325 research outputs found

    Historical biogeography of the squids from the family Loliginidae (Teuthoidea: Myopsida)

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    Indexación: Scopus.According to the vicariant hypothesis proposed by Brakoniecki (1986) the closure of the Sea of Tethys and the opening of the Atlantic Ocean would play an important role in the history of squids of the family Loliginidae, which is reflected in its current neritic distribution. Our study evaluated this hypothesis and alternative ideas to understand the historical biogeography of loliginid squids. This work is based on a phylogenetic hypothesis rebuilt with mitochondrial and nuclear sequences that incorporates the estimation of divergence times and ancestral distribution. Our results sustain that the squids of the family Loliginidae would have originated in the Western Pacific during the Late Paleocene about 59 My, following, during their diversification, at least 20 dispersion and 6 vicariant events. The first vicariant event fragments the ancestral distribution, remaining the ancestor of Sepioteuthis in the south and the subfamily Loligininae in the north. Successive events of dispersion, and some of vicariance (unrelated with the movement of tectonic plates and opening of the Atlantic Ocean), modeled it distribution. Our inference suggest a different origin compared to proposed by Brakoniecki (Tethys Sea), consistent with a center of origin that supports the most diversity of the family, with a predominance of dispersion processes over vicariant events, which explain the present distribution pattern.http://www.lajar.cl/pdf/imar/v45n1/Art%C3%ADculo_45_1_11.pd

    Generalized Brans-Dicke cosmology in the presence of matter and dark energy

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    We study the Generalized Brans-Dicke cosmology in the presence of matter and dark energy. Of particular interest for a constant Brans-Dicke parameter, the de Sitter space has also been investigated.Comment: 9 page

    Body mass index, but not FTO genotype or major depressive disorder, influences brain structure

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    Obesity and major depressive disorder (MDD) are highly prevalent and often comorbid health conditions. Both are associated with differences in brain structure and are genetically influenced. Yet, little is known about how obesity, MDD, and known risk genotypes might interact in the brain. Subjects were 81 patients with MDD (mean age 48.6 years) and 69 matched healthy controls (mean age 51.2 years). Subjects underwent 1.5T magnetic resonance imaging, genotyping for the fat mass and obesity associated (FTO) gene rs3751812 polymorphism, and measurements for body mass index (BMI). We conducted a whole brain voxelwise analysis using tensor-based morphometry (TBM) to examine the main and interaction effects of diagnosis, BMI and FTO genotype. Significant effects of BMI were observed across widespread brain regions, indicating reductions in predominantly subcortical and white matter areas associated with increased BMI, but there was no influence of MDD or FTO rs3751812 genotype. There were no significant interaction effects. Within MDD patients, there was no effect of current depressive symptoms; however the use of antidepressant medication was associated with reductions in brain volume in the frontal lobe and cerebellum. Obesity affects brain structure in both healthy participants and MDD patients; this influence may account for some of the brain changes previously associated with MDD. BMI and the use of medication should ideally be measured and controlled for when conducting structural brain imaging research in MDD

    The molecular basis and biologic significance of the β-dystroglycan-emerin interaction

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    β-dystroglycan (β-DG) assembles with lamins A/C and B1 and emerin at the nuclear envelope (NE) to maintain proper nuclear architecture and function. To provide insight into the nuclear function of β-DG, we characterized the interaction between β-DG and emerin at the molecular level. Emerin is a major NE protein that regulates multiple nuclear processes and whose deficiency results in Emery–Dreifuss muscular dystrophy (EDMD). Using truncated variants of β-DG and emerin, via a series of in vitro and in vivo binding experiments and a tailored computational analysis, we determined that the β-DG–emerin interaction is mediated at least in part by their respective transmembrane domains (TM). Using surface plasmon resonance assays we showed that emerin binds to β-DG with high affinity (KD in the nanomolar range). Remarkably, the analysis of cells in which DG was knocked out demonstrated that loss of β-DG resulted in a decreased emerin stability and impairment of emerin-mediated processes. β-DG and emerin are reciprocally required for their optimal targeting within the NE, as shown by immunofluorescence, western blotting and immunoprecipitation assays using emerin variants with mutations in the TM domain and B-lymphocytes of a patient with EDMD. In summary, we demonstrated that β-DG plays a role as an emerin interacting partner modulating its stability and function

