3,668 research outputs found
Testing AutoTrace: A Machine-learning Approach to Automated Tongue Contour Data Extraction
The Programme and Abstract booklet can be viewed at: http://www.qmu.ac.uk/casl/conf/ultrafest_2013/docs/Ultrafest%20abstract%20booklet.pdfOral Presentationpublished_or_final_versio
Sub-Planck spots of Schroedinger cats and quantum decoherence
Heisenberg's principle states that the product of uncertainties of
position and momentum should be no less than Planck's constant . This is
usually taken to imply that phase space structures associated with sub-Planck
() scales do not exist, or, at the very least, that they do not
matter. I show that this deeply ingrained prejudice is false: Non-local
"Schr\"odinger cat" states of quantum systems confined to phase space volume
characterized by `the classical action' develop spotty structure
on scales corresponding to sub-Planck . Such
structures arise especially quickly in quantum versions of classically chaotic
systems (such as gases, modelled by chaotic scattering of molecules), that are
driven into nonlocal Schr\"odinger cat -- like superpositions by the quantum
manifestations of the exponential sensitivity to perturbations. Most
importantly, these sub-Planck scales are physically significant: determines
sensitivity of a quantum system (or of a quantum environment) to perturbations.
Therefore sub-Planck controls the effectiveness of decoherence and
einselection caused by the environment. It may also be relevant in
setting limits on sensitivity of Schr\"odinger cats used as detectors.Comment: Published in Nature 412, 712-717 (2001
Anatomy of quantum chaotic eigenstates
The eigenfunctions of quantized chaotic systems cannot be described by
explicit formulas, even approximate ones. This survey summarizes (selected)
analytical approaches used to describe these eigenstates, in the semiclassical
limit. The levels of description are macroscopic (one wants to understand the
quantum averages of smooth observables), and microscopic (one wants
informations on maxima of eigenfunctions, "scars" of periodic orbits, structure
of the nodal sets and domains, local correlations), and often focusses on
statistical results. Various models of "random wavefunctions" have been
introduced to understand these statistical properties, with usually good
agreement with the numerical data. We also discuss some specific systems (like
arithmetic ones) which depart from these random models.Comment: Corrected typos, added a few references and updated some result
How do you say ‘hello’? Personality impressions from brief novel voices
On hearing a novel voice, listeners readily form personality impressions of that speaker. Accurate or not, these impressions are known to affect subsequent interactions; yet the underlying psychological and acoustical bases remain poorly understood. Furthermore, hitherto studies have focussed on extended speech as opposed to analysing the instantaneous impressions we obtain from first experience. In this paper, through a mass online rating experiment, 320 participants rated 64 sub-second vocal utterances of the word ‘hello’ on one of 10 personality traits. We show that: (1) personality judgements of brief utterances from unfamiliar speakers are consistent across listeners; (2) a two-dimensional ‘social voice space’ with axes mapping Valence (Trust, Likeability) and Dominance, each driven by differing combinations of vocal acoustics, adequately summarises ratings in both male and female voices; and (3) a positive combination of Valence and Dominance results in increased perceived male vocal Attractiveness, whereas perceived female vocal Attractiveness is largely controlled by increasing Valence. Results are discussed in relation to the rapid evaluation of personality and, in turn, the intent of others, as being driven by survival mechanisms via approach or avoidance behaviours. These findings provide empirical bases for predicting personality impressions from acoustical analyses of short utterances and for generating desired personality impressions in artificial voices
Prospects for terahertz imaging the human skin cancer with the help of gold-nanoparticles-based terahertz-to-infrared converter
The design is suggested, and possible operation parameters are discussed, of
an instrument to inspect a skin cancer tumour in the terahertz (THz) range,
transferring the image into the infrared (IR) and making it visible with the
help of standard IR camera. The central element of the device is the THz-to-IR
converter, a Teflon or silicon film matrix with embedded 8.5 nm diameter gold
nanoparticles. The use of external THz source for irradiating the biological
tissue sample is presumed. The converter's temporal characteristics enable its
performance in a real-time scale. The details of design suited for the
operation in transmission mode (in vitro) or on the human skin in reflection
mode {in vivo) are specified.Comment: To be published in the proceedings of the FANEM2018 workshop - Minsk,
3-5 June 201
The semi-classical expansion and resurgence in gauge theories: new perturbative, instanton, bion, and renormalon effects
We study the dynamics of four dimensional gauge theories with adjoint
