1,490 research outputs found

    The star cluster system of the 3 Gyr old merger remnant NGC 1316: Clues from optical and near-infrared photometry

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    The giant merger remnant galaxy NGC 1316 (Fornax A) is an ideal probe for studying the long-term effects of a past major merger on star cluster systems, given its spectroscopically derived merger age of ~3 Gyr which we reported in a recent paper. Here we present new ground-based, large-area optical and near-IR imaging of star clusters in NGC 1316, complemented with deep HST/WFPC2 imaging. We find that the optical-near-IR colours and luminosities of the brightest ~10 clusters in NGC 1316 are consistent with those of intermediate-age (2-3 Gyr) populations. Unlike `normal' giant ellipticals, the B-I colour distribution of clusters in NGC 1316 is not clearly bimodal. However, the luminosity functions (LFs) of the blue and red parts of the cluster colour distribution are different: The red cluster LF is well represented by a power law with index -1.2 +/- 0.3, extending to about 1.5 mag brighter (in B) than those of typical giant ellipticals. In contrast, the shape of the blue cluster LF is consistent with that of `normal' spiral and elliptical galaxies. We conclude that the star cluster system of NGC 1316 is a combination of a population of age ~3 Gyr having roughly solar metallicity and a population of old, metal-poor clusters which probably belonged to the pre-merger galaxies. After the 3 Gyr old, metal-rich clusters fade to an age of 10 Gyr, they will form a red `peak' in a bimodal cluster colour distribution. This `red peak' will have a colour consistent with that found in `normal, old' giant ellipticals of the same galaxy luminosity (taking age dimming into account). These features of the star cluster system of NGC 1316 are fully consistent with scenarios for forming `normal' giant elliptical galaxies through gas-rich mergers at look-back times \ga 10 Gyr.Comment: 21 pages, LaTeX format, figures included using psfig.sty. Accepted by MNRAS. Abstract below is abridged (full abstract in paper). Used 8-bit mapping to limit size of figures (24-bit mapping in MNRAS paper

    Velocity dispersion estimates of APM galaxy clusters

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    We present 83 new galaxy radial velocities in the field of 18 APM clusters with redshifts between 0.06 and 0.13. The clusters have Abell identifications and the galaxies were selected within 0.75 h1^{-1}Mpc in projection from their centers. We derive new cluster velocity dispersions for 13 clusters using our data and published radial velocities. We analyze correlations between cluster velocity dispersions and cluster richness counts as defined in Abell and APM catalogs. The correlations show a statistically significant trend although with a large scatter suggesting that richness is a poor estimator of cluster mass irrespectively of cluster selection criteria and richness definition. We find systematically lower velocity dispersions in the sample of Abell clusters that do not fulfill APM cluster selection criteria suggesting artificially higher Abell richness counts due to contamination by projection effects in this subsample.Comment: Accepted for publication in MNRA

    The Stellar Populations of NGC 3109: Another Dwarf Irregular Galaxy with a Population II Stellar Halo

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    We have obtained V and I-band photometry for about 17500 stars in the field of the dwarf irregular galaxy NGC3109, located in the outskirts of the Local Group. The photometry allows us to study the stellar populations present inside and outside the disk of this galaxy. From the VI color-magnitude diagram we infer metallicities and ages for the stellar populations in the main body and in the halo of NGC3109. The stars in the disk of this galaxy have a wide variety of ages, including very young stars with approximately 10^7 yr. Our main result is to establish the presence of a halo consisting of population II stars, extending out to about 4.5 arcmin (or 1.8 kpc) above and below the plane of this galaxy. For these old stars we derive an age of > 10 Gyr and a metallicity of [Fe/H] = -1.8 +/- 0.2. We construct a deep luminosity function, obtaining an accurate distance modulus (m-M)_0 = 25.62 +/- 0.1 for this galaxy based on the I-magnitude of the red giant branch (RGB) tip and adopting E(V-I) = 0.05.Comment: Accepted for publication in the Astronomical Journal 23 pages, latex, 12 Figures (Fig 1 not available in electronic format

