Abstract
The saffron finch, Sicalis flaveola, a passerine bird, can be found in nearly all Brazilian territory and is also raised in captivity. The objective of this work was to determine the prevalence and load of oocysts in captive saffron finches in the municipality of Campos dos Goytacazes, state of Rio de Janeiro and in free-living saffron finches in the municipality of Eugenopolis, state of Minas Gerais. In this analysis, 30 captive and 30 wild birds were assessed. Feces eliminated in a 24-hour period were collected and weighed to determine the number of oocysts per gram of feces (OoPG). Statistical analyses were performed using Microsoft Excel and GraphPad Prism Software. All birds in the present study were positive for one or more species of coccidia. Captive birds had a mean total oocyst count higher than that of wild birds. No significant differences in OoPG counts were observed when comparing males and females or captive and wild birds. We can conclude that due to the fact that birds both eat and defecate in their cages, it is essential to keep them as clean as possible, since captive birds have a higher prevalence of coccidia.
Keywords:
OoPg; Passeriformes; oocysts; feces
Resumo
Canário-da-terra, Sicalis flaveola, uma ave passeriforme, está presente na natureza em praticamente todo o território brasileiro, além de ser criada em cativeiro. O objetivo deste trabalho foi determinar a prevalência e carga de oocistos em canários-da-terra de cativeiro, no município de Campos dos Goytacazes, estado do Rio de Janeiro. E de canários-da-terra de vida livre no município Eugenopolis, estado de Minas Gerais. Para isso, foram utilizadas 30 aves de cativeiro e 30 de vida livre. Fezes eliminadas durante 24h foram coletadas e pesadas para a realização da contagem de oocistos por grama de fezes (OoPG). Análises estatísticas foram feitas com o auxílio do Software Microsoft Excel e Graphpad Prism. Todas as aves do presente estudo estavam positivas para uma ou mais espécie de coccídio. As aves de cativeiro apresentaram média de contagem total de oocistos maior do que as aves de vida livre. Não foi observada diferença significativa nas contagens de OoPG com relação ao sexo e à origem das aves de cativeiro ou de vida livre. Pode-se concluir que, devido ao fato das aves comerem e defecarem em suas gaiolas, é essencial mantê-las as mais limpas possíveis, uma vez que as aves em cativeiro apresentam maior prevalência de coccídios.
Palavras-chave:
OoPg; Passeriformes; oocistos; fezes
The saffron finch, Sicalis flaveola, is a small, bright yellow neotropical passerine native to South America, ranging from Argentina to Venezuela; introduced populations also exist in other locales, including Puerto Rico, Jamaica, and Hawaii. The birds travel in pairs or small flocks, forage for insects and seeds on the ground, and visit feeders in suburban backyards (Rising, 2011Rising JD. Family Emberizidae (buntings and new world sparrows). In: del Hoyo J, Elliott A, Sargatal J, Christie DA. Handbook of the birds of the world. Tanagers to new world blackbirds. Vol. 16. Barcelona: Lynx Edicions; 2011. p. 633-634.).
Coccidia are a highly diverse subclass of protozoan obligate intracellular parasites of domestic and wild animals (Ruggiero et al., 2015Ruggiero MA, Gordon DP, Orrell TM, Bailly N, Bourgoin T, Brusca RC, et al. Correction: a higher level classification of all living organisms. PLoS One 2015; 10(4): e0130114. http://doi.org/10.1371/journal.pone.0130114. PMid:26068874.
http://doi.org/10.1371/journal.pone.0130...
; Fayer, 1980Fayer R. Epidemiology of protozoan infection the coccidia. Vet Parasitol 1980; 6(1-3): 75-103. http://doi.org/10.1016/0304-4017(80)90039-4.
http://doi.org/10.1016/0304-4017(80)9003...
