Uso do complexo enzimático solid state fermentation (SSF) em rações para tilápia do Nilo

Detalhes bibliográficos
Ano de defesa: 2011
Autor(a) principal: Moura, Guilherme de Souza
Orientador(a): Lanna, Eduardo Arruda Teixeira lattes
Banca de defesa: Abreu, Márvio Lobão Teixeira de lattes, Seixas Filho, José Teixeira de lattes, Albino, Luiz Fernando Teixeira lattes
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Viçosa
Programa de Pós-Graduação: Doutorado em Zootecnia
Departamento: Genética e Melhoramento de Animais Domésticos; Nutrição e Alimentação Animal; Pastagens e Forragicul
País: BR
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: http://locus.ufv.br/handle/123456789/1782
Resumo: In the first experiment aimed to evaluate the stability of the enzyme complex SSF (solid state fermentation) during the feed processing and storage time. Two diets were formulated with the same nutritional composition, being a diet free of SSF and the other containing 50g of SSF/kg of diet. The samples were collected during the following processing steps: mixing, after pelleting and then dried. To evaluate the storage time, was considered as day one, ready to feed after drying. On this day, two samples were being kept in a room with ambient temperature of 25oC and another kept in a freezer at-18oC. Sub-samples were taken in the 15th, 30th, 45th and 60th day. All samples from the processing stage and storage period were sent to the laboratory, measured the activity of the following enzymes: α-galactosidase, endoglucanase (carboxy-methyl-cellulase), xylanase, sucrase, amylase, lipase and trypsin. For all control samples, were not observed activities of the enzymes analyzed. Among the steps of mixing and post oven there were no differences, except for α-galactosidase and lipase activities that were observed reduction and sucrase that was observed increase in activity. There were no effects for the activities of endoglucanase, sucrase, xylanase, amylase and trypsin between the first (after oven) and the 60th day of the trial for the storage temperature of 25°C. For the storage temperature of -18°C, no differences were observed only in relation to the activities of endoglucanase and xylanase between the first and last day. Comparison between the two treatments (-25oC and 18oC) was only observed effect on the activity of galactosidase and trypsin at 60 days. For all enzymes of the SSF there was no difference in the period from 30 to 45 days of storage. It is concluded that the enzymes studied the SSF enzyme complex remain stable during the processing of pelleted feed at 55°C, maintaining activity for at least 60 days when stored at temperatures up to 25oC. For the second trial aimed to evaluate the effects of enzyme complex SSF in diets for Nile tilapia and the availability of sucrose and monosaccharides in these chime. We used 360 fish with an average weight ranging from 4.43 ± 70g in a completely randomized design with six treatments (0, 50, 100, 150, 200 and 250 ppm), six replicates, totaling 10 fish per experimental unit. At 60 days of the experiment was evaluated: initial weight, final weight, weight gain, feed conversion, specific growth rate and survival. For evaluation of sucrose, glucose and fructose present in the chyme, every 15 days, it was sacrificed a fish of each experimental unit. The levels of these carbohydrates were measured by HPLC. There was a linear effect of treatment according to final weight and weight gain. For the other performance parameters, no effect was observed. For sucrose and glucose levels of chime was observed quadratic effect as a function of treatment, while levels of fructose increased linearly. It is concluded that the enzyme complex SSF improves performance and increases the availability of sucrose and monosaccharides in the chime of Nile tilapia. The third trial evaluated the effects of the enzyme complex SSF on nutrient and gross energy digestibility in diets for Nile tilapia. A total of 72 males of Nile tilapia with average weight of 204.30 ± 17.2 g were randomly assigned to six tanks adapted for digestibility trial. The experimental diets were isonitrogenous (30% CP) and isocaloric (3,000 kcal DE / kg), supplemented with the enzyme complex SSF levels of 0, 50, 100, 150, 200 and 250 ppm. The apparent digestibility was measured by the indirect method using chromium oxide (Cr2O3) as an indicator of digestibility. Each tank received a treatment and stool collections were performed during the night (19:00, 11:00, 02:00 and 05:00). The study was conducted during nine days, with six treatments and three replicates. It is concluded that the addition of the enzyme complex in the diet improves the apparent digestibility of dry matter, crude protein, gross energy, calcium and phosphorus.
