467 research outputs found

    Realization of BEC-BCS crossover physics in a compact oven-loaded magneto-optic trap apparatus

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    We report on a simple oven-loaded magneto-optical trap (MOT) apparatus for the creation of both molecular Bose-Einstein condensates (mBEC) and degenerate Fermi gases (DFGs) of lithium. The apparatus does not require a Zeeman slower or a 2D MOT nor does it require any separation or differential pumping between the effusive atom source and the science chamber. The result is an exceedingly simple, inexpensive, and compact vacuum system ideal for miniaturization. We discuss our work in the context of other realizations of quantum degenerate gases by evaporation in optical dipole traps and illustrate that our apparatus meets the key requirements of atom number and trap lifetime. We also demonstrate with this system the production of a mBEC, and we use it to observe the pairing gap of a strongly interacting two-component DFG in the BEC-BCS crossover regime.Comment: 12 pages, 7 figure

    Andromeda II as a merger remnant

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    Using N-body simulations we study the origin of prolate rotation recently detected in the kinematic data for And II, a dSph satellite of M31. We propose an evolutionary model for the origin of And II involving a merger between two disky dwarf galaxies whose structural parameters differ only in their disk scale lengths. The dwarfs are placed on a radial orbit towards each other with their angular momenta inclined by 45 deg to the orbital plane and by 90 deg with respect to each other. After 5 Gyr of evolution the merger remnant forms a stable triaxial galaxy with rotation only around the longest axis. The origin of this rotation is naturally explained as due to the symmetry of the initial configuration which leads to the conservation of angular momentum components along the direction of the merger. The stars originating from the two dwarfs show significantly different surface density profiles while having very similar kinematics in agreement with the properties of separate stellar populations in And II. We also study an alternative scenario for the formation of And II, via tidal stirring of a disky dwarf galaxy. While intrinsic rotation occurs naturally in this model as a remnant of the initial rotation of the disk, it is mostly around the shortest axis of the stellar component. The rotation around the longest axis is induced only occasionally and remains much smaller that the system's velocity dispersion. We conclude that although tidal origin of the velocity distribution in And II cannot be excluded, it is much more naturally explained within the scenario involving a past merger event. Thus, in principle, the presence of prolate rotation in dSph galaxies of the Local Group and beyond may be used as an indicator of major mergers in their history or even as a way to distinguish between the two scenarios of their formation.Comment: 5 pages, 6 figures, accepted for publication in MNRAS Letter

    Clinicoprognostical features of endometrial cancer patients with somatic mtDNA mutations

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    Somatic mitochondrial DNA (mtDNA) mutations have been found in a subset of endometrial cancers (EC) from different populations. We have investigated the relationship between mtDNA changes and clinical and pathological variables of women affected by EC. mtDNA mutations were detected both in early (3/32; 9%) and in advanced (1/8; 12%) stages of uterine tumors. However, patients carrying the mtDNA mutations or the normal mtDNA sequence had indistinguishable clinicopathological data, including age, clinical stage, histological grade and type or depth of myometrial invasion. It is noteworthy that mtDNA mutations were not detected in hyperplastic endometrial tissues or in ECs coexisting with hyperplasia, nor in a single case of endometrial stromal sarcoma. LOH at the tumor suppressor genes RB1 and TP53 as well as p16INK4A alterations (LOH, gene deletion) were found in tumors carrying mtDNA mutations. These results suggest that somatic mtDNA mutations are detected in a subset of ECs, although they are unrelated to clinicopathological variables of cancer
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