RESUMO

There are few scientific reports on the histology of the phallus of ratite birds. The aim of this study was to conduct a histochemical analysis to determine the distribution of smooth muscle cells and the volumetric density (Vv) of the fibres of the elastic system in the ostrich phallus. Adult ostriches, 14 months old, were used. The phalluses were fixed in Bouin's solution and then transferred to a buffered formalin solution. They were then processed using standard histological stains for paraffin and slices were obtained. The following techniques were performed: HE, Picrosirius red, Alcian Blue at pH 1.0 and 2.5. The Periodic acid-Schiff reagent and Weigert's Resorcin-Fuchsin with previous oxidation were performed. The M42 test system was used to quantify the elastic system fibres. For immunohistochemical analysis, an anti alpha smooth muscle actin monoclonal antibody was used. The surface of the phallus is covered by a non-keratinized stratified squamous epithelium, which becomes stratified cylindrical in the region of the spermatic sulcus. No glands associated with the connective tissue were observed. The Vv of the elastic system fibres was 4.75%. Smooth muscle cells were visualized only in the walls of blood vessels through immunostaining, with an absence in the lymphatic sinuses. Despite similarities with other birds, such as the presence of a fibrous external axis, a lymphatic core, and a spermatic groove, the ostrich phallus shows marked differences, including the absence of an elastic core, a non-keratinized lining epithelium, and the absence of glands throughout its extension.

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The bone texture of Rhea americana was evaluated through the examination of a postnatal ontogenetic series. The hind limb bone surfaces of specimens of one, three and five months old, and adults were compared to characterize each stage according to the morphological features generated by their differential ossification. The results suggest a similar process of tissue maturation concerning neognathous birds, although with some differences. A spongy or striated surface with abundant pores in the femur and longitudinal grooves in the tibiotarsus and tarsometatarsus characterizes chicks. Vascularity decreases, and the bone texture gradually changes acquiring a more homogeneous surface, to eventually reach the smooth appearance of adult bones. The establishment of particular textures corresponding to different bones and ontogenetic stages permits the accurate interpretation of remains in ecological, archaeological and paleontological contexts in which bones are fragmented and/or incomplete.

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The greater rhea, Rhea americana, is a wild ratite of high scientific importance and significant and zootechnical value, especially considering the current development state of Brazilian poultry production, where research aimed at increasing the productivity of these animals has become extremely relevant. Studies concerning fetal attachments and embryonic development are paramount, as they can provide essential information concerning reproductive and nutritional animal management. However, a lack of information on greater rhea fetal morphology is noted. Therefore, the aim of the present study was to establish a standard model for fetal attachments in this species. Greater rhea eggs were incubated from 0 to 36 days, and macroscopic and microscopic embryonic attachment characterizations were performed. Histologically, all embryonic annexes exhibit germ layers, namely the ectoderm (outer layer), mesoderm (middle layer) and endoderm (inner layer). The findings indicate that greater rhea development patterns are similar to other birds.

RESUMO

The objective was to characterize morphological, morphometric, and ultrastructural changes in rhea spermatozoa between the epididymis and the vas deferens. Sperm samples were collected from the reproductive tracts of seven adult individuals and evaluated for sperm characteristics using brightfield microscopy as well as ultrastructural features using scanning electron microscopy (SM). Mean sperm count tended to increase in the vas deferens (378.0 ± 135.0 × 106) compared to the epididymis (201.0 ± 77.4 × 106). Percentages of motile sperm grew from 37.0 ± 4.9% in the epididymis to 58.5 ± 7.7% in the vas deferens. The proportion of normal spermatozoa was 75.6 ± 1.8% and most common defects were bent tails (9.7 ± 0.9%). However, these proportions were not different between epididymis and vas deferens. SM analysis revealed further features of rhea spermatozoa. Normal rhea spermatozoa were threadlike with an acrosome (0.95 ± 0.0 µm), head (7.53 ± 0.01 µm), midpiece (2.08 ± 0.01 µm), and tail (30.7 ± 0.06 µm). Lengths of sperm acrosome, head, midpiece, and tail were longer in the vas deferens compared to the epididymis. Our findings suggest that rhea spermatozoa undergo a maturation process during the passage from the epididymis to the vas deferens.

RESUMO

The objectives of the study were to (1) describe the kinematic parameters of spermatozoa (2) compare methods of evaluating sperm viability (3) validate assays of functionality and integrity of the sperm membrane and (4) evaluate possible changes between spermatozoa from the epididymis and the vas deferens of the greater rhea. Semen samples were recovered from 7 adult individuals. Sperm motility was characterized by adjusting the set-up for Computer-assisted semen analysis (CASA) to that new species. For sperm viability evaluation, smears of bromophenol blue and eosin-nigrosine dyes were used. Five solutions of different osmolarities were then tested for the hypoosmotic swelling test (HOST). The combination of fluorescent probes (propidium iodide - IP and Hoechst 33342) was also used to assess plasma membrane integrity. Data were presented as mean ± SEM. Rhea spermatozoa from the vas deferens had an overall motility of 14.6 ± 2.5%. The bromophenol blue staining technique revealed that 64.6 ± 5.2% sperm were viable, while that proportion was 72.1 ± 2.5% using eosin-nigrosine. An average of 77.6 ± 4.8% of spermatozoa reacted to the HOST with distilled water at 0 mOsm/l. Fluorescent probes indicated that 65.3 ± 2.6% of spermatozoa had intact membranes. Interestingly, no statistical differences were observed between the parameters analyzed in the epididymal spermatozoa and the vas deferens. These new assays set reference values that can now be used to further exploration of sperm handling conditions and freezing protocols in rheas.

