1,026 research outputs found
Magnetorotational Instability in Core-Collapse Supernovae
We discuss the relevance of the magnetorotational instability (MRI) in
core-collapse supernovae (CCSNe). Our recent numerical studies show that in
CCSNe, the MRI is terminated by parasitic instabilities of the Kelvin-Helmholtz
type. To determine whether the MRI can amplify initially weak magnetic fields
to dynamically relevant strengths in CCSNe, we performed three-dimensional
simulations of a region close to the surface of a differentially rotating
proto-neutron star in non-ideal magnetohydrodynamics with two different
numerical codes. We find that under the conditions prevailing in proto-neutron
stars, the MRI can amplify the magnetic field by (only) one order of magnitude.
This severely limits the role of MRI channel modes as an agent amplifying the
magnetic field in proto-neutron stars starting from small seed fields.Comment: Proceedings in Acta Physica Polonica B, Proceedings Supplement, Vol.
10, No. 2, p.361, 4 pages, 1 figur
Pleuritis en la Valencia romana
X Congreso Nacional de Paleopatología. Univesidad Autónoma de Madrid, septiembre de 200
Shine bright or live long: substituent effects in [Cu(N^N)(P^P)]+-based light-emitting electrochemical cells where N^N is a 6-substituted 2,2'-bipyridine
We report [Cu(P^P)(N^N)][PF6] complexes with P^P = bis(2-(diphenylphosphino)phenyl)ether (POP) or 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos) and N^N = 6-methyl-2,2′-bipyridine (Mebpy), 6-ethyl-2,2′-bipyridine (Etbpy), 6,6′-dimethyl-2,2′-bipyridine (Me2bpy) or 6-phenyl-2,2′-bipyridine (Phbpy). The crystal structures of [Cu(POP)(Phbpy)][PF6]·Et2O, [Cu(POP)(Etbpy)][PF6]·Et2O, [Cu(xantphos)(Me2bpy)][PF6], [Cu(xantphos)(Mebpy)][PF6]·CH2Cl2·0.4Et2O, [Cu(xantphos)(Etbpy)][PF6]·CH2Cl2·1.5H2O and [Cu(xantphos)(Phbpy)][PF6] are described; each copper(I) centre is distorted tetrahedral. In the crystallographically determined structures, the N^N domain in [Cu(xantphos)(Phbpy)]+ and [Cu(POP)(Phbpy)]+ is rotated ∼180° with respect to its orientation in [Cu(xantphos)(Mebpy)]+, [Cu(POP)(Etbpy)]+ and [Cu(xantphos)(Etbpy)]+; in each complex containing xantphos, the xanthene ‘bowl’ retains the same conformation in the solid-state structures. The two conformers resulting from the 180° rotation of the N^N ligand were optimized at the B3LYP-D3/(6-31G**+LANL2DZ) level and are close in energy for each complex. Variable temperature NMR spectroscopy evidences the presence of two conformers of [Cu(xantphos)(Phbpy)]+ in solution which are related by inversion of the xanthene unit. The complexes exhibit MLCT absorption bands in the range 378 to 388 nm, and excitation into each MLCT band leads to yellow emissions. Photoluminescence quantum yields (PLQYs) increase from solution to thin-film and powder; the highest PLQYs are observed for powdered [Cu(xantphos)(Mebpy)][PF6] (34%), [Cu(xantphos)(Etbpy)][PF6] (37%) and [Cu(xantphos)(Me2bpy)][PF6] (37%) with lifetimes of 9.6–11 μs. Density functional theory calculations predict that the emitting triplet (T1) involves an electron transfer from the Cu–P^P environment to the N^N ligand and therefore shows a 3MLCT character. T1 is calculated to be ∼0.20 eV lower in energy than the first singlet excited state (S1). The [Cu(P^P)(N^N)][PF6] ionic transition-metal (iTMC) complexes were tested in light-emitting electrochemical cells (LECs). Turn-on times are fast, and the LEC with [Cu(xantphos)(Me2bpy)][PF6] achieves a maximum efficacy of 3.0 cd A−1 (luminance = 145 cd m−2) with a lifetime of 1 h; on going to the [Cu(xantphos)(Mebpy)][PF6]-based LEC, the lifetime exceeds 15 h but at the expense of the efficacy (1.9 cd A−1). The lifetimes of LECs containing [Cu(xantphos)(Etbpy)][PF6] and [Cu(POP)(Etbpy)][PF6] exceed 40 and 80 h respectively
Estimation of the mechanical properties of the eye through the study of its vibrational modes
Measuring the eye's mechanical properties in vivo and with minimally invasive
techniques can be the key for individualized solutions to a number of eye
pathologies. The development of such techniques largely relies on a
computational modelling of the eyeball and, it optimally requires the synergic
interplay between experimentation and numerical simulation. In Astrophysics and
