3,208 research outputs found

    Enhancement of the Dark Matter Abundance Before Reheating: Applications to Gravitino Dark Matter

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    In the first stages of inflationary reheating, the temperature of the radiation produced by inflaton decays is typically higher than the commonly defined reheating temperature TRH(ΓϕMP)1/2T_{RH} \sim (\Gamma_\phi M_P)^{1/2} where Γϕ\Gamma_\phi is the inflaton decay rate. We consider the effect of particle production at temperatures at or near the maximum temperature attained during reheating. We show that the impact of this early production on the final particle abundance depends strongly on the temperature dependence of the production cross section. For σvTn/Mn+2\langle \sigma v \rangle \sim T^n/M^{n+2}, and for n<6n < 6, any particle produced at TmaxT_{\rm max} is diluted by the later generation of entropy near TRHT_{RH}. This applies to cases such as gravitino production in low scale supersymmetric models (n=0n=0) or NETDM models of dark matter (n=2n=2). However, for n6n\ge6 the net abundance of particles produced during reheating is enhanced by over an order of magnitude, dominating over the dilution effect. This applies, for instance to gravitino production in high scale supersymmetry models where n=6n=6.Comment: 16 pages, 5 figure

    Post-Inflationary Gravitino Production Revisited

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    We revisit gravitino production following inflation. As a first step, we review the standard calculation of gravitino production in the thermal plasma formed at the end of post-inflationary reheating when the inflaton has completely decayed. Next we consider gravitino production prior to the completion of reheating, assuming that the inflaton decay products thermalize instantaneously while they are still dilute. We then argue that instantaneous thermalization is in general a good approximation, and also show that the contribution of non-thermal gravitino production via the collisions of inflaton decay products prior to thermalization is relatively small. Our final estimate of the gravitino-to-entropy ratio is approximated well by a standard calculation of gravitino production in the post-inflationary thermal plasma assuming total instantaneous decay and thermalization at a time t1.2/Γϕt \simeq 1.2/\Gamma_\phi. Finally, in light of our calculations, we consider potential implications of upper limits on the gravitino abundance for models of inflation, with particular attention to scenarios for inflaton decays in supersymmetric Starobinsky-like models.Comment: 34 pages, 7 figures, uses psfra

    Analysis of the biofilm proteome of Xylella fastidiosa

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    <p>Abstract</p> <p>Background</p> <p><it>Xylella fastidiosa </it>is limited to the xylem of the plant host and the foregut of insect vectors (sharpshooters). The mechanism of pathogenicity of this bacterium differs from other plant pathogens, since it does not present typical genes that confer specific interactions between plant and pathogens (avr and/or hrp). The bacterium is injected directly into the xylem vessels where it adheres and colonizes. The whole process leads to the formation of biofilms, which are considered the main mechanism of pathogenicity. Cells in biofilms are metabolically and phenotypically different from their planktonic condition. The mature biofilm stage (phase of higher cell density) presents high virulence and resistance to toxic substances such as antibiotics and detergents. Here we performed proteomic analysis of proteins expressed exclusively in the mature biofilm of <it>X. fastidiosa </it>strain 9a5c, in comparison to planktonic growth condition.</p> <p>Results</p> <p>We found a total of 456 proteins expressed in the biofilm condition, which correspond to approximately 10% of total protein in the genome. The biofilm showed 37% (or 144 proteins) different protein than we found in the planktonic growth condition. The large difference in protein pattern in the biofilm condition may be responsible for the physiological changes of the cells in the biofilm of <it>X. fastidiosa</it>. Mass spectrometry was used to identify these proteins, while real-time quantitative polymerase chain reaction monitored expression of genes encoding them. Most of proteins expressed in the mature biofilm growth were associated with metabolism, adhesion, pathogenicity and stress conditions. Even though the biofilm cells in this work were not submitted to any stress condition, some stress related proteins were expressed only in the biofilm condition, suggesting that the biofilm cells would constitutively express proteins in different adverse environments.</p> <p>Conclusions</p> <p>We observed overexpression of proteins related to quorum sensing, proving the existence of communication between cells, and thus the development of structuring the biofilm (mature biofilm) leading to obstruction of vessels and development of disease. This paper reports a first proteomic analysis of mature biofilm of <it>X. fastidiosa</it>, opening new perspectives for understanding the biochemistry of mature biofilm growth in a plant pathogen.</p

    Nutritional reserves of Vochysiaceae seeds: chemical diversity and potential economic uses