RESUMO

The purpose of this research was to study the histology and describe the microscopy findings of the epididymis epithelium of greater Rhea americana at three time periods: November 2005 (n=14), December 2006 (n= 20), and May 2007 (n= 20), to observe and compare the differences that occurred. We studied the epididymis from 54 rheas, bred in Santa Maria, Rio Grande do Sul, Brazil. The epididymis were collected during commercial slaughter and fixed in bouin. Optical microscopy was used to measure the cellular structure, types of cells, tubules, and stereological values like the epididymis epithelium diameters, lumen, thickness, and relative volume of the tissue structure. Additionally, electron microscopy was studied. In December 2006 and May 2007, the means of the epididymis tubular diameter were: 79.1 and 58.1 µm, epithelium thickness: 24.0 and 52.2 µm, and lumen diameter: 55.0 and 5.8 µm, respectively. Regarding the volumetric proportion, we reported the following values: epithelium volume 36.2 and 80.4%, lumen without spermatozoon 19.6 and 3.0%, lumen with spermatozoon 5.4 and 0.0%, interstitium 35.4 and 12.0%, blood vessels 3.5 and 4.6%, structures in cellular superficies 1.4 and 0%, lamina 1.4 and 3.2%, and artifacts 0.3 and 1.3%, respectively. The epididymis ducts had a circular form in transverse sections with spermatozoon only in November 2005 and December 2006. The Rheas epididymis morphology was found to be similar to ostriches, roosters, and Japanese quail. Here, we present data from stereological microscopy (tubular diameter, epithelium thickness, and lumen diameter), volumetric proportion (epithelium, lumen without spermatozoon, lumen with spermatozoon, interstitium, blood vessels, structures in cellular superficies; cilium, estereocilium, and lamina) in this species during the repose and sexual activity period (reproductive season).(AU)

O objetivo desta pesquisa foi estudar a histologia e descrever os achados microscópicos do epitélio epidídimo de ema em três períodos: novembro/2005 (n = 14), dezembro/2006 (n = 20) e maio/2007 (n = 20), para observação e comparação das diferenças que ocorreram nesses tempos distintos. Estudamos o epidídimo de 54 animais, criados em Santa Maria, RS. Durante o abate comercial, os epidídimos foram coletados e fixados em Bouin. A microscopia óptica mede a estrutura celular, tipos de células, túbulos e valores estereológicos, como os diâmetros do epitélio do epidídimo, lúmen, espessura, volume relativo da estrutura do tecido. Em dezembro/2006 e maio/2007, as médias do diâmetro tubular do epidídimo foram: 79,1 e 58,1µm, espessura do epitélio: 24,0 e 52,2µm, diâmetro do lúmen: 55,0 e 5,8µm, respectivamente. Em relação à proporção volumétrica, encontramos os seguintes valores: volume epitelial 36,2 e 80,4%, lúmen sem espermatozoide 19,6 e 3,0%, lúmen com espermatozoide 5,4 e 0,0%, intestínio 35,4 e 12,0%, vasos sanguíneos 3,5 e 4,6%, estruturas celulares superfícies 1,4 e 0%, lâmina 1,4 e 3,2%, artefatos 0,3 e 1,3%, respectivamente. Os ductos do epidídimo apresentaram forma circular em cortes transversais com espermatozoide apenas em novembro/2005 e dezembro/2006. A morfologia do epidídimo de Rhea foi semelhante ao avestruz, galo e codornas japonesas. Apresentamos dados de microscopia estereológica (diâmetro tubular, espessura do epitélio, diâmetro do lúmen), proporção volumétrica, em porcentagem (epitélio, lúmen sem espermatozóide, lúmen com espermatozoide, intestório, vasos sanguíneos, estruturas em superfícies celulares - cílio - estereocílio, lâmina e artefatos) nesta espécie nos períodos de repouso e atividade sexual (estação reprodutiva).(AU)

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ABSTRACT: The purpose of this research was to study the histology and describe the microscopy findings of the epididymis epithelium of greater Rhea americana at three time periods: November 2005 (n=14), December 2006 (n= 20), and May 2007 (n= 20), to observe and compare the differences that occurred. We studied the epididymis from 54 rheas, bred in Santa Maria, Rio Grande do Sul, Brazil. The epididymis were collected during commercial slaughter and fixed in bouin. Optical microscopy was used to measure the cellular structure, types of cells, tubules, and stereological values like the epididymis epithelium diameters, lumen, thickness, and relative volume of the tissue structure. Additionally, electron microscopy was studied. In December 2006 and May 2007, the means of the epididymis tubular diameter were: 79.1 and 58.1 µm, epithelium thickness: 24.0 and 52.2 µm, and lumen diameter: 55.0 and 5.8 µm, respectively. Regarding the volumetric proportion, we reported the following values: epithelium volume 36.2 and 80.4%, lumen without spermatozoon 19.6 and 3.0%, lumen with spermatozoon 5.4 and 0.0%, interstitium 35.4 and 12.0%, blood vessels 3.5 and 4.6%, structures in cellular superficies 1.4 and 0%, lamina 1.4 and 3.2%, and artifacts 0.3 and 1.3%, respectively. The epididymis ducts had a circular form in transverse sections with spermatozoon only in November 2005 and December 2006. The Rhea's epididymis morphology was found to be similar to ostriches, roosters, and Japanese quail. Here, we present data from stereological microscopy (tubular diameter, epithelium thickness, and lumen diameter), volumetric proportion (epithelium, lumen without spermatozoon, lumen with spermatozoon, interstitium, blood vessels, structures in cellular superficies; cilium, estereocilium, and lamina) in this species during the repose and sexual activity period (reproductive season).

RESUMO: O objetivo desta pesquisa foi estudar a histologia e descrever os achados microscópicos do epitélio epidídimo de ema em três períodos: novembro/2005 (n = 14), dezembro/2006 (n = 20) e maio/2007 (n = 20), para observação e comparação das diferenças que ocorreram nesses tempos distintos. Estudamos o epidídimo de 54 animais, criados em Santa Maria, RS. Durante o abate comercial, os epidídimos foram coletados e fixados em Bouin. A microscopia óptica mede a estrutura celular, tipos de células, túbulos e valores estereológicos, como os diâmetros do epitélio do epidídimo, lúmen, espessura, volume relativo da estrutura do tecido. Em dezembro/2006 e maio/2007, as médias do diâmetro tubular do epidídimo foram: 79,1 e 58,1µm, espessura do epitélio: 24,0 e 52,2µm, diâmetro do lúmen: 55,0 e 5,8µm, respectivamente. Em relação à proporção volumétrica, encontramos os seguintes valores: volume epitelial 36,2 e 80,4%, lúmen sem espermatozoide 19,6 e 3,0%, lúmen com espermatozoide 5,4 e 0,0%, intestínio 35,4 e 12,0%, vasos sanguíneos 3,5 e 4,6%, estruturas celulares superfícies 1,4 e 0%, lâmina 1,4 e 3,2%, artefatos 0,3 e 1,3%, respectivamente. Os ductos do epidídimo apresentaram forma circular em cortes transversais com espermatozoide apenas em novembro/2005 e dezembro/2006. A morfologia do epidídimo de Rhea foi semelhante ao avestruz, galo e codornas japonesas. Apresentamos dados de microscopia estereológica (diâmetro tubular, espessura do epitélio, diâmetro do lúmen), proporção volumétrica, em porcentagem (epitélio, lúmen sem espermatozóide, lúmen com espermatozoide, intestório, vasos sanguíneos, estruturas em superfícies celulares - cílio - estereocílio, lâmina e artefatos) nesta espécie nos períodos de repouso e atividade sexual (estação reprodutiva).

