3,398 research outputs found
Deep SOAR follow-up photometry of two Milky Way outer-halo companions discovered with Dark Energy Survey
We report the discovery of a new star cluster, DESâ3, in the constellation of Indus, and deeper observations of the previously identified satellite DESâJ0222.7â5217 (EridanusâIII). DESâ3 was detected as a stellar overdensity in first-year Dark Energy Survey data, and confirmed with deeper photometry from the 4.1-m Southern Astrophysical Research (SOAR) telescope. The new system was detected with a relatively high significance and appears in the DES images as a compact concentration of faint blue point sources. We determine that DESâ3 is located at a heliocentric distance of â76.2âkpc and it is dominated by an old (â9.8âGyr) and metal-poor ([Fe/H] â â1.84) population. While the age and metallicity values of DESâ3 are comparable to typical globular clusters (objects with a high stellar density, stellar mass of âŒ10^5 Mâ and luminosity M_V ⌠â7.3), its half-light radius (r_h ⌠6.87âpc) and luminosity (M_V ⌠â1.7) are more indicative of faint star cluster. Based on the angular size, DESâ3, with a value of r_h ⌠0.â31, is among the smallest faint star clusters known to date. Furthermore, using deeper imaging of DESâJ0222.7â5217 taken with the SOAR telescope, we update structural parameters and perform the first isochrone modelling. Our analysis yields the first age (â12.6âGyr) and metallicity ([Fe/H] â â2.01) estimates for this object. The half-light radius (r_h â 11.24âpc) and luminosity (M_V â â2.4) of DESâJ0222.7â5217 suggest that it is likely a faint star cluster. The discovery of DESâ3 indicates that the census of stellar systems in the Milky Way is still far from complete, and demonstrates the power of modern wide-field imaging surveys to improve our knowledge of the Galaxyâs satellite population
Why one-size-fits-all vaso-modulatory interventions fail to control glioma invasion: in silico insights
There is an ongoing debate on the therapeutic potential of vaso-modulatory
interventions against glioma invasion. Prominent vasculature-targeting
therapies involve functional tumour-associated blood vessel deterioration and
normalisation. The former aims at tumour infarction and nutrient deprivation
medi- ated by vascular targeting agents that induce occlusion/collapse of
tumour blood vessels. In contrast, the therapeutic intention of normalising the
abnormal structure and function of tumour vascular net- works, e.g. via
alleviating stress-induced vaso-occlusion, is to improve chemo-, immuno- and
radiation therapy efficacy. Although both strategies have shown therapeutic
potential, it remains unclear why they often fail to control glioma invasion
into the surrounding healthy brain tissue. To shed light on this issue, we
propose a mathematical model of glioma invasion focusing on the interplay
between the mi- gration/proliferation dichotomy (Go-or-Grow) of glioma cells
and modulations of the functional tumour vasculature. Vaso-modulatory
interventions are modelled by varying the degree of vaso-occlusion. We
discovered the existence of a critical cell proliferation/diffusion ratio that
separates glioma invasion re- sponses to vaso-modulatory interventions into two
distinct regimes. While for tumours, belonging to one regime, vascular
modulations reduce the tumour front speed and increase the infiltration width,
for those in the other regime the invasion speed increases and infiltration
width decreases. We show how these in silico findings can be used to guide
individualised approaches of vaso-modulatory treatment strategies and thereby
improve success rates
Impact assessment of interregional government transfers in Brazil: an input-output approach
Redistributive policies carried out by the central government through interregional government transfers is a relevant feature of the Brazilian federal fiscal system. Regional shares of the central government revenues in the poorer regions have been recurrently smaller than the shares of central government expenditures in those regions. Appeal to core-periphery outcomes could be made, as SĂŁo Paulo, the wealthiest state in the country, concentrated, in 2005, over 40% of total Federal tax revenue, receiving less than 35% of Federal expenditures. These figures suggest a redistribution of public funds from the spatial economic core of the economy to the peripheral areas. This paper investigates the role interregional transfers play in the redistribution of activities in the country, using an interregional input-output approach. Counterfactual simulations allow us to estimate some costs and benefits, for the core and periphery respectively, from such fiscal mechanisms.Interregional government transfers, input-output analysis, impact analysis, Brazilian economy
SLOCC determinant invariants of order 2^{n/2} for even n qubits
In this paper, we study SLOCC determinant invariants of order 2^{n/2} for any
even n qubits which satisfy the SLOCC determinant equations. The determinant
invariants can be constructed by a simple method and the set of all these
determinant invariants is complete with respect to permutations of qubits.
SLOCC entanglement classification can be achieved via the vanishing or not of
the determinant invariants. We exemplify the method for several even number of
qubits, with an emphasis on six qubits.Comment: J. Phys. A: Math. Theor. 45 (2012) 07530
The Visibility Graph: a new method for estimating the Hurst exponent of fractional Brownian motion
Fractional Brownian motion (fBm) has been used as a theoretical framework to
study real time series appearing in diverse scientific fields. Because its
intrinsic non-stationarity and long range dependence, its characterization via
the Hurst parameter H requires sophisticated techniques that often yield
ambiguous results. In this work we show that fBm series map into a scale free
visibility graph whose degree distribution is a function of H. Concretely, it
is shown that the exponent of the power law degree distribution depends
linearly on H. This also applies to fractional Gaussian noises (fGn) and
generic f^(-b) noises. Taking advantage of these facts, we propose a brand new
methodology to quantify long range dependence in these series. Its reliability
is confirmed with extensive numerical simulations and analytical developments.
Finally, we illustrate this method quantifying the persistent behavior of human
gait dynamics.Comment: 5 pages, submitted for publicatio
Chaos control in random Boolean networks by reducing mean damage percolation rate
Chaos control in Random Boolean networks is implemented by freezing part of
the network to drive it from chaotic to ordered phase. However, controlled
nodes are only viewed as passive blocks to prevent perturbation spread. This
paper proposes a new control method in which controlled nodes can exert an
active impact on the network. Controlled nodes and frozen values are
deliberately selected according to the information of connection and Boolean
functions. Simulation results show that the number of nodes needed to achieve
control is largely reduced compared to previous method. Theoretical analysis is
also given to estimate the least fraction of nodes needed to achieve control.Comment: 10 pages, 2 figure
Reply to Harwood et al.: Alternative functional conformations of native human α<inf>2</inf>-macroglobulin
Cryo-EM structures show the mechanistic basis of pan-peptidase inhibition by human α<inf>2</inf>-macroglobulin
Human α2-macroglobulin (hα2M) is a multidomain protein with a plethora of essential functions, including transport of signaling molecules and endopeptidase inhibition in innate immunity. Here, we dissected the molecular mechanism of the inhibitory function of the âŒ720-kDa hα2M tetramer through eight cryo-electron microscopy (cryo-EM) structures of complexes from human plasma. In the native complex, the hα2M subunits are organized in two flexible modules in expanded conformation, which enclose a highly porous cavity in which the proteolytic activity of circulating plasma proteins is tested. Cleavage of bait regions exposed inside the cavity triggers rearrangement to a compact conformation, which closes openings and entraps the prey proteinase. After the expanded-to-compact transition, which occurs independently in the four subunits, the reactive thioester bond triggers covalent linking of the proteinase, and the receptor-binding domain is exposed on the tetramer surface for receptor-mediated clearance from circulation. These results depict the molecular mechanism of a unique suicidal inhibitory trap
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