628 research outputs found

    The Veneziano amplitude in AdS5×_5 \timesS3^3 from an 8-dimensional effective action

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    We study four-point functions of arbitrary half-BPS operators in a 4-dimensional N=2\mathcal{N}=2 SCFT with flavour group SO(8)SO(8) at genus-zero and strong 't Hooft coupling, corresponding - via AdS/CFT - to the (α′\alpha' expansion of the) Veneziano amplitude on an AdS5×_5 \timesS3^3 background. We adapt a procedure first proposed by Abl, Heslop and Lipstein in the context of AdS5×_5 \timesS5^5, and postulate the existence of an effective action in terms of an 88-dimensional scalar field valued in the adjoint of the flavour group. The various Kaluza-Klein correlators can then be computed by uplifting the standard AdS/CFT prescription to the full product geometry with AdS bulk-to-boundary propagators and Witten diagrams replaced by suitable AdS5×_5 \timesS3^3 versions. After elucidating the main features of the procedure, valid at all orders in α′\alpha', we show explicit results up to order α′5\alpha'^{5}. The results provide further evidence of a novel relation between AdS×\timesS and flat amplitudes - which made its first appearance in N=4\mathcal{N}=4 SYM - that is perhaps the most natural extension of the well known flat-space limit proposed by Penedones to cases where AdS and S have the same radius.Comment: 34 page

    BCJ relations in AdS5×S3{AdS}_5 \times S^3 and the double-trace spectrum of super gluons

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    We revisit the four-point function of super gluons in AdS5×S3AdS_5 \times S^3 in the spirit of the large pp formalism and show how the integrand of a generalised Mellin transform satisfies various non-trivial properties such as U(1)U(1) decoupling identity, BCJ relations and colour-kinematic duality, in a way that directly mirrors the analogous relations in flat space. We unmix the spectrum of double-trace operators at large NN and find all anomalous dimensions at leading order. The anomalous dimensions follow a very simple pattern, resembling those of other theories with hidden conformal symmetries.Comment: 9 page

    Evolución de los ácidos grasos en el mesocarpo del níspero (Mespilus germanica. L.) a diferentes estados de maduración

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    The fatty acid composition of medlar (Mespilus germanica L.) varied significantly among the ripening stages sampled at 157, 172 and 187 DAFs (days after full bloom). Twenty-one different fatty acids were detected in preclimacteric fruit and 17 when the climacteric began. Principal fatty acids, determined in medlar fruit harvested from October (157 and 172 DAFs) to November (187 DAF) were mainly palmitic acid (16:0), linoleic acid (18:2n-6), and a-linolenic acid (18:3n-3). While the content of saturated fatty acids [palmitic acid (16:0) and stearic acid (18:0)] increased, the content of the essential polyunsaturated fatty acids [linoleic acid (18:2n-6) and linolenic acid (18:3n-3)] decreased through ripening, in parallel with pulp darkening. The percentage of linoleic acid and a-linolenic acid in ripe, hard fruits was 60.0 and 13.5 % of dry wt at 157 DAF which decreased throughout ripening, remaining at 28.7 and 5.6 % of dry wt, respectively, in the fully softened and darkened pulp. A marked decreases in the double bond index, percentage of unsaturation and the ratio of unsaturation/saturation were also seen throughout the medlar ripening. The contribution of unsaturated fatty acid to the total fatty acid content decreased markedly as the medlar fruit became progressively softer and darkened.La composición en ácidos grasos del níspero (Mespilus germanica L.) varió significativamente entre los estados de maduración muestreados a los 157, 172 y 187 DAFs (días después de la floración). Veinte y un ácidos grasos diferentes fueron detectados en el fruto preclimatérico y 17 cuando comenzó el climaterio. Los ácidos grasos principales encontrados en nísperos, recolectados desde Octubre (157 y 172 DAFs) hasta Noviembre (187 DAF), fueron principalmente ácido palmítico (16:0), ácido linoléico (18:2n-6), y ácido a-linolénico (18:3n-3). En tanto que el contenido en ácidos grasos saturados (ácido palmítico (16:0) y ácido esteárico (18:0)) aumentó, el contenido en ácidos grasos esenciales (ácido linoleico (18:2n-6) y ácido linolénico (18:3n-6)) disminuyó durante la maduración, en paralelo con el oscurecimiento de la pulpa. El porcentaje de ácido linoleico y de ácido a-linolénico en frutos maduros sin reblandecer fue de 60.0 y 13.5 % del peso seco a 157 DAF, disminuyendo durante la maduración, y permaneciendo a 28.7 y 56 % del peso seco, respectivamente, en la pulpa completamente blanda y oscura. También se observó durante la maduración del níspero una marcada disminución en el número de dobles enlaces, en el tanto por ciento de instauración y en la relación instauración / saturación. La contribución de los ácidos grasos insaturados al contenido de ácidos grasos totales disminuyó marcadamente cuando el níspero comenzó progresivamente a reblandecerse y oscurecerse

