20 research outputs found
Hydraulic and thermal impact modelling at the scale of the geothermal heating doublet in the Paris Basin, France
13 pagesInternational audienceThe Paris Basin is extensively developed for the geothermal district heating (GDH) of approximately 150 000 dwellings. As of late 2010, thirty four GDH systems apply the doublet concept in the Paris suburban area and mine the heat of the Dogger reservoir, a limestone formation of Mid-Jurassic age at depths ranging from 1500 to 2000 m. As the brine is fully reinjected, cold water bodies progressively invade the reservoir around injector wells inducing both thermal and hydraulic interactions at the doublet scale. The premature production well cooling and the sustainable development of the resource highlight two critical parameters, the thermal breakthrough time (tB) and the extent of the cooled fluid bubble(S) respectively. First, a set of benchtest simulations was launched to compare the sensitivities of tB and S parameters to selected reservoir conceptual model typologies. These simulations were applied on a GDH doublet undergoing a suspected thermal breakthrough. Five reservoir modelling teams validated their “in house” simulations by (i) checking an analytical (Gringarten-Sauty, 1979) solution, and (ii) testing three candidate reservoir structures on the doublet considered remotely located (i.e. not interfering with nearby exploitations) for a first step. The outcome resulted in a rewarding insight into the variability of simulation outputs. An additional segment will enable the actors to compare their modelling expertise on the same doublet considered in interaction with the other GDH operations located in its environment. Second, BRGM carried out a survey towards various rehabilitation schemes (a new doublet or a triplet) and their contribution toward sustainability standards. From a hypothetical, twenty five year life, doublet simulation, an initial hydraulic/temperature field was derived. Then, several new well locations were simulated and isotherms, alongside production well cooling kinetics, compared accordingly. A two-stage rehabilitation scheme, i.e. triplet then a new doublet, seems to reconcile the resource longevity and the economic demand. Further work is required to compare the different designs with a method integrating both the impact of the geothermal exploitation on the resource and the lifetime of the exploitation in a single mathematical factor
How digital/physical toolkits integrated in consumer products empower users to self-design their uses: A theoretical framework for use generation
International audienceMaking use of the modern design theories like C-K theory, we propose, in this paper to develop a theoretical framework that permit to understand thoroughly the design activities presently carried by digital/physical toolkits. Then, we apply it on two sets of design tools embedded in the ADIDAS One running shoes and the EMOTIO software. Relying on the findings, we consider managerial implications for firms attempting to integrate digital/physical toolkits into their products at low risk
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A Versatile Class of Cell Surface Directional Motors Gives Rise to Gliding Motility and Sporulation in <i>Myxococcus xanthus</i>
<div><p>Eukaryotic cells utilize an arsenal of processive transport systems to deliver macromolecules to specific subcellular sites. In prokaryotes, such transport mechanisms have only been shown to mediate gliding motility, a form of microbial surface translocation. Here, we show that the motility function of the <i>Myxococcus xanthus</i> Agl-Glt machinery results from the recent specialization of a versatile class of bacterial transporters. Specifically, we demonstrate that the Agl motility motor is modular and dissociates from the rest of the gliding machinery (the Glt complex) to bind the newly expressed Nfs complex, a close Glt paralogue, during sporulation. Following this association, the Agl system transports Nfs proteins directionally around the spore surface. Since the main spore coat polymer is secreted at discrete sites around the spore surface, its transport by Agl-Nfs ensures its distribution around the spore. Thus, the Agl-Glt/Nfs machineries may constitute a novel class of directional bacterial surface transporters that can be diversified to specific tasks depending on the cognate cargo and machinery-specific accessories.</p></div
The AglRQS motor rotates the Nfs complex around the spore surface.
<p>(A) NfsD-mCherry moves in orbital trajectories around the surface of 4-h-old spores. Observation of dynamic NfsD-mCherry clusters at different focal planes, middle (i) and top (ii) sections of a spore. For each time lapse, trajectories were computed by summing the different time points in consecutive frames and shown in “fire” colors to the right. Scale bar = 1 µm. (B) Instantaneous speed histogram of tracked NfsD-mCherry clusters over time in WT spores and in the different mutants. (C) Distance from the origin of NfsD-mCherry clusters in WT spores and different mutants. (D) Mean square displacement (MSD) of NfsD-mCherry clusters over time in WT spores and in the different mutants. (E) NfsD-mCherry rotation is abolished by CCCP. (F) Rotation of NfsD-mCherry requires AglQ. (G) Movement of NfsD-mCherry in the <i>exoA</i> mutant.</p
Phase specific interactions between Agl and Glt/Nfs promote motility or sporulation.
<p>The Agl motor (yellow), a three protein MotAB-like channel harvests the pmf and interacts either with Glt (orange) or Nfs (light blue) to transport slime (red) or the Exo polymer (blue) depending on the growth phase. Both Glt and Nfs are shown spanning the entire cell surface because they both contain predicted inner and outer membrane proteins. The connection between the Glt complex and the MreB cytoskeleton is shown in black. IM, inner membrane; OM, outer membrane; the PG is not represented because its connection with Glt is unresolved and spores apparently lack PG. In both cases, the transport mechanism remains to be elucidated. In motile cells, the current model proposes that Glt proteins and attached slime (orange-red dots circled in black) traffic along a closed loop helix (grey) and generate propulsion as they interact with the underlying substratum. At the lagging cell pole, the motility complexes become de-activated (orange circles), potentially by removing their connection to slime, which thus becomes deposited on the substrate. In spores, Nfs proteins may associate with Exo polymers following their secretion by the Exo export machinery (green). Distributed Agl motor units could move Exo-linked Nfs complexes from one motor to the next, guided by the Exo polymer.</p
The Agl interacts with Nfs to promote spore coat assembly.
