, introns 3 and 4 of the wc-1 gene were alternatively spliced. As the result of alternative splicing (AS), six transcript variants were identified, encoding different lengths of deduced polypeptides (from 1,044 to 1,065aa). Ratios of the wc-1 gene transcript variants in the RNA population were the same in the sporulated and non-sporulated PN-w isolate Sn37-1 and the sporulated PN-w isolate S-79-1, grown under light/dark conditions. The AS of the wc-1 gene may control various light-dependent reactions in PN-w, which leads to diverse morphological, physiological and pathological characters for pathogen infection and spread. Based on the nucleotide and deduced amino acid sequences, the wc-1 gene in cereal Phaeosphaeria pathogens was diverse. It appeared that the deduced wc-1 polypeptide sequences of P. avenaria f. sp. avenaria (Paa), P. avenaria f. sp. triticea (Pat1 and Pat3) and barley biotype P. nodorum (PN-b) were more closely related than PN-w and Phaeosphaeeria sp. (P-rye) from Poland. Based on the wc-1 deduced polypeptide sequences, P. avenaria f. sp. triticea (Pat2) from foxtail barley (Hordeum jubatum L.) was evolutionary well separated from the other cereal Phaeosphaeria pathogens

    The σ\sigma pole in J/ψ→ωπ+π−J/\psi \to \omega \pi^+ \pi^-

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    Using a sample of 58 million J/ψJ/\psi events recorded in the BESII detector, the decay J/ψ→ωπ+π−J/\psi \to \omega \pi^+ \pi^- is studied. There are conspicuous ωf2(1270)\omega f_2(1270) and b1(1235)πb_1(1235)\pi signals. At low ππ\pi \pi mass, a large broad peak due to the σ\sigma is observed, and its pole position is determined to be (541±39)(541 \pm 39) - ii (252±42)(252 \pm 42) MeV from the mean of six analyses. The errors are dominated by the systematic errors.Comment: 15 pages, 6 figures, submitted to PL

    Spin-dependent cross sections from the three-body photodisintegration of He 3 at incident energies of 12.8 and 14.7 MeV

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    The first measurement of the three-body photodisintegration of polarized 3He using a circularly polarized photon beam has been performed at incident energies of 12.8 and 14.7 MeV. This measurement was carried out at the high-intensity γ-ray source located at Triangle Universities Nuclear Laboratory. A high-pressure 3He target, polarized via spin exchange optical pumping with alkali metals, was used in the experiment. The spin-dependent double- and single-differential cross sections from 3He(γ,n)pp for laboratory angles varying from 30° to 165° are presented and compared with state-of-the-art three-body calculations. The data reveal the importance of including the Coulomb interaction between protons in the three-body calculations

    Direct Measurements of the Branching Fractions for D0→K−e+ÎœeD^0 \to K^-e^+\nu_e and D0→π−e+ÎœeD^0 \to \pi^-e^+\nu_e and Determinations of the Form Factors f+K(0)f_{+}^{K}(0) and f+π(0)f^{\pi}_{+}(0)

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    The absolute branching fractions for the decays D0→K−e+ÎœeD^0 \to K^-e ^+\nu_e and D0→π−e+ÎœeD^0 \to \pi^-e^+\nu_e are determined using 7584±198±3417584\pm 198 \pm 341 singly tagged Dˉ0\bar D^0 sample from the data collected around 3.773 GeV with the BES-II detector at the BEPC. In the system recoiling against the singly tagged Dˉ0\bar D^0 meson, 104.0±10.9104.0\pm 10.9 events for D0→K−e+ÎœeD^0 \to K^-e ^+\nu_e and 9.0±3.69.0 \pm 3.6 events for D0→π−e+ÎœeD^0 \to \pi^-e^+\nu_e decays are observed. Those yield the absolute branching fractions to be BF(D0→K−e+Îœe)=(3.82±0.40±0.27)BF(D^0 \to K^-e^+\nu_e)=(3.82 \pm 0.40\pm 0.27)% and BF(D0→π−e+Îœe)=(0.33±0.13±0.03)BF(D^0 \to \pi^-e^+\nu_e)=(0.33 \pm 0.13\pm 0.03)%. The vector form factors are determined to be ∣f+K(0)∣=0.78±0.04±0.03|f^K_+(0)| = 0.78 \pm 0.04 \pm 0.03 and ∣f+π(0)∣=0.73±0.14±0.06|f^{\pi}_+(0)| = 0.73 \pm 0.14 \pm 0.06. The ratio of the two form factors is measured to be ∣f+π(0)/f+K(0)∣=0.93±0.19±0.07|f^{\pi}_+(0)/f^K_+(0)|= 0.93 \pm 0.19 \pm 0.07.Comment: 6 pages, 5 figure

    Measurements of J/psi Decays into 2(pi+pi-)eta and 3(pi+pi-)eta

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    Based on a sample of 5.8X 10^7 J/psi events taken with the BESII detector, the branching fractions of J/psi--> 2(pi+pi-)eta and J/psi-->3(pi+pi-)eta are measured for the first time to be (2.26+-0.08+-0.27)X10^{-3} and (7.24+-0.96+-1.11)X10^{-4}, respectively.Comment: 11 pages, 6 figure

    Study of J/ψ→ωK+K−J/\psi \to \omega K^+K^-

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    New data are presented on J/ψ→ωK+K−J/\psi \to \omega K^+K^- from a sample of 58M J/ψJ/\psi events in the upgraded BES II detector at the BEPC. There is a conspicuous signal for f0(1710)→K+K−f_0(1710) \to K^+K^- and a peak at higher mass which may be fitted with f2(2150)→KKˉf_2(2150) \to K\bar K. From a combined analysis with ωπ+π−\omega \pi ^+ \pi ^- data, the branching ratio BR(f0(1710)→ππ)/BR(f0(1710)→KKˉ)BR(f_0(1710)\to\pi\pi)/BR(f_0(1710) \to K\bar K) is <0.11< 0.11 at the 95% confidence level.Comment: 11 pages, 5 figures. Submitted to Phys. Lett.

    Search for the Lepton Flavor Violation Processes J/ψ→J/\psi \to Ότ\mu\tau and eτe\tau

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    The lepton flavor violation processes J/ψ→ΌτJ/\psi \to \mu\tau and eτe\tau are searched for using a sample of 5.8×107\times 10^7 J/ψJ/\psi events collected with the BESII detector. Zero and one candidate events, consistent with the estimated background, are observed in J/ψ→Ότ,τ→eΜˉeΜτJ/\psi \to \mu\tau, \tau\to e\bar\nu_e\nu_{\tau} and J/ψ→eτ,τ→ΌΜˉΌΜτJ/\psi\to e\tau, \tau\to\mu\bar\nu_{\mu}\nu_{\tau} decays, respectively. Upper limits on the branching ratios are determined to be Br(J/ψ→Ότ)<2.0×10−6Br(J/\psi\to\mu\tau)<2.0 \times 10^{-6} and Br(J/ψ→eτ)<8.3×10−6Br(J/\psi \to e\tau) < 8.3 \times10^{-6} at the 90% confidence level (C.L.).Comment: 9 pages, 2 figure

    BESII Detector Simulation

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    A Monte Carlo program based on Geant3 has been developed for BESII detector simulation. The organization of the program is outlined, and the digitization procedure for simulating the response of various sub-detectors is described. Comparisons with data show that the performance of the program is generally satisfactory.Comment: 17 pages, 14 figures, uses elsart.cls, to be submitted to NIM
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