). Although little is known about avian coccidia in wild birds worldwide, in captive birds, low levels of coccidia are common and harmless in most bird species (Greiner & Ritchie, 1994Greiner EC, Ritchie BW. Parasites. In: Ritchie BW, Harrison GL, Harrison LR. Avian medicine: principles and application. Lake Worth: Wingers Publishing; 1994. p. 1007-1029.), but severe infections are known to cause severe endemic disease in captive birds (Schoener et al., 2013Schoener ER, Alley MR, Howe L, Castro I. Coccidia species in endemic and native New Zealand passerines. Parasitol Res 2013; 112(5): 2027-2036. http://doi.org/10.1007/s00436-013-3361-z. PMid:23468142.
http://doi.org/10.1007/s00436-013-3361-z...
).
Until 2011, only Isospora sicalisi and Isospora cetasiensis were reported in S. flaveola (Coelho et al., 2011Coelho CD, Berto BP, Neves DM, Oliveira VM, Flausino W, Lopes CWG. Two new Isospora species from the saffron finch, Sicalis flaveola in Brazil. Acta Parasitol 2011; 56(3): 239-244. http://doi.org/10.2478/s11686-011-0051-9.
http://doi.org/10.2478/s11686-011-0051-9...
); however, more recently, Isospora bertoi and Eimeria flaveola were reported in birds of this species that lived free between the border of the Northwest of the State of Rio de Janeiro and Zona da Mata of Minas Gerais, Brazil (Gallo et al., 2022Gallo SSM, de Oliveira FCR, Elizeu TKS, Ederli NB. A new species of Eimeria Schneider, 1875 from the saffron finch, Sicalis flaveola (Aves: Passeriformes) in Brazil. Acta Parasitol 2022; 67(3): 1199-1205. http://doi.org/10.1007/s11686-022-00566-w. PMid:35589907.
http://doi.org/10.1007/s11686-022-00566-...
; Oliveira et al., 2023Oliveira FCR, Gallo SSM, Elizeu TKS, Ederli NB. Isospora bertoi n. sp. of the saffron finch, Sicalis flaveola (Aves: Passeriformes) from Brazil. Braz J Biol 2023; 83: e270649. http://doi.org/10.1590/1519-6984.270649. PMid:37222367.
http://doi.org/10.1590/1519-6984.270649...
). Recently, Cryptosporidium andersoni was diagnosed in a saffron finch from a commercial establishment in northern Rio de Janeiro (Oliveira et al., 2022Oliveira FCR, Gallo SSM, Elizeu TKS, Ederli NB. Molecular and phylogenetic characterization of Cryptosporidium species in the saffron finch Sicalis flaveola. BMC Vet Res 2022; 18(1): 449. http://doi.org/10.1186/s12917-022-03553-5. PMid:36564739.
http://doi.org/10.1186/s12917-022-03553-...
).
This study was conducted to determine the prevalence and load of oocysts in the feces of wild saffron finch S. flaveola from the state of Minas Gerais and captive saffron finch in Campos dos Goytacazes, in the state of Rio de Janeiro.
A total of 60 adults saffron finches, S. flaveola, were included in the study, of which 30 were raised in breeding cages and commercial establishments in the municipality of Campos dos Goytacazes, Rio de Janeiro, Brazil. The other 30 birds were free-living and inhabited peri-urban and rural regions of the municipality of Eugenopolis, Minas Gerais and were captured with mist nets. After capture, the birds were individually housed for 24 hours in cages with water and food ad libitum. This study was approved by the Biodiversity Authorization and Information System (SISBIO) under protocol n° 78,016–1/2022, and all experimental protocols were approved by the ethics committee for the use of animals (protocol n° 523). The distinction between the sex of adult birds was possible because they present marked sexual dimorphism in the coloration of their plumage (Benítez Saldívar & Massoni, 2018Benítez Saldívar MJ, Massoni V. Lack of conspecific visual discrimination between second-year males and females in the Saffron Finch. PLoS One 2018; 13(12): e0209549. http://doi.org/10.1371/journal.pone.0209549. PMid:30589869.
http://doi.org/10.1371/journal.pone.0209...