    Phase angle correlates with n-3 fatty acids and cholesterol in red cells of Nigerian children with sickle cell disease

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    OBJECTIVE: To determine the cholesterol content and fatty acid composition of red cell membrane phospholipids (PL) of children with sickle cell disease (SCD) and to correlate these levels with whole body phase angle that is related to the integrity and function of cell membranes. STUDY DESIGN: Blood samples were obtained from 69 children with SCD and 72 healthy age- and gender-matched controls in Nigeria for the determination of the cholesterol content and proportions of fatty acids in red cell PL. Bioelectrical impedance analysis was used to obtain resistance (R) and reactance (Xc) from which phase angle was calculated as arctan Xc/R. Cholesterol (normalized to lipid phosphorus) and the proportions of individual fatty acids were correlated with phase angle. RESULTS: The proportions of palmitic (p < 0.001), stearic acid (p = 0.003) and cholesterol (p < 0.001) were significantly higher in the red cells of children with SCD, whereas the proportions of arachidonic acid and docosahexaenoic acid were reduced (p = 0.03 and < 0.001, respectively) compared to controls. The phase angle was inversely correlated with the proportions of palmitic acid (p = 0.03) and oleic acid (p < 0.001) and cholesterol (p = 0.003). Three n-3 polyunsaturated fatty acids-eicosapentaenoic acid, docosapentaenoic acid and docosahexaenoic acid- were positively correlated with phase angle (p < 0.001). CONCLUSIONS: The fatty acid composition and cholesterol content of tissue membranes in SCD correlate with the phase shift measured by bioelectrical impedance analysis. Phase angle measurements may provide a non-invasive method for monitoring interventions aimed at altering the lipid composition of membranes

    Towards A Microgrid Based Residential Home Energy Management Using Genetic Algorithm

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    This paper proposes a load scheduling approach for a residential home in an islanded PV microgrid scenario based on a Genetic Algorithm (GA). The primary aim is to inform on how a Demand Side Management (DSM) could reduce the capital cost of the residential home energy use and operational cost of the microgrid by minimizing the use of fossil fuel generator. The research study proposes and describes the design for load allocation to achieve utilization of solar PV resources optimally. The proposed scheme is based on the time-of-use (TOU) and improvement of electricity users' comfort. The demonstration of the concept is presented and discussed based on a single smart home scenario using a solar PV microgrid and battery in a rural community of Enugu State, Nigeria

    Lymph node homing cells biologically enriched for γδ T cells express multiple genes from the T19 repertoire

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    Sheep γδ T cells have been shown serologically to express T19, a membrane protein of 180-200 kDa which is a member of the scavenger receptor superfamily. Previous work from this laboratory resulted in the detection of a multigene family of T19-like genes in the sheep genome. In this study nucleotide sequences from several T19 genes were determined and are reported along with the corresponding segments of a number of expressed mRNA molecules. A segment of a single sheep T19-like gene was sequenced and these data, along with the corresponding sequences from cloned T19-like cDNA molecules from sheep and cow, were used to design an ollgonucleotide primer system suitable for amplification of corresponding segments of many T19 genes and their cDNAs. Between 30 and 40% of cloned T19 genes were amenable to amplification using the selected primers, and sequence analysis of cloned PCR products confirmed that different T19 genes encode unique amino acid sequences. The expression of multiple T19 genes was established using cDNA molecules obtained from a single sample of sheep lymphocyte mRNA. The possible role of the T19 family of genes is discusse

    The Genomic Diversity and Phylogenetic Relationship in the Family Iridoviridae

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    The Iridoviridae family are large viruses (∼120–200 nm) that contain a linear double-stranded DNA genome. The genomic size of Iridoviridae family members range from 105,903 bases encoding 97 open reading frames (ORFs) for frog virus 3 to 212,482 bases encoding 211 ORFs for Chilo iridescent virus. The family Iridoviridae is currently subdivided into five genera: Chloriridovirus, Iridovirus, Lymphocystivirus, Megalocytivirus, and Ranavirus. Iridoviruses have been found to infect invertebrates and poikilothermic vertebrates, including amphibians, reptiles, and fish. With such a diverse array of hosts, there is great diversity in gene content between different genera. To understand the origin of iridoviruses, we explored the phylogenetic relationship between individual iridoviruses and defined the core-set of genes shared by all members of the family. In order to further explore the evolutionary relationship between the Iridoviridae family repetitive sequences were identified and compared. Each genome was found to contain a set of unique repetitive sequences that could be used in future virus identification. Repeats common to more than one virus were also identified and changes in copy number between these repeats may provide a simple method to differentiate between very closely related virus strains. The results of this paper will be useful in identifying new iridoviruses and determining their relationship to other members of the family
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