9 research outputs found

    Forecasting the Arrival Time of Coronal Mass Ejections: Analysis of the CCMC CME Scoreboard

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    Accurate forecasting of the properties of coronal mass ejections (CMEs) as they approach Earth is now recognized as an important strategic objective for both NOAA and NASA. The time of arrival of such events is a key parameter, one that had been anticipated to be relatively straightforward to constrain. In this study, we analyze forecasts submitted to the Community Coordinated Modeling Center at NASA's Goddard Space Flight Center over the last 6 years to answer the following questions: (1) How well do these models forecast the arrival time of CME-driven shocks? (2) What are the uncertainties associated with these forecasts? (3) Which model(s) perform best? (4) Have the models become more accurate during the past 6 years? We analyze all forecasts made by 32 models from 2013 through mid-2018, and additionally focus on 28 events, all of which were forecasted by six models. We find that the models are generally able to predict CME-shock arrival times, in an average sense, to within 10 hr, but with standard deviations often exceeding 20 hr. The best performers, on the other hand, maintained a mean error (bias) of 1 hr, a mean absolute error of 13 hr, and a precision (standard deviation) of 15 hr. Finally, there is no evidence that the forecasts have become more accurate during this interval. We discuss the intrinsic simplifications of thevarious models analyzed, the limitations of this investigation, and suggest possible paths to improve these forecasts in the future

    Neuron-Targeted Caveolin-1 Improves Molecular Signaling, Plasticity, and Behavior Dependent on the Hippocampus in Adult and Aged Mice

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    BACKGROUND: Studies in vitro demonstrate that neuronal membrane/lipid rafts (MLRs) establish cell polarity by clustering pro-growth receptors and tethering cytoskeletal machinery necessary for neuronal sprouting. However, the effect of MLR and MLR-associated proteins on neuronal aging is unknown. METHODS: Here we assessed the impact of neuron-targeted overexpression of a MLR scaffold protein, caveolin-1 (via a synapsin promoter; SynCav1), in the hippocampus in vivo in adult (6-months-old) and aged (20-month-old) mice on biochemical, morphologic and behavioral changes. RESULTS: SynCav1 resulted in increased expression of Cav-1, MLRs, and MLR-localization of Cav-1 and tropomyosin-related kinase B (TrkB) receptor independent of age and time post gene transfer. Cav-1 overexpression in adult mice enhanced dendritic arborization within the apical dendrites of hippocampal CA1 and granule cell neurons, effects that were also observed in aged mice, albeit to a lesser extent, indicating preserved impact of Cav-1 on structural plasticity of hippocampal neurons with age. Cav-1 overexpression enhanced contextual fear memory in adult and aged mice demonstrating improved hippocampal function. CONCLUSIONS: Neuron-targeted overexpression of Cav-1 in the adult and aged hippocampus enhances functional MLRs with corresponding roles in cell signaling and protein trafficking. The resultant structural alterations in hippocampal neurons in vivo are associated with improvements in hippocampal dependent learning and memory. Our findings suggest Cav-1 as a novel therapeutic strategy in disorders involving impaired hippocampal function

    Price-Fixing Overcharges: Legal and Economic Evidence

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