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spelling Moura, Guilherme de Souzahttp://lattes.cnpq.br/0412709903933194Donzele, Juarez Lopeshttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4787766D0Oliveira, Maria Goreti de Almeidahttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4790894D6Lanna, Eduardo Arruda Teixeirahttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4788116T3Abreu, Márvio Lobão Teixeira dehttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4701110A0Seixas Filho, José Teixeira dehttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4782867P1Albino, Luiz Fernando Teixeirahttp://lattes.cnpq.br/79305405180872672015-03-26T12:54:39Z2012-07-172015-03-26T12:54:39Z2011-09-22MOURA, Guilherme de Souza. Use of enzyme complex solid state fermentation (SSF) in diets for Nile tilapia. 2011. 80 f. Tese (Doutorado em Genética e Melhoramento de Animais Domésticos; Nutrição e Alimentação Animal; Pastagens e Forragicul) - Universidade Federal de Viçosa, Viçosa, 2011.http://locus.ufv.br/handle/123456789/1782In the first experiment aimed to evaluate the stability of the enzyme complex SSF (solid state fermentation) during the feed processing and storage time. Two diets were formulated with the same nutritional composition, being a diet free of SSF and the other containing 50g of SSF/kg of diet. The samples were collected during the following processing steps: mixing, after pelleting and then dried. To evaluate the storage time, was considered as day one, ready to feed after drying. On this day, two samples were being kept in a room with ambient temperature of 25oC and another kept in a freezer at-18oC. Sub-samples were taken in the 15th, 30th, 45th and 60th day. All samples from the processing stage and storage period were sent to the laboratory, measured the activity of the following enzymes: α-galactosidase, endoglucanase (carboxy-methyl-cellulase), xylanase, sucrase, amylase, lipase and trypsin. For all control samples, were not observed activities of the enzymes analyzed. Among the steps of mixing and post oven there were no differences, except for α-galactosidase and lipase activities that were observed reduction and sucrase that was observed increase in activity. There were no effects for the activities of endoglucanase, sucrase, xylanase, amylase and trypsin between the first (after oven) and the 60th day of the trial for the storage temperature of 25°C. For the storage temperature of -18°C, no differences were observed only in relation to the activities of endoglucanase and xylanase between the first and last day. Comparison between the two treatments (-25oC and 18oC) was only observed effect on the activity of galactosidase and trypsin at 60 days. For all enzymes of the SSF there was no difference in the period from 30 to 45 days of storage. It is concluded that the enzymes studied the SSF enzyme complex remain stable during the processing of pelleted feed at 55°C, maintaining activity for at least 60 days when stored at temperatures up to 25oC. For the second trial aimed to evaluate the effects of enzyme complex SSF in diets for Nile tilapia and the availability of sucrose and monosaccharides in these chime. We used 360 fish with an average weight ranging from 4.43 ± 70g in a completely randomized design with six treatments (0, 50, 100, 150, 200 and 250 ppm), six replicates, totaling 10 fish per experimental unit. At 60 days of the experiment was evaluated: initial weight, final weight, weight gain, feed conversion, specific growth rate and survival. For evaluation of sucrose, glucose and fructose present in the chyme, every 15 days, it was sacrificed a fish of each experimental unit. The levels of these carbohydrates were measured by HPLC. There was a linear effect of treatment according to final weight and weight gain. For the other performance