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Registro Completo |
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Biblioteca(s): |
Embrapa Uva e Vinho. |
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Data corrente: |
04/11/2009 |
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Data da última atualização: |
29/07/2022 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
GIACOMINI, R.; MORO, L.; SPAGNOL, F.; VIEIRA, R. D.; ANTONIOLLI, L. R.; NICKEL, O.; FIALHO, F. B.; FIORAVANÇO, J. C. |
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Afiliação: |
ROSANE GIACOMINI, CNPQ; LAÍS MORO, IFRS-BG; FERNANDO SPAGNOL, UERGS; ROBERTA D'ÁVILA VIEIRA, IFRS-BG; LUCIMARA ROGERIA ANTONIOLLI, CNPUV; OSMAR NICKEL, CNPUV; FLAVIO BELLO FIALHO, CNPUV; JOAO CAETANO FIORAVANCO, CNPUV. |
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Título: |
Qualidade de frutos provenientes de macieiras com infecções virais. |
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Ano de publicação: |
2009 |
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Fonte/Imprenta: |
In: ENCONTRO DE INICIAÇÃO CIENTÍFICA DA EMBRAPA UVA E VINHO, 7.; ENCONTRO DE PÓS-GRADUANDOS DA EMBRAPA UVA E VINHO, 3., 2009, Bento Gonçalves. Resumos... Bento Gonçalves: Embrapa Uva e Vinho, 2009. |
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Páginas: |
p. 49. |
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Idioma: |
Português |
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Conteúdo: |
Com o objetivo de avaliar a qualidade de maçãs ?Maxi Gala? provenientes de plantas com infecções virais, foram colhidos frutos de plantas sadias (T1) e de plantas infectadas com diferentes combinações virais: CL+SG+SP (T2); SG+SP (T3); SP (T4). Os frutos foram avaliados na colheita e após 60 e 120 dias de refrigeração. Após cada período, os frutos foram mantidos por 10 dias sob temperatura ambiente, de forma a simular o período de comercialização. Os tratamentos SG+SP+MV (T5) e SP+MV (T6) foram avaliados somente na colheita. O delineamento experimental foi o inteiramente casualizado, com 4 repetições de 5 frutos. Foram avaliados os atributos de qualidade: perda de massa, firmeza de polpa, SS, AT, ratio e coloração da epiderme. |
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Palavras-Chave: |
Anais; CNPUV; IC; Iniciação cientifica. |
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Thesagro: |
Doença de planta; Fruticultura; Maçã; Qualidade; Vírus. |
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Categoria do assunto: |
F Plantas e Produtos de Origem Vegetal |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/573909/1/Resumos-7IC-2009-fINAL3-1-49.pdf
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Marc: |
LEADER 01720nam a2200313 a 4500
001 1573909
005 2022-07-29
008 2009 bl uuuu u00u1 u #d
100 1 $aGIACOMINI, R.
245 $aQualidade de frutos provenientes de macieiras com infecções virais.$h[electronic resource]
260 $aIn: ENCONTRO DE INICIAÇÃO CIENTÍFICA DA EMBRAPA UVA E VINHO, 7.; ENCONTRO DE PÓS-GRADUANDOS DA EMBRAPA UVA E VINHO, 3., 2009, Bento Gonçalves. Resumos... Bento Gonçalves: Embrapa Uva e Vinho$c2009
300 $ap. 49.
520 $aCom o objetivo de avaliar a qualidade de maçãs ?Maxi Gala? provenientes de plantas com infecções virais, foram colhidos frutos de plantas sadias (T1) e de plantas infectadas com diferentes combinações virais: CL+SG+SP (T2); SG+SP (T3); SP (T4). Os frutos foram avaliados na colheita e após 60 e 120 dias de refrigeração. Após cada período, os frutos foram mantidos por 10 dias sob temperatura ambiente, de forma a simular o período de comercialização. Os tratamentos SG+SP+MV (T5) e SP+MV (T6) foram avaliados somente na colheita. O delineamento experimental foi o inteiramente casualizado, com 4 repetições de 5 frutos. Foram avaliados os atributos de qualidade: perda de massa, firmeza de polpa, SS, AT, ratio e coloração da epiderme.
650 $aDoença de planta
650 $aFruticultura
650 $aMaçã
650 $aQualidade
650 $aVírus
653 $aAnais
653 $aCNPUV
653 $aIC
653 $aIniciação cientifica
700 1 $aMORO, L.
700 1 $aSPAGNOL, F.
700 1 $aVIEIRA, R. D.
700 1 $aANTONIOLLI, L. R.
700 1 $aNICKEL, O.
700 1 $aFIALHO, F. B.
700 1 $aFIORAVANÇO, J. C.
