242 research outputs found
SiO Maser Survey of IRAS Sources in the Inner Galactic Disk
We have surveyed 401 color selected IRAS sources in the Galactic disk in the
SiO J=1--0 v= 1 and 2 maser lines at 43 GHz, resulting in 254 (239 new)
detections. The observed sources lie mostly in a strip of the inner Galactic
disk with boundaries -10<l<40 deg and |b|<3 deg. This survey provides radial
velocities of inner-disk stars for which optical measurements cannot be made
due to interstellar extinction. The SiO -- diagram in the area lv$ map does, indicating a slight difference of stellar
type between SiO and OH emitting stars. After identifying all of the SiO
detected sources in the 2MASS near-infrared catalog, we computed their
luminosity distances based on the infrared fluxes. We then mapped these objects
onto the first quadrant of the Galactic plane. Combining the distances with the
SiO radial-velocities, we obtained a pattern speed for SiO maser sources,
Omega_P=21 (+- 13) km s^{-1} kpc^{-1}, between the distances 1 and 5.5 kpc,
without the use of any dynamical models. The increase of the pattern speed
toward the Galactic center (up to 60 km s^{-1} kpc^{-1} between the distances,
5.5 and 7 kpc) suggests the presence of two pattern speeds in the Galaxy.Comment: 38 page 9 figures, high res. eps files are available as NRO report
No. 608 (http://www.nro.nao.ac.jp/library/report/list.html). PASJ 56 No. 4 in
pres
SiO Maser Survey of the Large-Amplitude Variables in the Galactic Center
We have surveyed ~400 known large-amplitude variables within 15' of the
galactic center in the SiO J=1--0 v=1 and 2 maser lines at 43 GHz, resulting in
179 detections. SiO lines were also detected from 16 other resulting in 180
detections. SiO lines were also detected from 16 other sources, which are
located within 20" (the telescope half beamwidth) of the program objects. The
detection rate of 48 percent is comparable to that obtained in Bulge IRAS
source surveys. Among the SiO detections, five stars have radial velocities
greater than 200 km/s. The SiO detection rate increases steeply with the period
of light variation, particularly for stars with P>500 d, where it exceeds 80%.
We found that, at a given period, the SiO detection rate is approximately three
times that for OH. These facts suggest that the large-amplitude variables in
the Nuclear Disk region are AGB stars similar in their overall properties to
the inner and outer Bulge IRAS/SiO sources. From the set of radial velocity
data, the mass distribution within 30 pc of the galactic center is derived by a
new method which is based on the collisionless Boltzmann equation integrated
along the line of sight. The mass within 30 pc is about 6.4 [\pm 0.7] \times
10^7 M_{\odot} and the mass of the central black hole is 2.7 [\pm 1.3] \times
10^6 M_{\odot}. Consideration of the line-of-sight velocity of each star and
its potential energy leads to the conclusion that the five high-velocity stars
come from galactocentric distances as high as 300 pc. The high-velocity
subsample of stars with negative radial velocities exhibits a tendency to have
brighter K magnitudes than the subsample of stars with positive velocities. The
origin of these high-velocity stars is discussed.Comment: Hires. figures are available as No.604 of NRO report at
http://www.nro.nao.ac.jp/library/report/list.html . PASJ 56 (april 28 issue)
in pres
Detections of SiO Masers from the Large-Amplitude Variables in the Galactic Nuclear Disk
We have surveyed known large-amplitude variables within 15' of the Galactic
center in the SiO J=1-0 v=1 and 2 maser lines at 43 GHz, resulting in 79
detections and 58 non-detections. The detection rate of 58 percent is
comparable to that obtained in Bulge IRAS source surveys. SiO lines were also
detected from four other sources near the program objects. The SiO detection
rate increases steeply with the period, particularly for stars with P>500 d,
where it exceeds 80%. We found at a given period that the SiO detection rate is
approximately double that for OH. These facts suggest that the large-amplitude
variables in the Nuclear Disk region are AGB stars similar in their overall
properties to the inner and outer bulge IRAS/SiO sources.Comment: 5 pages, 2 figures, 1 Table. PASJ 54, No 2 April 25 issue in pres
Outflows from the high-mass protostars NGC 7538 IRS1/2 observed with bispectrum speckle interferometry -- Signatures of flow precession
NGC 7538 IRS1 is a high-mass (approx. 30 M_sun) protostar with a CO outflow,
an associated UCHII region, and a linear methanol maser structure, which might
trace a Keplerian-rotating circumstellar disk. The directions of the various
associated axes are misaligned with each other. We investigate the
near-infrared morphology of the source to clarify the relations among the
various axes. K'-band bispectrum speckle interferometry was performed at two
6-meter-class telescopes -- the BTA 6m telescope and the 6.5m MMT.