<p>(A) Sporulation titers after heat and sonication counted by DAPI staining in various strains. Corresponding DAPI-staining images are shown. Note the 10<sup>2</sup> spores/ml detection limit of the assay. Scale bar = 5 µm. (B) Thin sections of myxospores observed by transmission electron microscopy. WT, <i>aglQ</i>, <i>nfsD</i>, and <i>exoA</i> strains were observed 24 h after the induction of sporulation. Arrows point to spore coat material that detaches from the surface of sporulating cells in <i>aglQ</i> and <i>nfsD</i> mutants. Scale bars = 0.1 µm. (C) GSLI-FITC staining of the spore coat material. WT, <i>aglQ</i>, <i>nfsD</i>, and <i>exoA</i> strains were observed 4 h after the induction of sporulation. Scale bar = 1 µm. (D) AglR interacts with GltG and NfsG in a bacterial two hybrid assay.</p
The Nfs complex transports the spore coat polymer at the surface of the developing spores.
<p>(A) Snapshots of two beads moving on spore surface. Two beads are attached to a WT spore; another bead is stuck to the bottom of flow chamber providing a fixed reference. The bead in focus is tracked using the low-powered laser as in the Methods section. Both beads move independently at different times (arrows). Scale bar = 1 µm. (B) Speed histogram of tracked polystyrene beads at the spore surface: WT spores, <i>exoA</i> spores, <i>exoA</i> spores in the presence of CCCP (10 µM), and <i>exoA aglQ</i> spores. WT spores in the presence of CCCP and <i>aglQ</i> spores yielded similar results as the <i>exoA</i> CCCP and <i>exoA aqlQ</i> spores and are therefore not represented for improved clarity. (C) Dynamics of NfsD-mCherry and GSLI-FITC on a sporulating cell. A time lapse of a 4-h-old sporulating cell is shown with its corresponding kymograph. The white arrow points to the dissociation of the red and green signals. Scale bar = 1 µm.</p
The Agl-Nfs machinery is sporulation-specific.
<p>(A) <i>nfs</i> and <i>glt</i> genes are differentially regulated during sporulation. Expression of NfsD, GltD, and AglQ as inferred from the measurements of relative single cell mCherry/sfGFP fluorescence intensities over time after sporulation induction. Shown are the average fluorescence intensity ratios (measured intensity/maximum intensity) of 25 cells for each time points. (B) Time course of AglQ-sfGFP (left), GltD-mCherry (middle panel), and NfsD-mCherry (right panel) dynamics during sporulation.</p
La grotte du Taillis des Coteaux à Antigny (Vienne) : intérêts d'une séquence originale à la structuration des premiers temps du Magdalénien
The cave of Le Taillis des Coteaux, Antigny (Vienne, France) was discovered in 1998 and excavations began in 2000. The preserved stratigraphy is exceptional as it represents almost the whole Upper Palaeolithic, from the Aurignacian to the Middle Magdalenian, through the Gravettian, Badegoulian and Lower Magdalenian. The latter provides an archaeological assemblage with original typo-technological features evoking the Magdalenian. However, its dating to around 17 000 BP is close to the Badegoulian. The main characteristics of the lithic industry are described, particularly the bladelet production. Its relationship with the Lower Magdalenian is also discussed.La grotte du Taillis des Coteaux à Antigny (Vienne), découverte en 1998 et fouillée depuis 2000, conserve une stratigraphie exceptionnelle comprenant la quasi-totalité du Paléolithique supérieur, depuis l’Aurignacien jusqu’au Magdalénien moyen, en passant par le Gravettien, le Badegoulien et le Magdalénien inférieur. Ce dernier livre un assemblage archéologique aux caractères typotechnologiques originaux, riche en microlamelles à dos, évoquant le Magdalénien, mais dont les datations autour de 17000 BP se rapprochent plutôt du Badegoulien. Cela conduit les auteurs à se demander si le fort investissement dans la production lamellaire serait une spécificité magdalénienne et, par conséquent, un de ses caractères d’identification. En d’autres termes, ces industries à microlamelles à dos portent-elles déjà les caractères du Magdalénien?Soler Ludovic, Schmiti Aurore, Rambaud Delphine, Mistrot Vincent, Liolios Despina, Liard Morgane, Le Brun-Ricalens Foni, Laroulandie Véronique, Houmard Claire, Henry-Gambier Dominique, Guérin Samuel, Griggo Christophe, Berthet Anne-Laure, Langlais Mathieu, Gabilleau Joël, Brou Laurent, Primault Jérôme, Taborin Yvette, Vissac Carole. La grotte du Taillis des Coteaux à Antigny (Vienne) : intérêts d'une séquence originale à la structuration des premiers temps du Magdalénien. In: Bulletin de la Société préhistorique française, tome 104, n°4, 2007. pp. 743-758