376 research outputs found

    Automated ice-core layer-counting with strong univariate signals

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    We present an automated process for determining the annual layer chronology of an ice-core with a strong annual signal, utilising the hydrogen peroxide record from an Antarctic Peninsula ice-core as a test signal on which to count annual cycles and explain the methods. The signal is de-trended and normalised before being split into sections with a deterministic cycle count and those that need more attention. Possible reconstructions for the uncertain sections are determined which could be used as a visual aid for manual counting, and a simple method for assigning probability measures to each reconstruction is discussed. The robustness of this process is explored by applying it to versions of two different chemistry signals from the same stretch of the NGRIP (North Greenland Ice Core Project) ice-core, which shows more variation in annual layer thickness, with and without thinning to mimic poorer quality data. An adapted version of these methods is applied to the more challenging non-sea-salt sulphur signal from the same Antarctic Peninsula core from which the hydrogen peroxide signal was taken. These methods could readily be adapted for use on much longer datasets, thereby reducing manual effort and providing a robust automated layer-counting methodology

    A proposal of a Renormalization Group transformation

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    We propose a family of renormalization group transformations characterized by free parameters that may be tuned in order to reduce the truncation effects. As a check we test them in the three dimensional XY model. The Schwinger--Dyson equations are used to study the renormalization group flow.Comment: Contribution to Lattice'94. uuencoded postscript fil

    Guidance in author instructions of hematology and oncology journals: A cross sectional and longitudinal study.

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    The debate about the value of biomedical publications led to recommendations for improving reporting quality. It is unclear to what extent these recommendations have been endorsed by journals. We analyzed whether specific recommendations were included in author instructions, which journal characteristics were associated with their endorsement, how endorsement of the domains changed and whether endorsement was associated with change of impact factor between 2010 and 2015. We considered two study samples consisting of "Hematology" and "Oncology" journals of the Journal Citation Report 2008 and 2014, respectively. We extracted information regarding endorsement of the (1) recommendations of the International Committee of Medical Journal Editors, of (2) reporting guidelines, (3) requirement for trial registration and (4) disclosure of conflicts of interest. Data extraction was done by reading the author instructions before conducting a text search with keywords. We calculated a global generalized linear mixed effects model for endorsement of each of the four domains followed by separate multivariable logistic regression models and a longitudinal analysis. We defined endorsement as the author instructions saying that they approve the use of the recommendations. In 2015, the ICMJE recommendations were mentioned in author instructions of 156 journals (67.5%). CONSORT was referred to by 77 journals (33.3%); MOOSE, PRISMA, STARD and STROBE were referred to by less than 15% of journals. There were 99 journals (42.9%) that recommended or required trial registration, 211 (91.3%) required authors to disclose conflicts of interest. Journal impact factor, journal start year and geographical region were positively associated with endorsement of any of the four domains. The overall endorsement of all domains increased between 2010 and 2015. The endorsement of any domain in 2010 seemed to be associated with an increased impact factor in 2014. Hematology and oncology journals endorse major recommendations to various degrees. Endorsement is increasing slowly over time and might be positively associated with the journals' impact factor

