219 research outputs found

    The low mass population of the Vela OB2 association from Gaia

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    The first Gaia Data Release presents an opportunity to characterise the low-mass population of OB associations, providing larger statistical samples and better constraints on the formation and evolution of clusters and associations. Using previously known low mass members in a small region of Vela OB2 we have designed selection criteria that combine Gaia and 2MASS photometry, independently of any astrometric information, to identify low-mass pre-main-sequence (PMS) stars over the wider association area. Our method picks out the known clusters of young stars around Velorum and NGC-2547, but also identifies other over-densities that may represent previously unknown clusters. There are clear differences in the spatial distributions of the low-mass and the high-mass OB populations, suggesting either that the structure and dynamics of these populations has evolved separately or that the initial mass function can vary considerably on small scales within a single association

    The dynamics of the γ Vel cluster and nearby Vela OB2 association

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    The kinematics of low-mass stars in nearby OB associations can provide clues about their origins and evolution. Combining the precise positions, proper motions, and parallaxes given in the second Gaia Data Release with radial-velocity measurements obtained with the Hermes spectrograph at the Anglo-Australian Telescope, we have an opportunity to study in detail the kinematics of low-mass stars belonging to the nearby γ Vel cluster and the Vela OB2 association it is projected against. The presence of lithium is used to confirm the youth of our targets. We separate our sample into the cluster and association populations based on the Gaia-ESO Survey membership probabilities their parallaxes, and kinematics. We find strong evidence for expansion in the OB association population with at least 4σ significance along all three axes, though the expansion is notably anisotropic. We discuss these results in the context of cluster and association dispersal theories

    An anomalous extinction law in the Cep OB3b young cluster: Evidence for dust processing during gas dispersal

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    © 2014. The American Astronomical Society. All rights reserved. We determine the extinction law through Cep OB3b, a young cluster of 3000 stars undergoing gas dispersal. The extinction is measured toward 76 background K giants identified with MMT/Hectospec spectra. Color excess ratios were determined toward each of the giants using V and R photometry from the literature, g, r, i, and z photometry from the Sloan Digital Sky Survey and J, H, and Ks photometry from the Two Micron All Sky Survey. These color excess ratios were then used to construct the extinction law through the dusty material associated with Cep OB3b. The extinction law through Cep OB3b is intermediate between the RV = 3.1 and RV = 5 laws commonly used for the diffuse atomic interstellar medium and dense molecular clouds, respectively. The dependence of the extinction law on line-of-sight AV is investigated and we find the extinction law becomes shallower for regions with AV > 2.5 mag. We speculate that the intermediate dust law results from dust processing during the dispersal of the molecular cloud by the cluster.Support for this work was provided by the National Science Foundation award AST-1009564. This research has made use of the NASA/IPAC Infrared Science Archive, which is operated by the Jet Propulsion Laboratory, California Institute of Technology, under contract with the National Aeronautics and Space Administration. This publication makes use of data products from the Two Micron All Sky Survey, which is a joint project of the University of Massachusetts and the Infrared Processing and Analysis Center/California Institute of Technology, funded by the National Aeronautics and Space Administration and the National Science Foundation and JPL support from SAO/JPL SV4-74011. Funding for SDSS-III has been provided by the Alfred P. Sloan Foundation, the Participating Institutions, the National Science Foundation, and the U.S. Department of Energy Office of Science. The SDSS-III web site is http://www.sdss3.org/. SDSS-III is managed by the Astrophysical Research Consortium for the Participating Institutions of the SDSS-III Collaboration including the University of Arizona, the Brazilian Participation Group, Brookhaven National Laboratory, University of Cambridge, Carnegie Mellon University, University of Florida, the French Participation Group, the German Participation Group, Harvard University, the Instituto de Astrofisica de Canarias, the Michigan State/Notre Dame/JINA Participation Group, Johns Hopkins University, Lawrence Berkeley National Laboratory, Max Planck Institute for Astrophysics, Max Planck Institute for Extraterrestrial Physics, New Mexico State University, New York University, Ohio State University, Pennsylvania State University, University of Portsmouth, Princeton University, the Spanish Participation Group, University of Tokyo, University of Utah, Vanderbilt University, University of Virginia, University of Washington, and Yale University

