12 research outputs found

    MICROSPRAY SIMULATION OF DENSE GAS DISPERSION IN COMPLEX TERRAIN

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    An extended validation of the new Lagrangian particle model MicroSpray version for dense gas simulation is proposed. MicroSpray simulates the dense gas dispersion in situations characterized by the presence of buildings, other obstacles, complex terrain, and possible occurrence of low wind speed conditions. Its performances are compared to a chlorine railway accident (Macdona), to a field experiment (Kit Fox) and to an atmospheric CFD model

    Effects of in vitro contamination by Brucella Abortus on mice and cows embryos

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    On a cultivĂ© in vitro des embryons de souris et de vache, Ă  zone pellucide intacte, dans des milieux contenant 101 Ă  105 brucella par mi pour tester la viabilitĂ© et les risques de contamination de ces embryons aprĂšs contact prolongĂ© de 24 h et 48 h. Il en ressort que : — pour de faibles concentrations en brucella (101 Ă  102 b/ml), la viabilitĂ© des embryons est peu modifiĂ©e par rapport aux tĂ©moins ; — dans nos conditions expĂ©rimentales, aucun embryon n’a Ă©tĂ© conta minĂ© aprĂšs 48 heures de contact quelle que soit la concentration en brucella et en particulier celles-ci ne sont pas adsorbĂ©es sur la zone pellucide ; — dix lavages successifs des embryons contaminĂ©s, mĂȘme Ă  des concentrations elevĂ©es sont suffisants pour Ă©liminer les brucella du milieu de transfert (effet dilution) Ă  condition de respecter le protocole proposĂ©. En conclusion, il paraĂźt possible d'utiliser des vaches brucelliques de haute valeur gĂ©nĂ©tique comme donneuses d’embryons, sans risque de transmission de cette maladie aux receveuses et aux futurs produits.In vitro cultures of mice (as a model) and cows embryos with intact zona pellucida have been performed in media containing 101 to 105 brucella per ml. This was aimed at evaluating both viability and risks of contamination of these embryos after 24 or 48 h of such cultures. It was found : (1) with low concentrations of brucella (101 - 10- b./ml, embryo viability was not affected when compared to that of controls ; (2) in our experimental conditions, no embryo was found to be contaminated after 48 h whatever was the brucella concentration in the culture medium ; in particular, brucella were not adsorbed on the zona pellucida ; (3) ten consecutive washings of the embryos initially inserted in a brucella-infected medium (at any of the concentrations studied) are definitely sufficient to eliminate all brucella from the transfer medium under strict conditions defined in the present paper. In conclusion, embryos from cows with high breeding values but unfortunately affected with brucellosis may be transferred with no risk of contamination neither to the embryo nor to the recipient

    New lagrangian approach for wet plume modelling

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    International audienceA new version of the lagrangian dispersion modelling system Micro-SWIFT-SPRAY (MSS developed by ARIA Technologies and ARIANET) has been developed in order to allow simulation of wet plume, microorganisms, insecticide or pesticide dispersion. For all these applications, it is necessary to take into account both gas and liquid phase evolution including mass and heat transfer. In the particular case of microorganisms distinct behaviors potentially occur when transported by the liquid and/or the gas phase. Following the MSS lagrangian approach, it is easy to define a mass quantity of vapor and a large number of droplets of the same diameter by a virtual particle. Hence a spectrum of different size of droplets can be model using several virtual particles. The development of the new module consists of modelling the physical phenomenon of evaporation and condensation inside a wet plume taking into account temperature and humidity of ambient atmosphere. Microphysics of droplet is solved using the classical laws of evaporation/condensation processes in the surrounding atmosphere. The calculated evaporation rate allows to estimate the diameter evolution and the temperature inside the droplet. The difficulty consists in characterizing the surrounding atmosphere. The interaction between droplets and ambient humidity has been performed on an eulerian frame. Two methods of two way coupling have been tested on academic cases (0D). The proposed paper will present the two approaches and the obtained results

    Acceleration of simulations by application of a kernel method in a high-resolution Lagrangian Particle Dispersion model.

