147 research outputs found

    Operator representation and logistic extension of elementary cellular automata

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    We redefine the transition function of elementary cellular automata (ECA) in terms of discrete operators. The operator representation provides a clear hint about the way systems behave both at the local and the global scale. We show that mirror and complementary symmetric rules are connected to each other via simple operator transformations. It is possible to decouple the representation into two pairs of operators which are used to construct a periodic table of ECA that maps all unique rules in such a way that rules having similar behavior are clustered together. Finally, the operator representation is used to implement a generalized logistic extension to ECA. Here a single tuning parameter scales the pace with which operators iterate the rules. We show that, as this parameter is tuned, many rules of ECA undergo multiple phase transitions between periodic, locally chaotic, chaotic and complex (Class 4) behavior

    Le TBI : un nouvel instrument pour innover l’enseignement / apprentissage du FLE

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    Le dispositif techno-pédagogique proposé dans cet article, sollicite pleinement le Tableau Blanc Interactif (TBI). Il vise le développement de capacités d’expression et de communication en langue française dans des situations d’apprentissage concrètes, et approfondit la réflexion sur le fonctionnement de la langue. L’engagement sociocognitif de l’apprenant y est tout particulièrement sollicité pour qu’il puisse donner plus de sens à son apprentissage. Sur un plan purement théorique, c’est aussi l’occasion de considérer les différentes actions pédagogiques qu’il est possible d’envisager avec le TBI en classe de FLE

    Minimizing equipment and energy cost in mixed 10G and 100G/200G filterless horseshoe networks with hierarchical OTN boards

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    Emerging 5G services are changing the way operators manage and optimize their optical metro networks, and the transmission technology and network design process must be tailored to the specific conditions in this segment of the network. Ensuring cost-efficient and energy-efficient network design requires novel approaches that optimize across all network layers. Therefore, to moderate the growth of operators’ expenses, in this paper, we investigate low-cost and energy-efficient cross-layer deployment of hierarchical optical transport network (OTN) boards minimizing equipment and energy consumption cost in mixed 10G and 100G/200G filterless metro networks. We propose an integer linear programming (ILP) model and a genetic algorithm (GA) approach that decide: (i) the node structure by deploying various stacked OTN boards (performing traffic-grooming at the electrical layer) and (ii) lightpath establishment considering coherent and non-coherent transmission technologies. Simulative results on real filterless horseshoe networks with real traffic matrices show that our proposed approaches achieve up to 50% cost savings compared to real-world benchmark deployments

    Cs-induced charge transfer on (2x4)-GaAs(001) studied by photoemission

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    Cesium adsorption on 2x4 GaAs (001) was studied by photoemission and low energy electron diffraction. The different Cs induced changes of the As 3d and Ga 3d core level spectra show that charge transfer is almost complete for Ga surface sites, but is negligible to surface As at a coverage smaller than 0.3 ML. The situation is opposite for a coverage larger than 0.3ML, at which transfer occurs to As but no longer to Ga. Charge transfer to As atoms leads to disordering and destabilization and induces surface conversion from the As-rich surface to the Ga-rich 4x2 one after annealing at a reduced temperature of 450 C

    The Potamophylax nigricornis group (Trichoptera, Limnephilidae): resolution of phylogenetic species by fine structure analysis

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    Applying the phylogenetic species concept and the sexual selection theory we have reviewed some natal aspects of incipient species and their accelerated evolution. How can we recognise early stages of divergence? Which selection pressures are at work during speciation? Which pathways accelerate the speed of speciation? Which kinds of trait variabilities makes difficult to find initial split criteria? Elaborating the principles of Fine Structure Analysis (FSA) and the morphological Initial Split Criteria (ISP) it was discovered that the European spring dwelling caddisfly Potamophylax nigricornis doesn’tbelong to a single species. It represents an entire species group with seventeen peripatric species evolving on the southernperipheries of the distributional area. Four new species subgroups have been erected: Potamophylax nigricornis new species subgroup, P. elegantulus new species subgroup, P. horgos new species subgroup, P. simas new species subgroup. Eleven new species have been described: Potamophylax apados sp. nov., P. fules sp. nov., P. fureses sp. nov., P. hasas sp. novov., P. horgos sp. nov., P. kethas sp. nov., P. lemezes sp. nov., P. peremes sp. nov., P. simas sp. nov., P. tuskes sp. nov., P. ureges sp. nov. One Potamophylax sp. nov. has been differentiated and three new species status have been documented:Potamophylax elegantulus (Klapálek) stat. n., P. mista (Navás) stat. nov., P. testaceus (Zetterstedt) stat. nov

    Identification and characterization of an inhibitory fibroblast growth factor receptor 2 (FGFR2) molecule, up-regulated in an Apert Syndrome mouse model

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    AS (Apert syndrome) is a congenital disease composed of skeletal, visceral and neural abnormalities, caused by dominant-acting mutations in FGFR2 [FGF (fibroblast growth factor) receptor 2]. Multiple FGFR2 splice variants are generated through alternative splicing, including PTC (premature termination codon)-containing transcripts that are normally eliminated via the NMD (nonsense-mediated decay) pathway. We have discovered that a soluble truncated FGFR2 molecule encoded by a PTC-containing transcript is up-regulated and persists in tissues of an AS mouse model. We have termed this IIIa–TM as it arises from aberrant splicing of FGFR2 exon 7 (IIIa) into exon 10 [TM (transmembrane domain)]. IIIa–TM is glycosylated and can modulate the binding of FGF1 to FGFR2 molecules in BIAcore-binding assays. We also show that IIIa–TM can negatively regulate FGF signalling in vitro and in vivo. AS phenotypes are thought to result from gain-of-FGFR2 signalling, but our findings suggest that IIIa–TM can contribute to these through a loss-of-FGFR2 function mechanism. Moreover, our findings raise the interesting possibility that FGFR2 signalling may be a regulator of the NMD pathway
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