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                <text>&lt;strong&gt;Bioconversiones para la revalorizaci&amp;oacute;n de glicerol:s&amp;iacute;ntesis de &amp;aacute;cido L-l&amp;aacute;ctico utilizando una cascada biosint&amp;eacute;tica&lt;/strong&gt;</text>
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                <text>El glicerol es un subproducto inevitable de la producci&amp;oacute;n de biodi&amp;eacute;sel. Una gran cantidad de este producto es generado durante la transesterificaci&amp;oacute;n de grasas y aceites con alcohol. El exceso de oferta y la limitada demanda de este producto afectan directamente los costos de producci&amp;oacute;n del biodi&amp;eacute;sel. Sin embargo, el glicerol puede ser convertido a productos de m&amp;aacute;s alto valor agregado mediante procesos puramente qu&amp;iacute;micos o mediante biotransformaciones. Los bioprocesos verdes, tales como las reacciones biocatal&amp;iacute;ticas, son capaces de modificar selectivamente sustratos polifuncionales debido a su alta eficiencia catal&amp;iacute;tica, selectividad inherente y f&amp;aacute;cil o nulo procesamiento downstream. Adem&amp;aacute;s, las biotransformaciones se realizan bajo condiciones suaves con menores requerimientos energ&amp;eacute;ticos, ofreciendo tecnolog&amp;iacute;as medioambientalmente limpias. Las nuevas tendencias en bioconversiones marcan el acoplamiento de procesos biocatal&amp;iacute;ticos enzim&amp;aacute;ticos a procesos fermentativos como una soluci&amp;oacute;n de gran potencial en la bios&amp;iacute;ntesis secuencial de productos biotecnol&amp;oacute;gicos. En esta tesis se propuso una ruta biosint&amp;eacute;tica mixta novedosa para la s&amp;iacute;ntesis de &amp;aacute;cido L-l&amp;aacute;ctico a partir de glicerol crudo, subproducto de la industria del biodi&amp;eacute;sel. Nuestro enfoque incluy&amp;oacute; el uso de biocatalizadores inmovilizados microbiol&amp;oacute;gicos y enzim&amp;aacute;ticos mediante estrategias que aportaron estabilidad y la posibilidad de reutilizaci&amp;oacute;n en aras de conversiones m&amp;aacute;s verdes y econ&amp;oacute;micas.</text>
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>The performance of a group of density functional methods of progressive complexity for the description of the ClO bond in a series of chlorine oxides was investigated. The simplest ClO radical species as well as the two isomeric structures XClO/ClOX for each X=H, Cl and O were studied using the PW91, TPSS, B3LYP, PBE0, M06, M06-2X, BMK and B2PLYP functionals. Geometry optimizations as well as reaction enthalpies and enthalpies of formation for each species were calculated using Pople basis sets and the (aug)-cc-pVnZ Dunning sets, with n=2-6. For the calculation of enthalpies of formation, atomization as well as isodesmic reactions were employed. Both the precision of the methods with respect to the increase of the basis sets, as well as their accuracy, were gauged by comparing the results with the more accurate CCSD(T) calculations, performed using the same basis sets as for the DFT methods. The results obtained employing composite chemical methods (G4, CBS-QB3 and W1BD) were also used for the comparisons, as well as the experimental results when they are available. The results obtained show that error compensation is the key for successful description of molecular properties (geometries and energies) by carefully selecting method and basis sets. In general, expansion of the one-electron basis set to the limit of completeness does not improve results at the DFT level, but just the opposite. The enthalpies of formation calculated at the CCSD(T)/aug-cc-pV6Z for the species considered are generally in agreement with experimental determinations, and the most accurate derived theoretically up to present. Different sources of error in the calculations are discussed in detail.</text>
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                  <text>Contiene la producción científica nacional de los profesionales químicos e investigadores, durante el período 1929 hasta la fecha.</text>
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                <text>&lt;strong&gt;Characterization of the cellulase-secretome produced by the Antarctic bacterium Flavobacterium sp. AUG42&lt;/strong&gt;</text>
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                <text>CARBONO</text>
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                <text>Flavobacterium sp. AUG42 is a cellulase-producing bacterium isolated from the Antarctic oligochaete Grania sp. (Annelida). In this work, we report that AUG42 produces a glycoside hydrolase cocktail with CMCase, PASCase and cellobiase activities (optimum pHs and temperatures ranging from 5.5 to 6.5 and 40 to 50&amp;thinsp;&amp;deg;C, respectively). The time-course analyses of the bacterial growth and cellulase production showed that the cocktail has maximal activity at the stationary phase when growing at 16&amp;thinsp;&amp;deg;C with filter paper as a cellulosic carbon source, among the tested substrates. The analyses of the CAZome and the identification of secreted proteins by shotgun Mass Spectrometry analysis showed that five glycoside hydrolyses are present in the bacterial secretome, which probably cooperate in the degradation of the cellulosic substrates. Two of these glycoside hydrolyses may harbor putative carbohydrate binding modules, both with a cleft-like active site. The cellulolytic cocktail was assayed in saccharification experiments using carboxymethylcellulose as a substrate and results showed the release of glucose (a fermentable sugar) and other reducing-sugars, after 24&amp;thinsp;h incubation. The ecological relevance of producing cellulases in the Antarctic environment, as well as their potential use in the bio-refinery industry, are discussed.</text>
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                <text>&lt;strong&gt;Herrera, Lorena.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Bra&amp;ntilde;a, Victoria.&lt;/strong&gt;</text>
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                <text>&lt;a title="Curriculum Vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=729d3d9bb07d7be0ba5e4dc762c01e29" target="_self"&gt;&lt;strong&gt;Franco Fraguas, Laura.&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;strong&gt;Castro-Sowinski, Susana&lt;/strong&gt;</text>
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                <text>Microbiological Research v.223-225, 2019. -- p. 13-21</text>
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            <name>Rights</name>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>DOI: 10.1016/j.micres.2019.03.009</text>
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                  <text>Versiones electrónicas de las tesis de doctorado, maestría y trabajos de diploma de la Facultad de Química, Universidad de la República (UdelaR).&#13;
Incluye únicamente trabajos hasta el año 2023. Los trabajos posteriores se encuentran disponibles en el Repositorio Colibrí.</text>
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                <text>&lt;strong&gt;Implementaci&amp;oacute;n y desarrollo de metodolog&amp;iacute;as radiosint&amp;eacute;ticas para la incorporaci&amp;oacute;n de 11C en mol&amp;eacute;culas org&amp;aacute;nicas&lt;/strong&gt;</text>
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                <text>QU&amp;Iacute;MICA ORG&amp;Aacute;NICA DEL CARBONO</text>
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                <text>RADIOQU&amp;Iacute;MICA</text>
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                <text>MEDICINA NUCLEAR PET</text>
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                <text>El estudio de nuevos radiotrazadores para PET es un &amp;aacute;rea mundialmente muy activa que requiere de un trabajo multidisciplinario y que implica desde la selecci&amp;oacute;n de los blancos moleculares, la s&amp;iacute;ntesis org&amp;aacute;nica, la marcaci&amp;oacute;n utilizando metodolog&amp;iacute;as automatizadas que minimicen la irradiaci&amp;oacute;n del operador y el desarrollo de metodolog&amp;iacute;as de evaluaci&amp;oacute;n fisicoqu&amp;iacute;mica y biol&amp;oacute;gicas compatibles con los cortos per&amp;iacute;odos de semidesintegraci&amp;oacute;n de los radionucleidos. Dentro de &amp;eacute;stos &amp;uacute;ltimos, el 11C ocupa un lugar fundamental por sus ventajas, pero tambi&amp;eacute;n por sus limitaciones. El 11C permite realizar marcaciones isot&amp;oacute;picas, con lo cual se logran radiotrazadores sin modificaciones fisicoqu&amp;iacute;micas significativas respecto a las mol&amp;eacute;culas end&amp;oacute;genas cuyo metabolismo se desea estudiar. Por otra parte, el 11C puede ser obtenido con buenos rendimientos en los ciclotrones comercialmente disponibles, y su radioqu&amp;iacute;mica ha sido bien estudiada y desarrollada a lo largo de las cuatro &amp;uacute;ltimas d&amp;eacute;cadas. La principal limitante de su uso radica fundamentalmente en el corto per&amp;iacute;odo de semidesintegraci&amp;oacute;n (20.4 minutos), y es lo que supone un desaf&amp;iacute;o para el radioqu&amp;iacute;mico que desarrolla m&amp;eacute;todos de marcaci&amp;oacute;n con 11C. La metodolog&amp;iacute;a m&amp;aacute;s utilizada para introducir 11C en mol&amp;eacute;culas org&amp;aacute;nicas a ser utilizadas como radiotrazadores PET, es a trav&amp;eacute;s de reacciones de 11C-metilaci&amp;oacute;n con