Low-power continuous-wave all-optical magnetic switching in ferromagnetic nanoarrays

All-optical magnetic switching promises ultrafast magnetization control without a magnetic field. Existing schemes typically require power-hungry femtosecond-pulsed lasers and complex magnetic materials. Here, we demonstrate deterministic, all-optical magnetic switching in simple ferromagnetic nanomagnets (Ni81Fe19, Ni50Fe50) with sub-diffraction limit dimensions using a focused low-power, linearly polarized continuous-wave laser. Isolated nanomagnets are switched across a range of dimensions, laser wavelengths, and powers. All square-geometry artificial spin ice vertex configurations are written at low powers (2.74 mW). Usually, switching with linearly polarized light is symmetry forbidden; here, the laser spot has a similar size to the nanomagnets, producing an absorption distribution that depends on the nanoisland-spot displacement. We attribute the deterministic switching to the transient dynamics of this asymmetric absorption. No switching is observed in Co or Ni nanostructures, suggesting the multi-species nature of NiFe plays a role. These results usher in inexpensive, low-power, optically controlled devices with impact across data storage, neuromorphic computation, and reconfigurable magnonics

Bone-protective effects of bioactive fractions and ingredients in Sambucus williamsii HANCE

2011-2012 > Academic research: refereed > Publication in refereed journalVersion of RecordPublishe

Livenet: A low-latency video transport network for large-scale live streaming

Low-latency live streaming has imposed stringent latency requirements on video transport networks. In this paper we report on the design and operation of the Alibaba low-latency video transport network, LiveNet. LiveNet builds on a flat CDN overlay with a centralized controller for global optimization. As part of this, we present our design of the global routing computation and path assignment, as well as our fast data transmission architecture with fine-grained control of video frames. The performance results obtained from three years of operation demonstrate the effectiveness of LiveNet in improving CDN performance and QoE metrics. Compared with our prior state-of-The-Art hierarchical CDN deployment, LiveNet halves the CDN delay and ensures 98% of views do not experience stalls and that 95% can start playback within 1 second. We further report our experiences of running LiveNet over the last 3 years

Saliency Benchmarking Made Easy: Separating Models, Maps and Metrics

Dozens of new models on fixation prediction are published every year and compared on open benchmarks such as MIT300 and LSUN. However, progress in the field can be difficult to judge because models are compared using a variety of inconsistent metrics. Here we show that no single saliency map can perform well under all metrics. Instead, we propose a principled approach to solve the benchmarking problem by separating the notions of saliency models, maps and metrics. Inspired by Bayesian decision theory, we define a saliency model to be a probabilistic model of fixation density prediction and a saliency map to be a metric-specific prediction derived from the model density which maximizes the expected performance on that metric given the model density. We derive these optimal saliency maps for the most commonly used saliency metrics (AUC, sAUC, NSS, CC, SIM, KL-Div) and show that they can be computed analytically or approximated with high precision. We show that this leads to consistent rankings in all metrics and avoids the penalties of using one saliency map for all metrics. Our method allows researchers to have their model compete on many different metrics with state-of-the-art in those metrics: "good" models will perform well in all metrics.Comment: published at ECCV 201

Low-power continuous-wave all-optical magnetic switching in ferromagnetic nanoarrays

All-optical magnetic switching promises ultrafast magnetization control without a magnetic field. Existing schemes typically require power-hungry femtosecond-pulsed lasers and complex magnetic materials. Here, we demonstrate deterministic, all-optical magnetic switching in simple ferromagnetic nanomagnets (Ni81Fe19, Ni50Fe50) with sub-diffraction limit dimensions using a focused low-power, linearly polarized continuous-wave laser. Isolated nanomagnets are switched across a range of dimensions, laser wavelengths, and powers. All square-geometry artificial spin ice vertex configurations are written at low powers (2.74 mW). Usually, switching with linearly polarized light is symmetry forbidden; here, the laser spot has a similar size to the nanomagnets, producing an absorption distribution that depends on the nanoisland-spot displacement. We attribute the deterministic switching to the transient dynamics of this asymmetric absorption. No switching is observed in Co or Ni nanostructures, suggesting the multi-species nature of NiFe plays a role. These results usher in inexpensive, low-power, optically controlled devices with impact across data storage, neuromorphic computation, and reconfigurable magnonics

