5,697 research outputs found

    The Daugavet equation for operators not fixing a copy of C(S)C(S)

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    We prove the norm identity ∥Id+T∥=1+∥T∥\|Id+T\| = 1+\|T\|, which is known as the Daugavet equation, for operators TT on C(S)C(S) not fixing a copy of C(S)C(S), where SS is a compact metric space without isolated points

    Climate Change Research in View of Bibliometrics

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    This bibliometric study of a large publication set dealing with research on climate change aims at mapping the relevant literature from a bibliometric perspective and presents a multitude of quantitative data: (1) The growth of the overall publication output as well as (2) of some major subfields, (3) the contributing journals and countries as well as their citation impact, and (4) a title word analysis aiming to illustrate the time evolution and relative importance of specific research topics. The study is based on 222,060 papers published between 1980 and 2014. The total number of papers shows a strong increase with a doubling every 5-6 years. Continental biomass related research is the major subfield, closely followed by climate modeling. Research dealing with adaptation, mitigation, risks, and vulnerability of global warming is comparatively small, but their share of papers increased exponentially since 2005. Research on vulnerability and on adaptation published the largest proportion of very important papers. Research on climate change is quantitatively dominated by the USA, followed by the UK, Germany, and Canada. The citation-based indicators exhibit consistently that the UK has produced the largest proportion of high impact papers compared to the other countries (having published more than 10,000 papers). The title word analysis shows that the term climate change comes forward with time. Furthermore, the term impact arises and points to research dealing with the various effects of climate change. Finally, the term model and related terms prominently appear independent of time, indicating the high relevance of climate modeling.Comment: 40 pages, 6 figures, and 4 table

    Introducing CitedReferencesExplorer (CRExplorer): A program for Reference Publication Year Spectroscopy with Cited References Standardization

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    We introduce a new tool - the CitedReferencesExplorer (CRExplorer, www.crexplorer.net) - which can be used to disambiguate and analyze the cited references (CRs) of a publication set downloaded from the Web of Science (WoS). The tool is especially suitable to identify those publications which have been frequently cited by the researchers in a field and thereby to study for example the historical roots of a research field or topic. CRExplorer simplifies the identification of key publications by enabling the user to work with both a graph for identifying most frequently cited reference publication years (RPYs) and the list of references for the RPYs which have been most frequently cited. A further focus of the program is on the standardization of CRs. It is a serious problem in bibliometrics that there are several variants of the same CR in the WoS. In this study, CRExplorer is used to study the CRs of all papers published in the Journal of Informetrics. The analyses focus on the most important papers published between 1980 and 1990.Comment: Accepted for publication in the Journal of Informetric

    Dose-response relationship and low dose extrapolatioin in chemical carcinogenesis

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    Data supporting various dose-response relationships in chemical carcinogenesis are summarized. General principles are derived to explain the relationships between exposure dose, DNA adduct level, induction of genetic changes, and tumor incidence. Some mechanistic aspects of epigenetic carcinogens (stimulation of cell division and maldifferentiation) are analyzed in a similar way. In a homogeneous population, non-linearities are frequent. They are due to phenomena of induction or saturation of enzymatic activities and to the multi-step nature of carcinogenesis: if a carcinogen accelerates more than one step, the superposition of the dose-response curves for the individual steps can result in an exponential relationship. A fourth power of the dose was the maximum seen in animals (formaldehyde). At the lowest dose levels, a proportionality between dose and tumor induction is postulated independent of the mechanism of action if the carcinogen accelerates the endogenous process responsible for spontaneous tumor formation. Low-dose thresholds are expected only for situations where the carcinogen acts in a way that has no endogenous counterpart. Epidemlological studies in humans show linear dose-response curves in all but two investigations. The difference from the strongly non-linear slopes seen in animal studies could be due to the heterogeneity of the human population: if the individual sensitivity to a carcinogen is governed by a large number of genetic and life-style factors, the non-linearities will tend to cancel each other out and the dose-response curve becomes ‘quasi-linear
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