1,474 research outputs found
Are Coronae of Magnetically Active Stars Heated by Flares? III. Analytical Distribution of Superimposed Flares
(abridged) We study the hypothesis that observed X-ray/extreme ultraviolet
emission from coronae of magnetically active stars is entirely (or to a large
part) due to the superposition of flares, using an analytic approach to
determine the amplitude distribution of flares in light curves. The
flare-heating hypothesis is motivated by time series that show continuous
variability suggesting the presence of a large number of superimposed flares
with similar rise and decay time scales. We rigorously relate the amplitude
distribution of stellar flares to the observed histograms of binned counts and
photon waiting times, under the assumption that the flares occur at random and
have similar shapes. Applying these results to EUVE/DS observations of the
flaring star AD Leo, we find that the flare amplitude distribution can be
represented by a truncated power law with a power law index of 2.3 +/- 0.1. Our
analytical results agree with existing Monte Carlo results of Kashyap et al.
(2002) and Guedel et al. (2003). The method is applicable to a wide range of
further stochastically bursting astrophysical sources such as cataclysmic
variables, Gamma Ray Burst substructures, X-ray binaries, and spatially
resolved observations of solar flares.Comment: accepted for publication in Ap
Exact quantum dynamics of bosons with finite-range time-dependent interactions of harmonic type
The exactly solvable quantum many-particle model with harmonic one- and
two-particle interaction terms is extended to include time-dependency. We show
that when the external trap potential and finite-range interparticle
interaction have a time-dependency the exact solutions of the corresponding
time-dependent many-boson Schr\"odinger equation are still available. We use
these exact solutions to benchmark the recently developed multiconfigurational
time-dependent Hartree method for bosons (MCTDHB) [Phys. Rev. Lett. {\bf 99},
030402 (2007), Phys. Rev. A {\bf 77}, 033613 (2008)]. In particular, we
benchmark the MCTDHB method for: (i) the ground state; (ii) the breathing
many-body dynamics activated by a quench scenario where the interparticle
interaction strength is suddenly turned on to a finite value; (iii) the
non-equilibrium dynamic for driven scenarios where both the trap- and
interparticle-interaction potentials are {\it time-dependent}. Excellent
convergence of the ground state and dynamics is demonstrated. The great
relevance of the self-consistency and time-adaptivity, which are the intrinsic
features of the MCTDHB method, is demonstrated by contrasting the MCTDHB
predictions and those obtained within the standard full configuration
interaction method spanning the Fock space of the same size, but utilizing as
one-particle basis set the fixed-shape eigenstates of the one-particle
potential. Connections of the model's results to ultra-cold Bose-Einstein
condensed systems are addressed.Comment: 31 pages, 5 figure
MaxDIA enables library-based and library-free data-independent acquisition proteomics
MaxDIA is a software platform for analyzing data-independent acquisition (DIA) proteomics data within the MaxQuant software environment. Using spectral libraries, MaxDIA achieves deep proteome coverage with substantially better coefficients of variation in protein quantification than other software. MaxDIA is equipped with accurate false discovery rate (FDR) estimates on both library-to-DIA match and protein levels, including when using whole-proteome predicted spectral libraries. This is the foundation of discovery DIA-hypothesis-free analysis of DIA samples without library and with reliable FDR control. MaxDIA performs three- or four-dimensional feature detection of fragment data, and scoring of matches is augmented by machine learning on the features of an identification. MaxDIA's bootstrap DIA workflow performs multiple rounds of matching with increasing quality of recalibration and stringency of matching to the library. Combining MaxDIA with two new technologies-BoxCar acquisition and trapped ion mobility spectrometry-both lead to deep and accurate proteome quantification. The software platform MaxDIA streamlines analysis of data-independent acquisition proteomics
Ferromagnetic transition metal implanted ZnO: a diluted magnetic semiconductor?
