The Cultural Evolution of Democracy: Saltational Changes in A Political Regime Landscape

Transitions to democracy are most often considered the outcome of historical modernization processes. Socio-economic changes, such as increases in per capita GNP, education levels, urbanization and communication, have traditionally been found to be correlates or ‘requisites’ of democratic reform. However, transition times and the number of reform steps have not been studied comprehensively. Here we show that historically, transitions to democracy have mainly occurred through rapid leaps rather than slow and incremental transition steps, with a median time from autocracy to democracy of 2.4 years, and overnight in the reverse direction. Our results show that autocracy and democracy have acted as peaks in an evolutionary landscape of possible modes of institutional arrangements. Only scarcely have there been slow incremental transitions. We discuss our results in relation to the application of phylogenetic comparative methods in cultural evolution and point out that the evolving unit in this system is the institutional arrangement, not the individual country which is instead better regarded as the ‘host’ for the political system

Level structure above the 17(+) isomeric state in Tm-152(69)83

Excited states above the 17(+) isomeric state in the proton-rich nucleus Tm-152 were established by employing the recoil-isomer tagging technique. Data were collected using the JUROGAM gamma-ray array and the GREAT spectrometer together with the recoil ion transport unit (RITU) gas-filled recoil separator and analyzed to identify the prompt and delayed gamma decays from the levels in Tm-152. Shell-model calculations, either in a large valence space or in a reduced model space with five protons in the pi 0h(11)(/2) orbital and one neutron in the nu 1 f(7/2) orbital, agree with the observed energies of the yrast levels up to angular momentum J = 21. The observation of near degeneracies in the energy spectrum can be attributed to specific components of the proton-neutron interaction. The isomeric decay of the 17(+) level is not reproduced in the shell-model calculations as it arises from a delicate balance between hindrance due to seniority selection rules and enhancement due to configuration mixing.Peer reviewe

Fusogenic membrane glycoprotein-mediated tumour cell fusion activates human dendritic cells for enhanced IL-12 production and T-cell priming

Fusogenic membrane glycoproteins (FMG) are a family of viral genes that, when expressed in tumour cells, trigger extensive cell to cell fusion and subsequent cell death. Gene therapy approaches using FMG are also potentially immunogenic, since syncitia generated ex vivo can be therapeutic as antitumour vaccines in murine models. This study has addressed the mechanisms responsible for the immunogenicity of FMG-mediated cell death, and its applicability to human immune priming. We show that fusion of human Mel888 melanoma cells following transfection with FMG can reverse the suppressive effects of Mel888 on dendritic cells (DC) phenotype, and potentiate IL-12 production by DC on activation in a cell contact-dependent manner. DC loaded with fusing, but not intact, tumour cells primed a naive, tumour-specific cytotoxic T-cell response, which was MHC class I-restricted and associated with production of high levels of IFN and, later, IL-5. Fusing cells were an effective source of antigen for DC cross-priming and presentation of the melanoma-specific antigen gp100 to a specific T-cell clone. These data show, in a human system, that FMG represent an immunogenic, as well as cytotoxic, gene therapy for cancer, reversing the inhibitory effects of tumour cells on DC to potentiate IL-12 production and naive T-cell priming.<br/