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 | Acesso ao texto completo restrito à biblioteca da Embrapa Hortaliças. Para informações adicionais entre em contato com cnph.biblioteca@embrapa.br. |
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Registro Completo |
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Biblioteca(s): |
Embrapa Hortaliças. |
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Data corrente: |
20/06/2007 |
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Data da última atualização: |
20/06/2007 |
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Autoria: |
ANDRADE JÚNIOR, V. C. de; YURI, J. E.; NUNES, U. R.; PIMENTA, F. L.; MATOS, C. de S. M. de; FLORIO, F. C. de A.; MADEIRA, D. M. |
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Título: |
Emprego de tipos de coberturta de canteiro no cultivo de alface. |
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Ano de publicação: |
2005 |
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Fonte/Imprenta: |
Horticultura Brasileira, Brasília, DF, v. 23, n. 4, p. 899-903, out./dez. 2005. |
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Idioma: |
Português |
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Thesagro: |
Alface; Cobertura do Solo; Lactuca Sativa; Produtividade. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 00674naa a2200229 a 4500
001 1780118
005 2007-06-20
008 2005 bl uuuu u00u1 u #d
100 1 $aANDRADE JÚNIOR, V. C. de
245 $aEmprego de tipos de coberturta de canteiro no cultivo de alface.
260 $c2005
650 $aAlface
650 $aCobertura do Solo
650 $aLactuca Sativa
650 $aProdutividade
700 1 $aYURI, J. E.
700 1 $aNUNES, U. R.
700 1 $aPIMENTA, F. L.
700 1 $aMATOS, C. de S. M. de
700 1 $aFLORIO, F. C. de A.
700 1 $aMADEIRA, D. M.
773 $tHorticultura Brasileira, Brasília, DF$gv. 23, n. 4, p. 899-903, out./dez. 2005.
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Embrapa Hortaliças (CNPH) |
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Biblioteca(s): |
Embrapa Caprinos e Ovinos. |
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Data corrente: |
17/09/2013 |
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Data da última atualização: |
17/05/2022 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
LIMA, J. T. M.; FONSECA, J. F. da; ESTEVES, L. V.; PENEIRAS, A. B. V.; LIMA, M. S. D.; BRANDÃO, F. Z. |
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Afiliação: |
J. T. M. Lima, Fluminense Federal University, Niterói, Rio de Janeiro, Brazil; JEFERSON FERREIRA DA FONSECA, CNPC; L. V. Esteves, Fluminense Federal University - Niterói, Rio de Janeiro, Brazil; A. B. V. Peneiras, Fluminense Federal University - Niterói, Rio de Janeiro, Brazil; M. S. D. Lima, Fluminense Federal University - Niterói, Rio de Janeiro, Brazil; F. Z. Brandão, Fluminense Federal University - Niterói, Rio de Janeiro, Brazil. |
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Título: |
Duration of estrus and time of ovulation in superovulated Santa Inês ewes. |
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Ano de publicação: |
2013 |
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Fonte/Imprenta: |
Reproduction, Fertility and Development, v. 25, n. 1, p. 151, 2013. |
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DOI: |
http://dx.doi.org/10.1071/RDv25n1Ab8 |
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Idioma: |
Inglês |
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Conteúdo: |
Abstract: The aim of this study was to determine the intervals between sponge removal and the onset of estrus, sponge removal and the first detected ovulation, and onset of estrus and the first ovulation, and also to determine the duration of estrus, in superovulated Santa Inês ewes subjected to natural mating (NM) and AI. The trial was done in July and February at Cachoeiras de Macacu?Rio de Janeiro (22°27'S, 43°39'W). Fifteen non-pregnant Santa Inês ewes, age 3.4 ± 1.4 years, weighing 47.8 ± 6.3 kg, with 3.3 ± 0.4 body condition score (scale of 1 to 5), were randomly assigned to 2 groups. Both groups were superovulated using the same protocol and were mated in a crossover design by NM and laparoscopic AI. Estrus was synchronized using intravaginal sponges (60 mg of medroxyprogesterone acetate; Progespon®, Schering Plough Animal Health, São Paulo, Brazil) inserted (Day 0) and maintained for 6 days. On Day 5, the ewes received IM injections of 300 IU of eCG (Novormon®, Schering Plough Animal Health) and 0.0375 mg of