Book Reviews

Review of Prehistory, by Derek Roe; Aspects of Prehistory, by Grahame Clark; World Prehistory, by Grahame Clark; Introductory Readings in Archaeology, by Brian M. Fagan, ed.; The Origins of Civilization, by Carroll L. Riley; The Archaeology of Early Man, by J. M. Coles and E. S. Higgs; Shipwrecks and Archaeology, by Peter Throckmorton; A History of Dyed Textiles, by Stuart Robinson; Food in Antiquity, by Don and Patricia Brothwell; World Archaeology, Vol. 1, nos. 1, 2, 3, by Roy Hodson and Colin Platt, eds.; The Structure and Growth of Australia's Aboriginal Population, by F. Lancaster Jones; Attitudes and Social Conditions, by Ronald Taft, John L. M. Dawson, and Pamela Beasley; Aboriginal Settlements, by J. P. M. Long; The Destruction of Aboriginal Society, by C. D. Rowley; Aboriginal Advancement to Integration, by H. P. Schapper

Form Factors for B -> pi l nu-bar_l and B -> K* gamma Decays on the Lattice

We present a unified method for analysing form factors in B -> pi l nu-bar_l and B -> K* gamma decays. The analysis provides consistency checks on the q^2 and 1/M extrapolations necessary to obtain the physical decay rates. For the first time the q^2 dependence of the form factors is obtained at the B scale. In the B -> pi l nu-bar_l case, we show that pole fits to f^+ may not be consistent with the q^2 behaviour of f^0, leading to a possible factor of two uncertainty in the decay rate and hence in the value of |V_{ub}|^2 deduced from it. For B -> K* gamma, from the combined analysis of form factors T_1 and T_2, we find the hadronisation ratio R_{K^*} of the exclusive B -> K* gamma to the inclusive b -> s gamma rates is of order 35% or 15% for constant and pole-type behaviour of T_2 respectively.Comment: 13 pages, uuencoded compressed postscript file (including five figures). Also available from http://wwwhep.phys.soton.ac.uk/hepwww/papers/shep9509

Spinor condensates and light scattering from Bose-Einstein condensates

These notes discuss two aspects of the physics of atomic Bose-Einstein condensates: optical properties and spinor condensates. The first topic includes light scattering experiments which probe the excitations of a condensate in both the free-particle and phonon regime. At higher light intensity, a new form of superradiance and phase-coherent matter wave amplification were observed. We also discuss properties of spinor condensates and describe studies of ground--state spin domain structures and dynamical studies which revealed metastable excited states and quantum tunneling.Comment: 58 pages, 33 figures, to appear in Proceedings of Les Houches 1999 Summer School, Session LXXI

Whole-genome sequencing reveals host factors underlying critical COVID-19

Critical COVID-19 is caused by immune-mediated inflammatory lung injury. Host genetic variation influences the development of illness requiring critical care1 or hospitalization2,3,4 after infection with SARS-CoV-2. The GenOMICC (Genetics of Mortality in Critical Care) study enables the comparison of genomes from individuals who are critically ill with those of population controls to find underlying disease mechanisms. Here we use whole-genome sequencing in 7,491 critically ill individuals compared with 48,400 controls to discover and replicate 23 independent variants that significantly predispose to critical COVID-19. We identify 16 new independent associations, including variants within genes that are involved in interferon signalling (IL10RB and PLSCR1), leucocyte differentiation (BCL11A) and blood-type antigen secretor status (FUT2). Using transcriptome-wide association and colocalization to infer the effect of gene expression on disease severity, we find evidence that implicates multiple genes—including reduced expression of a membrane flippase (ATP11A), and increased expression of a mucin (MUC1)—in critical disease. Mendelian randomization provides evidence in support of causal roles for myeloid cell adhesion molecules (SELE, ICAM5 and CD209) and the coagulation factor F8, all of which are potentially druggable targets. Our results are broadly consistent with a multi-component model of COVID-19 pathophysiology, in which at least two distinct mechanisms can predispose to life-threatening disease: failure to control viral replication; or an enhanced tendency towards pulmonary inflammation and intravascular coagulation. We show that comparison between cases of critical illness and population controls is highly efficient for the detection of therapeutically relevant mechanisms of disease