15,810 research outputs found
Adaptive Optics Near-Infrared Spectroscopy of the Sgr A* Cluster
We present K-band ~ 2600 spectroscopy of five stars
(K ~ 14 - 16 mag) within 0.''5 of Sgr A*, the radio source associated with the
compact massive object suspected to be a 2.6 x 10 \msun black hole at the
center of our Galaxy. High spatial resolution of ~ 0.''09, and good strehl
ratios of ~ 0.2 achieved with adaptive optics on the 10-meter Keck telescope
make it possible to measure moderate-resolution spectra of these stars
individually for the first time. Two stars (S0-17 and S0-18) are identified as
late-type stars by the detection of CO bandhead absorption in their spectra.
Their absolute K magnitudes and CO bandhead absorption strengths are consistent
with early K giants. Three stars (S0-1, S0-2, and S0-16), with r
0.0075 pc (~ 0.''2) from Sgr A*, lack CO bandhead absorption, confirming the
results of earlier lower spectral and lower spatial resolution observations
that the majority of the stars in the Sgr A* Cluster are early-type stars. The
absolute K magnitudes of the early-type stars suggest that they are late O -
early B main sequence stars of ages 20 Myr. The presence of young stars in
the Sgr A* Cluster, so close to the central supermassive black hole, poses the
intriguing problem of how these stars could have formed, or could have been
brought, within its strong tidal field.Comment: 19 pages, 8 figures, 2 tables. Accepted for publication in Ap
Potassium Relationships of Three Ohio Soils
Author Institution: The Ohio State University Agricultural Technical Institute; Department of Agronomy, The Ohio State UniversityThree Ohio soils, Hoytville clay, Brookston silty clay loam, and Wooster silt loam located at various branches of the Ohio Agricultural Research and Development Center, were studied. Bulk samples from each horizon were tested for exchangeable basic cations, pH, sulfuric acid extractable potassium (K+), and particle-size distribution. The surface horizons of each soil were characterized by measurement of cation exchange capacity, quantity-intensity adsorption isotherms for K+ and x-ray diffraction of the clay ( times greater than that for Wooster. Hoytville clay was predominantly illitic while the Brookston and Wooster clays were of a more mixed mineralogical nature. The potassium content and crystallinity of the illite in the Hoytville clay is lower than those of the Brookston and Wooster clays
K-Band Spectroscopy of an Obscured Massive Stellar Cluster in the Antennae Galaxies (NGC 4038/4039) with NIRSPEC
We present infrared spectroscopy of the Antennae Galaxies (NGC 4038/4039)
with NIRSPEC at the W. M. Keck Observatory. We imaged the star clusters in the
vicinity of the southern nucleus (NGC 4039) in 0.39" seeing in K-band using
NIRSPEC's slit-viewing camera. The brightest star cluster revealed in the
near-IR (M_K(0) = -17.9) is insignificant optically, but coincident with the
highest surface brightness peak in the mid-IR (12-18 um) ISO image presented by
Mirabel et al (1998). We obtained high signal-to-noise 2.03-2.45 um spectra of
the nucleus and the obscured star cluster at R = 1900.
The cluster is very young (age ~ 4 Myr), massive (M ~ 16E6 M_sun), and
compact (density ~ 115 M_sun pc^(-3) within a 32 pc half-light radius),
assuming a Salpeter IMF (0.1-100 M_sun). Its hot stars have a radiation field
characterized by T_eff ~ 39,000 K, and they ionize a compact HII region with
n_e ~ 10^4 cm^(-3). The stars are deeply embedded in gas and dust (A_V = 9-10
mag), and their strong FUV field powers a clumpy photodissociation region with
densities n_H > 10^5 cm^(-3) on scales of ~ 200 pc, radiating L{H_2 1-0 S(1)}=
9600 L_sun.Comment: 4 pages, 4 embedded figures, uses emulateapj.sty. To appear in ApJL.
Also available at http://astro.berkeley.edu/~agilber
The molecular genetic analysis of the expanding pachyonychia congenita case collection
BACKGROUND: Pachyonychia congenita (PC) is a rare autosomal dominant keratinizing disorder characterized by severe, painful, palmoplantar keratoderma and nail dystrophy, often accompanied by oral leucokeratosis, cysts and follicular keratosis. It is caused by mutations in one of five keratin genes: KRT6A, KRT6B, KRT6C, KRT16 or KRT17. OBJECTIVES: To identify mutations in 84 new families with a clinical diagnosis of PC, recruited by the International Pachyonychia Congenita Research Registry during the last few years. METHODS: Genomic DNA isolated from saliva or peripheral blood leucocytes was amplified using primers specific for the PC-associated keratin genes and polymerase chain reaction products were directly sequenced. RESULTS: Mutations were identified in 84 families in the PC-associated keratin genes, comprising 46 distinct keratin mutations. Fourteen were previously unreported mutations, bringing the total number of different keratin mutations associated with PC to 105. CONCLUSIONS: By identifying mutations in KRT6A, KRT6B, KRT6C, KRT16 or KRT17, this study has confirmed, at the molecular level, the clinical diagnosis of PC in these families
The neuropathology of kuru and variant Creutzfeldt–Jakob disease
A comparison of the pathological profiles of two spongiform encephalopathies with a similar presumptive route of infection was performed. Archival kuru and recent variant Creutzfeldt–Jakob disease (vCJD) cases reveal distinct lesional differences, particularly with respect to prion protein, suggesting that the strain of agent is important in determining the phenotype. Genotype analysis of the polymorphism on codon 129 reveals (in conjunction with updated information from more kuru cases) that all three genotypes (VV, MV and MM (where M is methionine and V is valine)) are detected in kuru with some preference for MM homozygosity. The presence of valine does not therefore appear to determine peripheral selection of PrPCJD. vCJD remains restricted to date to MM homozygosity on codon 129. It remains to be determined whether this genotype is dictating a shorter incubation period
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