266 research outputs found

    Spatiotemporal Variability in Biomass and Forage Quality Across a Temperate Landscape with Heterogeneous Phenology Patterns (Poster)

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    Although spatial and temporal heterogeneity in grassland biomass and forage quality is well-recognized to play an important role in migratory ungulate population dynamics, attempts to directly quantify biomass and forage quality across temperate landscapes throughout the growing season are limited. It is generally recognized that biomass and forage quality are directly related to phenology, but little is known about how seasonal biomass and forage quality differs across land use and biophysical gradients with varying phenology patterns. This study uses field estimates of biomass, chlorophyll concentration, crude protein, and in vitro dry matter digestibility collected from 20, 250m2 grassland plots throughout the summers of 2013 and 2014 to quantify how biomass and forage quality differ across land uses and biophysical gradients in the migratory elk (Cervus elaphus) range in the Upper Yellowstone River Basin. Key findings were that irrigated agriculture had overall greater and longer available biomass and forage quality throughout the growing season compared to private and public grasslands with natural phenology patterns. And that areas that begin growth later in the season had overall greater biomass and forage quality than areas with mid and early phenology characteristics, but availability was shorter. These results suggest that seasonal patterns of biomass and forage quality differ with phenological characteristics across temperate landscapes. This information should be incorporated in our understanding of spatiotemporal patterns of vegetation important for studying migratory ungulate ecology and predicting the effects of climate change and human land use on vegetation dynamics in temperate landscapes

    Spatial Variation in Distribution and Growth Patterns of Old Growth Strip-Bark Pines

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    Postindustrial rises in CO2 have the potential to confound the interpretation of climatically sensitive tree-ring chronologies. Increased growth rates observed during the 20th century in strip-bark trees have been attributed to CO2 fertilization. Absent in the debate of CO2 effects on tree growth are spatially explicit analyses that examine the proximate mechanisms that lead to changes in rates of tree growth. Twenty-seven pairs of strip-bark and companion entire-bark trees were analyzed in a spatially explicit framework for abiotic environmental correlates. The strip-bark tree locations were not random but correlated to an abiotic proxy for soil moisture. The strip-bark trees showed a characteristic increase in growth rates after about 1875. Furthermore, the difference in growth rates between the strip-bark trees and entire-bark companions increased with increasing soil moisture. A possible mechanism for these findings is that CO2 is affecting water-use efficiency, which in turn affects tree-ring growth. These results point to the importance of accounting for microsite variability in analyzing the potential role of CO2 in governing growth responses

    Method for culturing Candidatus Ornithobacterium hominis.

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    Candidatus Ornithobacterium hominis has been detected in nasopharyngeal microbiota sequence data from around the world. This report provides the first description of culture conditions for isolating this bacterium. The availability of an easily reproducible culture method is expected to facilitate deeper understanding of the clinical significance of this species

    The Ursinus Weekly, April 28, 1978

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    Ursinus news in brief: Fire wakes New Dorm; Muds victorious; Faculty members promoted; Ec student cited; Files accessible; Weekly to change name; Hash bash • Richter outlines proposed changes • Judiciary Board revived • Reaction to Richter encouraging, optimistic • Comment: The Happy days • Letters to the editor: Necessary repair?; Fletcher controversy; Curriculum force in gear; And again; Student comments; Alumni speaks; Staff member reacts • Finally an answer: a modest proposal • Top tunes • Language action group: Dubious privilege • Cub and Key present alumni • Renaissance: Changing with the seasons • Apology • Women\u27s lacrosse cradles to Cape Cod • B-ball banquet • Muds win big • Lacrosse wrap-up • Ursinus track: 3-2 • Widener takes two • Tennis team optimistichttps://digitalcommons.ursinus.edu/weekly/1085/thumbnail.jp