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Registro original: |
Embrapa Uva e Vinho (CNPUV) |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Caprinos e Ovinos. Para informações adicionais entre em contato com cnpc.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Caprinos e Ovinos. |
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Data corrente: |
09/04/2010 |
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Data da última atualização: |
25/09/2019 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
Internacional - A |
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Autoria: |
FONSECA, J. F. da; BRUSCHI, J. H.; SANTOS, I. C. C.; VIANA, J. H. M.; MAGALHÃES, A. C. M. |
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Afiliação: |
JEFERSON FERREIRA DA FONSECA, CNPC; JOSE HENRIQUE BRUSCHI, CNPGL; Tecnopec, São Paulo, SP; JOAO HENRIQUE MOREIRA VIANA, CNPGL; UFV, Viçosa, MG. |
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Título: |
Induction of estrus in non-lactating dairy goats with different estrous synchrony protocols. |
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Ano de publicação: |
2005 |
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Fonte/Imprenta: |
Animal Reproduction Science, v. 85, n. 1/2, p. 117-124, Jan. 2005. |
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DOI: |
10.1016/j.anireprosci.2004.03.005 |
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Idioma: |
Inglês |
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Conteúdo: |
The objective of this experiment was to determine the effect of prepartum lipid supplementation on the number and quality of embryos recovered following ovarian super-ovulation in postpartum suckled beef cows. Mature cows (n = 40) were assigned to one of two treatments (lipid versus. no lipid) and supplemented for approximately 40 days prior to calving. Supplements provided to cows were isocaloric and isonitrogenous. The treatment group was fed 1.6 kg hd?1 per day of whole soybeans (WSB; 19.8% ether extract, and 41.8% crude protein) and the control group received a supplement consisting of 1.8 kg hd?1 day of a soybean meal and soy?hull combination (SBS; 2.15% EE and 36.81% CP). Cows were synchronized using a GnRH [Cystorelin® 100 ?g im]?GnRH?PGF2? [Lutalyse® 25 mg im] protocol. Cows were administered two injections of GnRH seven days apart and PG seven days after the second GnRH injection. Twenty-eight cows (WSB, n = 15; SBS, n = 13) responded to estrus synchronization and were superstimulated. Super-ovulation was initiated on day 8?10 of the synchronized cycle by twice-daily injections of pFSH (Pluset®) over four days in decreasing doses using a total of 608.4 IU per cow. Prostaglandin F2? was administered 96 and 108 h after super-stimulation was initiated with FSH. Days postpartum (WSB = 59 days; SBS = 57 days) at initiation of FSH treatments were similar (P > 0.10) for both treatments. Cows were monitored for estrus activity by the HeatWatch® Estrus Detection System. Twenty-seven cows (WSB, n = 15; SBS, n = 12) exhibited estrus after FSH and inseminated at 0, 12, and 24 h after the onset of estrus with 1, 2, and 1 units of semen, respectively. Embryos were recovered and evaluated 7?8 days later. Only cows that responded to FSH and that were inseminated were used for statistical analysis. Data were analyzed using the General Linear Models Procedure of SAS. Body condition scores did not differ (P > 0.10) between treatments when cows were evaluated at the initiation of the experiment, two weeks prior to calving, and at initiation of superovulation with FSH. Estrous cyclicity prior to the initiation of estrus synchronization did not differ (P > 0.10) between treatments. There was no difference (P > 0.10) between treatments in recovery of total embryos (WSB, 14.7 ± 3.5; SBS, 17.5 ± 3.0), transferable embryos (WSB, 10.3 ± 2.5; SBS, 13.6 ± 2.6), degenerate embryos (WSB, 3.3 ± 1.1; SBS, 1.6 ± 1.7) or unfertilized ova (WSB, 1.1 ± 0.5; SBS, 2.3 ± 1.2). Cows that were supplemented with whole soybeans prior to parturition failed to produce an increased total number of ova or transferable embryos following super-ovulation. MenosThe objective of this experiment was to determine the effect of prepartum lipid supplementation on the number and quality of embryos recovered following ovarian super-ovulation in postpartum suckled beef cows. Mature cows (n = 40) were assigned to one of two treatments (lipid versus. no lipid) and supplemented for approximately 40 days prior to calving. Supplements provided to cows were isocaloric and isonitrogenous. The treatment group was fed 1.6 kg hd?1 per day of whole soybeans (WSB; 19.8% ether extract, and 41.8% crude protein) and the control group received a supplement consisting of 1.8 kg hd?1 day of a soybean meal