parameters, no effect was observed. For sucrose and glucose levels of chime was observed quadratic effect as a function of treatment, while levels of fructose increased linearly. It is concluded that the enzyme complex SSF improves performance and increases the availability of sucrose and monosaccharides in the chime of Nile tilapia. The third trial evaluated the effects of the enzyme complex SSF on nutrient and gross energy digestibility in diets for Nile tilapia. A total of 72 males of Nile tilapia with average weight of 204.30 ± 17.2 g were randomly assigned to six tanks adapted for digestibility trial. The experimental diets were isonitrogenous (30% CP) and isocaloric (3,000 kcal DE / kg), supplemented with the enzyme complex SSF levels of 0, 50, 100, 150, 200 and 250 ppm. The apparent digestibility was measured by the indirect method using chromium oxide (Cr2O3) as an indicator of digestibility. Each tank received a treatment and stool collections were performed during the night (19:00, 11:00, 02:00 and 05:00). The study was conducted during nine days, with six treatments and three replicates. It is concluded that the addition of the enzyme complex in the diet improves the apparent digestibility of dry matter, crude protein, gross energy, calcium and phosphorus.No primeiro experimento, objetivou-se avaliar a estabilidade ao processamento de ração e ao tempo de estocagem do complexo enzimático SSF (solid state fermentation). Foram formuladas duas dietas com composição nutricional idêntica, sendo uma dieta isenta de SSF e a outra contendo 50g/Kg de inclusão deste complexo enzimático. As amostras foram coletadas durante as seguintes etapas de processamento: mistura, após a peletização e após secagem em estufa. Para avaliação do tempo de estocagem, foi considerado como dia um, a ração pronta após secagem. Neste dia, foram feitas duas amostragens, sendo uma mantida em sala com temperatura ambiente de 25oC e outra mantida em freezer a -18oC. Foram feitas sub-amostragens no 15o, 30o, 45o e 60o dia. Em todas as amostras foram mensuradas a atividade das seguintes enzimas: α-galactosidase, endoglucanase (carboxi-metil-celulase), xilanase, sacarase, amilase, lipase e tripsina. Para todas as amostras de controle, não foram observados atividades das enzimas analisadas. Entre as etapas de mistura e pós estufa não houve diferenças, exceto para a α-galactosidase e a lipase que foram observados redução na atividade e a sacarase que foi observado aumento na atividade. Não foram verificados efeitos para as atividades de endoglucanase, sacarase, xilanase, amilase e tripsina entre o primeiro (após estufa) e o 60o dia de experimento para a temperatura de estocagem de 25ºC. Para à temperatura de estocagem de -18ºC, não foi observado diferenças somente em relação às atividades de endoglucanase e xilanase entre o primeiro e o último dia. Quanto à comparação entre os dois tratamentos térmicos (25oC e -18oC), somente foi observada efeito para a atividade de galactosidase e tripsina aos 60 dias. Para todas as enzimas do SSF não houve diferença no período de 30 e 45 dias de estocagem. Conclui-se que as enzimas estudadas do complexo enzimático SSF permanecem estáveis durante o processamento de rações peletizadas à 55oC, mantendo a atividade por no mínimo 60 dias quando estocadas em ambiente de até 25oC. Para o segundo experimento, objetivou-se avaliar os efeitos do complexo enzimático SSF em rações para tilápias do Nilo e a disponibilização de sacarose e monossacarídeos no quimo destas. Foram utilizados 360 peixes com peso médio variando entre 70g ± 4,43 em um delineamento inteiramente casualizado, com seis tratamentos (0, 50, 100, 150, 200 e 250 ppm), seis repetições, totalizando 10 peixes por unidade experimental. Aos 60 dias do experimento foi avaliado: peso inicial, peso final, ganho de peso, conversão