Investigation of Hamamatsu H8500 phototubes as single photon detectors

We have investigated the response of a significant sample of Hamamatsu H8500 MultiAnode PhotoMultiplier Tubes (MAPMTs) as single photon detectors, in view of their use in a ring imaging Cherenkov counter for the CLAS12 spectrometer at the Thomas Jefferson National Accelerator Facility. For this, a laser working at 407.2nm wavelength was employed. The sample is divided equally into standard window type, with a spectral response in the visible light region, and UV-enhanced window type MAPMTs. The studies confirm the suitability of these MAPMTs for single photon detection in such a Cherenkov imaging application

Test of the CLAS12 RICH large scale prototype in the direct proximity focusing configuration

A large area ring-imaging Cherenkov detector has been designed to provide clean hadron identification capability in the momentum range from 3 GeV/c up to 8 GeV/c for the CLAS12 experiments at the upgraded 12 GeV continuous electron beam accelerator facility of Jefferson Laboratory. The adopted solution foresees a novel hybrid optics design based on aerogel radiator, composite mirrors and high-packed and high-segmented photon detectors. Cherenkov light will either be imaged directly (forward tracks) or after two mirror reflections (large angle tracks). We report here the results of the tests of a large scale prototype of the RICH detector performed with the hadron beam of the CERN T9 experimental hall for the direct detection configuration. The tests demonstrated that the proposed design provides the required pion-to-kaon rejection factor of 1:500 in the whole momentum range.Comment: 15 pages, 23 figures, to appear on EPJ

Explanation of the activity sensitivity of Mn I 5394.7 \AA

There is a long-standing controversy concerning the reason why the Mn I 5394.7 A line in the solar irradiance spectrum brightens more at larger activity than most other photospheric lines. The claim that this activity sensitivity is caused by spectral interlocking to chromospheric emission in Mg II h & k is disputed. Classical one-dimensional modeling is used for demonstration; modern three-dimensional MHD simulation for verification and analysis. The Mn I 5394.7 A line thanks its unusual sensitivity to solar activity to its hyperfine structure. This overrides the thermal and granular Doppler smearing through which the other, narrower, photospheric lines lose such sensitivity. We take the nearby Fe I 5395.2 A line as example of the latter and analyze the formation of both lines in detail to demonstrate and explain granular Doppler brightening. We show that this affects all narrow lines. Neither the chromosphere nor Mg II h & k play a role, nor is it correct to describe the activity sensitivity of Mn I 5394.7 A through plage models with outward increasing temperature contrast. The Mn I 5394.7 A line represents a proxy diagnostic of strong-field magnetic concentrations in the deep solar photosphere comparable to the G band and the blue wing of H-alpha, but not a better one than these. The Mn I lines are more promising as diagnostic of weak fields in high-resolution Stokes polarimetry.Comment: 12 pages, 8 figures, accepted by A&

Photospheric Dynamic Model of Magnetic Reconnection

We present a dynamic model of the atmospheric magnetic field in which magnetic loop footpoints are controlled by photospheric flows computed through a N-body algorithm. This simulation reproduces a system whose behaviour is characterized by small scale (e.g., granular) advection flows that interact to form large spatial organization scales (e.g., meso- and super-granulation). In this model the passive advection of magnetic footpoints through photospheric spatio-temporal correlated flows causes the magnetic field to reconfigure as a consequence of magnetic reconnection processes. This approach, based on the dynamic model of multiple magnetic loops tep{b8 Hu03} and on an advective-interaction model proposed by tet{b8 Ra03}, naturally accounts for the observed probability distribution functions and waiting time statistics of the emitted magnetic energy

MiR-203 controls proliferation, migration and invasive potential of prostate cancer cell lines

Prostate cancers show a slow progression from a local lesion (primary tumor) to a metastatic and hormone-resistant phenotype. After an initial step of hyperplasia, in a high percentage of cases a neoplastic transformation event occurs that, less frequently, is followed by epithelial to mesenchymal transition and invasion of healthy tissues (usually bones). MicroRNA-203 (miR-203) is a tumor suppressor microRNA often silenced in different malignancies. Here, we show that miR-203 is downregulated in clinical primary prostatic tumors compared to normal prostate tissue, and in metastatic prostate cancer cell lines compared to normal epithelial prostatic cells. Overexpression of miR-203 in brain or bone metastatic prostate cell lines (DU145 and PC3) is sufficient to induce a mesenchymal to epithelial transition with inhibition of cell proliferation, migration and invasiveness. We have identified CKAP2, LASP1, BIRC5, WASF1, ASAP1 and RUNX2 as new miR-203 direct target mRNAs involved in these events. Therefore, miR-203 could be a potentially new prognostic marker and therapeutic target in metastatic prostate cancer

MiR-203 controls proliferation, migration and invasive potential of prostate cancer cell lines

Prostate cancers show a slow progression from a local lesion (primary tumor) to a metastatic and hormone-resistant phenotype. After an initial step of hyperplasia, in a high percentage of cases a neoplastic transformation event occurs that, less frequently, is followed by epithelial to mesenchymal transition and invasion of healthy tissues (usually bones). MicroRNA-203 (miR-203) is a tumor suppressor microRNA often silenced in different malignancies. Here, we show that miR-203 is downregulated in clinical primary prostatic tumors compared to normal prostate tissue, and in metastatic prostate cancer cell lines compared to normal epithelial prostatic cells. Overexpression of miR-203 in brain or bone metastatic prostate cell lines (DU145 and PC3) is sufficient to induce a mesenchymal to epithelial transition with inhibition of cell proliferation, migration and invasiveness. We have identified CKAP2, LASP1, BIRC5, WASF1, ASAP1 and RUNX2 as new miR-203 direct target mRNAs involved in these events. Therefore, miR-203 could be a potentially new prognostic marker and therapeutic target in metastatic prostate cancer