los precursores radiactivos secundarios [11C]CH3I o [11C]CH3OTf. Estos precursores est&amp;aacute;n disponibles en plataformas comerciales, su radioqu&amp;iacute;mica ha sido bien estudiada y por ello su utilizaci&amp;oacute;n es mundialmente muy amplia. Un gran n&amp;uacute;mero de radiotrazadores PET se sintetizan utilizando estos dos precursores radioactivos, y a la fecha se utilizan para la producci&amp;oacute;n de todos los radiof&amp;aacute;rmacos de 11C en uso precl&amp;iacute;nico y cl&amp;iacute;nico en el Centro Uruguayo de Imagenolog&amp;iacute;a Molecular (CUDIM). Sin embargo, su aplicabilidad est&amp;aacute; limitada a mol&amp;eacute;culas nucleof&amp;iacute;licas conteniendo los hetero&amp;aacute;tomos O, N o S. Otros precursores tales como el [11]CO2, [11C]CO, o el [11C]CN- permiten la obtenci&amp;oacute;n de mol&amp;eacute;culas marcadas en otros grupos funcionales, con lo que se ampl&amp;iacute;a el espectro de estructuras conteniendo 11C y las aplicaciones de las mismas. Teniendo en cuenta lo anterior, es que en el presente trabajo se plantea la posibilidad de trabajar en el CUDIM con precursores de 11C alternativos a [11C]CH3I o [11C]CH3OTf. Como punto de partida del trabajo se propuso al [11C]CN- (com&amp;uacute;nmente referido como [11C]HCN o [11C]NH4CN) como precursor radiactivo. En la Qu&amp;iacute;mica Org&amp;aacute;nica tradicional, el ani&amp;oacute;n CN- es un sint&amp;oacute;n atractivo, pues permite la formaci&amp;oacute;n de un enlace C-C por sustituci&amp;oacute;n nucleof&amp;iacute;lica sobre estructuras que presenten la funci&amp;oacute;n C-X (X = hal&amp;oacute;geno u otros grupos salientes). El grupo nitrilo tambi&amp;eacute;n est&amp;aacute; presente en un importante n&amp;uacute;mero de f&amp;aacute;rmacos y compuestos de inter&amp;eacute;s biol&amp;oacute;gico. El uso del precursor [11C]CN- permite obtener radiotrazadores atractivos para el diagn&amp;oacute;stico mediante PET de alteraciones metab&amp;oacute;licas y otros fen&amp;oacute;menos patol&amp;oacute;gicos. La s&amp;iacute;ntesis de mol&amp;eacute;culas de importancia bioqu&amp;iacute;mica tales como 1-[11C]amino&amp;aacute;cidos 1-[11C]glucosa, 1-[11C]&amp;aacute;cidos grasos, entre otros ha sido descrita en la literatura. CUDIM cuenta con una plataforma automatizada (m&amp;oacute;dulo ProCab&amp;reg;) capaz de convertir qu&amp;iacute;micamente el [11C]CO2 en [11C]CN-, por lo que el trabajo comenz&amp;oacute; realizando un estudio de algunas variables de la producci&amp;oacute;n de este precursor en nuestra plataforma. Se 20 determin&amp;oacute; que la robustez de la misma depende fundamentalmente de su frecuencia de uso, y de finos ajustes en par&amp;aacute;metros f&amp;iacute;sicos tales como el flujo de los gases utilizados. En condiciones optimizadas, el m&amp;oacute;dulo ProCab&amp;reg; es capaz de transformar [11C]CO2 en [11C]CN- con un rendimiento radioqu&amp;iacute;mico de aproximadamente 30% (corregido) en no m&amp;aacute;s de 10 minutos. El [11C]CN- as&amp;iacute; producido, se utiliz&amp;oacute; en un sistema modelo de reactividad, logr&amp;aacute;ndose obtener D,L-1-[11C]Fenilalanina, utilizando para la misma una plataforma automatizada TRACERlab&amp;reg; FX C Pro. En una segunda etapa, se trabaj&amp;oacute; con [11C]CO2 como precursor radiactivo, de acuerdo a la metodolog&amp;iacute;a com&amp;uacute;nmente conocida como &amp;ldquo;fijaci&amp;oacute;n-reducci&amp;oacute;n de [11C]CO2&amp;rdquo;. La radioqu&amp;iacute;mica de fijaci&amp;oacute;n o incorporaci&amp;oacute;n de [11C]CO2 es un terreno f&amp;eacute;rtil para la obtenci&amp;oacute;n eficiente de radiotrazadores PET, al punto que es referida por algunos reconocidos investigadores como el &amp;ldquo;Renacimiento de la Qu&amp;iacute;mica PET&amp;rdquo;. Tradicionalmente, el uso de [11C]CO2 se encontraba limitado a la reacci&amp;oacute;n de Grignard para la s&amp;iacute;ntesis de &amp;aacute;cidos 11C-carbox&amp;iacute;licos. Aun cuando esta t&amp;eacute;cnica ha sido y es extensamente empleada, posee desventajas en cuanto a la inestabilidad inherente de los precursores org&amp;aacute;nicos empleados, y la escasa variabilidad estructural de los radiotrazadores obtenidos. Recientemente ha habido avances significativos en la incorporaci&amp;oacute;n de 11C en mol&amp;eacute;culas org&amp;aacute;nicas utilizando [11C]CO2, para dar estructuras moleculares tales como ureas, carbamatos, oxazolidinonas y &amp;aacute;cidos carbox&amp;iacute;licos, o su incorporaci&amp;oacute;n y posterior reducci&amp;oacute;n para obtener especies N-11C-metiladas. Dado el alto n&amp;uacute;mero de radiof&amp;aacute;rmacos de uso cl&amp;iacute;nico que poseen el grupo 11C-metilo, se considera muy ventajoso sintetizarlos a partir de [11C]CO2 en lugar de los agentes 11C-metilantes tradicionales ([11C]MeI o [11C]MeOTf). El uso directo de [11C]CO2 y de modalidades de reacci&amp;oacute;n &amp;ldquo;one-pot&amp;rdquo; minimiza el n&amp;uacute;mero de pasos sint&amp;eacute;ticos, y presupone un aumento de los rendimientos de s&amp;iacute;ntesis, lo que se traduce en una mayor actividad final disponible para estudios precl&amp;iacute;nicos o cl&amp;iacute;nicos. En tal sentido, se propuso estudiar condiciones para llevar a cabo y optimizar reacciones de incorporaci&amp;oacute;n de [11C]CO2 y su posterior reducci&amp;oacute;n con el fin de contar con metodolog&amp;iacute;as eficientes aplicables a la s&amp;iacute;ntesis de 11C-radiotrazadores. Para el trabajo con [11C]CO2 se utiliz&amp;oacute; tambi&amp;eacute;n la plataforma automatizada TRACERlab&amp;reg;, con m&amp;iacute;nimas modificaciones de tal manera de dirigir el [11C]CO2 purificado a un reactor de marcaci&amp;oacute;n. Se estudi&amp;oacute; la fisicoqu&amp;iacute;mica de su captura en soluci&amp;oacute;n. Se evaluaron tres sistemas radioqu&amp;iacute;micos para promover la incorporaci&amp;oacute;n reductiva de [11C]CO2 en un sistema modelo de reactividad compuesto por 4-toluidina: i) DBU / PhSiH3, ii) IPr carbeno / PhSiH3 y iii) TBAF / PhSiH3. Para cada uno de ellos se estudi&amp;oacute; la influencia de factores f&amp;iacute;sicos y qu&amp;iacute;micos, tanto en la pureza radioqu&amp;iacute;mica de la amina 11C-metilada como en su rendimiento radioqu&amp;iacute;mico. Dos de ellos (IPr / PhSiH3 y TBAF / PhSiH3) se aplicaron a la s&amp;iacute;ntesis del radiotrazador PET [11C]PiB. Mediante el uso de [11C]CO2 / TBAF / PhSiH3 en diglyme, a 150 &amp;ordm;C por 1 min, se logr&amp;oacute; marcar [11C]PiB en un 14.8% de rendimiento radioqu&amp;iacute;mico, con actividad molar de 61 GBq/&amp;mu;mol. Si bien este valor es aparentemente bajo por el uso directo de [11C]CO2, el rendimiento radioqu&amp;iacute;mico del [11C]PiB producido de esta forma duplica al del m&amp;eacute;todo de 11C-metilaci&amp;oacute;n con [11C]CH3OTf actualmente utilizado en CUDIM. La aplicaci&amp;oacute;n de esta metodolog&amp;iacute;a permiti&amp;oacute; desarrollar un m&amp;eacute;todo novedoso de preparaci&amp;oacute;n para este 21 radiof&amp;aacute;rmaco, junto con su control de calidad en un contexto precl&amp;iacute;nico. La validaci&amp;oacute;n de este proceso en el marco del &amp;aacute;rea de Pr</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Assessment of antioxidant, antidiabetic, antiobesity, and anti-inflammatory properties of a Tannat winemaking by-product&lt;/strong&gt;</text>
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                <text>Winemaking industry produces large amounts of by-products (grape pomace or marc) every year, making necessary a sustainable management of such waste. Among red wines, Tannat variety possesses a unique polyphenolic profile. Consequently, the study of the bioactive properties of its by-product and the extraction optimization of its bioactive compounds is of great interest to state its health promoting potential. In this study, different extraction processes were tested: maceration with ethanol (95%), ultrasound-assisted ethanolic extraction optimization with surface methodology, ultrasound-assisted aqueous extraction, and hydro-alcoholic-acid extraction (EHAA). Using this last extraction procedure, higher polyphenolic content (11.459 &amp;plusmn; 1.048 g GAE/100 g of dry extract), monomeric anthocyanins (2.030 &amp;plusmn; 0.085 g Cyd/100 g of dry extract), antioxidant capacity (0.474 &amp;plusmn; 0.036 mg/mL for ABTS and 0.715 &amp;plusmn; 0.063 &amp;micro;mol TE/mg of dry extract for ORAC-FL), &amp;alpha;-glucosidase (IC50 888.5 &amp;plusmn; 79.3 &amp;micro;g/mL), and pancreatic lipase inhibition capacity (IC50 2431.0 &amp;plusmn; 79.9 &amp;micro;g/mL) were found on Tannat grape skin. Considering as a whole, these results may imply a great antidiabetic and antiobesity potential. Moreover, EHAA showed to have anti-inflammatory capacity (IC50 587 &amp;micro;g/mL) on RAW 264.7 cells. In summary, EHAA possesses great potential as a functional ingredient for prevention and/or treatment of chronic diseases.</text>
