5,115 research outputs found
The Effective temperature scale of M dwarfs from spectral synthesis
We present a comparison of low-resolution spectra of 60 stars covering the
whole M-dwarf sequence. Using the most recent PHOENIX BT-Settl stellar model
atmospheres (see paper by F. Allard, in this book) we do a first quantitative
compari- son to our observed spectra in the wavelength range 550-950 nm. We
perform a first confrontation between models and observations and we assign an
effective tempera- tures to the observed M-dwarfs. Teff-spectral type relations
are then compared with the published ones. This comparison also aims at
improving the models' opacities.Comment: To be published in the on-line version of the Proceedings of Cool
Stars 16 (ASP Conference Series) New version with bibliography correcte
A library of near-infrared integral field spectra of young M-L dwarfs
We present a library of near-infrared (1.1-2.45 microns) medium-resolution
(R~1500-2000) integral field spectra of 15 young M6-L0 dwarfs, composed of
companions with known ages and of isolated objects. We use it to (re)derive the
NIR spectral types, luminosities and physical parameters of the targets, and to
test (BT-SETTL, DRIFT-PHOENIX) atmospheric models. We derive infrared spectral
types L0+-1, L0+-1, M9.5+-0.5, M9.5+-0.5, M9.25+-0.25, M8+0.5-0.75, and
M8.5+-0.5 for AB Pic b, Cha J110913-773444, USco CTIO 108B, GSC 08047-00232 B,
DH Tau B, CT Cha b, and HR7329B, respectively. BT-SETTL and DRIFT-PHOENIX
models yield close Teff and log g estimates for each sources. The models seem
to evidence a 600-300+600 K drop of the effective temperature at the M-L
transition. Assuming the former temperatures are correct, we derive new mass
estimates which confirm that DH Tau B, USco CTIO 108B, AB Pic b, KPNO Tau 4,
OTS 44, and Cha1109 lay inside or at the boundary of the planetary mass range.
We combine the empirical luminosities of the M9.5-L0 sources to the Teff to
derive semi-empirical radii estimates that do not match "hot-start"
evolutionary models predictions at 1-3 Myr. We use complementary data to
demonstrate that atmospheric models are able to reproduce the combined optical
and infrared spectral energy distribution, together with the near-infrared
spectra of these sources simultaneously. But the models still fail to represent
the dominant features in the optical. This issue casts doubts on the ability of
these models to predict correct effective temperatures from near-infrared
spectra alone. We advocate the use of photometric and spectroscopic data
covering a broad range of wavelengths to study the properties of very low mass
young companions to be detected with the planet imagers (Subaru/SCExAO,
LBT/LMIRCam, Gemini/GPI, VLT/SPHERE).Comment: 27 pages, 14 tables, 19 figures, accepted for publication in
Astronomy & Astrophysic
Active split-ring metamaterial slabs for magnetic resonance imaging
In this work, it is analyzed the ability of split-ring metamaterial slabs
with zero/high permeability to reject/confine the radiofrequency magnetic field
in magnetic resonance imaging systems. Using an homogenization procedure,
split-ring slabs have been designed and fabricated to work in a 1.5T system.
