56 research outputs found

    Measurement of B(D_s+ -> mu+ nu_mu)/B(D_s+ -> phi mu+ nu_mu) and Determination of the Decay Constant f_{D_s}

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    We have observed 23.2±6.0−0.9+1.023.2 \pm 6.0_{-0.9}^{+1.0} purely-leptonic decays of Ds+−>μ+νμD_s^+ -> \mu^+ \nu_\mu from a sample of muonic one prong decay events detected in the emulsion target of Fermilab experiment E653. Using the Ds+−>ϕμ+νμD_s^+ -> \phi \mu^+ \nu_\mu yield measured previously in this experiment, we obtain B(Ds+−−>μ+νμ)/B(Ds+−−>ϕμ+νμ)=0.16±0.06±0.03B(D_s^+ --> \mu^+ \nu_\mu) / B(D_s^+ --> \phi \mu^+ \nu_\mu) =0.16 \pm 0.06 \pm 0.03. In addition, we extract the decay constant fDs=194±35±20±14MeVf_{D_s}=194 \pm 35 \pm 20 \pm 14 MeV.Comment: 15 pages including one figur

    Contemporary global movement of emerging plant diseases

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    Plant diseases are a significant constraint to agricultural productivity. Exotic plant diseases pose a continued threat to profitable agriculture in the United States. The extent of this threat has increased dramatically in the 1980s and 1990s due to the expansion of international trade in agricultural products and frequent movement of massive volume of people and goods across national boundaries. Introduction of new diseases has not only caused farm losses, but has also diminished export revenue since phytosanitary issues are linked to international commerce. Plant pathogens and their vectors have also moved across national boundaries, sometimes naturally and at other times influenced by the recent changes in trade practices. Sorghum ergot, Karnal bunt of wheat, potato late blight, and citrus tristeza are some of the most recent examples of enhanced importance of diseases due to the introduction of plant pathogens or vectors

    Pathogenic variability in monoconidial isolates of the sorghum anthracnose fungus Colletotrichum graminicola from single lesions and from monoconidial cultures.

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    A patogenidade de culturas c sub-culturas monospóricas de Colletotrichum graminicola obtidas de uma única lesão c de isolamentos monospóricos das cultivares de sorgo Tx623 e SC748-5 foi avaliada em 5 cultivares diferenciadoras. Isolados foram separados em diferentes fenótipos de virulência, indicando a ocorrência de instabilidade patogenica em isolados deste patógeno. Reversão de um estado de virulência para um de virulência foi observada para alguns isolados.199

    Registration of Tx2935 through Tx2944 Sorghum Germplasm

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    Registration of 16 Sorghum Germplasm Lines

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    Relations among sorghum ergot strains from the United States, Mexico, Puerto Rico, Bolivia, India and Australia

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    Sorghum ergot, initially restricted to Asia and Africa, was recently found in the Americas and Australia. Three species causing the disease have been reported: Claviceps sorghi in India, C. sorghicola in Japan, and C. africana in all ergot-positive countries. The objective of our study was to study the intraspecific variation in C. africana isolates in the Americas, Africa, India, and Australia. We confirmed C. africana, C. sorghi, and C. sorghicola as different species using differences in nucleotide sequences of internal transcribed spacer 1 and 5.8S rDNA regions. Sequences of this region obtained from the representative American, Indian, and Australian isolates of C. africana were identical. In addition, random amplified polymorphic DNA (RAPD) banding patterns of sorghum ergot pathogen isolates from the United States, Mexico, Puerto Rico, Bolivia, Australia, and India were evaluated with nearly 100 primers. A total of 65 primers gave identical patterns for all isolates, which confirmed that all were C. africana. The identity of RAPD pattern and rDNA sequence of Indian isolates with those of C. africana confirmed that the species is now present in India. Only 20 primers gave small pattern differences and 7 of them were used for routine testing. All of the American isolates were identical and three isolates of the same type were also found in South Africa, suggesting Africa as the origin of the invasion clone in the Americas. Australian and Indian isolates were distinguishable by a single band difference; therefore, migration from the Asian region to Australia is suspected. Another distinct group was found in Africa. Cluster analysis of the informative bands revealed that the American and African group are on the same moderately (69%) supported clade. Isolates from Australia and India belonged to another clade
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