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                <text>European Food Research and Technology v. 245, no. 8, 2019. -- p. 1539-1551</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>A regional raw clay was used as the starting material to prepare iron-pillared clays with different iron contents. The catalytic activity of these materials was tested in the heterogeneous photo-Fenton process, applied to the degradation of 2-chlorophenol chosen as the model pollutant. Different catalyst loads between 0.2 and 1.0 g L&amp;minus;1 and pH values between 3.0 and 7.0 were studied. The local volumetric rate of photon absorption (LVRPA) in the reactor was evaluated solving the radiative transfer equation applying the discrete ordinate method and using the optical properties of the catalyst suspensions. The photonic and quantum efficiencies of the 2-chlorophenol degradation depend on both the catalyst load and the iron content of the catalyst. The higher values for these parameters, 0.080 mol Einstein&amp;minus;1 and 0.152 mol Einstein&amp;minus;1, respectively, were obtained with 1.0 g L&amp;minus;1 of the catalyst with the higher iron content (17.6%). For the mineralization process, photonic and quantum efficiencies depend mainly on the catalyst load. Therefore, it was possible to employ a natural and cheap resource from the region to obtain pillared clay-based catalysts to degrade organic pollutants in water</text>
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&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>We present a complete all-electron density functional theory/ab initio study of structural and electronic properties at pure In(111) and Cd-doped In(111) surfaces, enabling a deep analysis of the electric field gradient (EFG) in these systems. We explained, from first-principles, results of previously performed key time-differential perturbed &amp;gamma;-&amp;gamma; angular correlations experiments [W. K&amp;ouml;rner et al., Phys. Rev. Lett. 49, 1735 (1982)] on In111 isotopes (which decay to Cd111 impurity probe-atoms) deposited onto the In(111) surface of thin films under ultrahigh vacuum, adding inactive indium layer by layer, carefully designed to determine the EFG at different depths from the surface. We confirmed the existence of only two hyperfine interactions, one related with Cd111 probes localized at the two more superficial In sites (HFIS), and the other related with probes localized in any of the other inequivalent In sites existing from the surface towards the bulk (HFIB). In the case of HFIS, V33 is oriented normal to the (111) surface, and for HFIB we found a V33 orientation parallel to the [001] axis and coincident with the orientation predicted for both the pure and Cd-doped In bulk (not determined experimentally at present), enabling us to confirm the experimental assignment of HFIB. The axial symmetry that the EFG has in pure and Cd-doped In bulk systems is broken when the surface is generated and is recovered as the probe (In or Cd, respectively) goes deeper from the surface into the bulk. We separated the structural and electronic effects and their sources in the pure and Cd-doped In(111) surface. For the Cd-doped systems we confirm the experimental ratio |V33S/V33B|&amp;asymp;4, showing that light structural modifications have in important impact on the Cd p-states distribution, which governs the V33 behavior. Finally, from the combination of the predicted V33 for the Cd-doped systems as a function of the depth of the Cd localization from the surface with the experimental fractions of HFIS and HFIB, we demonstrated that a single 3-&amp;Aring; active monolayer was enough to explain the origin of these fractions (in discrepancy with the previous interpretation of the experiments), proposing a deposition rate for the inactive In layers, in agreement with the experimental fraction evolution as a function of inactive In deposition.</text>
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                <text>&lt;strong&gt;Darriba, Germ&amp;aacute;n N.&lt;/strong&gt;</text>
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                <text>Physical Review B v. 99, no. 19, 2019, -- e195435</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Determination of multiclass, semi-polar pesticide residues in fatty fish muscle tissue by gas and liquid chromatography mass spectrometry&lt;/strong&gt;</text>
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                <text>With the aim of monitoring multiclass semi-polar pesticide residues in freshwater fatty fish, two QuEChERS approaches (so-called acetate buffered and unbuffered versions) were evaluated for the determination of 77 pesticide residues. Compounds were selected according to the dominant rainfed agriculture activities in South America. Unbuffered QuEChERS was finally chosen for validation purposes owing that it provided the best results in terms of recovery yields. Method performance was evaluated in two instrumental systems, liquid chromatography &amp;ndash; tandem mass spectrometry (LC&amp;ndash;MS/MS) in Scheduled MRM&amp;trade; algorithm available on hybrid quadrupole &amp;ndash; linear ion trap (QLIT) instrument, and gas chromatography &amp;ndash; mass spectrometry (GC&amp;ndash;MS) under selected ion monitoring (SIM) mode. Spiking experiments were carried out to determine the trueness, precision, linearity, limit of quantification of the method as well as matrix effect. The Unbuffered QuECHERS method described here: &amp;bull; Was validated for the analysis of 67 pesticide residues in fish muscle tissue. &amp;bull; Presented quantification limits in the range 1&amp;ndash;15&amp;thinsp;&amp;mu;g&amp;thinsp;kg&amp;minus;1 for the vast majority of the studied compounds. &amp;bull; Enable environmental monitoring of pesticide residues in fish due to their low LOQs.</text>
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                <text>&lt;strong&gt;Collazo, Marcos&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Alonso, Beatriz&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Ernst Godoy, Federico.&lt;/strong&gt;</text>
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                <text>MethodsX v. 6, 2019. -- p. 929-937</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>DOI: 10.1016/j.mex.2019.04.014</text>
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                  <text>Bibliografía Nacional Química</text>
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                  <text>Contiene la producción científica nacional de los profesionales químicos e investigadores, durante el período 1929 hasta la fecha.</text>
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                <text>&lt;strong&gt;An overview of environmental arsenic issues and exposure risks in Uruguay&lt;/strong&gt;</text>
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                <text>BIBLIOGRAFIA NACIONAL QUIMICA</text>
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                <text>ARSENICO</text>
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                <text>AGUA POTABLE</text>
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                <text>CONTAMINACION AMBIENTAL</text>
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                <text>Evidence for low-dose health effects of Arsenic (As) in humans is still controversial and presents a major public health issue in several countries worldwide. It is not clear yet, whether there is a lower safe threshold for arsenic in drinking water among other possible sources such as food, below which, exposures are not harmful. In Uruguay, safe drinking water is supplied to 94% of the population by a state company (OSE) and As levels in workplaces and food are officially regulated. This paper aims to present and discuss the issues regarding arsenic exposure risks to the environment and human population, which are being addressed in a multidisciplinary manner in Uruguay since 2007. An overview is given on both the background and the current situation, presenting reports and research studies conducted on these problems by various academic, state, and private institutions that deal with regulations, surveillance, and health care. Scientific research on geogenic As levels in groundwater indicates As levels above those recommended by the WHO for drinking water (10 &amp;mu;g L-1) in different Uruguayan aquifers. There is a lack of baseline studies concerning Uruguayan residents that are exposed to As in drinking water over time. Furthermore, there is a need for data on environmental chemical exposure that could be associated with disease or death in the country. In addition, only a few As risk exposure assessment studies in children, adults, and workers using biomarkers in urine are available. Furthermore, this paper presents As levels in a rice growing region and the spatial distribution of groundwater arsenic data compared to a national cancer atlas database as ongoing research advances. Multidisciplinary research projects and local future actions are also described. This contribution constitutes a first attempt to develop a feasible health risk assessment of low-dose arsenic exposure in this Latin-American country</text>
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                <text>&lt;a title="Curriculum Vitae" href="https://www.google.com/url?sa=t&amp;amp;rct=j&amp;amp;q=&amp;amp;esrc=s&amp;amp;source=web&amp;amp;cd=1&amp;amp;cad=rja&amp;amp;uact=8&amp;amp;ved=2ahUKEwjTxtTB4r_mAhVqHrkGHWs1D3IQFjAAegQIARAH&amp;amp;url=https%3A%2F%2Fexportcvuy.anii.org.uy%2FCvEstatico%2F%3FurlId%3D634eb781f2cbe0d939cf790644adfaec018225d86b7ceb9ac4a95b88749360897f4225dcae0a8b722897405f0b4e3c4d378c7b82cb9ce488150ff125f878119e%26formato%3Dpdf%26convocatoria%3D21&amp;amp;usg=AOvVaw3cYnv5j9twWXIbaNQrV5ev" target="_self"&gt;&lt;strong&gt;Ma&amp;ntilde;ay, Nelly.&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;a title="Curriculum Vitae" href="https://www.google.com/url?sa=t&amp;amp;rct=j&amp;amp;q=&amp;amp;esrc=s&amp;amp;source=web&amp;amp;cd=1&amp;amp;cad=rja&amp;amp;uact=8&amp;amp;ved=2ahUKEwjUpbHa5r_mAhXnK7kGHWGCAqYQFjAAegQIAhAH&amp;amp;url=https%3A%2F%2Fexportcvuy.anii.org.uy%2FCvEstatico%2F%3FurlId%3D61479bcedba0147d3c3d319c58b33c3b8097d0e921a472a96c977f72410c865c0f760872b9315b74ede8b43e4be18142c73316e553e66830ee9d5a4c2cfdd139%26formato%3Dpdf%26convocatoria%3D21&amp;amp;usg=AOvVaw27Y3Lz3kXq6ufLaHD6Mkxc" target="_self"&gt;&lt;strong&gt;Pist&amp;oacute;n, Mariela&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;strong&gt;C&amp;aacute;ceres, M.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Pizzorno, P.&lt;/strong&gt;</text>
