5,364 research outputs found
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On Visible Homelessness and the Micro-Aesthetics of Public Space
In this article, we investigate the circumstances that have produced the current municipal regulatory approach to homelessness in the City of Melbourne, Victoria, and the ways in which visibly homeless people are policed through a micro-aesthetics of their presence in public space, which involves the monitoring of their bodily demeanour and their physical possessions. Our study contributes to and draws from a range of debates, including studies of the governmental conjunction of poverty and crime, analysis of the co-implication of law and spatiality, research on the criminalisation of homelessness and homeless people, and the burgeoning criminological interest in the significance of the visual field for our understandings of crime and criminality. This article recounts how homelessness, public space and questions of aesthetics have recently coalesced in debates about the regulation of homelessness in the public space of Melbourne’s city centre. It approaches the issues through comparative consideration of genres of municipal management frameworks in other jurisdictions, detailed textual consideration of the Protocol on Homelessness in the City of Melbourne and an empirical study of visible homelessness in the public places of central Melbourne
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Computationally Directed Discovery of MoBi\u3csub\u3e2\u3c/sub\u3e
Incorporating bismuth, the heaviest element stable to radioactive decay, into new materials enables the creation of emergent properties such as permanent magnetism, superconductivity, and nontrivial topology. Understanding the factors that drive Bi reactivity is critical for the realization of these properties. Using pressure as a tunable synthetic vector, we can access unexplored regions of phase space to foster reactivity between elements that do not react under ambient conditions. Furthermore, combining computational and experimental methods for materials discovery at high-pressures provides broader insight into the thermodynamic landscape than can be achieved through experiment alone, informing our understanding of the dominant chemical factors governing structure formation. Herein, we report our combined computational and experimental exploration of the Mo–Bi system, for which no binary intermetallic structures were previously known. Using the ab initio random structure searching (AIRSS) approach, we identified multiple synthetic targets between 0–50 GPa. High-pressure in situ powder X-ray diffraction experiments performed in diamond anvil cells confirmed that Mo–Bi mixtures exhibit rich chemistry upon the application of pressure, including experimental realization of the computationally predicted CuAl2-type MoBi2 structure at 35.8(5) GPa. Electronic structure and phonon dispersion calculations on MoBi2 revealed a correlation between valence electron count and bonding in high-pressure transition metal–Bi structures as well as identified two dynamically stable ambient pressure polymorphs. Our study demonstrates the power of the combined computational–experimental approach in capturing high-pressure reactivity for efficient materials discovery
Effects of immediate postexercise carbohydrate ingestion with and without protein on neutrophil degranulation
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Evidence of Molecular Evolution Driven by Recombination Events Influencing Tropism in a Novel Human Adenovirus that Causes Epidemic Keratoconjunctivitis
In 2005, a human adenovirus strain (formerly known as HAdV-D22/H8 but renamed here HAdV-D53) was isolated from an outbreak of epidemic keratoconjunctititis (EKC), a disease that is usually caused by HAdV-D8, -D19, or -D37, not HAdV-D22. To date, a complete change of tropism compared to the prototype has never been observed, although apparent recombinant strains of other viruses from species Human adenovirus D (HAdV-D) have been described. The complete genome of HAdV-D53 was sequenced to elucidate recombination events that lead to the emergence of a viable and highly virulent virus with a modified tropism. Bioinformatic and phylogenetic analyses of this genome demonstrate that this adenovirus is a recombinant of HAdV-D8 (including the fiber gene encoding the primary cellular receptor binding site), HAdV-D22, (the ε determinant of the hexon gene), HAdV-D37 (including the penton base gene encoding the secondary cellular receptor binding site), and at least one unknown or unsequenced HAdV-D strain. Bootscanning analysis of the complete genomic sequence of this novel adenovirus, which we have re-named HAdV-D53, indicated at least five recombination events between the aforementioned adenoviruses. Intrahexon recombination sites perfectly framed the ε neutralization determinant that was almost identical to the HAdV-D22 prototype. Additional bootscan analysis of all HAdV-D hexon genes revealed recombinations in identical locations in several other adenoviruses. In addition, HAdV-D53 but not HAdV-D22 induced corneal inflammation in a mouse model. Serological analysis confirmed previous results and demonstrated that HAdV-D53 has a neutralization profile representative of the ε determinant of its hexon (HAdV-D22) and the fiber (HAdV-D8) proteins. Our recombinant hexon sequence is almost identical to the hexon sequences of the HAdV-D strain causing EKC outbreaks in Japan, suggesting that HAdV-D53 is pandemic as an emerging EKC agent. This documents the first genomic, bioinformatic, and biological descriptions of the molecular evolution events engendering an emerging pathogenic adenovirus
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Predicting the Next Eye Pathogen: Analysis of a Novel Adenovirus