Active elements consisting of pairs of crossed diodes are inserted in the
split-rings. With these elements, the permeability of the slabs can be
automatically switched between a unity value when interacting with the strong
excitation field of the transmitting body coil, and zero or high values when
interacting with the weak field produced by protons in tissue. Experiments are
shown for different configurations where these slabs can help to locally
increase the signal-to-noise-ratio.Comment: 6 pages, 4 figure
Molecular phylogeny of brachiopods and phoronids based on nuclear-encoded small subunit ribosomal RNA gene sequences
Brachiopod and phoronid phylogeny is inferred from SSU rDNA sequences of 28 articulate and nine inarticulate brachiopods, three phoronids, two ectoprocts and various outgroups, using gene trees reconstructed by weighted parsimony, distance and maximum likelihood methods. Of these sequences, 33 from brachiopods, two from phoronids and one each from an ectoproct and a priapulan are newly determined. The brachiopod sequences belong to 31 different genera and thus survey about 10% of extant genus-level diversity. Sequences determined in different laboratories and those from closely related taxa agree well, but evidence is presented suggesting that one published phoronid sequence (GenBank accession UO12648) is a brachiopod-phoronid chimaera, and this sequence is excluded from the analyses. The chiton, Acanthopleura, is identified as the phenetically proximal outgroup; other selected outgroups were chosen to allow comparison with recent, non-molecular analyses of brachiopod phylogeny. The different outgroups and methods of phylogenetic reconstruction lead to similar results, with differences mainly in the resolution of weakly supported ancient and recent nodes, including the divergence of inarticulate brachiopod sub-phyla, the position of the rhynchonellids in relation to long- and short-looped articulate brachiopod clades and the relationships of some articulate brachiopod genera and species. Attention is drawn to the problem presented by nodes that are strongly supported by non-molecular evidence but receive only low bootstrap resampling support. Overall, the gene trees agree with morphology-based brachiopod taxonomy, but novel relationships are tentatively suggested for thecideidine and megathyrid brachiopods. Articulate brachiopods are found to be monophyletic in all reconstructions, but monophyly of inarticulate brachiopods and the possible inclusion of phoronids in the inarticulate brachiopod clade are less strongly established. Phoronids are clearly excluded from a sister-group relationship with articulate brachiopods, this proposed relationship being due to the rejected, chimaeric sequence (GenBank UO12648). Lineage relative rate tests show no heterogeneity of evolutionary rate among articulate brachiopod sequences, but indicate that inarticulate brachiopod plus phoronid sequences evolve somewhat more slowly. Both brachiopods and phoronids evolve slowly by comparison with other invertebrates. A number of palaeontologically dated times of earliest appearance are used to make upper and lower estimates of the global rate of brachiopod SSU rDNA evolution, and these estimates are used to infer the likely divergence times of other nodes in the gene tree. There is reasonable agreement between most inferred molecular and palaeontological ages. The estimated rates of SSU rDNA sequence evolution suggest that the last common ancestor of brachiopods, chitons and other protostome invertebrates (Lophotrochozoa and Ecdysozoa) lived deep in Precambrian time. Results of this first DNA-based, taxonomically representative analysis of brachiopod phylogeny are in broad agreement with current morphology-based classification and systematics and are largely consistent with the hypothesis that brachiopod shell ontogeny and morphology are a good guide to phylogeny
Deep near-IR observations of the Globular Cluster M4: Hunting for Brown Dwarfs
We present an analysis of deep HST/WFC3 near-IR (NIR) imaging data of the
globular cluster M4. The best-photometry NIR colour-magnitude diagram (CMD)
clearly shows the main sequence extending towards the expected end of the
Hydrogen-burning limit and going beyond this point towards fainter sources. The
white dwarf sequence can be identified. As such, this is the deepest NIR CMD of
a globular cluster to date. Archival HST optical data were used for
proper-motion cleaning of the CMD and for distinguishing the white dwarfs (WDs)
from brown dwarf (BD) candidates. Detection limits in the NIR are around F110W
approx 26.5 mag and F160W approx27 mag, and in the optical around F775W approx
28 mag. Comparing our observed CMDs with theoretical models, we conclude that
we have reached beyond the H-burning limit in our NIR CMD and are probably just
above or around this limit in our optical-NIR CMDs. Thus, any faint NIR sources
that have no optical counterpart are potential BD candidates, since the optical
data are not deep enough to detect them. We visually inspected the positions of
NIR sources which are fainter than the H-burning limit in F110W and for which
the optical photometry did not return a counterpart. We found in total five
sources for which we did not get an optical measurement. For four of these five
sources, a faint optical counterpart could be visually identified, and an upper
optical magnitude was estimated. Based on these upper optical magnitude limits,
we conclude that one source is likely a WD, one source could either be a WD or
BD candidate, and the remaining two sources agree with being BD candidates. For
only one source no optical counterpart could be detected, which makes this
source a good BD candidate. We conclude that we found in total four good BD
candidates.Comment: ApJ accepted, 28 pages including 16 figure
D 4.1: Protocol for converting data sources into common standards for input into WP3 and WP9 : Version 3.0 Document date: 2009-10-10
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