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Registro completo
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Biblioteca (s) : |
INIA La Estanzuela. |
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Fecha : |
08/05/2017 |
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Actualizado : |
08/05/2017 |
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Tipo de producción científica : |
Artículos en Revistas Indexadas Internacionales |
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Autor : |
PEDROSO, P. M. O.; SANTOS, M. V. B.; SEUS, V. G.; SILVA, R. M. M. DA; RIET-CORREA, F.; MACÊDO, J. T. S. A. |
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Afiliación : |
FRANKLIN RIET-CORREA AMARAL, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay. |
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Título : |
Intoxicação por metternichia princeps (Solanaceae) em caprinos no Estado da Bahia. |
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Fecha de publicación : |
2015 |
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Fuente / Imprenta : |
Pesquisa Veterinária Brasileira, Rio de Janeiro v. 35, n. 5, p. 448-450, maio 2015. |
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Idioma : |
Español |
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Contenido : |
Descreve-se um surto de intoxicação por Metternichia princeps em caprinos no Estado da Bahia. De oito caprinos, três morreram, dos quais dois foram necropsiados; cinco não adoeceram. Os principais sinais clínicos caracterizaram-se por secreção nasal mucosa, emagrecimento, diarreia, apatia, debilidade leve, andar cambaleante, flexão dos membros torácicos e pélvicos, decúbito esterno-abdominal e decúbito lateral, seguidos de morte após aproximadamente dois dias de evolução clínica. Na necropsia foi observado edema pulmonar, hidrotórax, hidropericárdio, ascite, rins pálidos, edema perirrenal e hemorragias no tecido subcutâneo. Microscopicamente nos rins havia acentuada necrose de coagulação do epitélio tubular e túbulos com regeneração do epitélio. No pulmão havia acentuada congestão associada a edema interalveolar e interseptal. Na bioquímica sanguínea observou-se aumento na ureia, creatinina e creatinina fosfoquinase. |
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Palabras claves : |
Intoxicação por planta; Metternichia princeps; Northeastern Brazil; Plant poisoning; Pulmonary edema. |
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Thesagro : |
Edema pulmonar; Nefrose; Nephrosis; Planta tóxica; Poisonous plants; Ruminante; Ruminants; Solanaceae. |
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Asunto categoría : |
-- |
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URL : |
http://www.ainfo.inia.uy/digital/bitstream/item/6768/1/Pesq.-Vet.-Bras.-355p.448-450-maio-2015.pdf
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Marc : |
LEADER 01949naa a2200337 a 4500
001 1057185
005 2017-05-08
008 2015 bl uuuu u00u1 u #d
100 1 $aPEDROSO, P. M. O.
245 $aIntoxicação por metternichia princeps (Solanaceae) em caprinos no Estado da Bahia.$h[electronic resource]
260 $c2015
520 $aDescreve-se um surto de intoxicação por Metternichia princeps em caprinos no Estado da Bahia. De oito caprinos, três morreram, dos quais dois foram necropsiados; cinco não adoeceram. Os principais sinais clínicos caracterizaram-se por secreção nasal mucosa, emagrecimento, diarreia, apatia, debilidade leve, andar cambaleante, flexão dos membros torácicos e pélvicos, decúbito esterno-abdominal e decúbito lateral, seguidos de morte após aproximadamente dois dias de evolução clínica. Na necropsia foi observado edema pulmonar, hidrotórax, hidropericárdio, ascite, rins pálidos, edema perirrenal e hemorragias no tecido subcutâneo. Microscopicamente nos rins havia acentuada necrose de coagulação do epitélio tubular e túbulos com regeneração do epitélio. No pulmão havia acentuada congestão associada a edema interalveolar e interseptal. Na bioquímica sanguínea observou-se aumento na ureia, creatinina e creatinina fosfoquinase.
650 $aEdema pulmonar
650 $aNefrose
650 $aNephrosis
650 $aPlanta tóxica
650 $aPoisonous plants
650 $aRuminante
650 $aRuminants
650 $aSolanaceae
653 $aIntoxicação por planta
653 $aMetternichia princeps
653 $aNortheastern Brazil
653 $aPlant poisoning
653 $aPulmonary edema
700 1 $aSANTOS, M. V. B.