Recently theoretical works predict that some semiconductors (e.g. ZnO) doped
with magnetic ions are diluted magnetic semiconductors (DMS). In DMS magnetic
ions substitute cation sites of the host semiconductor and are coupled by free
carriers resulting in ferromagnetism. One of the main obstacles in creating DMS
materials is the formation of secondary phases because of the solid-solubility
limit of magnetic ions in semiconductor host. In our study transition metal
ions were implanted into ZnO single crystals with the peak concentrations of
0.5-10 at.%. We established a correlation between structural and magnetic
properties. By synchrotron radiation X-ray diffraction (XRD) secondary phases
(Fe, Ni, Co and ferrite nanocrystals) were observed and have been identified as
the source for ferromagnetism. Due to their different crystallographic
orientation with respect to the host crystal these nanocrystals in some cases
are very difficult to be detected by a simple Bragg-Brentano scan. This results
in the pitfall of using XRD to exclude secondary phase formation in DMS
materials. For comparison, the solubility of Co diluted in ZnO films ranges
between 10 and 40 at.% using different growth conditions pulsed laser
deposition. Such diluted, Co-doped ZnO films show paramagnetic behaviour.
However, only the magnetoresistance of Co-doped ZnO films reveals possible s-d
exchange interaction as compared to Co-implanted ZnO single crystals.Comment: 27 pages, 8 figure
International Veterinary Epilepsy Task Force recommendations for systematic sampling and processing of brains from epileptic dogs and cats
Traditionally, histological investigations of the epileptic brain are required to identify epileptogenic brain lesions, to evaluate the impact of seizure activity, to search for mechanisms of drug-resistance and to look for comorbidities. For many instances, however, neuropathological studies fail to add substantial data on patients with complete clinical work-up. This may be due to sparse training in epilepsy pathology and or due to lack of neuropathological guidelines for companion animals.
The protocols introduced herein shall facilitate systematic sampling and processing of epileptic brains and therefore increase the efficacy, reliability and reproducibility of morphological studies in animals suffering from seizures.
Brain dissection protocols of two neuropathological centres with research focus in epilepsy have been optimised with regards to their diagnostic yield and accuracy, their practicability and their feasibility concerning clinical research requirements.
The recommended guidelines allow for easy, standardised and ubiquitous collection of brain regions, relevant for seizure generation. Tissues harvested the prescribed way will increase the diagnostic efficacy and provide reliable material for scientific investigations
International Veterinary Epilepsy Task Force Consensus Proposal: Outcome of therapeutic interventions in canine and feline epilepsy
Common criteria for the diagnosis of drug resistance and the assessment of outcome are needed urgently as a prerequisite for standardized evaluation and reporting of individual therapeutic responses in canine epilepsy. Thus, we provide a proposal for the definition of drug resistance and partial therapeutic success in canine patients with epilepsy. This consensus statement also suggests a list of factors and aspects of outcome, which should be considered in addition to the impact on seizures. Moreover, these expert recommendations discuss criteria which determine the validity and informative value of a therapeutic trial in an individual patient and also suggest the application of individual outcome criteria. Agreement on common guidelines does not only render a basis for future optimization of individual patient management, but is also a presupposition for the design and implementation of clinical studies with highly standardized inclusion and exclusion criteria. Respective standardization will improve the comparability of findings from different studies and renders an improved basis for multicenter studies. Therefore, this proposal provides an in-depth discussion of the implications of outcome criteria for clinical studies. In particular ethical aspects and the different options for study design and application of individual patient-centered outcome criteria are considered
International Veterinary Epilepsy Task Force recommendations for a veterinary epilepsy-specific MRI protocol
Epilepsy is one of the most common chronic neurological diseases in veterinary practice. Magnetic resonance imaging (MRI) is regarded as an important diagnostic test to reach the diagnosis of idiopathic epilepsy. However, given that the diagnosis requires the exclusion of other differentials for seizures, the parameters for MRI examination should allow the detection of subtle lesions which may not be obvious with existing techniques. In addition, there are several differentials for idiopathic epilepsy in humans, for example some focal cortical dysplasias, which may only apparent with special sequences, imaging planes and/or particular techniques used in performing the MRI scan. As a result, there is a need to standardize MRI examination in veterinary patients with techniques that reliably diagnose subtle lesions, identify post-seizure changes, and which will allow for future identification of underlying causes of seizures not yet apparent in the veterinary literature.
