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The proper motion of HV2112: A TZO candidate in the SMC
The candidate Thorne-\.Zytkow object (T\.ZO), HV2112, is becoming a
well-studied if enigmatic object. A key point of its candidacy as a T\.ZO is
whether or not it resides in the Small Magellanic Cloud (SMC). HV2112 has
detections in a series of photometric catalogues which have resulted in
contradictory estimates of its proper motion and, therefore, its membership
within the SMC. This letter seeks to resolve the issue of the SMC membership of
HV2112 through a reanalysis of extant photometric data. We also demonstrate the
difficulties and downfalls inherent in considering a range of catalogue proper
motions. We conclude that the proper motion, and associated ancillary radial
velocity, positional and photometric properties, are fully consistent with
HV2112 being within the SMC and thus it remains a candidate T\.ZO.This work is based on observations collected at the European Organisation for Astronomical Research in the Southern Hemisphere under ESO programme(s) 179.B-2003 and was partly supported by the European Union FP7 programme through ERC grant number 320360. RGI thanks the STFC for funding for his Rutherford fellowship. CAT thanks Churchill College for his fellowship. This research has made use of the VizieR catalogue access tool (A&AS, 143, 23), the Aladin sky atlas and the SIMBAD data base developed and operated at CDS, Strasbourg, France. The Digitized Sky Surveys (DSS) were produced at the Space Telescope Science Institute under US Government grant NAG W-2166.This is the final version of the article. It first appeared from Oxford University Press via http://dx.doi.org/10.1093/mnrasl/slw03
Ozone-depleting substances (ODSs) and related chemicals
The amended and adjusted Montreal Protocol continues to be successful at reducing emissions and atmospheric abundances of most controlled ozone-depleting substances (ODSs).Global Ozone Research and Monitoring Projec
Core-collapse supernova progenitor constraints using the spatial distributions of massive stars in local galaxies
We study the spatial correlations between the H emission and
different types of massive stars in two local galaxies, the Large Magellanic
Cloud (LMC) and Messier 33. We compare these to correlations derived for
core-collapse supernovae (CCSNe) in the literature to connect CCSNe of
different types with the initial masses of their progenitors and to test the
validity of progenitor mass estimates which use the pixel statistics method. We
obtain samples of evolved massive stars in both galaxies from catalogues with
good spatial coverage and/or completeness, and combine them with coordinates of
main-sequence stars in the LMC from the SIMBAD database. We calculate the
spatial correlation of stars of different classes and spectral types with
H emission. We also investigate the effects of distance, noise and
positional errors on the pixel statistics method. A higher correlation with
H emission is found to correspond to a shorter stellar lifespan, and we
conclude that the method can be used as an indicator of the ages, and therefore
initial masses, of SN progenitors. We find that the spatial distributions of
type II-P SNe and red supergiants of appropriate initial mass (9
) are consistent with each other. We also find the distributions of
type Ic SNe and WN stars with initial masses 20
consistent, while supergiants with initial masses around 15 are a
better match for type IIb and II-L SNe. The type Ib distribution corresponds to
the same stellar types as type II-P, which suggests an origin in interacting
binaries. On the other hand, we find that luminous blue variable stars show a
much stronger correlation with H emission than do type IIn SNe.ERC, STF
Future Cities: Asserting Public Governance
The smart city has become a main prism through which urban futures are viewed. With it comes the promise of big data technology enabling more resource-efficient urban systems and improved governance. Increasingly, however, this technocentric view is being challenged, at least rhetorically, by seeking to place people at the heart of smart city development. Yet, especially in the case of the UK, such development typically takes place within a governance context which marginalises established planning and decision processes, thus arguably weakening public accountability. Moreover, the norms of engagement change in that citizens are assigned more of an entrepreneurial role as co-producers of data-driven information. It becomes necessary, therefore, to reconsider as well as reinvigorate the place of the public in the future city. This article seeks to do so by making the case, on one hand, for strengthening institutional frameworks and, on the other, advancing a more active role for citizens to become involved in actualising and scrutinising future cities
