69 research outputs found

    Are empirical equations an appropriate tool to assess separation distances to avoid odour annoyance?

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    Annoyance due to environmental odour exposure is in many jurisdictions evaluated by a yes/no decision. Such a binary decision has been typically achieved via odour impact criteria (OIC) and, when applicable, the resultant separation distances between emission sources and residential areas. If the receptors lie inside the required separation distance, odour exposure is characterised with the potential of causing excessive annoyance. The state-of-the-art methodology to determine separation distances is based on two general steps: (i) calculation of the odour exposure (time series of ambient odour concentrations) using dispersion models and (ii) determination of separation distances through the evaluation of this odour exposure by OIC. Regarding meteorological input data, dispersion models need standard meteorological observations and/or atmospheric stability typically on an hourly basis, which requires expertise in this field. In the planning phase, and as a screening tool, an educated guess of the necessary separation distances to avoid annoyance is in some cases sufficient. Therefore, empirical equations (EQs) are in use to substitute the more time-consuming and costly application of dispersion models. Because the separation distance shape often resembles the wind distribution of a site, wind data should be included in such approaches. Otherwise, the resultant separation distance shape is simply given by a circle around the emission source. Here, an outline of selected empirical equations is given, and it is shown that only a few of them properly reflect the meteorological situation of a site. Furthermore, for three case studies, separation distances as calculated from empirical equations were compared against those from Gaussian plume and Lagrangian particle dispersion models. Overall, our results suggest that some empirical equations reach their limitation in the sense that they are not successful in capturing the inherent complexity of dispersion models. However, empirical equations, developed for Germany and Austria, have the potential to deliver reasonable results, especially if used within the conditions for which they were designed. The main advantage of empirical equations lies in the simplification of the meteorological input data and their use in a fast and straightforward approach

    Caracterização da autoincompatibilidade em populações segregantes de macieira via marcadores de DNA para alelos S.

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    Abstract - The objective of this study was to characterize the parents and respective populations of apple trees regarding S-alleles to confirm their genealogy and to evaluate the efficiency of the molecular markers used. Sixteen specific sets of primers were used for identification of apple S-alleles by PCR. Two segregating populations of the Epagri Apple Breeding Program resulting from crosses between ?Fred Hough? × ?Monalisa? and ?M-11/00? × ?M-13/91? were evaluated. The expected segregations are 1:1:1:1 for full compatibility and 1:1 for semi-compatibility, which can be confirmed by the X2 test. The ?Fred Hough? (S5 S19) × ?Monalisa? (S2 S10) cross proved to be fully compatible; and two triploids were identified among the hybrids as well. The ?M-11/00? (S3 S19) × ?M-13/91? (S3 S5 ) cross was characterized as semi-compatible based on DNA markers, and the segregation of the S-alleles in the hybrids was 1:1, as expected. The segregation of the DNA markers occurred together with their respective S-alleles: S2, S3 , S5 , S10, and S19. Thus, characterization of the S-alleles not only allowed identification of compatibility between parents but also identified contaminations in segregating populations. Index terms: Malus × domestica Borkh., S genotype, S-RNase, allele-specific PCR, segregation. Caracterização da autoincompatibilidade em populações segregantes de macieira via marcadores de DNA para alelos S Resumo - O objetivo deste trabalho foi caracterizar genitores e respectivas populações de macieiras quanto aos alelos S para confirmar sua genealogia e para avaliar a eficiência dos marcadores moleculares utilizados. Conjuntos específicos de iniciadores foram utilizados para a identificação dos alelos S via PCR. Foram avaliadas duas populações segregantes do Programa de Melhoramento Genético de Macieira da Epagri resultantes dos cruzamentos entre ?Fred Hough? × ?Monalisa? e ?M-11/00? × ?M-13/91?. As segregações esperadas são 1:1:1:1 para compatibilidade total e 1:1 para semi compatibilidade, que podem ser confirmadas pelo teste X2 . O cruzamento ?Fred Hough? (S5 S19) × ?Monalisa? (S2 S10) foi identificado como totalmente compatível, e foram identificados dois triploides entre os híbridos. O cruzamento entre ?M-11/00? (S3 S19) × ?M-13/91? (S3 S5 ) mostrou-se semicompatível baseado nos marcadores moleculares, e a segregação dos alelos S nos híbridos foi de 1:1, como esperado. A segregação dos marcadores de DNA para S2 , S3, S5, S10 e S19 ocorreujuntamente com seus respectivos alelos S. Dessa forma, a caracterização dos alelos S, além de permitir identificar a compatibilidade entre os genitores, serviu para identificar contaminações em populações segregantes. Termos para indexação: Malus × domestica Borkh., genótipo S, S-RNase, PCR alelo-específico, segregação. 1 Industrial biotechnologist, M.Sc. Doctora

