University of Warsaw

About: University of Warsaw is a education organization based out in Warsaw, Poland. It is known for research contribution in the topics: Population & Large Hadron Collider. The organization has 20832 authors who have published 56617 publications receiving 1185084 citations. The organization is also known as: Uniwersytet Warszawski & Warsaw University.

MOA-2011-BLG-262Lb: A Sub-Earth-Mass Moon Orbiting a Gas Giant Primary or a High Velocity Planetary System in the Galactic Bulge

Abstract: We present the first microlensing candidate for a free-floating exoplanet-exomoon system, MOA-2011-BLG-262, with a primary lens mass of M host ~ 4 Jupiter masses hosting a sub-Earth mass moon. The argument for an exomoon hinges on the system being relatively close to the Sun. The data constrain the product ML πrel where ML is the lens system mass and πrel is the lens-source relative parallax. If the lens system is nearby (large πrel), then ML is small (a few Jupiter masses) and the companion is a sub-Earth-mass exomoon. The best-fit solution has a large lens-source relative proper motion, μrel = 19.6 ± 1.6 mas yr–1, which would rule out a distant lens system unless the source star has an unusually high proper motion. However, data from the OGLE collaboration nearly rule out a high source proper motion, so the exoplanet+exomoon model is the favored interpretation for the best fit model. However, there is an alternate solution that has a lower proper motion and fits the data almost as well. This solution is compatible with a distant (so stellar) host. A Bayesian analysis does not favor the exoplanet+exomoon interpretation, so Occam's razor favors a lens system in the bulge with host and companion masses of and , at a projected separation of AU. The existence of this degeneracy is an unlucky accident, so current microlensing experiments are in principle sensitive to exomoons. In some circumstances, it will be possible to definitively establish the mass of such lens systems through the microlensing parallax effect. Future experiments will be sensitive to less extreme exomoons.

Masses and Orbital Constraints for the OGLE-2006-BLG-109Lb,c Jupiter/Saturn Analog Planetary System

Abstract: We present a new analysis of the Jupiter+Saturn analog system, OGLE-2006-BLG-109Lb,c, which was the first double planet system discovered with the gravitational microlensing method. This is the only multi-planet system discovered by any method with measured masses for the star and both planets. In addition to the signatures of two planets, this event also exhibits a microlensing parallax signature and finite source effects that provide a direct measure of the masses of the star and planets, and the expected brightness of the host star is confirmed by Keck AO imaging, yielding masses of , Mb = 231 ± 19 M ⊕, and Mc = 86 ± 7 M ⊕. The Saturn-analog planet in this system had a planetary light-curve deviation that lasted for 11 days, and as a result, the effects of the orbital motion are visible in the microlensing light curve. We find that four of the six orbital parameters are tightly constrained and that a fifth parameter, the orbital acceleration, is weakly constrained. No orbital information is available for the Jupiter-analog planet, but its presence helps to constrain the orbital motion of the Saturn-analog planet. Assuming co-planar orbits, we find an orbital eccentricity of and an orbital inclination of . The 95% confidence level lower limit on the inclination of i > 49° implies that this planetary system can be detected and studied via radial velocity measurements using a telescope of 30 m aperture.

ASASSN-15oi: a rapidly evolving, luminous tidal disruption event at 216 Mpc

Abstract: We present ground-based and Swift photometric and spectroscopic observations of the tidal disruption event (TDE) ASASSN-15oi, discovered at the center of 2MASX J20390918-3045201 ($d\simeq216$ Mpc) by the All-Sky Automated Survey for SuperNovae (ASAS-SN). The source peaked at a bolometric luminosity of $L\simeq1.9\times10^{44}$ ergs s$^{-1}$ and radiated a total energy of $E\simeq5.0\times10^{50}$ ergs over the $\sim3.5$ months of observations. The early optical/UV emission of the source can be fit by a blackbody with temperature increasing from $T\sim2\times10^4$ K to $T\sim6\times10^4$ K while the luminosity declines from $L\simeq1.9\times10^{44}$ ergs s$^{-1}$ to $L\simeq2.8\times10^{43}$ ergs s$^{-1}$, requiring the photosphere to be shrinking rapidly. The optical/UV luminosity decline is broadly consistent with an exponential decline, $L\propto e^{-t/t_0}$, with $t_0\simeq35$ days. ASASSN-15oi also exhibits roughly constant soft X-ray emission that is significantly weaker than the optical/UV emission. Spectra of the source show broad helium emission lines and strong blue continuum emission in early epochs, although these features fade rapidly and are not present $\sim3$ months after discovery. The early spectroscopic features and color evolution of ASASSN-15oi are consistent with a TDE, but the rapid spectral evolution is unique among optically-selected TDEs.

A concept for G protein activation by G protein-coupled receptor dimers: the transducin/rhodopsin interface.

Abstract: G protein-coupled receptors (GPCRs) are ubiquitous and essential in modulating virtually all physiological processes. These receptors share a similar structural design consisting of the seven-transmembrane α-helical segments. The active conformations of the receptors are stabilized by an agonist and couple to structurally highly conserved heterotrimeric G proteins. One of the most important unanswered questions is how GPCRs couple to their cognate G proteins. Phototransduction represents an excellent model system for understanding G protein signaling, owing to the high expression of rhodopsin in rod photoreceptors and the multidisciplinary experimental approaches used to study this GPCR. Here, we describe how a G protein (transducin) docks on to an oligomeric GPCR (rhodopsin), revealing structural details of this critical interface in the signal transduction process. This conceptual model takes into account recent structural information on the receptor and G protein, as well as oligomeric states of GPCRs.