Time, spatial, and spectral resolution of the Halpha line-formation region of Deneb and Rigel with the VEGA/CHARA interferometer

BA-type supergiants are amongst the most optically-bright stars. They are observable in extragalactic environments, hence potential accurate distance indicators. Emission activity in the Halpha line of the BA supergiants Rigel (B8Ia) and Deneb (A2Ia) is indicative of presence of localized time-dependent mass ejections. Here, we employ optical interferometry to study the Halpha line-formation region in these stellar environments. High spatial- (0.001 arcsec) and spectral- (R=30 000) resolution observations of Halpha were obtained with the visible recombiner VEGA installed on the CHARA interferometer, using the S1S2 array-baseline (34m). Six independent observations were done on Deneb over the years 2008 and 2009, and two on Rigel in 2009. We analyze this dataset with the 1D non-LTE radiative-transfer code CMFGEN, and assess the impact of the wind on the visible and near-IR interferometric signatures, using both Balmer-line and continuum photons. We observe a visibility decrease in Halpha for both Rigel and Deneb, suggesting that the line-formation region is extended (1.5-1.75 R*). We observe a significant visibility decrease for Deneb in the SiII6371 line. We witness time variations in the differential phase for Deneb, implying an inhomogeneous and unsteady circumstellar environment, while no such variability is seen in differential visibilities. Radiative-transfer modeling of Deneb, with allowance for stellar-wind mass loss, accounts fairly well for the observed decrease in the Halpha visibility. Based on the observed differential visibilities, we estimate that the mass-loss rate of Deneb has changed by less than 5%

Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as Hypertension Susceptibility Genes in Han Chinese with a Genome-Wide Gene-Based Association Study

Hypertension is a complex disorder with high prevalence rates all over the world. We conducted the first genome-wide gene-based association scan for hypertension in a Han Chinese population. By analyzing genome-wide single-nucleotide-polymorphism data of 400 matched pairs of young-onset hypertensive patients and normotensive controls genotyped with the Illumina HumanHap550-Duo BeadChip, 100 susceptibility genes for hypertension were identified and also validated with permutation tests. Seventeen of the 100 genes exhibited differential allelic and expression distributions between patient and control groups. These genes provided a good molecular signature for classifying hypertensive patients and normotensive controls. Among the 17 genes, IGF1, SLC4A4, WWOX, and SFMBT1 were not only identified by our gene-based association scan and gene expression analysis but were also replicated by a gene-based association analysis of the Hong Kong Hypertension Study. Moreover, cis-acting expression quantitative trait loci associated with the differentially expressed genes were found and linked to hypertension. IGF1, which encodes insulin-like growth factor 1, is associated with cardiovascular disorders, metabolic syndrome, decreased body weight/size, and changes of insulin levels in mice. SLC4A4, which encodes the electrogenic sodium bicarbonate cotransporter 1, is associated with decreased body weight/size and abnormal ion homeostasis in mice. WWOX, which encodes the WW domain-containing protein, is related to hypoglycemia and hyperphosphatemia. SFMBT1, which encodes the scm-like with four MBT domains protein 1, is a novel hypertension gene. GRB14, TMEM56 and KIAA1797 exhibited highly significant differential allelic and expressed distributions between hypertensive patients and normotensive controls. GRB14 was also found relevant to blood pressure in a previous genetic association study in East Asian populations. TMEM56 and KIAA1797 may be specific to Taiwanese populations, because they were not validated by the two replication studies. Identification of these genes enriches the collection of hypertension susceptibility genes, thereby shedding light on the etiology of hypertension in Han Chinese populations

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