545 research outputs found
The Hard X-ray Emission of Cen A
The radio galaxy Cen A has been detected all the way up to the TeV energy
range. This raises the question about the dominant emission mechanisms in the
high-energy domain. Spectral analysis allows us to put constraints on the
possible emission processes. Here we study the hard X-ray emission as measured
by INTEGRAL in the 3-1000 keV energy range, in order to distinguish between a
thermal and non-thermal inverse Compton process. The hard X-ray spectrum of Cen
A shows a significant cut-off at energies Ec = 434 (+106 -73) keV with an
underlying power law of photon index 1.73 +- 0.02. A more physical model of
thermal Comptonisation (compPS) gives a plasma temperature of kT = 206+-62 keV
within the optically thin corona with Compton parameter y = 0.42 (+0.09 -0.06).
The reflection component is significant at the 1.9 sigma level with R = 0.12
(+0.09 -0.10), and a reflection strength R>0.3 can be excluded on a 3 sigma
level. Time resolved spectral studies show that the flux, absorption, and
spectral slope varied in the range f(3-30 keV) = (1.2 - 9.2)e-10 erg/cm**2/s,
NH = (7 - 16)e22 1/cm**2, and photon index 1.75 - 1.87. Extending the cut-off
power law or the Comptonisation model to the gamma-ray range shows that they
cannot account for the high-energy emission. On the other hand, also a broken
or curved power law model can represent the data, therefore a non-thermal
origin of the X-ray to GeV emission cannot be ruled out. The analysis of the
SPI data provides no sign of significant emission from the radio lobes and
gives a 3 sigma upper limit of f(40-1000 keV) < 0.0011 ph/cm**2/s. While
gamma-rays, as detected by CGRO and Fermi, are caused by non-thermal (jet)
processes, the main process in the hard X-ray emission of Cen A is still not
unambiguously determined, being either dominated by thermal inverse Compton
emission, or by non-thermal emission from the base of the jet.Comment: 8 pages, 6 figures, accepted for publication in A&
The ultra-compact binary 4U1850-087 observed with INTEGRAL: hard X-ray emission from an X-ray burster
The X-ray burster 4U1850-087, located in the Galactic globular cluster
NGC6712, is an ultracompact binary (orbital period~21 min),likely harbouring a
degenerate companion.The source has been observed at soft gamma-rays several
times with the INTEGRAL satellite,during the monitoring of the Galactic plane,
with an unprecedented exposure time.We analysed all available INTEGRAL
observations, with the main aim of studying the long-term behaviour of this
Galactic bulge X-ray burster.The spectral results are based on the systematic
analysis of all INTEGRAL observations covering the source position performed
between March 2003 and November 2005.The source X-ray emission is hard and is
observed, for the first time, up to 100keV.A broad-band spectrum obtained
combining the INTEGRAL spectrum together with a quasi-simultaneous XMM-Newton
observation performed in September 2003 is well modeled with a disk-blackbody
emission (with kTin=0.8keV) together with a power-law (photon index=2.1).The
2-100keV luminosity is 1.5E36 erg/s (assuming a distance of 6.8kpc).Comment: Accepted for publication in Astronomy & Astrophysic
Revisiting the exercise heart rate-music tempo preference relationship
In the present study, we investigated a hypothesized quartic relationship (meaning three inflection points) between exercise heart rate (HR) and preferred music tempo. Initial theoretical predictions suggested a positive linear relationship (Iwanaga, 1995a, 1995b); however, recent experimental work has shown that as exercise HR increases, step changes and plateaus that punctuate the profile of music tempo preference may occur (Karageorghis, Jones, & Stuart, 2008). Tempi bands consisted of slow (95â100 bpm), medium
(115â120 bpm), fast (135â140 bpm), and very fast (155â160 bpm) music. Twenty-eight active undergraduate students cycled at exercise intensities representing 40, 50, 60, 70, 80, and 90% of their maximal HR reserve while their music preference was assessed using a 10-point scale. The Exercise Intensity x Music Tempo interaction was significant, F(6.16, 160.05) = 7.08, p < .001, ηp 2 =.21, as was the test for both cubic and quartic trajectories in the exercise HRâpreferred-music-tempo relationship (p < .001). Whereas slow tempo music was not preferred at any exercise intensity, preference for fast tempo increased, relative to medium and very fast tempo music, as exercise intensity increased. The implications for the prescription of music in exercise and physical activity contexts are discussed
