913 research outputs found
Faire un stage de recherche à LAM. Entretien avec Arnaud Dupuy, stagiaire LAM
No full textFree consultation with a Doctor of mobile health team has Madagacar. Author : Docteur Ando. Licence : CC BY SA. https://commons.wikimedia.org/wiki/File:Free_consultation_with_a_Doctor_of_mobile_health_team_has_Madagacar.jpg En mai-juin 2019, Arnaud Dupuy a accompli un stage au laboratoire Les Afriques dans le monde, encadré par Jean-Philippe Berrou, enseignant-chercheur en économie. Il a été impliqué dans deux programmes de recherches pluridisciplinaires concernant l’aire africaine. Qu’est..
Dutch space; interview with Arnaud de Jong, CEO
No full textDutch Space, the largest space company in the Netherlands and part of Airbus Defence and Space, appointed a new CEO last year. The Leonardo Times sat down with the CEO Arnaud de Jong for an interview. We discuss his career, developments in Dutch Space, his take on competition in the commercial space domain and his future outlook on European and International space markets.Aerospace Engineerin
Arnaud François
No full textArnaud François, born in 1978, is a professor of philosophy at the University of Poitiers. He is the author of several books and articles on Bergson, Schopenhauer and Nietzsche, as well as of works on the philosophy of health. He is currently exploring, at the junction between philosophy and literature, the work of Émile Zola. He is, with Ondřej Švec, co-president of the Organisation Francophone pour la Formation et la Recherche Européennes en Sciences humaines (OFFRES), an academic collabora..
Interview with Arnaud Lechevalier on Social Europe
No full textHeike Wieters and Dominique Gareis of Saisir l'Europe - axis Social State have recently conducted an Interview with Arnaud Lechevalier (Maitre de Conferences, Université Paris 1 Panthéon-Sorbonne, researcher at the Laboratoire Interdisciplinaire pour la Sociologie Economique, CNAM-CNRS and at the Centre Marc Bloch, co-author (with Jan Wielgohs, Europa University Viadrina) of the edited volume Social Europe: A Dead End. What the Eurozone Crisis is doing to Europe’s Social Dimension, on social ..
St Arnaud total count grid geodetic
No full textMaintenance and Update Frequency: notPlannedStatement: This St Arnaud total count grid geodetic is an airborne-derived radiometric terrestrial dose rate grid for the St Arnaud Infill merge, 1990 survey. The survey was acquired under the project No. 1345 for the geological survey of VIC. The grid has a cell size of 0.00042 degrees (approximately 42m). A total of 18970 line-kilometres of data at a line spacing between 200m and 400m, and 100m terrain clearance were acquired to produce this grid. The terrestrial dose rate grid is derived as a linear combination of the filtered K, U and Th grids. Details of the specifications of individual airborne surveys can be found in the Fourteenth Edition of the Index of Airborne Geophysical Surveys (Percival, 2014). This Index is also available online at http://pid.geoscience.gov.au/dataset/79134.