Complementary IRAC images from the Spitzer Space Telescope Archive were used to
relate the structures detected with the outflow at larger scales. High-dynamic
range images show fan-shaped outflow structure in which we detect 18 stars and
several blobs of diffuse emission. We interpret the misalignment of various
outflow axes in the context of a disk precession model, including numerical
hydrodynamic simulations of the molecular emission. The precession period is
approx. 280 years and its half-opening angle is 40 degrees. A possible
triggering mechanism is non-coplanar tidal interaction of an (undiscovered)
close companion with the circumbinary protostellar disk. Our observations
resolve the nearby massive protostar NGC 7538 IRS2 as a close binary with
separation of 195 mas. We find indications for shock interaction between the
outflow activities in IRS1 and IRS2. Indications of outflow precession have
been discovered to date in a number of massive protostars, all with large
precession angles 20--45 degrees. This might explain the difference between the
outflow widths in low- and high-mass stars and add support to a common
collimation mechanism.Comment: 20 pages; 8 figures; Accepted by A&A on April 10, 2006; Image quality
reduced due to astro-ph file size limitations; Please download a version with
high-quality images from
http://www.mpifr-bonn.mpg.de/staff/tpreibis/ngc7538.pd
The 2006 Radio Outburst of a Microquasar Cyg X-3: Observation and Data
We present the results of the multi-frequency observations of radio outburst
of the microquasar Cyg X-3 in February and March 2006 with the Nobeyama 45-m
telescope, the Nobeyama Millimeter Array, and the Yamaguchi 32-m telescope.
Since the prediction of a flare by RATAN-600, the source has been monitored
from Jan 27 (UT) with these radio telescopes. At the eighteenth day after the
quench of the activity, successive flares exceeding 1 Jy were observed
successfully. The time scale of the variability in the active phase is
presumably shorter in higher frequency bands.
We also present the result of a follow-up VLBI observation at 8.4 GHz with
the Japanese VLBI Network (JVN) 2.6 days after the first rise. The VLBI image
exhibits a single core with a size of <8 mas (80 AU). The observed image was
almost stable, although the core showed rapid variation in flux density. No jet
structure was seen at a sensitivity of K.Comment: 17 pages,6 figures; accepted by PAS
Very compact radio emission from high-mass protostars. II. Dust disks and ionized accretion flows
This paper reports 43 GHz imaging of the high-mass protostars W33A, AFGL 2591
and NGC 7538 IRS9 at 0.04'' and 0.6'' resolution. In each case, weak (~mJy),
compact (~100 AU) emission is detected, which has an elongated shape (axis
ratio ~3). For AFGL 2591 and NGC 7538 IRS9, the emission is single-peaked,
while for the highest luminosity source, W33A, a `mini-cluster' of three
sources is detected. The derived sizes, flux densities, and broad-band radio
spectra of the sources support recent models where the initial expansion of HII
regions around very young O-type stars is prevented by stellar gravity. In
these models, accretion flows onto high-mass stars originate in large-scale
molecular envelopes and become ionized close to the star. These models
reproduce our observations of ionized gas as well as the structure of the
molecular envelopes of these sources on 10^3--10^4 AU scales derived previously
from single-dish submillimeter continuum and line mapping. For AFGL 2591, the
43 GHz flux density is also consistent with dust emission from a disk seen in
near-infrared `speckle' images. However, the alignment of the 43 GHz emission
with the large-scale molecular outflow argues against an origin in a disk for