; Cruz-Bernate et al., 2023Cruz-Bernate L, Espinosa-Bravo C, Rivera-Gutiérrez HF. Does cryptic dichromatism exist in the Saffron Finch (Sicalis flaveola)? Colorimetric variables and the avian visual model. Avian Res 2023; 14: 100127. http://doi.org/10.1016/j.avrs.2023.100127.
http://doi.org/10.1016/j.avrs.2023.10012...
).
Feces from 24 hours after capture were collected from the bottom of each cage and were placed in 15 mL tubes, identified, placed in an isothermal box with ice and immediately transported to the Núcleo de Pesquisas Avançadas em Parasitologia (NUPAP) at the Universidade Estadual do Norte Fluminense Darcy Ribeiro (UENF) in the Municipality of Campos dos Goytacazes, Rio de Janeiro, Brazil.
A portion of the fecal samples from all captured birds were filtered through double gauze, mixed with 2.5% potassium dichromate (K2Cr2O7), placed in a Petri dish and incubated at 23–28 °C until 70% of the oocysts were sporulated. Oocysts were retrieved by the flotation method with Sheather’s sugar solution and examined microscopically using the method described by Duszynski & Wilber (1997)Duszynski DW, Wilber PG. A guideline for the preparation of species descriptions in the Eimeriidae. J Parasitol 1997; 83(2): 333-336. http://doi.org/10.2307/3284470. PMid:9105325.
http://doi.org/10.2307/3284470...
.
Fecal oocyst counts were performed by Wisconsin sugar flotation method with oocysts recovery at 20 min. The number of oocysts per gram of feces (OoPG) was calculated as the total count of oocysts divided by the total weight of the sample in grams (Tookhy et al., 2022Tookhy NA, Nakamura Y, Wasim WA. Recovery rates of Eimeria Oocysts from cattle feces by wisconsin sugar flotation method. Afghan Res J Nat Sci 2022; 3(1): 01-05.). The mean number, standard deviation, minimum and maximum value of observed oocysts were calculated using Microsoft Excel 2013™ software (Microsoft, Redmond, WA, USA). Student's t test was the statistical method used to compare means between groups of captive and free-living birds. For this, the GraphPad Prism 5™ program (GraphPad Software, SD, USA) was used and 95% confidence intervals were computed.
Among the captive birds, 26 (87%) had sexual dimorphism, where 21 (70%) were males and five (17%) were females; however, in four (13%) of these birds, it was not possible to determine the sex (Table 1). Of the wild birds (Figure 1), nine (30%) were identified as males, 14 (47%) as females, and in seven (23%), it was not possible to identify the sex of the captured bird (Table 2).
Oocysts per gram of feces (OoPG) of captive saffron finches, Sicalis flaveola, in relation to sexual dimorphism.
Wild saffron finches, Sicalis flaveola, captured in Eugenopolis, state of Minas Gerais, Brazil. In a, male specimen and in b, female specimen.
Oocysts per gram of feces (OoPG) of wild saffron finches Sicalis flaveola in relation to sexual dimorphism.
All birds in the present study were positive for one or more species of coccidia, thus indicating a prevalence of 100%. From captive birds, it was possible to collect an average of 2.74 (1.10-6.28) grams of feces, with a total oocyst count ranging from four to 16,886 and an average of 2,660 oocysts shed in 24 hours. The OoPG count ranged from 2 to 4311 with a mean of 862 (Table 1).
From wild birds kept in cages for 24 hours, it was possible to collect an average of 2.05 (0.5-6.0) grams of feces. In these feces, 5 to 10,049 oocysts were counted per bird, with an average of 2003 shed oocysts. For this group of birds, the OoPG ranged from 3 to 3377 with a measured average of 985 oocysts (Table 2).
No significant differences were observed in the OoPG count of the saffron finch based on the sex of birds raised in captivity (P=0.0967) or captured from the wild (P=0.3731), or when the prevalence of all birds was analyzed as a single group (P=0.7683). (Table 3).
No significant difference was observed in the OoPG counts (P=0.6689) of the saffron finch by origin (captive vs. wild; Table 4).
Frequency of oocysts per gram of feces (OoPG) in relation to the origin of saffron finches, Sicalis flaveola.
