213 research outputs found

    Tank-treading of microcapsules in shear flow

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    International audienceWe investigated experimentally the deformation of soft microcapsules and the dynamics of their membrane in simple shear flows. Firstly, the tank-treading motion, i.e. the rotation of the membrane, was visualized and quantified by tracking particles included in the membrane by a new protocol. The period of membrane rotation increased quadratically with the extension of the large axis. The tracking of the distance between two close micro-particles showed membrane contraction at the tips and stretching on the sides, a specific property of soft particles such as capsules. Present experimental results are discussed in regard to previous numerical simulations. This analysis showed that the variation of the tank-treading period with the Taylor parameter (deformation) cannot be explained by purely elastic membrane models. It suggests a strong effect of membrane viscosity whose order of magnitude is determined. Secondly, two distinct shapes of sheared microcapsules were observed. For moderate deformations, the shape was a steady ellipsoid in the shear plane. For larger deformations, the capsule became asymmetric and presented a S-like shape. When the viscous shear stress increased by three orders of magnitude, the small axis decreased by 70 % whereas the large axis increased by 100% before any break-up. The inclination angle decreased from 40 ‱ to 8 ‱ , almost aligned with the flow direction as expected by theory/numerics on capsules and experiments/theory/numerics on drops and vesicles. Whatever the microcapsule size and the concentration of proteins, the characteristic lengths of the shape, the Taylor parameter and the inclination angle satisfy master curves versus the longest axis or the normalized shear stress or the capillary number in agreement with theory for non negligible membrane viscosity in the regime of moderate deformations. Finally, we observed that very small deviation from sphericity gave rise to swinging motion, i.e. shape oscillations, in the small deformation regime. In conclusion, this study of tank-treading motion supports the role of membrane viscosity on the dynamics of microcapsules in shear flow by both independent methods which compare experimental data with numerical results in the regime of large deformations and with the theory in the regime of moderate deformations

    Ecological niches of open ocean phytoplankton taxa:Niches of open ocean phytoplankton

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    International audienceWe characterize the realized ecological niches of 133 phytoplankton taxa in the open ocean based on observations from the MAREDAT initiative and a statistical species distribution model (MaxEnt). The models find that the physical conditions (mixed layer depth, temperature, light) govern large-scale patterns in phyto-plankton biogeography over nutrient availability. Strongest differences in the realized niche centers were found between diatoms and coccolithophores. Diatoms (87 species) occur in habitats with significantly lower temperatures, light intensity and salinity, with deeper mixed layers, and with higher nitrate and silicate concentrations than coccolithophores (40 species). However, we could not statistically separate the realized niches of coccolithophores from those of diazotrophs (two genera) and picophytoplankton (two genera). Phaeocystis (two species) niches only clearly differed from diatom niches for temperature. While the realized niches of diatoms cover the majority of niche space, the niches of picophytoplankton and coccolithophores spread across an intermediate fraction and diazotroph and colonial Phaeocystis niches only occur within a relatively confined range of environmental conditions in the open ocean. Our estimates of the realized niches roughly match the predictions of Reynolds' C-S-R model for the global ocean, namely that taxa classified as nutrient stress tolerant have niches at lower nutrient and higher irradiance conditions than light stress tolerant taxa. Yet, there is considerable within-class variability in niche centers, and many taxa occupy broad niches, suggesting that more complex approaches may be necessary to capture all aspects of phytoplankton ecology

    Synoptic-to-planetary scale wind variability enhances phytoplankton biomass at ocean fronts

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    In nutrient-limited conditions, phytoplankton growth at fronts is enhanced by winds, which drive upward nutrient fluxes via enhanced turbulent mixing and upwelling. Hence, depth-integrated phytoplankton biomass can be 10 times greater at isolated fronts. Using theory and two-dimensional simulations with a coupled physical-biogeochemical ocean model, this paper builds conceptual understanding of the physical processes driving upward nutrient fluxes at fronts forced by unsteady winds with timescales of 4–16 days. The largest vertical nutrient fluxes occur when the surface mixing layer penetrates the nutricline, which fuels phytoplankton in the mixed layer. At a front, mixed layer deepening depends on the magnitude and direction of the wind stress, cross-front variations in buoyancy and velocity at the surface, and potential vorticity at the base of the mixed layer, which itself depends on past wind events. Consequently, mixing layers are deeper and more intermittent in time at fronts than outside fronts. Moreover, mixing can decouple in time from the wind stress, even without other sources of physical variability. Wind-driven upwelling also enhances depth-integrated phytoplankton biomass at fronts; when the mixed layer remains shallower than the nutricline, this results in enhanced subsurface phytoplankton. Oscillatory along-front winds induce both oscillatory and mean upwelling. The mean effect of oscillatory vertical motion is to transiently increase subsurface phytoplankton over days to weeks, whereas slower mean upwelling sustains this increase over weeks to months. Taken together, these results emphasize that wind-driven phytoplankton growth is both spatially and temporally intermittent and depends on a diverse combination of physical processes.DBW was supported by the National Science Foundation postdoctoral research fellowship program, award number 1421125. J.R.T. was supported by the Natural Environment Research Council, award NE/J010472/1

    Chirality scenario of the spin-glass ordering

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    Detailed account is given of the chirality scenario of experimental spin-glass transitions. In this scenario, the spin glass order of weakly anisotropic Heisenberg-like spin-glass magnets including canonical spin glasses are essentially chirality driven. Recent numerical and experimental results are discussed in conjunction with this scenario.Comment: Submitted to J. Phys. Soc. Japan "Special Issue on Frustration