Controlling Cherenkov angles with resonance transition radiation

Cherenkov radiation provides a valuable way to identify high energy particles in a wide momentum range, through the relation between the particle velocity and the Cherenkov angle. However, since the Cherenkov angle depends only on material's permittivity, the material unavoidably sets a fundamental limit to the momentum coverage and sensitivity of Cherenkov detectors. For example, Ring Imaging Cherenkov detectors must employ materials transparent to the frequency of interest as well as possessing permittivities close to unity to identify particles in the multi GeV range, and thus are often limited to large gas chambers. It would be extremely important albeit challenging to lift this fundamental limit and control Cherenkov angles as preferred. Here we propose a new mechanism that uses constructive interference of resonance transition radiation from photonic crystals to generate both forward and backward Cherenkov radiation. This mechanism can control Cherenkov angles in a flexible way with high sensitivity to any desired range of velocities. Photonic crystals thus overcome the severe material limit for Cherenkov detectors, enabling the use of transparent materials with arbitrary values of permittivity, and provide a promising option suited for identification of particles at high energy with enhanced sensitivity.Comment: There are 16 pages and 4 figures for the manuscript. Supplementary information with 18 pages and 5 figures, appended at the end of the file with the manuscript. Source files in Word format converted to PDF. Submitted to Nature Physic

A Novel Splicing Mutation Alters DSPP Transcription and Leads to Dentinogenesis Imperfecta Type II

Dentinogenesis imperfecta (DGI) type II is an autosomal dominant disease characterized by a serious disorders in teeth. Mutations of dentin sialophosphoprotein (DSPP) gene were revealed to be the causation of DGI type II (DGI-II). In this study, we identified a novel mutation (NG_011595.1:g.8662T>C, c.135+2T>C) lying in the splice donor site of intron 3 of DSPP gene in a Chinese Han DGI-II pedigree. It was found in all affected subjects but not in unaffected ones or other unrelated healthy controls. The function of the mutant DSPP gene, which was predicted online and subsequently confirmed by in vitro splicing analysis, was the loss of splicing of intron 3, leading to the extended length of DSPP mRNA. For the first time, the functional non-splicing of intron was revealed in a novel DSPP mutation and was considered as the causation of DGI-II. It was also indicated that splicing was of key importance to the function of DSPP and this splice donor site might be a sensitive mutation hot spot. Our findings combined with other reports would facilitate the genetic diagnosis of DGI-II, shed light on its gene therapy and help to finally conquer human diseases

Capture barrier of Sn-related DX centers in AlGaAs epilayers

Thermal capture and emission processes of Sn-related DX centers in AlxGa1-xAs (x = 0.26) were measured by a constant capacitance (CC) voltage transient in various temperatures, By employing a Laplace defect spectroscopic (LDS) method, the non-exponential transients were decomposed into several discrete exponential components. The results shown that more exponential components appeared in the small emission rate region as capture period increased. This indicates that electrons preferentially fill shallow energy levels due to their lower capture barriers. Discrete exponential components of the capture process were identified and four of their barriers were preliminarily measured to be about 0.14, 0.15, 0.16, and 0.17 eV, respectively

Histone Deacetylases Regulate Gonadotropin-Releasing Hormone I Gene Expression via Modulating Otx2-Driven Transcriptional Activity

BACKGROUND: Precise coordination of the hypothalamic-pituitary-gonadal axis orchestrates the normal reproductive function. As a central regulator, the appropriate synthesis and secretion of gonadotropin-releasing hormone I (GnRH-I) from the hypothalamus is essential for the coordination. Recently, emerging evidence indicates that histone deacetylases (HDACs) play an important role in maintaining normal reproductive function. In this study, we identify the potential effects of HDACs on Gnrh1 gene transcription. METHODOLOGY/PRINCIPAL FINDINGS: Inhibition of HDACs activities by trichostatin A (TSA) and valproic acid (VPA) promptly and dramatically repressed transcription of Gnrh1 gene in the mouse immortalized mature GnRH neuronal cells GT1-7. The suppression was connected with a specific region of Gnrh1 gene promoter, which contains two consensus Otx2 binding sites. Otx2 has been known to activate the basal and also enhancer-driven transcription of Gnrh1 gene. The transcriptional activity of Otx2 is negatively modulated by Grg4, a member of the Groucho-related-gene (Grg) family. In the present study, the expression of Otx2 was downregulated by TSA and VPA in GT1-7 cells, accompanied with the opposite changes of Grg4 expression. Chromatin immunoprecipitation and electrophoretic mobility shift assays demonstrated that the DNA-binding activity of Otx2 to Gnrh1 gene was suppressed by TSA and VPA. Overexpression of Otx2 partly abolished the TSA- and VPA-induced downregulation of Gnrh1 gene expression. CONCLUSIONS/SIGNIFICANCE: Our data indicate that HDAC inhibitors downregulate Gnrh1 gene expression via repressing Otx2-driven transcriptional activity. This study should provide an insight for our understanding on the effects of HDACs in the reproductive system and suggests that HDACs could be potential novel targets for the therapy of GnRH-related diseases