In captive and wild, in general, prevalences of 9% for Isospora sicalisi, 47% for Isospora cetasiensis and 7% for Isospora bertoi were identified. A prevalence of 37% of oocysts of the species Eimeria flaveola was also observed.
Isospora sicalisi oocysts had a prevalence of 32% in captive birds and 1% in wild birds, while I. cetasiensis oocysts had a prevalence of 68% in captive birds and 39% in wild birds. In wild birds, 2% of I. sicalisi oocysts and 2% of I. cetasiensis oocysts with polar granules were observed, a morphological characteristic not yet reported for these species. For oocysts of I. bertoi and E. flaveola, prevalences of 9% and 48%, respectively, were calculated in wild birds.
The high prevalence rate (100%) of oocysts in both captive and wild birds in the present study did not corroborate the findings of Coelho et al. (2011)Coelho CD, Berto BP, Neves DM, Oliveira VM, Flausino W, Lopes CWG. Two new Isospora species from the saffron finch, Sicalis flaveola in Brazil. Acta Parasitol 2011; 56(3): 239-244. http://doi.org/10.2478/s11686-011-0051-9.
http://doi.org/10.2478/s11686-011-0051-9...
, who reported a prevalence of 69% in captive S. flaveola. This may support the hypothesis of Alasadiy et al. (2022)Alasadiy DKY, Mahmood RM, Naji Alhasnawi A. A comparative study of parasitic infections in domestic and wild pigeons in Iraq. Arch Razi Inst 2022; 77(2): 709-715. http://doi.org/10.22092/ari.2022.357105.1976. PMid:36284957.
http://doi.org/10.22092/ari.2022.357105....
: a greater prevalence of these coccidia is related to climatic conditions such as humidity and temperature, which under ideal conditions are more suitable for the development of parasitism than the sex of the host. These same researchers reported that captive birds had a greater chance of infection because they are confined to small areas with larger groups of individuals, contrary to what Rising (2011)Rising JD. Family Emberizidae (buntings and new world sparrows). In: del Hoyo J, Elliott A, Sargatal J, Christie DA. Handbook of the birds of the world. Tanagers to new world blackbirds. Vol. 16. Barcelona: Lynx Edicions; 2011. p. 633-634. observed in nature, and this increases the possibility of ingestion of large numbers of oocysts. This finding was supported by the results of our study, although no significant difference by group was detected in this analysis.
Isospora bertoi and E. flaveola, recently described in wild birds (Gallo et al., 2022Gallo SSM, de Oliveira FCR, Elizeu TKS, Ederli NB. A new species of Eimeria Schneider, 1875 from the saffron finch, Sicalis flaveola (Aves: Passeriformes) in Brazil. Acta Parasitol 2022; 67(3): 1199-1205. http://doi.org/10.1007/s11686-022-00566-w. PMid:35589907.
http://doi.org/10.1007/s11686-022-00566-...
; Oliveira et al., 2023Oliveira FCR, Gallo SSM, Elizeu TKS, Ederli NB. Isospora bertoi n. sp. of the saffron finch, Sicalis flaveola (Aves: Passeriformes) from Brazil. Braz J Biol 2023; 83: e270649. http://doi.org/10.1590/1519-6984.270649. PMid:37222367.
http://doi.org/10.1590/1519-6984.270649...
), were not observed in the feces of birds from Campos dos Goytacazes. Although Cryptosporidium spp. was also not observed, we cannot infer that the birds in this project did not harbor this parasite in their feces since the coprological analyses were performed by common optical microscopy, which is not the appropriate diagnostic method for detecting this parasite. Isospora sicalisi and I. cetasiensis, two species described by Coelho et al. (2011)Coelho CD, Berto BP, Neves DM, Oliveira VM, Flausino W, Lopes CWG. Two new Isospora species from the saffron finch, Sicalis flaveola in Brazil. Acta Parasitol 2011; 56(3): 239-244. http://doi.org/10.2478/s11686-011-0051-9.
http://doi.org/10.2478/s11686-011-0051-9...
in a study of captive S. flaveola, 26 birds were assessed and 69% (18) were infected by I. cetasiensis and 12% (3) by I. sicalisi. Our research corroborates the study by Coelho and collaborators, since among the 30 captive birds in our study, I. cetasiensis was more prevalent (68%) compared to I. sicalisi (32%). Similarly, we found that I. cetasiensis was more prevalent (39%) in wild birds than I. sicalisi (1%).