    Risk of COVID-19 after natural infection or vaccination

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    BACKGROUND: While vaccines have established utility against COVID-19, phase 3 efficacy studies have generally not comprehensively evaluated protection provided by previous infection or hybrid immunity (previous infection plus vaccination). Individual patient data from US government-supported harmonized vaccine trials provide an unprecedented sample population to address this issue. We characterized the protective efficacy of previous SARS-CoV-2 infection and hybrid immunity against COVID-19 early in the pandemic over three-to six-month follow-up and compared with vaccine-associated protection. METHODS: In this post-hoc cross-protocol analysis of the Moderna, AstraZeneca, Janssen, and Novavax COVID-19 vaccine clinical trials, we allocated participants into four groups based on previous-infection status at enrolment and treatment: no previous infection/placebo; previous infection/placebo; no previous infection/vaccine; and previous infection/vaccine. The main outcome was RT-PCR-confirmed COVID-19 \u3e7-15 days (per original protocols) after final study injection. We calculated crude and adjusted efficacy measures. FINDINGS: Previous infection/placebo participants had a 92% decreased risk of future COVID-19 compared to no previous infection/placebo participants (overall hazard ratio [HR] ratio: 0.08; 95% CI: 0.05-0.13). Among single-dose Janssen participants, hybrid immunity conferred greater protection than vaccine alone (HR: 0.03; 95% CI: 0.01-0.10). Too few infections were observed to draw statistical inferences comparing hybrid immunity to vaccine alone for other trials. Vaccination, previous infection, and hybrid immunity all provided near-complete protection against severe disease. INTERPRETATION: Previous infection, any hybrid immunity, and two-dose vaccination all provided substantial protection against symptomatic and severe COVID-19 through the early Delta period. Thus, as a surrogate for natural infection, vaccination remains the safest approach to protection. FUNDING: National Institutes of Health

    Inhibiting androgen receptor nuclear entry in castration-resistant prostate cancer

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    Clinical resistance to the second-generation antiandrogen enzalutamide in castration resistant prostate cancer (CRPC), despite persistent androgen receptor (AR) activity in tumors, highlights the unmet medical need for next generation antagonists. We have identified and characterized tetra-aryl cyclobutanes (CBs) as a new class of competitive AR antagonists that exhibit a unique mechanism of action. These CBs are structurally distinct from current antiandrogens (hydroxyflutamide, bicalutamide, and enzalutamide), and inhibit AR-mediated gene expression, cell proliferation, and tumor growth in several models of CRPC. Conformational profiling revealed that CBs stabilize an AR conformation resembling an unliganded receptor. Using a variety of techniques, it was determined that the AR:CB complex was not recruited to AR-regulated promoters and, like apo AR, remains sequestered in the cytoplasm bound to heat shock proteins. Thus, we have identified third generation AR antagonists whose unique mechanism of action suggests that they may have therapeutic potential in CRPC

    HpARI protein secreted by a helminth parasite suppresses interleukin-33

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    Infection by helminth parasites is associated with amelioration of allergic reactivity, but mechanistic insights into this association are lacking. Products secreted by the mouse parasite Heligmosomoides polygyrus suppress type 2 (allergic) immune responses through interference in the interleukin-33 (IL-33) pathway. Here, we identified H. polygyrus Alarmin Release Inhibitor (HpARI), an IL-33-suppressive 26-kDa protein, containing three predicted complement control protein (CCP) modules. In vivo, recombinant HpARI abrogated IL-33, group 2 innate lymphoid cell (ILC2) and eosinophilic responses to Alternaria allergen administration, and diminished eosinophilic responses to Nippostrongylus brasiliensis, increasing parasite burden. HpARI bound directly to both mouse and human IL-33 (in the cytokine's activated state) and also to nuclear DNA via its N-terminal CCP module pair (CCP1/2), tethering active IL-33 within necrotic cells, preventing its release, and forestalling initiation of type 2 allergic responses. Thus, HpARI employs a novel molecular strategy to suppress type 2 immunity in both infection and allergy. Osbourn et al identified HpARI, a protein secreted by a helminth parasite that is capable of suppressing allergic responses. HpARI binds to IL-33 (a critical inducer of allergy) and nuclear DNA, preventing the release of IL-33 from necrotic epithelial cells

    Populist Mobilization: A New Theoretical Approach to Populism*

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/112280/1/j.1467-9558.2011.01388.x.pd
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