For DNA viruses, genetic recombination, addition, and deletion represent important evolutionary mechanisms. Since these genetic alterations can lead to new, possibly severe pathogens, we applied a systems biology approach to study the pathogenicity of a novel human adenovirus with a naturally occurring deletion of the canonical penton base Arg-Gly-Asp (RGD) loop, thought to be critical to cellular entry by adenoviruses. Bioinformatic analysis revealed a new highly recombinant species D human adenovirus (HAdV-D60). A synthesis of in silico and laboratory approaches revealed a potential ocular tropism for the new virus. In vivo, inflammation induced by the virus was dramatically greater than that by adenovirus type 37, a major eye pathogen, possibly due to a novel alternate ligand, Tyr-Gly-Asp (YGD), on the penton base protein. The combination of bioinformatics and laboratory simulation may have important applications in the prediction of tissue tropism for newly discovered and emerging viruses
The effects of postexercise feeding on saliva antimicrobial proteins
The purpose of this study was to determine the effects of a carbohydrate (CHO) and protein (PRO) drink consumed immediately after endurance exercise on saliva antimicrobial proteins known to be important for host defense. Eleven male runners ran for 2 hr at 75% VO2max on 2 occasions and immediately postexercise were provided, in randomized order, either a placebo solution (CON) or a CHO-PRO solution containing 1.2 g CHO/kg body mass (BM) and 0.4 g PRO/kg BM (CHO-PRO). The solutions were flavor and volume equivalent (12 ml/kg BM). Saliva flow rate, lysozyme, α-amylase, and secretory (S) IgA concentrations were determined from unstimulated saliva samples collected preexercise, immediately postexercise, and every 30 min until 180 min postexercise. CHO-PRO ingestion immediately postexercise resulted in a lower saliva flow rate than with CON at 30 and 60 min postexercise. Saliva lysozyme concentration increased immediately postexercise in both trials compared with preexercise (p< .05), and CHO-PRO ingestion immediately postexercise resulted in a higher saliva lysozyme concentration in the first hour of recovery than with CON (125% greater at 30 min, 94% greater at 60 min; p< .01). Saliva SIgA concentration decreased below preexercise concentrations 90–150 min postexercise (p< .001), with no effect of CHO-PRO. Saliva α-amylase activity was unaffected by exercise or CHO-PRO refeeding. CHO-PRO refeeding did not alter the secretion rates of any saliva variables during recovery. In conclusion, immediate refeeding with CHO-PRO evoked a greater saliva lysozyme concentration during the first hour of recovery after prolonged exercise than ingestion of placebo but had minimal impact on saliva α-amylase and SIgA responses.</jats:p
A New 5-Flavour LO Analysis and Parametrization of Parton Distributions in the Real Photon
New, radiatively generated, LO quark (u,d,s,c,b) and gluon densities in a
real, unpolarized photon are presented. We perform a global 3-parameter fit,
based on LO DGLAP evolution equations, to all available data for the structure
function F2^gamma(x,Q^2). We adopt a new theoretical approach called ACOT(chi),
originally introduced for the proton, to deal with the heavy-quark thresholds.
This defines our basic model (CJKL model), which gives a very good description
of the experimental data on F2^gamma(x,Q^2), for both Q^2 and x dependences.
For comparison we perform a standard fit using the Fixed Flavour-Number Scheme
(FFNS_CJKL model), updated with respect to the previous fits of this type. We
show the superiority of the CJKL fit over the FFNS_CJKL one and other LO fits
to the F2^gamma(x,Q^2) data. The CJKL model gives also the best description of
the LEP data on the Q^2 dependence of the F2^gamma, averaged over various
x-regions, and the F_2,c^gamma, which were not used directly in the fit.
Finally, a simple analytic parametrization of the resulting parton densities
obtained with the CJKL model is given.Comment: 43 pages, RevTeX4 using axodraw style, 3 tex and 12 postscript
figures, version submitted to Phys. Rev. D, small text changes, one reference
added, FORTRAN program available at http://www.fuw.edu.pl/~pjank/param.html
and at http://www-zeuthen.desy.de/~alorca/id4.htm
Designing magnetic properties in CrSBr through hydrostatic pressure and ligand substitution
The ability to control magnetic properties of materials is crucial for
fundamental research and underpins many information technologies. In this
context, two-dimensional materials are a particularly exciting platform due to
their high degree of tunability and ease of implementation into nanoscale
devices. Here we report two approaches for manipulating the A-type
antiferromagnetic properties of the layered semiconductor CrSBr through
hydrostatic pressure and ligand substitution. Hydrostatic pressure compresses
the unit cell, increasing the interlayer exchange energy while lowering the
N\'eel temperature. Ligand substitution, realized synthetically through Cl
alloying, anisotropically compresses the unit cell and suppresses the
Cr-halogen covalency, reducing the magnetocrystalline anisotropy energy and
decreasing the N\'eel temperature. A detailed structural analysis combined with
first-principles calculations reveal that alterations in the magnetic
properties are intricately related to changes in direct Cr-Cr exchange
interactions and the Cr-anion superexchange pathways. Further, we demonstrate
that Cl alloying enables chemical tuning of the interlayer coupling from
antiferromagnetic to ferromagnetic, which is unique amongst known
two-dimensional magnets. The magnetic tunability, combined with a high ordering
temperature, chemical stability, and functional semiconducting properties, make
CrSBr an ideal candidate for pre- and post-synthetic design of magnetism in
two-dimensional materials.Comment: Main text: 17 pages, 4 figures. Supporting Information: 34 pages, 32
figures, 4 table
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