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    The role of microscale atmospheric dispersion modelling is becoming increasingly important in air quality assessment, especially in residential areas, for regulatory purposes and to project pollution control strategies. Consequently, the use of these models in long-term studies and forecasting systems is growing. However, this modelling can be challenging because of the amount of time and CPU required for the simulations, especially if the computational domain has a significant extension. This article describes the application of a concentration calculation methodology to reduce the computational time needed by microscale Lagrangian Particle Dispersion Models (LPDMs). These models normally estimate the concentration with the box counting method: a 3D mesh is set, and the density is computed counting particles in each box. An alternative method based on the use of the statistical technique of kernel density estimation is proposed to determine the concentration from the particles’ position. The kernel method allows for a reduction of computational particles emitted during the simulation, guaranteeing a similar accuracy to that of box counting method. It enables therefore to optimize the overall simulation time and the required CPUs in order to improve time and cost, enhancing the efficiency of models and widening their application fields. The use of the kernel method to perform high-resolution simulations took the first steps with an application inside the LPDM of PMSS (Parallel-Micro-SWIFT-SPRAY) system to evaluate road traffic gases emissions in urban areas, enabling an 80% simulation time reduction. In this article, additional features of this method are developed within the Micro-SPRAY model and validated against two new test cases. The test cases consider microscale simulations of industrial sources emitting gases and particles, evaluated both inside a domain divided in tiles and inside a nested domains configuration. The existing kernel method is enhanced in order to estimate the pollutant concentrations of point sources and to compute also the corresponding deposition at building-resolving scale and in nested domains with different horizontal resolution

    Effets de la contamination expérimentale in vitro des embryons de souris et de brebis par Campylobacter fetus

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    Effects of Campylobacter fetus in vitro experimental infection of mice and ewes embryos. A total of 350 ZP-I, days 3-5 mice embryos were collected and subdivided as follows : 184 were exposed to C. fetus ss fetus compared to 46 controls (non contaminated) and 182 exposed to C. fetus ss venerealis compared to 48 controls. In addition, 164 ZP-I, day 6 sheep embryos were collected and contaminated with C. fetus ss fetus compared to 51 control embryos. The mice embryos were submitted for 48 hours at 37°C to a range of 0.01-100 IDso and the sheep embryos to a range of 0.1-100 ID50. After 48 hours, the non-degenerated embryos were washed, homogeneized and then cultured simultaneously to the washing fluids for search of Campylobacter fetus. After 48 hours, a dose-effect on the survival rate of the embryos (p < 0.001) and a duration-effect (p < 0.01) of the contamination are shown both for mice and sheep embryos for the two species of Campylobacter fetus. No Campylobacter fetus either in mice or sheep were isolated in the last washing mediums nor in the homogeneized embryos.Un ensemble de 460 embryons de souris de 3 Ă  5 jours, Ă  zone pellucide intacte, ont Ă©tĂ© collectĂ©s et exposĂ©s Ă  une contamination expĂ©rimentale in vitro par C. fetus ss fetus (n = 184, 1 lot tĂ©moin = 46 embryons) et par C. fetus ss venerealis (n = 182, 1 lot tĂ©moin = 48 embryons). Semblablement, 164 embryons de brebis ont Ă©tĂ© parallĂšlement exposĂ©s dans les mĂȘmes conditions Ă  C. fetus ss fetus, et SI embryons ont servi de tĂ©moins. Les embryons ont Ă©tĂ© exposĂ©s pendant 48 heures Ă  37 °C, Ă  des doses variant entre 0,01 et 100 DIES50 pour les embryons de souris et entre 0,1 et 100 DIES50 pour les embryons de brebis. AprĂšs l’épreuve infectante, les embryons vivants ont Ă©tĂ© lavĂ©s, broyĂ©s et mis en culture, ainsi que les liquides de lavage, en vue de la recherche de C. fetus. AprĂšs 48 heures d’incubation, on constate un effet de la durĂ©e de l’énreuve infectante (p < 0.01) et un effet de la dose (p < 0.001) sur la survie embryonnaire pour tous les embryons et pour les deux espĂšces bactĂ©riennes testĂ©es. AprĂšs lavage et broyage, aucun embryon n’était contaminĂ© par Campylobacter fetus.GuĂ©rin Bernard, Builly J. P., Humblot P., Nibart M., Thibier Michel. Effets de la contamination expĂ©rimentale in vitro des embryons de souris et de brebis par Campylobacter fetus. In: Bulletin de l'AcadĂ©mie VĂ©tĂ©rinaire de France tome 141 n°1, 1988. pp. 63-78
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