481 research outputs found
The radio lighthouse CU Virginis: the spindown of a single main sequence star
The fast rotating star CU Virginis is a magnetic chemically peculiar star
with an oblique dipolar magnetic field. The continuum radio emission has been
interpreted as gyrosyncrotron emission arising from a thin magnetospheric
layer. Previous radio observations at 1.4 GHz showed that a 100% circular
polarized and highly directive emission component overlaps to the continuum
emission two times per rotation, when the magnetic axis lies in the plane of
the sky. This sort of radio lighthouse has been proposed to be due to cyclotron
maser emission generated above the magnetic pole and propagating
perpendicularly to the magnetic axis. Observations carried out with the
Australia Telescope Compact Array at 1.4 and 2.5 GHz one year after this
discovery show that this radio emission is still present, meaning that the
phenomenon responsible for this process is steady on a timescale of years. The
emitted radiation spans at least 1 GHz, being observed from 1.4 to 2.5 GHz. On
the light of recent results on the physics of the magnetosphere of this star,
the possibility of plasma radiation is ruled out. The characteristics of this
radio lighthouse provides us a good marker of the rotation period, since the
peaks are visible at particular rotational phases. After one year, they show a
delay of about 15 minutes. This is interpreted as a new abrupt spinning down of
the star. Among several possibilities, a quick emptying of the equatorial
magnetic belt after reaching the maximum density can account for the magnitude
of the breaking. The study of the coherent emission in stars like CU Vir, as
well as in pre main sequence stars, can give important insight into the angular
momentum evolution in young stars. This is a promising field of investigation
that high sensitivity radio interferometers such as SKA can exploit.Comment: Accepted to MNRAS, 8 pages, 7 figures, updated versio
Transport, Metabolism, and Function of Thyroid Hormones in the Developing Mammalian Brain
Ever since the discovery of thyroid hormone deficiency as the primary cause of cretinism in the second half of the 19th century, the crucial role of thyroid hormone (TH) signaling in embryonic brain development has been established. However, the biological understanding of TH function in brain formation is far from complete, despite advances in treating thyroid function deficiency disorders. The pleiotropic nature of TH action makes it difficult to identify and study discrete roles of TH in various aspect of embryogenesis, including neurogenesis and brain maturation. These challenges notwithstanding, enormous progress has been achieved in understanding TH production and its regulation, their conversions and routes of entry into the developing mammalian brain. The endocrine environment has to adjust when an embryo ceases to rely solely on maternal source of hormones as its own thyroid gland develops and starts to produce endogenous TH. A number of mechanisms are in place to secure the proper delivery and action of TH with placenta, blood-brain interface, and choroid plexus as barriers of entry that need to selectively transport and modify these hormones thus controlling their active levels. Additionally, target cells also possess mechanisms to import, modify and bind TH to further fine-tune their action. A complex picture of a tightly regulated network of transport proteins, modifying enzymes, and receptors has emerged from the past studies. TH have been implicated in multiple processes related to brain formation in mammals—neuronal progenitor proliferation, neuronal migration, functional maturation, and survival—with their exact roles changing over developmental time. Given the plethora of effects thyroid hormones exert on various cell types at different developmental periods, the precise spatiotemporal regulation of their action is of crucial importance. In this review we summarize the current knowledge about TH delivery, conversions, and function in the developing mammalian brain. We also discuss their potential role in vertebrate brain evolution and offer future directions for research aimed at elucidating TH signaling in nervous system development
Marginally low mass ratio close binary system V1191 Cyg
In this study, we present photometric and spectroscopic variations of the
extremely small mass ratio () late-type contact binary system
\astrobj{V1191 Cyg}. The parameters for the hot and cooler companions have been
determined as = 0.13 (1) , = 1.29 (8)
, = 0.52 (15) , = 1.31 (18)
, = 0.46 (25) , = 2.71 (80)
, the separation of the components is = 2.20(8) and
the distance of the system is estimated as 278(31) pc. Analyses of the times of
minima indicates a period increase of
days/yr that reveals a very high mass transfer rate of
/yr from the less massive
component to the more massive one. New observations show that the depths of the
minima of the light curve have been interchanged.Comment: Accepted for publication in New Astronomy, 16 pages, 2 figures, 4
table
The Lorentz force in atmospheres of CP stars: Aurigae
Several dynamical processes may induce considerable electric currents in the
atmospheres of magnetic chemically peculiar (CP) stars. The Lorentz force,
which results from the interaction between the magnetic field and the induced
currents, modifies the atmospheric structure and induces characteristic
rotational variability of the hydrogen Balmer lines. To study this phenomena we
have initiated a systematic spectroscopic survey of the Balmer lines variation
in magnetic CP stars. In this paper we continue presentation of results of the
program focusing on the high-resolution spectral observations of A0p star \aur
(HD 40312). We have detected a significant variability of the H,
H, and H spectral lines during full rotation cycle of the star.
