Abstract Wire-Cell is a 3D event reconstruction package for liquid argon time projection chambers. Through geometry, time, and drifted charge from multiple readout wire planes, 3D space points with associated charge are reconstructed prior to the pattern recognition stage. Pattern recognition techniques, including track trajectory and d Q /d x (ionization charge per unit length) fitting, 3D neutrino vertex fitting, track and shower separation, particle-level clustering, and particle identification are then applied on these 3D space points as well as the original 2D projection measurements. A deep neural network is developed to enhance the reconstruction of the neutrino interaction vertex. Compared to traditional algorithms, the deep neural network boosts the vertex efficiency by a relative 30% for charged-current ν e interactions. This pattern recognition achieves 80–90% reconstruction efficiencies for primary leptons, after a 65.8% (72.9%) vertex efficiency for charged-current ν e (ν μ ) interactions. Based on the resulting reconstructed particles and their kinematics, we also achieve 15-20% energy reconstruction resolutions for charged-current neutrino interactions.
more »
« less
Unsupervised vessel trajectory reconstruction
A trajectory is a sequence of observations in time and space, for examples, the path formed by maritime vessels, orbital debris, or aircraft. It is important to track and reconstruct vessel trajectories using the Automated Identification System (AIS) data in real-world applications for maritime navigation safety. In this project, we use the National Science Foundation (NSF)'s Algorithms for Threat Detection program (ATD) 2019 Challenge AIS data to develop novel trajectory reconstruction method. Given a sequence ofNunlabeled timestamped observations, the goal is to track trajectories by clustering the AIS points with predicted positions using the information from the true trajectoriesΧ. It is a natural way to connect the observed pointxîwith the closest point that is estimated by using the location, time, speed, and angle information from a set of the points under considerationxi∀i∈ {1, 2, …,N}. The introduced method is an unsupervised clustering-based method that does not train a supervised model which may incur a significant computational cost, so it leads to a real-time, reliable, and accurate trajectory reconstruction method. Our experimental results show that the proposed method successfully clusters vessel trajectories.
more »
« less
- Award ID(s):
- 1924792
- PAR ID:
- 10479167
- Publisher / Repository:
- Frontiers
- Date Published:
- Journal Name:
- Frontiers in Applied Mathematics and Statistics
- Volume:
- 9
- ISSN:
- 2297-4687
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Abstract The overarching goal of this study is to effect the elimination of platinum from adducts withcis–C≡C−Pt−C≡C‐ linkages, thereby generating novel conjugated polyynes. Thus, the bis(hexatriynyl) complextrans‐(p‐tol3P)2Pt((C≡C)3H)2is treated with 1,3‐diphosphines R2C(CH2PPh2)2to generate (R2C(CH2PPh2)2)2Pt((C≡C)3H)2(14; R=c,n‐Bu;e,p‐tolCH2). These condense with the diiodide complexes R2C(CH2PPh2)2PtI2(9 a,c) in the presence of CuI (cat.) and excess HNEt2to give the title macrocycles [(R2C(CH2PPh2)2)Pt(C≡C)3]4(16 c,e) as adducts of the byproduct [H2NEt2]+I−(30–66 %). DOSY NMR experiments establish that this association is maintained in solution, but NaOAc removes the ammonium salt. The bis(triethylsilylpolyynyl) complexes (n‐Bu2C(CH2PPh2)2)Pt((C≡C)nSiEt3)2(n=2, 3) are synthesized analogously to14 c. They react with I2at rt to give mainly the diiodide complex9 cand the coupling product Et3Si(C≡CC≡C)nSiEt3. The possibility of competing reactions giving IC≡C species is investigated. Analogous reactions of the Pt4C24macrocycle16 calso give9 c, but no sp13C NMR signals or mass spectrometric Cxz+ions (x=24–100) could be detected. It is proposed that some cyclo[24]carbon is generated, but then rapidly converts to other forms of elemental carbon. No cyclotetracosane (C24H48) is detected when this sequence is carried out in the presence of PtO2and H2.more » « less
-
Abstract The objective of the cyclotron radiation emission spectroscopy (CRES) technology is to build precise particle energy spectra. This is achieved by identifying the start frequencies of charged particle trajectories which, when exposed to an external magnetic field, leave semi-linear profiles (called tracks) in the time–frequency plane. Due to the need for excellent instrumental energy resolution in application, highly efficient and accurate track reconstruction methods are desired. Deep learning convolutional neural networks (CNNs) - particularly suited to deal with information-sparse data and which offer precise foreground localization—may be utilized to extract track properties from measured CRES signals (called events) with relative computational ease. In this work, we develop a novel machine learning based model which operates a CNN and a support vector machine in tandem to perform this reconstruction. A primary application of our method is shown on simulated CRES signals which mimic those of the Project 8 experiment—a novel effort to extract the unknown absolute neutrino mass value from a precise measurement of tritiumβ−-decay energy spectrum. When compared to a point-clustering based technique used as a baseline, we show a relative gain of 24.1% in event reconstruction efficiency and comparable performance in accuracy of track parameter reconstruction.more » « less
-
A long-standing issue about the correct identification of an important starting reagent, iron(III) hexafluoroacetylacetonate, Fe(hfac)3(1), has been resolved. Thetris-chelated mononuclear complex was found to crystallize in two polymorph modifications which can be assigned as the low-temperature (1-L) monoclinicP21/nand the high-temperature (1-H) trigonalP\overline{3}. Low-temperature polymorph1-Lwas found to transform to1-Hupon sublimation at 44 °C. Two modifications are clearly distinguished by powder X-ray diffraction (PXRD), single-crystal X-ray diffraction, differential scanning calorimetry (DSC), and melting-point measurements. On the other hand, the two forms share similar characteristics in direct analysis in real-time mass spectrometry (DART-MS), attenuated total reflection (ATR) spectroscopy, and some physical properties, such as color, volatility, sensitivity, and solubility. Analysis of the literature and some of our preliminary data strongly suggest that the appearance of two polymorph modifications for trivalent metal (both transition and main group) hexafluoroacetylacetonates is a common case for several largely used complexes not yet accounted for in the crystallographic databases.more » « less
-
The crystal structures of two intermediates, 4-amino-3,5-difluorobenzonitrile, C7H4F2N2(I), and ethyl 4-amino-3,5-difluorobenzoate, C9H9F2NO2(II), along with a visible-light-responsive azobenzene derivative, diethyl 4,4′-(diazene-1,2-diyl)bis(3,5-difluorobenzoate), C18H14F4N2O4(III), obtained by four-step synthetic procedure, were studied using single-crystal X-ray diffraction. The molecules ofIandIIdemonstrate the quinoid character of phenyl rings accompanied by the distortion of bond angles related to the presence of fluorine substituents in the 3 and 5 (ortho) positions. In the crystals ofIandII, the molecules are connected by N—H...N, N—H...F and N—H...O hydrogen bonds, C—H...F short contacts, and π-stacking interactions. In crystal ofIII, only stacking interactions between the molecules are found.more » « less
An official website of the United States government