cloprostenol (Prolise®, Tecnopec, São Paulo, Brazil). Twelve hours after sponge removal, 0.025 mg of gonadorelin acetate (Gestran®, Tecnopec) was administered IM. Superovulation started 60 h after sponge removal and consisted of 5 IU kg -1 of porcine FSH (pFSH; Pluset®, Hertape Calier, Minas Gerais, Brazil) IM in 6 decreasing doses (25, 25, 15, 15, 10, and 10%) at 12-h intervals. At the first pFSH dose, new sponges were inserted. At the fifth pFSH dose, 0.0375 mg of cloprostenol was administered IM and the sponges were removed. After the sponge removal, the NM group was exposed to rams twice per day for mating, until the end of estrus. In the AI group, estrus was detected using a teaser with the penis diverted. The females were permitted to be mounted twice per day until the end of estrus, and were inseminated with frozen-thawed semen 24 and 36 h after the end of superovulation. The follicular development and ovulation time were observed using real-time ultrasonography (8.0 MHz Pie Medical®, Aquila Vet, Tokyo, Japan) at 12-h intervals. For statistical analysis, a Student's t-test was performed (5% significance level) using the BioEstat program. Results are presented as mean ± standard deviation. The time from sponge removal to onset of estrus and the duration of estrus did not differ between NM and AI groups (31.79 ± 5.94 v. 25.25 ± 10.38 h and 29.89 ± 11.54 v. 26.66 ± 8.67 h, respectively). The time from sponge removal to ovulation and from onset of estrus to the first ovulation were shorter (P < 0.001) in the NM group (32.11 ± 12.72 v. 56.48 ± 15.39 h and 8.61 ± 5.99 v. 32.25 ± 18.57 h, respectively). The time from sponge removal to ovulation in July and February was 56.07 ± 7.27 versus 56.83 ± 20.72 in the AI group and 29.54 ± 0.56 versus 33.83 ± 19.02 in the NM group, respectively, suggesting that the season of the year in a tropical region did not influence the ovulation time for each treatment. Possibly, the mechanical stimulation induced by the contact of the penis with the vagina fornix and by the accessory sex glands fluids in mating hastened the ovulation time in the NM group. The service can shorten the time of ovulation. MenosAbstract: The aim of this study was to determine the intervals between sponge removal and the onset of estrus, sponge removal and the first detected ovulation, and onset of estrus and the first ovulation, and also to determine the duration of estrus, in superovulated Santa Inês ewes subjected to natural mating (NM) and AI. The trial was done in July and February at Cachoeiras de Macacu?Rio de Janeiro (22°27'S, 43°39'W). Fifteen non-pregnant Santa Inês ewes, age 3.4 ± 1.4 years, weighing 47.8 ± 6.3 kg, with 3.3 ± 0.4 body condition score (scale of 1 to 5), were randomly assigned to 2 groups. Both groups were superovulated using the same protocol and were mated in a crossover design by NM and laparoscopic AI. Estrus was synchronized using intravaginal sponges (60 mg of medroxyprogesterone acetate; Progespon®, Schering Plough Animal Health, São Paulo, Brazil) inserted (Day 0) and maintained for 6 days. On Day 5, the ewes received IM injections of 300 IU of eCG (Novormon®, Schering Plough Animal Health) and 0.0375 mg of cloprostenol (Prolise®, Tecnopec, São Paulo, Brazil). Twelve hours after sponge removal, 0.025 mg of gonadorelin acetate (Gestran®, Tecnopec) was administered IM. Superovulation started 60 h after sponge removal and consisted of 5 IU kg -1 of porcine FSH (pFSH; Pluset®, Hertape Calier, Minas Gerais, Brazil) IM in 6 decreasing doses (25, 25, 15, 15, 10, and 10%) at 12-h intervals. At the first pFSH dose, new sponges were inserted. At the fifth pFSH dose, 0.0375 mg... Mostrar Tudo |
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Palavras-Chave: |
Oestrus synchronization; Raça Santa Inês; Superovulated females. |
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Thesagro: |
Ciclo estral; Ovelha; Ovino; Ovulação; Reprodução animal; Superovulação. |
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Thesaurus NAL: |
Ovulation; Reproduction; Sheep; Superovulation. |
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Categoria do assunto: |
L Ciência Animal e Produtos de Origem Animal |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/89520/1/rac-Duration-of-estrus.pdf
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Marc: |
LEADER 04210nam a2200337 a 4500
001 1966395
005 2022-05-17
008 2013 bl uuuu u00u1 u #d
024 7 $ahttp://dx.doi.org/10.1071/RDv25n1Ab8$2DOI
100 1 $aLIMA, J. T. M.