This variability is interpreted in the framework of the model atmosphere
analysis, which accounts for the Lorentz force effects. Both the inward and
outward directed Lorentz forces are considered under the assumption of the
axisymmetric dipole or dipole+quadrupole magnetic field configurations. We
demonstrate that only the model with the outward directed Lorentz force in the
dipole+quadrupole configuration is able to reproduce the observed hydrogen line
variation. These results present new strong evidences for the presence of
non-zero global electric currents in the atmosphere of an early-type magnetic
star.Comment: 10 figure
Pion-Lambda-Sigma Coupling Extracted from Hyperonic Atoms
The latest measurements of the atomic level width in Sigma-hyperonic Pb atom
offer the most accurate datum in the region of low-energy Sigma-hyperon
physics. Atomic widths are due to the conversion of Sigma-nucleon into
Lambda-nucleon. In high angular momentum states this conversion is dominated by
the one-pion exchange. A joint analysis of the data of the scattering of
negative-Sigma on proton converting into a Lambda and a neutron and of the
atomic widths allows to extract a pseudovector pion-hyperon-Sigma coupling
constant of 0.048 with a statistical error of +-0.005 and a systematic one of
+-0.004. This corresponds to a pseudoscalar coupling constant of 13.3 with a
statistical uncertainty of 1.4 and a systematic one of 1.1.Comment: 12 pages, 1 figure, Use of Revtex.st
Advances in chemical and biological methods to identify microorganisms—from past to present
Fast detection and identification of microorganisms is a challenging and significant feature from industry to medicine. Standard approaches are known to be very time-consuming and labor-intensive (e.g., culture media and biochemical tests). Conversely, screening techniques demand a quick and low-cost grouping of bacterial/fungal isolates and current analysis call for broad reports of microorganisms, involving the application of molecular techniques (e.g., 16S ribosomal RNA gene sequencing based on polymerase chain reaction). The goal of this review is to present the past and the present methods of detection and identification of microorganisms, and to discuss their advantages and their limitations.C.F.R. would like to thank the Portuguese Foundation for Science and Technology (FCT–Portugal) for the C.F.R. for the project UID/EQU/00511/2019—Laboratory for Process Engineering, Environment, Biotechnology, and Energy—LEPABE funded by national funds through FCT/MCTES (PIDDAC) and N.M. for the Strategic project ref. UID/BIM/04293/2013 and “NORTE2020 - Programa Operacional Regional do Norte” (NORTE-01-0145-FEDER-000012)
Longitudinal Analysis of Quality of Life, Clinical, Radiographic, Echocardiographic, and Laboratory Variables in Dogs with Preclinical Myxomatous Mitral Valve Disease Receiving Pimobendan or Placebo: The EPIC Study
Background: Changes in clinical variables associated with the administration of pimobendan to dogs with preclinical myxomatous mitral valve disease (MMVD) and cardiomegaly have not been described.
Objectives: To investigate the effect of pimobendan on clinical variables and the relationship between a change in heart size and the time to congestive heart failure (CHF) or cardiac-related death (CRD) in dogs with MMVD and cardiomegaly. To determine whether pimobendan-treated dogs differ from dogs receiving placebo at onset of CHF.
Animals: Three hundred and fifty-four dogs with MMVD and cardiomegaly.
Materials and Methods: Prospective, blinded study with dogs randomized (ratio 1:1) to pimobendan (0.4-0.6 mg/kg/d) or placebo. Clinical, laboratory, and heart-size variables in both groups were measured and compared at different time points (day 35 and onset of CHF) and over the study duration. Relationships between short-term changes in echocardiographic variables and time to CHF or CRD were explored.
Results: At day 35, heart size had reduced in the pimobendan group:median change in (Delta) LVIDDN -0.06 (IQR:-0.15 to + 0.02), P < 0.0001, and LA:Ao -0.08 (IQR:-0.23 to + 0.03), P < 0.0001. Reduction in heart size was associated with increased time to CHF or CRD. Hazard ratio for a 0.1 increase in Delta LVIDDN was 1.26, P = 0.0003. Hazard ratio for a 0.1 increase in Delta LA:Ao was 1.14, P = 0.0002. At onset of CHF, groups were similar.
Conclusions and Clinical Importance: Pimobendan treatment reduces heart size. Reduced heart size is associated with improved outcome. At the onset of CHF, dogs treated with pimobendan were indistinguishable from those receiving placebo
Effect of Pimobendan in Dogs with Preclinical Myxomatous Mitral Valve Disease and Cardiomegaly: The EPIC Study - A Randomized Clinical Trial
Background: Pimobendan is effective in treatment of dogs with congestive heart failure (CHF) secondary to myxomatous mitral valve disease (MMVD). Its effect on dogs before the onset of CHF is unknown. Hypothesis/Objectives: Administration of pimobendan (0.4-0.6 mg/kg/d in divided doses) to dogs with increased heart size secondary to preclinical MMVD, not receiving other cardiovascular medications, will delay the onset of signs of CHF, cardiac-related death, or euthanasia. Animals: 360 client-owned dogs with MMVD with left atrial-to-aortic ratio >= 1.6, normalized left ventricular internal diameter in diastole >= 1.7, and vertebral heart sum >10.5. Methods: Prospective, randomized, placebo-controlled, blinded, multicenter clinical trial. Primary outcome variable was time to a composite of the onset of CHF, cardiac-related death, or euthanasia. Results: Median time to primary endpoint was 1228 days (95% CI: 856-NA) in the pimobendan group and 766 days (95% CI: 667-875) in the placebo group (P = .0038). Hazard ratio for the pimobendan group was 0.64 (95% CI: 0.47-0.87) compared with the placebo group. The benefit persisted after adjustment for other variables. Adverse events were not different between treatment groups. Dogs in the pimobendan group lived longer (median survival time was 1059 days (95% CI: 952-NA) in the pimobendan group and 902 days (95% CI: 747-1061) in the placebo group) (P = .012). Conclusions and Clinical Importance: Administration of pimobendan to dogs with MMVD and echocardiographic and radiographic evidence of cardiomegaly results in prolongation of preclinical period and is safe and well tolerated. Prolongation of preclinical period by approximately 15 months represents substantial clinical benefit
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