481 research outputs found
Mean first-passage time of surface-mediated diffusion in spherical domains
We present an exact calculation of the mean first-passage time to a target on
the surface of a 2D or 3D spherical domain, for a molecule alternating phases
of surface diffusion on the domain boundary and phases of bulk diffusion. The
presented approach is based on an integral equation which can be solved
analytically. Numerically validated approximation schemes, which provide more
tractable expressions of the mean first-passage time are also proposed. In the
framework of this minimal model of surface-mediated reactions, we show
analytically that the mean reaction time can be minimized as a function of the
desorption rate from the surface.Comment: to appear in J. Stat. Phy
Kinetics of active surface-mediated diffusion in spherically symmetric domains
We present an exact calculation of the mean first-passage time to a target on
the surface of a 2D or 3D spherical domain, for a molecule alternating phases
of surface diffusion on the domain boundary and phases of bulk diffusion. We
generalize the results of [J. Stat. Phys. {\bf 142}, 657 (2011)] and consider a
biased diffusion in a general annulus with an arbitrary number of regularly
spaced targets on a partially reflecting surface. The presented approach is
based on an integral equation which can be solved analytically. Numerically
validated approximation schemes, which provide more tractable expressions of
the mean first-passage time are also proposed. In the framework of this minimal
model of surface-mediated reactions, we show analytically that the mean
reaction time can be minimized as a function of the desorption rate from the
surface.Comment: Published online in J. Stat. Phy
Occupation times of random walks in confined geometries: From random trap model to diffusion limited reactions
We consider a random walk in confined geometry, starting from a site and
eventually reaching a target site. We calculate analytically the distribution
of the occupation time on a third site, before reaching the target site. The
obtained distribution is exact, and completely explicit in the case or
parallepipedic confining domains. We discuss implications of these results in
two different fields: The mean first passage time for the random trap model is
computed in dimensions greater than 1, and is shown to display a non-trivial
dependence with the source and target positions ; The probability of reaction
with a given imperfect center before being trapped by another one is also
explicitly calculated, revealing a complex dependence both in geometrical and
chemical parameters
Mesoscale texture of cement hydrates
Strength and other mechanical properties of cement and concrete rely upon the formation of calcium-silicate-hydrates (C-S-H) during cement hydration. Controlling structure and properties of the C-S-H phase is a challenge, due to the complexity of this hydration product and of the mechanisms that drive its precipitation from the ionic solution upon dissolution of cement grains in water. Departing from traditional models mostly focused on length scales above the micrometer, recent research addressed the molecular structure of C-S-H. However, small-angle neutron scattering, electron- microscopy imaging, and nanoindentation experiments suggest that its mesoscale organization, extending over hundreds of nanometers, may be more important. Here we unveil the C-S-H mesoscale texture, a crucial step to connect the fundamental scales to the macroscale of engineering properties. We use simulations that combine information of the nanoscale building units of C-S-H and their effective interactions, obtained from atomistic simulations and experiments, into a statistical physics framework for aggregating nanoparticles. We compute small-angle scattering intensities, pore size distributions, specific surface area, local densities, indentation modulus, and hardness of the material, providing quantitative understanding of different experimental investigations. Our results provide insight into how the heterogeneities developed during the early stages of hydration persist in the structure of C-S-H and impact the mechanical performance of the hardened cement paste. Unraveling such links in cement hydrates can be groundbreaking and controlling them can be the key to smarter mix designs of cementitious materials
Irreversible Aging Dynamics and Generic Phase Behavior of Aqueous Suspensions of Laponite
In this work we study the aging behavior of aqueous suspension of Laponite
having 2.8 weight % concentration using rheological tools. At various salt
concentration all the samples demonstrate orientational order when observed
using crossed polarizers. In rheological experiments we observe inherent
irreversibility in the aging dynamics which forces the system not to rejuvenate
to the same state in the shear melting experiment carried out at a later date
since preparation. The extensive rheological experiments carried out as a
function of time elapsed since preparation demonstrate the self similar trend
in the aging behavior irrespective of the concentration of salt. We observe
that the exploration of the low energy states as a function of aging time is
only kinetically affected by the presence of salt. We estimate that the energy
barrier to attain the low energy states decreases linearly with increase in the
concentration of salt. The observed superposition of all the elapsed time and
the salt concentration dependent data suggests that the aging that occurs in
low salt concentration systems over a very long period is qualitatively similar
to the aging behavior observed in systems with high salt concentration over a
shorter period.Comment: 27 pages, 8 figures. Langmuir, in pres
Diffusion on random site percolation clusters. Theory and NMR microscopy experiments with model objects
Quasi two-dimensional random site percolation model objects were fabricate
based on computer generated templates. Samples consisting of two compartments,
a reservoir of HO gel attached to a percolation model object which was
initially filled with DO, were examined with NMR (nuclear magnetic
resonance) microscopy for rendering proton spin density maps. The propagating
proton/deuteron inter-diffusion profiles were recorded and evaluated with
respect to anomalous diffusion parameters. The deviation of the concentration
profiles from those expected for unobstructed diffusion directly reflects the
anomaly of the propagator for diffusion on a percolation cluster. The fractal
dimension of the random walk, , evaluated from the diffusion measurements
on the one hand and the fractal dimension, , deduced from the spin density
map of the percolation object on the other permits one to experimentally
compare dynamical and static exponents. Approximate calculations of the
propagator are given on the basis of the fractional diffusion equation.
