Scaling limit for a drainage network model

We consider the two dimensional version of a drainage network model introduced by Gangopadhyay, Roy and Sarkar, and show that the appropriately rescaled family of its paths converges in distribution to the Brownian web. We do so by verifying the convergence criteria proposed by Fontes, Isopi, Newman and Ravishankar.Comment: 15 page

Temperature dependent carrier lifetime studies of Mo in crystalline silicon

The capture cross sections of both electronsσn and holes σp were determined for interstitialmolybdenum in crystalline silicon over the temperature range of −110 to 150 °C. Carrier lifetimemeasurements were performed on molybdenum-contaminated silicon using a temperature controlled photoconductance instrument. Injection dependent lifetime spectroscopy was applied at each temperature to calculate σp and σn. This analysis involved a novel approach that independently determined the capture cross sections at each temperature assuming a known defect density and thermal velocity. Since the energy state is in the lower half of the bandgap, the determination of σp is unaffected by the defect energy at all temperatures, and σp is found to decrease with temperature in a fashion consistent with excitonic Auger capture. At temperatures below 0 °C, the determination of σn is also unaffected by the defect energy due to the suppression of thermal emission, and σn decreases with temperature as well. It is shown that a projection of σn to higher temperature suggests the defect has an energy of 0.375 eV above the valance band edge of silicon.D.M. likes to thank the Australian Research Council for fellowship and G.C. likes to thank “CrystalClear Integrated Project” Contract No. SES6-CT_2003-502583 funded by the European Commission

Neighbourhood branding and urban regeneration: performing the 'right to the brand' in Casilino, Rome

In the last decade, many cities have experimented with small-scale initiatives aimed at enhancing the quality of life of residents; these initiatives have somehow fostered a reconceptualization of the term, as well as practice, of urban regeneration. In this context, the role of civic networks in bringing forward experiments in the production of alternative imaginaries and place-making has gained a major role, in particular in marginal neighbourhoods. By focusing on a case study in the eastern periphery of Rome, the paper explores the case of citizen-led neighbourhood branding, highlighting open issues and ambiguities in claiming a 'right to the brand'

Introduction to the special issue: between practices and policies. Rethinking urban regeneration in Southern European cities after the crisis

This Special Issue explores new approaches to urban regeneration, and potentially give new meanings to the term itself, as it appears in the context of austerity urbanism. In particular, the aim of this Special Issue is to offer a Southern European perspective of the nexus between the withdrawal of the State from urban governance, and of the new forms of cooperation arising from civil society, thus presenting original research material, and innovative perspectives, for current debates in urban studies

Targeting RAGE prevents muscle wasting and prolongs survival in cancer cachexia

Background: Cachexia, a multifactorial syndrome affecting more than 50% of patients with advanced cancer and responsible for ~20% of cancer-associated deaths, is still a poorly understood process without a standard cure available. Skeletal muscle atrophy caused by systemic inflammation is a major clinical feature of cachexia, leading to weight loss, dampening patients' quality of life, and reducing patients' response to anticancer therapy. RAGE (receptor for advanced glycation end-products) is a multiligand receptor of the immunoglobulin superfamily and a mediator of muscle regeneration, inflammation, and cancer. Methods: By using murine models consisting in the injection of colon 26 murine adenocarcinoma (C26-ADK) or Lewis lung carcinoma (LLC) cells in BALB/c and C57BL/6 or Ager−/− (RAGE-null) mice, respectively, we investigated the involvement of RAGE signalling in the main features of cancer cachexia, including the inflammatory state. In vitro experiments were performed using myotubes derived from C2C12 myoblasts or primary myoblasts isolated from C57BL/6 wild type and Ager−/− mice treated with the RAGE ligand, S100B (S100 calcium-binding protein B), TNF (tumor necrosis factor)α±IFN (interferon) γ, and tumour cell- or masses-conditioned media to analyse hallmarks of muscle atrophy. Finally, muscles of wild type and Ager−/− mice were injected with TNFα/IFNγ or S100B in a tumour-free environment. Results: We demonstrate that RAGE is determinant to activate signalling pathways leading to muscle protein degradation in the presence of proinflammatory cytokines and/or tumour-derived cachexia-inducing factors. We identify the RAGE ligand, S100B, as a novel factor able to induce muscle atrophy per se via a p38 MAPK (p38 mitogen-activated protein kinase)/myogenin axis and STAT3 (signal transducer and activator of transcription 3)-dependent MyoD (myoblast determination protein 1) degradation. Lastly, we found that in cancer conditions, an increase in serum levels of tumour-derived S100B and HMGB1 (high mobility group box 1) occurs leading to chronic activation/overexpression of RAGE, which induces hallmarks of cancer cachexia (i.e. muscle wasting, systemic inflammation, and release of tumour-derived pro-cachectic factors). Absence of RAGE in mice translates into reduced serum levels of cachexia-inducing factors, delayed loss of muscle mass and strength, reduced tumour progression, and increased survival. Conclusions: RAGE is a molecular determinant in inducing the hallmarks of cancer cachexia, and molecular targeting of RAGE might represent a therapeutic strategy to prevent or counteract the cachectic syndrome

The asymptotic shape theorem for the frog model on finitely generated abelian groups

We study the frog model on Cayley graphs of groups with polynomial growth rate $D \geq 3$. The frog model is an interacting particle system in discrete time. We consider that the process begins with a particle at each vertex of the graph and only one of these particles is active when the process begins. Each activated particle performs a simple random walk in discrete time activating the inactive particles in the visited vertices. We prove that the activation time of particles grows at least linearly and we show that in the abelian case with any finite generator set the set of activated sites has a limiting shape.Comment: The original publication is available at www.esaim-ps.or

Ultrafast Momentum Imaging of Pseudospin-Flip Excitations in Graphene

The pseudospin of Dirac electrons in graphene manifests itself in a peculiar momentum anisotropy for photo-excited electron-hole pairs. These interband excitations are in fact forbidden along the direction of the light polarization, and are maximum perpendicular to it. Here, we use time- and angle-resolved photoemission spectroscopy to investigate the resulting unconventional hot carrier dynamics, sampling carrier distributions as a function of energy and in-plane momentum. We first show that the rapidly-established quasi-thermal electron distribution initially exhibits an azimuth-dependent temperature, consistent with relaxation through collinear electron-electron scattering. Azimuthal thermalization is found to occur only at longer time delays, at a rate that depends on the substrate and the static doping level. Further, we observe pronounced differences in the electron and hole dynamics in n-doped samples. By simulating the Coulomb- and phonon-mediated carrier dynamics we are able to disentangle the influence of excitation fluence, screening, and doping, and develop a microscopic picture of the carrier dynamics in photo-excited graphene. Our results clarify new aspects of hot carrier dynamics that are unique to Dirac materials, with relevance for photo-control experiments and optoelectronic device applications.Comment: 23 pages, 12 figure