RESUMO

O avestruz africano é uma ave ratita da família Struthionidae. As características anatômicas do encéfalo do avestruz foram investigadas neste artigo. Vinte encéfalos de avestruzes adultos (dez machos e dez fêmeas), fixados em formaldeído a 10%, foram analisados neste estudo. Foram obtidas as medidas do encéfalo: comprimento e largura total do encéfalo, comprimento, largura e altura dos hemisférios cerebrais direito e esquerdo, comprimento e largura do cerebelo, comprimento e largura dos lobos ópticos direito e esquerdo. Também foram aferidos o comprimento e a largura do crânio. Os resultados para cada variável foram expressos em média e em desvio padrão. Através do teste t de Student não-pareado as variáveis foram comparadas entre os sexos e entre os antímeros. Considerou-se p<0,05 como significante. O comprimento e largura do encéfalo dos machos foram de 5,57 cm ± 0,23 cm e de 4,19 cm ± 0,16 cm, respectivamente. Nas fêmeas o comprimento e largura do encéfalo foram de 5,56 cm ± 0,23 cm e de 4,18 cm ± 0,16 cm respectivamente. O comprimento do hemisfério cerebral direito foi de 3,41 cm ± 0,13 cm nos machos e de 3,39 cm ± 0,12 cm nas fêmeas, já no esquerdo foi de 3,35 cm ± 0,14 cm nos machos e de 3,34 cm ± 0,05 cm nas fêmeas. A largura do hemisfério cerebral direito foi de 2,27 cm ± 0,17 cm nos machos e de 2,25 ± 0,14 cm nas fêmeas, e do esquerdo foi de 2,25 cm ± 0,11 cm nos machos e de 2,27 cm ± 0,11 cm nas fêmeas. A altura do hemisfério cerebral direito foi de 2,08 cm ± 0,23 cm nos machos e de 2,07 cm ± 0,21 cm nas fêmeas e do hemisfério cerebral esquerdo foi de 2,05 cm ± 0,22 cm nos machos e de 2,05 cm ± 0,22 nas fêmeas. O comprimento do cerebelo foi de 2,45 cm ± 0,32 cm nos machos e de 2,44 cm ± 0,32 cm nas fêmeas, e sua largura foi de 1,59 cm ± 0,16 cm nos machos e de 1,58 cm ± 0,15 cm nas fêmeas. O comprimento do lobo óptico direito foi de 1,30 cm ± 0,06 nos machos e de 1,30 cm ± 0,06 cm nas fêmeas, já o comprimento do lobo óptico esquerdo foi de 1,24 cm ± 0,07 cm nos machos e de 1,23 cm ± 0,67 cm nas fêmeas. A largura do lobo óptico direito foi de 1,08 cm ± 0,07 cm nos machos e de 1,08 cm ± 0,07 cm nas fêmeas e largura do lobo óptico esquerdo foi de 1,08 cm ± 0,07 cm nos machos e de 1,08 cm ± 0,07 cm nas fêmeas. A superfície do cérebro do avestruz é lisa sem qualquer giro ou sulco. A média do comprimento dos crânios dos machos é maior que a das fêmeas. Em relação aos 20 encéfalos analisados o lobo óptico direito é maior que o esquerdo. Houve correlação linear positiva entre a largura do crânio com a largura do cerebelo.(AU)

The african ostrich is a ratite bird in the family Struthionidae. The anatomical features of the African ostrich brain were investigated in this study. Twenty adult ostrich heads (10 males and 10 females), fixed in 10% formaldehyde, were analyzed in this study. The measures of the brain were obtained: length and total width of the brain, length, width and height of the right and left cerebral hemispheres, length and width of the cerebellum, length and width of the right and left optical lobes. The length and width of the skull were also measured. Results for each variable were expressed as mean and standard deviation. Through unpaired Student's ttest the variables were compared between sexes and between antimers. Statistical significance was considered as p<0,05. The length and width of the male encephalus was 5.57 ± 0.23 cm and 4.19 ± 0.16, respectively. In females, the length and width of the encephalus were 5.56 ± 0.23 and 4.18 ± 0.16 respectively. The length of the right cerebral hemisphere was 3.41 ± 0.13 in males and 3.39 ± 0.12 in females, while in the left it was 3.35 ± 0.14in males and 3.34 ± 0.05 in females. The width of the right cerebral hemisphere was 2.27 ± 0.17 in males and 2.25 ± 0.14 in females, and the left was 2.25 ± 0.11 in males and 2.27 ± 0.11 in females. The height of the right cerebral hemisphere was 2.08 ± 0.23 in males and 2.07 ± 0.21 in females and the left cerebral hemisphere was 2.05 ± 0.22 in males and 2.05 ± 0.22 in females. The length of the cerebellum was 2.45 ± 0.32 in males and 2.44 ± 0.32 in females, and its width was 1.59 ± 0.16 in males and 1.58 ± 0.15 in females. The length of the right optic lobe was 1.30 ± 0.06 in males and 1.30 ± 0.06 in females, while the length of the left optic lobe was 1.24 ± 0.07 in males and 1.23 ± 0.67 in females. The width of the right optic lobe was 1.08 ± 0.07 in males and 1.08 ± 0.07 in females and the width of the left optic lobe was 1.08 ± 0.07 in males and 1.08 ± 0.07 in females. The surface of the ostrich brain is smooth without any gyrus or sulcus. The average length of the skulls of males is greater than that of females. In relation to the 20 encephalus analyzed, the right optic lobe is larger than the left. There was a positive linear correlation between the width of the skull and the width of the cerebellum.(AU)