Furthermore, the ordinary diffusion equation was solved numerically for the
corresponding initial and boundary conditions for comparison. The anomalous
diffusion constant was evaluated and is compared to the Brownian case. Some ad
hoc correction of the propagator is shown to pay tribute to the finiteness of
the system. In this way, anomalous solutions of the fractional diffusion
equation could experimentally be verified for the first time.Comment: REVTeX, 12 figures in GIF forma
Accentuating institutional brands: A multimodal analysis of the homepages of selected South African universities
In seeking to disentangle themselves from the constraints of apartheid, South African
universities have immersed themselves in an identity modification process in which they not only
seek to redress the past, but also to reposition their identities as equal opportunity and non-racial
institutions. In this paper, we investigate how the University of the Western Cape, the University
of Cape Town and Stellenbosch University have used visual and verbal semiotics to re-design
their identities on their homepages to appeal to diverse national and international clients. Using
Multimodal Discourse Analysis (MDA), we show how the multi-semiotic choices work together on
the homepages to give the universities differentiated, competitive, powerful and attractive brands.
We conclude that the homepages blended cultural semiotic artefacts, historical, global and transformational
discourses, and architectural landscapes to construct different brand identities that, in turn,
rebrand the universities from edifices of apartheid education to equal opportunity institutions
Chitin recognition via chitotriosidase promotes pathologic type-2 helper T cell responses to cryptococcal infection
Pulmonary mycoses are often associated with type-2 helper T (Th2) cell responses. However, mechanisms of Th2 cell accumulation are multifactorial and incompletely known. To investigate Th2 cell responses to pulmonary fungal infection, we developed a peptide-MHCII tetramer to track antigen-specific CD4+ T cells produced in response to infection with the fungal pathogen Cryptococcus neoformans. We noted massive accruement of pathologic cryptococcal antigen-specific Th2 cells in the lungs following infection that was coordinated by lung-resident CD11b+ IRF4-dependent conventional dendritic cells. Other researchers have demonstrated that this dendritic cell subset is also capable of priming protective Th17 cell responses to another pulmonary fungal infection, Aspergillus fumigatus. Thus, higher order detection of specific features of fungal infection by these dendritic cells must direct Th2 cell lineage commitment. Since chitin-containing parasites commonly elicit Th2 responses, we hypothesized that recognition of fungal chitin is an important determinant of Th2 cell-mediated mycosis. Using C. neoformans mutants or purified chitin, we found that chitin abundance impacted Th2 cell accumulation and disease. Importantly, we determined Th2 cell induction depended on cleavage of chitin via the mammalian chitinase, chitotriosidase, an enzyme that was also prevalent in humans experiencing overt cryptococcosis. The data presented herein offers a new perspective on fungal disease susceptibility, whereby chitin recognition via chitotriosidase leads to the initiation of harmful Th2 cell differentiation by CD11b+ conventional dendritic cells in response to pulmonary fungal infection
Automated Analysis of Cryptococcal Macrophage Parasitism Using GFP-Tagged Cryptococci
The human fungal pathogens Cryptococcus neoformans and C. gattii cause life-threatening infections of the central nervous system. One of the major characteristics of cryptococcal disease is the ability of the pathogen to parasitise upon phagocytic immune effector cells, a phenomenon that correlates strongly with virulence in rodent models of infection. Despite the importance of phagocyte/Cryptococcus interactions to disease progression, current methods for assaying virulence in the acrophage system are both time consuming and low throughput. Here, we introduce the first stable and fully characterised GFP–expressing derivatives of two widely used cryptococcal strains: C. neoformans serotype A type strain H99 and C. gattii serotype B type strain R265. Both strains show unaltered responses to environmental and host stress conditions and no deficiency in virulence in the macrophage model system. In addition, we report the development of a method to effectively and rapidly investigate macrophage parasitism by flow cytometry, a technique that preserves the accuracy of current approaches but offers a four-fold improvement in speed
CD56 is a pathogen recognition receptor on human natural killer cells
Aspergillus (A.) fumigatus is an opportunistic fungal mold inducing invasive aspergillosis (IA) in immunocompromised patients. Although antifungal activity of human natural killer (NK) cells was shown in previous studies, the underlying cellular mechanisms and pathogen recognition receptors (PRRs) are still unknown. Using flow cytometry we were able to show that the fluorescence positivity of the surface receptor CD56 significantly decreased upon fungal contact. To visualize the interaction site of NK cells and A. fumigatus we used SEM, CLSM and dSTORM techniques, which clearly demonstrated that NK cells directly interact with A. fumigatus via CD56 and that CD56 is re-organized and accumulated at this interaction site time-dependently. The inhibition of the cytoskeleton showed that the receptor re-organization was an active process dependent on actin re-arrangements. Furthermore, we could show that CD56 plays a role in the fungus mediated NK cell activation, since blocking of CD56 surface receptor reduced fungal mediated NK cell activation and reduced cytokine secretion. These results confirmed the direct interaction of NK cells and A. fumigatus, leading to the conclusion that CD56 is a pathogen recognition receptor. These findings give new insights into the functional role of CD56 in the pathogen recognition during the innate immune response
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