Reference:
Percival, P.J., 2014. Index of airborne geophysical surveys (Fourteenth Edition).The radiometric, or gamma-ray spectrometric method, measures the natural variations in the gamma-rays detected near the Earth's surface as the result of the natural radioactive decay of potassium (K), uranium (U) and thorium (Th). The data collected are processed via standard methods to ensure the response recorded is that due only to the rocks in the ground. The results produce datasets that can be interpreted to reveal the geological structure of the sub-surface. The processed data is checked for quality by GA geophysicists to ensure that the final data released by GA are fit-for-purpose. The terrestrial dose rate grid is derived as a linear combination of the filtered K, U and Th grids. A low pass filter is applied to this grid to generate the filtered terrestrial dose rate grid.<br/>This St Arnaud total count grid geodetic has a cell size of 0.00042 degrees (approximately 42m) and shows the terrestrial dose rate of the St Arnaud Infill merge, 1990. The data used to produce this grid was acquired in 1990 by the VIC Government, and consisted of 18970 line-kilometres of data at a line spacing between 200m and 400m, and 100m terrain clearance
Dendropaemon (Coprophanaeoides) furtadoi Genier & Arnaud, new species
No full text5. Dendropaemon (Coprophanaeoides) furtadoi Génier & Arnaud, new species (Figs. 5, 48– 49, 156) Type locality. Diamantino, Mato Grosso, Brasil. Diagnosis. Differs from nearly all other species in the genus by its long elytral pilosity combined with the sharply carinate lateral edge of the pronotal lateral depressions. The much less pilose dorsum, especially the nearly glabrous eighth elytral interval will separate D. furtadoi from D. pilosissimus and the much less heavily punctate pronotal disc will separate it from D. carinifer. From its sister species, D. cribrosus, the straight clypeal edge on each side of the clypeal teeth combined with the distinctly anteriorly convergent pronotal lateral edges and less defined elytral striae will set it apart. Description. Male holotype (Fig. 5). Body. Body large, length 15.0 mm, maximum width 8.0 mm; body subrectangular in dorsal view; dorsum narrowly flat. Color. Dorsal surface dark brown to black, glossy, with green metallic sheen; head black along anterior edge of clypeus, metallic green on remaining surface; pronotum with green metallic sheen except for anteromedian carina, on anterior portion of disc and surface adjacent to lateral fossae; elytra with uniform green metallic sheen; ventrum with faint greenish and coppery metallic sheen; pygidium with green metallic sheen; legs with coppery and greenish metallic sheen on femora and tibiae. Head. Clypeus gena arcuate, clypeus straight between clypeogenal junction and lateral emargination of clypeal teeth, anterior portion upturned; clypeal teeth acutely triangular; clypeal median emargination v-shaped, clypeal edge acutely notched on external side of each clypeal tooth, clypeal teeth ventral surface lacking carina, clypeal margin ill-defined, lacking sharp carina posteriorly, clypeal surface with transverse blunt rugulae anteriorly and small setiferous tubercles posteriorly; clypeogenal suture well-defined, bluntly carinate internally; genal surface with small setiferous tubercles, lacking distinct transverse carina, simply convex; clypeofrontal carina rather low, approximately 4 times wider than high, straight in dorsal view, simply carinate, clypeofrontal carina apical edge slightly trilobate in frontal view; eyes large in dorsal view, interocular ratio 4.0. Pronotum. Pronotum transverse in dorsal view, pronotal width/length ratio 1.6; disc of pronotum minutely punctate basally with large confluent setiferous puncture medially changing into dense squamose and setiferous rugulae anteriorly, with an ill-defined shallow longitudinal depression on posterior half; pronotal anterior margin only slightly wider and flat lateral to eye; anterior portion with a tri-sinuous carina, carina produced into a tubercle medially; anterior angles surface finely granulate, similar to lateral margin along posterior edge of anterior margin; lateral fossae oval, bordered laterally by a sharp carina and anteriorly by a blunt tubercle; lateral portions strongly explanate; pronotal basal fossae ill-defined, slightly concave; posterior margin well-defined and crenulate, with several long setae. Elytra. Elytra approximately as long as wide in dorsal view, elytral combined width/length