150 research outputs found
Performance Verification of the FlashCam Prototype Camera for the Cherenkov Telescope Array
The Cherenkov Telescope Array (CTA) is a future gamma-ray observatory that is
planned to significantly improve upon the sensitivity and precision of the
current generation of Cherenkov telescopes. The observatory will consist of
several dozens of telescopes with different sizes and equipped with different
types of cameras. Of these, the FlashCam camera system is the first to
implement a fully digital signal processing chain which allows for a traceable,
configurable trigger scheme and flexible signal reconstruction. As of autumn
2016, a prototype FlashCam camera for the medium-sized telescopes of CTA nears
completion. First results of the ongoing system tests demonstrate that the
signal chain and the readout system surpass CTA requirements. The stability of
the system is shown using long-term temperature cycling.Comment: 5 pages, 13 figures, Proceedings of the 9th International Workshop on
Ring Imaging Cherenkov Detectors (RICH 2016), Lake Bled, Sloveni
The Optical System for the Large Size Telescope of the Cherenkov Telescope Array
The Large Size Telescope (LST) of the Cherenkov Telescope Array (CTA) is
designed to achieve a threshold energy of 20 GeV. The LST optics is composed of
one parabolic primary mirror 23 m in diameter and 28 m focal length. The
reflector dish is segmented in 198 hexagonal, 1.51 m flat to flat mirrors. The
total effective reflective area, taking into account the shadow of the
mechanical structure, is about 368 m. The mirrors have a sandwich structure
consisting of a glass sheet of 2.7 mm thickness, aluminum honeycomb of 60 mm
thickness, and another glass sheet on the rear, and have a total weight about
47 kg. The mirror surface is produced using a sputtering deposition technique
to apply a 5-layer coating, and the mirrors reach a reflectivity of 94%
at peak. The mirror facets are actively aligned during operations by an active
mirror control system, using actuators, CMOS cameras and a reference laser.
Each mirror facet carries a CMOS camera, which measures the position of the
light spot of the optical axis reference laser on the target of the telescope
camera. The two actuators and the universal joint of each mirror facet are
respectively fixed to three neighboring joints of the dish space frame, via
specially designed interface plate.Comment: In Proceedings of the 34th International Cosmic Ray Conference
(ICRC2015), The Hague, The Netherlands. All CTA contributions at
arXiv:1508.0589
FlashCam: a fully-digital camera for the medium-sized telescopes of the Cherenkov Telescope Array
The FlashCam group is currently preparing photomultiplier-tube based cameras
proposed for the medium-sized telescopes (MST) of the Cherenkov Telescope Array
(CTA). The cameras are designed around the FlashCam readout concept which is
the first fully-digital readout system for Cherenkov cameras, based on
commercial FADCs and FPGAs as key components for the front-end electronics
modules and a high performance camera server as back-end. This contribution
describes the progress of the full-scale FlashCam camera prototype currently
under construction, as well as performance results also obtained with earlier
demonstrator setups. Plans towards the production and implementation of
FlashCams on site are also briefly presented.Comment: 8 pages, 6 figures. In Proceedings of the 34th International Cosmic
Ray Conference (ICRC2015), The Hague, The Netherlands. All CTA contributions
at arXiv:1508.0589
FlashCam: A fully digital camera for CTA telescopes
The future Cherenkov Telescope Array (CTA) will consist of several tens of
telescopes of different mirror sizes. CTA will provide next generation
sensitivity to very high energy photons from few tens of GeV to >100 TeV.
Several focal plane instrumentation options are currently being evaluated
inside the CTA consortium. In this paper, the current status of the FlashCam
prototyping project is described. FlashCam is based on a fully digital camera
readout concept and features a clean separation between photon detector plane
and signal digitization/triggering electronics.Comment: In Proceedings of the 2012 Heidelberg Symposium on High Energy
Gamma-Ray Astronomy. All CTA contributions at arXiv:1211.184
The Cherenkov Telescope Array Large Size Telescope
The two arrays of the Very High Energy gamma-ray observatory Cherenkov
Telescope Array (CTA) will include four Large Size Telescopes (LSTs) each with
a 23 m diameter dish and 28 m focal distance. These telescopes will enable CTA
to achieve a low-energy threshold of 20 GeV, which is critical for important
studies in astrophysics, astroparticle physics and cosmology. This work
presents the key specifications and performance of the current LST design in
the light of the CTA scientific objectives.Comment: 4 pages, 5 figures, In Proceedings of the 33rd International Cosmic
Ray Conference (ICRC2013), Rio de Janeiro (Brazil). All CTA contributions at
arXiv:1307.223
Linking Inflammation to Natural Killer T Cell Activation
Immune activation is often associated with inflammation, but inflammation's role in the expansion of antigen-specific immune responses remains unclear. This primer focuses on recent findings that show how specific natural killer T cells are activated by inflammatory messengers, thus illuminating the cellular and molecular links between immunity and inflammation
Search for Daily Modulation of MeV Dark Matter Signals with DAMIC-M
Dark Matter (DM) particles with sufficiently large cross sections may scatter
as they travel through Earth's bulk. The corresponding changes in the DM flux
give rise to a characteristic daily modulation signal in detectors sensitive to
DM-electron interactions. Here, we report results obtained from the first
underground operation of the DAMIC-M prototype detector searching for such a
signal from DM with MeV-scale mass. A model-independent analysis finds no
modulation in the rate of 1 events with periods in the range 1-48 h. We
then use these data to place exclusion limits on DM in the mass range [0.53,
2.7] MeV/c interacting with electrons via a dark photon mediator. Taking
advantage of the time-dependent signal we improve by 2 orders of
magnitude on our previous limit obtained from the total rate of 1 events,
using the same data set. This daily modulation search represents the current
strongest limit on DM-electron scattering via ultralight mediators for DM
masses around 1 MeV/c
Thymic Alterations in GM2 Gangliosidoses Model Mice
BACKGROUND: Sandhoff disease is a lysosomal storage disorder characterized by the absence of β-hexosaminidase and storage of GM2 ganglioside and related glycolipids. We have previously found that the progressive neurologic disease induced in Hexb(-/-) mice, an animal model for Sandhoff disease, is associated with the production of pathogenic anti-glycolipid autoantibodies. METHODOLOGY/PRINCIPAL FINDINGS: In our current study, we report on the alterations in the thymus during the development of mild to severe progressive neurologic disease. The thymus from Hexb(-/-) mice of greater than 15 weeks of age showed a marked decrease in the percentage of immature CD4(+)/CD8(+) T cells and a significantly increased number of CD4(+)/CD8(-) T cells. During involution, the levels of both apoptotic thymic cells and IgG deposits to T cells were found to have increased, whilst swollen macrophages were prominently observed, particularly in the cortex. We employed cDNA microarray analysis to monitor gene expression during the involution process and found that genes associated with the immune responses were upregulated, particularly those expressed in macrophages. CXCL13 was one of these upregulated genes and is expressed specifically in the thymus. B1 cells were also found to have increased in the thy mus. It is significant that these alterations in the thymus were reduced in FcRγ additionally disrupted Hexb(-/-) mice. CONCLUSIONS/SIGNIFICANCE: These results suggest that the FcRγ chain may render the usually poorly immunogenic thymus into an organ prone to autoimmune responses, including the chemotaxis of B1 cells toward CXCL13
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