20 research outputs found
Recommended from our members
Towards a Comprehensive View of Accretion, Inner Disks, and Extinction in Classical T Tauri Stars: An ODYSSEUS Study of the Orion OB1b Association
The coevolution of T Tauri stars and their surrounding protoplanetary disks dictates the timescales of planet formation. In this paper, we present magnetospheric accretion and inner disk wall model fits to near-UV (NUV) to near-IR (NIR) spectra of nine classical T Tauri stars in Orion OB1b as part of the Outflows and Disks around Young Stars: Synergies for the Exploration of ULLYSES Spectra (ODYSSEUS) survey. Using NUV–optical spectra from the Hubble UV Legacy Library of Young Stars as Essential Standards (ULLYSES) Director's Discretionary Program and optical–NIR spectra from the PENELLOPE VLT Large Programme, we find that the accretion rates of these targets are relatively high for the region's intermediate age of 5.0 Myr; rates are in the range of (0.5–17.2) × 10−8 M☉ yr−1, with a median value of 1.2 × 10−8 M☉ yr−1. The NIR excesses can be fit with 1200–1800 K inner disk walls located at 0.05–0.10 au from the host stars. We discuss the significance of the choice in extinction law, as the measured accretion rate depends strongly on the adopted extinction value. This analysis will be extended to the complete sample of T Tauri stars being observed through ULLYSES to characterize accretion and inner disks in star-forming regions of different ages and stellar populations.
</p
Histo-Blood Group Gene Polymorphisms as Potential Genetic Modifiers of Infection and Cystic Fibrosis Lung Disease Severity
The pulmonary phenotype in cystic fibrosis (CF) is variable; thus, environmental and genetic factors likely contribute to clinical heterogeneity. We hypothesized that genetically determined ABO histo-blood group antigen (ABH) differences in glycosylation may lead to differences in microbial binding by airway mucus, and thus predispose to early lung infection and more severe lung disease in a subset of patients with CF. infection in the severe or mild groups. Multivariate analyses of other clinical phenotypes, including gender, asthma, and meconium ileus demonstrated no differences between groups based on ABH type. infection, nor was there any association with other clinical phenotypes in a group of 808 patients homozygous for the ΔF508 mutation