Comment on Mie Scattering from a Sonoluminescing Bubble with High Spatial and Temporal Resolution [Physical Review E 61, 5253 (2000)]

A key parameter underlying the existence of sonoluminescence (SL)is the time relative to SL at which acoustic energy is radiated from the collapsed bubble. Light scattering is one route to this quantity. We disagree with the statement of Gompf and Pecha that -highly compressed water causes the minimum in scattered light to occur 700ps before SL- and that this effect leads to an overestimate of the bubble wall velocity. We discuss potential artifacts in their experimental arrangement and correct their description of previous experiments on Mie scattering.Comment: 10 pages, 2 figure

Oligopsony With Fixed Market Supply

This paper analyzes oligopsonistic price competition under a fixed input supply constraint. Firms simultaneously and noncooperatively choose input prices. A highest offer first allocation rule determines each firm\u27s share of the fixed supply. Under this rule, if a firm offers a particularly low price, then it may be shut out of the market. Moreover, low offer prices cannot be sustained in the market as a whole since firms have an incentive to outbid their rival(s) and increase individual market share. A pure strategy Nash equilibrium exists if the number of competing firms is sufficiently large. When this condition is satisfied, all equilibrium prices are near the firms\u27 marginal valuation of input: The market outcome is approximately Walrasian

Inflammation in the CNS: advancing the field using intravital imaging

Inflammation of the CNS can have devastating, long-lived, and in some cases fatal consequences for patients. The stimuli that can induce CNS inflammation are diverse, and include infectious agents, autoimmune responses against CNS-expressed antigens, and sterile inflammation following ischemia or traumatic injury. In these conditions, cells of the immune system play central roles in promulgation and resolution of the inflammatory response. However, the immunological mechanisms at work in these diverse responses differ according to the nature of the response. Our understanding of the actions of immune cells in the CNS has been restricted by the difficulty in visualising leukocytes as they undergo recruitment from the cerebral microvasculature and following their entry into the CNS parenchyma. However, advances in in vivo microscopy over the last 10-15 years have overcome many of these difficulties, and studies using these forms of microscopy have revealed a wealth of new information regarding the cellular and molecular mechanisms of CNS inflammation. This Research Topic brings together state of the art reviews examining the use of in vivo imaging in investigating inflammation and leukocyte behaviour in the CNS. Papers in this Research Topic describe how in vivo microscopy has increased our understanding of the actions of immune cells in the inflamed CNS, following various stimuli including autoimmunity, infection and sterile inflammation

Episcopic 3D Imaging Methods: Tools for Researching Gene Function

This work aims at describing episcopic 3D imaging methods and at discussing how these methods can contribute to researching the genetic mechanisms driving embryogenesis and tissue remodelling, and the genesis of pathologies. Several episcopic 3D imaging methods exist. The most advanced are capable of generating high-resolution volume data (voxel sizes from 0.5x0.5x1 µm upwards) of small to large embryos of model organisms and tissue samples. Beside anatomy and tissue architecture, gene expression and gene product patterns can be three dimensionally analyzed in their precise anatomical and histological context with the aid of whole mount in situ hybridization or whole mount immunohistochemical staining techniques. Episcopic 3D imaging techniques were and are employed for analyzing the precise morphological phenotype of experimentally malformed, randomly produced, or genetically engineered embryos of biomedical model organisms. It has been shown that episcopic 3D imaging also fits for describing the spatial distribution of genes and gene products during embryogenesis, and that it can be used for analyzing tissue samples of adult model animals and humans. The latter offers the possibility to use episcopic 3D imaging techniques for researching the causality and treatment of pathologies or for staging cancer. Such applications, however, are not yet routine and currently only preliminary results are available. We conclude that, although episcopic 3D imaging is in its very beginnings, it represents an upcoming methodology, which in short terms will become an indispensable tool for researching the genetic regulation of embryo development as well as the genesis of malformations and diseases

Warfare in Late Neolithic\Early Chalcolithic Pisidia, southwestern Turkey. Climate induced social unrest in the late 7th millennium calBC

This paper proposes an association between climate forcing connected with the 8200 calBP ‘climate event’ and a postulated phase of internecine warfare and population collapse at Late Neolithic/Early Chalcolithic sites in Pisidia, southwestern Turkey. A summary of this evidence is provided and a hypothetical scenario considered in the context of contemporaneous developments in neighbouring regions

Non-ergodicity of a globular protein extending beyond its functional timescale

Internal motions of folded proteins have been assumed to be ergodic, i.e., that the dynamics of a single protein molecule averaged over a very long time resembles that of an ensemble. Here, by performing single-molecule fluorescence resonance energy transfer (smFRET) experiments and molecular dynamics (MD) simulations of a multi-domain globular protein, cytoplasmic protein-tyrosine phosphatase (SHP2), we demonstrate that the functional inter-domain motion is observationally non-ergodic over the time spans 1012 to 107 s and 101 to 102 s. The difference between observational non-ergodicity and simple non-convergence is discussed. In comparison, a single-strand DNA of similar size behaves ergodically with an energy landscape resembling a one-dimensional linear chain. The observed non-ergodicity results from the hierarchical connectivity of the high-dimensional energy landscape of the protein molecule. As the characteristic time for the protein to conduct its dephosphorylation function is 10 s, our findings suggest that, due to the non-ergodicity, individual, seemingly identical protein molecules can be dynamically and functionally different