Atomic jet from SMM1 (FIRS1) in Serpens uncovers non-coeval binary companion

We report on the detection of an atomic jet associated with the protostellar source SMM1 (FIRS1) in Serpens. The jet is revealed in [FeII] and [NeII] line maps observed with Spitzer/IRS, and further confirmed in HiRes IRAC and MIPS images. It is traced very close to SMM1 and peaks at ~5 arcsec" from the source at a position angle of $\sim 125 degrees. In contrast, molecular hydrogen emission becomes prominent at distances > 5" from the protostar and extends at a position angle of 160 degrees. The morphological differences suggest that the atomic emission arises from a companion source, lying in the foreground of the envelope surrounding the embedded protostar SMM1. In addition the molecular and atomic Spitzer maps disentangle the large scale CO (3-2) emission observed in the region into two distinct bipolar outflows, giving further support to a proto-binary source setup. Analysis at the peaks of the [FeII] jet show that emission arises from warm and dense gas (T ~1000 K, n(electron) 10^5 - 10^6 cm^-3). The mass flux of the jet derived independently for the [FeII] and [NeII] lines is 10^7 M(sun)/yr, pointing to a more evolved Class~I/II protostar as the driving source. All existing evidence converge to the conclusion that SMM1 is a non-coeval proto-binary source.Comment: 10 pages, 7 figures, 1 table. Accepted for publication in Astronomy \& Astrophysic

Water destruction by X-rays in young stellar objects

We study the H2O chemistry in star-forming environments under the influence of a central X-ray source and a central far ultraviolet (FUV) radiation field. The gas-phase water chemistry is modeled as a function of time, hydrogen density and X-ray flux. To cover a wide range of physical environments, densities between n_H = 10^4-10^9 cm^-3 and temperatures between T = 10-1000 K are studied. Three different regimes are found: For T < 100 K, the water abundance is of order 10^-7-10^-6 and can be somewhat enhanced or reduced due to X-rays, depending on time and density. For 100 K < T < 250 K, H2O is reduced from initial x(H2O) ~ 10^-4 following ice evaporation to x(H2O) ~ 10^-6 for F_X > 10^-3 ergs s-1 cm^-2 (t = 10^4 yrs) and for F_X > 10^-4 ergs s^-1 cm^-2 (t = 10^5 yrs). At higher temperatures (T > 250 K) and hydrogen densities, water can persist with x(H2O) ~ 10^-4 even for high X-ray fluxes. The X-ray and FUV models are applied to envelopes around low-mass Class 0 and I young stellar objects (YSOs). Water is destroyed in both Class 0 and I envelopes on relatively short timescales (t ~ 5000 yrs) for realistic X-ray fluxes, although the effect is less prominent in Class 0 envelopes due to the higher X-ray absorbing densities there. FUV photons from the central source are not effective in destroying water. The average water abundance in Class I sources for L_X > 10^27 ergs s^-1 is predicted to be x(H2O) < 10^-6.Comment: 12 pages, 14 figures, Accepted for publication in A&

Lower bounds for the first eigenvalue of the magnetic Laplacian

We consider a Riemannian cylinder endowed with a closed potential 1-form A and study the magnetic Laplacian with magnetic Neumann boundary conditions associated with those data. We establish a sharp lower bound for the first eigenvalue and show that the equality characterizes the situation where the metric is a product. We then look at the case of a planar domain bounded by two closed curves and obtain an explicit lower bound in terms of the geometry of the domain. We finally discuss sharpness of this last estimate.Comment: Replaces in part arXiv:1611.0193

QTL Analysis of Vernalisation Requirement and Heading Traits in \u3cem\u3eFestuca Pratensis\u3c/em\u3e Huds.

The transition from the vegetative phase to the reproductive phase occurs as a result of environmental and endogenous stimuli. In Festuca pratensis, low temperature and/or short days over a certain period (primary induction) followed by long days (secondary induction) will lead to heading and flowering (Heide, 1988). We present results from QTL mapping of vernalisation requirement and heading traits and mapping of the Vrn-1 ortholog in F. pratensis