Generation of long-living entanglement using cold trapped ions with pair cat states

With the reliance in the processing of quantum information on a cold trapped ion, we analyze the entanglement entropy in the ion-field interaction with pair cat states. We investigate a long-living entanglement allowing the instantaneous position of the center-of-mass motion of the ion to be explicitly time dependent. An analytic solution for the system operators is obtained. We show that different nonclassical effects arise in the dynamics of the population inversion, depending on the initial states of the vibrational motion. We study in detail the entanglement degree and demonstrate how the input pair cat state is required for initiating the long living entanglement. This long living entanglement is damp out with an increase in the number difference $q$. Owing to the properties of entanglement measures, the results are checked using another entanglement measure (high order linear entropy).Comment: 15 pages, 7 figures, Sub. Appl. Phys. B: Laser and Optic

Evolution of a pathogen population in host mixtures : simple race - complex race competition.

International audienc

Evolution of a pathogen population in host mixtures : rate of emergence of complex races

International audienc

Identification of common bean alleles resistant to anthracnose using RAPD

RAPD markers were identified close to common bean alleles responsible for resistance to the fungus Colletotrichum lindemuthianum and may be useful in selecting plants resistant to this pathogen. DNA from F2 plants of the crosses Carioca 300V x P45, Carioca 300V x Ouro and P24 x Ouro was amplified by RAPD. Line P45 has the Co.4 allele for resistance, and the Ouro cultivar has the Co.5 allele. The primer OPC08 amplified a DNA fragment of about 1059 bp linked to the Co.4 allele. The recombination frequency was 0.133 (SE = 0.039; 95% CI = 0.056-0.211). Using the primer OPF10 a DNA fragment of about 912 bp was amplified and found to be associated with the Co.5 allele. The recombination frequency was 0.115 (SE = 0.038; 95% CI = 0.041-0.189). A second marker (1122 pb) amplified by the OPR03 primer was identified in the population P24 x Ouro. The recombination frequency for this marker was 0.363 (SE = 0.081; 95% CI = 0.205-0.522). Both these markers flanked the Co.5 allele. The markers identified in this study may be useful in identifying lines with the Co.4 and Co.5 alleles.<br>Marcadores RAPD foram identificados próximos de alelos do feijão responsáveis pela resistência ao Colletotrichum lindemuthianum, visando auxiliar na seleção de plantas resistentes ao patógeno. Empregou-se o método dos bulks segregantes de DNA extraídos de plantas F2 dos seguintes cruzamentos: Carioca 300V x P45, Carioca 300V x Ouro e P24 x Ouro. A linhagem P45 é portadora do alelo Co.4 de resistência e o cultivar Ouro é portador do alelo Co.5, os quais foram marcados. Procedeu-se à reação RAPD dos bulks e foi identificado o iniciador OPC08 que amplificou um fragmento de DNA com cerca de 1059 pb, ligado ao alelo Co.4. A freqüência de recombinação foi de 0,133 (erro padrão 0,039) e o intervalo de confiança foi 0,056 e 0,211, com 95% de probabilidade. Em relação ao alelo Co.5 foi identificado um fragmento de DNA amplificado pelo iniciador OPF10 com cerca de 912 pb, na análise dos bulks provenientes dos cruzamentos Carioca 300V x Ouro e P24 x Ouro. A freqüência de recombinação foi de 0,115 (erro padrão 0,038) e o intervalo de confiança foi 0,041 e 0,189. Um segundo marcador foi identificado a partir da análise da população P24 x Ouro, resultante da amplificação pelo iniciador OPR03, e possui cerca de 1122 pb. A freqüência de recombinação foi 0,363 (erro padrão 0,081) e o intervalo de confiança variou de 0,205 a 0,522. Constatou-se que esses dois marcadores estão flanqueando o alelo Co.5 e a seleção de plantas resistentes de uma população F2 por meio dos marcadores será eficiente em 83% dos casos

The effect of potato variety mixtures on epidemics of late blight, in relation to plot size and level of resistance

Potatoes of a number of varieties of contrasting levels of resistance were planted in pure or mixed stands in four experiments over 3 years. Three experiments compared the late blight severity and progress in mixtures with that in pure stands. Disease on susceptible or moderately resistant varieties typical of those in commercial use was similar in mixtures and pure stands. In 2 of 3 years, there were slight reductions on cv. Sante, which is moderately susceptible, in mixture with cv. Cara, which is moderately resistant. Cara was unaffected by this mixture. Mixtures of an immune or near-immune partner with Cara or Sante substantially reduced disease on the latter. The effect of the size of plots of individual varieties or mixtures on blight severity was compared in two experiments. Larger plots had a greater area under the disease progress curve, but the average rate of disease progress was greater in smaller plots; this may be because most disease progress took place later, under more favourable conditions, in the smaller plots. In one experiment, two planting densities were used. Density had no effect on disease and did not interact with mixture effects. The overall conclusion is that, while mixtures of potato varieties may be desirable for other reasons, they do not offer any improvement on the average of the disease resistance of the components