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Free, publicly-accessible full text available March 18, 2023
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Free, publicly-accessible full text available March 18, 2023
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Free, publicly-accessible full text available October 25, 2022
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Context. The PSR J2222−0137 binary system has a set of features that make it a unique laboratory for tests of gravity theories. Aims. To fully exploit the system’s potential for these tests, we aim to improve the measurements of its physical parameters, spin and orbital orientation, and post-Keplerian parameters, which quantify the observed relativistic effects. Methods. We describe an improved analysis of archival very long baseline interferometry (VLBI) data, which uses a coordinate convention in full agreement with that used in timing. We have also obtained much improved polarimetry of the pulsar with the Five hundred meter Aperture Spherical Telescopemore »Free, publicly-accessible full text available October 1, 2022
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Mobile edge computing (MEC) is an emerging paradigm that integrates computing resources in wireless access networks to process computational tasks in close proximity to mobile users with low latency. In this paper, we propose an online double deep Q networks (DDQN) based learning scheme for task assignment in dynamic MEC networks, which enables multiple distributed edge nodes and a cloud data center to jointly process user tasks to achieve optimal long-term quality of service (QoS). The proposed scheme captures a wide range of dynamic network parameters including non-stationary node computing capabilities, network delay statistics, and task arrivals. It learns themore »
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Booker, S (Ed.)Applying enzymatic reactions to produce useful molecules is a central focus of chemical biology. Iron and 2-oxoglutarate (Fe/2OG) enzymes are found in all kingdoms of life and catalyze a broad array of oxidative transformations. Herein, we demonstrate that the activity of an Fe/2OG enzyme can be redirected when changing the targeted carbon hybridization from sp3 to sp2. During leucine 5-hydroxylase catalysis, installation of an olefin group onto the substrate redirects the Fe(IV)−oxo species reactivity from hydroxylation to asymmetric epoxidation. The resulting epoxide subsequently undergoes intramolecular cyclization to form the substituted piperidine, 2S,5S-hydroxypipecolic acid.