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                <text>&lt;a title="Curriculum Vitae" href="https://exportcvuy.anii.org.uy/cv/?ca84b28131b8efed34167ae10248c656ff79f6f431726f73fdd8c44a23a4fa44a73be1d51fa2a55b8b46f6d41be849f47df0616955c90c6098e2b7de9fadc19c" target="_self"&gt;&lt;strong&gt;B&amp;uuml;hl, V&amp;aacute;lery.&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;p&gt;Science of the Total Environment&amp;nbsp; v. 686, 2019. --p. 590-598&lt;/p&gt;</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Herein we report the synthesis, characterization, and photophysical and biological evaluation of the complexes Ln(DBM)3(RPhen) (Ln = Sm, R = H; Ln = Sm, Eu, Tb, R = 5-NH2) stabilized by three &amp;beta;-diketonate units (DBM) and a phenanthroline (RPhen) derivative, with the aim of contributing to the development of lanthanide-based compounds with potential application as anticancer agents. The UV-vis spectra of [Sm(DBM)3(Phen)], [Sm(DBM)3(NH2Phen)], [Eu(DBM)3(NH2Phen)] and [Tb(DBM)3(NH2Phen)] measured in DMSO and PBS showed a strong absorption band centered at ca. 350 nm in both solvents. In DMSO, all lanthanide compounds except [Sm(DBM)3(Phen)] show a ligand centered emission band at ca. 520 nm. In PBS only sharp emission peaks are detected. The complexes show similar cytotoxic effects in A2780 ovarian cancer cells, presenting IC50 values at 24 h in the range 16&amp;ndash;27 &amp;mu;M. The measurement of the cellular uptake of the complexes in the A2780 cells by inductively coupled plasma mass spectrometry (ICP-MS) revealed preferential accumulation at the membrane and cytoskeleton, with the exception of [Sm(DBM)3(Phen)] that presented higher accumulation in the cytosol than in the cell membranes. All the evaluated lanthanide complexes showed low nuclear uptake, although not negligible. Spectroscopic studies on the interaction of the complexes with calf thymus DNA (ctDNA) revealed a moderate affinity with apparent binding constants in the 104 M&amp;minus;1 range. Complexes bind DNA not by intercalation but probably by electrostatic interactions. A morphological evaluation of the cells treated with the different complexes by electron microscopy (TEM/SEM) proved that all of them induce mitochondrial alterations, which seemed more pronounced for the NH2Phen complexes. In addition, the complex [Eu(DBM)3(NH2Phen)] presented lysosomal uptake that might explain its augmented cytotoxicity.</text>
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                <text>&lt;a title="Curriculum Vitae" href="https://exportcvuy.anii.org.uy/CvEstatico/?urlId=6bb5dcce3e2559101357796ca4a2b2d4c9ba6b3a978a0bd4c5dab0107081b73e1ff46dcf49a7de2b571ff7980c4a01789f09f1d7eac1b879a8553641f940b9a5&amp;amp;formato=pdf&amp;amp;convocatoria=21" target="_self"&gt;&lt;strong&gt;Gambino, Dinorah.&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>Dalton Transactions v. 48, no. 14, 2019. -- p. 4611-4624</text>
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                <text>Royal Society of Chemistry</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>&lt;strong&gt;Assessing multimetric trophic state variability during an ENSO event in a large estuary (R&amp;iacute;o de la Plata, South America)&lt;/strong&gt;</text>
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                <text>During the &amp;ldquo;El Ni&amp;ntilde;o&amp;rdquo;- Southern Oscillation (ENSO) event 2009&amp;ndash;2010, trophic state uni (TSI&amp;rsquo;s) and multimetric (TRIX&amp;rsquo;s) indexes were determined in the north coast of the R&amp;iacute;o de la Plata (RdlP). The relationships of such indexes with the hydrological, physical and chemical parameters were explored to identify climatic variability or anthropogenic effects on the eutrophication process. Eleven oceanographic sampling campaigns at 25 stations were conducted along the north coast of RdlP from 2009 to 2011. Temperature, salinity and oxygen saturation, water transparency (Secchi depth), chlorophyll (Chl a) content and total nutrient concentrations (total nitrogen and phosphorous) were determined. Trophic indexes (TSI Chl a, TSI TP, TRIX NP-Voll. and TRIX NP-Mvdeo.) were quantified and the RdlP flow was measured. RdlP flow showed significant differences between ENSO phases, with higher values during &amp;ldquo;El Ni&amp;ntilde;o&amp;rdquo; (EN), negative and significant correlations with salinity, Secchi depth and positive with total nutrients. The trophic status indexes showed spatial and temporal variability and associations with flow, physical and chemical parameters. Trophic state indexes showed spatial and temporal heterogeneity and were strongly associated to environmental conditions (hydrological and seasonal oscillations) during the study period but also to the anthropogenic factors affecting the north coast of RdlP. The system has been classified as mesotrophic to hypertrophic, depending on the selected indicator. According to these results, we suggest the use of a multimetric trophic state indicator, i.e., the TRIX index, as explains better the causes and effects of the eutrophication processes. To implement the TRIX index, (TRIX NP-Mvdeo.) we suggest researchers to consider a large number of local records (Chl a, nutrients, oxygen) at seasonal scales. This index is adapted to the environmental conditions of the study zone and complemented with other community structure indexes, and should be used for eutrophication assessment programs in the north coast of RdlP.</text>
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                <text>&lt;strong&gt;Brugnoli, E.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Muniz, P.&lt;/strong&gt;</text>
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&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Pd nanoparticles anchored on Nb-doped TiO2 with functionalized carbon support (denoted as Pd/Nb&amp;ndash;TiO2&amp;ndash;C) is synthesized through a controllable hydrolysis and impregnation method. The as-synthesized catalyst is characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). Pd nanoparticles exhibit a uniform distribution with an average particle size of 3 nm. The electrochemical performance is tested by cyclic voltammetry (CV) and chronoamperometry (CA). Compared with Pd supported by functionalized carbon (Pd/C), Pd/Nb&amp;ndash;TiO2&amp;ndash;C demonstrates 15.7% higher metallic Pd content, 23% higher electrochemical active surface area, 75% higher current density in ethanol electro-oxidation, 5% higher durability, and better tolerance of carbonaceous species. The performance enhancement is attributed to the increased conductivity from Nb-doping and the synergistic effect between Pd and TiO2.</text>
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                <text>&lt;strong&gt;Brasil, L. M. M.&lt;/strong&gt;</text>
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                <text>Renewable Energy and Power Quality Journal v. 17, 2019. -- p. 480-482</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
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&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>In the present study, synthesis, characterization, and the antibacterial activity of silver nanoparticles from native isolate of Corynebacterium glutamicum has been reported. Silver nanoparticles were synthesized by challenging the dried biomass of C. glutamicum with aqueous diamine silver ([Ag (NH3)2]+) containing 1 mM AgNO3. Synthesized silver nanoparticles (AgNPs) were characterized by ultraviolet&amp;ndash;visible spectroscopy and energy-dispersive X-ray (EDX) spectroscopy analysis. Morphological study of silver nanoparticles was carried out using transmission electron microscopy (TEM) and scanning electron microscope (SEM). The spherical morphology of silver nanoparticles was confirmed from SEM image. The TEM image showed the average particle size of silver nanoparticles was about 15 nm. Silver nanoparticles synthesized from C. glutamicum were found to have enhanced antimicrobial activity against selected pathogenic strains. Silver nanoparticles from pure strains of Corynebacterium species was done by many investigators, but as per the present literature, this is the first report on the production of silver nanoparticles using a native strain of Corynebacterium.</text>