    Properties of Flares-Generated Seismic Waves on the Sun

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    The solar seismic waves excited by solar flares (``sunquakes'') are observed as circular expanding waves on the Sun's surface. The first sunquake was observed for a flare of July 9, 1996, from the Solar and Heliospheric Observatory (SOHO) space mission. However, when the new solar cycle started in 1997, the observations of solar flares from SOHO did not show the seismic waves, similar to the 1996 event, even for large X-class flares during the solar maximum in 2000-2002. The first evidence of the seismic flare signal in this solar cycle was obtained for the 2003 ``Halloween'' events, through acoustic ``egression power'' by Donea and Lindsey. After these several other strong sunquakes have been observed. Here, I present a detailed analysis of the basic properties of the helioseismic waves generated by three solar flares in 2003-2005. For two of these flares, X17 flare of October 28, 2003, and X1.2 flare of January 15, 2005, the helioseismology observations are compared with simultaneous observations of flare X-ray fluxes measured from the RHESSI satellite. These observations show a close association between the flare seismic waves and the hard X-ray source, indicating that high-energy electrons accelerated during the flare impulsive phase produced strong compression waves in the photosphere, causing the sunquake. The results also reveal new physical properties such as strong anisotropy of the seismic waves, the amplitude of which varies significantly with the direction of propagation. The waves travel through surrounding sunspot regions to large distances, up to 120 Mm, without significant decay. These observations open new perspectives for helioseismic diagnostics of flaring active regions on the Sun and for understanding the mechanisms of the energy release and transport in solar flares.Comment: 12 pages, 4 figures, submitted to Ap

    The four dimensional site-diluted Ising model: a finite-size scaling study

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    Using finite-size scaling techniques, we study the critical properties of the site-diluted Ising model in four dimensions. We carry out a high statistics Monte Carlo simulation for several values of the dilution. The results support the perturbative scenario: there is only the Ising fixed point with large logarithmic scaling corrections. We obtain, using the Perturbative Renormalization Group, functional forms for the scaling of several observables that are in agreement with the numerical data.Comment: 30 pages, 8 postscript figure

    Monte Carlo Renormalization Group Analysis of Lattice ϕ4\phi^4 Model in D=3,4D=3,4

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    We present a simple, sophisticated method to capture renormalization group flow in Monte Carlo simulation, which provides important information of critical phenomena. We applied the method to D=3,4D=3,4 lattice ϕ4\phi^4 model and obtained renormalization flow diagram which well reproduces theoretically predicted behavior of continuum ϕ4\phi^4 model. We also show that the method can be easily applied to much more complicated models, such as frustrated spin models.Comment: 13 pages, revtex, 7 figures. v1:Submitted to PRE. v2:considerably reduced redundancy of presentation. v3:final version to appear in Phys.Rev.

    Sleep onset problems and subcortical development in infants later diagnosed with autism spectrum disorder

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    Objective: Sleep patterns in children with autism spectrum disorder (ASD) appear to diverge from typical development in the second or third year of life. Little is known, however, about the occurrence of sleep problems in infants who later develop ASD and possible effects on early brain development. In a longitudinal neuroimaging study of infants at familial high or low risk for ASD, parent-reported sleep onset problems were examined in relation to subcortical brain volumes in the first 2 years of life. Methods: A total of 432 infants were included across three study groups: infants at high risk who developed ASD (N=71), infants at high risk who did not develop ASD (N=234), and infants at low risk (N=127). Sleep onset problem scores (derived from an infant temperament measure) were evaluated in relation to longitudinal high-resolution T1 and T2 structural imaging data acquired at 6, 12, and 24 months of age. Results: Sleep onset problems were more common at 6–12 months among infants who later developed ASD. Infant sleep onset problems were related to hippocampal volume trajectories from 6 to 24 months only for infants at high risk who developed ASD. Brain-sleep relationships were specific to the hippocampus; no significant relationships were found with volume trajectories of other subcortical structures examined (the amygdala, caudate, globus pallidus, putamen, and thalamus). Conclusions: These findings provide initial evidence that sleep onset problems in the first year of life precede ASD diagnosis and are associated with altered neurodevelopmental trajectories in infants at high familial risk who go on to develop ASD. If replicated, these findings could provide new insights into a potential role of sleep difficulties in the development of ASD

    Investigating the validity of the DN4 in a consecutive population of patients with chronic pain

