On the comparison of analog and digital SiPM readout in terms of expected timing performance

AbstractIn time of flight positron emission tomography (TOF-PET) and in particular for the EndoTOFPET-US Project (Frisch, 2013 [1]), and other applications for high energy physics, the multi-digital silicon photomultiplier (MD-SiPM) was recently proposed (Mandai and Charbon, 2012 [2]), in which the time of every single photoelectron is being recorded. If such a photodetector is coupled to a scintillator, the largest and most accurate timing information can be extracted from the cascade of the scintillation photons, and the most probable time of positron emission determined. The readout concept of the MD-SiPM is very different from that of the analog SiPM, where the individual photoelectrons are merely summed up and the output signal fed into the readout electronics. We have developed a comprehensive Monte Carlo (MC) simulation tool that describes the timing properties of the photodetector and electronics, the scintillation properties of the crystal and the light transfer within the crystal. In previous studies we have compared MC simulations with coincidence time resolution (CTR) measurements and found good agreement within less than 10% for crystals of different lengths (from 3mm to 20mm) coupled to SiPMs from Hamamatsu. In this work we will use the developed MC tool to directly compare the highest possible time resolution for both the analog and digital readout of SiPMs with different scintillator lengths. The presented studies reveal that the analog readout of SiPMs with microcell signal pile-up and leading edge discrimination can lead to nearly the same time resolution as compared to the maximum likelihood time estimation applied to MD-SiPMs. Consequently there is no real preference for either a digital or analog SiPM for the sake of achieving highest time resolution. However, the best CTR in the analog SiPM is observed for a rather small range of optimal threshold values, whereas the MD-SiPM provides stable CTR after roughly 20 registered photoelectron timestamps in the time estimator

Studies of the effect of charged hadrons on lead tungstate crystals

Scintillating crystals are used for calorimetry in several high-energy physics experiments. For some of them, performance has to be ensured in difficult operating conditions, like a high radiation environment, very large particle fluxes and high collision rates. Results are presented here from a thorough series of measurements concerning mainly the effect of charged hadrons on lead tungstate. It is also shown how these results can be used to predict the effect on crystals due to a given flux of particles.Comment: Submitted to Proceedings Calor 2008 - XIII International Conference on Calorimetry in High Energy Physics, Pavia (Italy) 26-30 May 2008. To be published in Journal of Physics: Conference Series (8 pages, 16 figures

Ce-doped LuAG single-crystal fibers grown from the melt for high-energy physics

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Location of the Energy Levels of the Rare-Earth Ion in BaF2 and CdF2

The location of the energy levels of rare-earth (RE) elements in the energy band diagram of BaF2 and CdF2 crystals is determined. The role of RE3+ and RE2+ ions in the capture of charge carriers, luminescence, and the formation of radiation defects is evaluated. It is shown that the substantial difference in the luminescence properties of BaF2:RE and CdF2:RE is associated with the location of the excited energy levels in the band diagram of the crystals

Ultrafast emission from colloidal nanocrystals under pulsed X-ray excitation

Fast timing has emerged as a critical requirement for radiation detection in medical and high energy physics, motivating the search for scintillator materials with high light yield and fast time response. However, light emission rates from conventional scintillation mechanisms fundamentally limit the achievable time resolution, which is presently at least one order of magnitude slower than required for next-generation detectors. One solution to this challenge is to generate an intense prompt signal in response to ionizing radiation. In this paper, we present colloidal semiconductor nanocrystals (NCs) as promising prompt photon sources. We investigate two classes of NCs: two-dimensional CdSe nanoplatelets (NPLs) and spherical CdSe/CdS core/giant shell quantum dots (GS QDs). We demonstrate that the emission rates of these NCs under pulsed X-ray excitation are much faster than traditional mechanisms in bulk scintillators, i.e. 5d-4f transitions. CdSe NPLs have a sub-100 ps effective decay time of 77 ps and CdSe/CdS GS QDs exhibit a sub-ns value of 849 ps. Further, the respective CdSe NPL and CdSe/CdS GS QD X-ray excited photoluminescence have the emission characteristics of excitons (X) and multiexcitons (MX), with the MXs providing additional prospects for fast timing with substantially shorter lifetimes

A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutation.

