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Jet-like correlations with neutral pion triggers in pp and central Pb–Pb collisions at 2.76 TeV
(2016)
We present measurements of two-particle correlations with neutral pion trigger particles of transverse momenta 8<pTtrig<16 GeV/c and associated charged particles of 0.5<pTassoc<10 GeV/c versus the azimuthal angle difference Δφ at midrapidity in pp and central Pb–Pb collisions at √sNN=2.76 TeV with ALICE. The new measurements exploit associated charged hadrons down to 0.5 GeV/c, which significantly extends our previous measurement that only used charged hadrons above 3 GeV/c. After subtracting the contributions of the flow background, v2 to v5, the per-trigger yields are extracted for |Δφ|<0.7 on the near and for |Δφ−π|<1.1 on the away side. The ratio of per-trigger yields in Pb–Pb to those in pp collisions, IAA, is measured on the near and away side for the 0–10% most central Pb–Pb collisions. On the away side, the per-trigger yields in Pb–Pb are strongly suppressed to the level of IAA≈0.6 for pTassoc>3 GeV/c, while with decreasing momenta an enhancement develops reaching about 5 at low pTassoc. On the near side, an enhancement of IAA between 1.2 at the highest to 1.8 at the lowest pTassoc is observed. The data are compared to parton-energy-loss predictions of the JEWEL and AMPT event generators, as well as to a perturbative QCD calculation with medium-modified fragmentation functions. All calculations qualitatively describe the away-side suppression at high pTassoc. Only AMPT captures the enhancement at low pTassoc, both on the near and away side. However, it also underpredicts IAA above 5 GeV/c, in particular on the near-side.
The inclusive J/ψ production has been studied in Pb–Pb and pp collisions at the centre-of-mass energy per nucleon pair √sNN=5.02 TeV, using the ALICE detector at the CERN LHC. The J/ψ meson is reconstructed, in the centre-of-mass rapidity interval 2.5<y<4 and in the transverse-momentum range pT<12 GeV/c, via its decay to a muon pair. In this Letter, we present results on the inclusive J/ψ cross section in pp collisions at √s=5.02 TeV and on the nuclear modification factor RAA. The latter is presented as a function of the centrality of the collision and, for central collisions, as a function of the transverse momentum pT of the J/ψ. The measured RAA values indicate a suppression of the J/ψ in nuclear collisions and are then compared to our previous results obtained in Pb–Pb collisions at √sNN=2.76 TeV. The ratio of the RAA values at the two energies is also computed and compared to calculations of statistical and dynamical models. The numerical value of the ratio for central events (0–10% centrality) is 1.17±0.04(stat)±0.20(syst). In central events, as a function of pT, a slight increase of RAA with collision energy is visible in the region 2<pT<6 GeV/c. Theoretical calculations qualitatively describe the measurements, within uncertainties.
As an integral part of ALICE, the dedicated heavy ion experiment at CERN’s Large Hadron Collider, the Transition Radiation Detector (TRD) contributes to the experiment’s tracking, triggering and particle identification. Central element in the TRD’s processing chain is its trigger and readout processor, the Global Tracking Unit (GTU). The GTU implements fast triggers on various signatures, which rely on the reconstruction of up to 20 000 particle track segments to global tracks, and performs the buffering and processing of event raw data as part of a complex detector readout tree.
The high data rates the system has to handle and its dual use as trigger and readout processor with shared resources and interwoven processing paths require the GTU to be a unique, high-performance parallel processing system. To achieve high data taking efficiency, all elements of the GTU are optimized for high running stability and low dead time.
The solutions presented in this thesis for the handling of readout data in the GTU, from the initial reception to the final assembly and transmission to the High-Level Trigger computer farm, address all these aspects. The presented concepts employ multi-event buffering, in-stream data processing, extensive embedded diagnostics, and advanced features of modern FPGAs to build a robust high-performance system that can conduct the high- bandwidth readout of the TRD with maximum stability and minimized dead time. The work summarized here not only includes the complete process from the conceptual layout of the multi-event data handling and segment control, but also its implementation, simulation, verification, operation and commissioning. It also covers the system upgrade for the second data taking period and presents an analysis of the actual system performance.
The presented design of the GTU’s input stage, which is comprised of 90 FPGA-based nodes, is built to support multi-event buffering for the data received from the 18 TRD supermodules on 1080 optical links at the full sender aggregate net bandwidth of 2.16 Tbit/s. With careful design of the control logic and the overall data path, the readout on the 18 concentrator nodes of the supermodule stage can utilize an effective aggregate output bandwidth of initially 3.33 GiB/s, and, after the successful readout bandwidth upgrade, 6.50 GiB/s via 18 optical links. The high possible readout link utilization of more than 99 % and the intermediate buffering of events on the GTU helps to keep the dead time associated with the local event building and readout typically below 10%. The GTU has been used for production data taking since start-up of the experiment and ever since performs the event buffering, local event building and readout for the TRD in a correct, efficient and highly dependable fashion.
Background The connection of the variable part of the heavy chain (VH) and and the variable part of the light chain (VL) by a peptide linker to form a consecutive polypeptide chain (single chain antibody, scFv) was a breakthrough for the functional production of antibody fragments in Escherichia coli. Being double the size of fragment variable (Fv) fragments and requiring assembly of two independent polypeptide chains, functional Fab fragments are usually produced with significantly lower yields in E. coli. An antibody design combining stability and assay compatibility of the fragment antigen binding (Fab) with high level bacterial expression of single chain Fv fragments would be desirable. The desired antibody fragment should be both suitable for expression as soluble antibody in E. coli and antibody phage display. Results Here, we demonstrate that the introduction of a polypeptide linker between the fragment difficult (Fd) and the light chain (LC), resulting in the formation of a single chain Fab fragment (scFab), can lead to improved production of functional molecules. We tested the impact of various linker designs and modifications of the constant regions on both phage display efficiency and the yield of soluble antibody fragments. A scFab variant without cysteins (scFabdeltaC) connecting the constant part 1 of the heavy chain (CH1) and the constant part of the light chain (CL) were best suited for phage display and production of soluble antibody fragments. Beside the expression system E.coli, the new antibody format was also expressed in Pichia pastoris. Monovalent and divalent fragments (DiFabodies) as well as multimers were characterised. Conclusion A new antibody design offers the generation of bivalent Fab derivates for antibody phage display and production of soluble antibody fragments. This antibody format is of particular value for high throughput proteome binder generation projects, due to the avidity effect and the possible use of common standard sera for detection.