347 research outputs found

    Adsorción-desorción de los metales pesados Pb(II) y Hg(II) por modelos de partículas coloidales del suelo

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    4 páginas, 2 figuras, 1 tabla, 3 referencias.-- Publicado en el Capítulo IV: Contaminación y Medio Ambiente.-- Trabajo presentado a la XVII Reunión Científica de la Sociedad Española de Arcillas, celebrada en Elche (Alicante) y Castellón, del 27-29 de noviembre de 2002.El destino de los metales pesados en el medio ambiente está controlado por las reacciones de adsorción a los coloides del suelo. Por otro lado, las interacciones entre los constituyentes del suelo pueden alterar significativamente la cantidad y naturaleza de la superficie expuesta por los coloides del suelo para la adsorción de contaminantes. Por tanto, las predicciones sobre la extensión de la adsorción basadas en la suma de las capacidades adsorbentes de los constituyentes individuales del suelo pueden desviarse de lo que ocurre en la naturaleza (1). En la bibliografia han sido poco estudiadas las interacciones entre contaminantes y adsorbentes polifásicos, aunque en la última década ha aumentado la atención dada al estudio del comportamiento de modelos de asociaciones coloidales para obtener una interpretación más realista del proceso de adsorción en el suelo (2). En este trabajo se han determinado las capacidades adsorbentes de modelos de partículas coloidales binarias y ternarias que contienen montmorillonita (SW), ferrihidrita (Fh) y ácido húmico (AH) para dos contaminantes inorgánicos, los metales pesados Pb(lI) y Hg(II), Y se compararon con las capacidades de adsorción de los constituyentes individuales. Las partículas modelos se prepararon en el laboratorio y se caracterizaron por análisis elemental, espectroscopía infrarroja, difracción de rayos X y medidas de superficie específica. Se estudió la adsorción-desorción de Pb(lI) y Hg(ll) por parte de los diferentes adsorbentes y se utilizaron las técnicas de espectroscopía infrarroja y difracción de rayos X para analizar los mecanismos de interacción.Este trabajo ha sido financiado por el proyecto del MCYT REN2001-1700-C02- 01/TECNO y por el grupo RNM124 del PAI de la Junta de AndalucíaPeer reviewe

    Characterization of Benzoyl Saxitoxin Analogs from the Toxigenic Marine Dinoflagellate Gymnodinium catenatum by Hydrophilic Interaction Liquid Ion-Chromatography-Tandem Mass Spectrometry

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    The chain-forming marine dinoflagellate Gymnodinium catenatum Graham has a remarkable capacity to produce a wide array of neurotoxic alkaloids associated with Paralytic Shellfish Poisoning (PSP). More than a decade ago, a completely new group of benzoyl saxitoxin analogs produced exclusively by this species was discovered, but the exact structural assignments and diversity among global population has remained elusive and nconfirmed in most cases. In the current study, fifteen among eighteen hypothetical benzoyl analogs were partially purified and identified from cultured isolates of G. catenatum from the Pacific coast of Mexico. Combined serial application of flash chromatography, preparative liquid chromatography and tandem mass spectrometry (LC-MS/MS) in multiple steps yielded a richness of benzoyl analogs that has not been reported nor confirmed before. Two sub-fractions were analyzed by 1H-NMR; results from one fraction showed a probable AMX pattern for three protons, consistent with the presence of a 3,4-dihydroxylated benzoyl ring. These findings could be interpreted to correct the 2,4-dihydroxylated structure previously proposed for the GCa benzoyl analog series. The revised and enhanced structural information on proposed benzoyl derivatives is necessary to provide further insights into biogeographical diversity of these potentially potent toxins produced by marine dinoflagellates and their role in seafood safety

    A turn-on fluorescent solid-sensor for Hg(II) detection

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    A rhodamine organosilane derivative (Rh-UTES) has been obtained by one-pot synthesis. The chemical structure of Rh-UTES was confirmed by nuclear magnetic resonance (NMR) and infrared (FTIR) techniques. To obtain an inorganic-organic hybrid sensor, Rh-UTES was covalently immobilized on a porous silicon microcavity (PSiMc) via triethoxysilane groups. The attachment of the organic derivative into PSiMc was confirmed by FTIR, specular reflectance, and scanning electron microscopy (SEM). The optical performance of Rh-UTES receptor for Hg2+ detection was investigated by fluorescent spectroscopy and microscopy. Upon the addition of increasing amounts of Hg2+ ions, a remarkable enhancement in emission intensity was produced in both systems. In the solid phase, an increase of integrated fluorescent emission of 0.12- and 0.15-fold after Hg2+ receptor coordination was observed. The light harvesting capability of PSiMc devices allowed obtaining an enhanced fluorescent emission after Rh-UTES immobilization (277-fold). The fluorescence microscopy of hybrid PSiMc sensor provided an optical qualitative test for Hg2+ detection.A rhodamine organosilane derivative (Rh-UTES) has been obtained by one-pot synthesis. The chemical structure of Rh-UTES was confirmed by nuclear magnetic resonance (NMR) and infrared (FTIR) techniques. To obtain an inorganic-organic hybrid sensor, Rh-UTES was covalently immobilized on a porous silicon microcavity (PSiMc) via triethoxysilane groups. The attachment of the organic derivative into PSiMc was confirmed by FTIR, specular reflectance, and scanning electron microscopy (SEM). The optical performance of Rh-UTES receptor for Hg2+ detection was investigated by fluorescent spectroscopy and microscopy. Upon the addition of increasing amounts of Hg2+ ions, a remarkable enhancement in emission intensity was produced in both systems. In the solid phase, an increase of integrated fluorescent emission of 0.12- and 0.15-fold after Hg2+ receptor coordination was observed. The light harvesting capability of PSiMc devices allowed obtaining an enhanced fluorescent emission after Rh-UTES immobilization (277-fold). The fluorescence microscopy of hybrid PSiMc sensor provided an optical qualitative test for Hg2+ detection