Modeling the early stage of DNA sequence recognition within RecA nucleoprotein filaments
Homologous recombination is a fundamental process enabling the repair of double-strand breaks with a high degree of fidelity. In prokaryotes, it is carried out by RecA nucleofilaments formed on single-stranded DNA (ssDNA). These filaments incorporate genomic sequences that are homologous to the ssDNA and exchange the homologous strands. Due to the highly dynamic character of this process and its rapid propagation along the filament, the sequence recognition and strand exchange mechanism remains unknown at the structural level. The recently published structure of the RecA/DNA filament active for recombination (Chen et al., Mechanism of homologous recombination from the RecA-ssDNA/dsDNA structure, Nature 2008, 453, 489) provides a starting point for new exploration of the system. Here, we investigate the possible geometries of association of the early encounter complex between RecA/ssDNA filament and double-stranded DNA (dsDNA). Due to the huge size of the system and its dense packing, we use a reduced representation for protein and DNA together with state-of-the-art molecular modeling methods, including systematic docking and virtual reality simulations. The results indicate that it is possible for the double-stranded DNA to access the RecA-bound ssDNA while initially retaining its WatsonâCrick pairing. They emphasize the importance of RecA L2 loop mobility for both recognition and strand exchange
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A variant in long palate, lung and nasal epithelium clone 1 is associated with cholera in a Bangladeshi population
Vibrio cholerae causes a dehydrating diarrheal illness that can be rapidly fatal in the absence of specific treatment. The organism is an historic scourge and, like similar infectious diseases, may have influenced the evolution of the human genome. We report here the results of the first candidate gene association study of cholera. In a family-based study of 76 pedigrees from Dhaka, Bangladesh, we evaluated the association between cholera and five candidate genesâthe cystic fibrosis transmembrane receptor; lactoferrin; long palate, lung and nasal epithelium clone 1 (LPLUNC1); estrogen-related receptor alpha and calcium-activated chloride channel 1. We found a significant association with a marker in the promoter region of LPLUNC1 (rs11906665), a member of a family of evolutionarily conserved innate immunity proteins. An earlier microarray-based study of duodenal biopsies showed significantly increased expression of LPLUNC1 in cholera patients compared with healthy control subjects. Our results suggest that variation in host innate immune responses may influence the outcome of exposure to V. cholerae in an endemic setting.Organismic and Evolutionary BiologyOther Research Uni
Preventable hospital admissions among the homeless in California: A retrospective analysis of care for ambulatory care sensitive conditions
Background
Limited research exists that investigates hospital admissions for ambulatory care sensitive conditions (ACSCs) among the homeless, who frequently lack a usual source of care. This study profiled ACSC admissions for homeless patients.
Methods
Bivariate analyses and logistic regression were completed to investigate ACSC and non-ACSC admissions among homeless patients using the 2010 California State Inpatient Database.
Results
Homeless patients admitted for an ACSC were mostly male, non-Hispanic white, and on average 49.9ĂąâŹËyears old. In the predictive model, the odds of an ACSC admission among homeless patients increased when they were black, admitted to the emergency department or transferred from another health facility. Having Medicare was associated with a decreased odds of an ACSC admission.
Conclusions
Specific characteristics are associated with a greater likelihood of an ACSC admission. Research should examine how these characteristics contribute to ACSC hospitalizations and findings should be linked to programs designed to serve as a safety-net for homeless patients to reduce hospitalizations
Hard X-ray emission from the Galactic ridge
We present results of a study of the Galactic ridge X-ray emission (GRXE) in
hard X-rays performed with the IBIS telescope aboard INTEGRAL. The imaging
capabilities of this coding aperture telescope make it possible to account for
the flux from bright Galactic point sources whereas the wide field of view
permits to collect large flux from the underlying GRXE. Extensive study of the
IBIS/ISGRI detector background allowed us to construct a model that predicts
the detector count rate with % accuracy in the energy band 17-60 keV.
