Chiral Dirac fermions on the lattice using Geometric Discretisation

A new approach to the problem of doubling is presented with the Dirac-Kahler (DK) theory as a starting point and using Geometric Discretisation providing us with a new way of extracting the Dirac field in the discrete setting of a hyper-cubic complex.Comment: Lattice2003(Chiral), 3 page

The Phase Diagrams of the Schwinger and Gross-Neveu Models with Wilson Fermions

A new method to analytically determine the partition function zeroes of weakly coupled theories on finite-size lattices is developed. Applied to the lattice Schwinger model, this reveals the possible absence of a phase transition at fixed weak coupling. We show how finite-size scaling techniques on small or moderate lattice sizes may mimic the presence of a spurious phase transition. Application of our method to the Gross-Neveu model yields a phase diagram consistent with that coming from a saddle point analysis.Comment: Talk at LATTICE99, 3 pages, 2 figure

Adaptive Step Size for Hybrid Monte Carlo Algorithm

We implement an adaptive step size method for the Hybrid Monte Carlo a lgorithm. The adaptive step size is given by solving a symmetric error equation. An integr ator with such an adaptive step size is reversible. Although we observe appreciable variations of the step size, the overhead of the method exceeds its benefits. We propose an explanation for this phenomenon.Comment: 13 pages, 5 Postscript figures, late

Glueball spectrum based on a rigorous three-dimensional relativistic equation for two-gluon bound states II: calculation of the glueball spectrum

In the preceding paper, a rigorous three-dimensional relativistic equation for two-gluon bound states was derived from the QCD with massive gluons and represented in the angular momentum representation. In order to apply this equation to calculate the glueball spectrum, in this paper, the equation is recast in an equivalent three-dimensional relativistic equation satisfied by the two-gluon positive energy state amplitude. The interaction Hamiltonian in the equation is exactly derived and expressed as a perturbative series. The first term in the series describes the one-gluon exchange interaction which includes fully the retardation effect in it. This term plus the linear confining potential are chosen to be the interaction Hamiltonian and employed in the practical calculation. With the integrals containing three and four spherical Bessel functions in the QCD vertices being analytically calculated, the interaction Hamiltonian is given an explicit expression in the angular momentum representation. Numerically solving the relativistic equation with taking the contributions arising from the retardation effect and the longitudinal mode of gluon fields into account, a set of masses for the $0^{++},0^{-+},1^{++},1^{-+},2^{++}$ and $2^{-+\text{}}$ glueball states are obtained and are in fairly good agreement with the predictions given by the lattice simulatio

Glueball spectrum based on a rigorous three-dimensional relativistic equation for two-gluon bound states I: Derivation of the relativistic equation

A rigorous three-dimensional relativistic equation satisfied by two-gluon bound states is derived from the QCD with massive gluons. With the gluon fields and the quark fields being expanded in terms of the gluon multipole fields and the spherical Dirac spinors respectively, the equation is well established in the angular momentum representation and hence is much convenient for solving the problem of two-gluon glueball spectra. In particular, the interaction kernel in the equation is exactly derived and given a closed expression which includes all the interactions taking place in the two-gluon glueballs. The kernel contains only a few types of Green's functions and commutators. Therefore, it is not only easily calculated by the perturbation method, but also provides a suitable basis for nonperturbative investigations

The Kentucky Noisy Monte Carlo Algorithm for Wilson Dynamical Fermions

We develop an implementation for a recently proposed Noisy Monte Carlo approach to the simulation of lattice QCD with dynamical fermions by incorporating the full fermion determinant directly. Our algorithm uses a quenched gauge field update with a shifted gauge coupling to minimize fluctuations in the trace log of the Wilson Dirac matrix. The details of tuning the gauge coupling shift as well as results for the distribution of noisy estimators in our implementation are given. We present data for some basic observables from the noisy method, as well as acceptance rate information and discuss potential autocorrelation and sign violation effects. Both the results and the efficiency of the algorithm are compared against those of Hybrid Monte Carlo. PACS Numbers: 12.38.Gc, 11.15.Ha, 02.70.Uu Keywords: Noisy Monte Carlo, Lattice QCD, Determinant, Finite Density, QCDSPComment: 30 pages, 6 figure

