Institution
University of Bremen
Education•Bremen, Germany•
About: University of Bremen is a education organization based out in Bremen, Germany. It is known for research contribution in the topics: Population & Context (language use). The organization has 14563 authors who have published 37279 publications receiving 970381 citations. The organization is also known as: Universität Bremen.
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TL;DR: The agent-based and density-based modeling frameworks including the cases of multidimensional opinions and heterogeneous bounds ousting Monte Carlo style and master equation style are presented.
Abstract: Models of continuous opinion dynamics under bounded confidence have been presented independently by Krause and Hegselmann and by Deffuant et al in 2000. They have raised a fair amount of attention in the communities of social simulation, sociophysics and complexity science. The researchers working on it come from disciplines as physics, mathematics, computer science, social psychology and philosophy.
Agents hold continuous opinions which they can gradually adjust if they hear the opinions of others. The idea of bounded confidence is that agents only interact if they are close in opinion to each other. Usually, the models are analyzed with agent-based simulations in a Monte-Carlo style, but they can also be reformulated on the agent's density in the opinion space in a master-equation style. This paper is to present the agent-based and density-based modeling frameworks including the cases of multidimensional opinions and heterogeneous bounds of confidence; second, to give the bifurcation diagrams of cluster configuration in the homogeneous model with uniformly distributed initial opinions; third to review the several extensions and the evolving phenomena which have been studied so far; and fourth to state some basic open questions.
494 citations
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University of Bremen1, University of Tübingen2, Autonomous University of Barcelona3, University of Kiel4, Oregon State University5, Alfred Wegener Institute for Polar and Marine Research6, Commonwealth Scientific and Industrial Research Organisation7, Aix-Marseille University8, Cardiff University9, Australian National University10, University of Barcelona11, National Taiwan Ocean University12, University of Bordeaux13, Université du Québec à Montréal14, University of Bergen15, University of Cambridge16, University of Limerick17, Newcastle University18, University of Sfax19, Dalhousie University20, University of Liverpool21, Université du Québec22, National Oceanography Centre23, Geoscience Australia24, University of California, Davis25
TL;DR: This article presented an updated synthesis of sea surface temperatures during the Last Glacial Maximum, rigorously defined as the period between 23 and 19 thousand years before present, from the Multiproxy Approach for the Reconstruction of the Glacial Ocean Surface (MARGO) project.
Abstract: Observation-based reconstructions of sea surface temperature from relatively stable periods in the past, such as the Last Glacial Maximum, represent an important means of constraining climate sensitivity and evaluating model simulations1. The first quantitative global reconstruction of sea surface temperatures during the Last Glacial Maximum was developed by the Climate Long-Range Investigation, Mapping and Prediction (CLIMAP) project in the 1970s and 1980s (refs 2, 3). Since that time, several shortcomings of that earlier effort have become apparent4. Here we present an updated synthesis of sea surface temperatures during the Last Glacial Maximum, rigorously defined as the period between 23 and 19 thousand years before present, from the Multiproxy Approach for the Reconstruction of the Glacial Ocean Surface (MARGO) project5. We integrate microfossil and geochemical reconstructions of surface temperatures and include assessments of the reliability of individual records. Our reconstruction reveals the presence of large longitudinal gradients in sea surface temperature in all of the ocean basins, in contrast to the simulations of the Last Glacial Maximum climate available at present6, 7.
493 citations
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TL;DR: This work demonstrates that surface-chemistry-driven actuation can be realized in high-surface-area materials such as nanoporous gold, and achieves reversible strain amplitudes of the order of a few tenths of a per cent by alternating exposure of nanoporous Au to ozone and carbon monoxide.
Abstract: Although actuation in biological systems is exclusively powered by chemical energy, this concept has not been realized in man-made actuator technologies, as these rely on generating heat or electricity first. Here, we demonstrate that surface-chemistry-driven actuation can be realized in high-surface-area materials such as nanoporous gold. For example, we achieve reversible strain amplitudes of the order of a few tenths of a per cent by alternating exposure of nanoporous Au to ozone and carbon monoxide. The effect can be explained by adsorbate-induced changes of the surface stress, and can be used to convert chemical energy directly into a mechanical response, thus opening the door to surface-chemistry-driven actuator and sensor technologies.
