Inner disk clearing around the Herbig Ae star HD139614: Evidence for a planet-induced gap?
ASTRONOMY & ASTROPHYSICS
Authors: Matter, A.; Labadie, L.; Augereau, J. C.; Kluska, J.; Crida, A.; Carmona, A.; Gonzalez, J. F.; Thi, W. F.; Le Bouquin, J. -B.; Olofsson, J.; Lopez, B.
Abstract
Spatially resolving the inner dust cavity (or gap) of the so-called (pre-) transitional disks is a key to understanding the connection between the processes of planetary formation and disk dispersal. The disk around the Herbig star HD139614 is of particular interest since it presents a pretransitional nature with an au-sized gap structure that is spatially resolved by mid-infrared interferometry in the dust distribution. With the aid of new near-infrared interferometric observations, we aim to characterize the 0.1-10 au region of the HD 139614 disk further and then identify viable mechanisms for the inner disk clearing. We report the first multiwavelength modeling of the interferometric data acquired on HD 139614 with the VLTI instruments PIONIER, AMBER, and MIDI, complemented by Herschel/PACS photometric measurements. We first performed a geometrical modeling of the new near-infrared interferometric data, followed by radiative transfer modeling of the complete dataset using the code RADMC3D. We confirm the presence of a gap structure in the warm mu m-sized dust distribution, extending from about 2.5 au to 6 au, and constrained the properties of the inner dust component: e.g., a radially increasing dust surface density profile, and a depletion in dust of similar to 10(3) relative to the outer disk. Since self-shadowing and photoevaporation appears unlikely to be responsible for the au-sized gap of HD 139614, we thus tested if dynamical clearing could be a viable mechanism using hydrodynamical simulations to predict the structure of the gaseous disk. Indeed, a narrow au-sized gap is consistent with the expected effect of the interaction between a single giant planet and the disk. Assuming that small dust grains are well coupled to the gas, we found that an approximately 3 M-jup planet located at similar to 4.5 au from the star could, in less than 1 Myr, reproduce most of the aspects of the dust surface density profile, while no significant depletion (in gas) occurred in the inner disk, in contrast to the dust. However, this "dust-depleted" inner disk could be explained by the expected dust filtration by the gap and the efficient dust growth/fragmentation occurring in the inner disk regions. Our results support the hypothesis of a giant planet opening a gap and shaping the inner region of the HD 139614 disk. This makes HD 139614 an exciting candidate specifically for witnessing planet-disk interaction.
Combination of palmoplantar keratoderma and hair shaft anomalies, the warning signal of severe arrhythmogenic cardiomyopathy: a systematic review on genetic desmosomal diseases
JOURNAL OF MEDICAL GENETICS
Authors: Polivka, Laura; Bodemer, Christine; Hadj-Rabia, Smail
Abstract
Inherited desmosomal diseases are characterised by skin and/or cardiac features. Dermatological features might be a clue in the determination of the underlying life-threatening cardiac disease. This article aims to propose a dermatological algorithm for the diagnosis of desmosomal diseases after a systematic review of published articles. Palmoplantar keratoderma (PPK), hair shaft anomalies and skin fragility are the major features in the 458 patients analysed. Isolated PPK or isolated hair shaft anomalies are associated with a desmosomal disease limited to skin. The combination of PPK and hair shaft anomalies was recorded in 161 patients, and this association is at high risk of cardiac disease (129/161, 80.1%). Skin features had led to cardiac monitoring in only 2.3% of those patients. We delineated three major phenotypes: the PPK-hair shaft anomalies-non-fragile skin subtype (77%), always associated with cardiac involvement; the PPK-hair shaft anomalies-skin fragility-normal cardiac function subtype (19.9%), frequently associated with PKP1 mutations; the PPK-hair shaft anomalies-skin fragility-cardiac involvement subtype (3.1%), always due to DSP mutations. Three mutation hotspots in DSP and JUP account for 90.8% of the patients with cardiac involvement. The combination of PPK and hair shaft anomalies justifies long-term cardiac monitoring.