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O avestruz africano é uma ave ratita da família Struthionidae. As características anatômicas do encéfalo do avestruz foram investigadas neste artigo. Vinte encéfalos de avestruzes adultos (dez machos e dez fêmeas), fixados em formaldeído a 10%, foram analisados neste estudo. Foram obtidas as medidas do encéfalo: comprimento e largura total do encéfalo, comprimento, largura e altura dos hemisférios cerebrais direito e esquerdo, comprimento e largura do cerebelo, comprimento e largura dos lobos ópticos direito e esquerdo. Também foram aferidos o comprimento e a largura do crânio. Os resultados para cada variável foram expressos em média e em desvio padrão. Através do teste t de Student não-pareado as variáveis foram comparadas entre os sexos e entre os antímeros. Considerou-se p<0,05 como significante. O comprimento e largura do encéfalo dos machos foram de 5,57 cm ± 0,23 cm e de 4,19 cm ± 0,16 cm, respectivamente. Nas fêmeas o comprimento e largura do encéfalo foram de 5,56 cm ± 0,23 cm e de 4,18 cm ± 0,16 cm respectivamente. O comprimento do hemisfério cerebral direito foi de 3,41 cm ± 0,13 cm nos machos e de 3,39 cm ± 0,12 cm nas fêmeas, já no esquerdo foi de 3,35 cm ± 0,14 cm nos machos e de 3,34 cm ± 0,05 cm nas fêmeas. A largura do hemisfério cerebral direito foi de 2,27 cm ± 0,17 cm nos machos e de 2,25 ± 0,14 cm nas fêmeas, e do esquerdo foi de 2,25 cm ± 0,11 cm nos machos e de 2,27 cm ± 0,11 cm nas fêmeas. A altura do hemisfério cerebral direito foi de 2,08 cm ± 0,23 cm nos machos e de 2,07 cm ± 0,21 cm nas fêmeas e do hemisfério cerebral esquerdo foi de 2,05 cm ± 0,22 cm nos machos e de 2,05 cm ± 0,22 nas fêmeas. O comprimento do cerebelo foi de 2,45 cm ± 0,32 cm nos machos e de 2,44 cm ± 0,32 cm nas fêmeas, e sua largura foi de 1,59 cm ± 0,16 cm nos machos e de 1,58 cm ± 0,15 cm nas fêmeas. O comprimento do lobo óptico direito foi de 1,30 cm ± 0,06 nos machos e de 1,30 cm ± 0,06 cm nas fêmeas, já o comprimento do lobo óptico esquerdo foi de 1,24 cm ± 0,07 cm nos machos e de 1,23 cm ± 0,67 cm nas fêmeas. A largura do lobo óptico direito foi de 1,08 cm ± 0,07 cm nos machos e de 1,08 cm ± 0,07 cm nas fêmeas e largura do lobo óptico esquerdo foi de 1,08 cm ± 0,07 cm nos machos e de 1,08 cm ± 0,07 cm nas fêmeas. A superfície do cérebro do avestruz é lisa sem qualquer giro ou sulco. A média do comprimento dos crânios dos machos é maior que a das fêmeas. Em relação aos 20 encéfalos analisados o lobo óptico direito é maior que o esquerdo. Houve correlação linear positiva entre a largura do crânio com a largura do cerebelo.

The african ostrich is a ratite bird in the family Struthionidae. The anatomical features of the African ostrich brain were investigated in this study. Twenty adult ostrich heads (10 males and 10 females), fixed in 10% formaldehyde, were analyzed in this study. The measures of the brain were obtained: length and total width of the brain, length, width and height of the right and left cerebral hemispheres, length and width of the cerebellum, length and width of the right and left optical lobes. The length and width of the skull were also measured. Results for each variable were expressed as mean and standard deviation. Through unpaired Student's ttest the variables were compared between sexes and between antimers. Statistical significance was considered as p<0,05. The length and width of the male encephalus was 5.57 ± 0.23 cm and 4.19 ± 0.16, respectively. In females, the length and width of the encephalus were 5.56 ± 0.23 and 4.18 ± 0.16 respectively. The length of the right cerebral hemisphere was 3.41 ± 0.13 in males and 3.39 ± 0.12 in females, while in the left it was 3.35 ± 0.14in males and 3.34 ± 0.05 in females. The width of the right cerebral hemisphere was 2.27 ± 0.17 in males and 2.25 ± 0.14 in females, and the left was 2.25 ± 0.11 in males and 2.27 ± 0.11 in females. The height of the right cerebral hemisphere was 2.08 ± 0.23 in males and 2.07 ± 0.21 in females and the left cerebral hemisphere was 2.05 ± 0.22 in males and 2.05 ± 0.22 in females. The length of the cerebellum was 2.45 ± 0.32 in males and 2.44 ± 0.32 in females, and its width was 1.59 ± 0.16 in males and 1.58 ± 0.15 in females. The length of the right optic lobe was 1.30 ± 0.06 in males and 1.30 ± 0.06 in females, while the length of the left optic lobe was 1.24 ± 0.07 in males and 1.23 ± 0.67 in females. The width of the right optic lobe was 1.08 ± 0.07 in males and 1.08 ± 0.07 in females and the width of the left optic lobe was 1.08 ± 0.07 in males and 1.08 ± 0.07 in females. The surface of the ostrich brain is smooth without any gyrus or sulcus. The average length of the skulls of males is greater than that of females. In relation to the 20 encephalus analyzed, the right optic lobe is larger than the left. There was a positive linear correlation between the width of the skull and the width of the cerebellum.

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The objective of this study was to describe emus' breeding performance in Brazil at different ages, grouped in couples or colonies. The duration of the breeding season and the production of eggs per female housed were recorded, and the productivity and breeding variables were associated with the variation of the photoperiod. The total production of the flock was 180 eggs, and the breeding season lasted 167 days (April-September), a period with an average of 11 h and 11min of daylight. The breeding season lasted 113, 133 and 82 days, the numbers of eggs produced per female were 7.29, 25.67 and 17.3, and productivity values were 31.6, 38.6, and 45.4% in the groups of birds with ages of two, four and seven years, respectively. The breeding season in 2016 occurred between April and August in Brazil. Older birds tended to start breeding later. The production rate observations indicated that earlier peak production was associated with lower egg production potential. Finally, there was a tendency for better breeding performance of birds housed in couples than in groups with more birds.(AU)