    Effect of zinc intake on growth in infants: A meta-analysis

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    A systematic review and meta-analysis of available randomized controlled trials (RCTs) was conducted to evaluate the effect of zinc (Zn) intake on growth in infants. Out of 5500 studies identified through electronic searches and reference lists, 19 RCTs were selected after applying the exclusion/inclusion criteria. The influence of Zn intake on growth was considered in the overall meta-analysis. Other variables were also taken into account as possible effect modifiers: doses of Zn intake, intervention duration, nutritional status, and risk of bias. From each select growth study, final measures of weight, length, mid upper arm circumference (MUAC), head circumference, weight for age z-score (WAZ), length for age z-score (LAZ), and weight for length z-score (WLZ) were assessed. Pooled β and 95% confidence interval (CI) were calculated. Additionally, we carried out a sensitivity analysis. Zn intake was not associated with weight, length, MUAC, head circumference, and LAZ in the pooled analyses. However, Zn intake had a positive and statistically effect on WAZ (β = 0.06; 95%CI 0.02 to 0.10) and WLZ (β = 0.05; 95%CI 0.01 to 0.08). The dose–response relationship between Zn intake and these parameters indicated that a doubling of Zn intake increased WAZ and WLZ by approximately 4%. Substantial heterogeneity was present only in length analyses (I2 = 45%; p = 0.03). Zn intake was positively associated with length values at short time (four to 20 weeks) (β = 0.01; CI 95% 0 to 0.02) and at medium doses of Zn (4.1 to 8 mg/day) (β = 0.003; CI 95% 0 to 0.01). Nevertheless, the effect magnitude was small. Our results indicate that Zn intake increases growth parameters of infants. Nonetheless, interpretation of these results should be carefully considered

    Triplets of Quasars at high redshift I: Photometric data

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    We have conducted an optical and infrared imaging in the neighbourhoods of 4 triplets of quasars. R, z', J and Ks images were obtained with MOSAIC II and ISPI at Cerro Tololo Interamerican Observatory. Accurate relative photometry and astrometry were obtained from these images for subsequent use in deriving photometric redshifts. We analyzed the homogeneity and depth of the photometric catalog by comparing with results coming from the literature. The good agreement shows that our magnitudes are reliable to study large scale structure reaching limiting magnitudes of R = 24.5, z' = 22.5, J = 20.5 and Ks = 19.0. With this catalog we can study the neighbourhoods of the triplets of quasars searching for galaxy overdensities such as groups and galaxy clusters.Comment: The paper contains 12 figures and 3 table

    Cluster vs. Field Elliptical Galaxies and Clues on their Formation

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    Using new observations for a sample of 931 early-type galaxies we investigate whether the \mg2--\so relation shows any dependence on the local environment. The galaxies have been assigned to three different environments depending on the local overdensity: clusters, groups, and field, having used our completeredshift database to guide the assignment of galaxies. It is found that cluster, group and field early-type galaxies follow almost identical \mg2--\so\ relations, with the largest \mg2 zero-point difference (clusters minus field) being only 0.007±0.0020.007\pm 0.002 mag. No correlation of the residuals is found with the morphological type or the bulge to disk ratio. Using stellar population models in a differential fashion, this small zero-point difference implies a luminosity-weighted age difference of only 1\sim 1 Gyr between the corresponding stellar populations, with field galaxies being younger. The mass-weighted age difference could be significantly smaller, if minor events of late star formation took place preferentially in field galaxies. We combine these results with the existing evidence for the bulk of stars in cluster early-type galaxies having formed at very high redshift, and conclude that the bulk of stars in galactic spheroids had to form at high redshifts (z\gsim 3), no matter whether such spheroids now reside in low or high density regions. The cosmological implications of these findings are briefly discussed.Comment: 16 pages, 2 figures, accepted for publication in the ApJ.

