240 research outputs found

    Antimony and bismuth oxide cluster ions

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    The formation of charged antimony and bismuth oxide clusters in a pulsed arc cluster ion source (PACIS) has been studied with time-of-Ñight mass spectrometric techniques. We compare series of antimony and bismuth oxide cluster anions with their known cationic counterparts. The anionic series and (M 2 O 3 ) n MO 2h ave been predicted proceeding from the known cationic series and n Ob y adding O2~and have been experimentally established. All these series contain the metal atoms (M \ Sb or Bi) in the formal oxidation state ]3. However, only in the case of antimony, oxygen rich oxide clusters appear, that can be explained with a gradual transition in the oxidation number from ]3 to ]5 of single antimony atoms in the cluster. To estimate the inÑuence of the special oxide formation conditions comparative investigations with the PACIS and a laser vaporisation cluster source have been carried out for bismuth oxide cations. The similar oxide cluster distributions at comparable oxygen availability display clearly that the special thermodynamical stability of the discussed magic clusters is the signiÐcant driving force for their formation

    Measuring Political Deliberation: A Discourse Quality Index

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    In this paper, we develop a discourse quality index (DQI) that serves as a quantitative measure of discourse in deliberation. The DQI is rooted in Habermas' discourse ethics and provides an accurate representation of the most important principles underlying deliberation. At the same time, the DQI can be shown to be a reliable measurement instrument due to its focus on observable behavior and its detailed coding instructions. We illustrate the DQI for a parliamentary debate in the British House of Commons. We show that the DQI yields reliable data and we discuss how these data could be used in subsequent analysis. We conclude by discussing some limitations of the DQI and by identifying some areas in which it could prove useful. Introduction Over the past decade, deliberative politics has moved to the forefront of political theory. 1 Deliberation implies that political decision-making is or should be 'talk-centric' rather than 'vote-centric Despite the advances in the political theory of deliberation and despite deliberative theorists' claims about the importance of discourse, empirically 2 This is partially a reflection of the continued predominance of social choice theory and other theories that treat preferences as given and view decision-making as a process of preference aggregation. However, a larger issue may be the dearth of measurement instruments that allow researchers to operationalize and quantify the quality of discourse, and that open up deliberation for empirical research. In this article, we develop a measurement instrument of deliberative quality -the discourse quality index (DQI). This measurement instrument has the advantage that it is theoretically grounded, finding its origins in Habermas (1981, 1990, 1991, 1992, 1995, 1996) as well as other theorists. At the same time, the DQI can be applied easily and reliably to a wide range of deliberative contexts. Thus, the DQI opens up deliberation for empirical research, allowing this research to interface with political theory. We should point out at the outset that this is a measurement paper. We lack the space to investigate actually the impact of discourse quality on political outcomes. Although many theorists believe that deliberative politics leads to better outcomes, there is no consensus on this matter, with some arguing vociferously that an automatic connection between deliberation and just outcomes cannot be presumed We organize this article as follows. First, we discuss the criteria that a measure of the nature of discourse should satisfy. Next, we discuss two past efforts at measuring deliberation. Third, we discuss the theoretical foundation of the DQI. Having laid the groundwork, we then provide a detailed discussion of the DQI. This is followed by an empirical illustration that shows the coding procedures as well as the measurement properties of the DQI. We then discuss how the DQI can be employed in empirical research. We conclude by discussing some limitations of the DQI and opportunities for its use. Measurement Criteria A measure of the nature of discourse can serve as a bridge between political theory and empirical scholarship only if it does justice to the former and provides guidance to the latter. We believe, therefore, that such a measure should meet four different criteria: (1) it should be theoretically grounded, (2) it should tap into observable phenomena, (3) it should be general, and (4) it should be reliable. The first criterion is essential because it concerns the validity of the discourse measure. An improperly grounded measure lacks construct validity, would be of little practical use and would fail to convince theorists. The complication here is the lack of agreement among political theorists about what constitute deliberation and discourse. One could attempt to develop a measure that captures all of the different conceptions of these concepts, but this would result in an instrument that is too complex to be of practical value and one that lacks internal consistency (since the different theories are not necessarily compatible). Our approach is different; we have selected a particular theory of deliberation, one that is most closely associated with The second to fourth criteria speak to the empirical power of a discourse measure. Most importantly, the measurement instrument should tap into observable discourse behavior. This is essential if the measurement instrument is to produce reliable data and if it is to convince empirical scholars. In addition, an ideal measure of discourse quality should be general, so that it can be transported from one research domain to the next. Finally, such a measure should be reliable. This requires not only that it is based on observable behavior, but also that its coding instructions are specific, and that its coding categories are sufficiently clear that different coders could agree on the classification of the same discourse. Of course, reliable measurement is never guaranteed, so that empirical reliability assessments should be a standard practice in discourse analysis. Below, we shall argue that the DQI meets these criteria. However, before outlining the logic of this measure, we should review past efforts at measuring discourse. As we shall see, these efforts leave considerable room for improvement