    Fine-mapping of 5q12.1-13.3 unveils new genetic contributors to caries

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    Caries is a multifactorial disease and little is still known about the host genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified the interval 5q12.1–5q13.3 as linked to low caries susceptibility in Filipino families. Here we fine-mapped this region in order to identify genetic contributors to caries susceptibility. Four hundred and seventy-seven subjects from 72 pedigrees with similar cultural and behavioral habits and limited access to dental care living in the Philippines were studied. DMFT scores and genotype data of 75 single-nucleotide polymorphisms were evaluated in the Filipino families with the Family-Based Association Test. For replication purposes, a total 1,467 independent subjects from five different populations were analyzed in a case-control format. In the Filipino cohort, statistically significant and borderline associations were found between low caries experience and four genes spanning 13 million base pairs (PART1, ZSWIM6, CCNB1, and BTF3). We were able to replicate these results in some of the populations studied. We detected PART1 and BTF3 expression in whole saliva, and the expression of BTF3 was associated with caries experience. Our results suggest BTF3 may have a functional role in protecting against caries.Fil: Shimizu, T.. Nihon University of Dentistry; JapónFil: Deeley, K.. University of Pittsburgh; Estados UnidosFil: Briseño Ruiz, J.. University of Pittsburgh; Estados UnidosFil: Faraco Junior, I. M.. University of Pittsburgh; Estados UnidosFil: Poletta, Fernando Adrián. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. CEMIC-CONICET. Centro de Educaciones Médicas e Investigaciones Clínicas "Norberto Quirno". CEMIC-CONICET.; ArgentinaFil: Brancher, J. A.. Pontifical Catholic University of Paraná; BrasilFil: Pecharki, G. D.. Pontifical Catholic University of Paraná; BrasilFil: Küchler, E. C.. Universidade Federal Fluminense; BrasilFil: Tannure, P. N.. Universidade Federal do Rio de Janeiro; BrasilFil: Lips, A.. Universidade Federal do Rio de Janeiro; BrasilFil: Vieira, T. C. S.. Universidade Federal Fluminense; BrasilFil: Patir, A.. Istanbul Medipol Universit; TurquíaFil: Yildirim, M.. Istanbul University; TurquíaFil: Mereb, J. C.. Centro de Educación Médica e Investigaciones Clínicas “Norberto Quirno”; ArgentinaFil: Resick, J. M.. University of Pittsburgh; Estados UnidosFil: Brandon, C. A.. University of Pittsburgh; Estados UnidosFil: Cooper, M. E.. University of Pittsburgh; Estados UnidosFil: Seymen, F.. Istanbul University; TurquíaFil: Costa, M. C.. Universidade Federal do Rio de Janeiro; BrasilFil: Granjeiro, J. M.. Universidade Federal Fluminense; BrasilFil: Trevilatto, P. C.. Pontifical Catholic University of Paraná; BrasilFil: Orioli, I. M.. Universidade Federal do Rio de Janeiro; Brasil. Centro de Educación Médica e Investigaciones Clínicas “Norberto Quirno”; ArgentinaFil: Castilla, Eduardo Enrique. Instituto Oswaldo Cruz; Brasil. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. CEMIC-CONICET. Centro de Educaciones Médicas e Investigaciones Clínicas "Norberto Quirno". CEMIC-CONICET.; ArgentinaFil: Marazita, M. L.. University of Pittsburgh; Estados UnidosFil: Vieira, A. R.. University of Pittsburgh; Estados Unido

    Enamel Formation Genes Influence Enamel Microhardness Before and After Cariogenic Challenge

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    There is evidence for a genetic component in caries susceptibility, and studies in humans have suggested that variation in enamel formation genes may contribute to caries. For the present study, we used DNA samples collected from 1,831 individuals from various population data sets. Single nucleotide polymorphism markers were genotyped in selected genes (ameloblastin, amelogenin, enamelin, tuftelin, and tuftelin interacting protein 11) that influence enamel formation. Allele and genotype frequencies were compared between groups with distinct caries experience. Associations with caries experience can be detected but they are not necessarily replicated in all population groups and the most expressive results was for a marker in AMELX (p = 0.0007). To help interpret these results, we evaluated if enamel microhardness changes under simulated cariogenic challenges are associated with genetic variations in these same genes. After creating an artificial caries lesion, associations could be seen between genetic variation in TUFT1 (p = 0.006) and TUIP11 (p = 0.0006) with enamel microhardness. Our results suggest that the influence of genetic variation of enamel formation genes may influence the dynamic interactions between the enamel surface and the oral cavity. © 2012 Shimizu et al

    Enamel Formation Genes Influence Enamel Microhardness Before and After Cariogenic Challenge

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    Abstract There is evidence for a genetic component in caries susceptibility, and studies in humans have suggested that variation in enamel formation genes may contribute to caries. For the present study, we used DNA samples collected from 1,831 individuals from various population data sets. Single nucleotide polymorphism markers were genotyped in selected genes (ameloblastin, amelogenin, enamelin, tuftelin, and tuftelin interacting protein 11) that influence enamel formation. Allele and genotype frequencies were compared between groups with distinct caries experience. Associations with caries experience can be detected but they are not necessarily replicated in all population groups and the most expressive results was for a marker in AMELX (p = 0.0007). To help interpret these results, we evaluated if enamel microhardness changes under simulated cariogenic challenges are associated with genetic variations in these same genes. After creating an artificial caries lesion, associations could be seen between genetic variation in TUFT1 (p = 0.006) and TUIP11 (p = 0.0006) with enamel microhardness. Our results suggest that the influence of genetic variation of enamel formation genes may influence the dynamic interactions between the enamel surface and the oral cavity

    Contratos de licenciamento de propriedade industrial: autonomia privada e ordem pública

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    - Divulgação dos SUMÁRIOS das obras recentemente incorporadas ao acervo da Biblioteca Ministro Oscar Saraiva do STJ. Em respeito à Lei de Direitos Autorais, não disponibilizamos a obra na íntegra.- Localização na estante: 347.77(81) B816
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