Insights from Amphioxus into the Evolution of Vertebrate Cartilage
Central to the story of vertebrate evolution is the origin of the vertebrate head, a problem difficult to approach using paleontology and comparative morphology due to a lack of unambiguous intermediate forms. Embryologically, much of the vertebrate head is derived from two ectodermal tissues, the neural crest and cranial placodes. Recent work in protochordates suggests the first chordates possessed migratory neural tube cells with some features of neural crest cells. However, it is unclear how and when these cells acquired the ability to form cellular cartilage, a cell type unique to vertebrates. It has been variously proposed that the neural crest acquired chondrogenic ability by recruiting proto-chondrogenic gene programs deployed in the neural tube, pharynx, and notochord. To test these hypotheses we examined the expression of 11 amphioxus orthologs of genes involved in neural crest chondrogenesis. Consistent with cellular cartilage as a vertebrate novelty, we find that no single amphioxus tissue co-expresses all or most of these genes. However, most are variously co-expressed in mesodermal derivatives. Our results suggest that neural crest-derived cartilage evolved by serial cooption of genes which functioned primitively in mesoderm
Binary companions of nearby supernova remnants found with Gaia
© ESO, 2017. Aims. We search for runaway former companions of the progenitors of nearby Galactic core-collapse supernova remnants (SNRs) in the Tycho-Gaia astrometric solution (TGAS). Methods. We look for candidates among a sample of ten SNRs with distances 2kpc, taking astrometry and G magnitude from TGAS and B,V magnitudes from the AAVSO Photometric All-Sky Survey (APASS). A simple method of tracking back stars and finding the closest point to the SNR centre is shown to have several failings when ranking candidates. In particular, it neglects our expectation that massive stars preferentially have massive companions. We evolve a grid of binary stars to exploit these covariances in the distribution of runaway star properties in colour - magnitude - ejection velocity space. We construct an analytic model which predicts the properties of a runaway star, in which the model paramet ers are the location in the grid of progenitor binaries and the properties of the SNR. Using nested sampling we calculate the Bayesian evidence for each candidate to be the runaway and simultaneously constrain the properties of that runaway and of the SNR itself. Results. We identify four likely runaway companions of the Cygnus Loop (G074.0-08.5), HB 21 (G089.0+ 04.7), S147 (G180.0+ 01.7) and the Monoceros Loop (G205.5+ 00.5). HD 37424 has previously been suggested as the companion of S147, however the other three stars are new candidates. The favoured companion of HB 21 is the Be star BD+50 3188 whose emission-line features could be explained by pre-supernova mass transfer from the primary. There is a small probability that the 2M candidate runaway TYC 2688-1556-1 associated with the Cygnus Loop is a hypervelocity star. If the Monoceros Loop is related to the on-going star formation in the Mon OB2 association, the progenitor of the Monoceros Loop is required to be more massive than 40M which is in tension with the posterior for our candidate runaway star HD 261393.DPB is grateful to the Science and Technology Facilities Council (STFC) for providing Ph.D. funding. M.F. is supported by a Royal Society – Science Foundation Ireland University Research Fellowship. This work was partly supported by the European Union FP7 programme through ERC grant number 320360. RGI thanks the STFC for funding his Rutherford fellowship under grant ST/L003910/1 and Churchill College, Cambridge for his fellowship
Molecular and cellular mechanisms underlying the evolution of form and function in the amniote jaw.