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                <text>Switchgrass (Panicum virgatum) is a perennial grass highly valued as an energy crop resource for the production of bioethanol due to its high carbohydrate content, fast growth, and ability to grow in lands that cannot support crop or food production. In the present study, this biomass was submitted to steam explosion pretreatment in a semi-continuous pre-pilot reactor with the aim of obtaining a pretreated solid with high digestibility for enzymatic hydrolysis. Different conditions of temperature (170&amp;ndash;200 &amp;deg;C) and residence time (5&amp;ndash;15 min), leading to different severity factors (2.76&amp;ndash;4.12) were used for steam explosion pretreatment, which were combined through a 22 central composite design. The results revealed that both variables had great influence in the process, affecting both the biomass structure and the saccharification yield, as a consequence. However, in the range of values evaluated in this study, the effect of the temperature was more prominent than the effect of the residence time. The best saccharification yield (88.3%) was obtained when using the biomass pretreated at 200 &amp;deg;C for 10 min. Similar result was obtained using a commercial cellulose pulp as feedstock for enzymatic hydrolysis, confirming that the best conditions for switchgrass pretreatment in the pre-pilot scale were successfully established.</text>
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&lt;p&gt;&lt;strong&gt; ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>The dissipation of 4 commercial pre-harvest pesticides used in two Citrus species under field conditions is presented. The influence of agroecological region, the Citrus species and weather conditions on abamectin, spinosad, imidacloprid and difenoconazole dissipation rate on fruits were evaluated. A validated ethyl acetate method coupled to liquid chromatography-tandem mass spectrometry allowed the determination of pesticide residues having recoveries of 72&amp;ndash;115%, relative standard deviations &amp;le;16% and quantification limits below the international Maximum Residue Levels (MRLs). After 35&amp;ndash;40 days from pesticides spraying, all residues were below the international required MRL. For each citrus species, the influence of the agroecological region on the pesticide dissipation was assessed. Film-protected fruits against direct radiation and rain showed higher residue levels of imidacloprid and spinosad than the non-protected ones. Either for orange or mandarin, abamectin residues were detectable only at the first day after application. These findings provide useful information to state safer pre harvest intervals and to ensure food safety and compliance with good agricultural practices.</text>
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                <text>&lt;a title="Curriculum Vitae" href="https://www.google.com/url?sa=t&amp;amp;rct=j&amp;amp;q=&amp;amp;esrc=s&amp;amp;source=web&amp;amp;cd=1&amp;amp;cad=rja&amp;amp;uact=8&amp;amp;ved=2ahUKEwjFsIWj5r_mAhVkIbkGHf6iB7QQFjAAegQIBRAH&amp;amp;url=https%3A%2F%2Fexportcvuy.anii.org.uy%2FCvEstatico%2F%3FurlId%3Dfda2ddd3225e35b6cd0dd11333996b08c4f2ec35ccdbe92a4a51420f1bc7853e8c31c9c047392931df7517b95a6a8bc0513e278125b0cdd382223a0af2e3d381%26formato%3Dpdf%26convocatoria%3D21&amp;amp;usg=AOvVaw27THRXuO9wnELzxGIHdvMy" target="_self"&gt;&lt;strong&gt;P&amp;eacute;rez Parada, Andr&amp;eacute;s&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;strong&gt;Rivas, Fernando.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;&lt;a title="Curriculum Vitae" href="https://exportcvuy.anii.org.uy/CvEstatico/?urlId=efdc2e4d27c46568e51501a117c8d64c661d28215277fe2b1621ea4a392338f0bd55c3b410eb66c8bd85997e02d92a5828f529ff076bd0478d3b4ffd01ec2037&amp;amp;formato=pdf&amp;amp;convocatoria=21" target="_self"&gt;Heinzen, Horacio.&lt;/a&gt;&lt;/strong&gt;</text>
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                <text>Scientia Horticulturae&amp;nbsp; v. 248, 2019. -- p. 34-40</text>
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                <text>Scientia Horticulturae v. 248, 2019. -- p. 34-40</text>
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            <description>Information about rights held in and over the resource</description>
            <elementTextContainer>
              <elementText elementTextId="532988">
                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Ingl&amp;eacute;s</text>
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                <text>DOI: 10.1016/j.scienta.2018.12.053</text>
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                <text>Uruguay</text>
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        <name>Naranjas</name>
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        <name>Pesticidas</name>
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        <name>Residuos de pesticidas</name>
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        <name>Uruguay</name>
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                  <text>Bibliografía Nacional Química</text>
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                  <text>Contiene la producción científica nacional de los profesionales químicos e investigadores, durante el período 1929 hasta la fecha.</text>
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                  <text>Departamento de Documentación y Biblioteca</text>
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          <description>If the image is of an object, state the type of object, such as painting, sculpture, paper, photo, and additional data</description>
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                <text>&lt;strong&gt;Inefficient and abortive classical complement pathway activation by the calcium inositol hexakisphosphate component of the Echinococcus granulosus laminated layer&lt;/strong&gt;</text>
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                <text>ENFERMEDADES PARASITARIAS</text>
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                <text>ECHINOCOCCUS GRANULOSUS</text>
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                <text>EQUINOCOSIS QUISTICA</text>
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                <text>BIBLIOGRAFIA NACIONAL QUIMICA</text>
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                <text>Persistent extracellular tissue-dwelling pathogens face the challenge of antibody-dependent activation of the classical complement pathway (CCP). A prime example of this situation is the larva of the cestode Echinococcus granulosus sensu lato, causing cystic echinococcosis. This tissue-dwelling, bladder-like larva is bounded by a cellular layer protected by the outermost acellular &amp;ldquo;laminated layer&amp;rdquo; (LL), to which host antibodies bind. The LL is made up of a mucin meshwork and interspersed nano-deposits of calcium inositol hexakisphosphate (calcium InsP6). We previously reported that calcium InsP6 bound C1q, apparently initiating CCP activation. The present work dissects CCP activation on the LL. Most of the C1 binding activity in the LL corresponded to calcium InsP6, and this binding was enhanced by partial proteolysis of the mucin meshwork. The remaining C1 binding activity was attributable to host antibodies, which included CCP-activating IgG isotypes. Calcium InsP6 made only a weak contribution to early CCP activation on the LL, suggesting inefficient C1 complex activation as reported for other polyanions. CCP activation on calcium InsP6 gave rise to a dominant population of C3b deposited onto calcium InsP6 itself that appeared to be quickly inactivated. Apparently as a result of inefficient initiation plus C3b inactivation, calcium InsP6 made no net contribution to C5 activation. We propose that the LL protects the underlying parasite cells from CCP activation through the combined effects of inefficient permeation of C1 through the mucins and C1 retention on calcium InsP6. This mechanism does not result in C5 activation, which is known to drive parasite-damaging inflammation.</text>
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                <text>&lt;strong&gt;Barrios, Anabella A.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Grezzi, Leticia&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Miles, Sebasti&amp;aacute;n&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Mariconti, Mara&lt;/strong&gt;</text>
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                <text>&lt;a title="Curriculum Vitae" href="https://exportcvuy.anii.org.uy/CvEstatico/?urlId=8077d6141c1946a30df792835b6b6ef857fe8ef0419315625ad1c8238bb9aca6cff0e2e3a0117a509b98df7dc5fd1db6728b0697ffb3f71b1ca9ceb5260c5454&amp;amp;formato=pdf&amp;amp;convocatoria=21" target="_self"&gt;&lt;strong&gt;Mourglia Ettlin, Gustavo Daniel.&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>&lt;strong&gt;Seoane, Paula I.&lt;/strong&gt;</text>
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                <text>&lt;a title="Curriculum Vitae" href="https://www.google.com/url?sa=t&amp;amp;rct=j&amp;amp;q=&amp;amp;esrc=s&amp;amp;source=web&amp;amp;cd=1&amp;amp;cad=rja&amp;amp;uact=8&amp;amp;ved=2ahUKEwiR-faO27_mAhUAGrkGHbG5AxwQFjAAegQIBBAH&amp;amp;url=https%3A%2F%2Fexportcvuy.anii.org.uy%2Fpdf%2F%3Fc855a45b7dae1af50c961a96b5eb15c26a7b943e53f84d972caa0f9ce21ec5f03ef21e57ce461b5656b60c7a13dbc71dbc1dad52a109e231d5b638ac5639067d&amp;amp;usg=AOvVaw2-p60bssNmxkcYsJPe3H-P" target="_self"&gt;&lt;strong&gt;Alvaro, D&amp;iacute;az&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>Immunobiology v.224, no.5, 2019. -- p. 710-719</text>
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              <elementText elementTextId="533012">
                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>DOI:10.1016/j.imbio.2019.05.009</text>
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                <text>&lt;strong&gt;Characterizing Honeybee Cuticular Hydrocarbons During Foraging&lt;/strong&gt;</text>
