Commissioning of the ATLAS Trigger Event Selection with Single‐Beam and Cosmic Rays

ATLAS is one of the two general‐purpose detectors at the Large Hadron Collider (LHC). The trigger system needs to efficiently reject a huge rate of background events and still select potentially interesting ones with good efficiency. After a first processing level using custom electronics, the trigger event selection is made by the High Level Trigger (HLT) system, implemented in software. To reduce the processing time to manageable levels, the HLT uses seeded, step‐wise and fast selection algorithms, aiming at the earliest possible rejection of background events. The ATLAS trigger event selection is based on the reconstruction of potentially interesting physical objects like electrons, muons, jets etc. The recent LHC startup and short single‐beam run provided the first test of the trigger system against real data. Following this period, ATLAS continued to collect cosmic‐ray events for detector alignment and calibration purposes. Both running periods provided very important data to commission the trigger reconstruction and selection algorithms. Several tracking, muon‐finding, and calorimetry algorithms, constituting the first ATLAS trigger menu, were exercised online. The trigger decision was used to stream the events into separate samples. This event streaming facilitated the commissioning of the different ATLAS sub‐detectors. This paper will give an overview of the trigger design and its innovative features. It wil l focus on the valuable experience gained in running the trigger reconstruction and event selection in the fast‐changing environment of the detector commissioning

