290 research outputs found

    How Luhmann’s systems theory can inform gambling studies

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    Gambling and problem gambling studies tend to be characterised by individual-based approaches both theoretically and methodologically, while sociological approaches remain underutilised or even marginal. In this study, we discuss the potential of Niklas Luhmann’s systems theory in the analysis of gambling. As opposed to positivist or individualistic approaches, Luhmann’s work is strongly constructivist: neither systems nor their components are seen to be made up of individuals. Using systems theory in informing gambling research distances the research interests from individuals and directs it towards societal mechanisms, structures, and processes. Therefore, a systems theoretical approach can offer novel tools to study gambling, but also the paradigm of gambling research itself. This paper demonstrates how systems theory can critically inform gambling research through five operationalisations: gambling as a system, the gambling experience, the regulation of gambling economies, gambling providers as organisations, and systems theory as a methodological program. These five operationalisations can serve as an important window to widen perspectives on gambling.Peer reviewe

    Anfälligkeit von Leguminosen gegenüber Meloidogyne hapla

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    Green manure legumes are a necessary element of organic crop rotations. However, they are able to propagate nematodes especially Meloidogyne and Paratylenchus species. The results of a pot experiment showed that plant species of the genera Pisum, Vicia, Trifolium had a higher propagation rate of Meloidogyne hapla than salad Latuca sativa while plant species of the genera Medicago and Melilotus were less susceptible to infestation of nematodes. It is concluded that crop rotation management especially in vegetable production has to consider the different susceptibility of the legumes and further research has to test more species and varieties

    Caspofungin for treatment of invasive aspergillosis in Germany: results of a pre-planned subanalysis of an international registry

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    <p>Abstract</p> <p>Background</p> <p>This study is a pre-planned country-specific subanalysis of results in Germany from a multinational multicenter registry to prospectively assess real-world experience with caspofungin administered for treatment of proven or probable invasive aspergillosis (IA).</p> <p>Methods</p> <p>Data from patients treated with caspofungin for a single episode of IA were collected. Effectiveness was determined by the local investigator as favorable (complete or partial response) or unfavorable (stable disease, failure or death) at the end of caspofungin therapy. Descriptive statistics with binomial exact confidence intervals were employed.</p> <p>Results</p> <p>Forty-two consecutive patients were identified in three German centers. Three patients (7%) had proven IA and 39/42 (93%) had probable IA (modified European Organization for Research and Treatment of Cancer/Mycosis Study Group (EORTC/MSG) criteria). Forty-one patients had pulmonary IA and one had tracheal IA. Caspofungin monotherapy was received by 36/42 patients (86%); of these, 26/36 (72%) received salvage therapy. A favorable response was observed in 29/42 patients (69%; 95% CI 53 to 82%); of these, 21/29 (72%) had a complete and 8/29 (28%) a partial response. Favorable response rate was 69% in patients with monotherapy (95% CI 52% to 84%; 25/36 patients), and 67% in patients receiving combination therapy (95% CI 22% to 96%; 4/6 patients). Favorable response rate in patients with first line therapy was 64% (95% CI 31% to 89%; 7/11 patients), and 73% in patients with second line therapy (95% CI 54% to 88%; 20/30 patients). No adverse events were reported. In total, 35/42 patients (83%; 95% CI 69 to 93%) survived seven days after completion of caspofungin therapy.</p> <p>Conclusions</p> <p>These real-life findings in Germany are consistent with the international findings from this registry and with findings from randomized studies.</p

    Tree insect pests and pathogens: a global systematic review of their impacts in urban areas

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    Trees contribute greatly to urban environments and human well-being, yet relatively little is known about the extent to which a rising incidence of tree insect pests and pathogens may be affecting these contributions. To address this issue, we undertook a systematic review and synthesis of the diverse global empirical evidence on the impacts of urban tree insect pests and pathogens, using bibliographic databases. Following screening and appraisal of over 3000 articles from a wide range of fields, 100 studies from 28 countries, spanning 1979–2021, were conceptually sorted into a three-part framework: (1) environmental impacts, representing 95 of the studies, including those reporting on tree damage, mortality, reduced growth, and changes in tree function; (2) social impacts were reported by 35 of studies, including on aesthetics, human health, and safety hazards; and (3) economic impacts, reported in 24 of studies, including on costs of pest management, and economic losses. There has been a considerable increase in urban impact studies since 2011. Evidence gaps exist on impacts on climate-regulating capacity, including temperature regulation, water retention, soil erosion, and wind protection, but also on specific hazards, nuisances, human well-being, property damages, and hazard liabilities. As a knowledge synthesis, this article presents the best available evidence of urban tree insect / pathogen impacts to guide policy, management and further research. It will enable us to better forecast how growing threats will affect the urban forest and plan for these eventualities