There is a need for a standardized veterinary epilepsy-specific MRI protocol which will facilitate more detailed examination of areas susceptible to generating and perpetuating seizures, is cost efficient, simple to perform and can be adapted for both low and high field scanners. Standardisation of imaging will improve clinical communication and uniformity of case definition between research studies. A 6–7 sequence epilepsy-specific MRI protocol for veterinary patients is proposed and further advanced MR and functional imaging is reviewed
Decreased CD90 expression in human mesenchymal stem cells by applying mechanical stimulation
BACKGROUND: Mesenchymal stem cells (MSC) are multipotent cells which can differentiate along osteogenic, chondrogenic, and adipogenic lineages. The present study was designed to investigate the influence of mechanical force as a specific physiological stress on the differentiation of (MSC) to osteoblast-like cells. METHODS: Human MSC were cultured in osteoinductive medium with or without cyclic uniaxial mechanical stimulation (2000 μstrain, 200 cycles per day, 1 Hz). Cultured cells were analysed for expression of collagen type I, osteocalcin, osteonectin, and CD90. To evaluate the biomineral formation the content of bound calcium in the cultures was determined. RESULTS: After 14 days in culture immunfluorescence staining revealed enhancement of collagen type I and osteonectin expression in response to mechanical stimulation. In contrast, mechanically stimulated cultures stained negative for CD90. In stimulated and unstimulated cultures an increase in the calcium content over time was observed. After 21 days in culture the calcium content in mechanical stimulated cultures was significantly higher compared to unstimulated control cultures. CONCLUSION: These results demonstrate the influence of mechanical force on the differentiation of human MSC into osteoblast-like cells in vitro. While significant enhancement of the biomineral formation by mechanical stimulation is not detected before 21 days, effects on the extracellular matrix became already obvious after 14 days. The decrease of CD90 expression in mechanically stimulated cultures compared to unstimulated control cultures suggests that CD90 is only transiently expressed expression during the differentiation of MSC to osteoblast-like cells in culture
A New Method to Predict the Epidemiology of Fungal Keratitis by Monitoring the Sales Distribution of Antifungal Eye Drops in Brazil
Purpose: Fungi are a major cause of keratitis, although few medications are licensed for their treatment. The aim of this study is to observe the variation in commercialisation of antifungal eye drops, and to predict the seasonal distribution of fungal keratitis in Brazil. Methods: Data from a retrospective study of antifungal eye drops sales from the only pharmaceutical ophthalmologic laboratory, authorized to dispense them in Brazil (Opthalmos) were gathered. These data were correlated with geographic and seasonal distribution of fungal keratitis in Brazil between July 2002 and June 2008. Results: A total of 26,087 antifungal eye drop units were sold, with a mean of 2.3 per patient. There was significant variation in antifungal sales during the year (p < 0.01). A linear regression model displayed a significant association between reduced relative humidity and antifungal drug sales (R-2 = 0.17, p < 0.01). Conclusions: Antifungal eye drops sales suggest that there is a seasonal distribution of fungal keratitis. A possible interpretation is that the third quarter of the year (a period when the climate is drier), when agricultural activity is more intense in Brazil, suggests a correlation with a higher incidence of fungal keratitis. A similar model could be applied to other diseases, that are managed with unique, or few, and monitorable medications to predict epidemiological aspects.Conselho Nacional de Desenvolvimento Cientifico e TecnologicoConselho Nacional de Desenvolvimento Cientifico e Tecnologico [302005/2009-9]Fundacao de Apoio ao Ensino, Pesquisa e Assistencia do Hospital das Clinicas da Faculdade de Medicina de Ribeirao Preto da Universidade de Sao PauloFundacao de Apoio ao Ensino, Pesquisa e Assistencia do Hospital das Clinicas da Faculdade de Medicina de Ribeirao Preto da Universidade de Sao Paul
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