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                <text>Honeybees (Apis mellifera) adjust their time and effort during foraging activity. Their metabolic rates together with body temperature rise while gathering profitable resources. These physiological changes may result in a differential cuticular profile, which in turn may bear communicational value. We evaluated if sucrose concentration of collected food affects the cuticular chemistry of honeybees during foraging. We trained bees to artificial feeders with high (2 M) and low (0.5 M) sucrose concentrations, and captured the active foragers for surface extraction of cuticular compounds. We sampled foragers just after feeding, before taking-off towards the hive, and upon landing at the hive entrance, before entering the hive. Through gas chromatography-mass spectrometry analysis of cuticular extracts, we identified and quantified 48 compounds, including cuticular hydrocarbons (CHCs) and volatiles associated with exocrine glands. We found that higher sucrose concentrations resulted in increased amounts of alkanes and alkenes in the surface extracts of foragers captured at the hive entrance, but not at the feeding site. Our results suggest that the differences that have been reported for CHCs in waggle-dancing honey bees can be already found once they return to the hive from profitable food sources.</text>
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                <text>Sociobiology v. 66,no. 1, 2019.-- p.97-106</text>
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              <elementText elementTextId="544879">
                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>DOI: 10.13102/sociobiology.v66i1.2977</text>
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                <text>&lt;strong&gt;An In Silico Study of the Citrus Dioxygenases CCD4 family Substrates&lt;/strong&gt;</text>
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                <text>The coloration of Citrus fruits is related with the concentration of carotenoids, isoprenoid pigments of 40 carbon atoms (C40). Rodrigo et al. and Ma et al. reported a CCD4-type citrus dioxygenase responsible for the generation of C30 apocarotenoids providing a reddish-orange pigmentation to the peel of many mandarins and oranges. Among them, CCD4b was the first case described of a dioxygenase that cleaves carotenoids C40 in the double bond 7', 8' or 7, 8, generating &amp;beta;-citraurin or 8-&amp;beta;-apocarotenal. Here we report the three-dimensional structures of CCD4a and CCD4b, modeled by sequence homology (2BIW) and validated by molecular dynamics (MD). Docking calculations were performed in CCD4a and CCD4b structures with thousands of rotated initial carotenoid conformations and all the possible poses in the active site were found. The interaction energy was measured by means of ASE scoring, Amber99 refinement and London &amp;Delta;G rescoring. For the case of CCD4a model, the results showed London &amp;Delta;G score of -19, -17 and -15&amp;thinsp;kcal/mol for zeaxanthin, &amp;beta;-cryptoxanthin and &amp;beta;-carotene, respectively. The same sequence in the estimated interaction strength for the three ligands was obtained using MD. The interaction energy of CCD4b indicated that, in agreement with experimental data, zeaxanthin and &amp;beta;-cryptoxanthin could be cleaved by the enzyme, &amp;beta;- and &amp;alpha;-carotene have chances to be oxidized and lycopene has not good interaction energy to be predicted as substrate. These findings will be discussed considering the potential in vivo substrates and products, and the physiological role in Citrus fruits. Communicated by Ramaswamy H. Sarma.</text>
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                <text>&lt;strong&gt;Vega Teijido, Mauricio&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Cantero, Jorge&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;L&amp;oacute;pez, Carolina&lt;/strong&gt;</text>
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                <text>Journal of Biomolecular Structure &amp;amp; Dynamics v. 37, no, 8, 2019. -- p. 2086-2097</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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          <description>If the image is of an object, state the type of object, such as painting, sculpture, paper, photo, and additional data</description>
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                <text>&lt;strong&gt;S&amp;iacute;ntesis y caracterizaci&amp;oacute;n de boratos de zinc con aplicaci&amp;oacute;n en ciencia de materiales&lt;/strong&gt;</text>
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                <text>QU&amp;Iacute;MICA ANAL&amp;Iacute;TICA</text>
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                <text>BORATOS DE ZINC</text>
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                <text>NANOQU&amp;Iacute;MICA</text>
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                <text>SINTESIS DE COMPUESTOS INORG&amp;Aacute;NICOS</text>
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                <text>APLICACI&amp;Oacute;N EN MICROBIOLOG&amp;Iacute;A</text>
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                <text>ZINC</text>
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                <text>En este trabajo de tesis se han explorado dos metodolog&amp;iacute;as en la b&amp;uacute;squeda de la obtenci&amp;oacute;n de nanopart&amp;iacute;culas de boratos de zinc. Estas metodolog&amp;iacute;as fueron planteadas para lograr sintetizar fases de boratos de zinc en distintos rangos de temperaturas, lo que brinda grandes posibilidades en el desarrollo de aplicaciones tecnol&amp;oacute;gicas. Empleando la s&amp;iacute;ntesis por combusti&amp;oacute;n de gel asistida se pretendi&amp;oacute; sintetizar boratos de zinc a temperatura mayores a 250 &amp;deg;C, para los cuales se esperaba obtener nanopart&amp;iacute;culas que fueran importantes en el desarrollo de nuevos aditivos de materiales que se preparan a altas temperaturas, por ejemplo, pl&amp;aacute;sticos. A partir de las s&amp;iacute;ntesis asistidas por micelas reversas, se pretendi&amp;oacute; obtener boratos de zinc a baja temperatura, por ejemplo, los aminoboratos de zinc [Zn(NH3)3B4O5(OH)4]&amp;middot;H2O (ZB1) y Zn3(H2B3O7)2&amp;middot;2NH3&amp;middot;4H2O (ZB2), reportados previamente durante mi trabajo de Licenciatura en Qu&amp;iacute;mica. Mediante la metodolog&amp;iacute;a de combusti&amp;oacute;n de gel asistida se logr&amp;oacute; sintetizar la fase ZnB4O7. Los resultados presentados para estas s&amp;iacute;ntesis son contundentes respecto a los procesos qu&amp;iacute;micos que tienen lugar en el sistema estudiado. El medio reductor ofrecido por la alta concentraci&amp;oacute;n de amonio da lugar a la formaci&amp;oacute;n de carbono amorfo que permanece como principal impureza en las muestras obtenidas, no siendo posible la obtenci&amp;oacute;n de nanopart&amp;iacute;culas de boratos de zinc. La obtenci&amp;oacute;n de ZB2 por m&amp;eacute;todos de baja temperatura fue posible a partir de un sistema coloidal mantenido por agitaci&amp;oacute;n formado por agua, CTAB, hexano y diferentes alcoholes como cosurfactantes. Para estos sistemas se obtuvo la fase cristalina ZB2 con tama&amp;ntilde;os entre 100 y 1000 nm, report&amp;aacute;ndose tama&amp;ntilde;os menores a 150 nm cuando se emple&amp;oacute; isopropanol como cosurfactante. Tambi&amp;eacute;n se sintetiz&amp;oacute; la fase ZB2 en un medio de micelas reversas. Este &amp;uacute;ltimo es uno de los logros m&amp;aacute;s importantes de este trabajo, ya que se consigui&amp;oacute; estabilizar un sistema de micelas reversas y obtener un producto con un tama&amp;ntilde;o de part&amp;iacute;cula menor a 150 nm. Este trabajo es un aporte importante en la qu&amp;iacute;mica b&amp;aacute;sica de estos sistemas, abriendo puertas a futuros estudios de s&amp;iacute;ntesis en sistemas de micelas reversas. La metodolog&amp;iacute;a utilizada para determinar las condiciones de formaci&amp;oacute;n de micelas reversas es extrapolable a cualquier sistema de obtenci&amp;oacute;n de compuestos qu&amp;iacute;micos a partir de una soluci&amp;oacute;n acuosa con par&amp;aacute;metros de concentraci&amp;oacute;n y fuera i&amp;oacute;nica adecuados. Los estudios microbiol&amp;oacute;gicos realizados sobre la fase ZB2 permitieron confirmar la actividad antif&amp;uacute;ngica y antibacteriana presentada por este compuesto y su dependencia con el tama&amp;ntilde;o de part&amp;iacute;cula.</text>
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                <text>&lt;strong&gt;Imer, Marcos&lt;/strong&gt;</text>
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                <text>Montevideo: UdelaR-Facultad de Qu&amp;iacute;mica</text>
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            <name>Date</name>
            <description>A point or period of time associated with an event in the lifecycle of the resource</description>
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                <text>2019</text>
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            <name>Rights</name>
            <description>Information about rights held in and over the resource</description>
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              <elementText elementTextId="518201">
