Printer Friendly

Ipomoea brasiliana poisoning on buck reproduction/Efeitos da intoxicacao por Ipomoea brasiliana na reproducao de caprinos.


Swainsonine-containing plants comprise a group of several poisonous weeds that harm grasslands and impact animal husbandry development worldwide (COOK et al., 2014). These plants belong to three genera of the Fabaceae family (Astragalus, Oxytropis, and Swainsona) (BURROWS & TYRL, 2012; COOK et al., 2009; COOK et al., 2013), one genus of the Convolvulaceae family (Ipomoea) and one genus of the Malvaceae family (Sida) (OLIVEIRA JUNIOR et al., 2013). These plants are distributed in the United States, Canada, Mexico, Brazil, Russia, Spain, Ireland, Morocco, Egypt, Australia and China (JUNG et al., 2011; COOK et al., 2013; OLIVEIRA JUNIOR et al., 2013).

Ipomoea brasiliana (Mart. ex Choisy) Meisn., (previously reported as Ipomoea aff. verbascoidea and Ipomoea marcellia) (MENDONCA et al., 2012; ROCHA et al., 2016), is a decumbent upright shrub that grows up to 1-5m in height with oblong or oval-circular leaves and has solitary purple or lilac flowers (AUSTIN et al. 2015) and is an important poisonous plant of grazing livestock in the northeastern semi-arid region of Brazil (MENDONCA et al., 2012; LIMA et al., 2013). Ipomea brasiliana is known to contain swainsonine and calystegines, two important toxins that are associated with the development of lysosomal storage disease in ruminants (COLEGATE et al., 1979; STEGELMEIER et al., 2008; MENDONCA et al., 2012).

Swainsonine is an inhibitor of lysosomal a-mannosidase, Golgi mannosidase II and other calystegines that are potent glycosidase inhibitors, and it is suggested that these inhibitors disrupt intestinal glycosidases, lysosomal function, and glycoprotein processing, leading to enzymatic dysfunction and accumulation of complex oligosaccharides in the lysosomes of nervous and epithelial cells (COLEGATE et al., 1979; DORLING et al., 1980; STEGELMEIER et al., 2008). Recent research has demonstrated that swainsonine is a fungal-endophyte-derived secondary metabolite and is not produced by the host plant. The presence of endophyte fungi has been demonstrated in species of Astragalus, Oxytropis, Swainsona and Ipomoea (BRAUN et al., 2003; PRYOR et al., 2009; HAO et al., 2012; COOK et al., 2013). However, it has been suggested that calystegines are secondary metabolites derived from plants because these toxins are present in plants derived from fungicide-treated seeds (COOK et al., 2013).

Clinical effects of Ipomoea spp. poisoning on the nervous system in ruminants and horses are well established in Brazil and are similar to those caused by other swainsonine containing plants worldwide. Despite causing a neurological syndrome, swainsonine-containing plants also have severe adverse effects on the reproductive function of livestock. All aspects of reproduction can be affected. Neurological dysfunction also inhibits normal reproductive behavior, and some of these effects are permanent and progressive (PANTER et al., 1989; PANTER et al., 1999; HUEZA et al., 2007; WU et al., 2016).

In this article, we aimed to characterize the clinical changes and microscopic lesions of the reproductive system of bucks poisoned by I. brasiliana.


Leaves of Ipomoea brasiliana (voucher no. 50017) were collected in the municipality of Sertania-PE (Figure 1A). Samples were dried in the shade and crushed in a mill until a powder was formed, and then, the powder was mixed and packed in plastic bags. The weight of the dried leaves represented 40% of the green leaves' original weight. concentration of swainsonine was determined from the pool of desiccated powder of I. brasiliana leaves as previously described by GARDNER et al. (2001).

In the experiment, nine male Saanen goats that were clinically healthy, aged 6-9 months and weighed between 16-21kg were used. Goats were weighed at the beginning and end of the experiment to estimate the weight gain due to the media and standard deviation. Thirty days before the beginning of the experiment, goats received an antiparasitic medication, were randomly numbered and kept in individual stalls for adaptation and clinical observation. Early in the morning, goats received a commercial ration, mineral salt for goats, Tifton hay (Cynodon dactylon) and water ad libitum.

