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Ultrastructural aspects of the tongue in Magellanic Penguins Spheniscus magellanicus (Forster, 1781)/Aspectos ultraestruturais da lingua de Pinguim-de-Magalhaes Spheniscus magellanicus (Forster, 1781).

Introduction

In consideration the characteristics of the various phylogenetic groups of vertebrates, locomotion and feeding has featured for having a great influence on the evolution of adaptations and subsequent patterns of evolutionary process. Changes in eating habits reflect the phylogeny to some degree, so that detailed studies of these changes may elucidate the selective factors responsible for various adaptive events. What determines prey and habitat strongly influence, through natural selection, on feeding behavior and, ultimately, the function and morphology of feeding mechanisms (OZETI; WAKE, 1969).

Comparative studies on the tongue of different vertebrate species suggest morphological adaptations throughout the evolutionary process. These evolutionary changes are considered the bases for the progress in food intake and occupation of different habitats (EMURA et al., 2009a and b; 2010; IWASAKI, 2002).

The development of the upper and lower jaws of birds into beaks and the absence of teeth, lips and cheeks limit the manipulation of foods (REECE, 1996). The lingual apparatus is responsible for the regulation of these functions, consists of various elements that influence one another mechanically, such as cartilaginous and bony skeletal elements, muscles and salivary glands (HOMBERGER; MEYERS, 1989)

The tongue of birds show highly diversified morphology in terms of size, shape and structure (ERDOGAN et al., 2012; MCLELLAND, 1979), and may reflect the type of diet and the mode of feeding in these animals. Harrison (1964) grouped the tongue of birds in five categories according to the adaptive characteristics: adapted to capture, handling and swallowing of food, gustation and touch, and nest building.

Morphophysiological studies on the structure of bird tongues demonstrate that, in general, the tongue is found in the lower jaw and has, many times, the shape of the beak. It is divided into apex, body and root (CAMPBELL; LACK, 1985; EMURA et al., 2008a; 2009a and b; ERDOGAN; IWASAKI, 2014; GUIMARAES et al., 2009; KOENING; LIEBIG, 2001; MCLELLAND, 1990; VOLLMERHAUS; SINOWATZ, 1992).

Penguins of the Spheniscidae family are pelagic birds that are totally adapted to the marine environment. They make up a group of birds that lost the ability to fly and, in order to find their food in the sea, they are adapted to swimming and diving (BANNASCH, 1986; HILDEBRAND, 1974). However, like all the birds, they come back to land to lay and incubate their eggs (SILVA FILHO; RUOPPOLO, 2007).

The Magellanic penguins (Spheniscus magellanicus) inhabit the cold regions of the coasts of Argentina and Chile (BINGHAM, 2002). During their reproductive period, they migrate to the north of the continent in the search for greater availability of food (PUTZ et al., 2000; STOKES et al., 1998), reaching the southern and southwestern coastal areas of Brazil (ROOS, 2008; SILVA FILHO; RUOPPOLO, 2007). It is the most abundant penguin species in temperate regions, with a world population estimated in 1,300,000 of couples (MADER et al., 2010). However, according to the IUCN (2011), this species is considered near threatened of extinction.

Among the food preferences of this species are mainly the fish, cephalopods and shellfish (SCHIAVINI et al., 2005; YOFRE et al., 1983). According to Kobayashi et al (1998), the tongue of the penguins generally presents adaptations to this type of food, with rigid and sharp papillae that enable the capture of the slippery prey. Considering the adaptive morphological characteristics of the penguins, the objectives of the present study were to describe the morphology of the tongue of Magellanic penguins, considering the importance of the adaptation of this organ in the collection of food, and to compare these data with descriptions of other bird species in the literature.

Material and Methods

Six tongue of juveniles Magellanic penguins (Spheniscus magellanicus), the collection of veterinary anatomy laboratory of the Faculty of Veterinary Medicine and Animal Science of the University of Sao Paulo, were analyzed. After being removed from the oral cavity, tongues were photographed and sent to macroscopic analysis, to light microscopy and scanning electron microscopy.

