39 research outputs found

    Hysteresis, Avalanches, and Disorder Induced Critical Scaling: A Renormalization Group Approach

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    We study the zero temperature random field Ising model as a model for noise and avalanches in hysteretic systems. Tuning the amount of disorder in the system, we find an ordinary critical point with avalanches on all length scales. Using a mapping to the pure Ising model, we Borel sum the 6ϵ6-\epsilon expansion to O(ϵ5)O(\epsilon^5) for the correlation length exponent. We sketch a new method for directly calculating avalanche exponents, which we perform to O(ϵ)O(\epsilon). Numerical exponents in 3, 4, and 5 dimensions are in good agreement with the analytical predictions.Comment: 134 pages in REVTEX, plus 21 figures. The first two figures can be obtained from the references quoted in their respective figure captions, the remaining 19 figures are supplied separately in uuencoded forma

    Clinical Heterogeneity of Autosomal Recessive Spastic Paraplegias: Analysis of 106 Patients in 46 Families

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    Background Hereditary spastic paraplegias (HSPs) are a heterogeneous group of neurodegenerative disorders characterized by progressive and predominant spasticity of the lower limbs, in which dominant, recessive, and X-linked forms have been described. While autosomal dominant HSP has been extensively studied, autosomal recessive HSP is less well known and is considered a rare condition. Objective To analyze the clinical presentation in a large group of patients with autosomal recessive HSP from Portugal and Algeria to define homogeneous groups that could serve as a guide for future molecular studies. Results Clinical features in 106 patients belonging to 46 Portuguese and Algerian families with autosomal recessive HSP are presented, as well as the results of molecular studies in 23 of these families. Five phenotypes are defined: (1) pure early-onset families, (2) pure late-onset families, (3) complex families with mental retardation, (4) complex families with mental retardation and peripheral neuropathy, and (5) complex families with cerebellar ataxia. Six additional families have specific complex presentations, each of which is unique in the present series. Pyramidal signs in the upper limbs and pes cavus are frequent findings, while pseudobulbar signs, including dysarthria, dysphagia, and brisk jaw jerks, are more frequent in the complex forms. The complex forms have a poorer prognosis, while pure forms, particularly those with early onset, are more benign. One Algerian pure early-onset kindred was linked to the locus on chromosome 8, previously reported in 4 Tunisian families. Two of the Portuguese kindreds with complex forms (one with mental retardation and the other associated with hypoplasia of the corpus callosum) showed linkage to the locus recently identified on chromosome 16. Conclusions Although autosomal recessive HSP represents a heterogeneous group of diseases, some phenotypes can be defined by analyzing a large group of patients. The fact that only one Algerian family was linked to chromosome 8 suggests that this is a rare localization even in kindreds with the same ethnic background. Linkage to chromosome 16 was found in 2 clinically diverse Portuguese kindreds, illustrating that this locus is also rare and may correspond to different phenotypes.This study was supported by Généthon, Paris, France; and 2 grants from the Portuguese Foundation for Science and Technology and the Portuguese Health Administration (projects STRDA/C/SAU/277/92 and PECS/C/SAU/219/95)

    The evolving SARS-CoV-2 epidemic in Africa: Insights from rapidly expanding genomic surveillance

