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We conclude our investigations on the QCD cross-over transition temperatures with 2+1 staggered flavours and one-link stout improvement. We extend our previous two studies [Phys. Lett. B643 (2006) 46, JHEP 0906:088 (2009)] by choosing even finer lattices (N_t=16) and we work again with physical quark masses. These new results [for details see JHEP 1009:073,2010] support our earlier findings. We compare them with the published results of the hotQCD collaboration. All these results are confronted with the predictions of the Hadron Resonance Gas model and Chiral Perturbation Theory for temperatures below the transition region. Our results can be reproduced by using the physical spectrum. The findings of the hotQCD collaboration can be recovered only by using a distorted spectrum. This analysis provides a simple explanation for the observed discrepancy in the transition T between our and the hotQCD collaborations.
We have studied the 3-flavor, finite temperature, QCD phase transition with staggred fermions on an $ N_t=4$ lattice. By studying a variety of quark masses we have located the critical point, $m_c$, where the first order 3-flavor transition ends as l
We present our initial study of the electromagnetic splittings of charged and neutral mesons, and the violation of Dashens theorem. Hadron masses are calculated on MILC N_f=2+1 QCD ensembles at lattice spacing approx 0.15fm, together with quenched no
We present a full result for the 2+1 flavor QCD equation of state. All the systematics are controlled, the quark masses are set to their physical values, and the continuum extrapolation is carried out. This extends our previous studies [JHEP 0601:089
We present an update of our study of high temperature QCD with three flavors of quarks, using a Symanzik improved gauge action and the Asqtad staggered quark action. Simulations are being carried out on lattices with Nt=4, 6 and 8 for the case of thr
The QCD phase diagram at imaginary chemical potential exhibits a rich structure and studying it can constrain the phase diagram at real values of the chemical potential. Moreover, at imaginary chemical potential standard numerical techniques based on