O objetivo deste estudo foi descrever o desempenho reprodutivo de emus de diferentes idades, agrupados em casais ou em colônias, no Brasil. A duração da estação reprodutiva e a produção de ovos por fêmea alojada foram registradas, a produtividade e as variáveis reprodutivas foram associadas às variações no fotoperíodo. A produção total do lote de aves foi de 180 ovos, e a estação reprodutiva durou 167 dias (abril-setembro), período que apresentou fotoperíodo médio de 11 horas e 11 minutos. Nos grupos de aves de dois, quatro e sete anos de idade, a estação reprodutiva durou 113,, 133 e 82 dias, o número de ovos por fêmea foi de 7,29, 25,67 e 17,3 e a produtividade foi de 31,6, 38,6 e 45,4%, respectivamente. A estação reprodutiva em 2016 ocorreu entre abril e agosto no Brasil. Aves mais velhas tenderam a iniciar o período reprodutivo mais tarde. As observações na taxa de produção podem indicar que quanto mais precoce o pico produtivo, menor o potencial de produção de ovos em emus. Houve a tendência ao melhor desempenho reprodutivo das aves alojadas em casais em comparação com as alojadas em colônias.(AU)

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Background: The Rhea americana americana is a wild bird belonging to the group of Ratites, and is important from the scientific point of view given their adaptability to captivity. Considering that information about its morphology is important for the viability of domesticating the species, the aim of this study was to macroscopically identify the brain regions, as well as the cerebral arteries and the cerebral arterial circuit in order to establish the cerebral vascular pattern and systematization.Materials, Methods & Results: Twenty one brains from young and adult Greater Rheas of both sexes were used from animals that had died due to natural causes and were then kept in a freezer. The specimens were thawed and incised in the cervical region to allow exposure of the left common carotid artery, which was cannulated. The vascular system was rinsed with 0.9% saline solution, then perfused with latex Neoprene 650 stained with red pigment. The animals were subsequently fixed in 3.7% aqueous formaldehyde solution for 72 h, and then they were dissected by removing the bones from the skull cap. The brains were analyzed, and the structures were identified, photographed, schematized and denominated. Morphometric measurements were performed on the basilar and cerebellar ventral caudal arteries, recording the values of length and width in millimeters with the aid of a digital caliper. The brain was divided into: telencephalon, diencephalon, brainstem and cerebellum; while externally, the observed structures are: olfactory bulbs, optical lobes, optic nerves, optic chiasm, pituitary and pineal glands. Vascularization was performed by the following arteries: ventral spinal artery, basilar artery, ventricular cerebellar arteries, medium ventricular cerebellar arteries, caudal branches of the carotid arteries of the brain, ventral mesencephalic artery, cerebral caudal arteries, rostral branches of the carotid arteries of the brain, middle cerebral arteries,[...](AU)

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Background: The Rhea americana americana is a wild bird belonging to the group of Ratites, and is important from the scientific point of view given their adaptability to captivity. Considering that information about its morphology is important for the viability of domesticating the species, the aim of this study was to macroscopically identify the brain regions, as well as the cerebral arteries and the cerebral arterial circuit in order to establish the cerebral vascular pattern and systematization.Materials, Methods & Results: Twenty one brains from young and adult Greater Rheas of both sexes were used from animals that had died due to natural causes and were then kept in a freezer. The specimens were thawed and incised in the cervical region to allow exposure of the left common carotid artery, which was cannulated. The vascular system was rinsed with 0.9% saline solution, then perfused with latex Neoprene 650 stained with red pigment. The animals were subsequently fixed in 3.7% aqueous formaldehyde solution for 72 h, and then they were dissected by removing the bones from the skull cap. The brains were analyzed, and the structures were identified, photographed, schematized and denominated. Morphometric measurements were performed on the basilar and cerebellar ventral caudal arteries, recording the values of length and width in millimeters with the aid of a digital caliper. The brain was divided into: telencephalon, diencephalon, brainstem and cerebellum; while externally, the observed structures are: olfactory bulbs, optical lobes, optic nerves, optic chiasm, pituitary and pineal glands. Vascularization was performed by the following arteries: ventral spinal artery, basilar artery, ventricular cerebellar arteries, medium ventricular cerebellar arteries, caudal branches of the carotid arteries of the brain, ventral mesencephalic artery, cerebral caudal arteries, rostral branches of the carotid arteries of the brain, middle cerebral arteries,[...]

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Abstract Today, blood tests are an indispensable tool in avian medicine. This study aimed to describe and compare hematological and morphometric data of erythrocytes, leukocytes and thrombocytes of rhea, Rhea americana. To do so, 58 rheas of both sexes on two farms, one in Cachoeiro do Itapemirim, Espírito Santo (ES), and the other in São Carlos, São Paulo (SP), were selected. Blood samples were taken and their RBC counts, PCV and Hb levels were determined and used in hematimetric index calculations. The total and differentiated leukocyte counts and the TPP and fibrinogen serum levels were also obtained. The results from the two farms analyzed were compared by means of the t test. There were differences in the parameters of the erythrocyte series between the two flocks because of a process of hypochromic macrocytic anemia observed among the rheas in ES. The values for the erythrocyte series and indexes were: RBC, 2.81 ± 0.15 x106/μl; PCV, 44.20 ± 2.86%; Hb, 12.12 ± 0.74 g/dL; MCV, 15.75 ± 0.89 fL; MCH, 43.18 ± 1.82 pg; and MCHC, 27.44 ± 0.80 g/dL. The values for the leukocyte series were: WBC, 12,072 ± 4116 /μL; heterophils, 64.10 ± 9.90%; eosinophils, 2.05 ± 2.06%; monocytes, 6.40 ± 2.99%; lymphocytes, 26.93 ± 9.62%; and basophils, 0.52 ± 1.27%. These can all be suggested as references for rheas reared in Brazil. Statistical differences were observed in erythrocyte length measurements, which were higher in the rheas in SP than in those in ES. Regarding width, the heterophils, lymphocytes and monocytes of the birds in ES were statistically greater than those of the birds in SP. It was concluded that rheas may exhibit morphometric alterations to blood cells and differences in blood elements according to the type of management to which they are subjected.