ratio 1.2; elytral base distinctly marginate; elytral striae 1–4 moderately wide basally, narrower and ill-defined on posterior half, evenly impressed throughout, elytral striae 5 similar to 4 on disc, strial punctures fine, well-defined and setiferous, adjacent strial edge feebly encroaching on interval, stria 1 weakly impressed apically, going straight to elytral apical margin; interstriae slightly convex, minutely punctate and with few larger setiferous punctures along striae, surface glossy. Thoracic sterna. Proepisternal carina absent; metasternal median lobe angularly produced anteromedially, ventral ridge well-defined, y-shaped. Legs. Profemur posterior surface slightly but distinctly convex and glabrous internally, posterointernal margin rather thin, uneven, internal edge rather wide, with a contiguous row of setae along anterointernal edge and few scattered long setae on anterior half, remaining surface with irregular ill-defined punctures and glossy. Protibia with four teeth on lateral edge; internal basal angle lobate; anterior surface with long aligned row of setae internally, surface glossy or feebly microsculptured between punctures; posterior surface with some ill-defined irregular punctures externally to median carina, surface glossy between punctures, with a single interrupted setal row along lateral teeth. Mesofemur angularly produced on anterointernal edge apically. Mesotibia rather short, gradually widening toward apex in anterior view; anteroapical edge slightly sinuate in anterior view, anteroapical row of setae complete; apicoanterior edge circularly indented internally; external edge more or less rounded, with several large elongate setiferous punctures. Mesotarsus similar in shape to metatarsus, 3 -segmented, first segment moderately elongate, approximately two times as long as wide at apex. Metafemur internal edge nearly straight and lateral edge arcuate, lacking distinct depressed area anterointernally before apex, apicoposterior edge unmodified, anterior surface with a well-defined sulcus on more than half the length. Metatibia moderately slender, slightly widening toward apex in anterior view, anterior surface with distinct row of setae, surface glossy, metatibial posterior surface flat between longitudinal row of setae and lateral edge, with ill-defined microsculpture. Metatarsus 3 -segmented, first segment moderately elongate, approximately two times as long as wide at apex, with anterointernal carina well defined and almost reaching apical edge. Abdominal sternites. Sternites 3–6 longitudinally flat; sternites 4–6 with 1–3 unaligned rows of setae laterally, narrowly glabrous on segment 4 and with a single row of setae medially on segments 5–6; sternite 7 approximately longitudinally flat medially, shorter than segment 6 along midline; pygidium minutely punctate on disc. Male genitalia (Figs. 48–49). Parameres simply rounded apically in dorsal view; surface smooth, glossy apically. Measurements (1 male). Length: 15.0 mm. Primary type data. Holotype male (CEMT): [BRASIL: MT/ Diamantino/ X. 1984 / E. Furtado]; [WORLD / SCARAB./ DATABASE/ WSD00016761]; [HOLOTYPE / Dendropaemon / furtadoi n.sp. / Génier & Arnaud, 2014]. Material examined. Primary type only. Etymology. Furtadoi, a patronym in honor of Eurides Furtado of Diamantino (Mato Grosso) who was very hospitable during a visit of one of the author (FG) and also the collector of the only known specimen of this species. Natural history. Unknown. Remarks. Female and variation unknown. In addition to the characters mentioned in the diagnosis, this species also differs in having the lateral pronotal fossae bordered anteriorly by a much larger tubercles and the posterior pronotal margin is twice as wide in posterior view as in D. cribrosus. Because a single male specimen of this species is known it is difficult to assess if this is due to the allometric scaling.Published as part of François Génier & Patrick Arnaud, 2016, Dendropaemon Perty, 1830: taxonomy, systematics and phylogeny of the morphologically most derived phanaeine genus (Coleoptera: Scarabaeidae, Scarabaeinae, Phanaeini) in Zootaxa 4099 (1) on pages 14-15, DOI: 10.11646/zootaxa.4099.1.1, http://zenodo.org/record/26827
Dendropaemon (Onthoecus) lydiae Genier & Arnaud, new species