    Presencia de toxinas tipo benzoato en una cepa de Gymnodinium catenatum (Dinophyceae) aislada de Manzanillo, Colima, México

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    The extract of a Gymnodinium catenatum strain, isolated from Manzanillo, Colima, in the Mexican Pacific coast, was analized by nuclear magnetic resonance (1 H-NMR) to determine the presence of benzoate-type analogs. The extract was fractioned using solid-phase extraction (SPE) partitioning on a C-18 cartridge, using a stepwise gradient from 0 to 100% (v/v). Fraction 2 (10% methanol) showed two aromatic doublet signals at 7.91 and 7.53 ppm, consistent with an AABB system, corresponding to a para substituted bencenic ring, attributed to the hydroxybenzoate moiety on C-17 of the toxin basic structure. These findings indicate the presence of benzoate type analogs in this Mexican strain. These analogs have been poorly studied, and the report on their existence in our country is of great importance because they could represent a public health risk, but in the other hand, their existence generates the opportunity to continue the research to determine their toxicity in mammals and, eventually, their pharmacological potential.Se analizó, por espectroscopía de resonancia magnética nuclear de protón (1 H-RMN), el extracto de una cepa de Gymnodinium catenatum Graham, aislada de las costas de Manzanillo, Colima, para determinar la existencia de toxinas tipo benzoato. El extracto fue fraccionado con un gradiente ascendente de metanol de 0 a 100% (v/v) por extracción en fase sólida con cartuchos LC-18 en pasos de 10%. La fracción 2 (10% metanol) exhibió dos señales dobles centradas en 7.91 y 7.53 ppm, correspondientes a un sistema AABB, que confirmó la presencia de un anillo bencénico para sustituido, atribuido al p-hidroxibenzoato en el carbono 17 del esqueleto base de la toxina. Con ello se confirmó la presencia de análogos tipo benzoato en la cepa de Gymnodinium catenatum proveniente de esta zona del Pacífico Mexicano, los cuales han sido poco estudiados, y el hecho de detectarlos en cepas de México es importante por el peligro potencial que representan para la salud pública. Asímismo, se generó la oportunidad de continuar estudiando estos compuestos, tanto para determinar su toxicidad en mamíferos como para, eventualmente, conocer su potencial farmacológico

    PREVALENCE OF ANTIBODIES AGAINST AVIAN PARAMYXOVIRUS TYPE 1 IN BACKYARD TURKEYS IN FOUR PROVINCES OF LIMA, PERU

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    El objetivo del presente estudio fue determinar la prevalencia de anticuerpos contra Paramixovirus Aviar Tipo 1 (APMV-1) en pavos de crianza familiar (n=388) en cuatro provincias del departamento de Lima (Lima, Huaral, Huaura y Barranca), Perú. Las mues- tras fueron colectadas durante los meses de agosto a diciembre de 2008, y fueron anali- zadas mediante la prueba serológica de Inhibición de la Hemoaglutinación. Se encontró una prevalencia de 3.9%, observándose que 15/388 pavos presentaron títulos de anticuerpos compatibles a un desafío viral con cepas de campo del PMVA-1. La mayor frecuencia de muestras positivas (10/15) se observó en la provincia de Lima, mientras que no se tuvo muestras positivas en la provincia de Barranca. Se concluye que los pavos de crianza familiar de tres provincias de Lima estuvieron expuestos a alguna cepa de PMVA-l, constituyendo un reservorio del virus.The objective of the study was to determine the prevalence of antibodies against avian Paramyxovirus type 1 (APMV-1) in backyard turkeys (n=388) in four provinces of Lima, Peru (Lima, Huaral, Huaura, and Barranca). Blood samples were collected from August to December 2008 and analyzed by hemagglutination inhibition test. The resulting seroprevalence was 3.9% as 15/388 turkeys showed antibody titers consistent with a viral challenge of APMV-1. The highest frequency of positive samples (10/15) was observed in the province of Lima, whereas none sample was positive in the Barranca province. It is concluded that backyard turkeys in three provinces of Lima were exposed to some strains of PMVA-l, constituting a reservoir of virus