Hybrid Monte Carlo with Fat Link Fermion Actions

The use of APE smearing or other blocking techniques in lattice fermion actions can provide many advantages. There are many variants of these fat link actions in lattice QCD currently, such as FLIC fermions. The FLIC fermion formalism makes use of the APE blocking technique in combination with a projection of the blocked links back into the special unitary group. This reunitarisation is often performed using an iterative maximisation of a gauge invariant measure. This technique is not differentiable with respect to the gauge field and thus prevents the use of standard Hybrid Monte Carlo simulation algorithms. The use of an alternative projection technique circumvents this difficulty and allows the simulation of dynamical fat link fermions with standard HMC and its variants. The necessary equations of motion for FLIC fermions are derived, and some initial simulation results are presented. The technique is more general however, and is straightforwardly applicable to other smearing techniques or fat link actions

Strong Decays of Strange Quarkonia

In this paper we evaluate strong decay amplitudes and partial widths of strange mesons (strangeonia and kaonia) in the 3P0 decay model. We give numerical results for all energetically allowed open-flavor two-body decay modes of all nsbar and ssbar strange mesons in the 1S, 2S, 3S, 1P, 2P, 1D and 1F multiplets, comprising strong decays of a total of 43 resonances into 525 two-body modes, with 891 numerically evaluated amplitudes. This set of resonances includes all strange qqbar states with allowed strong decays expected in the quark model up to ca. 2.2 GeV. We use standard nonrelativistic quark model SHO wavefunctions to evaluate these amplitudes, and quote numerical results for all amplitudes present in each decay mode. We also discuss the status of the associated experimental candidates, and note which states and decay modes would be especially interesting for future experimental study at hadronic, e+e- and photoproduction facilities. These results should also be useful in distinguishing conventional quark model mesons from exotica such as glueballs and hybrids through their strong decays.Comment: 69 pages, 5 figures, 39 table

Effectiveness of targeted enhanced terminal room disinfection on hospital-wide acquisition and infection with multidrug-resistant organisms and Clostridium difficile: a secondary analysis of a multicentre cluster randomised controlled trial with crossover design (BETR Disinfection)

Background: The hospital environment is a source of pathogen transmission. The effect of enhanced disinfection strategies on the hospital-wide incidence of infection has not been investigated in a multicentre, randomised controlled trial. We aimed to assess the effectiveness of four disinfection strategies on hospital-wide incidence of multidrug-resistant organisms and Clostridium difficile in the Benefits of Enhanced Terminal Room (BETR) Disinfection study. Methods: We did a prespecified secondary analysis of the results from the BETR Disinfection study, a pragmatic, multicentre, crossover cluster-randomised trial that assessed four different strategies for terminal room disinfection in nine hospitals in the southeastern USA. Rooms from which a patient with a specific infection or colonisation (due to the target organisms C difficile, meticillin-resistant Staphylococcus aureus, vancomycin-resistant enterococci (VRE), or multidrug-resistant Acinetobacter spp) was discharged were terminally disinfected with one of four strategies: standard disinfection (quaternary ammonium disinfectant, except for C difficile, for which 10% hypochlorite [bleach] was used; reference); standard disinfection and disinfecting ultraviolet light (UV-C), except for C difficile, for which bleach and UV-C was used (UV strategy); 10% hypochlorite (bleach strategy); and bleach and UV-C (bleach and UV strategy). We randomly assigned the sequence of strategies for each hospital (1:1:1:1), and each strategy was used for 7 months, including a 1-month wash-in period and 6 months of data collection. The prespecified secondary outcomes were hospital-wide, hospital-acquired incidence of all target organisms (calculated as number of patients with hospital-acquired infection with a target organism per 10 000 patient days), and hospital-wide, hospital-acquired incidence of each target organism separately. BETR Disinfection is registered with ClinicalTrials.gov, number NCT01579370. Findings: Between April, 2012, and July, 2014, there were 271 740 unique patients with 375 918 admissions. 314 610 admissions met all inclusion criteria (n=73 071 in the reference study period, n=81 621 in the UV study period, n=78 760 in the bleach study period, and n=81 158 in the bleach and UV study period). 2681 incidenct cases of hospital-acquired infection or colonisation occurred during the study. There was no significant difference in the hospital-wide risk of target organism acquisition between standard disinfection and the three enhanced terminal disinfection strategies for all target multidrug-resistant organisms (UV study period relative risk [RR] 0·89, 95% CI 0·79–1·00; p=0·052; bleach study period 0·92, 0·79–1·08; p=0·32; bleach and UV study period 0·99, 0·89–1·11; p=0·89). The decrease in risk in the UV study period was driven by decreases in risk of acquisition of C difficile (RR 0·89, 95% CI 0·80–0·99; p=0·031) and VRE (0·56, 0·31–0·996; p=0·048). Interpretation: Enhanced terminal room disinfection with UV in a targeted subset of high-risk rooms led to a decrease in hospital-wide incidence of C difficile and VRE. Enhanced disinfection overcomes limitations of standard disinfection strategies and is a potential strategy to reduce the risk of acquisition of multidrug-resistant organisms and C difficile. Funding: US Centers for Disease Control and Prevention

