Manioc : Portail | resultats 341 - 360 pour la recherche: éruption

Éditeur(s) : HAL CCSD Elsevier
Résumé : Handheld energy dispersive portable X-ray spectrometers (pXRF) are generally designed and used for qualitative survey applications. We developed shipboard quantitative analysis protocols for pXRF and employed the instrument to make over 2000 individual abundance measurements for a selection of major and trace elements on over 1200 m of recovered core during the eight weeks of the International Ocean Discovery Program (IODP) Expedition 352 to the Izu-Bonin forearc. pXRF analytical performance, accuracy and precision were found to be the same on powdered rock samples and on freshly cut rock surfaces, and sample results were similar within error to measurements made via shipboard ICP-OES analysis save at low abundance levels for a few elements. Instrument performance was optimal for elements between Z = 19 and Z = 40, and the system yielded reproducible data for K, Ca, Ti, V, Cr, Mn, Fe, Cu, Zn, Rb, Sr, and Zr on both powdered samples and rock surfaces. Working curves developed via pXRF measurement of a suite of geologic standard reference materials and well-characterized lavas permitted accurate quantitative measurements for many of the examined elements on both sample powders and rock surfaces. Although pXRF has been sporadically employed on previous cruises, Expedition 352 is the first time a detailed, high-density chemostratigraphy of recovered core samples was collected using pXRF measurements of rock core surfaces. These high-resolution data allowed the recognition of chemically distinct eruptive units in near real-time. The rapid identification of geochemical trends vastly improved our selection of samples for shipboard and shore-based analysis, permitted a more comprehensive interpretation of our Expedition results, and provided key decision-making information for drilling operations.
ISSN: 0009-2541

hal-01553188
https://hal.archives-ouvertes.fr/hal-01553188
DOI : 10.1016/j.chemgeo.2017.01.007

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Numerical models of ionic diffusion in one and three dimensions: application to dehydration of mantle olivine
Auteur(s) : Thoraval, Catherine Demouchy, Sylvie
Auteurs secondaires : Géosciences Montpellier ; Université des Antilles et de la Guyane (UAG) - Institut national des sciences de l'Univers (INSU - CNRS) - Université de Montpellier (UM) - Centre National de la Recherche Scientifique (CNRS) Manteau et Interfaces ; Géosciences Montpellier ; Université des Antilles et de la Guyane (UAG) - Institut national des sciences de l'Univers (INSU - CNRS) - Université de Montpellier (UM) - Centre National de la Recherche Scientifique (CNRS) - Université des Antilles et de la Guyane (UAG) - Institut national des sciences de l'Univers (INSU - CNRS) - Université de Montpellier (UM) - Centre National de la Recherche Scientifique (CNRS)

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"The renewed activity of Pelée and Soufrière", Collier's Weekly, vol.XXIX, n°24

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Ruines du maître-autel de la cathédrale de Saint-Pierre. Martinique
Auteur(s) : Leboullanger

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Martinique. Saint-Pierre. Vue générale des ruines
Auteur(s) : Leboullanger

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Saint-Pierre. Arbres dévastés après l'éruption du 08 mai 1902

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Natural hazards in the French West Indies : an overall view ; Risques naturels dans les Antilles françaises: une vision d’ensemble ; Rischi naturali nelle Antille Francese: una visione globale
Auteur(s) : D'Ercole, Robert
Auteurs secondaires : Université des Antilles et de la Guyane (UAG) M. Panizza M. Soldati D. Barani

Éditeur(s) : HAL CCSD Dipartamento di Scienze della Terra, Università degli Studi di Modena
Résumé : International audience
The aim or this paper is to give an overall view of the natural hazards and risks affecting the French West Indies. These are mainly connected with hurricanes, volcanic eruptions and earthquakes which have caused several deaths and seriously weakened the local economy during the last three centuries. First of all the geological and geographical conditions which determine the natural predisposition of the French West Indies to geophysical and atmospheric hazards are described. Then the risk for the population is taken into account, both in terms of' the direct effects of the above mentioned hazards and of the side-effects, that is tidal waves, floods and mass movements. Finally the economic and social impact of natural disasters on the French West Indies and the difficulties arising in risk mitigation are shown.
Lo scopo di questo lavoro è di fornire un quadro generale dei rischi naturali che interessano le Antille Francese. Questi sono principalmente connessi con uragani, eruzioni vulcaniche e terremoti che, nel corso degli ultirni tre secoli hanno causato parecchi decessi e seriamente indebolito la economia locale. Vengono dapprima descritte le condizioni geologiche e geografiche che determinano la naturale predisposizione delle Antille Francese a minacche di tipo sia endogeno che esogeno. Viene poi considerato il rischio per la.popolazione, sia in termiini di effetti diretti dei fenomeni sopra citati che in termini di effetti marginali dovuti allo sviluppo di marernotti, alluvioni e frane. Infine viene considerato l’impatto sul tessuto sociale ed economico dei disastri di origine naturale nelle Antille Francese e le difficoltà che insorgono nella mitigazione del rischio.
The Erasmus 93-94 Programme in Geomorphology : Intensive Course in the French Antilles and Student Mobility