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    Contents of proteins, carbohydrates and oil of seeds of 57 individuals of Vochysiaceae, involving one species of Callisthene, six of Qualea, one of Salvertia and eight of Vochysia were determined. The main nutritional reserves of Vochysiaceae seeds are proteins (20% in average) and oils (21. 6%). Mean of carbohydrate contents was 5. 8%. Callisthene showed the lowest protein content (16. 9%), while Q. cordata was the species with the highest content (30% in average). The contents of ethanol soluble carbohydrates were much higher than those of water soluble carbohydrates. Oil contents lay above 20% for most species (30. 4% in V. pygmaea and V. pyramidalis seeds). The predominant fatty acids are lauric (Q. grandiflora), oleic (Qualea and Salvertia) or acids with longer carbon chains (Salvertia and a group of Vochysia species). The distribution of Vochysiaceae fatty acids suggests for seeds of some species an exploitation as food sources (predominance of oleic acid), for other species an alternative to cocoa butter (high contents or predominance of stearic acid) or the production of lubricants, surfactants, detergents, cosmetics and plastic (predominance of acids with C20 or C22 chains) or biodiesel (predominance of monounsaturated acids). The possibility of exploitation of Vochysiaceae products in a cultivation regimen and in extractive reserves is discussed.Teores de proteínas, carboidratos solúveis e óleos de sementes de 57 indivíduos de Vochysiaceae, compreendendo uma espécie de Callisthene, seis de Qualea, uma de Salvertia e oito de Vochysia foram determinados. As principais reservas de sementes de Vochysiaceae são proteínas (20% em média) e óleos (21, 6%). A média dos teores de carboidratos foi de 5, 8%. Callisthene apresentou o mais baixo teor de proteínas (16, 9%), enquanto Q. cordata foi a espécie com o mais elevado teor (30% em média). Teores de carboidratos solúveis em etanol foram muito superiores aos solúveis em água. Os teores de óleo foram superiores a 20% na maioria das espécies (30, 4% em V. pygmaea e V. pyramidalis). Ácidos graxos predominantes foram láurico (Q. grandiflora), oleico (Qualea e Salvertia) ou ácidos com cadeias mais longas (Salvertia e um grupo de espécies de Vochysia). A distribuição de ácidos graxos de Vochysiaceae sugere para as sementes de algumas espécies o uso em alimentação (predominância de ácido oléico), para outras, uma alternativa à manteiga de cacau (teores elevadosde ácido esteárico) ou produção de lubrificantes, tensoativos, detergentes, cosméticos e plásticos (predominância de ácidoscom cadeias C20 ou C22) ou biodiesel (predominância de ácidos monoinsaturados). Discute-se a possibilidade de aproveitamento de produtos de Vochysiaceae em regime de cultivo eem reservas extrativas.Conselho Nacional do Desenvolvimento Científico e Tecnológico (CNPq

    MOLYBDENUM CATALYZED ACID PEROXIDE BLEACHING OF EUCALYPTUS KRAFT PULP

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    Molybdenum catalyzed peroxide bleaching (PMo Stage) consists of pulp treatment with hydrogen peroxide under acidic conditions in the presence of a molybdenum catalyst. Molybdenum is applied in catalytic doses (50-200 mg/kg pulp) and may originate from various sources, including (NH4)6Mo7O24.4H2O, Na2MoO4.2H2O, siliconmolybdate, etc. This work is aimed at optimizing the PMo stage and evaluating its industrial application in the OAZDP sequence. Optimum PMo stage conditions for bleaching eucalyptus pulp were 90 ºC, pH 3.5, 2 h, 0.1 kg/adt Mo and 5 kg/adt H2O2. The PMo stage was more efficient to remove pulp hexenuronic acids than lignin. Its efficiency decreased with increasing pH in the range of 1.5-5.5, while it increased with increasing temperature and peroxide and molybdenum doses. The application of the PMo stage as replacement for the A-stage of the AZDP sequence significantly decreased chlorine dioxide demand. The PMo stage caused a decrease of 20-30% in the generation of organically bound chlorine. The quality parameters of the pulp produced during the PMo stage mill trial were comparable to those obtained with the reference A-stage

    Intelligent Fusion of Structural and Citation-Based Evidence for Text Classification

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    This paper investigates how citation-based information and structural content (e.g., title, abstract) can be combined to improve classification of text documents into predefined categories. We evaluate different measures of similarity, five derived from the citation structure of the collection, and three measures derived from the structural content, and determine how they can be fused to improve classification effectiveness. To discover the best fusion framework, we apply Genetic Programming (GP) techniques. Our empirical experiments using documents from the ACM digital library and the ACM classification scheme show that we can discover similarity functions that work better than any evidence in isolation and whose combined performance through a simple majority voting is comparable to that of Support Vector Machine classifiers

    Electrochemical and electrochromic properties of poly(4,4 dimethoxy 3'-methyl 2,2':5',2 terthiophene)

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    This work describes the electrochemical, spectroelectrochemical and electrochromic properties of poly(4,4 dimethoxy 3'-methyl 2,2':5',2 terthiophene) thin films. The effect of temperature on the electropolymerization was studied by cyclic voltammetry measured in situ. The temperatures used were -10, 0, 10, 20, and 40 ºC. Results indicate that the electropolymerization temperature directly affect the degree of chain organization. The optical response time for bleaching was 0.8 s and for coloring 0.3 s (for films synthesized at 40 ºC, 60 nm thick). After 1400 electrochromic cycles, the chromatic contrast at 570 nm changes from 31 to 14%. The coloration efficiency was enhanced as a function of redox cycling. This was probably caused by a decrease in the injected charge necessary for the color change, suggesting that the electroactive losses occurring during the cycles are related to sites not responsible for electrochromic contrast.Este trabalho descreve o estudo das propriedades eletroquímicas, espectroeletroquímicas e eletrocrômicas de filmes finos de poli(4,4 dimetoxi 3'-metil 2,2':5',2 tertiofeno). A voltametria cíclica in situ foi usada para estudar o efeito da temperatura sobre a eletropolimerização. As temperaturas utilizadas na deposição eletroquímica foram -10, 0, 10, 20 e 40 ºC. Os resultados indicaram que a temperatura de eletropolimerização afeta diretamente o grau de ordenamento molecular do polímero. O tempo de resposta eletrocrômico foi de 0,8 s para clareamento e 0,3 s para escurecimento (para filmes sintetizados a 40 ºC, espessura de 60 nm). Após 1400 ciclos eletrocrômicos, o contraste óptico a 570 nm diminuiu de 31 para 14%. A eficiência eletrocrômica foi intensificada em função do número de ciclos eletrocrômicos. Este fato foi provavelmente causado pela diminuição da carga injetada, necessária para a mudança de cor, sugerindo que as perdas na eletroatividade estão associadas a sítios que não são responsáveis pela mudança de coloração.733738Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES
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