After the adaptation period, goats were randomly assigned to three groups: Group I goats received the powder of desiccated I. brasiliana leaves containing 0.02% swainsonine at a dose of 4g/Kg (800 [micro]g swainsonine/Kg) mixed in their feed over 45 days and were euthanized on the 46th day of the experiment. Group II goats received the same daily dose of swainsonine for 45 days and were euthanized on the 120th day of the experiment. Group III goats were the control group; these goats received the same type of management, but they did not receive I. brasiliana and were euthanized on the 120th day of the experiment.

Goats of the three groups were examined in detail regarding their general condition, behavior, attitude, coordination, head posture, movement, appetite, mucous membrane color, rectal temperature, heart and respiratory rates, abdominal morphology, reticulum-rumen motility and physical appearance of their feces, urine and skin (RIET-CORREA et al. 2002; SMITH & SHERMAN 2009). An andrological exam was performed routinely, semen was collected using an artificial vagina and the analysis included the concentration, structure and motility of their spermatozoa according previous description (HAFEZ & HAFEZ, 2004). Values were expressed according to the mean; these means were compared by the Student's t test at 5% significance.

Before the beginning of the experiment, three andrological examinations were performed to verify the reproductive integrity of the animals. During the experiment, examinations were performed weekly, including general and physical examinations, palpation of the testicles, a behavioral examination to observe the presence of libido by observation of the courtship behavior and Flehmen reflex when placed next to a doe in heat, physical ability to perform a natural mount and spermogram.

For the determination of the serum testosterone levels, blood samples were obtained on the 15, 30, 45 days (Group I) and 15, 30, 45, 120 days (Group II and III) of the experiment. After centrifugation of 700g of blood for 15 minutes, the serum concentrations of testosterone were analyzed using an Elisa kit (testosterone[R], Biochem Diagnostics, Inc., Ontario, Canada) that had an analytical sensitivity of 0.022ng/mL, centesimal precision and intra-assay coefficient of variation of 9.6%.

For the histological characterization of the lesions, fragments of the male reproductive tract were routinely processed for a histopathology examination, immersed in methacrylate and stained with hematoxylin-floxin (TOLOSA, 2003). For morphometric analysis, 15 seminiferous tubules from each goat were photographed under microscopy with a 10x objective, after which the photomicrographs were used to measure the tubular diameter by means of ImagLab 3000 software. Duncan's Post-Hoc normality test was used for statistical analysis using ASSISTAT Version 7.7 beta software (2013).


Reproductive behavioral changes were observed starting on day 20 of the experiment in Group I and II goats. These changes were not uniform in goats from the experimental groups. One goat from Group I and two goats from Group II showed an absence of courtship behavior, absence of the Flehmen reflex, decrease or loss of libido and inability to perform mating. The remaining goats, despite the inability to perform mating, presented an abnormal courtship behavior, Flehmen reflex and libido. From the 20th to 34th days, the neurological clinical signs in both Group I and II were mild, and between the 35th and 37th days of the experiment, all goats presented severe clinical signs that were compatible with lysosomal storage disease; the main observed symptoms were motor incoordination, ataxia and dysmetria. These changes mainly resulted in the absence of libido and difficulty into mate (Figure 1B).

There was no significant difference related to the scrotal circumference between Groups I and II and the control group. There were also no changes related to the color and consistency of semen. The first changes in the seminal parameters, consisting of a discrete reduction of the semen volume and concentration of spermatozoa, were observed on the 14th day of the experiment in Group I and II goats. During this same period, there were slight reductions in swirling, motility and sperm vigor. On the 21st day of the experiment, these reductions were more severe and the number of major and minor defects in the spermatozoa were increased in goats poisoned by I. brasiliana. The main defects observed were cytoplasmatic droplets, prominent tails and bent tails. In group II goats, at 120 days of the experiment, there was no improvement related to the percentage of defects in the sperm morphology (Table 1).

Testosterone concentrations were statistically lower in the groups that received I. brasiliana than in the control group. Testosterone levels in the control group ranged from 15.1ng/mL to 15.8ng/mL. In the groups that received I. brasiliana, the concentration of testosterone decreased on the 15th day of the experiment to 10.9ng/mL and 13ng/ mL in Groups 1 and 2, respectively. Testosterone cooncentration decreased to 5.7ng/mL and 5.9ng/ mL on day 45 in Groups 1 and 2, respectively, and to 5.0ng/mL at day 120 in Group II.

