25 research outputs found

    Rare and Endangered Vetebrates of Ohio

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    Author Institution: U.S. Soil Conservation Service; Introductory Biology Program, The Ohio State University; School of Natural Resources, The Ohio State University; and Division of Wildlife, Ohio Department of Natural ResourcesThis paper, an annotated list of Ohio's rare and endangered vertebrate species, was compiled to supplement a similar national list and includes 10 mammals, 62 birds, 10 reptiles, 4 amphibians, and 33 fishes. Where possible, suggestions are made both as to causes of the rare or endangered status of these species and as to means of halting the trend. Ratings of endangered, rare, peripheral, or undetermined, as defined for the national classification, are given for each species

    Life History and Habits of the Cicada Killer in Ohio

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    Author Institution: Soil Conservation Servic

    Diffractive Production of bbˉb \bar b in Proton - Antiproton Collision at the Tevatron

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    We show that the cross section of the diffractive production of bbˉb \bar b can be described as the sum of two contributions: the first is proportional to the probability of finding a small size bbˉb \bar b color dipole in the fast hadron wave function before the interaction with a target, while the second is the bbˉb \bar b-production after or during the interaction with the target. The formulae are presented as well as the discussion of the interralation between these two contributions and the Ingelman- Schlein and coherent diffraction mechanisms. The main precdition is that the coherent diffraction mechanism dominates at least at the Tevatron Energies, giving the unique possibility to study it experimentally.Comment: 23 pages, 10 figures, latex fil

    Modulating Vascular Hemodynamics With an Alpha Globin Mimetic Peptide (HbαX)

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    The ability of hemoglobin to scavenge the potent vasodilator nitric oxide (NO) in the blood has been well established as a mechanism of vascular tone homeostasis. In endothelial cells, the alpha chain of hemoglobin (hereafter, alpha globin) and endothelial NO synthase form a macromolecular complex, providing a sink for NO directly adjacent to the production source. We have developed an alpha globin mimetic peptide (named HbαX) that displaces endogenous alpha globin and increases bioavailable NO for vasodilation. Here we show that, in vivo, HbαX administration increases capillary oxygenation and blood flow in arterioles acutely and produces a sustained decrease in systolic blood pressure in normal and angiotensin II-induced hypertensive states. HbαX acts with high specificity and affinity to endothelial NO synthase, without toxicity to liver and kidney and no effect on p50 of O binding in red blood cells. In human vasculature, HbαX blunts vasoconstrictive response to cumulative doses of phenylephrine, a potent constricting agent. By binding to endothelial NO synthase and displacing endogenous alpha globin, HbαX modulates important metrics of vascular function, increasing vasodilation and flow in the resistance vasculature
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