The Belle II Physics Book (Dec, 10.1093/ptep/ptz106, 2019) - correction

Autorzy: Kou, E., Urquijo, P., Altmannshofer, W., Beaujean, F., Bell, G., Beneke, M., Bigi, I.I., Bishara, F., Blanke, M., Bobeth, C., Bona, M., Brambilla, N., Braun, V.M., Brod, J., Buras, A.J., Cheng, H.Y., Chiang, C.W., Ciuchini, M., Colangelo, G., Crivellin, A., Czyz, H., Datta, A., De Fazio, F., Deppisch, T., Dolan, M.J., Evans, J., Fajfer, S., Feldmann, T., Godfrey, S., Gronau, M., Grossman, Y., Guo, F.K., Haisch, U., Hanhart, C., Hashimoto, S., Hirose, S., Hisano, J., Hofer, L., Hoferichter, M., Hou, W.S., Huber, T., Hurth, T., Jaeger, S., Jahn, S., Jamin, M., Jones, J., Jung, M., Kagan, A.L., Kahlhoefer, F., Kamenik, J.F., Kaneko, T., Kiyo, Y., Kokulu, A., Kosnik, N., Kronfeld, A.S., Ligeti, Z., Logan, H., Lu, C.D., Lubicz, V., Mahmoudi, F., Maltman, K., Mishima, S., Misiak, M., Moats, K., Moussallam, B., Nefediev, A., Nierste, U., Nomura, D., Offen, N., Olsen, S.L., Passemar, E., Paul, A., Paz, G., Petrov, A.A., Pich, A., Polosa, A.D., Pradler, J., Prelovsek, S., Procura, M., Ricciardi, G., Robinson, D.J., Roig, P., Rosiek, J., Schacht, S., Schmidt-Hoberg, K., Schwichtenberg, J., Sharpe, S.R., Shigemitsu, J., Shih, D., Shimizu, N., Shimizu, Y., Silvestrini, L., Simula, S., Smith, C., Stoffer, P., Straub, D., Tackmann, F.J., Tanaka, M., Tayduganov, A., Tetlalmatzi-Xolocotzi, G., Teubner, T., Vairo, A., Van Dyk, D., Virto, J., Was, Z., Watanabe, R., Watson, I., Westhoff, S., Zupan, J., Zwicky, R., Abudinén, F., Adachi, I., Adamczyk, K., Ahlburg, P., Aihara, H., Aloisio, A., Andricek, L., Anh Ky, N., Arndt, M., Asner, D.M., Atmacan, H., Aushev, T., Aushev, V., Ayad, R., Aziz, T., Baehr, S., Bahinipati, S., Bambade, P., Ban, Y., Barrett, M., Baudot, J., Behera, P., Belous, K., Bender, M., Bennett, J., Berger, M., Bernieri, E., Bernlochner, F.U., Bessner, M., Besson, D., Bettarini, S., Bhardwaj, V., Bhuyan, B., Bilka, T., Bilmis, S., Bilokin, S., Bonvicini, G., Bozek, A., Bračko, M., Branchini, P., Braun, N., Briere, R.A., Browder, T.E., Burmistrov, L., Bussino, S., Cao, L., Caria, G., Casarosa, G., Cecchi, C., Červenkov, D., Chang, M.-C., Chang, P., Cheaib, R., Chekelian, V., Chen, Y., Cheon, B.G., Chilikin, K., Cho, K., Choi, J., Choi, S.-K., Choudhury, S., Cinabro, D., Cremaldi, L.M., Cuesta, D., Cunliffe, S., Dash, N., De La Cruz Burelo, E., De Lucia, E., De Nardo, G., De Nuccio, M., De Pietro, G., De Yta Hernandez, A., Deschamps, B., Destefanis, M., Dey, S., Di Capua, F., Di Carlo, S., Dingfelder, J., Doležal, Z., Domínguez Jiménez, I., Dong, T.V., Dossett, D., Duell, S., Eidelman, S., Epifanov, D., Fast, J.E., Ferber, T., Fiore, S., Fodor, A., Forti, F., Frey, A., Frost, O., Fulsom, B.G., Gabriel, M., Gabyshev, N., Ganiev, E., Gao, X., Gao, B., Garg, R., Garmash, A., Gaur, V., Gaz, A., Geßler, T., Gebauer, U., Gelb, M., Gellrich, A., Getzkow, D., Giordano, R., Giri, A., Glazov, A., Gobbo, B., Godang, R., Gogota, O., Goldenzweig, P., Golob, B., Gradl, W., Graziani, E., Greco, M., Greenwald, D., Gribanov, S., Guan, Y., Guido, E., Guo, A., Halder, S., Hara, K., Hartbrich, O., Hauth, T., Hayasaka, K., Hayashii, H., Hearty, C., Heredia De La Cruz, I., Hernandez Villanueva, M., Hershenhorn, A., Higuchi, T., Hoek, M., Hollitt, S., Hong Van, N.T., Hsu, C.-L., Hu, Y., Huang, K., Iijima, T., Inami, K., Inguglia, G., Ishikawa, A., Itoh, R., Iwasaki, Y., Iwasaki, M., Jackson, P., Jacobs, W.W., Jaegle, I., Jeon, H.B., Ji, X., Jia, S., Jin, Y., Joo, C., Künzel, M., Kadenko, I., Kahn, J., Kakuno, H., Kaliyar, A.B., Kandra, J., Kang, K.H., Kato, Y., Kawasaki, T., Ketter, C., Khasmidatul, M., Kichimi, H., Kim, J.B., Kim, K.T., Kim, H.J., Kim, D.Y., Kim, K., Kim, Y., Kimmel, T.D., Kindo, H., Kinoshita, K., Konno, T., Korobov, A., Korpar, S., Kotchetkov, D., Kowalewski, R., Križan, P., Kroeger, R., Krohn, J.-F., Krokovny, P., Kuehn, W., Kuhr, T., Kulasiri, R., Kumar, M., Kumar, R., Kumita, T., Kuzmin, A., Kwon, Y.-J., Lacaprara, S., Lai, Y.-T., Lalwani, K., Lange, J.S., Lee, S.C., Lee, J.Y., Leitl, P., Levit, D., Levonian, S., Li, S., Li, L.K., Li, Y., Li, Y.B., Li, Q., Li Gioi, L., Libby, J., Liptak, Z., Liventsev, D., Longo, S., Loos, A., Lopez Castro, G., Lubej, M., Lueck, T., Luetticke, F., Luo, T., Müller, F., Müller, T., Macqueen, C., Maeda, Y., Maggiora, M., Maity, S., Manoni, E., Marcello, S., Marinas, C., Martinez Hernandez, M., Martini, A., Matvienko, D., Mckenna, J.A., Meier, F., Merola, M., Metzner, F., Miller, C., Miyabayashi, K., Miyake, H., Miyata, H., Mizuk, R., Mohanty, G.B., Moon, H.K., Moon, T., Morda, A., Morii, T., Mrvar, M., Muroyama, G., Mussa, R., Nakamura, I., Nakano, T., Nakao, M., Nakayama, H., Nakazawa, H., Nanut, T., Naruki, M., Nath, K.J., Nayak, M., Nellikunnummel, N., Neverov, D., Niebuhr, C., Ninkovic, J., Nishida, S., Nishimura, K., Nouxman, M., Nowak, G., Ogawa, K., Onishchuk, Y., Ono, H., Onuki, Y., Pakhlov, P., Pakhlova, G., Pal, B., Paoloni, E., Park, H., Park, C.-S., Paschen, B., Passeri, A., Paul, S., Pedlar, T.K., Perelló, M., Peruzzi, I.M., Pestotnik, R., Piilonen, L.E., Podesta Lerma, L., Popov, V., Prasanth, K., Prencipe, E., Prim, M., Purohit, M.V., Rabusov, A., Rasheed, R., Reiter, S., Remnev, M., Resmi, P.K., Ripp-Baudot, I., Ritter, M., Ritzert, M., Rizzo, G., Rizzuto, L., Robertson, S.H., Rodriguez Perez, D., Roney, J.M., Rosenfeld, C., Rostomyan, A., Rout, N., Rummel, S., Russo, G., Sahoo, D., Sakai, Y., Salehi, M., Sanders, D.A., Sandilya, S., Sangal, A., Santelj, L., Sasaki, J., Sato, Y., Savinov, V., Scavino, B., Schram, M., Schreeck, H., Schueler, J., Schwanda, C., Schwartz, A.J., Seddon, R.M., Seino, Y., Senyo, K., Seon, O., Seong, I.S., Sevior, M.E., Sfienti, C., Shapkin, M., Shen, C.P., Shimomura, M., Shiu, J.-G., Shwartz, B., Sibidanov, A., Simon, F., Singh, J.B., Sinha, R., Skambraks, S., Smith, K., Sobie, R.J., Soffer, A., Sokolov, A., Solovieva, E., Spruck, B., Stanič, S., Starič, M., Starinsky, N., Stolzenberg, U., Stottler, Z., Stroili, R., Strube, J.F., Stypula, J., Sumihama, M., Sumisawa, K., Sumiyoshi, T., Summers, D., Sutcliffe, W., Suzuki, S.Y., Tabata, M., Takahashi, M., Takizawa, M., Tamponi, U., Tan, J., Tanaka, S., Tanida, K., Taniguchi, N., Tao, Y., Taras, P., Tejeda Munoz, G., Tenchini, F., Tippawan, U., Torassa, E., Trabelsi, K., Tsuboyama, T., Uchida, M., Uehara, S., Uglov, T., Unno, Y., Uno, S., Ushiroda, Y., Usov, Y., Vahsen, S.E., Van Tonder, R., Varner, G., Varvell, K.E., Vinokurova, A., Vitale, L., Vos, M., Vossen, A., Waheed, E., Wakeling, H., Wan, K., Wang, M.-Z., Wang, X.L., Wang, B., Warburton, A., Webb, J., Wehle, S., Wessel, C., Wiechczynski, J., Wieduwilt, P., Won, E., Xu, Q., Xu, X., Yabsley, B.D., Yamada, S., Yamamoto, H., Yan, W., Yan, W., Yang, S.B., Ye, H., Yeo, I., Yin, J.H., Yonenaga, M., Yoshinobu, T., Yuan, W., Yuan, C.Z., Yusa, Y., Zakharov, S., Zani, L., Zeyrek, M., Zhang, J., Zhang, Y., Zhang, Y., Zhou, X., Zhukova, V., Zhulanov, V., Zupanc, A.This is a correction to: Progress of Theoretical and Experimental Physics, Volume 2019, Issue 12, December 2019, 123C01, https://doi.org/10.1093/ptep/ptz10