No significant differences were observed in the OoPG count of the saffron finch when assessed by sexual dimorphism, either among captive (Table 1) or wild birds (Table 2), or overall (Table 3). According to Brown et al. (2010)Brown MA, Ball SJ, Snow KR. Coccidian parasites of Bristish wild birds. J Nat Hist 2010; 44(43-44): 2669-2691. http://doi.org/10.1080/00222933.2010.501531.
http://doi.org/10.1080/00222933.2010.501...
, the general prevalence of infection does not seem to be influenced by the sex of the host, since the infection is significantly affected by direct contact with feces, type of food, use of parasiticides, type of enclosure and how often the cages are cleaned. In wild birds, however, infection can be influenced by the loss of natural habitats, population accumulation, illegal seizures, availability of food, shelter and climatic conditions (Friend & Franson, 1999Friend M, Franson JC. Intestinal coccidiosis In: Friend M, Franson JC. Field manual of wildlife diseases: general field and procedures and diseases of birds. Washington, Biological Resources Division; 1999. p. 207-213.; IUCN, 2002International Union for Conservation of Nature - IUCN. Guidelines the placement of confiscated animals. Re-introduction Specialist Group [online]. 2002. [cited 2023 Apr 8]. Available from: https://portals.iucn.org/library/node/8021
https://portals.iucn.org/library/node/80...
; Rising, 2011Rising JD. Family Emberizidae (buntings and new world sparrows). In: del Hoyo J, Elliott A, Sargatal J, Christie DA. Handbook of the birds of the world. Tanagers to new world blackbirds. Vol. 16. Barcelona: Lynx Edicions; 2011. p. 633-634.).
In the present study, no significant differences were observed in the OoPG counts (P=0.6689) of the saffron finch when the origin of the birds was considered (captive vs. wild; Table 4). Research carried out by Costa et al. (2010)Costa IA, Coelho CD, Bueno C, Ferreira I, Freire RB. Ocorrência de parasitos gastrintestinais em aves silvestres no município de Seropédica, Rio de Janeiro, Brasil. Cienc Anim Bras 2010; 11(4): 914-922. http://doi.org/10.5216/cab.v11i4.7164.
http://doi.org/10.5216/cab.v11i4.7164...
also demonstrated that wild and captive animals commonly had coccidia, but a significant difference in prevalence between them was not reported. Other authors, such as Quiroga et al. (2000)Quiroga MI, Alemañ N, Vázquez S, Nieto JM. Diagnosis of atoxoplasmosis in a canary (Serinus canarius) by histopathological and ultrastructural examination. Avian Dis 2000; 44(2): 465-469. http://doi.org/10.2307/1592564. PMid:10879930.
http://doi.org/10.2307/1592564...
and McQuistion (2000)McQuistion TE. The prevalence of coccidian parasites in passerine birds of South America. Trans Ill State Acad Sci 2000; 93(3): 221-227., reported that captive and wild passerines can be infected by coccidia regardless of their origin. Although no significant difference was detected by origin, it is still important to understand the impact on the infections caused in wild birds since little is known about the morphology of the oocysts of these birds (Greiner, 2008Greiner EC. Isospora, Atoxoplasma, and Sarcocystis. In: Atkinson CT, Thomas NJ, Hunder DB. Parasitic diseases of wild birds. 3rd ed. Ames: Wiley-Blackwell; 2008. p.108-119. http://doi.org/10.1002/9780813804620.ch5.
http://doi.org/10.1002/9780813804620.ch5...