SQSTM1 mutations, coding for the p62 protein, were identified as a monogenic cause of Paget disease of bone and of amyotrophic lateral sclerosis. More recently, SQSTM1 mutations were identified in few families with frontotemporal dementia. We report a new family carrying SQSTM1 mutation and presenting with a clinical phenotype of speech apraxia or atypical behavioral disorders, associated with early visuo-contructional deficits. This study further supports the implication of SQSTM1 in frontotemporal dementia, and enlarges the phenotypic spectrum associated with SQSTM1 mutations

In vivo imaging and quantitative analysis of leukocyte directional migration and polarization in inflamed tissue

Directional migration of transmigrated leukocytes to the site of injury is a central event in the inflammatory response. Here, we present an in vivo chemotaxis assay enabling the visualization and quantitative analysis of subtype-specific directional motility and polarization of leukocytes in their natural 3D microenvironment. Our technique comprises the combination of i) semi-automated in situ microinjection of chemoattractants or bacteria as local chemotactic stimulus, ii) in vivo near-infrared reflected-light oblique transillumination (RLOT) microscopy for the visualization of leukocyte motility and morphology, and iii) in vivo fluorescence microscopy for the visualization of different leukocyte subpopulations or fluorescence-labeled bacteria. Leukocyte motility parameters are quantified off-line in digitized video sequences using computer-assisted single cell tracking. Here, we show that perivenular microinjection of chemoattractants [macrophage inflammatory protein-1alpha (MIP-1alpha/Ccl3), platelet-activating factor (PAF)] or E. coli into the murine cremaster muscle induces target-oriented intravascular adhesion and transmigration as well as polarization and directional interstitial migration of leukocytes towards the locally administered stimuli. Moreover, we describe a crucial role of Rho kinase for the regulation of directional motility and polarization of transmigrated leukocytes in vivo. Finally, combining in vivo RLOT and fluorescence microscopy in Cx3CR1(gfp/gfp) mice (mice exhibiting green fluorescent protein-labeled monocytes), we are able to demonstrate differences in the migratory behavior of monocytes and neutrophils.Taken together, we propose a novel approach for investigating the mechanisms and spatiotemporal dynamics of subtype-specific motility and polarization of leukocytes during their directional interstitial migration in vivo

Sources of heterogeneity in human monocyte subsets

AbstractHuman monocytes are commonly defined and discriminated by the extent of their cell surface expression of CD14 and CD16, with associated differences in function and phenotype related to the intensity of expression of these markers. With increasing interest into the function and behaviour of monocytes, it is important to have a clear understanding of how differing strategies of analysis can affect results and how different protocols and population backgrounds can affect this highly morphogenic cell type.Using PBMCs from populations with differing ethnicities and histories of parasite exposure we have characterized monocyte phenotype based on intensity of CD14 and CD16 expression. Using the surface markers HLA-DR, CCR2 and CX3CR1, we compared monocyte phenotype between populations and further assessed changes in monocytes with freezing and thawing of PBMCs.Our results reveal that there is a progression of surface marker expression based on intensity of CD14 or CD16 expression, stressing the importance of careful gating of monocyte subtypes. Freezing and thawing of the PBMCs has no effect generally on the monocytes, although it does lead to a decrease in CD16 and CX3CR1 expression. We show that there are differences in the monocyte populations based on ethnicity and history of exposure to the common parasites Plasmodium falciparum and Schistosoma haematobium.This study highlights that blood monocytes consist of a continuous population of cells, within which the dominant phenotype may vary dependent on the background of the study population. Comparing results from monocyte studies therefore needs to be done with great care, as ethnic background of donor population, gating strategy and processing of PBMCs may all have an effect on outcome of monocyte phenotype