                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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            <name>Format</name>
            <description>The file format, physical medium, or dimensions of the resource</description>
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                <text>Papel</text>
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            <name>Language</name>
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                <text>Espa&amp;ntilde;ol</text>
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            <name>Type</name>
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        <name>Aplicación en Microbiologia</name>
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        <name>Boratos de Zinc</name>
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        <name>Nanoquímica</name>
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        <name>Química analítica</name>
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        <name>Sintesis de Compuestos Inorgánicoss</name>
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                  <text>Versiones electrónicas de las tesis de doctorado, maestría y trabajos de diploma de la Facultad de Química, Universidad de la República (UdelaR).&#13;
Incluye únicamente trabajos hasta el año 2023. Los trabajos posteriores se encuentran disponibles en el Repositorio Colibrí.</text>
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          <description>If the image is of an object, state the type of object, such as painting, sculpture, paper, photo, and additional data</description>
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                <text>&lt;strong&gt;Desarrollo de metodolog&amp;iacute;as analiticas para la determinaci&amp;oacute;n de contaminantes traza org&amp;aacute;nicos e inorg&amp;aacute;nicos en miel&lt;/strong&gt;</text>
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                <text>QU&amp;Iacute;MICA ANAL&amp;Iacute;TICA</text>
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                <text>CC-MS/-MS</text>
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                <text>METALES</text>
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                <text>ESPECTROMETRIA ATOMICA</text>
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                <text>Palabras clave: miel, determinaci&amp;oacute;n de metales, determinaci&amp;oacute;n de alcaloides pirrolizid&amp;iacute;nicos, an&amp;aacute;lisis en flujo, GC-MS, LC-MS/MS. El objetivo de esta tesis fue desarrollar metodolog&amp;iacute;as simples, r&amp;aacute;pidas, confiables y validadas que permitan la determinaci&amp;oacute;n en miel de dos grupos de analitos de inter&amp;eacute;s por su toxicidad, alcaloides pirrolizid&amp;iacute;nicos y metales. Con este prop&amp;oacute;sito, se busc&amp;oacute; simplificar la etapa de preparaci&amp;oacute;n de muestra y emplear t&amp;eacute;cnicas anal&amp;iacute;ticas simples, de bajo costo y f&amp;aacute;cilmente disponibles. Se exploraron entonces, diversas t&amp;eacute;cnicas tanto para la preparaci&amp;oacute;n de muestra como para la determinaci&amp;oacute;n. Para la preparaci&amp;oacute;n de muestra se emplearon t&amp;eacute;cnicas como la extracci&amp;oacute;n de punto nube, extracci&amp;oacute;n en fase s&amp;oacute;lida, microextracci&amp;oacute;n l&amp;iacute;quido-l&amp;iacute;quido dispersiva, extracci&amp;oacute;n del tipo QuEChERs y QuPPe. Las t&amp;eacute;cnicas empleadas para la determinaci&amp;oacute;n de los analitos de inter&amp;eacute;s fueron tambi&amp;eacute;n diversas dentro de la espectrometr&amp;iacute;a at&amp;oacute;mica y la cromatograf&amp;iacute;a. Se aplic&amp;oacute; espectrometr&amp;iacute;a de absorci&amp;oacute;n at&amp;oacute;mica de llama, espectrometr&amp;iacute;a de emisi&amp;oacute;n at&amp;oacute;mica de plasma de acoplamiento inductivo, cromatograf&amp;iacute;a de l&amp;iacute;quidos acoplada a detector de arreglo de diodos, de fluorescencia y a espectrometr&amp;iacute;a de masas y la cromatograf&amp;iacute;a gaseosa acoplada a espectrometr&amp;iacute;a de masas. Se aplicaron t&amp;eacute;cnicas de an&amp;aacute;lisis en flujo como el an&amp;aacute;lisis por inyecci&amp;oacute;n secuencial, el an&amp;aacute;lisis en flujo multiconmutado y plataformas mesoflu&amp;iacute;dicas como LOV. Se desarroll&amp;oacute; un m&amp;eacute;todo automatizado para la determinaci&amp;oacute;n de cadmio y plomo empleando LOV y como m&amp;eacute;todo de preparaci&amp;oacute;n de muestra extracci&amp;oacute;n en fase s&amp;oacute;lida empleando una resina de modo mixto, fase reversa e intercambio de cationes. 16 Desarrollo de metodolog&amp;iacute;as anal&amp;iacute;ticas para la determinaci&amp;oacute;n de contaminantes traza org&amp;aacute;nicos e inorg&amp;aacute;nicos en miel Desarrollo de metodolog&amp;iacute;as anal&amp;iacute;ticas para la determinaci&amp;oacute;n de contaminantes traza org&amp;aacute;nicos e inorg&amp;aacute;nicos en miel Se desarroll&amp;oacute; un m&amp;eacute;todo mecanizado para la determinaci&amp;oacute;n de cadmio empleando microextracci&amp;oacute;n l&amp;iacute;quido-l&amp;iacute;quido dispersiva cuyos par&amp;aacute;metros de desempe&amp;ntilde;o son adecuados al uso y en comparaci&amp;oacute;n con otros m&amp;eacute;todos reportados de similares caracter&amp;iacute;sticas, tiene un mejor desempe&amp;ntilde;o anal&amp;iacute;tico y mayor rapidez. Ambos m&amp;eacute;todos cumplen con la caracter&amp;iacute;stica de simplicidad en la preparaci&amp;oacute;n de muestra buscada y pueden ser empleados para evaluar la inocuidad de la miel desde el punto de vista de la contaminaci&amp;oacute;n por metales. Adem&amp;aacute;s, el m&amp;eacute;todo desarrollado a partir de la microextracci&amp;oacute;n l&amp;iacute;quido-l&amp;iacute;quido dispersiva por su rapidez, puede ser usado para evaluar episodios de contaminaci&amp;oacute;n donde las abejas act&amp;uacute;en como biomonitor a trav&amp;eacute;s de su producto la miel, y un n&amp;uacute;mero muy alto de muestras necesita ser procesado. Con respecto a los alcaloides pirrolizid&amp;iacute;nicos, se obtuvo como resultado de esta tesis un m&amp;eacute;todo para su determinaci&amp;oacute;n en miel empleando una variante de QuPPe (Quick Polar Pesticides Method) y cromatograf&amp;iacute;a de l&amp;iacute;quidos acoplada a espectrometr&amp;iacute;a de masas. La preparaci&amp;oacute;n de muestra consisti&amp;oacute; en la simple extracci&amp;oacute;n de los compuestos en acetonitrilo acidificado. Los m&amp;eacute;todos fueron optimizados aplicando dise&amp;ntilde;o de experimentos como dise&amp;ntilde;o factorial, completo o central compuesto, o de forma univariante. Una vez optimizados los m&amp;eacute;todos se validaron y aplicaron al an&amp;aacute;lisis de muestras del mercado. El desarrollo de esta tesis permiti&amp;oacute; entonces generar distintas metodolog&amp;iacute;as que pueden contribuir a garantizar la inocuidad de la miel tanto para su consumo como su comercio.</text>
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                <text>&lt;strong&gt;Sixto Anidos, Alexandra Mar&amp;iacute;a&lt;/strong&gt;</text>
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                <text>Montevideo: UdelaR-Facultad de Qu&amp;iacute;mica</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                  <text>Versiones electrónicas de las tesis de doctorado, maestría y trabajos de diploma de la Facultad de Química, Universidad de la República (UdelaR).&#13;
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                <text>&lt;strong&gt;Celulasas sicr&amp;oacute;filas, una innovaci&amp;oacute;n en la industria del bioetanol&lt;/strong&gt;</text>
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                <text>En este trabajo de tesis se han explorado dos metodolog&amp;iacute;as en la b&amp;uacute;squeda de la obtenci&amp;oacute;n de nanopart&amp;iacute;culas de boratos de zinc. Estas metodolog&amp;iacute;as fueron planteadas para lograr sintetizar fases de boratos de zinc en distintos rangos de temperaturas, lo que brinda grandes posibilidades en el desarrollo de aplicaciones tecnol&amp;oacute;gicas. Empleando la s&amp;iacute;ntesis por combusti&amp;oacute;n de gel asistida se pretendi&amp;oacute; sintetizar boratos de zinc a temperatura mayores a 250 &amp;deg;C, para los cuales se esperaba obtener nanopart&amp;iacute;culas que fueran importantes en el desarrollo de nuevos aditivos de materiales que se preparan a altas temperaturas, por ejemplo, pl&amp;aacute;sticos. A partir de las s&amp;iacute;ntesis asistidas por micelas reversas, se pretendi&amp;oacute; obtener boratos de zinc a baja temperatura, por ejemplo, los aminoboratos de zinc [Zn(NH3)3B4O5(OH)4]&amp;middot;H2O (ZB1) y Zn3(H2B3O7)2&amp;middot;2NH3&amp;middot;4H2O (ZB2), reportados previamente durante mi trabajo de Licenciatura en Qu&amp;iacute;mica. Mediante la metodolog&amp;iacute;a de combusti&amp;oacute;n de gel asistida se logr&amp;oacute; sintetizar la fase ZnB4O7. Los resultados presentados para estas s&amp;iacute;ntesis son contundentes respecto a los procesos qu&amp;iacute;micos que tienen lugar en el sistema estudiado. El medio reductor ofrecido por la alta concentraci&amp;oacute;n de amonio da lugar a la formaci&amp;oacute;n de carbono amorfo que permanece como principal impureza en las muestras obtenidas, no siendo posible la obtenci&amp;oacute;n de nanopart&amp;iacute;culas de boratos de zinc. La obtenci&amp;oacute;n de ZB2 por m&amp;eacute;todos