alimentar, taxa de crescimento específico e sobrevivência. Para avaliação de sacarose, glicose e frutose presente no quimo, a cada 15 dias, foi sacrificado um exemplar de cada unidade experimental. Os níveis destes carboidratos foram mensurados por meio de HPLC. Observou-se efeito linear em função do tratamento para peso final e ganho de peso. Para os demais parâmetros de desempenho, não foi verificado efeito. Quanto aos níveis de sacarose e de glicose no quimo foi observado efeito quadrático em função do tratamento, enquanto os níveis de frutose aumentaram linearmente. Conclui-se que o complexo enzimático SSF melhora o desempenho e aumenta a disponibilidade de sacarose e monossacarídeos no quimo de tilápias do Nilo. O terceiro experimento avaliou os efeitos do complexo enzimático SSF sobre a digestibilidade de nutrientes e de energia bruta em rações para tilápias do Nilo. Um total de 72 machos de tilápia do Nilo com peso médio de 204,30 ± 17,2 g foram distribuídas aleatoriamente em seis cubas adaptadas para ensaio de digestibilidade. As rações experimentais foram isoprotéicas (30% PB) e isoenergéticas (3.000 kcal de ED/ kg), sendo adicionado o complexo enzimático SSF nos níveis de 0, 50, 100, 150, 200 e 250 ppm. A digestibilidade aparente foi mensurada pelo método indireto sendo usado o óxido de cromo (Cr2O3) como indicador de digestibilidade. Cada cuba recebeu um tratamento e as coletas das fezes foram realizadas durante a noite (19:00, 11:00, 02:00 e 05:00). O estudo foi realizado durante nove dias, com seis tratamentos e 3 repetições. Conclui-se que a adição de complexo enzimático na ração melhora o coeficiente de digestibilidade aparente da matéria seca, proteína bruta, energia bruta, cálcio e fósforo.Conselho Nacional de Desenvolvimento Científico e Tecnológicoapplication/pdfporUniversidade Federal de ViçosaDoutorado em ZootecniaUFVBRGenética e Melhoramento de Animais Domésticos; Nutrição e Alimentação Animal; Pastagens e ForragiculOreochromis niloticusEnzimasFisiologia de peixesOreochromis niloticusEnzymeFish physiologyCNPQ::CIENCIAS AGRARIAS::ZOOTECNIA::NUTRICAO E ALIMENTACAO ANIMALUso do complexo enzimático solid state fermentation (SSF) em rações para tilápia do NiloUse of enzyme complex solid state fermentation (SSF) in diets for Nile tilapiainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/openAccessreponame:LOCUS Repositório Institucional da UFVinstname:Universidade Federal de Viçosa (UFV)instacron:UFVORIGINALtexto completo.pdfapplication/pdf282901https://locus.ufv.br//bitstream/123456789/1782/1/texto%20completo.pdf463cd250340430ba9ac0211a0f70b9a5MD51TEXTtexto completo.pdf.txttexto completo.pdf.txtExtracted texttext/plain137269https://locus.ufv.br//bitstream/123456789/1782/2/texto%20completo.pdf.txt0bfc78baca78c5f3d00b2fb9980d06f1MD52THUMBNAILtexto completo.pdf.jpgtexto completo.pdf.jpgIM Thumbnailimage/jpeg3635https://locus.ufv.br//bitstream/123456789/1782/3/texto%20completo.pdf.jpg80dab44a85a26f28b819fed647ee2f00MD53123456789/17822016-04-07 23:12:31.222oai:locus.ufv.br:123456789/1782Repositório InstitucionalPUBhttps://www.locus.ufv.br/oai/requestfabiojreis@ufv.bropendoar:21452016-04-08T02:12:31LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)false
dc.title.por.fl_str_mv Uso do complexo enzimático solid state fermentation (SSF) em rações para tilápia do Nilo
dc.title.alternative.eng.fl_str_mv Use of enzyme complex solid state fermentation (SSF) in diets for Nile tilapia
title Uso do complexo enzimático solid state fermentation (SSF) em rações para tilápia do Nilo
spellingShingle Uso do complexo enzimático solid state fermentation (SSF) em rações para tilápia do Nilo
Moura, Guilherme de Souza
Oreochromis niloticus
Enzimas
Fisiologia de peixes
Oreochromis niloticus
Enzyme
Fish physiology
CNPQ::CIENCIAS AGRARIAS::ZOOTECNIA::NUTRICAO E ALIMENTACAO ANIMAL
