108 research outputs found

    L’ANTHROPOCENE COMME RUPTURE DE L’HISTOIRE DE L’ECONOMIE

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    Si le passage Ă  l’AnthropocĂšne rĂ©vĂšle la capacitĂ© de l’homme Ă  transformer l’ensemble du systĂšme terrestre, les thĂ©ories Ă©conomiques ont de tout temps, minimisĂ© ce changement d’époque gĂ©ologique, prĂ©fĂ©rant focaliser leur attention sur la dynamique du systĂšme capitaliste ou la sacro-sainte croissance Ă©conomique. Si des limites Ă  la croissance sont bien mentionnĂ©es, elles restent cantonnĂ©es Ă  des contraintes socio-techniques (pĂ©nurie de main d'Ɠuvre, coĂ»t Ă©levĂ© du capital, prix des matiĂšres premiĂšres, faiblesse des investissements, absence de prise de risques des entrepreneurs
). Tout laisse Ă  penser que les sociĂ©tĂ©s, par essence Ă©conomiques, se seraient libĂ©rĂ©es des limites biophysiques. L’AnthropocĂšne montre au contraire que ces limites imposent un rĂ©encastrement de l’économie dans l’environnement et dans le social. La question du temps, souvent rĂ©duite au court terme et Ă  des questions de statique ou de dynamique dans la thĂ©orie Ă©conomique, impose de penser l’avenir, sans pour autant reposer sur une extrapolation du passĂ©. DĂšs lors, les thĂ©ories Ă©conomiques doivent proposer un corpus d’hypothĂšses et de concepts susceptibles de forger de nouveaux paradigmes, plus Ă  mĂȘme de se reprĂ©senter les futurs possible

    The composition of Saturn's rings

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    The origin and evolution of Saturn's rings is critical to understanding the Saturnian system as a whole. Here, we discuss the physical and chemical composition of the rings, as a foundation for evolutionary models described in subsequent chapters. We review the physical characteristics of the main rings, and summarize current constraints on their chemical composition. Radial trends are observed in temperature and to a limited extent in particle size distribution, with the C ring exhibiting higher temperatures and a larger population of small particles. The C ring also shows evidence for the greatest abundance of silicate material, perhaps indicative of formation from a rocky body. The C ring and Cassini Division have lower optical depths than the A and B rings, which contributes to the higher abundance of the exogenous neutral absorber in these regions. Overall, the main ring composition is strongly dominated by water ice, with minor silicate, UV absorber, and neutral absorber components. Sampling of the innermost D ring during Cassini's Grand Finale provides a new set of in situ constraints on the ring composition, and we explore ongoing work to understand the linkages between the main rings and the D ring. The D ring material is organic- and silicate-rich and water-poor relative to the main rings, with a large population of small grains. This composition may be explained in part by volatile losses in the D ring, and current constraints suggest some degree of fractionation rather than sampling of the bulk D ring material.Comment: Submitted to SSR for publication in the collection "New Vision of the Saturnian System in the Context of a Highly Dissipative Saturn

    ANNODIS : une approche outillée de l'annotation de structures discursives

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    International audienceThe ANNODIS project has two interconnected objectives: to produce a corpus of texts annotated at discourse-level, and to develop tools for corpus annotation and exploitation. Two sets of annotations are proposed, representing two complementary perspectives on discourse organisation: a bottom-up approach starting from minimal discourse units and building complex structures via a set of discourse relations; a top-down approach envisaging the text as a whole and using pre-identified cues to detect discourse macro-structures. The construction of the corpus goes hand in hand with the development of two interfaces: the first one supports manual annotation of discourse structures, and allows different views of the texts using NLP-based pre-processing; another interface will support the exploitation of the annotations. We present the discourse models and annotation protocols, and the interface which embodies them.Le projet ANNODIS vise la construction d'un corpus de textes annotĂ©s au niveau discursif ainsi que le dĂ©veloppement d'outils pour l'annotation et l'exploitation de corpus. Les annotations adoptent deux points de vue complĂ©mentaires : une perspective ascendante part d'unitĂ©s de discours minimales pour construire des structures complexes via un jeu de relations de discours ; une perspective descendante aborde le texte dans son entier et se base sur des indices prĂ©-identifiĂ©s pour dĂ©tecter des structures discursives de haut niveau. La construction du corpus est associĂ©e Ă  la crĂ©ation de deux interfaces : la premiĂšre assiste l'annotation manuelle des relations et structures discursives en permettant une visualisation du marquage issu des prĂ©traitements ; une seconde sera destinĂ©e Ă  l'exploitation des annotations. Nous prĂ©sentons les modĂšles et protocoles d'annotation Ă©laborĂ©s pour mettre en Ɠuvre, au travers de l'interface dĂ©diĂ©e, la campagne d'annotation

    Adrenocortical tumours in children and adolescents: The EXPeRT/PARTNER diagnostic and therapeutic recommendations