245 $aDuration of estrus and time of ovulation in superovulated Santa Inês ewes.$h[electronic resource]
260 $aReproduction, Fertility and Development, v. 25, n. 1, p. 151$c2013
520 $aAbstract: The aim of this study was to determine the intervals between sponge removal and the onset of estrus, sponge removal and the first detected ovulation, and onset of estrus and the first ovulation, and also to determine the duration of estrus, in superovulated Santa Inês ewes subjected to natural mating (NM) and AI. The trial was done in July and February at Cachoeiras de Macacu?Rio de Janeiro (22°27'S, 43°39'W). Fifteen non-pregnant Santa Inês ewes, age 3.4 ± 1.4 years, weighing 47.8 ± 6.3 kg, with 3.3 ± 0.4 body condition score (scale of 1 to 5), were randomly assigned to 2 groups. Both groups were superovulated using the same protocol and were mated in a crossover design by NM and laparoscopic AI. Estrus was synchronized using intravaginal sponges (60 mg of medroxyprogesterone acetate; Progespon®, Schering Plough Animal Health, São Paulo, Brazil) inserted (Day 0) and maintained for 6 days. On Day 5, the ewes received IM injections of 300 IU of eCG (Novormon®, Schering Plough Animal Health) and 0.0375 mg of cloprostenol (Prolise®, Tecnopec, São Paulo, Brazil). Twelve hours after sponge removal, 0.025 mg of gonadorelin acetate (Gestran®, Tecnopec) was administered IM. Superovulation started 60 h after sponge removal and consisted of 5 IU kg -1 of porcine FSH (pFSH; Pluset®, Hertape Calier, Minas Gerais, Brazil) IM in 6 decreasing doses (25, 25, 15, 15, 10, and 10%) at 12-h intervals. At the first pFSH dose, new sponges were inserted. At the fifth pFSH dose, 0.0375 mg of cloprostenol was administered IM and the sponges were removed. After the sponge removal, the NM group was exposed to rams twice per day for mating, until the end of estrus. In the AI group, estrus was detected using a teaser with the penis diverted. The females were permitted to be mounted twice per day until the end of estrus, and were inseminated with frozen-thawed semen 24 and 36 h after the end of superovulation. The follicular development and ovulation time were observed using real-time ultrasonography (8.0 MHz Pie Medical®, Aquila Vet, Tokyo, Japan) at 12-h intervals. For statistical analysis, a Student's t-test was performed (5% significance level) using the BioEstat program. Results are presented as mean ± standard deviation. The time from sponge removal to onset of estrus and the duration of estrus did not differ between NM and AI groups (31.79 ± 5.94 v. 25.25 ± 10.38 h and 29.89 ± 11.54 v. 26.66 ± 8.67 h, respectively). The time from sponge removal to ovulation and from onset of estrus to the first ovulation were shorter (P < 0.001) in the NM group (32.11 ± 12.72 v. 56.48 ± 15.39 h and 8.61 ± 5.99 v. 32.25 ± 18.57 h, respectively). The time from sponge removal to ovulation in July and February was 56.07 ± 7.27 versus 56.83 ± 20.72 in the AI group and 29.54 ± 0.56 versus 33.83 ± 19.02 in the NM group, respectively, suggesting that the season of the year in a tropical region did not influence the ovulation time for each treatment. Possibly, the mechanical stimulation induced by the contact of the penis with the vagina fornix and by the accessory sex glands fluids in mating hastened the ovulation time in the NM group. The service can shorten the time of ovulation.
650 $aOvulation
650 $aReproduction
650 $aSheep
650 $aSuperovulation
650 $aCiclo estral
650 $aOvelha
650 $aOvino
650 $aOvulação
650 $aReprodução animal
650 $aSuperovulação
653 $aOestrus synchronization
653 $aRaça Santa Inês
653 $aSuperovulated females
700 1 $aFONSECA, J. F. da
700 1 $aESTEVES, L. V.
700 1 $aPENEIRAS, A. B. V.
700 1 $aLIMA, M. S. D.
700 1 $aBRANDÃO, F. Z.
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