We present the results of the re-discovery of the decay $B^0 \to \pi^- \ell^+ \nu_\ell$ in 34.6 fb$^{-1}$ of Belle II data using hadronic $B$-tagging via the Full Event Interpretation algorithm. We observe 21 signal events on a background of 155 in a fit to the distribution of the square of the missing mass, $M_{\mathrm{miss}}^2$, with a significance of 5.69$\sigma$, and determine a total branching fraction of (1.58 $\pm$ 0.43$_{\mathrm{stat}}$ $\pm$ 0.07$_{\mathrm{sys}}$) $\times 10^{-4}$.
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Speech perception is known to rely on both auditory and visual information. However, sound specific somatosensory input has been shown also to influence speech perceptual processing (Ito et al., 2009). In the present study we addressed further the relationship between somatosensory information and speech perceptual processing by addressing the hypothesis that the temporal relationship between orofacial movement and sound processing contributes to somatosensory-auditory interaction in speech perception. We examined the changes in event-related potentials in response to multisensory synchronous (simultaneous) and asynchronous (90 ms lag and lead) somatosensory and auditory stimulation compared to individual unisensory auditory and somatosensory stimulation alone. We used a robotic device to apply facial skin somatosensory deformations that were similar in timing and duration to those experienced in speech production. Following synchronous multisensory stimulation the amplitude of the event-related potential was reliably different from the two unisensory potentials. More importantly, the magnitude of the event-related potential difference varied as a function of the relative timing of the somatosensory-auditory stimulation. Event-related activity change due to stimulus timing was seen between 160-220 ms following somatosensory onset, mostly around the parietal area. The results demonstrate a dynamic modulation of somatosensory-auditory convergence and suggest the contribution of somatosensory information for speech processing process is dependent on the specific temporal order of sensory inputs in speech production. International audience
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doi: 10.11575/prism/30622
handle: 1880/47438
In this paper, we explore physical layer cooperative communication in order to design network layer routing algorithms that are energy efficient. We assume each node in the network is equipped with a single omnidirectional antenna and that multiple nodes are able to coordinate their transmissions in order to take advantage of spatial diversity to save energy. Specifically, we consider cooperative diversity at physical layer and multi-hop routing at network layer, and formulate minimum energy routing as a joint optimization of the transmission power at the physical layer and the link selection at the network layer. We then show that as the network becomes larger, finding optimal cooperative routes becomes computationally intractable. As such, we develop a number of heuristic routing algorithms that have polynomial computational complexity, and yet achieve significant energy savings. Simulation results are also presented, which indicate that the proposed algorithms based on optimal power allocation significantly outperform existing algorithms based on equal power allocation, by more than 60% in some simulated scenarios. International audience Routing
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We report measurements of the $\bar{B}^0 \to D^{*+} \ell^{-} \bar��_l$ and $B^- \to D^{0} \ell^{-} \bar��_l$ processes using 34.6 fb$^{-1}$ of collision events recorded by the Belle II experiment at the SuperKEKB asymmetric-energy $e^+ e^-$ collider. For the $B^-\to D^{0}\ell^-\bar��_\ell$ channel, we present first studies that isolate this decay from other semileptonic processes and backgrounds. We report a measurement of the $\bar{B}^0 \to D^{*+} \ell^{-} \bar��_l$ branching fraction and obtain ${\cal B}(\bar{B}^0 \to D^{*+} \ell^{-} \bar��_l) = \left(4.60 \pm 0.05_{\mathrm{stat}}\pm0.17_{\mathrm{syst}} \pm 0.45_{��_s}\right) \%$, in agreement with the world average. Here, the uncertainties are statistical, systematic, and related to slow pion reconstruction, respectively. The systematic uncertainties are limited by the statistics of auxiliary measurements and will improve in the future. We also report differential branching fractions in five bins of the hadronic recoil parameter $w$ for $\bar{B}^0 \to D^{*+} \ell^{-} \bar��_l$, unfolded to account for resolution and efficiency effects. 19 pages, 6 figures
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We introduce Sleep, a new Python open-source graphical user interface (GUI) dedicated to visualization, scoring and analyses of sleep data. Among its most prominent features are: (1) Dynamic display of polysomnographic data, spectrogram, hypnogram and topographic maps with several customizable parameters, (2) Implementation of several automatic detection of sleep features such as spindles, K-complexes, slow waves, and rapid eye movements (REM), (3) Implementation of practical signal processing tools such as re-referencing or filtering, and (4) Display of main descriptive statistics including publication-ready tables and figures. The software package supports loading and reading raw EEG data from standard file formats such as European Data Format, in addition to a range of commercial data formats. Most importantly, Sleep is built on top of the VisPy library, which provides GPU-based fast and high-level visualization. As a result, it is capable of efficiently handling and displaying large sleep datasets. Sleep is freely available (http://visbrain.org/sleep) and comes with sample datasets and an extensive documentation. Novel functionalities will continue to be added and open-science community efforts are expected to enhance the capacities of this module.