Droits : info:eu-repo/semantics/OpenAccess
ISBN : 88-900094-0-3
hal-01191892
https://hal.archives-ouvertes.fr/hal-01191892
https://hal.archives-ouvertes.fr/hal-01191892/document
https://hal.archives-ouvertes.fr/hal-01191892/file/D%27Ercole%201995%20-%20Natural%20hazards%20in%20the%20French%20West%20Indies.pdf

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A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement
Auteur(s) : Prasad, Megana K. Geoffroy, Véronique Vicaire, Serge Jost, Bernard Dumas, Michael Le Gras, Stéphanie Switala, Marzena Gasse, Barbara
Auteurs secondaires : Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) ; Institut National de la Santé et de la Recherche Médicale (INSERM) - Centre National de la Recherche Scientifique (CNRS) DNA Microarrays and Sequencing Platform ; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) Evolution Paris Seine ; Université Nice Sophia Antipolis (UNS) ; Université Côte d'Azur (UCA) - Université Côte d'Azur (UCA) - Centre National de la Recherche Scientifique (CNRS) - Université des Antilles et de la Guyane (UAG) - Université Pierre et Marie Curie - Paris 6 (UPMC) Service de médecine infantile III et génétique clinique [CHRU Nancy] ; Hôpital d'Enfants Brabois [CHRU Nancy] ; Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy) - Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy) - Université de Lorraine (UL) Nutrition-Génétique et Exposition aux Risques Environnementaux (NGERE) ; Institut National de la Santé et de la Recherche Médicale (INSERM) - Université de Lorraine (UL) Service d'odontologie [CHU Nancy] ; Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy) Faculté de Chirurgie Dentaire Human Genetics Institute ; Heidelberg University

Éditeur(s) : HAL CCSD
Résumé : International audience
Background Orodental diseases include several clinically and genetically heterogeneous disorders that can present in isolation or as part of a genetic syndrome. Due to the vast number of genes implicated in these disorders, establishing a molecular diagnosis can be challenging. We aimed to develop a targeted next-generation sequencing (NGS) assay to diagnose mutations and potentially identify novel genes mutated in this group of disorders. Methods We designed an NGS gene panel that targets 585 known and candidate genes in orodental disease. We screened a cohort of 101 unrelated patients without a molecular diagnosis referred to the Reference Centre for Oro-Dental Manifestations of Rare Diseases, Strasbourg, France, for a variety of orodental disorders including isolated and syndromic amelogenesis imperfecta (AI), isolated and syndromic selective tooth agenesis (STHAG), isolated and syndromic dentinogenesis imperfecta, isolated dentin dysplasia, otodental dysplasia and primary failure of tooth eruption. Results We discovered 21 novel pathogenic variants and identified the causative mutation in 39 unrelated patients in known genes (overall diagnostic rate: 39%). Among the largest subcohorts of patients with isolated AI (50 unrelated patients) and isolated STHAG (21 unrelated patients), we had a definitive diagnosis in 14 (27%) and 15 cases (71%), respectively. Surprisingly, COL17A1 mutations accounted for the majority of autosomal-dominant AI cases. Conclusions We have developed a novel targeted NGS assay for the efficient molecular diagnosis of a wide variety of orodental diseases. Furthermore, our panel will contribute to better understanding the contribution of these genes to orodental disease. Trial registration numbers NCT01746121 and NCT02397824
Journal of Medical Genetics

hal-01272929
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01272929
DOI : 10.1136/jmedgenet-2015-103302
PUBMED : 26502894

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Saint-Pierre (Martinique). La Douane
Auteur(s) : H.K.

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