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    INTRODUCTION Investment in Africa over the past year with regard to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) sequencing has led to a massive increase in the number of sequences, which, to date, exceeds 100,000 sequences generated to track the pandemic on the continent. These sequences have profoundly affected how public health officials in Africa have navigated the COVID-19 pandemic. RATIONALE We demonstrate how the first 100,000 SARS-CoV-2 sequences from Africa have helped monitor the epidemic on the continent, how genomic surveillance expanded over the course of the pandemic, and how we adapted our sequencing methods to deal with an evolving virus. Finally, we also examine how viral lineages have spread across the continent in a phylogeographic framework to gain insights into the underlying temporal and spatial transmission dynamics for several variants of concern (VOCs). RESULTS Our results indicate that the number of countries in Africa that can sequence the virus within their own borders is growing and that this is coupled with a shorter turnaround time from the time of sampling to sequence submission. Ongoing evolution necessitated the continual updating of primer sets, and, as a result, eight primer sets were designed in tandem with viral evolution and used to ensure effective sequencing of the virus. The pandemic unfolded through multiple waves of infection that were each driven by distinct genetic lineages, with B.1-like ancestral strains associated with the first pandemic wave of infections in 2020. Successive waves on the continent were fueled by different VOCs, with Alpha and Beta cocirculating in distinct spatial patterns during the second wave and Delta and Omicron affecting the whole continent during the third and fourth waves, respectively. Phylogeographic reconstruction points toward distinct differences in viral importation and exportation patterns associated with the Alpha, Beta, Delta, and Omicron variants and subvariants, when considering both Africa versus the rest of the world and viral dissemination within the continent. Our epidemiological and phylogenetic inferences therefore underscore the heterogeneous nature of the pandemic on the continent and highlight key insights and challenges, for instance, recognizing the limitations of low testing proportions. We also highlight the early warning capacity that genomic surveillance in Africa has had for the rest of the world with the detection of new lineages and variants, the most recent being the characterization of various Omicron subvariants. CONCLUSION Sustained investment for diagnostics and genomic surveillance in Africa is needed as the virus continues to evolve. This is important not only to help combat SARS-CoV-2 on the continent but also because it can be used as a platform to help address the many emerging and reemerging infectious disease threats in Africa. In particular, capacity building for local sequencing within countries or within the continent should be prioritized because this is generally associated with shorter turnaround times, providing the most benefit to local public health authorities tasked with pandemic response and mitigation and allowing for the fastest reaction to localized outbreaks. These investments are crucial for pandemic preparedness and response and will serve the health of the continent well into the 21st century

    On route to chaos in stimulated Brillouin scattering with feedback

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    We theoretically analyse the dynamics of Brillouin scattering in Perot-Fabry fibre cavities. An original approach to the stability analysis of the steady state allows us to define the instability domain and to locate chaotic behaviours up to now attributed to Kerr effect. Numerical investigations give evidence of a Newhouse-Ruelle-Takens route to chaos, associated with the increase in the number of cavity modes under the gain curve

    Origine du brûlage de trou spectral dans les amplificateurs et générateurs Brillouin

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    De récentes expériences ont mis en évidence l'apparition d'un trou dans la courbe de gain de l'amplificateur Brillouin [1] et dans celle du générateur Brillouin [2]. Ce comportement est généralement interprété comme étant un effet lié à un élargissement inhomogène du gain. Pourtant, nous montrons que ce trou n'est aucunement lié à l'élargissement inhomogène mais qu'il est descriptible dans le cadre d'un gain homogène

    Bruit d'intensité dans les lasers Brillouin à fibre

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    Les caractéristiques du bruit d'intensité dans un laser Brillouin à fibre sont étudiées expérimentalement et théoriquement. Les fluctuations d'intensité de ce laser proviennent de deux sources de bruit : le bruit du laser de pompe et les fluctuations du coefficient de réinjection de la cavité. Le transfert du bruit d'une source sur l'intensité du laser Brillouin est défini par une fonction de gain qui a été déterminée expérimentalement et théoriquement

    Scaling of hysteresis in a multi-dimensional all-optical bistable system

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    We analyse the hysteresis enlargements of an optical bistable system involving three dynamical variables. We investigate, both experimentally and numerically, the local dynamics of the up- and down-switching process versus the sweeping frequency Ω of the control parameter. In particular, we delineate the domain of validity of the Ω2/3\Omega^{2/3} scaling law predicted for one-dimensional systems. At high sweeping frequency, we show the appearance of another asymptotic scaling low in Ω1/2\Omega^{1/2}. Thereafter, we analyse the global evolution of the hysteresis loop induced by these processes. At low frequency, a Ω2/3\Omega^{2/3} scaling law is retrieved, whereas at high frequency, the dynamical behaviour is shown to strongly depend on the particular shape of the bistability curve
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