The derived longitude and latitude profiles of the ridge emission are in good
agreement with the Galactic distribution of stars obtained from infrared
observations. This, along with the measured hard X-ray spectrum of the Galactic
ridge emission strongly indicates its stellar origin. The derived unit stellar
mass emissivity of the ridge in the energy band 17-60 keV, \lummass (assuming a bulge mass of )
agrees with that of local (in the Solar neigborhood) accreting magnetic white
dwarf binaries - dominant contributors to the GRXE at these energies. In
addition, the shape of the obtained GRXE spectrum can be used to determine the
average mass of white dwarfs in such systems in the Galaxy as \sim0.5
M_{\sun}. The total hard X-ray luminosity of the GRXE is \lum in the 17--60 keV band. At energies 70--200 keV
no additional contribution to the total emission of the Galaxy apart from the
detected point sources is seen.Comment: 13 pages, 19 figures, submitted to Astronomy and Astrophysic
Status of Muon Collider Research and Development and Future Plans
The status of the research on muon colliders is discussed and plans are
outlined for future theoretical and experimental studies. Besides continued
work on the parameters of a 3-4 and 0.5 TeV center-of-mass (CoM) energy
collider, many studies are now concentrating on a machine near 0.1 TeV (CoM)
that could be a factory for the s-channel production of Higgs particles. We
discuss the research on the various components in such muon colliders, starting
from the proton accelerator needed to generate pions from a heavy-Z target and
proceeding through the phase rotation and decay ()
channel, muon cooling, acceleration, storage in a collider ring and the
collider detector. We also present theoretical and experimental R & D plans for
the next several years that should lead to a better understanding of the design
and feasibility issues for all of the components. This report is an update of
the progress on the R & D since the Feasibility Study of Muon Colliders
presented at the Snowmass'96 Workshop [R. B. Palmer, A. Sessler and A.
Tollestrup, Proceedings of the 1996 DPF/DPB Summer Study on High-Energy Physics
(Stanford Linear Accelerator Center, Menlo Park, CA, 1997)].Comment: 95 pages, 75 figures. Submitted to Physical Review Special Topics,
Accelerators and Beam
Structural and Functional Insights into the Malaria Parasite Moving Junction Complex
Members of the phylum Apicomplexa, which include the malaria parasite Plasmodium, share many features in their invasion mechanism in spite of their diverse host cell specificities and life cycle characteristics. The formation of a moving junction (MJ) between the membranes of the invading apicomplexan parasite and the host cell is common to these intracellular pathogens. The MJ contains two key parasite components: the surface protein Apical Membrane Antigen 1 (AMA1) and its receptor, the Rhoptry Neck Protein (RON) complex, which is targeted to the host cell membrane during invasion. In particular, RON2, a transmembrane component of the RON complex, interacts directly with AMA1. Here, we report the crystal structure of AMA1 from Plasmodium falciparum in complex with a peptide derived from the extracellular region of PfRON2, highlighting clear specificities of the P. falciparum RON2-AMA1 interaction. The receptor-binding site of PfAMA1 comprises the hydrophobic groove and a region that becomes exposed by displacement of the flexible Domain II loop. Mutations of key contact residues of PfRON2 and PfAMA1 abrogate binding between the recombinant proteins. Although PfRON2 contacts some polymorphic residues, binding studies with PfAMA1 from different strains show that these have little effect on affinity. Moreover, we demonstrate that the PfRON2 peptide inhibits erythrocyte invasion by P. falciparum merozoites and that this strong inhibitory potency is not affected by AMA1 polymorphisms. In parallel, we have determined the crystal structure of PfAMA1 in complex with the invasion-inhibitory peptide R1 derived by phage display, revealing an unexpected structural mimicry of the PfRON2 peptide. These results identify the key residues governing the interactions between AMA1 and RON2 in P. falciparum and suggest novel approaches to antimalarial therapeutics
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