title_short Uso do complexo enzimático solid state fermentation (SSF) em rações para tilápia do Nilo
title_full Uso do complexo enzimático solid state fermentation (SSF) em rações para tilápia do Nilo
title_fullStr Uso do complexo enzimático solid state fermentation (SSF) em rações para tilápia do Nilo
title_full_unstemmed Uso do complexo enzimático solid state fermentation (SSF) em rações para tilápia do Nilo
title_sort Uso do complexo enzimático solid state fermentation (SSF) em rações para tilápia do Nilo
author Moura, Guilherme de Souza
author_facet Moura, Guilherme de Souza
author_role author
dc.contributor.authorLattes.por.fl_str_mv http://lattes.cnpq.br/0412709903933194
dc.contributor.author.fl_str_mv Moura, Guilherme de Souza
dc.contributor.advisor-co1.fl_str_mv Donzele, Juarez Lopes
dc.contributor.advisor-co1Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4787766D0
dc.contributor.advisor-co2.fl_str_mv Oliveira, Maria Goreti de Almeida
dc.contributor.advisor-co2Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4790894D6
dc.contributor.advisor1.fl_str_mv Lanna, Eduardo Arruda Teixeira
dc.contributor.advisor1Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4788116T3
dc.contributor.referee1.fl_str_mv Abreu, Márvio Lobão Teixeira de
dc.contributor.referee1Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4701110A0
dc.contributor.referee2.fl_str_mv Seixas Filho, José Teixeira de
dc.contributor.referee2Lattes.fl_str_mv http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4782867P1
dc.contributor.referee3.fl_str_mv Albino, Luiz Fernando Teixeira
dc.contributor.referee3Lattes.fl_str_mv http://lattes.cnpq.br/7930540518087267
contributor_str_mv Donzele, Juarez Lopes
Oliveira, Maria Goreti de Almeida
Lanna, Eduardo Arruda Teixeira
Abreu, Márvio Lobão Teixeira de
Seixas Filho, José Teixeira de
Albino, Luiz Fernando Teixeira
dc.subject.por.fl_str_mv Oreochromis niloticus
Enzimas
Fisiologia de peixes
topic Oreochromis niloticus
Enzimas
Fisiologia de peixes
Oreochromis niloticus
Enzyme
Fish physiology
CNPQ::CIENCIAS AGRARIAS::ZOOTECNIA::NUTRICAO E ALIMENTACAO ANIMAL
dc.subject.eng.fl_str_mv Oreochromis niloticus
Enzyme
Fish physiology
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS AGRARIAS::ZOOTECNIA::NUTRICAO E ALIMENTACAO ANIMAL
description In the first experiment aimed to evaluate the stability of the enzyme complex SSF (solid state fermentation) during the feed processing and storage time. Two diets were formulated with the same nutritional composition, being a diet free of SSF and the other containing 50g of SSF/kg of diet. The samples were collected during the following processing steps: mixing, after pelleting and then dried. To evaluate the storage time, was considered as day one, ready to feed after drying. On this day, two samples were being kept in a room with ambient temperature of 25oC and another kept in a freezer at-18oC. Sub-samples were taken in the 15th, 30th, 45th and 60th day. All samples from the processing stage and storage period were sent to the laboratory, measured the activity of the following enzymes: α-galactosidase, endoglucanase (carboxy-methyl-cellulase), xylanase, sucrase, amylase, lipase and trypsin. For all control samples, were not observed activities of the enzymes analyzed. Among the steps of mixing and post oven there were no differences, except for α-galactosidase and lipase activities that were observed reduction and sucrase that was observed increase in activity. There were no effects for the activities of endoglucanase, sucrase, xylanase, amylase and trypsin between the first (after oven) and the 60th day of the trial for the storage temperature of 25°C. For the storage temperature of -18°C, no differences were observed only in relation to the activities of endoglucanase and xylanase between the first and last day. Comparison