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Tag-side reconstruction is an important method for reconstructing $B$ meson decays with missing energy. The Belle II tag-side reconstruction algorithm, Full Event Interpretation, relies on a hierarchical reconstruction of $B$ meson decays with multivariate classification employed at each stage of reconstruction. Given the large numbers of classifiers employed and decay chains reconstructed, the performance of the algorithm on data and simulation differs significantly. Here, calibration factors are derived for hadronic tag-side $B$ decays by measuring a signal side decay, $B \rightarrow X\ell \nu$, in $34.6$ fb$^{-1}$ of Belle II data. For a very loose selection on the tag-side $B$ multivariate classifier, the calibration factors are $0.65 \pm 0.02$ and $0.83 \pm 0.03$ for tag-side $B^{+}$ and $B^{0}$ mesons, respectively.
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Solar photovoltaic (PV) technology is a means of increasing energy security whilst reducing the negative externalities of fossil fuel dependence. Programs, such as feed-in-tariffs (FITs) implemented in many countries for on-grid PV, provide economic incentives for investment. On the other hand, off-grid PV systems reduce energy poverty and increase both entrepreneurial productivity and return in rural isolated areas. Despite these social and economic justifications, there is still limited access to capital and appropriate financing mechanisms for the upfront cost, resulting in the slow uptake of solar PV under government programs, especially for poorer individuals. Peer-to-peer (P2P) lending networks represent an abundant untapped financial resource for accelerating the deployment of PV technology. This paper considers an innovative P2P lending framework for A) financing solar PV on-grid under a FIT program and B) off-grid for a small business, whilst distributing both the environmental and economic advantages throughout the entire population. The requirements and limitations of the proposed funding mechanisms are analyzed and conclusions are drawn. International audience
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pmid: 28972185
pmc: PMC5723990
Calcium (Ca
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pmid: 29845007
pmc: PMC5964622
Frontotemporal dementia (FTD) is a neurodegenerative disease with a strong genetic basis. Understanding the structural brain changes during pre-symptomatic stages may allow for earlier diagnosis of patients suffering from FTD; therefore, we investigated asymptomatic members of FTD families with mutations in C9orf72 and granulin (GRN) genes. Clinically asymptomatic subjects from families with C9orf72 mutation (15 mutation carriers, C9orf72+; and 23 non-carriers, C9orf72−) and GRN mutations (9 mutation carriers, GRN+; and 15 non-carriers, GRN−) underwent structural neuroimaging (MRI). Cortical thickness and subcortical gray matter volumes were calculated using FreeSurfer. Group differences were evaluated, correcting for age, sex and years to mean age of disease onset within the subject's family. Mean age of C9orf72+ and C9orf72− were 42.6 ± 11.3 and 49.7 ± 15.5 years, respectively; while GRN+ and GRN− groups were 50.1 ± 8.7 and 53.2 ± 11.2 years respectively. The C9orf72+ group exhibited cortical thinning in the temporal, parietal and frontal regions, as well as reduced volumes of bilateral thalamus and left caudate compared to the entire group of mutation non-carriers (NC: C9orf72− and GRN− combined). In contrast, the GRN+ group did not show any significant differences compared to NC. C9orf72 mutation carriers demonstrate a pattern of reduced gray matter on MRI prior to symptom onset compared to GRN mutation carriers. These findings suggest that the preclinical course of FTD differs depending on the genetic basis and that the choice of neuroimaging biomarkers for FTD may need to take into account the specific genes involved in causing the disease. Highlights • Patterns of brain atrophy differ in GRN & C9orf72 presymptomatic carriers. • Asymptomatic C9orf72+ carriers exhibit gray matter atrophy at a relatively early age. • GRN+ carrier did not demonstrate any significant gray matter changes despite being relatively older. • Preclinical course of FTD & the choice of imaging biomarker differ based on genetic mutations.
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We present the results of the re-discovery of the decay $B^0 \to \pi^- \ell^+ \nu_\ell$ in 34.6 fb$^{-1}$ of Belle II data using hadronic $B$-tagging via the Full Event Interpretation algorithm. We observe 21 signal events on a background of 155 in a fit to the distribution of the square of the missing mass, $M_{\mathrm{miss}}^2$, with a significance of 5.69$\sigma$, and determine a total branching fraction of (1.58 $\pm$ 0.43$_{\mathrm{stat}}$ $\pm$ 0.07$_{\mathrm{sys}}$) $\times 10^{-4}$.
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Speech perception is known to rely on both auditory and visual information. However, sound specific somatosensory input has been shown also to influence speech perceptual processing (Ito et al., 2009). In the present study we addressed further the relationship between somatosensory information and speech perceptual processing by addressing the hypothesis that the temporal relationship between orofacial movement and sound processing contributes to somatosensory-auditory interaction in speech perception. We examined the changes in event-related potentials in response to multisensory synchronous (simultaneous) and asynchronous (90 ms lag and lead) somatosensory and auditory stimulation compared to individual unisensory auditory and somatosensory stimulation alone. We used a robotic device to apply facial skin somatosensory deformations that were similar in timing and duration to those experienced in speech production. Following synchronous multisensory stimulation the amplitude of the event-related potential was reliably different from the two unisensory potentials. More importantly, the magnitude of the event-related potential difference varied as a function of the relative timing of the somatosensory-auditory stimulation. Event-related activity change due to stimulus timing was seen between 160-220 ms following somatosensory onset, mostly around the parietal area. The results demonstrate a dynamic modulation of somatosensory-auditory convergence and suggest the contribution of somatosensory information for speech processing process is dependent on the specific temporal order of sensory inputs in speech production. International audience
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