    The Target Silicon Detector for the FOCUS Spectrometer

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    We describe a silicon microstrip detector interleaved with segments of a beryllium oxide target which was used in the FOCUS photoproduction experiment at Fermilab. The detector was designed to improve the vertex resolution and to enhance the reconstruction efficiency of short-lived charm particles.Comment: 18 pages, 14 figure

    Observation of a 1750 MeV/c^2 Enhancement in the Diffractive Photoproduction of K^+K^-

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    Using the FOCUS spectrometer with photon beam energies between 20 and 160 \gev, we confirm the existence of a diffractively photoproduced enhancement in K+KK^+K^- at 1750 \mevcc with nearly 100 times the statistics of previous experiments. Assuming this enhancement to be a single resonance with a Breit-Wigner mass shape, we determine its mass to be 1753.5±1.5±2.31753.5\pm 1.5\pm 2.3 \mevcc and its width to be 122.2±6.2±8.0122.2\pm 6.2\pm 8.0 \mevcc. We find no corresponding enhancement at 1750 \mevcc in KKK^*K, and again neglecting any possible interference effects we place limits on the ratio Γ(X(1750)KK)/Γ(X(1750)K+K)\Gamma (X(1750) \to K^*K)/\Gamma (X(1750) \to K^+K^-). Our results are consistent with previous photoproduction experiments, but, because of the much greater statistics, challenge the common interpretation of this enhancement as the ϕ(1680)\phi (1680) seen in e+ee^+e^- annihilation experiments.Comment: 10 pages, 5 figure

    Measurement of the relative branching ratio BR(\Xi_c^+ \to p^+ K^-\pi^+)\BR(\Xi_c^+ \to \Xi^- \pi^+ \pi^+)

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    We report the observation of the Cabibbo suppressed decay \Xi_c^+ \to p K^-\pi^+ using data collected with the FOCUS spectrometer during the 1996--97 Fermilab fixed target run. We find a \Xi_c^+ signal peak of 202\pm35 events. We have measured the relative branching ratios BR(\Xi^+_c\to p K^-\pi^+)/BR(\Xi^+_c\to\Xi^-\pi^+\pi^+)= 0.234 \pm 0.047 \pm 0.022 and BR(\Xi^+_c\to p \bar{K}^*(892)^0)/BR(\Xi^+_c\to p K^-\pi^+)= 0.54 \pm 0.09 \pm 0.05 .Comment: 9 pages, 4 figure

    Search for CP violation in D0 and D+ decays

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    A high statistics sample of photoproduced charm particles from the FOCUS (E831) experiment at Fermilab has been used to search for CP violation in the Cabibbo suppressed decay modes D+ to K-K+pi+, D0 to K-K+ and D0 to pi-pi+. We have measured the following CP asymmetry parameters: A_CP(K-K+pi+) = +0.006 +/- 0.011 +/- 0.005, A_CP(K-K+) = -0.001 +/- 0.022 +/- 0.015 and A_CP(pi-pi+) = +0.048 +/- 0.039 +/- 0.025 where the first error is statistical and the second error is systematic. These asymmetries are consistent with zero with smaller errors than previous measurements.Comment: 12 pages, 4 figure

    A measurement of lifetime differences in the neutral D-meson system

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    Using a high statistics sample of photoproduced charm particles from the FOCUS experiment at Fermilab, we compare the lifetimes of neutral D mesons decaying via D0 to K- pi+ and K- K+ to measure the lifetime differences between CP even and CP odd final states. These measurements bear on the phenomenology of D0 - D0bar mixing. If the D0 to K-pi+ is an equal mixture of CP even and CP odd eigenstates, we measure yCP = 0.0342 \pm 0.0139 \pm 0.0074.Comment: 15 pages, 5 figure

    Evidence for a narrow dip structure at 1.9 GeV/c2^2 in 3π+3π3\pi^+ 3\pi^- diffractive photoproduction

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    A narrow dip structure has been observed at 1.9 GeV/c2^2 in a study of diffractive photoproduction of the  3π+3π~3\pi^+3\pi^- final state performed by the Fermilab experiment E687.Comment: The data of Figure 6 can be obtained by downloading the raw data file e687_6pi.txt. v5 (2nov2018): added Fig. 7, the 6 pion energy distribution as requested by a reade
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