No full text29. <i>Dendropaemon (Onthoecus) lydiae</i> Génier & Arnaud, new species <p>(Figs. 29, 88–89, 124, 159)</p> <p> <b>Type locality</b>. Cameta, Amazones.</p> <p> <b>Diagnosis.</b> The large size, rather thick body combined with the red to green metallic sheen will separate <i>D. lydiae</i> from most other species. It can be separated from <i>D. refulgens</i> by its less convex dorsum and much more robust posterior tibia which is completely covered with irregular sculpturing and punctures. Differs from <i>D. morettoi</i> by the shape of the anteromedian pronotal carina which is subangulate medially in female and is bordering anteriorly a distinct concavity in the male.</p> <p> <b>Description</b>. Male holotype (Fig. 29). <b>Body</b>. Body large, length 18.0 mm, maximum width 10.0 mm; body subrectangular; dorsum convex. <b>Color</b>. Dorsal surface black, glossy, with metallic sheen; head with red metallic sheen on posterior portion of clypeus, genae and frons; pronotum with red metallic sheen, except on anteromedian carina, small irregular area on disc and anterior to lateral fossae; elytra with red metallic sheen, except on humeral and apical umbone; ventrum dark brown to black; pygidium with red metallic sheen; legs black. <b>Head</b>. Clypeus broadly arcuate, anterior portion upturned; clypeal teeth obtusely triangular; clypeal median emargination broadly v-shaped, clypeal edge emarginate on external side of each clypeal tooth, clypeal teeth ventral surface with a fine v-shaped carina, clypeal margin ill-defined, bordered posteriorly by a more or less regular row of punctures, clypeal surface with transverse blunt rugulae; clypeogenal suture well-defined, bluntly carinate internally; genal surface with small and blunt irregular tubercles, lacking distinct transverse carina, concave laterally and convex internally; clypeofrontal carina rather low, approximately 4 times wider than high, slightly arcuate in dorsal view, simply carinate, clypeofrontal carina apical edge straight in frontal view; eyes small in dorsal view, interocular ratio 5.8. <b>Pronotum</b>. Pronotum transverse in dorsal view, pronotal width/length ratio 1.5; disc of pronotum finely punctate basally, punctures changing into fine blunt rugulae anterolaterally, with an ill-defined shallow longitudinal depression on posterior half; pronotal anterior margin slightly wider and concave lateral to eye; anterior portion with a strongly tri-sinuous carina transversally tuberculate medially; anterior angles surface with more or less rough and irregular fine tubercles, similar to lateral margin along posterior edge of anterior margin; lateral fossae simply rounded, concave; lateral portions slightly explanate; pronotal basal fossae well-defined, concave; posterior margin well-defined, lacking crenulation and setae. <b>Elytra</b>. Elytra approximately as long as wide in dorsal view, elytral combined width/length ratio 1.2; elytral base lacking distinct margin, simply convex; elytral striae 1–4 fine and well-defined, evenly impressed throughout, elytral striae 5 similar to 4 on disc, strial punctures minute, adjacent strial edge encroaching on interval, stria 1 well-defined apically, connecting to marginal stria; interstriae slightly convex, minutely punctate throughout, surface glossy. <b>Thoracic sterna</b>. Proepisternal carina reduced, present along coxal insertion only; metasternal median lobe angularly produced anteromedially, ventral ridge welldefined, v-shaped. <b>Legs</b>. Profemur posterior surface slightly but distinctly convex, rather coarsely punctate and glabrous internally, posterointernal margin rather thick, evenly developed, internal edge rather wide, with a contiguous row of setae along anterointernal edge and few scattered long setae on anterior half, remaining surface irregularly punctate. Protibia with four teeth on lateral edge; internal basal angle bluntly lobate; anterior surface with long aligned row of setae internally, surface glossy or feebly microsculptured between punctures; posterior surface with some well-defined punctures externally to median carina, surface between punctures finely and irregularly microsculptured, with a single interrupted setal row along lateral teeth. Mesofemur unmodified on anterointernal edge apically. Mesotibia rather short, gradually widening toward apex in anterior view; anteroapical edge slightly sinuate in anterior view, anteroapical row of setae complete; apicoanterior edge circularly indented internally; external edge more or less rounded, with several large elongate setiferous punctures. Mesotarsus similar in shape to metatarsus, 3-segmented, first segment moderately elongate, approximately two times as long as wide at apex. Metafemur elongate, internal and lateral