1,918 research outputs found

    Immediate effects of microclimate modification enhance native shrub encroachment

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    Shrubs have become more dense and expanded beyond their range all over the world for a variety of reasons including increased temperatures, overgrazing, and alteration of historical fire regime. Native shrubs have been encroaching on Virginia barrier island grasslands for over half a century for unknown reasons. Species composition, soil nutrients, leaf area index (LAI), and ground and air temperature were recorded across the shrub to grass transition and at free-standing shrubs in a coastal grassland in order to determine the effect of shrub encroachment on plant community and microclimate. Species richness was significantly lower inside shrub thickets. Soil water content, organic matter, nitrogen (N), carbon (C), and LAI were higher in shrub thickets and free-standing shrubs compared to grasslands. Summer and fall maximum temperatures were lower and more moderate where shrubs were present. Fall and winter minimum temperatures were highest inside shrub thickets. Native shrubs impact microclimate and species composition immediately upon encroachment. These shrubs lower overall species composition, increase soil nutrients and moisture, moderate summer temperature, and increase winter temperature, which has consequences on a larger scale. As barrier islands are critical for protecting marsh and mainland habitats, understanding this mechanism for shrub expansion is important to predict future encroachment of shrubs and displacement of grassland habitat

    Bostonia: v. 63, no. 3

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    Founded in 1900, Bostonia magazine is Boston University's main alumni publication, which covers alumni and student life, as well as university activities, events, and programs

    Heavy Scalar Top Quark Decays in the Complex MSSM: A Full One-Loop Analysis

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    We evaluate all two-body decay modes of the heavy scalar top quark in the Minimal Supersymmetric Standard Model with complex parameters (cMSSM) and no generation mixing. The evaluation is based on a full one-loop calculation of all decay channels, also including hard QED and QCD radiation. The renormalization of the complex parameters is described in detail. The dependence of the heavy scalar top quark decay on the relevant cMSSM parameters is analyzed numerically, including also the decay to Higgs bosons and another scalar quark or to a top quark and the lightest neutralino. We find sizable contributions to many partial decay widths and branching ratios. They are roughly of O(10%) of the tree-level results, but can go up to 30% or higher. These contributions are important for the correct interpretation of scalar top quark decays at the LHC and, if kinematically allowed, at the ILC. The evaluation of the branching ratios of the heavy scalar top quark will be implemented into the Fortran code FeynHiggs.Comment: 86 pages, 38 figures; minor changes, version published as Phys. Rev. D86 (2012) 03501

    Fast shower simulation in the ATLAS calorimeter

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    The time to simulate pp collisions in the ATLAS detector is largely dominated by the showering of electromagnetic particles in the heavy parts of the detector, especially the electromagnetic barrel and endcap calorimeters. Two procedures have been developed to accelerate the processing time of electromagnetic particles in these regions: (1) a fast shower parameterisation and (2) a frozen shower library. Both work by generating the response of the calorimeter to electrons and positrons with Geant 4, and then reintroduce the response into the simulation at runtime. In the fast shower parameterisation technique, a parameterisation is tuned to single electrons and used later by simulation. In the frozen shower technique, actual showers from low-energy particles are used in the simulation. Full Geant 4 simulation is used to develop showers down to ~1 GeV, at which point the shower is terminated by substituting a frozen shower. Judicious use of both techniques over the entire electromagnetic portion of the ATLAS calorimeter produces an important improvement of CPU time. We discuss the algorithms and their performance in this paper

    Mitigating alemtuzumab-associated autoimmunity in MS: A whack-a-mole B-cell depletion strategy

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    Objective: To determine whether the punctuated administration of low-dose rituximab, temporally linked to B-cell hyperrepopulation (defined when the return of CD19+ B cells approximates 40%-50% of baseline levels as measured before alemtuzumab treatment inception), can mitigate alemtuzumab-associated secondary autoimmunity. Methods: In this hypothesis-driven pilot study, 10 patients received low-dose rituximab (50-150 mg/m2), a chimeric anti-CD20 monoclonal antibody, after either their first or second cycles of alemtuzumab. These patients were then routinely assessed for the development of autoimmune disorders and safety signals related to the use of dual monoclonal antibody therapy. Results: Five patients received at least 1 IV infusion of low-dose rituximab, following alemtuzumab therapy, with a mean follow-up of 41 months. None of the 5 patients developed secondary autoimmune disorders. An additional 5 patients with follow-up over less than 24 months received at least 1 infusion of low-dose rituximab treatment following alemtuzumab treatment. No secondary autoimmune diseases were observed. Conclusions: An anti-CD20 whack-a-mole B-cell depletion strategy may serve to mitigate alemtuzumab-associated secondary autoimmunity in MS by reducing the imbalance in B- and T-cell regulatory networks during immune reconstitution. We believe that these observations warrant further investigation. Classification of evidence: This study provides Class IV evidence that for people with MS, low-dose rituximab following alemtuzumab treatment decreases the risk of alemtuzumab-associated secondary autoimmune diseases

    Eco-efficiency

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    none4openMassari, Stefania; Miglietta, Pier Paolo; De Leo, Federica; Ruberti, MarcelloMassari, Stefania; Miglietta, Pier Paolo; De Leo, Federica; Ruberti, Marcell

    Kynurenic acid as a biochemical factor underlying the association between Western-style diet and depression : a cross-sectional study

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    Consumption of a Western-style diet (WS-diet), high in saturated fat and added sugar, is associated with increased depression risk. However, the physiological mechanisms underlying the relationship requires elucidation. Diet can alter tryptophan metabolism along the kynurenine pathway (KP), potentially linking inflammation and depression. This study aimed to examine whether urinary inflammatory markers and KP metabolites differed according to WS-diet consumption and depression severity. Depression symptoms and habitual WS-diet consumption were assessed in 169 healthy adults aged 17–35 recruited from two experimental studies. Targeted metabolomics profiling of seven KP metabolites, ELISA-based assays of interleukin-6 (IL-6) and C-reactive protein (CRP) were performed using urine samples collected from the participants. Parametric tests were performed for group comparison and associations analysis. Multilevel mixed-effect modelling was applied to control for biases. Higher intake of WS-diet was associated with lower levels of neuroprotective kynurenic acid (KA; R = −0.17, p = 0.0236). There were no differences in IL-6 or CRP across diet groups (p > 0.05). Physical activity had negative associations with most KP metabolites. Mixed-effects regression analysis showed the glutamatergic inhibitor, KA, was the only biomarker to have a significant association with depression symptoms in a model adjusted for demographic and lifestyle variables: a unit increase in KA was associated with 0.21 unit decrease in Depression Anxiety and Stress Scale-21 depression score (p = 0.009). These findings suggest that urinary KA is associated with both habitual WS-diet intake, and levels of depression symptoms, independent of inflammation. Findings support the role of neuroprotection and glutamatergic modulation in depression. We propose that KA may act as endogenous glutamatergic inhibition in regulating depression severity in the absence of inflammation. Further comparison with blood-based markers will assist in validating the utility of non-invasive urine samples for measuring KP metabolites
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