    The structure and 3D kinematics of vela OB2

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    The kinematics of stars in OB associations can provide insights into their formation, dynamical evolution, and eventual fate. The low-mass stellar content of OB associations are sufficiently numerous as to provide a detailed sampling of their kinematic properties, however spectroscopy is required to confirm the youth of individual stars and to get 3D kinematics. In this paper, we present and analyse results from a large spectroscopic survey of Vela OB2 conducted using 2dF/HERMES on the AAT. This spectroscopy is used to confirm the youth of candidate young stars and determine radial velocities, which are combined with proper motions and parallaxes from Gaia to measure 3D positions and velocities. We identify multiple separate kinematic groups in the region, for which we measure velocity dispersions and infer their virial states. We measure expansion rates for all these groups and find strong evidence for anisotropic expansion in the Vela OB2 association of at least 11σ significance in all three dimensions, as well as some evidence for expansion in the γ Vel and P Puppis clusters. We trace back the motions of these groups into the past and find that the open cluster NGC 2547 is an interloper in the Vela OB2 region and actually formed >100 pc away from the association. We conclude that Vela OB2 must have formed with considerable spatial and kinematic substructure over a time-scale of ∼10 Myr, with clear temporal substructure within the association, but no clear evidence for an age gradient

    Deletion 22q13.3 syndrome

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    The deletion 22q13.3 syndrome (deletion 22q13 syndrome or Phelan-McDermid syndrome) is a chromosome microdeletion syndrome characterized by neonatal hypotonia, global developmental delay, normal to accelerated growth, absent to severely delayed speech, and minor dysmorphic features. The deletion occurs with equal frequency in males and females and has been reported in mosaic and non-mosaic forms. Due to lack of clinical recognition and often insufficient laboratory testing, the syndrome is under-diagnosed and its true incidence remains unknown. Common physical traits include long eye lashes, large or unusual ears, relatively large hands, dysplastic toenails, full brow, dolicocephaly, full cheeks, bulbous nose, and pointed chin. Behavior is autistic-like with decreased perception of pain and habitual chewing or mouthing. The loss of 22q13.3 can result from simple deletion, translocation, ring chromosome formation and less common structural changes affecting the long arm of chromosome 22, specifically the region containing the SHANK3 gene. The diagnosis of deletion 22q13 syndrome should be considered in all cases of hypotonia of unknown etiology and in individuals with absent speech. Although the deletion can sometimes be detected by high resolution chromosome analysis, fluorescence in situ hybridization (FISH) or array comparative genomic hybridization (CGH) is recommended for confirmation. Differential diagnosis includes syndromes associated with hypotonia, developmental delay, speech delay and/or autistic-like affect (Prader-Willi, Angelman, Williams, Smith-Magenis, Fragile X, Sotos, FG, trichorhinophalangeal and velocardiofacial syndromes, autism spectrum disorders, cerebral palsy). Genetic counseling is recommended and parental laboratory studies should be considered to identify cryptic rearrangements and detect parental mosaicism. Prenatal diagnosis should be offered for future pregnancies in those families with inherited rearrangements. Individuals with deletion 22q13 should have routine examinations by the primary care physician as well as genetic evaluations with referral to specialists if neurological, gastrointestinal, renal, or other systemic problems are suspected. Affected individuals benefit from early intervention programs, intense occupational and communication therapies, adaptive exercise and sport programs, and other therapies to strengthen their muscles and increase their communication skills. No apparent life-threatening organic abnormalities accompany the diagnosis of deletion 22q13

    Expanding associations in the Vela-Puppis region - 3D structure and kinematics of the young population