    Complementarity of experimental and lattice QCD data on pion parton distributions

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    We extract pion parton distribution functions (PDFs) in a Monte Carlo global QCD analysis of experimental data together with reduced Ioffe time pseudo-distributions and matrix elements of current-current correlators generated from lattice QCD. By including both experimental and lattice QCD data, our analysis rigorously quantifies both the uncertainties of the pion PDFs and systematic effects intrinsic to the lattice QCD observables. The reduced Ioffe time pseudo-distributions significantly decrease the uncertainties on the PDFs, while the current-current correlators are limited by the systematic effects associated with the lattice. Consistent with recent phenomenological determinations, the behavior of the valence quark distribution of the pion at large momentum fraction is found to be (1x)βeff\sim (1-x)^{ \beta_{\rm eff}} with βeff1.01.2\beta_{\rm eff} \approx 1.0-1.2.Comment: 46 pages, 15 figure

    Clinical and serological evaluation of a novel CENP-A peptide based ELISA

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    ABSTRACT: INTRODUCTION: Anti-centromere antibodies (ACA) are useful biomarkers in the diagnosis of systemic sclerosis (SSc). ACA are found in 20-40% of SSc patients and, albeit with lower prevalence, in patients with other systemic autoimmune rheumatic diseases. Historically, ACA were detected by indirect immunofluorescence (IIF) on HEp-2 cells and confirmed by immunoassays using recombinant CENP-B. The objective of this study was to evaluate a novel CENP-A peptide ELISA. METHODS: Sera collected from SSc patients (n=334) and various other diseases (n=619) and from healthy controls (n=175) were tested for anti-CENP-A antibodies by the novel CENP-A enzyme linked immunosorbent assay (ELISA). Furthermore, ACA were determined in the disease cohorts by IIF (ImmunoConcepts), CENP-B ELISA (Dr. Fooke), EliA(R) CENP (Phadia) and line-immunoassay (LIA, Mikrogen). Serological and clinical associations of anti-CENP-A with other autoantibodies were conducted in one participating centre. Inhibition experiments with either the CENP-A peptide or recombinant CENP-B were carried out to analyse the specificity of anti-CENP-A and -B antibodies. RESULTS: The CENP-A ELISA results were in good agreement with other ACA detection methods. According to the kappa method, the qualitative agreements were: 0.73 (vs. IIF), 0.81 (vs. LIA), 0.86 (vs. CENP-B ELISA) and 0.97 (vs. EliA(R) CENP). The quantitative comparison between CENP-A and CENP-B ELISA using 265 samples revealed a correlation value of rho=0.5 (by Spearman equation). The receiver operating characteristic analysis indicated that the discrimination between SSc patients (n=131) and various controls (n=134) was significantly better using the CENP-A as compared to CENP-B ELISA (p<0.0001). Modified Rodnan skin score was significantly lower in the CENP-A negative group compared to the positive patients (p=0.013). Inhibition experiments revealed no significant cross reactivity of anti-CENP-A and anti-CENP-B antibodies. Statistically relevant differences for gender ratio (p=0.0103), specific joint involvement (Jaccoud) (p=0.0006) and anti-phospholipid syndrome (p=0.0157) between ACA positive SLE patients and the entire SLE cohort were observed. CONCLUSION: Anti-CENP-A antibodies as determined by peptide ELISA represent a sensitive, specific and independent marker for the detection of ACA and are useful biomarkers for the diagnosis of SSc. Our data suggest that anti-CENP-A antibodies are a more specific biomarker for SSc than antibodies to CENP-B. Furthers studies are required to verify these findings.status: publishe
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