New routes to functionalised pyridines

A novel method of preparing substituted pyridines has been developed. This method uses readily available [3-ketoesters and amidrazone as starting materials. The pyridines obtained do not require purification and different substitution patterns, not available by known methods, can be obtained. The formation of 1,2,3-tricarbonyl compounds was achieved by oxidation of the alcohol precursors, following two different methods. a-Chloro-ct-acetoxy-f3-dicarbonyls were prepared in excellent yields and were shown to react as tricarbonyl equivalents in the formation of 1,2,4-triazines. Regioselective condensation reactions were observed between different amidrazones with tricarbonyl and tricarbonyl equivalents to produce a series of novel 1,2,4-triazines in good yields with no contamination by any regioisomer. When 1,2,4-triazines were obtained from a-chloro-a-acetoxy-P-dicarbonyls, 2.5 equivalents of amidrazone were required. However, decomposition of a-chloro-a-acetoxy-P-dicarbonyls prior to reaction with 1 equivalent of amidrazone yielded the 1,2,4-triazines in good yields. These 1,2,4-triazines underwent aza Diels-Alder cycloaddition reactions with 2,5- norbornadiene to give a series of novel 2,3,6-trisubstituted pyridines. The pyridines bearing electron withdrawing groups as substituents could also be obtained in a 'one- pot' reaction from their corresponding tricarbonyls or tricarbonyl derivatives. The 1,2,4- triazines bearing electron donating groups could be converted to their corresponding pyridines either by changing the reaction conditions or, when possible, by conversion of the electron donating group into a more electron withdrawing substituent by oxidation (e.g. sulphoxide substituent). Pyridines bearing a sulphoxide substituent undergo nucleophilic substitutions, giving great scope to introduce different functionality in the C-6 of the pyridines.EThOS - Electronic Theses Online ServiceGBUnited Kingdo