491 citations
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University of Bremen1, Duke University2, Max Planck Society3, University of Bristol4, University of Costa Rica5, Western Washington University6, University of Minnesota7, University of Bonn8, Karlsruhe Institute of Technology9, Free University of Berlin10, Oak Ridge National Laboratory11, Ulsan National Institute of Science and Technology12, University of Regensburg13, University of Warwick14, Los Alamos National Laboratory15, Claude Bernard University Lyon 116, University of Newcastle17, Dassault Systèmes18, Facultad de Ciencias Exactas y Naturales19, Argonne National Laboratory20, University of Luxembourg21
TL;DR: An overview of the recently developed capabilities of the DFTB+ code is given, demonstrating with a few use case examples, and the strengths and weaknesses of the various features are discussed, to discuss on-going developments and possible future perspectives.
Abstract: DFTB+ is a versatile community developed open source software package offering fast and efficient methods for carrying out atomistic quantum mechanical simulations. By implementing various methods approximating density functional theory (DFT), such as the density functional based tight binding (DFTB) and the extended tight binding method, it enables simulations of large systems and long timescales with reasonable accuracy while being considerably faster for typical simulations than the respective ab initio methods. Based on the DFTB framework, it additionally offers approximated versions of various DFT extensions including hybrid functionals, time dependent formalism for treating excited systems, electron transport using non-equilibrium Green’s functions, and many more. DFTB+ can be used as a user-friendly standalone application in addition to being embedded into other software packages as a library or acting as a calculation-server accessed by socket communication. We give an overview of the recently developed capabilities of the DFTB+ code, demonstrating with a few use case examples, discuss the strengths and weaknesses of the various features, and also discuss on-going developments and possible future perspectives.
491 citations
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TL;DR: Results are reported from analyses of IPLs in pure cultures of biogeochemically relevant prokaryotes and marine sediments by high-performance liquid chromatography/electrospray ionization ion-trap mass spectrometry (HPLC/ESI-IT-MSn) and analytical protocols are presented to decipher structural information from mass spectral data.
Abstract: Lipids from prokaryotic cell membranes can serve as sources of information on the biogeochemistry and microbial ecology of natural ecosystems. Traditionally, apolar derivatives of the intact polar membrane molecules, e.g., fatty acids, have been the major target of lipid-based biogeochemical studies. However, when still intact, i.e., as glycerol esters and ethers with attached polar headgroups, membrane lipids are diagnostic for living prokaryotes, which makes them excellent biomarkers for the study of in situ microbial processes in geological systems such as sediments or soils. Intact polar lipids (IPLs) are attractive analytical targets because they are taxonomically more specific than their apolar derivatives and avoid exclusion of signals from prokaryotes that primarily build their membranes with ether-bound lipids such as archaea and some bacteria. Here we report results from analyses of IPLs in pure cultures of biogeochemically relevant prokaryotes and marine sediments by high-performance liquid chromatography/electrospray ionization ion-trap mass spectrometry (HPLC/ESI-IT-MSn). This technique is suitable for screening of biomass and environmental samples for distinctive taxonomic structural features such as distribution of polar lipid headgroups, types of bonds between alkyl moiety and glycerol backbone, and the chain length and degree of unsaturation in the alkyl moieties. We present analytical protocols to decipher structural information from mass spectral data. The IPL contents in selected archaeal and bacterial species are diverse and qualify as molecular fingerprints. Applied to marine sediments, the approach provided detailed information on the dominant microbial groups. The IPLs from bacterial members of anaerobic methanotrophic communities in surface sediments at Hydrate Ridge resemble those found in Desulfosarcina variabilis. The presence of dietherglycerophospholipids, however, suggests the presence of other bacteria possibly affiliated with the deepest phylogenetic branches in the tree of life. Sediments from approximately 90 m below the seafloor on the Peruvian continental margin are dominated by intact archaeal tetraethers with glycosidically bound hexoses as headgroups, consistent with a significant fraction of the community being archaea. Additional calditol-based tetraethers imply that the sedimentary archaea are taxonomically linked to the crenarchaeal Sulfolobales.
486 citations
Authors
Showing all 14961 results
Name | H-index | Papers | Citations |
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Roger Y. Tsien | 163 | 441 | 138267 |
Klaus-Robert Müller | 129 | 764 | 79391 |
Ron Kikinis | 126 | 684 | 63398 |
Ulrich S. Schubert | 122 | 2229 | 85604 |
Andreas Richter | 110 | 769 | 48262 |
Michael Böhm | 108 | 755 | 66103 |
Juan Bisquert | 107 | 450 | 46267 |
John P. Sumpter | 101 | 266 | 46184 |
Jos Lelieveld | 100 | 570 | 37657 |
Michael Schulz | 100 | 759 | 50719 |
Peter Singer | 94 | 702 | 37128 |
Charles R. Tyler | 92 | 325 | 31724 |
John P. Burrows | 90 | 815 | 36169 |
Hans-Peter Kriegel | 89 | 444 | 73932 |
Harald Haas | 85 | 750 | 34927 |