At necropsy, no significant lesions were observed in the testicles, epididymis, vas deferens, vesicular glands, prostate, bulbourethral glands or penis of goats from Group I, II or III. The main histopathological findings observed in Group I and II goats consisted of cytoplasmic vacuolization of the germline and Sertoli cells, generalized impairment of spermatogonia maturation with exfoliation of degenerative cells, cell fragmentation, rare abnormal spermatocytes in the seminiferous lumen and disappearance of Leydig cells. In Group II goats, the pattern of lesions was quite different because they did not include vacuolization of the germline and Sertoli cells. In addition to the severe exfoliation of the degenerative and germinative epithelium, other alterations were observed, including a reduction in the number of spermatogonia and spermatocyte layers, accumulation of proteinaceous material in the lumen of the seminiferous tubules and absence of epithelial cell stereocilia in the epididymis (Figure 2).

On morphometrical analysis, the diameter of the seminiferous tubules lumen was significantly increased in goats that received I. brasiliana compared to control goats (Table 2). Typical lesions of lysosomal storage disease were previously reported and found in the cells of the central nervous system and epithelia of the liver, thyroid, pancreas and kidneys in Group I goats. No vacuolization was noted in the CNS or in other organs examined in Group II goats. In Group II, the lesions were mild and were only observed in the cerebellum and frontal and parietal cortexes, and the lesions consisted of neuronal necrosis as evidenced by the presence of small cell bodies with an eosinophilic and angular cytoplasm and pyknotic nucleus. Some residual spheroids and gliosis were also observed in the cerebellar peduncles. Additionally, a hypothyroidism was observed in these group.


In this study, the absence of courtship and Flehmen reflexes and decreased or lost libido were the main changes in the reproductive behavior of goats that consumed I. brasiliana. These changes were identified before clinical neurological signs and were severe. The inability to perform natural mating, identified after the 20th day of the experiment in Group I and II goats, probably represents the onset of cerebellar dysfunction, considering that severe clinical neurological signs, such as ataxia, hypermetria and motor incoordination, were only observed after the 35th day of the experiment. Additionally, it is important to know that goats that consume Ipomoea spp. for more than 45 days demonstrated neurological sequelae because there was sufficient encephalic neuronal loss/death; although, cytoplasmic vacuolization was not present upon histopathological analysis (BARBOSA et al., 2007; 2007; LIMA et al. 2013). At this point, the reproduction of goats was completely impaired by neurologic disease. Cerebellar damage also affected muscular function and contributed to the inability to mount and breed.

The low quality of the buck's semen poisoned by I. brasiliana resulted from lesions and could be characterized as a generalized impairment of spermatogonia maturation with exfoliation of degenerative cells and loss of seminiferous tubule cell layers (as observed in Table 2), including a loss of type A1 spermatogonia. The main mechanism responsible for the testicular degeneration observed in those goats, even in Group II goats, is probably related to vacuolar degeneration in the thyroids and hypothyroidism, which impairs reproduction when a decreased levels of serum T3 and T4 are present (WILSON, 1975). This fact is more relevant considering that goats are more susceptible to hypothyroidism than other domestic animals (MANSON AND WILKINSON, 1973). Similar results were reported in a previous study in which an increase of pathological spermatozoa in goats poisoned by I. carnea was associated with a decreased concentration of thyroid hormones (GOTARDO et al., 2014).

In the pathogenesis of reproductive alterations, it is important to remember that swainsonine is highly soluble in water, rapidly diffuses through the bloodstream of ruminants, and inhibits lysosomal [alpha]-mannosidases, lysosomal a-mannosidases II and enzymes of glycoprotein metabolism, which results in abnormal hormones as well as changes in cell membrane receptors. Specific spermatozoa lesions are related to the molecular changes caused by swainsonine, which hinder cell adhesion, communication and cellular movements (PANTER et al., 1999; MOREMEN, 2002). Additionally, the toxic effects of calystegines may be involved in pathogenesis because they are strong inhibitors of glycosidases, mainly [beta]-glucosidase and a-galactosidase, and it has been suggested that, in vivo, calystegines are likely to disrupt lysosomal function and glycoprotein processing (STEGELMEIER et al., 2008).

Results presented in this study confirm the hypothesis that I. brasiliana causes reproductive changes in bucks. Certain reproductive parameters of males may be affected within two weeks, and other effects, such as testicular dysfunction, may go unnoticed, especially under open pasture grazing of the plant in the field. Other species of swainonine-containing plants in Brazil, including I. riedelii, I. sericophyla, T. cordata and S. carpinifolia, may cause similar changes in the reproductive system of male goats. 10.1590/0103-8478cr20180061


We would like to thank the the Brazilian Agency Fundacao de Amparo a Ciencia e Tecnologia do Estado de Pernambuco (FACEPE) for providing a doctoral scholarship (Proc. IBPG-0760-5.05/09) and Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) (Finance Code 001).


