189 research outputs found

    Boundaries of Disk-like Self-affine Tiles

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    Let T:=T(A,D)T:= T(A, {\mathcal D}) be a disk-like self-affine tile generated by an integral expanding matrix AA and a consecutive collinear digit set D{\mathcal D}, and let f(x)=x2+px+qf(x)=x^{2}+px+q be the characteristic polynomial of AA. In the paper, we identify the boundary T\partial T with a sofic system by constructing a neighbor graph and derive equivalent conditions for the pair (A,D)(A,{\mathcal D}) to be a number system. Moreover, by using the graph-directed construction and a device of pseudo-norm ω\omega, we find the generalized Hausdorff dimension dimHω(T)=2logρ(M)/logq\dim_H^{\omega} (\partial T)=2\log \rho(M)/\log |q| where ρ(M)\rho(M) is the spectral radius of certain contact matrix MM. Especially, when AA is a similarity, we obtain the standard Hausdorff dimension dimH(T)=2logρ/logq\dim_H (\partial T)=2\log \rho/\log |q| where ρ\rho is the largest positive zero of the cubic polynomial x3(p1)x2(qp)xqx^{3}-(|p|-1)x^{2}-(|q|-|p|)x-|q|, which is simpler than the known result.Comment: 26 pages, 11 figure

    Hydrometeorological, glaciological and geospatial research data from the Peyto Glacier Research Basin in the Canadian Rockies

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    Canada First Research Excellent Fund’s Global Water Futures Programme, the National Sciences and Engineering Research Council of Canada’s Changing Cold Regions Network and Discovery Grants programme, the Canada Foundation for Innovation’s Canadian Rockies Hydrological Observatory, the Canada Research Chairs and Canada Excellence Research Chairs programmes, the Canadian Foundation for Climate and Atmospheric Sciences IP3 and WC2N networks, Natural Resources Canada, Environment Canada, Columbia Basin Trust, BC HydroPeer ReviewedThis paper presents hydrometeorological, glaciological and geospatial data from the Peyto Glacier Research Basin (PGRB) in the Canadian Rockies. Peyto Glacier has been of interest to glaciological and hydrological researchers since the 1960s, when it was chosen as one of five glacier basins in Canada for the study of mass and water balance during the International Hydrological Decade (IHD, 1965–1974). Intensive studies of the glacier and observations of the glacier mass balance continued after the IHD, when the initial seasonal meteorological stations were discontinued, then restarted as continuous stations in the late 1980s. The corresponding hydrometric observations were discontinued in 1977 and restarted in 2013. Datasets presented in this paper include high-resolution, co-registered digital elevation models (DEMs) derived from original air photos and lidar surveys; hourly off-glacier meteorological data recorded from 1987 to the present; precipitation data from the nearby Bow Summit weather station; and long-term hydrological and glaciological model forcing datasets derived from bias-corrected reanalysis products. These data are crucial for studying climate change and variability in the basin and understanding the hydrological responses of the basin to both glacier and climate change. The comprehensive dataset for the PGRB is a valuable and exceptionally long-standing testament to the impacts of climate change on the cryosphere in the high-mountain environment. The dataset is publicly available from Federated Research Data Repository at https://doi.org/10.20383/101.0259 (Pradhananga et al., 2020)

    Phospholipid dependent mechanism of smp24, an α-helical antimicrobial peptide from scorpion venom

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    Determining the mechanism of action of antimicrobial peptides (AMPs) is critical if they are to be developed into the clinical setting. In recent years high resolution techniques such as atomic force microscopy (AFM) have increasingly been utilised to determine AMP mechanism of action on planar lipid bilayers and live bacteria. Here we present the biophysical characterisation of a prototypical AMP from the venom of the North African scorpion Scorpio maurus palmatus termed Smp24. Smp24 is an amphipathic helical peptide containing 24 residues with a charge of + 3 and exhibits both antimicrobial and cytotoxic activity and we aim to elucidate the mechanism of action of this peptide on both membrane systems. Using AFM, quartz crystal microbalance-dissipation (QCM-D) and liposomal leakage assays the effect of Smp24 on prototypical synthetic prokaryotic (DOPG:DOPC) and eukaryotic (DOPE:DOPC) membranes has been determined. Our data points to a toroidal pore mechanism against the prokaryotic like membrane whilst the formation of hexagonal phase non-lamellar phase structures is seen in eukaryotic like membrane. Also, phase segregation is observed against the eukaryotic membrane and this study provides direct evidence of the same peptide having multiple mechanisms of action depending on the membrane lipid composition

    Fog computing security: a review of current applications and security solutions

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    Fog computing is a new paradigm that extends the Cloud platform model by providing computing resources on the edges of a network. It can be described as a cloud-like platform having similar data, computation, storage and application services, but is fundamentally different in that it is decentralized. In addition, Fog systems are capable of processing large amounts of data locally, operate on-premise, are fully portable, and can be installed on heterogeneous hardware. These features make the Fog platform highly suitable for time and location-sensitive applications. For example, Internet of Things (IoT) devices are required to quickly process a large amount of data. This wide range of functionality driven applications intensifies many security issues regarding data, virtualization, segregation, network, malware and monitoring. This paper surveys existing literature on Fog computing applications to identify common security gaps. Similar technologies like Edge computing, Cloudlets and Micro-data centres have also been included to provide a holistic review process. The majority of Fog applications are motivated by the desire for functionality and end-user requirements, while the security aspects are often ignored or considered as an afterthought. This paper also determines the impact of those security issues and possible solutions, providing future security-relevant directions to those responsible for designing, developing, and maintaining Fog systems

    Development of an In Vitro Model for the Multi-Parametric Quantification of the Cellular Interactions between Candida Yeasts and Phagocytes

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    We developed a new in vitro model for a multi-parameter characterization of the time course interaction of Candida fungal cells with J774 murine macrophages and human neutrophils, based on the use of combined microscopy, fluorometry, flow cytometry and viability assays. Using fluorochromes specific to phagocytes and yeasts, we could accurately quantify various parameters simultaneously in a single infection experiment: at the individual cell level, we measured the association of phagocytes to fungal cells and phagocyte survival, and monitored in parallel the overall phagocytosis process by measuring the part of ingested fungal cells among the total fungal biomass that changed over time. Candida albicans, C. glabrata, and C. lusitaniae were used as a proof of concept: they exhibited species-specific differences in their association rate with phagocytes. The fungal biomass uptaken by the phagocytes differed significantly according to the Candida species. The measure of the survival of fungal and immune cells during the interaction showed that C. albicans was the more aggressive yeast in vitro, destroying the vast majority of the phagocytes within five hours. All three species of Candida were able to survive and to escape macrophage phagocytosis either by the intraphagocytic yeast-to-hyphae transition (C. albicans) and the fungal cell multiplication until phagocytes burst (C. glabrata, C. lusitaniae), or by the avoidance of phagocytosis (C. lusitaniae). We demonstrated that our model was sensitive enough to quantify small variations of the parameters of the interaction. The method has been conceived to be amenable to the high-throughput screening of mutants in order to unravel the molecular mechanisms involved in the interaction between yeasts and host phagocytes
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