    Efecto de la reducción del peso molecular de quitosano obtenido de plumas de pota (Dosidicus gigas) utilizando dos métodos de despolimerización sobre su capacidad antimicrobiana

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    En esta investigación se obtuvo quitosano de diferente peso molecular (MW), usando ultrasonido con tiempos de exposición de 30, 60 y 90 minutos a una temperatura de 30, 45 y 60 °C, e irradiación ultravioleta (UV) con tiempos de exposición de 1, 2 y 3 minutos en presencia de peróxido de hidrogeno (H2O2) a concentraciones de 1, 2 y 3 %, como métodos de despolimerización del quitosano nativo extraído de la pluma de Dosidicus gigas (pota o calamar gigante), con un grado de desacetilación de 85,5 % y un peso molecular equivalente a 1 0554 78 Da. El tratamiento con ultrasonido a 40 kHz no generó una variación significativa en el Mw del quitosano, sin embargo, en el tratamiento con irradiación UV+H2O2 por 2 y 3 minutos se observó una disminución significativa del Mw hasta 431 536 Da. Se evaluó también la capacidad antimicrobiana (AC) del quitosano con diferente Mw frente a Staphilococus aureus (bacteria Gram positiva) y Klebsiella oxytoca (bacteria Gram negativa). El análisis de la AC refleja que para S. aureus la inhibición es estadísticamente igual, asimismo el quitosano sonicado por 30 minutos a 30 y 45 °C y el quitosano irradiado por 3 minutos con H2O2 al 3 %, generan inhibición significativa frente a K. oxytoca

    Updating the distribution of Dicrodon guttulatum Duméril & Bibron, 1839 (Reptilia, Teiidae) with a disjunct population in the eastern slope of the Peruvian Andes

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    We report a disjunct population of Dicrodon guttulatum Duméril & Bibron, 1839 on the eastern slope of the Cordillera Occidental in the inter-Andean Seasonally Dry Forests of the Marañón River, in the Departments of Cajamarca and Piura in northwestern Peru. We include an updated range distribution map using records from museum specimens, the Global Biodiversity Information Facility, and available photographic records on iNaturalist. In addition, we identify widespread cultivation of rice crops as the main threat to D. guttulatum in the inter-Andean Seasonally Dry Forests of the Marañón

    Axiomatic geometric formulation of electromagnetism with only one axiom: the field equation for the bivector field F with an explanation of the Trouton-Noble experiment

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    In this paper we present an axiomatic, geometric, formulation of electromagnetism with only one axiom: the field equation for the Faraday bivector field F. This formulation with F field is a self-contained, complete and consistent formulation that dispenses with either electric and magnetic fields or the electromagnetic potentials. All physical quantities are defined without reference frames, the absolute quantities, i.e., they are geometric four dimensional (4D) quantities or, when some basis is introduced, every quantity is represented as a 4D coordinate-based geometric quantity comprising both components and a basis. The new observer independent expressions for the stress-energy vector T(n)(1-vector), the energy density U (scalar), the Poynting vector S and the momentum density g (1-vectors), the angular momentum density M (bivector) and the Lorentz force K (1-vector) are directly derived from the field equation for F. The local conservation laws are also directly derived from that field equation. The 1-vector Lagrangian with the F field as a 4D absolute quantity is presented; the interaction term is written in terms of F and not, as usual, in terms of A. It is shown that this geometric formulation is in a full agreement with the Trouton-Noble experiment.Comment: 32 pages, LaTex, this changed version will be published in Found. Phys. Let

    Dietary Fat Patterns and Outcomes in Acute Pancreatitis in Spain

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    Background/Objective: Evidence from basic and clinical studies suggests that unsaturated fatty acids (UFAs) might be relevant mediators of the development of complications in acute pancreatitis (AP). Objective: The aim of this study was to analyze outcomes in patients with AP from regions in Spain with different patterns of dietary fat intake. Materials and Methods: A retrospective analysis was performed with data from 1,655 patients with AP from a Spanish prospective cohort study and regional nutritional data from a Spanish cross-sectional study. Nutritional data considered in the study concern the total lipid consumption, detailing total saturated fatty acids, UFAs and monounsaturated fatty acids (MUFAs) consumption derived from regional data and not from the patient prospective cohort. Two multivariable analysis models were used: (1) a model with the Charlson comorbidity index, sex, alcoholic etiology, and recurrent AP; (2) a model that included these variables plus obesity. Results: In multivariable analysis, patients from regions with high UFA intake had a significantly increased frequency of local complications, persistent organ failure (POF), mortality, and moderate-to-severe disease in the model without obesity and a higher frequency of POF in the model with obesity. Patients from regions with high MUFA intake had significantly more local complications and moderate-to-severe disease; this significance remained for moderate-to-severe disease when obesity was added to the model. Conclusions: Differences in dietary fat patterns could be associated with different outcomes in AP, and dietary fat patterns may be a pre-morbid factor that determines the severity of AP. UFAs, and particulary MUFAs, may influence the pathogenesis of the severity of AP
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