Calibration of <i>Herschel</i> SPIRE FTS observations at different spectral resolutions

The SPIRE Fourier Transform Spectrometer on-board the Herschel Space Observatory had two standard spectral resolution modes for science observations: high resolution (HR) and low resolution (LR), which could also be performed in sequence (H+LR). A comparison of the HR and LR resolution spectra taken in this sequential mode revealed a systematic discrepancy in the continuum level. Analysing the data at different stages during standard pipeline processing demonstrates that the telescope and instrument emission affect HR and H+LR observations in a systematically different way. The origin of this difference is found to lie in the variation of both the telescope and instrument response functions, while it is triggered by fast variation of the instrument temperatures. As it is not possible to trace the evolution of the response functions using housekeeping data from the instrument subsystems, the calibration cannot be corrected analytically. Therefore, an empirical correction for LR spectra has been developed, which removes the systematic noise introduced by the variation of the response functions

Connection Conditions and the Spectral Family under Singular Potentials

To describe a quantum system whose potential is divergent at one point, one must provide proper connection conditions for the wave functions at the singularity. Generalizing the scheme used for point interactions in one dimension, we present a set of connection conditions which are well-defined even if the wave functions and/or their derivatives are divergent at the singularity. Our generalized scheme covers the entire U(2) family of quantizations (self-adjoint Hamiltonians) admitted for the singular system. We use this scheme to examine the spectra of the Coulomb potential $V(x) = - e^2 / | x |$ and the harmonic oscillator with square inverse potential $V(x) = (m \omega^2 / 2) x^2 + g/x^2$, and thereby provide a general perspective for these models which have previously been treated with restrictive connection conditions resulting in conflicting spectra. We further show that, for any parity invariant singular potentials $V(-x) = V(x)$, the spectrum is determined solely by the eigenvalues of the characteristic matrix $U \in U(2)$.Comment: TeX, 18 page

Inflectional loci of scrolls

Let $X\subset \mathbb P^N$ be a scroll over a smooth curve $C$ and let \L=\mathcal O_{\mathbb P^N}(1)|_X denote the hyperplane bundle. The special geometry of $X$ implies that some sheaves related to the principal part bundles of \L are locally free. The inflectional loci of $X$ can be expressed in terms of these sheaves, leading to explicit formulas for the cohomology classes of the loci. The formulas imply that the only uninflected scrolls are the balanced rational normal scrolls.Comment: 9 pages, improved version. Accepted in Mathematische Zeitschrif

Kepler-1656b: a Dense Sub-Saturn With an Extreme Eccentricity

Kepler-1656b is a 5 $R_E$ planet with an orbital period of 32 days initially detected by the prime Kepler mission. We obtained precision radial velocities of Kepler-1656 with Keck/HIRES in order to confirm the planet and to characterize its mass and orbital eccentricity. With a mass of $48 \pm 4 M_E$, Kepler-1656b is more massive than most planets of comparable size. Its high mass implies that a significant fraction, roughly 80%, of the planet's total mass is in high density material such as rock/iron, with the remaining mass in a low density H/He envelope. The planet also has a high eccentricity of $0.84 \pm 0.01$, the largest measured eccentricity for any planet less than 100 $M_E$. The planet's high density and high eccentricity may be the result of one or more scattering and merger events during or after the dispersal of the protoplanetary disk.Comment: 10 pages, 6 figures, published in The Astronomical Journa

Hyperinsulinism-hyperammonaemia syndrome: novel mutations in the GLUD1 gene and genotype-phenotype correlations

Background: Activating mutations in the GLUD1 gene (which encodes for the intra-mitochondrial enzyme glutamate dehydrogenase, GDH) cause the hyperinsulinism–hyperammonaemia (HI/HA) syndrome. Patients present with HA and leucine-sensitive hypoglycaemia. GDH is regulated by another intra-mitochondrial enzyme sirtuin 4 (SIRT4). Sirt4 knockout mice demonstrate activation of GDH with increased amino acid-stimulated insulin secretion. Objectives: To study the genotype–phenotype correlations in patients with GLUD1 mutations. To report the phenotype and functional analysis of a novel mutation (P436L) in the GLUD1 gene associated with the absence of HA. Patients and methods: Twenty patients with HI from 16 families had mutational analysis of the GLUD1 gene in view of HA (n=19) or leucine sensitivity (n=1). Patients negative for a GLUD1 mutation had sequence analysis of the SIRT4 gene. Functional analysis of the novel P436L GLUD1 mutation was performed. Results: Heterozygous missense mutations were detected in 15 patients with HI/HA, 2 of which are novel (N410D and D451V). In addition, a patient with a normal serum ammonia concentration (21 µmol/l) was heterozygous for a novel missense mutation P436L. Functional analysis of this mutation confirms that it is associated with a loss of GTP inhibition. Seizure disorder was common (43%) in our cohort of patients with a GLUD1 mutation. No mutations in the SIRT4 gene were identified. Conclusion: Patients with HI due to mutations in the GLUD1 gene may have normal serum ammonia concentrations. Hence, GLUD1 mutational analysis may be indicated in patients with leucine sensitivity; even in the absence of HA. A high frequency of epilepsy (43%) was observed in our patients with GLUD1 mutations