    Functionals of the Brownian motion, localization and metric graphs

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    We review several results related to the problem of a quantum particle in a random environment. In an introductory part, we recall how several functionals of the Brownian motion arise in the study of electronic transport in weakly disordered metals (weak localization). Two aspects of the physics of the one-dimensional strong localization are reviewed : some properties of the scattering by a random potential (time delay distribution) and a study of the spectrum of a random potential on a bounded domain (the extreme value statistics of the eigenvalues). Then we mention several results concerning the diffusion on graphs, and more generally the spectral properties of the Schr\"odinger operator on graphs. The interest of spectral determinants as generating functions characterizing the diffusion on graphs is illustrated. Finally, we consider a two-dimensional model of a charged particle coupled to the random magnetic field due to magnetic vortices. We recall the connection between spectral properties of this model and winding functionals of the planar Brownian motion.Comment: Review article. 50 pages, 21 eps figures. Version 2: section 5.5 and conclusion added. Several references adde

    Buber, educational technology, and the expansion of dialogic space

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    Buber’s distinction between the ‘I-It’ mode and the ‘I-Thou’ mode is seminal for dialogic education. While Buber introduces the idea of dialogic space, an idea which has proved useful for the analysis of dialogic education with technology, his account fails to engage adequately with the role of technology. This paper offers an introduction to the significance of the I-It/I-Thou duality of technology in relation to opening dialogic space. This is followed by a short schematic history of educational technology which reveals the role technology plays, not only in opening dialogic space, but also in expanding dialogic space. The expansion of dialogic space is an expansion of what it means to be ‘us’ as dialogic engagement facilitates the incorporation, into our shared sense of identity, of aspects of reality that are initially experienced as alien or ‘other’. Augmenting Buber with an alternative understanding of dialogic space enables us to see how dialogue mediated by technology, as well as dialogue with monologised fragments of technology (robots), can, through education, lead to an expansion of what it means to be human

    Contribution of NFP LysM Domains to the Recognition of Nod Factors during the Medicago truncatula/Sinorhizobium meliloti Symbiosis

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    The root nodule nitrogen fixing symbiosis between legume plants and soil bacteria called rhizobia is of great agronomical and ecological interest since it provides the plant with fixed atmospheric nitrogen. The establishment of this symbiosis is mediated by the recognition by the host plant of lipo-chitooligosaccharides called Nod Factors (NFs), produced by the rhizobia. This recognition is highly specific, as precise NF structures are required depending on the host plant. Here, we study the importance of different LysM domains of a LysM-Receptor Like Kinase (LysM-RLK) from Medicago truncatula called Nod factor perception (NFP) in the recognition of different substitutions of NFs produced by its symbiont Sinorhizobium meliloti. These substitutions are a sulphate group at the reducing end, which is essential for host specificity, and a specific acyl chain at the non-reducing end, that is critical for the infection process. The NFP extracellular domain (ECD) contains 3 LysM domains that are predicted to bind NFs. By swapping the whole ECD or individual LysM domains of NFP for those of its orthologous gene from pea, SYM10 (a legume plant that interacts with another strain of rhizobium producing NFs with different substitutions), we showed that NFP is not directly responsible for specific recognition of the sulphate substitution of S. meliloti NFs, but probably interacts with the acyl substitution. Moreover, we have demonstrated the importance of the NFP LysM2 domain for rhizobial infection and we have pinpointed the importance of a single leucine residue of LysM2 in that step of the symbiosis. Together, our data put into new perspective the recognition of NFs in the different steps of symbiosis in M. truncatula, emphasising the probable existence of a missing component for early NF recognition and reinforcing the important role of NFP for NF recognition during rhizobial infection

    Seasonal variation in month of diagnosis in children with type 1 diabetes registered in 23 European centers during 1989-2008: little short-term influence of sunshine hours or average temperature

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    Background: The month of diagnosis in childhood type 1 diabetes shows seasonal variation. Objective: We describe the pattern and investigate if year-to-year irregularities are associated with meteorological factors using data from 50 000 children diagnosed under the age of 15 yr in 23 population-based European registries during 1989–2008. Methods: Tests for seasonal variation in monthly counts aggregated over the 20 yr period were performed. Time series regression was used to investigate if sunshine hour and average temperature data were predictive of the 240 monthly diagnosis counts after taking account of seasonality and long term trends. Results: Significant sinusoidal pattern was evident in all but two small centers with peaks in November to February and relative amplitudes ranging from ±11 to ±38% (median ±17%). However, most centers showed significant departures from a sinusoidal pattern. Pooling results over centers, there was significant seasonal variation in each age-group at diagnosis, with least seasonal variation in those under 5 yr. Boys showed greater seasonal variation than girls, particularly those aged 10–14 yr. There were no differences in seasonal pattern between four 5-yr sub-periods. Departures from the sinusoidal trend in monthly diagnoses in the period were significantly associated with deviations from the norm in average temperature (0.8% reduction in diagnoses per 1 °C excess) but not with sunshine hours. Conclusions: Seasonality was consistently apparent throughout the period in all age-groups and both sexes, but girls and the under 5 s showed less marked variation. Neither sunshine hour nor average temperature data contributed in any substantial way to explaining departures from the sinusoidal pattern
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