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    Adrenocortical tumours (ACTs) are rare during childhood. A complete surgical resection provides the best chance of cure, but the role and efficacy of the adjuvant therapy are still controversial. Various histologic criteria of malignancy for ACTs adopted in children do not facilitate comparative studies and are not completely shared. Therefore, a sharp demarcation between benign and malignant lesions has not been recognised, making it difficult to identify who potentially needs perioperative therapy. This manuscript presents the internationally harmonised recommendations for the diagnosis and treatment of ACTs in children and adolescents, established by the European Cooperative Study Group for Paediatric Rare Tumours (EXPeRT) group within the EU-funded project PARTNER (Paediatric Rare Tumours Network - European Registry)

    Potential Utility of Plasma P-Tau and Neurofilament Light Chain as Surrogate Biomarkers for Preventive Clinical Trials

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    OBJECTIVE: To test the utility of longitudinal changes in plasma phosphorylated tau 181 (p-tau181) and neurofilament light chain (NfL) as surrogate markers for clinical trials targeting cognitively unimpaired (CU) populations. METHODS: We estimated the sample size needed to test a 25% drug effect with 80% of power at a 0.05 level on reducing changes in plasma markers in CU participants from Alzheimer's Disease Neuroimaging Initiative database. RESULTS: We included 257 CU individuals (45.5% males; mean age = 73 [6] years; 32% ÎČ-amyloid [AÎČ] positive). Changes in plasma NfL were associated with age, whereas changes in plasma p-tau181 with progression to amnestic mild cognitive impairment. Clinical trials using p-tau181 and NfL would require 85% and 63% smaller sample sizes, respectively, for a 24-month than a 12-month follow-up. A population enrichment strategy using intermediate levels of AÎČ PET (Centiloid 20-40) further reduced the sample size of the 24-month clinical trial using p-tau181 (73%) and NfL (59%) as a surrogate. DISCUSSION: Plasma p-tau181/NfL can potentially be used to monitor large-scale population interventions in CU individuals. The enrollment of CU with intermediate AÎČ levels constitutes the alternative with the largest effect size and most cost-effective for trials testing drug effect on changes in plasma p-tau181 and NfL

    Global Patterns in Seasonal Activity of Influenza A/H3N2, A/H1N1, and B from 1997 to 2005: Viral Coexistence and Latitudinal Gradients

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    Despite a mass of research on the epidemiology of seasonal influenza, overall patterns of infection have not been fully described on broad geographic scales and for specific types and subtypes of the influenza virus. Here we provide a descriptive analysis of laboratory-confirmed influenza surveillance data by type and subtype (A/H3N2, A/H1N1, and B) for 19 temperate countries in the Northern and Southern hemispheres from 1997 to 2005, compiled from a public database maintained by WHO (FluNet). Key findings include patterns of large scale co-occurrence of influenza type A and B, interhemispheric synchrony for subtype A/H3N2, and latitudinal gradients in epidemic timing for type A. These findings highlight the need for more countries to conduct year-round viral surveillance and report reliable incidence data at the type and subtype level, especially in the Tropics

    Synergistic interventions to control COVID-19 : mass testing and isolation mitigates reliance on distancing

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    Stay-at-home orders and shutdowns of non-essential businesses are powerful, but socially costly, tools to control the pandemic spread of SARS-CoV-2. Mass testing strategies, which rely on widely administered frequent and rapid diagnostics to identify and isolate infected individuals, could be a potentially less disruptive management strategy, particularly where vaccine access is limited. In this paper, we assess the extent to which mass testing and isolation strategies can reduce reliance on socially costly non-pharmaceutical interventions, such as distancing and shutdowns. We develop a multi-compartmental model of SARS-CoV-2 transmission incorporating both preventative non-pharmaceutical interventions (NPIs) and testing and isolation to evaluate their combined effect on public health outcomes. Our model is designed to be a policy-guiding tool that captures important realities of the testing system, including constraints on test administration and non-random testing allocation. We show how strategic changes in the characteristics of the testing system, including test administration, test delays, and test sensitivity, can reduce reliance on preventative NPIs without compromising public health outcomes in the future. The lowest NPI levels are possible only when many tests are administered and test delays are short, given limited immunity in the population. Reducing reliance on NPIs is highly dependent on the ability of a testing program to identify and isolate unreported, asymptomatic infections. Changes in NPIs, including the intensity of lockdowns and stay at home orders, should be coordinated with increases in testing to ensure epidemic control; otherwise small additional lifting of these NPIs can lead to dramatic increases in infections, hospitalizations and deaths. Importantly, our results can be used to guide ramp-up of testing capacity in outbreak settings, allow for the flexible design of combined interventions based on social context, and inform future cost-benefit analyses to identify efficient pandemic management strategies

    Decrease of physical activity level in adolescents with limb fractures: an accelerometry-based activity monitor study

