276 research outputs found

    A Steady-State Picture of Solar Wind Acceleration and Charge State Composition Derived from a Global Wave-Driven MHD Model

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    The higher charge states found in slow (<<400km s−1^{-1}) solar wind streams compared to fast streams have supported the hypothesis that the slow wind originates in closed coronal loops, and released intermittently through reconnection. Here we examine whether a highly ionized slow wind can also form along steady and open magnetic field lines. We model the steady-state solar atmosphere using AWSoM, a global magnetohydrodynamic model driven by Alfv{\'e}n waves, and apply an ionization code to calculate the charge state evolution along modeled open field lines. This constitutes the first charge states calculation covering all latitudes in a realistic magnetic field. The ratios O+7/O+6O^{+7}/O^{+6} and C+6/C+5C^{+6}/C^{+5} are compared to in-situ Ulysses observations, and are found to be higher in the slow wind, as observed; however, they are under-predicted in both wind types. The modeled ion fractions of S, Si, and Fe are used to calculate line-of-sight intensities, which are compared to EIS observations above a coronal hole. The agreement is partial, and suggests that all ionization rates are under-predicted. Assuming the presence of suprathermal electrons improved the agreement with both EIS and Ulysses observations; importantly, the trend of higher ionization in the slow wind was maintained. The results suggest there can be a sub-class of slow wind that is steady and highly ionized. Further analysis shows it originates from coronal hole boundaries (CHB), where the modeled electron density and temperature are higher than inside the hole, leading to faster ionization. This property of CHBs is global, and observationally supported by EUV tomography.Comment: Submitted to the Astrophysical Journa

    ESPEN guidelines on definitions and terminology of clinical nutrition

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    BACKGROUND: A lack of agreement on definitions and terminology used for nutrition-related concepts and procedures limits the development of clinical nutrition practice and research. OBJECTIVE: This initiative aimed to reach a consensus for terminology for core nutritional concepts and procedures. METHODS: The European Society of Clinical Nutrition and Metabolism (ESPEN) appointed a consensus group of clinical scientists to perform a modified Delphi process that encompassed e-mail communication, face-to-face meetings, in-group ballots and an electronic ESPEN membership Delphi round. RESULTS: Five key areas related to clinical nutrition were identified: concepts; procedures; organisation; delivery; and products. One core concept of clinical nutrition is malnutrition/undernutrition, which includes disease-related malnutrition (DRM) with (eq. cachexia) and without inflammation, and malnutrition/undernutrition without disease, e.g. hunger-related malnutrition. Over-nutrition (overweight and obesity) is another core concept. Sarcopenia and frailty were agreed to be separate conditions often associated with malnutrition. Examples of nutritional procedures identified include screening for subjects at nutritional risk followed by a complete nutritional assessment. Hospital and care facility catering are the basic organizational forms for providing nutrition. Oral nutritional supplementation is the preferred way of nutrition therapy but if inadequate then other forms of medical nutrition therapy, i.e. enteral tube feeding and parenteral (intravenous) nutrition, becomes the major way of nutrient delivery. CONCLUSION: An agreement of basic nutritional terminology to be used in clinical practice, research, and the ESPEN guideline developments has been established. This terminology consensus may help to support future global consensus efforts and updates of classification systems such as the International Classification of Disease (ICD). The continuous growth of knowledge in all areas addressed in this statement will provide the foundation for future revisions

    A Global Two-temperature Corona and Inner Heliosphere Model: A Comprehensive Validation Study

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    The recent solar minimum with very low activity provides us a unique opportunity for validating solar wind models. During CR2077 (2008 November 20 through December 17), the number of sunspots was near the absolute minimum of solar cycle 23. For this solar rotation, we perform a multi-spacecraft validation study for the recently developed three-dimensional, two-temperature, Alfvén-wave-driven global solar wind model (a component within the Space Weather Modeling Framework). By using in situ observations from the Solar Terrestrial Relations Observatory (STEREO) A and B , Advanced Composition Explorer ( ACE ), and Venus Express , we compare the observed proton state (density, temperature, and velocity) and magnetic field of the heliosphere with that predicted by the model. Near the Sun, we validate the numerical model with the electron density obtained from the solar rotational tomography of Solar and Heliospheric Observatory /Large Angle and Spectrometric Coronagraph C2 data in the range of 2.4 to 6 solar radii. Electron temperature and density are determined from differential emission measure tomography (DEMT) of STEREO A and B Extreme Ultraviolet Imager data in the range of 1.035 to 1.225 solar radii. The electron density and temperature derived from the Hinode /Extreme Ultraviolet Imaging Spectrometer data are also used to compare with the DEMT as well as the model output. Moreover, for the first time, we compare ionic charge states of carbon, oxygen, silicon, and iron observed in situ with the ACE /Solar Wind Ion Composition Spectrometer with those predicted by our model. The validation results suggest that most of the model outputs for CR2077 can fit the observations very well. Based on this encouraging result, we therefore expect great improvement for the future modeling of coronal mass ejections (CMEs) and CME-driven shocks.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/98628/1/0004-637X_745_1_6.pd

    Solar interacting protons versus interplanetary protons in the core plus halo model of diffusive shock acceleration and stochastic re-acceleration