Geophysics the remote measurement of structural properties of the systems of
their realm is performed on the basis of (helio-)seismic techniques. As a
biomechanical system, the eyeball possesses normal vibrational modes
encompassing rich information about its structure and mechanical properties.
However, the integral analysis of the eyeball vibrational modes has not been
performed yet. Here we develop a new finite difference method to compute both
the spheroidal and, specially, the toroidal eigenfrequencies of the human eye.
Using this numerical model, we show that the vibrational eigenfrequencies of
the human eye fall in the interval 100 Hz - 10 MHz. We find that compressible
vibrational modes may release a trace on high frequency changes of the
intraocular pressure, while incompressible normal modes could be registered
analyzing the scattering pattern that the motions of the vitreous humour leave
on the retina. Existing contact lenses with embebed devices operating at high
sampling frequency could be used to register the microfluctuations of the
eyeball shape we obtain. We advance that an inverse problem to obtain the
mechanical properties of a given eye (e.g., Young's modulus, Poisson ratio)
measuring its normal frequencies is doable. These measurements can be done
using non-invasive techniques, opening very interesting perspectives to
estimate the mechanical properties of eyes in vivo. Future research might
relate various ocular pathologies with anomalies in measured vibrational
frequencies of the eye.Comment: Published in PLoS ONE as Open Access Research Article. 17 pages, 5
color figure
A new general relativistic magnetohydrodynamics code for dynamical spacetimes
We present a new numerical code that solves the general relativistic magneto-hydrodynamical (GRMHD) equations coupled to the Einstein equations for the evolution of a dynamical spacetime within a conformally-flat approximation. This code has been developed with the main objective of studying astrophysical scenarios in which both, high magnetic fields and strong gravitational fields appear, such as the magneto-rotational collapse of stellar cores, the collapsar model of GRBs, and the evolution of neutron stars. The code is based on an existing and thoroughly tested purely hydrodynamical code and on its extension to accommodate weakly magnetized fluids (passive magnetic-field approximation). These codes have been applied in the past to simulate the aforementioned scenarios with increasing levels of sophistication in the input physics. The numerical code we present here is based on high-resolution shock- capturing schemes to solve the GRMHD equations, which are cast in first-order, flux-conservative hyperbolic form, together with the flux constraint transport method to ensure the solenoidal condition of the magnetic field. Since the astrophysical applications envisaged do not deviate significantly from spherical symmetry, the conformal flatness condition approximation is used for the formulation of the Einstein equations; this has repeatedly shown to yield very good agreement with full general relativistic simulations of core- collapse supernovae and the evolution of isolated neutron stars. In addition, the code can handle several equations of state, from simple analytical expressions to microphysical tabulated ones. In this paper we present stringent tests of our new GRMHD numerical code, which show its ability to handle all aspects appearing in the astrophysical scenarios for which the code is intended, namely relativistic shocks, highly magnetized fluids, and equilibrium configurations of magnetized neutron stars. As an application, magneto- rotational core-collapse simulations of a realistic progenitor are presented and the results compared with our previous findings in the passive magnetic-field [email protected]; [email protected]
Phycomyces
This monographic review on a fungus is not addressed to mycologists. None of the authors has been trained or has otherwise acquired a general proficiency in mycology. They are motivated by a common interest in the performances of signal handling exhibited by the sense organs of all organisms and by the desire to attack these as yet totally obscure aspects of molecular biology by the study of a microorganism with certain desirable properties.
