Genuine Correlations in Hadronic Z0^0 Decays

Correlations among hadrons with the same electric charge produced in Z$^0$ decays are studied using the high statistics data collected from 1991 through 1995 with the OPAL detector at LEP. Normalized factorial cumulants up to fourth order are used to measure genuine pa rticle correlations as a function of the size of phase space domains in rapidity, azimuthal angle and transverse momentum. tein correlations. Some of the recently proposed algorithms to simulate Bose-Einstein effects, implemented in the Monte Carlo model \PYTHIA, reproduce reasonably well the me asured second- and higher-order correlations between particles with the same charge as well as those in all-charge particle multiplets.Comment: 6 pages, 4 figures (in ps), talk given at XXXI International Symposium on Multiparticle Dynamics, Sept 1-7, 2001, Datong China. See http://202.114.35.18

Bose-Einstein Correlations in e+e- -> W+W- at a Linear Collider

We show that the most popular method to simulate Bose-Einstein (BE) interference effects predicts negligible correlations between identical pions originating from the hadronic decay of different W's produced in e+e- -> W+W- -> 4 jets at typical linear collider energies.Comment: 5 pages, 2 eps figures, Proccedings of the Workshop "Physics Studies for a Future Linear Collider", QCD Working Group, 2000, DESY 123

How Can Viral Dynamics Models Inform Endpoint Measures in Clinical Trials of Therapies for Acute Viral Infections?

Acute viral infections pose many practical challenges for the accurate assessment of the impact of novel therapies on viral growth and decay. Using the example of influenza A, we illustrate how the measurement of infection-related quantities that determine the dynamics of viral load within the human host, can inform investigators on the course and severity of infection and the efficacy of a novel treatment. We estimated the values of key infection-related quantities that determine the course of natural infection from viral load data, using Markov Chain Monte Carlo methods. The data were placebo group viral load measurements collected during volunteer challenge studies, conducted by Roche, as part of the oseltamivir trials. We calculated the values of the quantities for each patient and the correlations between the quantities, symptom severity and body temperature. The greatest variation among individuals occurred in the viral load peak and area under the viral load curve. Total symptom severity correlated positively with the basic reproductive number. The most sensitive endpoint for therapeutic trials with the goal to cure patients is the duration of infection. We suggest laboratory experiments to obtain more precise estimates of virological quantities that can supplement clinical endpoint measurements

Quantum Weakly Nondeterministic Communication Complexity

We study the weakest model of quantum nondeterminism in which a classical proof has to be checked with probability one by a quantum protocol. We show the first separation between classical nondeterministic communication complexity and this model of quantum nondeterministic communication complexity for a total function. This separation is quadratic.Comment: 12 pages. v3: minor correction

Bayesian joint models with INLA exploring marine mobile predator-prey and competitor species habitat overlap

EPSRC grant Ecowatt 2050 EP/K012851/1 ACKNOWLEDGMENTS We would like to thank the associate editor and the anonymous reviewers for their useful and constructive suggestions which led to a considerable improvement of the manuscript. The authors would also like to thank the following people/organizations for making large datasets available for use in this paper: Mark Lewis (Joint Nature Conservation Committee), Philip Hammond (Scottish Oceans Institute, University of St. Andrews), Susan Lusseau (Marine Scotland Science), Darren Stevens (The Sir Alister Hardy Foundation for Ocean Science, PML), and Yuri Artioli (Plymouth Marine Laboratory). This work was supported by the Engineering and Physical Sciences Research Council (EcoWatt250; EPSRC EP/K012851/1).Peer reviewedPublisher PD

Large-scale albuminuria screen for nephropathy models in chemically induced mouse mutants

Background/Aim: Phenotype-driven screening of a great pool of randomly mutant mice and subsequent selection of animals showing symptoms equivalent to human kidney diseases may result in the generation of novel suitable models for the study of the pathomechanisms and the identification of genes involved in kidney dysfunction. Methods: We carried out a large-scale analysis of ethylnitrosourea (ENU)-induced mouse mutants for albuminuria by using qualitative SDS-polyacrylamide gel electrophoresis. Results: The primary albuminuria screen preceded the comprehensive phenotypic mutation analysis in a part of the mice of the Munich ENU project to avoid loss of mutant animals as a consequence of prolonged suffering from severe nephropathy. The primary screen detected six confirmed phenotypic variants in 2,011 G1 animals screened for dominant mutations and no variant in 48 G3 pedigrees screened for recessive mutations. Further breeding experiments resulted in two lines showing a low phenotypic penetrance of albuminuria. The secondary albuminuria screen was carried out in mutant lines which were established in the Munich ENU project without preceding primary albuminuria analysis. Two lines showing increased plasma urea levels were chosen to clarify if severe kidney lesions are involved in the abnormal phenotype. This analysis revealed severe albuminuria in mice which are affected by a recessive mutation leading to increased plasma urea and cholesterol levels. Conclusion: Thus, the phenotypic selection of ENU-induced mutants according to the parameter proteinuria in principle demonstrates the feasibility to identify nephropathy phenotypes in ENU-mutagenized mice. Copyright (C) 2005 S. Karger AG, Basel