fermions for all gauge groups, both in perturbation theory and
non-perturbatively, by using circle compactification with periodic boundary
conditions for the fermions. There are new gauge phenomena. We show that, to
all orders in perturbation theory, many gauge groups are Higgsed by the gauge
holonomy around the circle to a product of both abelian and nonabelian gauge
group factors. Non-perturbatively there are monopole-instantons with fermion
zero modes and two types of monopole-anti-monopole molecules, called bions. One
type are "magnetic bions" which carry net magnetic charge and induce a mass gap
for gauge fluctuations. Another type are "neutral bions" which are magnetically
neutral, and their understanding requires a generalization of multi-instanton
techniques in quantum mechanics - which we refer to as the
Bogomolny-Zinn-Justin (BZJ) prescription - to compactified field theory. The
BZJ prescription applied to bion-anti-bion topological molecules predicts a
singularity on the positive real axis of the Borel plane (i.e., a divergence
from summing large orders in peturbation theory) which is of order N times
closer to the origin than the leading 4-d BPST instanton-anti-instanton
singularity, where N is the rank of the gauge group. The position of the
bion--anti-bion singularity is thus qualitatively similar to that of the 4-d IR
renormalon singularity, and we conjecture that they are continuously related as
the compactification radius is changed. By making use of transseries and
Ecalle's resurgence theory we argue that a non-perturbative continuum
definition of a class of field theories which admit semi-classical expansions
may be possible.Comment: 112 pages, 7 figures; v2: typos corrected, discussion of
supersymmetric models added at the end of section 8.1, reference adde
HCV IRES manipulates the ribosome to promote the switch from translation initiation to elongation.
The internal ribosome entry site (IRES) of the hepatitis C virus (HCV) drives noncanonical initiation of protein synthesis necessary for viral replication. Functional studies of the HCV IRES have focused on 80S ribosome formation but have not explored its role after the 80S ribosome is poised at the start codon. Here, we report that mutations of an IRES domain that docks in the 40S subunit's decoding groove cause only a local perturbation in IRES structure and result in conformational changes in the IRES-rabbit 40S subunit complex. Functionally, the mutations decrease IRES activity by inhibiting the first ribosomal translocation event, and modeling results suggest that this effect occurs through an interaction with a single ribosomal protein. The ability of the HCV IRES to manipulate the ribosome provides insight into how the ribosome's structure and function can be altered by bound RNAs, including those derived from cellular invaders
Pharmacological levels of withaferin A (Withania somnifera) trigger clinically relevant anticancer effects specific to triple negative breast cancer cells
Withaferin A (WA) isolated from Withania somnifera (Ashwagandha) has recently become an attractive phytochemical under investigation in various preclinical studies for treatment of different cancer types. In the present study, a comparative pathway-based transcriptome analysis was applied in epithelial-like MCF-7 and triple negative mesenchymal MDA-MB-231 breast cancer cells exposed to different concentrations of WA which can be detected systemically in in vivo experiments. Whereas WA treatment demonstrated attenuation of multiple cancer hallmarks, the withanolide analogue Withanone (WN) did not exert any of the described effects at comparable concentrations. Pathway enrichment analysis revealed that WA targets specific cancer processes related to cell death, cell cycle and proliferation, which could be functionally validated by flow cytometry and real-time cell proliferation assays. WA also strongly decreased MDA-MB-231 invasion as determined by single-cell collagen invasion assay. This was further supported by decreased gene expression of extracellular matrix-degrading proteases (uPA, PLAT, ADAM8), cell adhesion molecules (integrins, laminins), pro-inflammatory mediators of the metastasis-promoting tumor microenvironment (TNFSF12, IL6, ANGPTL2, CSF1R) and concomitant increased expression of the validated breast cancer metastasis suppressor gene (BRMS1). In line with the transcriptional changes, nanomolar concentrations of WA significantly decreased protein levels and corresponding activity of uPA in MDA-MB-231 cell supernatant, further supporting its anti-metastatic properties. Finally, hierarchical clustering analysis of 84 chromatin writer-reader-eraser enzymes revealed that WA treatment of invasive mesenchymal MDA-MB-231 cells reprogrammed their transcription levels more similarly towards the pattern observed in non-invasive MCF-7 cells. In conclusion, taking into account that sub-cytotoxic concentrations of WA target multiple metastatic effectors in therapy-resistant triple negative breast cancer, WA-based therapeutic strategies targeting the uPA pathway hold promise for further (pre)clinical development to defeat aggressive metastatic breast cancer
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