All applicable national and institutional guidelines for the care and use of animals were followed. The animal procedures were approved by the Ethics Committee on the Use of Animals (UFPE Process Number 23076.047266/2016-11).


The authors declare no conflict of interest. The founding sponsors had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, and in the decision to publish the results.


All authors contributed equally for the conception and writing of the manuscript. All authors critically revised the manuscript and approved of the final version.


AUSTIN, D.F. et al. A synopsis of Ipomoea (Convolvulaceae) in the Americas: Further corrections, changes, and additions. Taxon, v. 64, p. 625-633, 2015. Available from: <>. Accessed: Jan. 23, 2018. doi: 10.12705/643.14.

BRAUN, K. et al. Production of swainsonine by fungal endophytes of locoweed. Mycological Research, v.107, p.980-988, 2003. Available from: <>. Accessed: Jan. 20, 2018. doi: 10.1017/s095375620300813x.

BURROWS, G.E.; TYRL, R.J. Toxic Plants of North America. Ames: Iowa State University Press, 2012. 1390p.

BARBOSA, R.C. et al. Experimental swainsonine poisoning in goats ingesting ingesting Ipomoea sericophylla and Ipomoea riedelii Ipomoea riedelii (Convolvulaceae). Pesquisa Veterinaria Brasileira, v. 27, p.409-414. Available from: < pdf_artigos/04-11-2007_15-30Vet%20421.pdf>. Accessed: May 09, 2018. doi: 1590/S0100-736X2007001000004.

COLEGATE, S.M. et al. A spectroscopic investigation of swainsonine: an a-mannosidase inhibitor isolated from Swainsona canescens. Australian Journal of Chemistry, v.32, p.2257-2264, 1979. Available from: <>. Accessed: Jan. 20, 2018. doi: 10.1071/CH9792257.

COOK D. et al. Swainsonine-containing plants and their relationship to endophytic fungi. Journal of Agricultural and Food Chemistry, v.62, p.7326-7334, 2009. Available from: <>. Accessed: Jan. 20, 2018. doi: 10.1021/jf501674r.

COOK, D. et al. Production of the alkaloid swainsonine by a fungal endosymbiont of the Ascomycete order Chaetothyriales in the host Ipomoea carnea. Journal of Agricultural and Food Chemistry, v.61, p.3797-3803, 2013. Available from: < ipdf/10.1021/jf4008423>. Accessed: Jan. 20, 2018. doi: 10.1021/ jf4008423.

COOK D. et al. Swainsonine-containing plants and their relationship to endophytic fungi. Journal of Agricultural and Food Chemistry, v.30, p. 7326-7334, 2014. Available from: < doi/10.1021/jf501674r>. Accessed: May 09, 2018. doi: 10.1021/ jf501674r.

DORLING, P.R. et al. Inhibition of lysosomal a-mannosidase by swainsonine, an indolizidine alkaloid isolated from Swainsona canescens. Biochemistry Journal, v.191, p.649-651, 1980. Available from: <>. Accessed: Jan. 20, 2018. doi: 10.1042/bj1910649.

GARDNER, D.R. et al. Analysis of swainsonine; extraction methods, detection, and measurement in populations of locoweeds (Oxytropis spp.). Journal of Agricultural and Food Chemistry, v.49, p.4573-4580, 2001. Available from: < pdf/10.1021/jf010596p>. Accessed: Jan. 20, 2018. doi: 10.1021/ jf010596p.

GOTARDO, A.T. et al. Endocrine disrupter action in ruminants: A study of the effects-of Ipomoea carnea in adult male goats. Small Ruminant Research, v. 119, p.81-87, 2014. Available from: <https:// pdf?code=rumin-site>. Accessed: May 09, 2018. doi: 10.1016/j. smallrumres.2014.02.003.

HAFEZ, E.S.E.; HAFEZ, B. Reproducao animal. Sao Paulo: Editora Manole, 2004. 513p.

HAO, L. et al. Isolation and identification of swainsonine-producing fungi found in locoweeds and their rhizosphere soil. African Journal of Microbiology Research, v.6, p.4959-4969, 2012. Available from: < AJMR/article-abstract/F96FA9126138>. Accessed: Jan. 20, 2018. doi: 10.5897/AJMR11.1572.

