4,446 research outputs found

    Neutral gas in Lyman-alpha emitting galaxies Haro 11 and ESO 338-IG04 measured through sodium absorption

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    Context. The Lyman alpha emission line of galaxies is an important tool for finding galaxies at high redshift, and thus probe the structure of the early universe. However, the resonance nature of the line and its sensitivity to dust and neutral gas is still not fully understood. Aims. We present measurements of the velocity, covering fraction and optical depth of neutral gas in front of two well known local blue compact galaxies that show Lyman alpha in emission: ESO 338-IG 04 and Haro 11. We thus test observationally the hypothesis that Lyman alpha can escape through neutral gas by being Doppler shifted out of resonance. Methods. We present integral field spectroscopy from the GIRAFFE/Argus spectrograph at VLT/FLAMES in Paranal, Chile. The excellent wavelength resolution allows us to accurately measure the velocity of the ionized and neutral gas through the H-alpha emission and Na D absorption, which traces the ionized medium and cold interstellar gas, respectively. We also present independent measurements with the VLT/X-shooter spectrograph which confirm our results. Results. For ESO 338-IG04, we measure no significant shift of neutral gas. The best fit velocity is -15 (16) km/s. For Haro 11, we see an outflow from knot B at 44 (13) km/s and infalling gas towards knot C with 32 (12) km/s. Based on the relative strength of the Na D absorption lines, we estimate low covering fractions of neutral gas (down to 10%) in all three cases. Conclusions. The Na D absorption likely occurs in dense clumps with higher column densities than where the bulk of the Ly-alpha scattering takes place. Still, we find no strong correlation between outflowing neutral gas and a high Lyman alpha escape fraction. The Lyman alpha photons from these two galaxies are therefore likely escaping due to a low column density and/or covering fraction.Comment: 9 pages, 3 figure

    High Resolution X-Ray Imaging of the Center of IC342

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    We presented the result of a high resolution (FWHM~0.5'') 12 ks Chandra HRC-I observation of the starburst galaxy IC342 taken on 2 April 2006. We identified 23 X-ray sources within the central 30' x 30' region of IC342. Our HRC-I observation resolved the historical Ultraluminous X-ray sources (ULX), X3, near the nucleus into 2 sources, namely C12 and C13, for the first time. The brighter source C12, with L(0.08-10keV)=(6.66\pm0.45)\times10^{38}ergs^-1, was spatially extended (~82 pc x 127 pc). From the astrometric registration of the X-ray image, C12 was at R.A.=03h:46m:48.43s, decl.=+68d05m47.45s, and was closer to the nucleus than C13. Thus we concluded that source was not an ULX and must instead be associated with the nucleus. The fainter source C13, with L(0.08-10keV)=(5.1\pm1.4) x 10^{37}ergs^-1 was consistent with a point source and located $6.51'' at P.A. 240 degree of C12. We also analyzed astrometrically corrected optical Hubble Space Telescope and radio Very Large Array images, a comparison with the X-ray image showed similarities in their morphologies. Regions of star formation within the central region of IC342 were clearly visible in HST H alpha image and this was the region where 3 optical star clusters and correspondingly our detected X-ray source C12 were observed. We found that a predicted X-ray emission from starburst was very close to the observed X-ray luminosity of C12, suggesting that nuclear X-ray emission in IC342 was dominated by starburst. Furthermore, we discussed the possibility of AGN in the nucleus of IC342. Although our data was not enough to give a firm existence of an AGN, it could not be discarded.Comment: 29 page, 8 figures, accepted by Ap

    Nuclear activity and massive star formation in the low luminosity AGN NGC4303: Chandra X-ray observations

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    We present evidence of the co-existence of either an AGN or an ultraluminous X-ray source (ULX), together with a young super stellar cluster in the 3 central parsecs of NGC4303. The galaxy contains a low luminosity AGN and hosts a number of starburst regions in a circumnuclear spiral, as well as in the nucleus itself. A high spatial resolution Chandra image of this source reveals that the soft X-ray emission traces the ultraviolet nuclear spiral down to a core, which is unresolved both in soft and hard X-rays. The astrometry of the X-ray core coincides with the UV core within the Chandra positioning accuracy. The total X-ray luminosity of the core, 1.5*10^{39} erg/s, is similar to that from some LINERs or from the weakest Seyferts detected so far. The soft X-rays in both the core and the extended structure surrounding it can be well reproduced by evolutionary synthesis models (which include the emission expected from single stars, the hot diffuse gas, supernova remnants and binary systems), consistent with the properties of the young stellar clusters identified in the UV. The hard X-ray tail detected in the core spectrum, however, most likely requires the presence of an additional source. This additional source could either be a weak active nucleus black hole or an ultraluminous X-ray object. The implications of these results are discussed.Comment: 37 pages, 7 figures, ApJ accepte

    Model-based Aeroservoelastic Design and Load Alleviation of Large Wind Turbine Blades