); other species (Gallo et al., 2022Gallo SSM, de Oliveira FCR, Elizeu TKS, Ederli NB. A new species of Eimeria Schneider, 1875 from the saffron finch, Sicalis flaveola (Aves: Passeriformes) in Brazil. Acta Parasitol 2022; 67(3): 1199-1205. http://doi.org/10.1007/s11686-022-00566-w. PMid:35589907.
http://doi.org/10.1007/s11686-022-00566-...
; Oliveira et al., 2023Oliveira FCR, Gallo SSM, Elizeu TKS, Ederli NB. Isospora bertoi n. sp. of the saffron finch, Sicalis flaveola (Aves: Passeriformes) from Brazil. Braz J Biol 2023; 83: e270649. http://doi.org/10.1590/1519-6984.270649. PMid:37222367.
http://doi.org/10.1590/1519-6984.270649...
) that have not yet been reported may be circulating among wild birds and may affect captive birds.
We can conclude that the total average count of oocysts was higher in captive birds due to the fact that they eat and defecate in their cages and are always in contact with infective oocysts. Inadequate management favors a greater prevalence of coccidia in captive birds, therefore, regular cleaning is an important part of bird's health and wellness. Furthermore, although coccidiosis may be a primary factor in mortality, its importance is also related to increasing the host's susceptibility to other diseases, thus reducing the chances of survival during periods of stress, both in the wild and in captivity.
Acknowledgements
The authors would like to thank CAPES (Coordination for the Improvement of Higher Education Personnel) for the financial support.
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How to cite: Oliveira FCR, Gallo SSM, Elizeu TKS, Ederli NB. Prevalence and parasite burden of oocysts in captive and free-living saffron finches, Sicalis flaveola. Braz J Vet Parasitol 2024; 33(2): e000524. https://doi.org/10.1590/S1984-29612024029
References
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» http://doi.org/10.22092/ari.2022.357105.1976 - Benítez Saldívar MJ, Massoni V. Lack of conspecific visual discrimination between second-year males and females in the Saffron Finch. PLoS One 2018; 13(12): e0209549. http://doi.org/10.1371/journal.pone.0209549 PMid:30589869.
» http://doi.org/10.1371/journal.pone.0209549 - Brown MA, Ball SJ, Snow KR. Coccidian parasites of Bristish wild birds. J Nat Hist 2010; 44(43-44): 2669-2691. http://doi.org/10.1080/00222933.2010.501531
» http://doi.org/10.1080/00222933.2010.501531 - Coelho CD, Berto BP, Neves DM, Oliveira VM, Flausino W, Lopes CWG. Two new Isospora species from the saffron finch, Sicalis flaveola in Brazil. Acta Parasitol 2011; 56(3): 239-244. http://doi.org/10.2478/s11686-011-0051-9
» http://doi.org/10.2478/s11686-011-0051-9 - Costa IA, Coelho CD, Bueno C, Ferreira I, Freire RB. Ocorrência de parasitos gastrintestinais em aves silvestres no município de Seropédica, Rio de Janeiro, Brasil. Cienc Anim Bras 2010; 11(4): 914-922. http://doi.org/10.5216/cab.v11i4.7164
» http://doi.org/10.5216/cab.v11i4.7164 - Cruz-Bernate L, Espinosa-Bravo C, Rivera-Gutiérrez HF. Does cryptic dichromatism exist in the Saffron Finch (Sicalis flaveola)? Colorimetric variables and the avian visual model. Avian Res 2023; 14: 100127. http://doi.org/10.1016/j.avrs.2023.100127
» http://doi.org/10.1016/j.avrs.2023.100127 - Duszynski DW, Wilber PG. A guideline for the preparation of species descriptions in the Eimeriidae. J Parasitol 1997; 83(2): 333-336. http://doi.org/10.2307/3284470 PMid:9105325.
» http://doi.org/10.2307/3284470 - Fayer R. Epidemiology of protozoan infection the coccidia. Vet Parasitol 1980; 6(1-3): 75-103. http://doi.org/10.1016/0304-4017(80)90039-4
» http://doi.org/10.1016/0304-4017(80)90039-4 - Friend M, Franson JC. Intestinal coccidiosis In: Friend M, Franson JC. Field manual of wildlife diseases: general field and procedures and diseases of birds Washington, Biological Resources Division; 1999. p. 207-213.
