1,395 research outputs found

    Informed perspectives on human annotation using neural signals

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    In this work we explore how neurophysiological correlates related to attention and perception can be used to better understand the image-annotation task. We explore the nature of the highly variable labelling data often seen across annotators. Our results indicate potential issues with regard to ‘how well’ a person manually annotates images and variability across annotators. We propose such issues arise in part as a result of subjectively interpretable instructions that may fail to elicit similar labelling behaviours and decision thresholds across participants. We find instances where an individual’s annotations differ from a group consensus, even though their EEG (Electroencephalography) signals indicate in fact they were likely in consensus with the group. We offer a new perspective on how EEG can be incorporated in an annotation task to reveal information not readily captured using manual annotations alone. As crowd-sourcing resources become more readily available for annotation tasks one can reconsider the quality of such annotations. Furthermore, with the availability of consumer EEG hardware, we speculate that we are approaching a point where it may be feasible to better harness an annotators time and decisions by examining neural responses as part of the process. In this regard, we examine strategies to deal with inter-annotator sources of noise and correlation that can be used to understand the relationship between annotators at a neural level

    PGI10 EXAMINATION OF RESOURCE UTILIZATION PATTERNS ACROSS SUBGROUPS OF GASTROESOPHAGEAL REFLUX DISEASE PATIENTS

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    Collapse of ρxx\rho_{xx} ringlike structures in 2DEGs under tilted magnetic fields

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    In the quantum Hall regime, the longitudinal resistivity ρxx\rho_{xx} plotted as a density--magnetic-field (n2DBn_{2D}-B) diagram displays ringlike structures due to the crossings of two sets of spin split Landau levels from different subbands [e.g., Zhang \textit{et al.}, Phys. Rev. Lett. \textbf{95}, 216801 (2005)]. For tilted magnetic fields, some of these ringlike structures "shrink" as the tilt angle is increased and fully collapse at θc6\theta_c \approx 6^\circ. Here we theoretically investigate the topology of these structures via a non-interacting model for the 2DEG. We account for the inter Landau-level coupling induced by the tilted magnetic field via perturbation theory. This coupling results in anti-crossings of Landau levels with parallel spins. With the new energy spectrum, we calculate the corresponding n2DBn_{2D}-B diagram of the density of states (DOS) near the Fermi level. We argue that the DOS displays the same topology as ρxx\rho_{xx} in the n2DBn_{2D}-B diagram. For the ring with filling factor ν=4\nu=4, we find that the anti-crossings make it shrink for increasing tilt angles and collapse at a large enough angle. Using effective parameters to fit the θ=0\theta = 0^\circ data, we find a collapsing angle θc3.6\theta_c \approx 3.6^\circ. Despite this factor-of-two discrepancy with the experimental data, our model captures the essential mechanism underlying the ring collapse.Comment: 3 pages, 2 figures; Proceedings of the PASPS V Conference Held in August 2008 in Foz do Igua\c{c}u, Brazi

    Local dimension and finite time prediction in spatiotemporal chaotic systems

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    We show how a recently introduced statistics [Patil et al, Phys. Rev. Lett. 81 5878 (2001)] provides a direct relationship between dimension and predictability in spatiotemporal chaotic systems. Regions of low dimension are identified as having high predictability and vice-versa. This conclusion is reached by using methods from dynamical systems theory and Bayesian modelling. We emphasize in this work the consequences for short time forecasting and examine the relevance for factor analysis. Although we concentrate on coupled map lattices and coupled nonlinear oscillators for convenience, any other spatially distributed system could be used instead, such as turbulent fluid flows.Comment: 5 pagers, 7 EPS figure

    Synergistic And Additive Effect Of Oregano Essential Oil And Biological Silver Nanoparticles Against Multidrug-resistant Bacterial Strains