Resumo Atualmente exames de sangue são ferramentas indispensáveis na medicina aviária. Este estudo teve como objetivo descrever e comparar valores hematológicos e morfométricos de eritrócitos, leucócitos e trombócitos de emas, Rhea americana. Para isso, foram selecionadas 58 emas de ambos os sexos de dois criatórios, um em Cachoeiro do Itapemirim, Espírito Santo (ES) e o outro em São Carlos, São Paulo (SP). Amostras de sangue foram coletadas e realizadas a hematimetria, Hto e dosagem de Hb que foram utilizados nos cálculos dos índices hematimétricos. Também foram efetuadas as contagens total e diferencial de leucócitos, além da dosagem de proteínas total e do fibrinogênio séricos. Os resultados referentes às duas propriedades analisadas foram comparados pelo Teste t. Ocorreram diferenças nos parâmetros da série vermelha entre as aves dos dois criatórios devido a um processo de anemia macrocítica hipocrômica observado nas emas do ES. Os valores para a série vermelha e índices hematimétricos como: hematimetria, 2,81±0,15 x106/μl; Hto, 44,20±2,86%; Hb, 12,12±0,74 g/dL; VCM, 15,75±0,89 fL; HCM, 43,18±1,82 pg; CHCM, 27,44±0,80, além dos valores da série branca como: leucometria total, 12.072±4.116/μL, heterofilo, 64,10±9,90%, eosinófilo, 2,05±2,06%, monócito, 6,40±2,99%, linfócito, 26,93±9,62%, basófilo, 0,52±1,27% foram sugeridos como os de referência para as emas criadas no Brasil. Diferenças estatísticas foram observadas no comprimento de eritrócitos, o qual estava maior nas emas de SP do que aquelas do ES. Em relação à largura, os heterófilos, linfócitos e monócitos das aves do ES foram estatisticamente maior do que aquelas das aves de SP. Concluiu-se que emas podem apresentar alterações morfométricas de células sanguíneas e diferenças nos elementos do sangue de acordo com o tipo de manejo a que são submetidos.

Assuntos

RESUMO

Today, blood tests are an indispensable tool in avian medicine. This study aimed to describe and compare hematological and morphometric data of erythrocytes, leukocytes and thrombocytes of rhea, Rhea americana. To do so, 58 rheas of both sexes on two farms, one in Cachoeiro do Itapemirim, Espيrito Santo (ES), and the other in Sمo Carlos, Sمo Paulo (SP), were selected. Blood samples were taken and their RBC counts, PCV and Hb levels were determined and used in hematimetric index calculations. The total and differentiated leukocyte counts and the TPP and fibrinogen serum levels were also obtained. The results from the two farms analyzed were compared by means of the t test. There were differences in the parameters of the erythrocyte series between the two flocks because of a process of hypochromic macrocytic anemia observed among the rheas in ES. The values for the erythrocyte series and indexes were: RBC, 2.81 ± 0.15 x106/l; PCV, 44.20 ± 2.86%; Hb, 12.12 ± 0.74 g/dL; MCV, 15.75 ± 0.89 fL; MCH, 43.18 ± 1.82 pg; and MCHC, 27.44 ± 0.80 g/dL. The values for the leukocyte series were: WBC, 12,072 ± 4116 /L; heterophils, 64.10 ± 9.90%; eosinophils, 2.05 ± 2.06%; monocytes, 6.40 ± 2.99%; lymphocytes, 26.93 ± 9.62%; and basophils, 0.52 ± 1.27%. These can all be suggested as references for rheas reared in Brazil. Statistical differences were observed in erythrocyte length measurements, which were higher in the rheas in SP than in those in ES. Regarding width, the heterophils, lymphocytes and monocytes of the birds in ES were statistically greater than those of the birds in SP. It was concluded that rheas may exhibit morphometric alterations to blood cells and differences in blood elements according to the type of management to which they are subjected.(AU)

Atualmente exames de sangue são ferramentas indispensáveis na medicina aviária. Este estudo teve como objetivo descrever e comparar valores hematológicos e morfométricos de eritrócitos, leucócitos e trombócitos de emas, Rhea americana. Para isso, foram selecionadas 58 emas de ambos os sexos de dois criatórios, um em Cachoeiro do Itapemirim, Espírito Santo (ES) e o outro em São Carlos, São Paulo (SP). Amostras de sangue foram coletadas e realizadas a hematimetria, Hto e dosagem de Hb que foram utilizados nos cálculos dos índices hematimétricos. Também foram efetuadas as contagens total e diferencial de leucócitos, além da dosagem de proteínas total e do fibrinogênio séricos. Os resultados referentes às duas propriedades analisadas foram comparados pelo Teste t. Ocorreram diferenças nos parâmetros da série vermelha entre as aves dos dois criatórios devido a um processo de anemia macrocítica hipocrômica observado nas emas do ES. Os valores para a série vermelha e índices hematimétricos como: hematimetria, 2,81±0,15 x106/μl; Hto, 44,20±2,86%; Hb, 12,12±0,74 g/dL; VCM, 15,75±0,89 fL; HCM, 43,18±1,82 pg; CHCM, 27,44±0,80, além dos valores da série branca como: leucometria total, 12.072±4.116/μL, heterofilo, 64,10±9,90%, eosinófilo, 2,05±2,06%, monócito, 6,40±2,99%, linfócito, 26,93±9,62%, basófilo, 0,52±1,27% foram sugeridos como os de referência para as emas criadas no Brasil. Diferenças estatísticas foram observadas no comprimento de eritrócitos, o qual estava maior nas emas de SP do que aquelas do ES. Em relação à largura, os heterófilos, linfócitos e monócitos das aves do ES foram estatisticamente maior do que aquelas das aves de SP. Concluiu-se que emas podem apresentar alterações morfométricas de células sanguíneas e diferenças nos elementos do sangue de acordo com o tipo de manejo a que são submetidos.(AU)