AFGL 2591 and NGC 7538 IRS9. In contrast, the outflow from W33A does not appear
to be collimated. Together with previously presented case studies of W3 IRS5
and AFGL 2136, our results indicate that the formation of stars and stellar
clusters with luminosities up to ~10^5 L0 proceeds through accretion and
produces collimated outflows as in the solar-type case, with the `additional
feature' that the accretion flow becomes ionized close to the star. Above ~10^5
L0, clusters of HII regions appear, and outflows are no longer collimated,
possibly as the result of mergers of protostars or pre-stellar cores.Comment: Accepted by A&A; 11 pages, 4 b/w figure
Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association
Inherited retinal disorder (IRD) is a leading cause of blindness, and CRX is one of a number of genes reported to harbour autosomal dominant (AD) and recessive (AR) causative variants. Eighteen patients from 13 families with CRX-associated retinal disorder (CRX-RD) were identified from 730 Japanese families with IRD. Ophthalmological examinations and phenotype subgroup classification were performed. The median age of onset/latest examination was 45.0/62.5 years (range, 15–77/25–94). The median visual acuity in the right/left eye was 0.52/0.40 (range, −0.08–2.00/−0.18–1.70) logarithm of the minimum angle of resolution (LogMAR) units. There was one family with macular dystrophy, nine with cone-rod dystrophy (CORD), and three with retinitis pigmentosa. In silico analysis of CRX variants was conducted for genotype subgroup classification based on inheritance and the presence of truncating variants. Eight pathogenic CRX variants were identified, including three novel heterozygous variants (p.R43H, p.P145Lfs*42, and p.P197Afs*22). A trend of a genotype-phenotype association was revealed between the phenotype and genotype subgroups. A considerably high proportion of CRX-RD in ADCORD was determined in the Japanese cohort (39.1%), often showing the mild phenotype (CORD) with late-onset disease (sixth decade). Frequently found heterozygous missense variants located within the homeodomain underlie this mild phenotype. This large cohort study delineates the disease spectrum of CRX-RD in the Japanese population
Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency
Biallelic variants in the EYS gene are a major cause of autosomal recessive inherited retinal disease (IRD), with a high prevalence in the Asian population. The purpose of this study was to identify pathogenic EYS variants, to determine the clinical/genetic spectrum of EYS-associated retinal disease (EYS-RD), and to discover disease-associated variants with relatively high allele frequency (1%-10%) in a nationwide Japanese cohort. Sixty-six affected subjects from 61 families with biallelic or multiple pathogenic/disease-associated EYS variants were ascertained by whole-exome sequencing. Three phenotype groups were identified in EYS-RD: retinitis pigmentosa (RP; 85.94%), cone-rod dystrophy (CORD; 10.94%), and Leber congenital amaurosis (LCA; 3.12%). Twenty-six pathogenic/disease-associated EYS variants were identified, including seven novel variants. The two most prevalent variants, p.(Gly843Glu) and p.(Thr2465Ser) were found in 26 and twelve families (42.6%, 19.7%), respectively, for which the allele frequency (AF) in the Japanese population was 2.2% and 3.0%, respectively. These results expand the phenotypic and genotypic spectrum of EYS-RD, accounting for a high proportion of EYS-RD both in autosomal recessive RP (23.4%) and autosomal recessive CORD (9.9%) in the Japanese population. The presence of EYS variants with relatively high AF highlights the importance of considering the pathogenicity of non-rare variants in relatively prevalent Mendelian disorders
- …