    The search for transient astrophysical neutrino emission with IceCube-DeepCore

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    We present the results of a search for astrophysical sources of brief transient neutrino emission using IceCube and DeepCore data acquired between 2012 May 15 and 2013 April 30. While the search methods employed in this analysis are similar to those used in previous IceCube point source searches, the data set being examined consists of a sample of predominantly sub-TeV muon-neutrinos from the Northern Sky (-5 degrees < delta < 90 degrees) obtained through a novel event selection method. This search represents a first attempt by IceCube to identify astrophysical neutrino sources in this relatively unexplored energy range. The reconstructed direction and time of arrival of neutrino events are used to search for any significant self-correlation in the data set. The data revealed no significant source of transient neutrino emission. This result has been used to construct limits at timescales ranging from roughly 1 s to 10 days for generic soft-spectra transients. We also present limits on a specific model of neutrino emission from soft jets in core-collapse supernovae

    Aging Differentially Affects Multiple Aspects of Vesicle Fusion Kinetics

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    How fusion pore formation during exocytosis affects the subsequent release of vesicle contents remains incompletely understood. It is unclear if the amount released per vesicle is dependent upon the nature of the developing fusion pore and whether full fusion and transient kiss and run exocytosis are regulated by similar mechanisms. We hypothesise that if consistent relationships exist between these aspects of exocytosis then they will remain constant across any age. Using amperometry in mouse chromaffin cells we measured catecholamine efflux during single exocytotic events at P0, 1 month and 6 months. At all ages we observed full fusion (amperometric spike only), full fusion preceded by fusion pore flickering (pre-spike foot (PSF) signal followed by a spike) and pure “kiss and run” exocytosis (represented by stand alone foot (SAF) signals). We observe age-associated increases in the size of all 3 modes of fusion but these increases occur at different ages. The release probability of PSF signals or full spikes alone doesn't alter across any age in comparison with an age-dependent increase in the incidence of “kiss and run” type events. However, the most striking changes we observe are age-associated changes in the relationship between vesicle size and the membrane bending energy required for exocytosis. Our data illustrates that vesicle size does not regulate release probability, as has been suggested, that membrane elasticity or flexural rigidity change with age and that the mechanisms controlling full fusion may differ from those controlling “kiss and run” fusion

    Characterization of Changes in Serum Anti-Glycan Antibodies in Crohn's Disease – a Longitudinal Analysis

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    INTRODUCTION: Anti-glycan antibodies are a promising tool for differential diagnosis and disease stratification of patients with Crohn's disease (CD). We longitudinally assessed level and status changes of anti-glycan antibodies over time in individual CD patients as well as determinants of this phenomenon. METHODS: 859 serum samples derived from a cohort of 253 inflammatory bowel disease (IBD) patients (207 CD, 46 ulcerative colitis (UC)) were tested for the presence of anti-laminarin (Anti-L), anti-chitin (Anti-C), anti-chitobioside (ACCA), anti-laminaribioside (ALCA), anti-mannobioside (AMCA) and anti-Saccharomyces cerevisiae (gASCA) antibodies by ELISA. All patients had at least two and up to eleven serum samples taken during the disease course. RESULTS: Median follow-up time for CD was 17.4 months (Interquartile range (IQR) 8.0, 31.6 months) and for UC 10.9 months (IQR 4.9, 21.0 months). In a subgroup of CD subjects marked changes in the overall immune response (quartile sum score) and levels of individual markers were observed over time. The marker status (positive versus negative) remained widely stable. Neither clinical phenotype nor NOD2 genotype was associated with the observed fluctuations. In a longitudinal analysis neither changes in disease activity nor CD behavior led to alterations in the levels of the glycan markers. The ability of the panel to discriminate CD from UC or its association with CD phenotypes remained stable during follow-up. In the serum of UC patients neither significant level nor status changes were observed. CONCLUSIONS: While the levels of anti-glycan antibodies fluctuate in a subgroup of CD patients the antibody status is widely stable over time

    Cannabinoid receptor CB1 mediates baseline and activity-induced survival of new neurons in adult hippocampal neurogenesis