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    Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Bacterial resistance to conventional antibiotics has become a clinical and public health problem, making therapeutic decisions more challenging. Plant compounds and nanodrugs have been proposed as potential antimicrobial alternatives. Studies have shown that oregano (Origanum vulgare) essential oil (OEO) and silver nanoparticles have potent antibacterial activity, also against multidrug-resistant strains; however, the strong organoleptic characteristics of OEO and the development of resistance to these metal nanoparticles can limit their use. This study evaluated the antibacterial effect of a two-drug combination of biologically synthesized silver nanoparticles (bio-AgNP), produced by Fusarium oxysporum, and OEO against Gram-positive and Gram-negative bacteria, including multidrug-resistant strains. OEO and bio-AgNP showed bactericidal effects against all 17 strains tested, with minimal inhibitory concentrations (MIC) ranging from 0.298 to 1.193 mg/mL and 62.5 to 250 mu M, respectively. Time-kill curves indicated that OEO acted rapidly (within 10 min), while the metallic nanoparticles took 4 h to kill Gram-negative bacteria and 24 h to kill Gram-positive bacteria. The combination of the two compounds resulted in a synergistic or additive effect, reducing their MIC values and reducing the time of action compared to bio-AgNP used alone, i.e., 20 min for Gram-negative bacteria and 7 h for Gram-positive bacteria. Scanning electron microscopy (SEM) revealed similar morphological alterations in Staphylococcus aureus (non-methicillin-resistant S. aureus, non-MRSA) cells exposed to three different treatments (OEO, bio-AgNP and combination of the two), which appeared cell surface blebbing. Individual and combined treatments showed reduction in cell density and decrease in exopolysaccharide matrix compared to untreated bacterial cells. It indicated that this composition have an antimicrobial activity against S. aureus by disrupting cells. Both compounds showed very low hemolytic activity, especially at MIC levels. This study7CNPq BIOTEC [402728/2013-0]Postgraduate Program in Microbiology of Universidade Estadual de LondrinaConselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq

    Migration- and exercise-induced changes to flight muscle size in migratory birds and association with \u3cem\u3eIGF1\u3c/em\u3e and \u3cem\u3emyostatin\u3c/em\u3e mRNA expression

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    Seasonal adjustments to muscle size in migratory birds may result from preparatory physiological changes or responses to changed workloads. The mechanisms controlling these changes in size are poorly understood. We investigated some potential mediators of flight muscle size (myostatin and insulin-like growth factor, IGF1) in pectoralis muscles of wild wintering or migrating white-throated sparrows (Zonotrichia albicollis), captive white-throated sparrows that were photoperiod manipulated to be in a `wintering\u27 or `migratory\u27 (Zugunruhe) state, and captive European starlings (Sturnus vulgaris) that were either exercised for 2 weeks in a wind tunnel or untrained. Flight muscle size increased in photo-stimulated `migrants\u27 and in exercised starlings. Acute exercise but not long-term training caused increased expression of IGF1, but neither caused a change in expression of myostatin or its metalloprotease activator TLL1. Photo-stimulated `migrant\u27 sparrows demonstrated increased expression of both myostatin and IGF1, but wild sparrows exhibited no significant seasonal changes in expression of either myostatin or IGF1. Additionally, in both study species we describe several splice variants of myostatin that are shared with distantly related bird species. We demonstrate that their expression patterns are not different from those of the typical myostatin, suggesting that they have no functional importance and may be mistakes of the splicing machinery. We conclude that IGF1 is likely to be an important mediator of muscle phenotypic flexibility during acute exercise and during endogenous, seasonal preparation for migration. The role of myostatin is less clear, but its paradoxical increase in photo-stimulated `migrants\u27 may indicate a role in seasonal adjustments of protein turnover

    Differential cellular FGF-2 upregulation in the rat facial nucleus following axotomy, functional electrical stimulation and corticosterone: a possible therapeutic target to Bell's palsy

