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Embryo transfer using cryopreserved Boer goat blastocystsLehloenya, KC, Greyling, JPC January 2010 (has links)
Abstract
The aim of this trial was to evaluate the effect of embryo cryopreservation techniques on the survivability of embryos and fertility following transfer to Boer goat does. The oestrous cycles of 27 mature recipients Boer goat does were synchronised using controlled internal drug release dispensers (CIDR’s) for 16 days. At CIDR removal, does were injected with 300 IU eCG. The recipient does were allocated to 3 groups (n = 9 per group), based on the technique of cryopreservation used for the embryos transferred. The in vivo produced embryos used were at blastocyst stage and surgically collected on day 6 following AI from Boer goat donors superovulated with pFSH. The first group received fresh embryos and served as the control, the second group of does received conventional slow frozen/thawed embryos and the third group received vitrified/thawed embryos. Two blastocysts were transferred per doe. A pregnancy rate of 85.7% (n = 6) was obtained following the transfer of fresh embryos and tended to be better than in does receiving slow frozen and vitrified embryos, (n = 4; 50.0% and n = 3; 37.5% does pregnant, respectively). The overall gestation period recorded for all does was 146.3 ± 3.0 d, with an overall litter size of 1.7 ± 0.5 being recorded. The kidding rate of the recipient does declined to 57.0% (4) and 25.0% (2) for fresh and conventional slow frozen groups, respectively. An embryo survival rate of 35.7% (n = 5) for fresh, 25.0% (n = 4) for conventional slow freezing and 31.3% (n = 5) for vitrification was recorded and was not affected by the number of CL’s present on the respective ovaries at the time of transfer. There was a tendency for more females to be born than males (ratio 1 : 2, male : female) but this could not be related to the cryopreservation technique. Although the pregnancy rate following the transfer of fresh embryos was satisfactory, the embryo survival rate following the transfer of either fresh or cryopreserved embryos tended to be less acceptable. More research is warranted with larger numbers of animals, directed at improving the survivability of embryos following fresh and cryopreserved goat embryo transfer.
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On the evolutionary history and population genetic structure of the North American mountain goat (Oreamnos americanus)Shafer, Aaron BA Unknown Date
No description available.
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Forage utilisation by dairy goatsBadamana, M. S. January 1987 (has links)
No description available.
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Determination of caprine serum albumin in milk using bromocresol green dyeOlaniyan, Benjamen Adekunle. January 1900 (has links)
Thesis (M.Sc.). / Written for the Dept. of Animal Science. Title from title page of PDF (viewed 2008/05/28). Includes bibliographical references.
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Acid adaptation of Escherichia coli 0157:H7 in fermented goat milkDlamini, Bhekisisa Chushuta. January 2008 (has links)
Thesis (M.Sc.)(Food Science)--University of Pretoria, 2008. / Includes summary. Includes bibliographical references. Available on the Internet via the World Wide Web.
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The quality and nutritive value of meat from male Boer and Australian feral goats /Pratiwi, Ni Made Werdi. January 2005 (has links) (PDF)
Thesis (Ph.D.) - University of Queensland, 2005. / Includes bibliography.
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Resistance of acid-adapted Escherichia coli O157:H7 to lactoperoxidase and heat in goat milk /Parry-Hanson, Angela Araba. January 2009 (has links)
Thesis (Ph.D.(Food science))-University of Pretoria, 2009. / Includes bibliographical references. Availalble in print and online.
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The impact of the combined lactoperoxidase and pasteurisation treatment on the safety of goat milk and cottage cheeseMariba, Onneile Jacqueline. January 2006 (has links)
Thesis (M.Inst.Agrar.)(Food Production)--University of Pretoria, 2006. / Includes summary. Includes bibliographical references. Available on the Internet via the World Wide Web.
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Curse KeepersFlaherty, John Martin 01 January 2008 (has links)
Curse Keepers is the first half of a novel that chronicles the story of a secret organization determined to keep the Chicago Cubs from winning the World Series and, thereby, forestalling the end of the world.
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Efeito da adição de Trolox® e catalase ao meio glicina-gema-leite sobre o sêmen caprino refrigerado por 24 ou 48 horas em sistema Equitainer®Sakashita, Sabrina Missae [UNESP] 25 August 2011 (has links) (PDF)
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sakashita_sm_me_botfmvz.pdf: 493745 bytes, checksum: b66b1a455367ff9bb2f050d0a9445f86 (MD5) / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / Objetivou-se determinar in vitro o efeito da adição de antioxidantes Trolox® e Catalase ao diluidor Glicina-Gema-Leite com 5% de gema de ovo, utilizado na refrigeração do sêmen caprino em sistema de Equitainer® por 24 ou 48 horas, avaliando-se a motilidade espermática determinada no sistema computadorizado (CASA), a integridade de membrana plasmática pela combinação dos corantes fluorescente iodeto de propídio e diacetato de carboxifluoresceína (IP+DIC), patologia espermática em câmara úmida em solução de gluteraldeído e após a refrigeração ao teste de exaustão em banho-maria (37ºC até 240 minutos). Para isso foi utilizado o sêmen em duplicata (12 amostras) de 6 caprinos Boer, coletados com vagina artificial e diluído na concentração final de 400x106 espermatozóides/mL em meio Glicose-Leite (GL) e nos diluidores Glicina-Gema-Leite com (GGLtc) e sem (GGL) antioxidantes Trolox® e Catalase. As análises foram realizadas no sêmen fresco, após diluição (pré-refrigeração), 24 e 48 horas pós-refrigeração no sistema Equitainer®, e durante o teste de exaustão nos tempos 30, 60, 120 e 240 minutos de incubação em banho-maria. Foi demonstrado que o diluidor GGLtc demonstrou melhor eficiência na proteção de acrossomo entre os diluidores. A adição de antioxidante ao diluidor GGL com 5% de gema de ovo foi capaz de manter baixo percentual de acrossomo lesado durante a refrigeração de até 48 horas e o sistema Equitainer® eficiente durante a refrigeração até 48 horas / The objetive was to determine in vitro the effect of adding antioxidant Trolox® and Catalase in the extender Glycine-Yolk-Milk with 5% of egg yolk, used in the goat semen cooling in Equitainer® system for 24 or 48 hours, evaluating sperm motility determined by the computerized semen analysis (CASA), the integrity of the plasma membrane by a combination of fluorescent carboxyfluorescein diacetato(DIC) and propidium iodide(IP), sperm pathology in the humid chamber in gluteraldehyde solution and after cooling to the exhaustion test in a water bath (37°C up to 240 minutes). For the semen that was used in duplicate (12 samples) for six Boer goats, collected with artificial vagina and diluted at a final concentration of 400x106 sperm/mL using extenders Glucose-Milk (GL) and Glycine-Yolk-Milk (GGLtc) and without (GGL) antioxidant Trolox® and Catalase. Analyses were performed in fresh semen, after diluition (pre-cooling) and 24 or 48 hours post cooling in Equitainer® system, and during the exhaustion test incubation in a water bath for 30, 60, 120 and 240 minutes. It has been shown that the extender GGLtc showed better efficiency in protection acrossome between the extenders. The addition of antioxidant in the GGL with 5% egg yolk (GGLtc) was able to maintain a low percentage of damaged acrossome during cooling up to 48 hours and the Equitainer® system during the cooling efficiency up to 48 hours
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