Diseño y construcción de un reactor mecatrónico para el crecimiento de películas delgadas por la técnica de recubrimiento por inmersión

The design and construction of an automated mechatronic system for the growth of thin films by the dip coating technique is presented. The system consists of a substrate-holder, which performs vertical movements between two adjustable positions. The movemSe presenta el diseño y construcción de un sistema mecatrónico automatizado para el crecimiento de películas delgadas mediante la técnica de recubrimiento por inmersión. El sistema consta de un soporte de sustrato, que realiza movimientos verticales entr

Pre-emptive Quality Control of a Misfolded Membrane Protein by Ribosome-Driven Effects.

Cells possess multiple mechanisms that protect against the accumulation of toxic aggregation-prone proteins. Here, we identify a pre-emptive pathway that reduces synthesis of membrane proteins that have failed to properly assemble in the endoplasmic reticulum (ER). We show that loss of the ER membrane complex (EMC) or mutation of the Sec61 translocon causes reduced synthesis of misfolded forms of the yeast ABC transporter Yor1. Synthesis defects are rescued by various ribosomal mutations, as well as by reducing cellular ribosome abundance. Genetic and biochemical evidence point to a ribosome-associated quality-control pathway triggered by ribosome collisions when membrane domain insertion and/or folding fails. In support of this model, translation initiation also contributes to synthesis defects, likely by modulating ribosome abundance on the message. Examination of translation efficiency across the yeast membrane proteome revealed that polytopic membrane proteins have relatively low ribosome abundance, providing evidence for translational tuning to balance protein synthesis and folding. We propose that by modulating translation rates of poorly folded proteins, cells can pre-emptively protect themselves from potentially toxic aberrant transmembrane proteins

Measurement of R(D) and R(D∗) with a semileptonic tagging method

The experimental results on the ratios of branching fractions R(D) = B(B¯ → Dτ − ν¯τ )/B(B¯ → D`− ν¯`) and R(D ∗ ) = B(B¯ → D ∗ τ − ν¯τ )/B(B¯ → D ∗ ` − ν¯`), where ` denotes an electron or a muon, show a long-standing discrepancy with the Standard Model predictions, and might hint to a violation of lepton flavor universality. We report a new simultaneous measurement of R(D) and R(D ∗ ), based on a data sample containing 772 × 106 BB¯ events recorded at the Υ(4S) resonance with the Belle detector at the KEKB e + e − collider. In this analysis the tag-side B meson is reconstructed in a semileptonic decay mode and the signal-side τ is reconstructed in a purely leptonic decay. The measured values are R(D) = 0.307 ± 0.037 ± 0.016 and R(D ∗ ) = 0.283 ± 0.018 ± 0.014, where the first uncertainties are statistical and the second are systematic. These results are in agreement with the Standard Model predictions within 0.2, 1.1 and 0.8 standard deviations for R(D), R(D ∗ ) and their combination, respectively. This work constitutes the most precise measurements of R(D) and R(D ∗ ) performed to date as well as the first result for R(D) based on a semileptonic tagging method

Measurement of R (D) and R (D∗) with a Semileptonic Tagging Method

The experimental results on the ratios of branching fractions R(D)=B(B→Dτ-ντ)/B(B→Dℓ-νℓ) and R(D∗)=B(B→D∗τ-ντ)/B(B→D∗ℓ-νℓ), where ℓ denotes an electron or a muon, show a long-standing discrepancy with the standard model predictions, and might hint at a violation of lepton flavor universality. We report a new simultaneous measurement of R(D) and R(D∗), based on a data sample containing 772×106 BB events recorded at the ϒ(4S) resonance with the Belle detector at the KEKB e+e- collider. In this analysis the tag-side B meson is reconstructed in a semileptonic decay mode and the signal-side τ is reconstructed in a purely leptonic decay. The measured values are R(D)=0.307±0.037±0.016 and R(D∗)=0.283±0.018±0.014, where the first uncertainties are statistical and the second are systematic. These results are in agreement with the standard model predictions within 0.2, 1.1, and 0.8 standard deviations for R(D), R(D∗), and their combination, respectively. This work constitutes the most precise measurements of R(D) and R(D∗) performed to date as well as the first result for R(D) based on a semileptonic tagging method