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    <p>Abstract</p> <p>Background</p> <p>The etiology of Bell's palsy can vary but anterograde axonal degeneration may delay spontaneous functional recovery leading the necessity of therapeutic interventions. Corticotherapy and/or complementary rehabilitation interventions have been employed. Thus the natural history of the disease reports to a neurotrophic resistance of adult facial motoneurons leading a favorable evolution however the related molecular mechanisms that might be therapeutically addressed in the resistant cases are not known. Fibroblast growth factor-2 (FGF-2) pathway signaling is a potential candidate for therapeutic development because its role on wound repair and autocrine/paracrine trophic mechanisms in the lesioned nervous system.</p> <p>Methods</p> <p>Adult rats received unilateral facial nerve crush, transection with amputation of nerve branches, or sham operation. Other group of unlesioned rats received a daily functional electrical stimulation in the levator labii superioris muscle (1 mA, 30 Hz, square wave) or systemic corticosterone (10 mgkg<sup>-1</sup>). Animals were sacrificed seven days later.</p> <p>Results</p> <p>Crush and transection lesions promoted no changes in the number of neurons but increased the neurofilament in the neuronal neuropil of axotomized facial nuclei. Axotomy also elevated the number of GFAP astrocytes (143% after crush; 277% after transection) and nuclear FGF-2 (57% after transection) in astrocytes (confirmed by two-color immunoperoxidase) in the ipsilateral facial nucleus. Image analysis reveled that a seven days functional electrical stimulation or corticosterone led to elevations of FGF-2 in the cytoplasm of neurons and in the nucleus of reactive astrocytes, respectively, without astrocytic reaction.</p> <p>Conclusion</p> <p>FGF-2 may exert paracrine/autocrine trophic actions in the facial nucleus and may be relevant as a therapeutic target to Bell's palsy.</p

    The September 2004 stench off the southern Malabar coast - A consequence of holococcolithophore bloom

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    During the third week of September 2004, particularly on 16th and 17th, an unusual and strong stench was reported from the coast at Kollam and Vizhinjam in Kerala (India). Local dailies reported that over 200 children, mostly below 15 years, complained of nausea, chest pain and short periods of breathlessness because of the stench. Many were hospitalized, but were discharged within a couple of hours. A press report stated that the stench was due to dead fish scattered on the beaches and in the water. The report linked the fish death to oxygen depletion and choking of fish gills. Both were reported to be possibly due to proliferation and eventual putrefaction of a fish-toxic alga Cochlodinium polykreikoides. Information was put up on the web that the bloom was caused by Karenia brevis, a toxic dinoflagellate. It was reported that the stench could be felt up to 5 km inland from the coast. On 20 September 2004, the Government of Kerala requested the National Institute of Oceanography (NIO), Goa to determine the cause of the phenomenon. In response, a team from NIO collected near-shore samples of water on 23 and 26 September off Vizhinjam, Shanghumugham and Kollam. During 3-7 October 2004, RV Sagar Sukti, a coastal research vessel of NIO, was used to collect samples in the waters offshore of Vizhinjam, Veli, Kollam in the depth zones of 20-50 m. The water samples collected on 23 and 26 September from the near-shore spots were analysed for various chemical (dissolved oxygen, hydrogen sulphide, nutrients, and salinity) and biological (microbiological, phytoplankton counting and identification) variables. Data from sea-level records at Cochin Port were also examined to learn about the possible evolution of physical conditions before and after the episode described above. In this preliminary report inferences based on analysis of the data is presented

    Epigenetics as a mechanism driving polygenic clinical drug resistance

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    Aberrant methylation of CpG islands located at or near gene promoters is associated with inactivation of gene expression during tumour development. It is increasingly recognised that such epimutations may occur at a much higher frequency than gene mutation and therefore have a greater impact on selection of subpopulations of cells during tumour progression or acquisition of resistance to anticancer drugs. Although laboratory-based models of acquired resistance to anticancer agents tend to focus on specific genes or biochemical pathways, such 'one gene : one outcome' models may be an oversimplification of acquired resistance to treatment of cancer patients. Instead, clinical drug resistance may be due to changes in expression of a large number of genes that have a cumulative impact on chemosensitivity. Aberrant CpG island methylation of multiple genes occurring in a nonrandom manner during tumour development and during the acquisition of drug resistance provides a mechanism whereby expression of multiple genes could be affected simultaneously resulting in polygenic clinical drug resistance. If simultaneous epigenetic regulation of multiple genes is indeed a major driving force behind acquired resistance of patients' tumour to anticancer agents, this has important implications for biomarker studies of clinical outcome following chemotherapy and for clinical approaches designed to circumvent or modulate drug resistance
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