and soy?hull combination (SBS; 2.15% EE and 36.81% CP). Cows were synchronized using a GnRH [Cystorelin® 100 ?g im]?GnRH?PGF2? [Lutalyse® 25 mg im] protocol. Cows were administered two injections of GnRH seven days apart and PG seven days after the second GnRH injection. Twenty-eight cows (WSB, n = 15; SBS, n = 13) responded to estrus synchronization and were superstimulated. Super-ovulation was initiated on day 8?10 of the synchronized cycle by twice-daily injections of pFSH (Pluset®) over four days in decreasing doses using a total of 608.4 IU per cow. Prostaglandin F2? was administered 96 and 108 h after super-stimulation was initiated with FSH. Days postpartum (WSB = 59 days; SBS = 57 days) at initiation of FSH treatments were similar (P > 0.10) for both treatments. Cows were monitored for estrus activity by the HeatWatch® Estrus Detection System. Twen... Mostrar Tudo |
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Palavras-Chave: |
Brasil; ECG; Estrous induction; Estrous synchrony protocols; Goat; Progestagen treatment. |
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Thesagro: |
Caprino; Ciclo estral; Indução; Reprodução animal; Sincronização do cio. |
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Thesaurus NAL: |
Animal reproduction; Artificial insemination; Brazil. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 03710naa a2200349 a 4500
001 1663671
005 2019-09-25
008 2005 bl uuuu u00u1 u #d
024 7 $a10.1016/j.anireprosci.2004.03.005$2DOI
100 1 $aFONSECA, J. F. da
245 $aInduction of estrus in non-lactating dairy goats with different estrous synchrony protocols.$h[electronic resource]
260 $c2005
520 $aThe objective of this experiment was to determine the effect of prepartum lipid supplementation on the number and quality of embryos recovered following ovarian super-ovulation in postpartum suckled beef cows. Mature cows (n = 40) were assigned to one of two treatments (lipid versus. no lipid) and supplemented for approximately 40 days prior to calving. Supplements provided to cows were isocaloric and isonitrogenous. The treatment group was fed 1.6 kg hd?1 per day of whole soybeans (WSB; 19.8% ether extract, and 41.8% crude protein) and the control group received a supplement consisting of 1.8 kg hd?1 day of a soybean meal and soy?hull combination (SBS; 2.15% EE and 36.81% CP). Cows were synchronized using a GnRH [Cystorelin® 100 ?g im]?GnRH?PGF2? [Lutalyse® 25 mg im] protocol. Cows were administered two injections of GnRH seven days apart and PG seven days after the second GnRH injection. Twenty-eight cows (WSB, n = 15; SBS, n = 13) responded to estrus synchronization and were superstimulated. Super-ovulation was initiated on day 8?10 of the synchronized cycle by twice-daily injections of pFSH (Pluset®) over four days in decreasing doses using a total of 608.4 IU per cow. Prostaglandin F2? was administered 96 and 108 h after super-stimulation was initiated with FSH. Days postpartum (WSB = 59 days; SBS = 57 days) at initiation of FSH treatments were similar (P > 0.10) for both treatments. Cows were monitored for estrus activity by the HeatWatch® Estrus Detection System. Twenty-seven cows (WSB, n = 15; SBS, n = 12) exhibited estrus after FSH and inseminated at 0, 12, and 24 h after the onset of estrus with 1, 2, and 1 units of semen, respectively. Embryos were recovered and evaluated 7?8 days later. Only cows that responded to FSH and that were inseminated were used for statistical analysis. Data were analyzed using the General Linear Models Procedure of SAS. Body condition scores did not differ (P > 0.10) between treatments when cows were evaluated at the initiation of the experiment, two weeks prior to calving, and at initiation of superovulation with FSH. Estrous cyclicity prior to the initiation of estrus synchronization did not differ (P > 0.10) between treatments. There was no difference (P > 0.10) between treatments in recovery of total embryos (WSB, 14.7 ± 3.5; SBS, 17.5 ± 3.0), transferable embryos (WSB, 10.3 ± 2.5; SBS, 13.6 ± 2.6), degenerate embryos (WSB, 3.3 ± 1.1; SBS, 1.6 ± 1.7) or unfertilized ova (WSB, 1.1 ± 0.5; SBS, 2.3 ± 1.2). Cows that were supplemented with whole soybeans prior to parturition failed to produce an increased total number of ova or transferable embryos following super-ovulation.
650 $aAnimal reproduction
650 $aArtificial insemination
650 $aBrazil
650 $aCaprino
650 $aCiclo estral
650 $aIndução
650 $aReprodução animal
650 $aSincronização do cio
653 $aBrasil
653 $aECG
653 $aEstrous induction
653 $aEstrous synchrony protocols
653 $aGoat
653 $aProgestagen treatment
700 1 $aBRUSCHI, J. H.
700 1 $aSANTOS, I. C. C.
700 1 $aVIANA, J. H. M.
700 1 $aMAGALHÃES, A. C. M.
773 $tAnimal Reproduction Science$gv. 85, n. 1/2, p. 117-124, Jan. 2005.
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