    Global transcriptome analysis of Lactococcus garvieae strains in response to temperature

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    Lactococcus garvieae is an important fish and an opportunistic human pathogen. The genomic sequences of several L. garvieae strains have been recently published, opening the possibility of global studies on the biology of this pathogen. In this study, a whole genome DNA microarray of two strains of L. garvieae was designed and validated. This DNA microarray was used to investigate the effects of growth temperature (18°C and 37°C) on the transcriptome of two clinical strains of L. garvieae that were isolated from fish (Lg8831) and from a human case of septicemia (Lg21881). The transcriptome profiles evidenced a strain-specific response to temperature, which was more evident at 18°C. Among the most significant findings, Lg8831 was found to up-regulate at 18°C several genes encoding different cold-shock and cold-induced proteins involved in an efficient adaptive response of this strain to low-temperature conditions. Another relevant result was the description, for the first time, of respiratory metabolism in L. garvieae, whose gene expression regulation was temperature-dependent in Lg21881. This study provides new insights about how environmental factors such as temperature can affect L. garvieae gene expression. These data could improve our understanding of the regulatory networks and adaptive biology of this important pathogen

    Multiple Sporadic Colorectal Cancers Display a Unique Methylation Phenotype

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    The members of the Gastrointestinal Oncology Group of the Spanish Gastroenterological Association are: Hospital 12 de Octubre, Madrid: Juan Diego Morillas (local coordinator), Raquel Muñoz, Marisa Manzano, Francisco Colina, Jose Díaz, Carolina Ibarrola, Guadalupe López, Alberto Ibáñez; Hospital Clínic, Barcelona: Antoni Castells (local coordinator), Virgínia Piñol, Sergi Castellví-Bel, Francesc Balaguer, Victoria Gonzalo, Teresa Ocaña, María Dolores Giráldez, Maria Pellisé, Anna Serradesanferm, Leticia Moreira, Miriam Cuatrecasas, Josep M. Piqué; Hospital Clínico Universitario, Zaragoza: Ángel Lanas (local coordinator), Javier Alcedo, Javier Ortego; Hospital Cristal-Piñor, Complexo Hospitalario de Ourense: Joaquin Cubiella (local coordinator), Ma Soledad Díez, Mercedes Salgado, Eloy Sánchez, Mariano Vega; Hospital del Mar, Barcelona: Montserrat Andreu (local coordinator), Anna Abuli, Xavier Bessa, Mar Iglesias, Agustín Seoane, Felipe Bory, Gemma Navarro, Beatriz Bellosillo, Josep Ma Dedeu, Cristina Álvarez, Begoña Gonzalez; Hospital San Eloy, Baracaldo and Hospital Donostia, CIBERehd, University of Country Basque, San Sebastián: Luis Bujanda (local coordinator) Ángel Cosme, Inés Gil, Mikel Larzabal, Carlos Placer, María del Mar Ramírez, Elisabeth Hijona, Jose M. Enríquez-Navascués, Jose L. Elosegui; Hospital General Universitario de Alicante: Artemio Payá (EPICOLON I local coordinator), Rodrigo Jover (EPICOLON II local coordinator), Cristina Alenda, Laura Sempere, Nuria Acame, Estefanía Rojas, Lucía Pérez-Carbonell; Hospital General de Granollers: Joaquim Rigau (local coordinator), Ángel Serrano, Anna Giménez; Hospital General de Vic: Joan Saló (local coordinator), Eduard Batiste-Alentorn, Josefina Autonell, Ramon Barniol; Hospital General Universitario de Guadalajara and Fundación para la Formación e Investigación Sanitarias Murcia: Ana María García (local coordinator), Fernando Carballo, Antonio Bienvenido, Eduardo Sanz, Fernando González, Jaime Sánchez, Akiko Ono; Hospital General Universitario de Valencia: Mercedes Latorre (local coordinator), Enrique Medina, Jaime Cuquerella, Pilar Canelles, Miguel Martorell, José Ángel García, Francisco Quiles, Elisa Orti; CHUVI-Hospital Meixoeiro, Vigo: EPICOLON I: Juan Clofent (local coordinator), Jaime Seoane, Antoni Tardío, Eugenia Sanchez; EPICOLON II: Ma Luisa de Castro (local coordinator), Antoni Tardío, Juan Clofent, Vicent Hernández; Hospital Universitari Germans Trias i Pujol, Badalona and Section of Digestive Diseases and Nutrition, University of Illinois at Chicago, Chicago, IL: Xavier Llor (local coordinator), Rosa M. Xicola, Marta Piñol, Mercè Rosinach, Anna