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The greater rhea (Rhea americana americana) is a bird of the Rheidae family, and is known as a ratite for being a flightless bird. This animal has great reproductive and productive potential, according to the products and by-products that it can provide such as meat, leather, feathers and fat which are very popular in the world market. Given its economic importance and lack of information in the literature on its morphology, especially in regard to its cardiovascular apparatus, this study aimed to describe the collateral arteries of the aortic arch, in order to establish the origin and distribution of arteries and thus contribute information to the biology of the species. The bodies of 20 young and adult rheas of both sexes which had died from natural causes and were being stored in a freezer at CEMAS / UFERSA were used. The study was approved by CEUA /UFERSA (Opinion No. 09/2015, process No. 23091.004968 / 2015-23). The animals were thawed and had the cannulated thoracic aorta artery and the vascular system perfused with Neoprene 450 latex colored with yellow pigment. Subsequently, the animals were fixed in 3.7% aqueous solution of formaldehyde, and after 72 hours dissections were carried out, images were obtained and schematic drawings were prepared. The right and left brachiocephalic trunks emerged from the aortic arch in 100% of the specimens from the right brachiocephalic trunk origined a common trunk the thyroid arteries, syringotracheal trunk, vertebral artery, superficial lateral cervical artery, basecervical artery, and ascending esophageal artery. The left brachiocephalic trunk collaterally stemmed in the left common carotid artery, which in turn led to the left internal carotid and a common trunk which stemmed the thyroid arteries, the syringotracheal trunk, vertebral artery, superficial lateral cervical artery, basecervical artery and descending esophageal artery. At the end of its trajectory, the right and left brachiocephalic trunks give rise to the right and left subclavian arteries, which in turn, stem the sternoclavicular, axillary, and intercostal arteries, pectoral trunk, cranial pectoral arteries, pectoral caudal artery and collateral branches of the pectoral trunk. Based on the results, it was concluded that the aortic arch in rheas issued right and left brachycephalic trunks.

A ema (Rhea americana americana) é uma ave da família Rheidae e por isto denominada de ratita, por não apresentar aptidões para o voo. Este animal tem grande potencial reprodutivo e produtivo, em função dos produtos e subprodutos que podem fornecer como carne, couro, penas e gordura muito procurados no mercado mundial. Dada a sua importância econômica e pela falta de informação na literatura sobre sua morfologia, principalmente no que diz respeito ao seu aparelho cardiovascular, objetivou-se descrever os ramos colaterais do arco aórtico, de modo a estabelecer a origem e distribuição destas artérias e, assim, contribuir com informações para a biologia da espécie. Foram utilizadas 20 emas jovens e adultas de ambos os sexos, oriundas do CEMAS/UFERSA, as quais vieram a óbito por causas naturais e que se encontravam armazenadas em freezer. A experimentação foi aprovada pela CEUA/UFERSA (Parecer n° 09/2015, processo n° 23091.004968/2015-23). Os animais foram descongelados e tiveram a artéria aorta torácica canulada e o sistema vascular perfundido com látex Neoprene 450 corado com pigmento amarelo. Posteriormente, os animais foram fixados em solução aquosa de formaldeído a 3,7% e após 72 horas realizaram-se as dissecações e obtenção de imagens fotográficas e elaboração de desenhos esquemáticos. Em 100% dos espécimes, emergiram a partir do arco aórtico os troncos braquiocefálicos direito e esquerdo. O tronco braquiocefálico direito emitiu colateralmente a partir de um tronco comum as artérias tireoide, tronco siringotraqueal, vertebral, cervical superficial lateral, basecervical e esofageana ascendente. Já o tronco braquiocefálico esquerdo emitiu colateralmente a artéria carótida comum esquerda, que por sua vez, originou a carótida interna esquerda e um tronco comum que emitiu as artérias tireoide, tronco siringotraqueal, vertebral, cervical superficial lateral, basecervical e esofageana descendente. No final de seu percurso, os troncos braquiocefálicos direito e esquerdo, originaram as artérias subclávias direita e esquerda, que por sua vez, emitiram as artérias esternoclaviculares, axilar, intercostal, tronco peitoral, peitorais craniais e peitoral caudal e ramos colaterais do tronco peitoral. Com base nos resultados, concluiu-se que, em emas, o arco aórtico emitiu os troncos braquicefálicos direito e esquerdo.

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Ostrich farming is an important livestock industry in different world regions with a diverse offer of products and services. In Colombia, as in other countries, this market led the importation of animals from countries like Canada, United States of America and South Africa for breeding objectives. With the animals, specific pathogens for these ratites could be introduced. Libyostrongylus spp. is a strongylid nematode with worldwide distribution, which can induce a severe disease and mortality in infected animals. Limited studies in Colombia have identified parasites in ostrich farming systems. The aim of this study was to identify parasites of the genus Libyostrongylus to a species level in faecal samples from ostrich farms in three departments of Colombia. Five ostrich farms from Boyacá, Meta and Tolima were sampled in 2011 and in 2013 to obtain fresh faecal samples which were further processed by flotation tests for egg visualization and faecal culture for infective larvae identification by morphological and morphometric parameters. One from the five farms, located in Meta department, was positive for strongylid eggs in both sampling periods. After faecal culture, infective larvae were identified as Libyostrongylus douglassii. These results corroborate previous records of Libyostrongylus in ostrich farms from Meta and confirms, for the first time, infection by L. douglassii in ratites from this region. Further studies must identify associated determinants for infection and its effects on the flock health and production.

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The aim of this study was to evaluate the morphogenesis of rheas reproduction equipment featuringgonadal differentiation phase. We used eight fetuses, obtained from eggs, the Study Group Preservation of WildAnimals UFPI. The animals were fixed in formalin 5% 70% alcohol, dissected and analyzed bystereomicroscopy. Fragments of the urogenital organs were dehydrated in alcohol, diaphanized in xyleneemblocados and subjected to 5μm sections stained with hematoxylin-eosin. It was found in fetus 14 days theurogenital structures as two elongated bodies, dorsally in the coelomic cavity, lateral to the midline, andflattened dorsoventrally, the urogenital ridge; 18 days were divided medially, forming new ventral massprimitive gonads and a dorsal primitive kidneys; 21 days, were completely separated, the lobate kidneys andgonads with smooth surfaces and fetus of 30 days was observed the evolution of the development of the gonads.The rhea sexual differentiation phase occurs on the 14th day of fetal development.