The sporangiophore of the fungus Phycomyces is a gigantic, single-celled, erect, cylindrical, aerial hypha. It is sensitive to at least four distinct stimuli: light, gravity, stretch, and some unknown stimulus by which it avoids solid objects. These stimuli control a common output, the growth rate, producing either temporal changes in growth rate or tropic responses.
We are interested in the output because it gives us information about the reception of the various signals. In the absence of external stimuli, the growth rate is controlled by internal signals keeping the network of biochemical processes in balance. The external stimuli interact with the internal signals. We wish to inquire into the early steps of this interaction. For light, for instance, the cell must have a receptor pigment as the first
mediator. What kind of a molecule is this pigment? Which organelle contains it? What chemical reaction happens after a light quantum has been absorbed? And how is the information introduced by this primary photochemical event amplified in a controlled manner and processed in the next step? How do a few quanta or a few molecules trigger macroscopic responses? Will we find ourselves confronted with devices wholly distinct from anything now known in biology
Identification of a microRNA signature for the diagnosis of fibromyalgia
Diagnosis of fibromyalgia (FM), a chronic musculoskeletal pain syndrome characterized by generalized body pain, hyperalgesia and other functional and emotional comorbidities, is a challenging process hindered by symptom heterogeneity and clinical overlap with other disorders. No objective diagnostic method exists at present. The aim of this study was to identify changes in miRNA expression profiles (miRNome) of these patients for the development of a quantitative diagnostic method of FM. In addition, knowledge of FM patient miRNomes should lead to a deeper understanding of the etiology and/or symptom severity of this complex disease.Genome-wide expression profiling of miRNAs was assessed in Peripheral Blood Mononuclear Cells (PBMCs) of FM patients (N=11) and population-age-matched controls (N=10) using human v16-miRbase 3D-Gene microarrays (Toray Industries, Japan). Selected miRNAs from the screen were further validated by RT-qPCR. Participating patients were long term sufferers (over 10 years) diagnosed by more than one specialist under 1990 American College of Rheumatology criteria.Microarray analysis of FM patient PBMCs evidenced a marked downregulation of hsa-miR223-3p, hsa-miR451a, hsa-miR338-3p, hsa-miR143-3p, hsa-miR145-5p and hsa-miR-21-5p (4-fold or more). All but the mildest inhibited miRNA, hsa-miR-21-5p, were validated by RT-qPCR. Globally, 20% of the miRNAs analyzed (233/1212) showed downregulation of at least 2-fold in patients. This might indicate a general de-regulation of the miRNA synthetic pathway in FM. No significant correlations between miRNA inhibition and FM cardinal symptoms could be identified. However, the patient with the lowest score for mental fatigue coincided with the mildest inhibition in four of the five miRNAs associated with the FM-group.We propose a signature of five strikingly downregulated miRNAs (hsa-miR223-3p, hsa-miR451a, hsa-miR338-3p, hsa-miR143-3p and hsa-miR145-5p) to be used as biomarkers of FM. Validation in larger study groups is required before the results can be transferred to the clinic.The study was funded by the Fundación Universidad Católica de Valencia “San Vicente Mártir”(UCV) Research Grant Program (2011-011-02, 2011-011-04 and 2012-011-008) the Fundación Cátedra Umivale at the UCV and the 3D-Gene International Competition Award to EOMedicin
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