The amniote jaw complex is a remarkable amalgamation of derivatives from distinct embryonic cell lineages. During development, the cells in these lineages experience concerted movements, migrations, and signaling interactions that take them from their initial origins to their final destinations and imbue their derivatives with aspects of form including their axial orientation, anatomical identity, size, and shape. Perturbations along the way can produce defects and disease, but also generate the variation necessary for jaw evolution and adaptation. We focus on molecular and cellular mechanisms that regulate form in the amniote jaw complex, and that enable structural and functional integration. Special emphasis is placed on the role of cranial neural crest mesenchyme (NCM) during the species-specific patterning of bone, cartilage, tendon, muscle, and other jaw tissues. We also address the effects of biomechanical forces during jaw development and discuss ways in which certain molecular and cellular responses add adaptive and evolutionary plasticity to jaw morphology. Overall, we highlight how variation in molecular and cellular programs can promote the phenomenal diversity and functional morphology achieved during amniote jaw evolution or lead to the range of jaw defects and disease that affect the human condition
Nanostructured 3D Constructs Based on Chitosan and Chondroitin Sulphate Multilayers for Cartilage Tissue Engineering
Nanostructured three-dimensional constructs combining layer-by-layer technology (LbL) and template leaching were processed and evaluated as possible support structures for cartilage tissue engineering. Multilayered constructs were formed by depositing the polyelectrolytes chitosan (CHT) and chondroitin sulphate (CS) on either bidimensional glass surfaces or 3D packet of paraffin spheres. 2D CHT/CS multi-layered constructs proved to support the attachment and proliferation of bovine chondrocytes (BCH). The technology was transposed to 3D level and CHT/CS multi-layered hierarchical scaffolds were retrieved after paraffin leaching. The obtained nanostructured 3D constructs had a high porosity and water uptake capacity of about 300%. Dynamical mechanical analysis (DMA) showed the viscoelastic nature of the scaffolds. Cellular tests were performed with the culture of BCH and multipotent bone marrow derived stromal cells (hMSCs) up to 21 days in chondrogenic differentiation media. Together with scanning electronic microscopy analysis, viability tests and DNA quantification, our results clearly showed that cells attached, proliferated and were metabolically active over the entire scaffold. Cartilaginous extracellular matrix (ECM) formation was further assessed and results showed that GAG secretion occurred indicating the maintenance of the chondrogenic phenotype and the chondrogenic differentiation of hMSCs
Historical greenhouse gas concentrations for climate modelling (CMIP6)
Atmospheric greenhouse gas (GHG) concentrations are at unprecedented, record-high levels compared to the last 800 000 years. Those elevated GHG concentrations warm the planet and – partially offset by net cooling effects by aerosols – are largely responsible for the observed warming over the past 150 years. An accurate representation of GHG concentrations is hence important to understand and model recent climate change. So far, community efforts to create composite datasets of GHG concentrations with seasonal and latitudinal information have focused on marine boundary layer conditions and recent trends since the 1980s. Here, we provide consolidated datasets of historical atmospheric concentrations (mole fractions) of 43 GHGs to be used in the Climate Model Intercomparison Project – Phase 6 (CMIP6) experiments. The presented datasets are based on AGAGE and NOAA networks, firn and ice core data, and archived air data, and a large set of published studies. In contrast to previous intercomparisons, the new datasets are latitudinally resolved and include seasonality. We focus on the period 1850–2014 for historical CMIP6 runs, but data are also provided for the last 2000 years. We provide consolidated datasets in various spatiotemporal resolutions for carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O), as well as 40 other GHGs, namely 17 ozone-depleting substances, 11 hydrofluorocarbons (HFCs), 9 perfluorocarbons (PFCs), sulfur hexafluoride (SF6), nitrogen trifluoride (NF3) and sulfuryl fluoride (SO2F2). In addition, we provide three equivalence species that aggregate concentrations of GHGs other than CO2, CH4 and N2O, weighted by their radiative forcing efficiencies. For the year 1850, which is used for pre-industrial control runs, we estimate annual global-mean surface concentrations of CO2 at 284.3 ppm, CH4 at 808.2 ppb and N2O at 273.0 ppb. The data are available at https://esgfnode.llnl.gov/search/input4mips/ and http://www.climatecollege.unimelb.edu.au/cmip6. While the minimum CMIP6 recommendation is to use the global- and annual-mean time series, modelling groups can also choose our monthly and latitudinally resolved concentrations, which imply a stronger radiative forcing in the Northern Hemisphere winter (due to the latitudinal gradient and seasonality)
All clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJD
Variant CJD (vCJD) is an incurable, infectious human disease, likely arising from the consumption of BSE-contaminated meat products. Whilst the epidemic appears to be waning, there is much concern that vCJD infection may be perpetuated in humans by the transfusion of contaminated blood products. Since 2004, several cases of transfusion-associated vCJD transmission have been reported and linked to blood collected from pre-clinically affected donors. Using an animal model in which the disease manifested resembles that of humans affected with vCJD, we examined which blood components used in human medicine are likely to pose the greatest risk of transmitting vCJD via transfusion. We collected two full units of blood from BSE-infected donor animals during the pre-clinical phase of infection. Using methods employed by transfusion services we prepared red cell concentrates, plasma and platelets units (including leucoreduced equivalents). Following transfusion, we showed that all components contain sufficient levels of infectivity to cause disease following only a single transfusion and also that leucoreduction did not prevent disease transmission. These data suggest that all blood components are vectors for prion disease transmission, and highlight the importance of multiple control measures to minimise the risk of human to human transmission of vCJD by blood transfusion
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