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    <p>Abstract</p> <p>Background</p> <p>Immobilization and associated periods of inactivity can cause osteopenia, the physiological response of the bone to disuse. Mechanical loading plays an essential role in maintaining bone integrity. Skeletal fractures represent one cause of reduction of the physical activity (PA) level in adolescents. The purpose of this study was to quantify the reduction of PA in adolescents with limb fractures during the cast immobilization period compared with healthy controls.</p> <p>Methods</p> <p>Two hundred twenty adolescents were divided into three groups: those with upper limb fractures (50 cases); lower limb fractures (50 cases); and healthy cases (120 cases). Patients and their healthy peers were matched for gender, age, and seasonal assessment of PA. PA level was assessed during cast immobilization by accelerometer. Time spent in PA in each of the different intensity levels - sedentary, light, moderate, and vigorous - was determined for each participant and expressed in minutes and as a percentage of total valid time.</p> <p>Results</p> <p>Reduction in PA during cast immobilization was statistically significant in patients with limb fractures compared to healthy controls. The total PA count (total number of counts/min) was significantly lower in those with upper and lower limb fractures (-30.1% and -62.4%, respectively) compared with healthy controls (p < 0.0001 and p = 0.0003, respectively). Time spent in moderate-to-vigorous PA by patients with upper and lower limb injuries decreased by 36.9% (<it>p </it>= 0.0003) and 76.6% (<it>p </it>< 0.0001), respectively, and vigorous PA was reduced by 41.4% (<it>p </it>= 0.0008) and 84.4% (<it>p </it>< 0.0001), respectively.</p> <p>Conclusions</p> <p>PA measured by accelerometer is a useful and valid tool to assess the decrease of PA level in adolescents with limb fractures. As cast immobilization and reduced PA are known to induce bone mineral loss, this study provides important information to quantify the decrease of skeletal loading in this patient population. The observed reduction of high intensity skeletal loading due to the decrease in vigorous PA may explain osteopenia due to disuse, and these data should be kept in mind by trauma practitioners to avoid any unnecessary prolongation of the cast immobilization period.</p

    Association of Phosphorylated Tau Biomarkers With Amyloid Positron Emission Tomography vs Tau Positron Emission Tomography

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    IMPORTANCE: The recent proliferation of phosphorylated tau (p-tau) biomarkers has raised questions about their preferential association with the hallmark pathologies of Alzheimer disease (AD): amyloid-ÎČ plaques and tau neurofibrillary tangles. OBJECTIVE: To determine whether cerebrospinal fluid (CSF) and plasma p-tau biomarkers preferentially reflect cerebral ÎČ-amyloidosis or neurofibrillary tangle aggregation measured with positron emission tomography (PET). DESIGN, SETTING, AND PARTICIPANTS: This was a cross-sectional study of 2 observational cohorts: the Translational Biomarkers in Aging and Dementia (TRIAD) study, with data collected between October 2017 and August 2021, and the Alzheimer's Disease Neuroimaging Initiative (ADNI), with data collected between September 2015 and November 2019. TRIAD was a single-center study, and ADNI was a multicenter study. Two independent subsamples were derived from TRIAD. The first TRIAD subsample comprised individuals assessed with CSF p-tau (p-tau181, p-tau217, p-tau231, p-tau235), [18F]AZD4694 amyloid PET, and [18F]MK6240 tau PET. The second TRIAD subsample included individuals assessed with plasma p-tau (p-tau181, p-tau217, p-tau231), [18F]AZD4694 amyloid PET, and [18F]MK6240 tau PET. An independent cohort from ADNI comprised individuals assessed with CSF p-tau181, [18F]florbetapir PET, and [18F]flortaucipir PET. Participants were included based on the availability of p-tau and PET biomarker assessments collected within 9 months of each other. Exclusion criteria were a history of head trauma or magnetic resonance imaging/PET safety contraindications. No participants who met eligibility criteria were excluded. EXPOSURES: Amyloid PET, tau PET, and CSF and plasma assessments of p-tau measured with single molecule array (Simoa) assay or enzyme-linked immunosorbent assay. MAIN OUTCOMES AND MEASURES: Associations between p-tau biomarkers with amyloid PET and tau PET. RESULTS: A total of 609 participants (mean [SD] age, 66.9 [13.6] years; 347 female [57%]; 262 male [43%]) were included in the study. For all 4 phosphorylation sites assessed in CSF, p-tau was significantly more closely associated with amyloid-PET values than tau-PET values (p-tau181 difference, 13%; 95% CI, 3%-22%; P = .006; p-tau217 difference, 11%; 95% CI, 3%-20%; P = .003; p-tau231 difference, 15%; 95% CI, 5%-22%; P < .001; p-tau235 difference, 9%; 95% CI, 1%-19%; P = .02) . These results were replicated with plasma p-tau181 (difference, 11%; 95% CI, 1%-22%; P = .02), p-tau217 (difference, 9%; 95% CI, 1%-19%; P = .02), p-tau231 (difference, 13%; 95% CI, 3%-24%; P = .009), and CSF p-tau181 (difference, 9%; 95% CI, 1%-21%; P = .02) in independent cohorts. CONCLUSIONS AND RELEVANCE: Results of this cross-sectional study of 2 observational cohorts suggest that the p-tau abnormality as an early event in AD pathogenesis was associated with amyloid-ÎČ accumulation and highlights the need for careful interpretation of p-tau biomarkers in the context of the amyloid/tau/neurodegeneration, or A/T/(N), framework
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