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    Neuropathic pain is clinically described as pain caused by a lesion or disease of the somatosensory nervous system. The aim of this study was to assess the validity of the Dutch version of the DN4, in a cross-sectional multicentre design, as a screening tool for detecting a neuropathic pain component in a large consecutive, not pre-stratified on basis of the target outcome, population of patients with chronic pain. Patients’ pain was classified by two independent (pain-)physicians as the gold standard. The analysis was initially performed on the outcomes of those patients (n = 228 out of 291) in whom both physicians agreed in their pain classification. Compared to the gold standard the DN4 had a sensitivity of 75% and specificity of 76%. The DN4-symptoms (seven interview items) solely resulted in a sensitivity of 70% and a specificity of 67%. For the DN4-signs (three examination items) it was respectively 75% and 75%. In conclusion, because it seems that the DN4 helps to identify a neuropathic pain component in a consecutive population of patients with chronic pain in a moderate way, a comprehensive (physical-) examination by the physician is still obligate

    Assessment of panobacumab as adjunctive immunotherapy for the treatment of nosocomial Pseudomonas aeruginosa pneumonia.

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    The fully human anti-lipopolysaccharide (LPS) immunoglobulin M (IgM) monoclonal antibody panobacumab was developed as an adjunctive immunotherapy for the treatment of O11 serotype Pseudomonas aeruginosa infections. We evaluated the potential clinical efficacy of panobacumab in the treatment of nosocomial pneumonia. We performed a post-hoc analysis of a multicenter phase IIa trial (NCT00851435) designed to prospectively evaluate the safety and pharmacokinetics of panobacumab. Patients treated with panobacumab (n = 17), including 13 patients receiving the full treatment (three doses of 1.2 mg/kg), were compared to 14 patients who did not receive the antibody. Overall, the 17 patients receiving panobacumab were more ill. They were an average of 72 years old [interquartile range (IQR): 64-79] versus an average of 50 years old (IQR: 30-73) (p = 0.024) and had Acute Physiology and Chronic Health Evaluation II (APACHE II) scores of 17 (IQR: 16-22) versus 15 (IQR: 10-19) (p = 0.043). Adjunctive immunotherapy resulted in an improved clinical outcome in the group receiving the full three-course panobacumab treatment, with a resolution rate of 85 % (11/13) versus 64 % (9/14) (p = 0.048). The Kaplan-Meier survival curve showed a statistically significantly shorter time to clinical resolution in this group of patients (8.0 [IQR: 7.0-11.5] versus 18.5 [IQR: 8-30] days in those who did not receive the antibody; p = 0.004). Panobacumab adjunctive immunotherapy may improve clinical outcome in a shorter time if patients receive the full treatment (three doses). These preliminary results suggest that passive immunotherapy targeting LPS may be a complementary strategy for the treatment of nosocomial O11 P. aeruginosa pneumonia

    Imaging Spectroscopy of a White-Light Solar Flare

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    We report observations of a white-light solar flare (SOL2010-06-12T00:57, M2.0) observed by the Helioseismic Magnetic Imager (HMI) on the Solar Dynamics Observatory (SDO) and the Reuven Ramaty High-Energy Solar Spectroscopic Imager (RHESSI). The HMI data give us the first space-based high-resolution imaging spectroscopy of a white-light flare, including continuum, Doppler, and magnetic signatures for the photospheric FeI line at 6173.34{\AA} and its neighboring continuum. In the impulsive phase of the flare, a bright white-light kernel appears in each of the two magnetic footpoints. When the flare occurred, the spectral coverage of the HMI filtergrams (six equidistant samples spanning \pm172m{\AA} around nominal line center) encompassed the line core and the blue continuum sufficiently far from the core to eliminate significant Doppler crosstalk in the latter, which is otherwise a possibility for the extreme conditions in a white-light flare. RHESSI obtained complete hard X-ray and \Upsilon-ray spectra (this was the first \Upsilon-ray flare of Cycle 24). The FeI line appears to be shifted to the blue during the flare but does not go into emission; the contrast is nearly constant across the line profile. We did not detect a seismic wave from this event. The HMI data suggest stepwise changes of the line-of-sight magnetic field in the white-light footpoints.Comment: 14 pages, 7 figures, Accepted by Solar Physic
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