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    <p>Abstract</p> <p>Background</p> <p>Adult neurogenesis is a particular example of brain plasticity that is partially modulated by the endocannabinoid system. Whereas the impact of synthetic cannabinoids on the neuronal progenitor cells has been described, there has been lack of information about the action of plant-derived extracts on neurogenesis. Therefore we here focused on the effects of Δ9-tetrahydrocannabinol (THC) and Cannabidiol (CBD) fed to female C57Bl/6 and Nestin-GFP-reporter mice on proliferation and maturation of neuronal progenitor cells and spatial learning performance. In addition we used cannabinoid receptor 1 (CB1) deficient mice and treatment with CB1 antagonist AM251 in Nestin-GFP-reporter mice to investigate the role of the CB1 receptor in adult neurogenesis in detail.</p> <p>Results</p> <p>THC and CBD differed in their effects on spatial learning and adult neurogenesis. CBD did not impair learning but increased adult neurogenesis, whereas THC reduced learning without affecting adult neurogenesis. We found the neurogenic effect of CBD to be dependent on the CB1 receptor, which is expressed over the whole dentate gyrus. Similarly, the neurogenic effect of environmental enrichment and voluntary wheel running depends on the presence of the CB1 receptor. We found that in the absence of CB1 receptors, cell proliferation was increased and neuronal differentiation reduced, which could be related to CB1 receptor mediated signaling in Doublecortin (DCX)-expressing intermediate progenitor cells.</p> <p>Conclusion</p> <p>CB1 affected the stages of adult neurogenesis that involve intermediate highly proliferative progenitor cells and the survival and maturation of new neurons. The pro-neurogenic effects of CBD might explain some of the positive therapeutic features of CBD-based compounds.</p

    Epigenetic Changes of CXCR4 and Its Ligand CXCL12 as Prognostic Factors for Sporadic Breast Cancer

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    Chemokines and their receptors are involved in the development and cancer progression. The chemokine CXCL12 interacts with its receptor, CXCR4, to promote cellular adhesion, survival, proliferation and migration. The CXCR4 gene is upregulated in several types of cancers, including skin, lung, pancreas, brain and breast tumors. In pancreatic cancer and melanoma, CXCR4 expression is regulated by DNA methylation within its promoter region. In this study we examined the role of cytosine methylation in the regulation of CXCR4 expression in breast cancer cell lines and also correlated the methylation pattern with the clinicopathological aspects of sixty-nine primary breast tumors from a cohort of Brazilian women. RT-PCR showed that the PMC-42, MCF7 and MDA-MB-436 breast tumor cell lines expressed high levels of CXCR4. Conversely, the MDA-MB-435 cell line only expressed CXCR4 after treatment with 5-Aza-CdR, which suggests that CXCR4 expression is regulated by DNA methylation. To confirm this hypothesis, a 184 bp fragment of the CXCR4 gene promoter region was cloned after sodium bisulfite DNA treatment. Sequencing data showed that cell lines that expressed CXCR4 had only 15% of methylated CpG dinucleotides, while the cell line that not have CXCR4 expression, had a high density of methylation (91%). Loss of DNA methylation in the CXCR4 promoter was detected in 67% of the breast cancer analyzed. The absence of CXCR4 methylation was associated with the tumor stage, size, histological grade, lymph node status, ESR1 methylation and CXCL12 methylation, metastasis and patient death. Kaplan-Meier curves demonstrated that patients with an unmethylated CXCR4 promoter had a poorer overall survival and disease-free survival. Furthermore, patients with both CXCL12 methylation and unmethylated CXCR4 had a shorter overall survival and disease-free survival. These findings suggest that the DNA methylation status of both CXCR4 and CXCL12 genes could be used as a biomarker for prognosis in breast cancer

    Chemotaxis of Cell Populations through Confined Spaces at Single-Cell Resolution

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    Cell migration is crucial for both physiological and pathological processes. Current in vitro cell motility assays suffer from various drawbacks, including insufficient temporal and/or optical resolution, or the failure to include a controlled chemotactic stimulus. Here, we address these limitations with a migration chamber that utilizes a self-sustaining chemotactic gradient to induce locomotion through confined environments that emulate physiological settings. Dynamic real-time analysis of both population-scale and single-cell movement are achieved at high resolution. Interior surfaces can be functionalized through adsorption of extracellular matrix components, and pharmacological agents can be administered to cells directly, or indirectly through the chemotactic reservoir. Direct comparison of multiple cell types can be achieved in a single enclosed system to compare inherent migratory potentials. Our novel microfluidic design is therefore a powerful tool for the study of cellular chemotaxis, and is suitable for a wide range of biological and biomedical applications
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