edges mostly parallel in ventral view, more than twice as long as wide, lacking distinct depressed area anterointernally before apex, apicoposterior edge lobate beyond tibial insertion, surface coarsely microsculptured, anterior surface with a row of irregular punctures, punctures not bordered anteriorly by a sharp and well-define sulcus. Metatibia robust, short, slightly widening toward apex in anterior view, anterior surface completely covered with irregular sculpturing and punctures, metatibial posterior surface concave between longitudinal row of setae and lateral edge, surface dull and irregularly punctate. Metatarsus 3-segmented (Fig. 124), first segment moderately elongate, approximately two times as long as wide at apex, with anterointernal carina ill-defined. <b>Abdominal sternites</b>. Sternites 3–6 longitudinally flat; sternites 4–6 with more than three unaligned row of setae laterally, glabrous medially; sternite 7 approximately longitudinally flat medially, subequal in length to segment 6 along midline; pygidium finely punctate on disc. <b>Male genitalia</b> (Figs. 88–89). Parameres concave before apex; with minute raspy tubercles apically.</p> <p> <b>Measurements</b> (3 males, 7 females). Length: male 17.0–18.0 (17.3±0.6), female 15.0–20.0 (18.3±2.0) mm.</p> <p> <b>Primary type data</b>. Holotype male (MNHN): [Cameta/ Amazones/ M. de Mathan]; Dendrop. refulgens Wth. / det. G. OLSOUFFIEFF] partly handwritten; [WORLD/ SCARAB./ DATABASE/ WSD00016632]; [HOLOTYPE / <i>Dendropaemon</i> / <i>lydiae n.sp.</i> / Génier & Arnaud, 2014] red card.</p> <p> <b>Material examined</b>. <b>BRAZIL</b>: ACRE, Parque Zoobotânico da Universidade Federal do Acre, Rio Branco, (9°57'8''S, 67°52'23''W), ii.1997, coll. F. Z. Vaz de Mello— 1 female (paratype) (CEMT); AMAZONAS, Cametá, (6°10'S, 64°14'W), [no date], coll. M. de Mathan— 1 male (holotype) (MNHN); Ega [=Tefé], (3°22'S, 64°42'W), [no date], coll. [anonymous]— 1 female (paratype) (MNHN); Lg. Galomãnha, Rio Unini, Resex Unini [= Reserva Extrativista Rio Unini], (1°37'S, 62°59'W), 13–28.vii.2004, coll. M.L. Oliveira, L. Aquino & A Silva-Filho— 1 female, 1 male (paratypes) (CEMT); Rio Parauary, (4°36'S, 57°47'W), 15.iii.1937, coll. Zellibor-Hauff— 1 female allotype (CMNC); MATO GROSSO, Municipio Cotriguaçu, (9°51'28''S, 58°24'50''W), v.2011, coll. R.E Vicente— 1 female (paratype) (CEMT); Vale da Solidão, Municipio Diamantino, (14°22'13''S, 56°7'12''W), 31.i.2009, coll. D.C.T. Oliveira— 1 male (paratype) (CEMT); PARÁ, Jacareacanga, (6°13'35''S, 57°46'9''W), xii.1972, coll. M. Alvarenga— 1 female (paratype) (CPFA); RORAIMA, Ilha de Maracá, (3°25'N, 61°40'W), ix.1996, coll. Ribeiro & Vaz-de-Mello— 1 female (paratype) (CEMT).</p> <p> <b>Etymology</b>. <i>Lydiae</i>, a patronym consisting of the Latinized form of the name Lydie. In honor of the late Lydie Arnaud, spouse of the junior author.</p> <p> <b>Natural history</b>. Unknown.</p> <p> <b>Remarks</b>. Females differs by their tri-sinuate anteromedian pronotal carina which is more evenly developed. In male the carina is strongly and transversally tuberculate medially and the carina is much reduced on a short distance on each side of the tubercle.</p> <p>The six known specimens are variable, and some might be recognized as representing distinct species once more material becomes available. However, at this time this variation will be treated as intraspecific. This variation is seen in leg morphology in the following form: in the holotype and the specimen from Roraima the metatibiae and metatarsi are significantly more slender.</p>Published as part of <i>François Génier & Patrick Arnaud, 2016, Dendropaemon Perty, 1830: taxonomy, systematics and phylogeny of the morphologically most derived phanaeine genus (Coleoptera: Scarabaeidae, Scarabaeinae, Phanaeini) in Zootaxa 4099 (1)</i> on pages 59-61, DOI: 10.11646/zootaxa.4099.1.1, <a href="http://zenodo.org/record/268274">http://zenodo.org/record/268274</a>
Ballarat - St Arnaud Region Gravity (P198344), gravity point data
No full textMaintenance and Update Frequency: notPlannedStatement: This Ballarat - St Arnaud Region Gravity (P198344), gravity point data contains ground gravity point data for the Ballarat - St Arnaud Region Gravity (P198344) survey acquired for Department of Minerals and Energy (Victoria). This dataset contains a total of 1112 point data values. The data is located in VIC and were acquired in 1983. The point located data were collected in traverses layout at an average station spacing of 50 metres.