- Gallo SSM, de Oliveira FCR, Elizeu TKS, Ederli NB. A new species of Eimeria Schneider, 1875 from the saffron finch, Sicalis flaveola (Aves: Passeriformes) in Brazil. Acta Parasitol 2022; 67(3): 1199-1205. http://doi.org/10.1007/s11686-022-00566-w PMid:35589907.
» http://doi.org/10.1007/s11686-022-00566-w - Greiner EC, Ritchie BW. Parasites. In: Ritchie BW, Harrison GL, Harrison LR. Avian medicine: principles and application Lake Worth: Wingers Publishing; 1994. p. 1007-1029.
- Greiner EC. Isospora, Atoxoplasma, and Sarcocystis In: Atkinson CT, Thomas NJ, Hunder DB. Parasitic diseases of wild birds. 3rd ed. Ames: Wiley-Blackwell; 2008. p.108-119. http://doi.org/10.1002/9780813804620.ch5
» http://doi.org/10.1002/9780813804620.ch5 - International Union for Conservation of Nature - IUCN. Guidelines the placement of confiscated animals. Re-introduction Specialist Group [online]. 2002. [cited 2023 Apr 8]. Available from: https://portals.iucn.org/library/node/8021
» https://portals.iucn.org/library/node/8021 - McQuistion TE. The prevalence of coccidian parasites in passerine birds of South America. Trans Ill State Acad Sci 2000; 93(3): 221-227.
- Oliveira FCR, Gallo SSM, Elizeu TKS, Ederli NB. Isospora bertoi n. sp. of the saffron finch, Sicalis flaveola (Aves: Passeriformes) from Brazil. Braz J Biol 2023; 83: e270649. http://doi.org/10.1590/1519-6984.270649 PMid:37222367.
» http://doi.org/10.1590/1519-6984.270649 - Oliveira FCR, Gallo SSM, Elizeu TKS, Ederli NB. Molecular and phylogenetic characterization of Cryptosporidium species in the saffron finch Sicalis flaveola. BMC Vet Res 2022; 18(1): 449. http://doi.org/10.1186/s12917-022-03553-5 PMid:36564739.
» http://doi.org/10.1186/s12917-022-03553-5 - Quiroga MI, Alemañ N, Vázquez S, Nieto JM. Diagnosis of atoxoplasmosis in a canary (Serinus canarius) by histopathological and ultrastructural examination. Avian Dis 2000; 44(2): 465-469. http://doi.org/10.2307/1592564 PMid:10879930.
» http://doi.org/10.2307/1592564 - Rising JD. Family Emberizidae (buntings and new world sparrows). In: del Hoyo J, Elliott A, Sargatal J, Christie DA. Handbook of the birds of the world. Tanagers to new world blackbirds Vol. 16. Barcelona: Lynx Edicions; 2011. p. 633-634.
- Ruggiero MA, Gordon DP, Orrell TM, Bailly N, Bourgoin T, Brusca RC, et al. Correction: a higher level classification of all living organisms. PLoS One 2015; 10(4): e0130114. http://doi.org/10.1371/journal.pone.0130114 PMid:26068874.
» http://doi.org/10.1371/journal.pone.0130114 - Schoener ER, Alley MR, Howe L, Castro I. Coccidia species in endemic and native New Zealand passerines. Parasitol Res 2013; 112(5): 2027-2036. http://doi.org/10.1007/s00436-013-3361-z PMid:23468142.
» http://doi.org/10.1007/s00436-013-3361-z - Tookhy NA, Nakamura Y, Wasim WA. Recovery rates of Eimeria Oocysts from cattle feces by wisconsin sugar flotation method. Afghan Res J Nat Sci 2022; 3(1): 01-05.
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Publication in this collection
17 June 2024 -
Date of issue
2024
History
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Received
15 Jan 2024 -
Accepted
16 Apr 2024