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    This paper presents an aeroservoelastic modeling approach for dynamic load alleviation in large wind turbines with trailing-edge aerodynamic surfaces. The tower, potentially on a moving base, and the rotating blades are modeled using geometrically non-linear composite beams, which are linearized around reference conditions with arbitrarily-large structural displacements. Time-domain aerodynamics are given by a linearized 3-D unsteady vortexlattice method and the resulting dynamic aeroelastic model is written in a state-space formulation suitable for model reductions and control synthesis. A linear model of a single blade is used to design a Linear-Quadratic-Gaussian regulator on its root-bending moments, which is finally shown to provide load reductions of about 20% in closed-loop on the full wind turbine non-linear aeroelastic model

    Scanning Electron Microscopy of 2,8-Dihydroxyadenine Crystals and Stones

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    The lack of purine salvage enzyme, adenine phosphoribosyltransferase (APRT), leads to 2,8-dihydroxyadenine stone formation and/or crystalluria because it is insoluble in urine. Urolithiasis composed of 2,8-dihydroxyadenine is not only formed in a complete defect of APRT, but also in a partial deficiency of this enzyme. The defect is inherited as an autosomal recessive trait, the homozygous state is associated with high urinary levels of 2,8-dihydroxyadenine and with crystalluria, calculus formation, and potential nephrotoxicity. Determination of the APRT activity will facilitate quantification of the enzyme deficiency and elucidation of the hereditary history. 2,8-dihydroxyadenine excretion in the 24-hour urine and its circadian rhythm were determined using a new method of high performance liquid chromatography determination. By means of a standard case presentation, we illustrate the analysis of urinary sediments and calculi as well as the scanning electron microscopic images of this kind of stone

    Patchy Reconnection in a Y-Type Current Sheet

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    We study the evolution of the magnetic field in a Y-type current sheet subject to a brief, localized magnetic reconnection event. The reconnection produces up- and down-flowing reconnected flux tubes which rapidly decelerate when they hit the Y-lines and underlying magnetic arcade loops at the ends of the current sheet. This localized reconnection outflow followed by a rapid deceleration reproduces the observed behavior of post-CME downflowing coronal voids. These simulations support the hypothesis that these observed coronal downflows are the retraction of magnetic fields reconnected in localized patches in the high corona.Comment: 4 pages, 3 figure

    The blackcap (Sylvia atricapilla) genome reveals a species-specific accumulation of LTR retrotransposons

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    Transposable elements are mobile genetic elements that have the ability to move around the genome, and as such can be a source of genome variability. Transposable elements (TEs) are ubiquitous and many are found within a wide variety of life. Based on their characteristics we can annotate TEs within the host genome and classify them into specific TE types and families. The increasing number of available high-quality genome references in recent years provides an excellent resource that will enhance the understanding of the role of recently active TEs on genetic variation and phenotypic evolution. Here we showcase this through a high-quality TE annotation of the Eurasian blackcap (Sylvia atricapilla), as our chromosome resolution reference genome allowed the reconstruction of difficult-to-assemble regions. We have the ability to distinguish species-specific and non-specific TEs. We investigate how these TE categories are distributed along the genome and evaluate their correlation with four genomic features: recombination rate, gene coverage, CpG island coverage and GC coverage. We found a marked difference between species-specific and non-specific TEs. While species-specific TEs were negatively correlated with both GC content and recombination rate, the correlation with recombination rate disappeared and turned positive for GC content when considering non-specific TEs

    The central role of IL-33/IL-1RL1 pathway in asthma:From pathogenesis to intervention

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    Interleukin-33 (IL-33), a member of the IL-1 family, and its cognate receptor, Interleukin-1 receptor like-1 (IL-1RL1 or ST2), are susceptibility genes for childhood asthma. In response to cellular damage, IL-33 is released from barrier tissues as an & lsquo;alarmin & rsquo; to activate the innate immune response. IL-33 drives type 2 responses by inducing signalling through its receptor IL-1RL1 in several immune and structural cells, thereby leading to type 2 cytokine and chemokine production. IL-1RL1 gene transcript encodes different isoforms generated through alternative splicing. Its soluble isoform, IL-1RL1-a or sST2, acts as a decoy receptor by sequestering IL-33, thereby inhibiting IL1RL1-b/IL-33 signalling. IL-33 and its receptor IL-1RL1 are therefore considered as putative biomarkers or targets for pharmacological intervention in asthma. This review will provide an overview of the genetics and biology of the IL-33/IL-1RL1 pathway in the context of asthma pathogenesis. It will discuss the potential and complexities of targeting the cytokine or its receptor, how genetics or biomarkers may inform precision medicine for asthma targeting this pathway, and the possible positioning of therapeutics targeting IL-33 or its receptor in the expanding landscape of novel biologicals applied in asthma management. (c) 2021 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/)
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