HUEZA, I.M. et al. Effect of Senna occidentalis seeds on immunity in broiler chickens. Journal of Veterinary Medicine A Physiology Pathology Clinical Medicine, v.54, p.179-185, 2007. Available from: <>. Accessed: Jan. 20, 2018. doi: 10.1111/j.1439-0442.2007.00917.x.

JUNG, J.K. et al. Distribution of phenolic compounds and antioxidative activities in parts of sweet potato (Ipomoea batata L.) plants and in home processed roots. Journal of Food Composition and Analysis. v. 24, p.29-37, 2011. Available from: <https://doi. org/10.1016/j.jfca.2010.03.025>. Accessed: Jan. 23, 2018. doi: 10.1016/j.jfca.2010.03.025.

LIMA, D.D.C.C. et al. Doenca de deposito lisossomal induzida pelo consumo de Ipomoea verbascoidea (Convolvulaceae) em caprinos no semiarido de Pernambuco. Pesquisa Veterinaria Brasileira, v.33, p.867-872, 2013. Available from: <http://dx.doi. org/10.1590/S0100-736X2013000700007>. Accessed: Jan. 20, 2018. doi: 10.1590/S0100736X2013000700007.

MANSON, R.; WILKINSON, J.S. 1973. The thyroid gland-a review. Australian Veterinary Journal, v. 49, p.44-49. Available from: < tb14680.x>. Accessed: May 09, 2018.

MENDONCA, F.S. et al. Alpha-mannosidosis in goats caused by the swainsonine-containing plant Ipomoea verbascoidea. Journal of Veterinary Diagnostic Investigation, v.24, p.90-95, 2012. Available from: <>. Accessed: Jan. 20, 2018. doi: 10.1177/1040638711425948.

MOREMEN, K.W. Golgi a-mannosidase II deficiency in vertebrate systems: Implications for asparagines-linked oligosaccharide processing in mammals. Biochimica et Biophysica Acta, v.1573, p.225-235, 2002. Available from: <>. Accessed: Jan. 20, 2018. doi: 10.1016/s03044165(02)00388-4.

OLIVEIRA JUNIOR, C.A. et al. Poisoning by swainsonine-containing plants in Brazil. Ciencia Rural, v.43, p.653-661, 2013. Available from: <>. Accessed: Jan. 20, 2018. doi: S0103-84782013000400014.

PANTER, K.E. et al. Transient testicular degeneration in rams fed locoweed (Astragalus lentiginosus). Veterinary and Human Toxicology, v.31, p.42-46, 1989. Available from: <https://www.>. Accessed: Jan. 23, 2018.

PANTER, K.E. et al. Locoweeds: Effects on reproduction in livestock. Journal Natural Toxins, v.8, p.53-62, 1999. Available from: <https://>. Accessed: Jan. 23, 2018.

PRYOR, B.M. et al. Undifilum, a new genus for endophytic Embellisia oxytropis and parasitic Helminthosporium bornmuelleri on legumes. Botany, v.87, p.178-194, 2009. Available from: <>. Accessed: Jan. 20, 2018. doi: 10.1139/B08-130.

RIET-CORREA et al. Importancia do exame clinico para o diagnostico das enfermidades do sistema nervoso em ruminantes e equideos. Pesquisa Veterinaria Brasileira, v.22, p.161-168, 2002. Available from: <>. Accessed: May 09, 2018. doi: 10.1590/S0100-736X2002000400006.

ROCHA, B.P. et al. Biopsia hepatica como metodo diagnostico para intoxicacao por plantas que contem swainsonina. Pesquisa Veterinaria Brasileira, v.36, p.373-377, 2016. Available from: <http://>. Accessed: Jan. 20, 2018. doi: 10.1590/S0100-736X2016000500003.

SMITH, M.C.; SHERMAN, D.M. Goat medicine. New Jersey: Wiley-Blackwell, 2009. 888p.

STEGELMEIER B.L. et al. The comparative pathology of the glycosidase inhibitors swainsonine, castanospermine, and calystegines A3, B2, and C1 in mice. Toxicology Pathology, v.36, p.651-659, 2008. Available from: <>. Accessed: Jan. 20, 2018. doi: 10.1177/0192623308317420.

TOLOSA, E.M.C. et al. Manual de Tecnicas para Histologia Normal e Patologica. Sao Paulo: Manole, 2003. 331p.

WILSON, J.C. 1975. Hypothyroidism in ruminants with special reference to foetal goitre. Veterinary Record, v. 97, p.161-164. Available from: <>. Accessed: May 09, 2018.