700 1 $aSEUS, V. G.
700 1 $aSILVA, R. M. M. DA
700 1 $aRIET-CORREA, F.
700 1 $aMACÊDO, J. T. S. A.
773 $tPesquisa Veterinária Brasileira, Rio de Janeiro$gv. 35, n. 5, p. 448-450, maio 2015.
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Registro original : |
INIA La Estanzuela (LE) |
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Registro completo
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Biblioteca (s) : |
INIA Las Brujas. |
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Fecha actual : |
02/02/2022 |
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Actualizado : |
02/02/2022 |
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Tipo de producción científica : |
Artículos en Revistas Indexadas Internacionales |
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Circulación / Nivel : |
Internacional - -- |
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Autor : |
TORRES, D.; DELGADO-CERRONE, L.; LUNA, L.; RESQUÍN, F.; AGUILAR, A.V.; SEBENN, A.M. |
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Afiliación : |
DIEGO GABRIEL TORRES DINI, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay; LEONARDO DELGADO-CERRONE, Instituto de Investigaciones Biológicas Clemente Estable (IIBCE), Av. Italia 3318, 11600 Montevideo, Uruguay.; LORENA LUNA, Centro Universitario de Tacuarembó (CUT), Ruta 5 Km 386, CEP 45000, Tacuarembó, TB, Uruguay; JOSE FERNANDO RESQUIN PEREZ, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay; ANANDA VIRGINIA AGUIAR, Empresa Brasileira de Pesquisa Agropecuária (EMBRAPA), Centro Nacional de Pesquisa de Florestas, Estrada da Ribeira, Km 111 - Bairro Guaraituba, 83411-000, Colombo, PR, Brazil.; ALEXANDRE MAGNO SEBBENN, Instituto Florestal de São Paulo, CP 1322, São Paulo, SP, 01059-970, Brazil. |
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Título : |
The traceability of Eucalyptus clones using molecular markers. |
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Fecha de publicación : |
2021 |
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Fuente / Imprenta : |
Silvae Genetica, 2021, 70(1) 217-225. OPEN ACCESS. https://doi.org/10.2478/sg-2021-0019 |
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DOI : |
10.2478/sg-2021-0019 |
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Idioma : |
Inglés |
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Notas : |
Article history: Published Online 25 Dec 2021.
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Corresponding author: Diego Torres-Dini, E-mail: diego.torres.dini@gmail.com |
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Contenido : |
ABSTRACT.- The improvement of Eucalyptus clones plays a crucial role in modern silviculture. This study used a set of 17 microsatellite loci to analyze the genetic diversity and structure of 107 elite clones (80 E. grandis and 27 E. globulus). All clones were cultivated in Uruguay and were sourced from three different providers. Using the fingerprinting technique, an exclusive molecular profile was assigned for each clone, and the genotyping reaction showed differences between the two species. The cumulative probability of identifying two random individuals that share the same genotype (???? ) with all 17 loci, was estimated as low for E. grandis (1.18×10-15) and E. globulus (4.03×10-14). The combined PIsibs was (1.05×10-5) and (2.17×10-5) for E. grandis and E. globulus, respectively. A total of 180 alleles were detected for E. grandis and 100 for E. globulus. We found a high mean number of alleles per locus (10 for E. grandis and 6 for E. globulus), and the results for mean polymorphic information content ( PIC ) were (0.648) and (0.548), respectively. The observed heterozygosity ( Ho ) ranged from 0.216 to 0.838 (mean = 0.509) for E. grandis and 0 to 1 (mean = 0.566) for E. globulus. Two core sets of seven EST-SSR loci were identified for each species. These markers revealed unambiguous fragment amplification, providing a minimum number of SSRs for effective clonal identification. The genetic structure analysis suggests that the germplasm of the E. grandis population is structured in four clusters, while the E. globulus population consists of two clusters.