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    With the first observations of solar γ-rays from the decay of pions, the relationship of protons producing ground level enhancements (GLEs) on the Earth to those of similar energies producing the γ-rays on the Sun has been debated. These two populations may be either independent and simply coincident in large flares, or they may be, in fact, the same population stemming from a single accelerating agent and jointly distributed at the Sun and also in space. Assuming the latter, we model a scenario in which particles are accelerated near the Sun in a shock wave with a fraction transported back to the solar surface to radiate, while the remainder is detected at Earth in the form of a GLE. Interplanetary ions versus ions interacting at the Sun are studied for a spherical shock wave propagating in a radial magnetic field through a highly turbulent radial ray (the acceleration core) and surrounding weakly turbulent sector in which the accelerated particles can propagate toward or away from the Sun. The model presented here accounts for both the first-order Fermi acceleration at the shock front and the second-order, stochastic re-acceleration by the turbulence enhanced behind the shock. We find that the re-acceleration is important in generating the γ-radiation and we also find that up to 10% of the particle population can find its way to the Sun as compared to particles escaping to the interplanetary space

    In vivo testing of novel vaccine prototypes against Actinobacillus pleuropneumoniae

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    Actinobacillus pleuropneumoniae (A. pleuropneumoniae) is a Gram-negative bacterium that represents the main cause of porcine pleuropneumonia in pigs, causing significant economic losses to the livestock industry worldwide. A. pleuropneumoniae, as the majority of Gram-negative bacteria, excrete vesicles from its outer membrane (OM), accordingly defined as outer membrane vesicles (OMVs). Thanks to their antigenic similarity to the OM, OMVs have emerged as a promising tool in vaccinology. In this study we describe the in vivo testing of several vaccine prototypes for the prevention of infection by all known A. pleuropneumoniae serotypes. Previously identified vaccine candidates, the recombinant proteins ApfA and VacJ, administered individually or in various combinations with the OMVs, were employed as vaccination strategies. Our data show that the addition of the OMVs in the vaccine formulations significantly increased the specific IgG titer against both ApfA and VacJ in the immunized animals, confirming the previously postulated potential of the OMVs as adjuvant. Unfortunately, the antibody response raised did not translate into an effective protection against A. pleuropneumoniae infection, as none of the immunized groups following challenge showed a significantly lower degree of lesions than the controls. Interestingly, quite the opposite was true, as the animals with the highest IgG titers were also the ones bearing the most extensive lesions in their lungs. These results shed new light on A. pleuropneumoniae pathogenicity, suggesting that antibody-mediated cytotoxicity from the host immune response may play a central role in the development of the lesions typically associated with A. pleuropneumoniae infections

    Comprehensive diagnostics of acute myeloid leukemia by whole transcriptome RNA sequencing

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    Acute myeloid leukemia (AML) is caused by genetic aberrations that also govern the prognosis of patients and guide risk-adapted and targeted therapy. Genetic aberrations in AML are structurally diverse and currently detected by different diagnostic assays. This study sought to establish whole transcriptome RNA sequencing as single, comprehensive, and flexible platform for AML diagnostics. We developed HAMLET (Human AML Expedited Transcriptomics) as bioinformatics pipeline for simultaneous detection of fusion genes, small variants, tandem duplications, and gene expression with all information assembled in an annotated, user-friendly output file. Whole transcriptome RNA sequencing was performed on 100 AML cases and HAMLET results were validated by reference assays and targeted resequencing. The data showed that HAMLET accurately detected all fusion genes and overexpression of EVI1 irrespective of 3q26 aberrations. In addition, small variants in 13 genes that are often mutated in AML were called with 99.2% sensitivity and 100% specificity, and tandem duplications in FLT3 and KMT2A were detected by a novel algorithm based on soft-clipped reads with 100% sensitivity and 97.1% specificity. In conclusion, HAMLET has the potential to provide accurate comprehensive diagnostic information relevant for AML classification, risk assessment and targeted therapy on a single technology platform

    Increased efficacy for in-house validation of real-time PCR GMO detection methods

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    To improve the efficacy of the in-house validation of GMO detection methods (DNA isolation and real-time PCR, polymerase chain reaction), a study was performed to gain insight in the contribution of the different steps of the GMO detection method to the repeatability and in-house reproducibility. In the present study, 19 methods for (GM) soy, maize canola and potato were validated in-house of which 14 on the basis of an 8-day validation scheme using eight different samples and five on the basis of a more concise validation protocol. In this way, data was obtained with respect to the detection limit, accuracy and precision. Also, decision limits were calculated for declaring non-conformance (>0.9%) with 95% reliability. In order to estimate the contribution of the different steps in the GMO analysis to the total variation variance components were estimated using REML (residual maximum likelihood method). From these components, relative standard deviations for repeatability and reproducibility (RSDr and RSDR) were calculated. The results showed that not only the PCR reaction but also the factors ‘DNA isolation’ and ‘PCR day’ are important factors for the total variance and should therefore be included in the in-house validation. It is proposed to use a statistical model to estimate these factors from a large dataset of initial validations so that for similar GMO methods in the future, only the PCR step needs to be validated. The resulting data are discussed in the light of agreed European criteria for qualified GMO detection methods
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