Enhanced terminal room disinfection and acquisition and infection caused by multidrug-resistant organisms and Clostridium difficile (the Benefits of Enhanced Terminal Room Disinfection study): a cluster-randomised, multicentre, crossover study

Background Patients admitted to hospital can acquire multidrug-resistant organisms and Clostridium difficile from inadequately disinfected environmental surfaces. We determined the effect of three enhanced strategies for terminal room disinfection (disinfection of a room between occupying patients) on acquisition and infection due to meticillin-resistant Staphylococcus aureus, vancomycin-resistant enterococci, C difficile, and multidrug-resistant Acinetobacter. Methods We did a pragmatic, cluster-randomised, crossover trial at nine hospitals in the southeastern USA. Rooms from which a patient with infection or colonisation with a target organism was discharged were terminally disinfected with one of four strategies: reference (quaternary ammonium disinfectant except for C difficile, for which bleach was used); UV (quaternary ammonium disinfectant and disinfecting ultraviolet [UV-C] light except for C difficile, for which bleach and UV-C were used); bleach; and bleach and UV-C. The next patient admitted to the targeted room was considered exposed. Every strategy was used at each hospital in four consecutive 7-month periods. We randomly assigned the sequence of strategies for each hospital (1:1:1:1). The primary outcomes were the incidence of infection or colonisation with all target organisms among exposed patients and the incidence of C difficile infection among exposed patients in the intention-to-treat population. This trial is registered with ClinicalTrials.gov, NCT01579370. Findings 31 226 patients were exposed; 21 395 (69%) met all inclusion criteria, including 4916 in the reference group, 5178 in the UV group, 5438 in the bleach group, and 5863 in the bleach and UV group. 115 patients had the primary outcome during 22 426 exposure days in the reference group (51·3 per 10 000 exposure days). The incidence of target organisms among exposed patients was significantly lower after adding UV to standard cleaning strategies (n=76; 33·9 cases per 10 000 exposure days; relative risk [RR] 0·70, 95% CI 0·50–0·98; p=0·036). The primary outcome was not statistically lower with bleach (n=101; 41·6 cases per 10 000 exposure days; RR 0·85, 95% CI 0·69–1·04; p=0·116), or bleach and UV (n=131; 45·6 cases per 10 000 exposure days; RR 0·91, 95% CI 0·76–1·09; p=0·303) among exposed patients. Similarly, the incidence of C difficile infection among exposed patients was not changed after adding UV to cleaning with bleach (n=38 vs 36; 30·4 cases vs 31·6 cases per 10 000 exposure days; RR 1·0, 95% CI 0·57–1·75; p=0·997). Interpretation A contaminated health-care environment is an important source for acquisition of pathogens; enhanced terminal room disinfection decreases this risk. Funding US Centers for Disease Control and Prevention