Roca, Elisenda Pons, José M. Hernández, Miquel A. Gassull; Hospital Universitari Mútua de Terrassa: Fernando Fernández-Bañares (local coordinator), Josep M. Viver, Antonio Salas, Jorge Espinós, Montserrat Forné, Maria Esteve; Hospital Universitari Arnau de Vilanova, Lleida: Josep M. Reñé (local coordinator), Carmen Piñol, Juan Buenestado, Joan Viñas; Hospital Universitario de Canarias: Enrique Quintero (local coordinator), David Nicolás, Adolfo Parra, Antonio Martín; Hospital Universitario La Fe, Valencia: Lidia Argüello (local coordinator), Vicente Pons, Virginia Pertejo, Teresa Sala; Hospital Sant Pau, Barcelona: Dolors Gonzalez (local coordinator), Eva Roman, Teresa Ramon, Maria Poca, Ma Mar Concepción, Marta Martin, Lourdes Pétriz; Hospital Xeral Cies, Vigo: Daniel Martinez (local coordinator); Fundacion Publica Galega de Medicina Xenomica (FPGMX), CIBERER, Genomic Medicine Group-University of Santiago de Compostela, Santiago de Compostela, Galicia, Spain: Ángel Carracedo (local coordinator), Clara Ruiz-Ponte, Ceres Fernández-Rozadilla, Ma Magdalena Castro; Hospital Universitario Central de Asturias: Sabino Riestra (local coordinator), Luis Rodrigo; Hospital de Galdácano, Vizcaya: Javier Fernández (local coordinator), Jose Luis Cabriada; Fundación Hospital de Calahorra (La Rioja) La Rioja: Luis Carreño (local coordinator), Susana Oquiñena, Federico Bolado; Hospital Royo Villanova, Zaragoza: Elena Peña (local coordinator), José Manuel Blas, Gloria Ceña, Juan José Sebastián; Hospital Universitario Reina Sofía, Córdoba: Antonio Naranjo (local coordinator).Epigenetics are thought to play a major role in the carcinogenesis of multiple sporadic colorectal cancers (CRC). Previous studies have suggested concordant DNA hypermethylation between tumor pairs. However, only a few methylation markers have been analyzed. This study was aimed at describing the epigenetic signature of multiple CRC using a genome-scale DNA methylation profiling. We analyzed 12 patients with synchronous CRC and 29 age-, sex-, and tumor location-paired patients with solitary tumors from the EPICOLON II cohort. DNA methylation profiling was performed using the Illumina Infinium HM27 DNA methylation assay. The most significant results were validated by Methylight. Tumors samples were also analyzed for the CpG Island Methylator Phenotype (CIMP); KRAS and BRAF mutations and mismatch repair deficiency status. Functional annotation clustering was performed. We identified 102 CpG sites that showed significant DNA hypermethylation in multiple tumors with respect to the solitary counterparts (difference in β value ≥0.1). Methylight assays validated the results for 4 selected genes (p = 0.0002). Eight out of 12(66.6%) multiple tumors were classified as CIMP-high, as compared to 5 out of 29(17.2%) solitary tumors (p = 0.004). Interestingly, 76 out of the 102 (74.5%) hypermethylated CpG sites found in multiple tumors were also seen in CIMP-high tumors. Functional analysis of hypermethylated genes found in multiple tumors showed enrichment of genes involved in different tumorigenic functions. In conclusion, multiple CRC are associated with a distinct methylation phenotype, with a close association between tumor multiplicity and CIMP-high. Our results may be important to unravel the underlying mechanism of tumor multiplicity.This work was supported by grants from the Hospital Clínic of Barcelona (Josep Font grant), Ministerio de Economí­a y Competitividad (SAF 2007-64873 and SAF2010-19273), Fundación Científica de la Asociación Española contra el Cáncer, and Instituto de Salud Carlos III (PI10/00384). “Cofinanciado por el Fondo Europeo de Desarrollo Regional (FEDER). Unión Europea. Una manera de hacer Europa”. CIBEREHD is funded by the Instituto de Salud Carlos III

    Elaboración de recursos docentes para la enseñanza presencial y semipresencial en el área de la Ingeniería Química empleando Jupyter Notebook

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    El objetivo principal de este proyecto es la elaboración de recursos docentes, para estudiantes y profesores, dentro del área de la Ingeniería Química, utilizando el software libre Jupyter Notebook, empleado bajo el lenguaje de programación Python
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