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The aim of this study was to evaluate the morphogenesis of rheas reproduction equipment featuringgonadal differentiation phase. We used eight fetuses, obtained from eggs, the Study Group Preservation of WildAnimals UFPI. The animals were fixed in formalin 5% 70% alcohol, dissected and analyzed bystereomicroscopy. Fragments of the urogenital organs were dehydrated in alcohol, diaphanized in xyleneemblocados and subjected to 5μm sections stained with hematoxylin-eosin. It was found in fetus 14 days theurogenital structures as two elongated bodies, dorsally in the coelomic cavity, lateral to the midline, andflattened dorsoventrally, the urogenital ridge; 18 days were divided medially, forming new ventral massprimitive gonads and a dorsal primitive kidneys; 21 days, were completely separated, the lobate kidneys andgonads with smooth surfaces and fetus of 30 days was observed the evolution of the development of the gonads.The rhea sexual differentiation phase occurs on the 14th day of fetal development.(AU)

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The purpose of this study was to study the microscopic morphology of the testicular parenchyma of Rhea americana birds. Fifty-four 2.5±0.5 year-old male adults bred in captivity. were used. During commercial slaughter, samples of testis were collected in November/2005, December/2006 and May/2007, in order to compare possible differences. The samples underwent optical microscopy analysis and measurements of seminiferous tubule (ST) total diameters, lumen, epithelium thickness and the relative volume of parenchyma. The ST had circular form in transverse cross sections. November/2005 and December/2006 samples had many types of germinative cells and spermatozoa in lumen, but in May/2007 the samples of epithelium were poor regarding meiotic and mitotic pictures, and it was difficult to find any spermatozoon; in many tubules the lumen was inexistent or diminished. In December/2006 and May/2007 the averages were: tubule diameter 110.3 and 5.3mµ, lumen 52.4 and 4.5mµ, epithelium thickness 57.8 and 0.7mµ respectively. The volumetric proportions were: seminiferous epithelium 75.6 and 75.9, cysts in epithelium 2.1 and 1.0, ST 93.3 and 84.0, interstitium 6.2 and 15.6 respectively. The sperm reserves were: 19.7±2 and 0±0 x109 sperm cells in December 2006 and May 2007 respectively. Microscopic measures of seminiferous tubules, spermatic cells and diameter of the nuclei were presented. These data confirm reproductive seasonality, with breeding season in spring-summer with sperm production. A great variation n parenchyma, when compared breeding was noticeable.(AU)

O objetivo do estudo foi estudar a morfologia microscópica do parênquima testicular de emas (Rhea americana). Foram utilizados 54 machos adultos criados em cativeiro de 2,5±0,5 anos de idade. Durante o abate comercial foram coletadas amostras de testículos em novembro/2005, dezembro/2006 e maio/2007, para efeitos de comparação. As amostras foram processadas e para microscopia ótica de rotina para análise. Foram medidas diâmetro total de túbulos seminíferos (ST), lúmen, espessura do epitélio e a proporção volumétrica dos componentes do parênquima. O ST apresentou forma circular nas seções transversais. Em novembro/2005 e dezembro/2006, se observaram os tipos de células germinativas e espermatozoides no lúmen. Em maio/2007, as amostras de epitélio se observaram escassas meioses e imagens de mitose e era difícil de ver qualquer espermatozoide, em muitos dos túbulos o lúmen era inexistentes ou diminuído de tamanho. Em dezembro/2006 e maio/2007, as médias das características estudadas foram: diâmetro dos túbulos 110,3 e 5,3 mµ, lúmen 52,4 e 4,5mµ, espessura do epitélio 57,8 e 0,7mµ, respectivamente. As proporções volumétricas foram: epitélio seminífero 75,6 e 75,9, cistos no epitélio 2,1 e 1,0, túbulos seminíferos 93,3 e 84,0, interstício 6,2 e 15,6, respectivamente. Foram apresentadas medidas microscópicas de túbulos seminíferos, diâmetro dos núcleos das espermátides. Estes dados confirmam a sazonalidade reprodutiva, com época de reprodução na primavera - verão, com a produção de esperma. Foi perceptível uma grande variação nas medidas do parênquima testicular, quando se comparou a estação reprodutiva.(AU)

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The cloacal bursa is an organ in fowls, which triggers lymphocyte maturation and transference to other tissues. Since there is scanty information on its morphology in wild species in spite of its importance in the fowls´ immunological system, current analysis describes the arterial vascularization of the cloacal bursa in the greater rhea. Twenty juvenile rheas (male and female), which died of natural causes, were obtained from the Center for the Multiplication of Wild Animals (CEMAS/UFERSA). The animals were dissected and their thoracic aorta cannulated and red-stained Latex Neoprene 650 was introduced. The cloacal bursa was irrigated from the terminal branches of the abdominal aorta similar to the caudal mesenteric artery and to the right and left internal iliac arteries. The right and left internal pudenda arteries originated from the right and left internal iliac arteries which, in their turn, gave rise to cloacalbursa arteries and to the right and left cloacal arteries in all studied animals. The caudal mesenteric artery contributed to the arterial blood of the cloacal bursa in almost all studied animals through the anastomosis of right or left internal pudenda artery, with direct branches to the cloacal bursa. The cloacal bursa of the greater rhea is irrigated by cloacal-bursa arteries and cloacal right and left and also by the mesenteric caudal artery, with small variations with regard to the number and layout of the anastomoses and branches from the arteries. The latter are specific characteristics and differentiate them from standards perceived in other fowls.

A bolsa cloacal é o órgão das aves responsável pela maturação e transferência de linfócitos para outros tecidos. Apesar da importância deste órgão nos mecanismos imunológicos das aves, são escassas as informações a respeito de sua morfologia em espécies silvestres, fato que ensejou descrever a vascularização arterial do mesmo em emas. Foram utilizadas 20 emas jovens (machos e fêmeas) obtidas no Centro de Multiplicação de Animais Silvestres (CEMAS/UFERSA), as quais vieram a óbito por causas naturais. Os animais foram dissecados e a aorta torácica canulada e perfundida com Látex Neoprene 650 corado com pigmento vermelho. Verificou-se que a irrigação da bolsa cloacal é originada a partir de ramos terminais da artéria aorta abdominal, tais como, as artérias ilíacas internas, direita e esquerda e a artéria mesentérica caudal. Das artérias ilíacas internas, direita e esquerda, originaram-se as artérias pudendas internas, direita e esquerda, que por sua vez deram origem às artérias bursocloacais e cloacais, direita e esquerda em todos os animais estudados. A artéria mesentérica caudal contribuiu com o aporte sanguíneo arterial da bolsa cloacal em quase todos os animais estudados, por meio de anastomose com a artéria pudenda interna direita ou com a artéria pudenda interna esquerda, mas também emitiu ramos diretamente a bolsa cloacal. A bolsa cloacal de emas é irrigada pelas artérias bursocloacais e cloacais direita e esquerda e ainda, pela artéria mesentérica caudal, podendo apresentar pequenas variações quanto ao número e disposição de anastomoses e ramos emitidos, peculiares à espécie, o que as diferenciam do padrão comumente reportado para outras aves.

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