between the two treatments (-25oC and 18oC) was only observed effect on the activity of galactosidase and trypsin at 60 days. For all enzymes of the SSF there was no difference in the period from 30 to 45 days of storage. It is concluded that the enzymes studied the SSF enzyme complex remain stable during the processing of pelleted feed at 55°C, maintaining activity for at least 60 days when stored at temperatures up to 25oC. For the second trial aimed to evaluate the effects of enzyme complex SSF in diets for Nile tilapia and the availability of sucrose and monosaccharides in these chime. We used 360 fish with an average weight ranging from 4.43 ± 70g in a completely randomized design with six treatments (0, 50, 100, 150, 200 and 250 ppm), six replicates, totaling 10 fish per experimental unit. At 60 days of the experiment was evaluated: initial weight, final weight, weight gain, feed conversion, specific growth rate and survival. For evaluation of sucrose, glucose and fructose present in the chyme, every 15 days, it was sacrificed a fish of each experimental unit. The levels of these carbohydrates were measured by HPLC. There was a linear effect of treatment according to final weight and weight gain. For the other performance parameters, no effect was observed. For sucrose and glucose levels of chime was observed quadratic effect as a function of treatment, while levels of fructose increased linearly. It is concluded that the enzyme complex SSF improves performance and increases the availability of sucrose and monosaccharides in the chime of Nile tilapia. The third trial evaluated the effects of the enzyme complex SSF on nutrient and gross energy digestibility in diets for Nile tilapia. A total of 72 males of Nile tilapia with average weight of 204.30 ± 17.2 g were randomly assigned to six tanks adapted for digestibility trial. The experimental diets were isonitrogenous (30% CP) and isocaloric (3,000 kcal DE / kg), supplemented with the enzyme complex SSF levels of 0, 50, 100, 150, 200 and 250 ppm. The apparent digestibility was measured by the indirect method using chromium oxide (Cr2O3) as an indicator of digestibility. Each tank received a treatment and stool collections were performed during the night (19:00, 11:00, 02:00 and 05:00). The study was conducted during nine days, with six treatments and three replicates. It is concluded that the addition of the enzyme complex in the diet improves the apparent digestibility of dry matter, crude protein, gross energy, calcium and phosphorus.
publishDate 2011
dc.date.issued.fl_str_mv 2011-09-22
dc.date.available.fl_str_mv 2012-07-17
2015-03-26T12:54:39Z
dc.date.accessioned.fl_str_mv 2015-03-26T12:54:39Z
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dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
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dc.identifier.citation.fl_str_mv MOURA, Guilherme de Souza. Use of enzyme complex solid state fermentation (SSF) in diets for Nile tilapia. 2011. 80 f. Tese (Doutorado em Genética e Melhoramento de Animais Domésticos; Nutrição e Alimentação Animal; Pastagens e Forragicul) - Universidade Federal de Viçosa, Viçosa, 2011.
dc.identifier.uri.fl_str_mv http://locus.ufv.br/handle/123456789/1782
identifier_str_mv MOURA, Guilherme de Souza. Use of enzyme complex solid state fermentation (SSF) in diets for Nile tilapia. 2011. 80 f. Tese (Doutorado em Genética e Melhoramento de Animais Domésticos; Nutrição e Alimentação Animal; Pastagens e Forragicul) - Universidade Federal de Viçosa, Viçosa, 2011.
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dc.publisher.department.fl_str_mv Genética e Melhoramento de Animais Domésticos; Nutrição e Alimentação Animal; Pastagens e Forragicul
publisher.none.fl_str_mv Universidade Federal de Viçosa
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