Terrain corrections were calculated using the INTREPID Geophysics software package. The processed data are checked by GA geophysicists using standard methods for assessing quality to ensure that the final data are fit-for-purpose.
All data are provided in EPSG:4283 coordinates, Australian Height Datum (AHD) and gravity datum of AAGD07. The units are degrees, meters, and micrometres per second squared, respectively.
Reference:
Intrepid Geophysics, http://www.intrepid-geophysics.com.Gravity data measures small changes in gravity due to changes in the density of rocks beneath the Earth's surface. The data collected are processed via standard methods to ensure the response recorded is that due only to the rocks in the ground. The results produce datasets that can be interpreted to reveal the geological structure of the sub-surface. The processed data is checked for quality by GA geophysicists to ensure that the final data released by GA are fit-for-purpose.<br/> This Ballarat - St Arnaud Region Gravity (P198344) contains a total of 1112 point data values acquired at a spacing of 50 metres. The data is located in VIC and were acquired in 1983, under project No. 198344 for Department of Minerals and Energy (Victoria)
St Arnaud detailed traverses, gravity (P198942), gravity point data
No full textMaintenance and Update Frequency: notPlannedStatement: This St Arnaud detailed traverses, gravity (P198942), gravity point data contains ground gravity point data for the St Arnaud detailed traverses, gravity (P198942) survey acquired for Department of Minerals and Energy (Victoria). This dataset contains a total of 925 point data values. The data is located in VIC and were acquired in 1989. The point located data were collected in traverses layout at an average station spacing of 100 metres.
Terrain corrections were calculated using the INTREPID Geophysics software package. The processed data are checked by GA geophysicists using standard methods for assessing quality to ensure that the final data are fit-for-purpose.
All data are provided in EPSG:4283 coordinates, Australian Height Datum (AHD) and gravity datum of AAGD07. The units are degrees, meters, and micrometres per second squared, respectively.
Reference:
Intrepid Geophysics, http://www.intrepid-geophysics.com.Gravity data measures small changes in gravity due to changes in the density of rocks beneath the Earth's surface. The data collected are processed via standard methods to ensure the response recorded is that due only to the rocks in the ground. The results produce datasets that can be interpreted to reveal the geological structure of the sub-surface. The processed data is checked for quality by GA geophysicists to ensure that the final data released by GA are fit-for-purpose.<br/> This St Arnaud detailed traverses, gravity (P198942) contains a total of 925 point data values acquired at a spacing of 100 metres. The data is located in VIC and were acquired in 1989, under project No. 198942 for Department of Minerals and Energy (Victoria)
New insights in viral infections after kidney transplantation : focus on cytomegalovirus, norovirus and BK virus
No full textThis work aims to provide new insights in three frequent viral infections after kidney transplantation (KT). We show that the de novo use of an mTOR inhibitor based immunosuppressive regimen is associated with a decreased incidence of cytomegalovirus disease after KT compared to the standard of care. We demonstrate that Norovirus is the leading cause of infectious diarrhea after KT and that pre-existing conditions determine the primary functional long-term consequences after post-KT diarrhea. We show that an aggressive minimization of immunosuppression to treat sustained BK virus (BKV) viremia does not improve long-term graft outcome compared to a more gradual reduction, but is associated with an increased risk of developing de novo donor specific antibodies. Finally, we show that urinary tract infection, BKV viremia and BKV nephropathy increase the urinary levels of CXCL9 and CXCL10. These confounding factors must be addressed before urinary CXCL9 and CXCL10 can be used as noninvasive diagnostic markers of acute rejection.(MED - Sciences médicales) -- UCL, 202
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