WU, C. et al. The toxicology mechanism of endophytic fungus and swainsonine in locoweed. Enviromental Toxicology and Pharmacology, v.47, p.38-46, 2016. Available from: <http://>. Accessed: Jan. 20, 2018. doi: 10.1016/j.etap.2016.08.018.

Ana Lizia Brito da Cunha (1) Juliana Pinto de Medeiros (2) Franklin Riet-Correa (3) Dale Gardner (4) Hisadora Advincula da Silva Chaves (5) Givaldo Bom da Silva Filho (5) Francisco de Assis Leite Souza (5) Joaquim Evencio Neto (5) Fabio de Souza Mendonca (5) *

(1) Programa de Pos-graduacao em Medicina Veterinaria, Universidade Federal Rural de Pernambuco (UFRPE), Recife, PE, Brasil.

(2) Centro de Ciencias Biologicas, Universidade Federal de Pernambuco (UFPE), Recife, PE, Brasil.

(3) National Institute of Agricutural Research (INIA), La Estanzuela, Colonia, Uruguay.

(4) Poisonous Plant Research Laboratory, Agricultural Research Service, United States Department of Agriculture, Logan, UT, USA.

(5) Laboratorio de Diagnostico Animal, Departamento de Morfologia e Fisiologia Animal (DMFA), Recife, PE, Brasil. E-mail:

* Corresponding author.

Caption: Figure 1-(A) Ipomoea brasiliana is a decumbent upright shrub up to 1-5m in height, with oblong or oval- circular leaves, solitary purple or lilac flowers, Municipality of Sertania, Pernambuco, Brazil. (B) Group I buck on the 20th day of the experiment still demonstrating libido, but with difficulty to perform natural mating.

Caption: Figure 2-Reproductive changes in goats poisoned by I. brasiliana. (A) Seminiferous tubules of control group with normal conjoined germinative epithelial cells and spermatozoa in the lumen. (B) Group II seminiferous tubules of goat with loss of cellular cohesion of the germinal epithelium, cytoplasmic vacuolization of spermatogonia and spermatocytes, sometimes with marginalized chromatin. (C) Epididymis of control group goat with intact epithelium and adequate concentration of spermatozoa in the lumen. (D). Epididymis of group II goat with cytoplasmic vacuolization of epithelial cells and oligospermia.
Table 1--Mean of the sperm parameters of Ipomoea brasiliana
poisoned goats.

Group   SP (cm)   Vol (mL)   C (x106sptz/ml)   MM (0-5)    Mot (%)

I       20.3 (a)  0.4 (a)        1.1 (a)       2.1 (a)    39.9 (a)
II      19.3 (a)  0.5 (a)        0.9 (a)       1.5 (a)    26.6 (a)
III      20.0a      1.0b          2.0b           4.4b       77.7b

Group    V (0-5)    Major defects (%)   Minor defects (%)

I        2.1 (a)         4.1 (a)             3.5 (a)
II       1.6 (a)         6.4 (b)             5.3 (b)
III       4.4b            3.2a                4.8ab

SP--scrotal perimeter, Vol--volume, C--concentration, MM--mass
motility, Mot--motility, V--vigor. Ab Means followed by different
letters in the same column differ from each other by Student's Test

Table 2--Mean values and standard deviation of the diameter
of the seminiferous tubules epithelial cells ([micro]m) of goats
poisoned by Ipomoea brasiliana.

Group      Mean      Standard Deviation

I       54.5 (a) *      [+ or -] 0.7
II      46.9 (ab)       [+ or -] 1.2
III     81.5 (abc)      [+ or -] 1.9

* (abc) Different letters in the same column indicate statistically
significant results. Duncan p<0.05.
COPYRIGHT 2018 Universidade Federal de Santa Maria
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2018 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:PATHOLOGY
Author:da Cunha, Ana Lizia Brito; de Medeiros, Juliana Pinto; Riet-Correa, Franklin; Gardner, Dale; Chaves,
Publication:Ciencia Rural
Date:Oct 1, 2018
Previous Article:Transmission of caprine arthritis encephalitis virus between sheep/ Transmissao do virus da artrite encefalite caprina entre ovinos.
Next Article:Hematological profile of captive bearded capuchin monkeys (Sapajus libidinosus) from Northeastern Brazil/Perfil hematologico de macacos-prego...

Terms of use | Privacy policy | Copyright © 2019 Farlex, Inc. | Feedback | For webmasters