Heavy Quarkonium

I review heavy quarkonium physics in view of recent experimental results. In particular, I discuss new results on spin singlet states, photon and hadronic transitions, D-states and discovery of yet unexplained narrow X(3872) state.Comment: 15 pages, 16 figures. 2nd version: minor changes in references and text. Invited talk presented at the 21st International Symposium On Lepton And Photon Interactions At High Energies (LP03) 11-16 August 2003, Batavia, Illinoi

The optimally-sampled galaxy-wide stellar initial mass function - Observational tests and the publicly available GalIMF code

Here we present a full description of the integrated galaxy-wide initial mass function (IGIMF) theory in terms of the optimal sampling and compare it with available observations. Optimal sampling is the method we use to discretize the IMF into stellar masses deterministically. Evidence has been indicating that nature may be closer to deterministic sampling as observations suggest a smaller scatter of various relevant observables than random sampling would give, which may result from a high level of self-regulation during the star formation process. The variation of the IGIMFs under various assumptions are documented. The results of the IGIMF theory are consistent with the empirical relation between the total mass of a star cluster and the mass of its most massive star, and the empirical relation between a galaxy's star formation rate (SFR) and the mass of its most massive cluster. Particularly, we note a natural agreement with the empirical relation between the IMF's power-law index and a galaxy's SFR. The IGIMF also results in a relation between the galaxy's SFR and the mass of its most massive star such that, if there were no binaries, galaxies with SFR $<10^{-4}$ M$_\odot$/yr should host no Type II supernova events. In addition, a specific list of initial stellar masses can be useful in numerical simulations of stellar systems. For the first time, we show optimally-sampled galaxy-wide IMFs (OSGIMF) which mimics the IGIMF with an additional serrated feature. Finally, A Python module, GalIMF, is provided allowing the calculation of the IGIMF and OSGIMF in dependence on the galaxy-wide SFR and metallicity.Comment: 15 pages, 15 figures, A&A, in press; paper remains unchanged (version1 equals version2); the GalIMF module is downloadable at githu

Mutations in Mtr4 Structural Domains Reveal Their Important Role in Regulating tRNA\u3csub\u3ei\u3c/sub\u3e \u3csup\u3eMet\u3c/sup\u3e Turnover in \u3cem\u3eSaccharomyces cerevisiae\u3c/em\u3e and Mtr4p Enzymatic Activities \u3cem\u3eIn Vitro\u3c/em\u3e

RNA processing and turnover play important roles in the maturation, metabolism and quality control of a large variety of RNAs thereby contributing to gene expression and cellular health. The TRAMP complex, composed of Air2p, Trf4p and Mtr4p, stimulates nuclear exosome-dependent RNA processing and degradation in Saccharomyces cerevisiae. The Mtr4 protein structure is composed of a helicase core and a novel so-called arch domain, which protrudes from the core. The helicase core contains highly conserved helicase domains RecA-1 and 2, and two structural domains of unclear functions, winged helix domain (WH) and ratchet domain. How the structural domains (arch, WH and ratchet domain) coordinate with the helicase domains and what roles they are playing in regulating Mtr4p helicase activity are unknown. We created a library of Mtr4p structural domain mutants for the first time and screened for those defective in the turnover of TRAMP and exosome substrate, hypomodified tRNAiMet. We found these domains regulate Mtr4p enzymatic activities differently through characterizing the arch domain mutants K700N and P731S, WH mutant K904N, and ratchet domain mutant R1030G. Arch domain mutants greatly reduced Mtr4p RNA binding, which surprisingly did not lead to significant defects on either in vivo tRNAiMet turnover, or in vitro unwinding activities. WH mutant K904N and Ratchet domain mutant R1030G showed decreased tRNAiMet turnover in vivo, as well as reduced RNA binding, ATPase and unwinding activities of Mtr4p in vitro. Particularly, K904 was found to be very important for steady protein levels in vivo. Overall, we conclude that arch domain plays a role in RNA binding but is largely dispensable for Mtr4p enzymatic activities, however the structural domains in the helicase core significantly contribute to Mtr4p ATPase and unwinding activities