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    Context. The Vela-Puppis region is known to host the Vela OB2 association as well as several young clusters featuring OB and pre-main-sequence stars. Several spatial and kinematic subgroups have been identified in recent years. Aims. By grouping stars based on their positions and velocity, we can address the question of the dynamical history of the region and the mechanisms that drove stellar formation. The Gaia DR2 astrometry and photometry enables us to characterise the 3D spatial and 3D kinematic distribution of young stars and to estimate the ages of the identified components. Methods. We used an unsupervised classification method to group stars based on their proper motions and parallax. We studied the expansion rates of the different identified groups based on 3D velocities and on corrected tangential velocities. We used theoretical isochrones to estimate ages. Results. The young stars can be separated into seven main groups of different ages and kinematical distribution. All groups are found to be expanding, although the expansion is mostly not isotropic. Conclusions. The size of the region, the age substructure, and the anisotropic expansion rates are compatible with a prolonged period of star formation in a turbulent molecular cloud. The current kinematics of the stars cannot be explained by internal processes alone (such as gas expulsion)

    Network capitalism and the role of strategy, contracts and performance expectations for Asia-Pacific innovation partnerships

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    © Springer Nature Singapore Pte Ltd. 2018. With the growth of emerging economies in Asia-Pacific over the last three decades collaboration with the aim of innovation between firms within and with partners outside the region have developed substantially. Not always have such partnerships fulfilled their anticipated strategic objectives. The literature suggests that the nature of market arrangements and the role of government within that system play a role, but also innate contracting practices and governance of innovation partnerships are related. Yet, our understanding about the specific relationships between these factors and the emerging partnership innovation culture that facilitates joint business activities in an Asia-Pacific context remains vague. In this conceptual chapter we suggest how characteristics of so called network capitalism in conjunction with the nature of contractual agreements between partners, the alignment of their innovation objectives and the ambiguity inherent in their mutual contributions to the partnership can be interpreted as indicators of joint innovation culture. However, while innovation partnerships generally may result to be bureaucratic, market, clan, or adhocracy, we discuss how in an Asia Pacific context, innovation partnerships are limited by the extent of codification and diffusion of information and the social embeddedness of economic transactions

    Absent otoacoustic emissions predict otitis media in young Aboriginal children: A birth cohort study in Aboriginal and non-Aboriginal children in an arid zone of Western Australia

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    AbstractBackground: Otitis media (OM) is the most common paediatric illness for which antibiotics areprescribed. In Australian Aboriginal children OM is frequently asymptomatic and starts at a youngerage, is more common and more likely to result in hearing loss than in non-Aboriginal children.Absent transient evoked otoacoustic emissions (TEOAEs) may predict subsequent risk of OM.Methods: 100 Aboriginal and 180 non-Aboriginal children in a semi-arid zone of WesternAustralia were followed regularly from birth to age 2 years. Tympanometry was conducted atroutine field follow-up from age 3 months. Routine clinical examination by an ENT specialist wasto be done 3 times and hearing assessment by an audiologist twice. TEOAEs were measured at ages<1 and 1–2 months. Cox proportional hazards model was used to investigate the associationbetween absent TEOAEs and subsequent risk of OM.Results: At routine ENT specialist clinics, OM was detected in 55% of 184 examinations inAboriginal children and 26% of 392 examinations in non-Aboriginal children; peak prevalence was72% at age 5–9 months in Aboriginal children and 40% at 10–14 months in non-Aboriginal children.Moderate-severe hearing loss was present in 32% of 47 Aboriginal children and 7% of 120 non-Aboriginal children aged 12 months or more.TEOAE responses were present in 90% (46/51) of Aboriginal children and 99% (120/121) of non-Aboriginal children aged <1 month and in 62% (21/34) and 93% (108/116), respectively, inAboriginal and non-Aboriginal children at age 1–2 months. Aboriginal children who failed TEOAEat age 1–2 months were 2.6 times more likely to develop OM subsequently than those who passed.Overall prevalence of type B tympanograms at field follow-up was 50% (n = 78) in Aboriginalchildren and 20% (n = 95) in non-Aboriginal children
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