de baja temperatura fue posible a partir de un sistema coloidal mantenido por agitaci&amp;oacute;n formado por agua, CTAB, hexano y diferentes alcoholes como cosurfactantes. Para estos sistemas se obtuvo la fase cristalina ZB2 con tama&amp;ntilde;os entre 100 y 1000 nm, report&amp;aacute;ndose tama&amp;ntilde;os menores a 150 nm cuando se emple&amp;oacute; isopropanol como cosurfactante. Tambi&amp;eacute;n se sintetiz&amp;oacute; la fase ZB2 en un medio de micelas reversas. Este &amp;uacute;ltimo es uno de los logros m&amp;aacute;s importantes de este trabajo, ya que se consigui&amp;oacute; estabilizar un sistema de micelas reversas y obtener un producto con un tama&amp;ntilde;o de part&amp;iacute;cula menor a 150 nm. Este trabajo es un aporte importante en la qu&amp;iacute;mica b&amp;aacute;sica de estos sistemas, abriendo puertas a futuros estudios de s&amp;iacute;ntesis en sistemas de micelas reversas. La metodolog&amp;iacute;a utilizada para determinar las condiciones de formaci&amp;oacute;n de micelas reversas es extrapolable a cualquier sistema de obtenci&amp;oacute;n de compuestos qu&amp;iacute;micos a partir de una soluci&amp;oacute;n acuosa con par&amp;aacute;metros de concentraci&amp;oacute;n y fuera i&amp;oacute;nica adecuados. Los estudios microbiol&amp;oacute;gicos realizados sobre la fase ZB2 permitieron confirmar la actividad antif&amp;uacute;ngica y antibacteriana presentada por este compuesto y su dependencia con el tama&amp;ntilde;o de part&amp;iacute;cula</text>
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                <text>&lt;strong&gt;Herrera, Lorena.&lt;/strong&gt;</text>
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                <text>Montevideo: Udelar-Facultad de Química</text>
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                <text>&lt;strong&gt;&lt;a title="Curriculum Vitae" href="http://buscadores.anii.org.uy/buscador_sni/exportador/ExportarPdf?hash=729d3d9bb07d7be0ba5e4dc762c01e29" target="_self"&gt;Franco Fraguas, Laura&lt;/a&gt;&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Castro, Susana&lt;/strong&gt;</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                <text>Microorganisms were isolated from industrial wool scouring effluents and from the soil adjacent to the wastewater treatment lagoon, both sterols-rich environments, in order to search for novel biocatalysts able to transform cholesterol. The isolates were identified on the basis of morphological and biochemical characteristics and phylogenetic analysis. Furthermore, a rapid and accurate bacteria identification by matrix assisted laser desorption/ionization-time-of-flight mass spectrometry was carried out. Bacteria and fungi including representatives of the genera Fusarium, Talaromyces, Trichoderma, Mucor, Aspergillus, Citrobacter, Proteus, Klebsiella, Exiguobacterium, Acinetobacter, Tsukamurella, Bacillus, and Streptomyces were found and evaluated for their ability to biotransform cholesterol by whole-cell treatment system. The results show that a Trichoderma koningiopsis strain, as well as two strains of Mucor circinelloides were able to transform cholesterol into value-added products. The major products were characterized as 7&amp;beta;-hydroxycholesterol, 4-cholesten-3-one, 5&amp;alpha;,6&amp;alpha;-epoxycholestan-3&amp;beta;-ol and 5&amp;beta;,6&amp;beta;-epoxycholestan-3&amp;beta;-ol. To the best of our knowledge, the present study is the first report of cholesterol biotransformation by representatives of Trichoderma and Mucor genera</text>
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                <text>&lt;strong&gt;Giorgi, Victoria&lt;/strong&gt;</text>
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&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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                  <text>Contiene la producción científica nacional de los profesionales químicos e investigadores, durante el período 1929 hasta la fecha.</text>
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                <text>&lt;strong&gt;Response of Diaphorina citri (Hemiptera: Liviidae) to volatiles characteristic of preferred citrus hosts&lt;/strong&gt;</text>
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                <text>PLAGAS</text>
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                <text>DIAPHORINA CITRI</text>
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                <text>The Asian citrus psyllid, Diaphorina citri, is currently the most important pest of citrus worldwide because it vectors &amp;lsquo;Candidatus Liberibacter&amp;rsquo; spp., the etiological agents of lethal Huanglongbing (HLB). Reduction of D. citri populations is a key component of HLB management. Identifying potential D. citri attractants, such as volatiles, could be useful for behavioral management of this insect. This could, for instance, enhance catches of adults on monitoring traps. The overall aim of this study was to investigate the response of D. citri to volatiles characteristic of preferred citrus hosts. An ancillary objective was to formulate a synthetic blend of volatiles based on preferred host odors that could enhance monitoring traps. Volatile collections of two preferred citrus species, Duncan grapefruit (Citrus paradise) and sweet orange (Citrus sinensis), were performed in aeration chambers and analyzed by gas chromatography-mass spectrometry. Based on the grapefruit volatile profile, a synthetic blend consisting in d-limonene (0.62 mg), methyl N-methylanthranilate (0.19 mg), &amp;beta;-ocimene (0.11 mg), &amp;beta;-elemene (0.02 mg), and &amp;beta;-caryophyllene (0.02 mg) was prepared in 9.9 mL of dichloromethane and evaluated for attractiveness, as well as the individual compounds, and compared with a positive control of natural volatiles collected from Citrus sinensis. Behavior of D. citri adults was evaluated in two-choice behavioral assays comparing response to lures with different combinations and dosages of the volatiles deployed on yellow sticky traps. Individually, neither d-limonene nor methyl N-methylanthranilate affected behavior of D. citri. However, these volatiles increased catches of D. citri, as compared with solvent control, when presented as components of the synthetic grapefruit blend, as did the natural citrus odor positive control. Importantly, catch of D. citri appeared to vary with the release rate of the identified grapefruit volatile blend, which was attractive at a 0.1 mg loading dosage, but repellent at a dosage only 1 log step higher.</text>
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                <text>&lt;strong&gt;Amor&amp;oacute;s, Mar&amp;iacute;a Eugenia&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Pereira das Neves, Virginia.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Rivas, Fernando.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Buenahora Acosta, Jos&amp;eacute; Hermes.&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Martini, Xavier&lt;/strong&gt;</text>
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                <text>&lt;strong&gt;Stelinski, Lukasz L&lt;/strong&gt;.</text>
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                <text>&lt;a title="Curriculum Vitae" href="https://www.google.com/url?sa=t&amp;amp;rct=j&amp;amp;q=&amp;amp;esrc=s&amp;amp;source=web&amp;amp;cd=1&amp;amp;cad=rja&amp;amp;uact=8&amp;amp;ved=2ahUKEwj1sfiR6L_mAhX2HbkGHfoOB6IQFjAAegQIAxAE&amp;amp;url=https%3A%2F%2Fexportcvuy.anii.org.uy%2FCvEstatico%2F%3FurlId%3D0ac67fcafcb05bf82a3b4f786e94421e55e9c32193a59fde55335950e4436b28365608365e898c13ec1423a96e4446d3e85ca026c37efbe62a5d1cfad62cc2ea%26formato%3Dpdf%26convocatoria%3D21&amp;amp;usg=AOvVaw01x06vB1PdGM_4930ySy_t" target="_self"&gt;&lt;strong&gt;Rossini, Carmen&lt;/strong&gt;&lt;/a&gt;</text>
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                <text>Arthropod-Plant Interactions v. 13, no. 3, 2019. -- p. 367-374</text>
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                <text>&lt;p&gt;&lt;strong&gt;Informaci&amp;oacute;n sobre Derechos de Autor&lt;/strong&gt;&lt;/p&gt;&#13;
&lt;p&gt;(Por favor lea este aviso antes de abrir los documentos u objetos)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;La legislaci&amp;oacute;n uruguaya protege el derecho&lt;/strong&gt; de autor sobre toda creaci&amp;oacute;n literaria, cient&amp;iacute;fica o art&amp;iacute;stica, tanto en lo que tiene que ver con sus derechos morales, como en lo referente a los derechos patrimoniales con sujeci&amp;oacute;n a lo establecido por el derecho com&amp;uacute;n y las siguientes leyes (LEY 9.739 DE 17 DE DICIEMBRE DE 1937 SOBRE PROPIEDAD LITERARIA Y ARTISTICA CON LAS MODIFICACIONES INTRODUCIDAS POR LA LEY DE DERECHO DE AUTOR Y DERECHOS CONEXOS No. 17.616 DE 10 DE ENERO DE 2003, LEY 17.805 DE 26 DE AGOSTO DE 2004, LEY 18.046 DE 24 DE OCTUBRE DE 2006)&lt;/p&gt;&#13;
&lt;p&gt;&lt;strong&gt;ADVERTENCIA -&lt;/strong&gt; La consulta de este documento queda condicionada a la aceptaci&amp;oacute;n de las siguientes condiciones de uso: Este documento es &amp;uacute;nicamente para usos privados enmarcados en actividades de investigaci&amp;oacute;n y docencia. No se autoriza su reproducci&amp;oacute;n con fines de lucro. Esta reserva de derechos afecta tanto los datos del documento como a sus contenidos. En la utilizaci&amp;oacute;n o cita de partes debe indicarse el nombre de la persona autora.&lt;/p&gt;</text>
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