© 2020 Diego Torres-Dini et al., published by Sciendo MenosABSTRACT.- The improvement of Eucalyptus clones plays a crucial role in modern silviculture. This study used a set of 17 microsatellite loci to analyze the genetic diversity and structure of 107 elite clones (80 E. grandis and 27 E. globulus). All clones were cultivated in Uruguay and were sourced from three different providers. Using the fingerprinting technique, an exclusive molecular profile was assigned for each clone, and the genotyping reaction showed differences between the two species. The cumulative probability of identifying two random individuals that share the same genotype (???? ) with all 17 loci, was estimated as low for E. grandis (1.18×10-15) and E. globulus (4.03×10-14). The combined PIsibs was (1.05×10-5) and (2.17×10-5) for E. grandis and E. globulus, respectively. A total of 180 alleles were detected for E. grandis and 100 for E. globulus. We found a high mean number of alleles per locus (10 for E. grandis and 6 for E. globulus), and the results for mean polymorphic information content ( PIC ) were (0.648) and (0.548), respectively. The observed heterozygosity ( Ho ) ranged from 0.216 to 0.838 (mean = 0.509) for E. grandis and 0 to 1 (mean = 0.566) for E. globulus. Two core sets of seven EST-SSR loci were identified for each species. These markers revealed unambiguous fragment amplification, providing a minimum number of SSRs for effective clonal identification. The genetic structure analysis suggests that the germplasm of the E. grandis population is st... Presentar Todo |
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Palabras claves : |
Clone; Clone certification; Genotyping; Identity; Multiplex; Nurseries; Traceability. |
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Asunto categoría : |
K01 Ciencias forestales - Aspectos generales |
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URL : |
https://sciendo.com/pdf/10.2478/sg-2021-0019
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Marc : |
LEADER 02660naa a2200289 a 4500
001 1062729
005 2022-02-02
008 2021 bl uuuu u00u1 u #d
024 7 $a10.2478/sg-2021-0019$2DOI
100 1 $aTORRES, D.
245 $aThe traceability of Eucalyptus clones using molecular markers.$h[electronic resource]
260 $c2021
500 $aArticle history: Published Online 25 Dec 2021. This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License. Corresponding author: Diego Torres-Dini, E-mail: diego.torres.dini@gmail.com
520 $aABSTRACT.- The improvement of Eucalyptus clones plays a crucial role in modern silviculture. This study used a set of 17 microsatellite loci to analyze the genetic diversity and structure of 107 elite clones (80 E. grandis and 27 E. globulus). All clones were cultivated in Uruguay and were sourced from three different providers. Using the fingerprinting technique, an exclusive molecular profile was assigned for each clone, and the genotyping reaction showed differences between the two species. The cumulative probability of identifying two random individuals that share the same genotype (???? ) with all 17 loci, was estimated as low for E. grandis (1.18×10-15) and E. globulus (4.03×10-14). The combined PIsibs was (1.05×10-5) and (2.17×10-5) for E. grandis and E. globulus, respectively. A total of 180 alleles were detected for E. grandis and 100 for E. globulus. We found a high mean number of alleles per locus (10 for E. grandis and 6 for E. globulus), and the results for mean polymorphic information content ( PIC ) were (0.648) and (0.548), respectively. The observed heterozygosity ( Ho ) ranged from 0.216 to 0.838 (mean = 0.509) for E. grandis and 0 to 1 (mean = 0.566) for E. globulus. Two core sets of seven EST-SSR loci were identified for each species. These markers revealed unambiguous fragment amplification, providing a minimum number of SSRs for effective clonal identification. The genetic structure analysis suggests that the germplasm of the E. grandis population is structured in four clusters, while the E. globulus population consists of two clusters. © 2020 Diego Torres-Dini et al., published by Sciendo
653 $aClone
653 $aClone certification
653 $aGenotyping
653 $aIdentity
653 $aMultiplex
653 $aNurseries
653 $aTraceability
700 1 $aDELGADO-CERRONE, L.
700 1 $aLUNA, L.
700 1 $aRESQUÍN, F.
700 1 $aAGUILAR, A.V.
700 1 $aSEBENN, A.M.
773 $tSilvae Genetica, 2021, 70(1) 217-225. OPEN ACCESS. https://doi.org/10.2478/sg-2021-0019
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