For light microscopy, tongues were fixed by immersion in formaldehyde 10%. After that, they were washed in running water, dehydrated in increasing concentrations of alcohol to 100%, diaphanized in xylol and embedded in Paraplast[R]. Samples were cut in sections of 5-pm in thickness, and were stained by Hematoxylin-Eosin (HE), Masson's Trichrome, and Picrosirius techniques.

For the scanning electron microscopy, samples were fixed in modified Karnovsky's fixative, containing 2.5 glutaraldehyde and 2% paraformaldehyde, according to Watanabe and Yimada (1983). After fixation, they were washed in distilled water and immersed in tannic acid 1% (MURAKAMI, 1974). For the analysis the epithelium-connective tissue interface, they were treated with NaOH 10% for 3-6 days at room temperature (OHTANI, 1987) in order to remove the epithelial layer and expose the surface of the lamina. Then, they were washed and submitted to post-fixation with osmium tetroxide 1% aqueous solution, washed in distilled water and immersed in tannic acid 1%.

After that, all samples were dehydrated in serial baths of alcohol from 60 to 100%, and dried in a critical point dryer. Later on, samples were mounted in metallic stubs, covered with gold, and analyzed and photographed in a MEV LEO 435VP electron microscope.

Results

The tongue of the Magellanic penguin has a fusiform shape with a round apex that is narrower that the root (Figure 1A, B and C), following the shape of the beak. As for size, it was observed that the tongue presented mean apex-root length of 4cm, occupying almost all the lower jaw.

All the dorsal surface of the tongue was composed only the filiform papillae distributed in longitudinally arranged rows. It was possible to observe a variation in the size of these papillae, with larger ones in the medial region, not in the root and apex. Although filiform papillae were caudally inclined, papillae located in the rows in the lateral margins of the tongue (right and left) were inclined latero-caudally (Figures 1 and 2C).

The epithelium of the tongue of the Magellanic penguin is stratified, with a thick keratin layer and presence of sloughing (Figure 2A, E, F and 3A). It was noted that the apex of the papillae was the region where most of the sloughing was found (Figure 2D, E and F), when compared with the body and base of the papillae and the floor of the tongue. No taste buds were observed in these papillae, which were characterized as mechanical papillae.

Below the thick epithelium of the lingual papillae, connective tissue rich in type I and III collagen fibers was observed, with predominance of type III fibers (Figures 2B and 3B) and absence of mucous glands. After the epithelium was removed, the floor of the tongue presented narrow parallel rows of longitudinally arranged connective papillae. The arrangement of the connective papillae followed the distribution of the epithelial papillae (Figure 3D, E and F). It was observed the presence of salivary glands in the whole extension of the tongue dorsal surface.

The ventral region did not show lingual papillae or connective papillae, but small cavities in the epithelium close to the apex of the tongue were observed (Figure 3G and H).

The cartilaginous skeleton, formed by hyaline cartilage, was observed in the medial region of the tongue, extending from the base to the apex. Striated skeletal muscle fibers were observed around the tongue cartilage (Figure 3A, C, G and H).

Discussion

The avian tongues exhibit adaptations specific for the collection, manipulation and swallowing of foods (ERDOGAN; IWASAKI, 2014; STURKIE, 2000). The diversity of feeding adaptations among birds is reflected in the form and function of their feeding apparatus, and morphological adaptations of avian tongues are also closely associated with discrete eating habits and lifestyle in different environments (EMURA et al., 2008a and b; NICKEL et al., 1977; PARCHAMI et al., 2010a and b).

Studies on the adaptive morphology of the tongue of vertebrates, such as the keratinization of the tongue epithelium during the adaptation to moist to dry conditions or to seawater, suggest an important role of this organ during the migration of vertebrates from freshwater to seawater or land (IWASAKI, 2002).

The tongue of the Magellanic penguin showed a highly keratinized epithelium both in the dorsal and ventral regions, as it was observed with other penguin species (KOBAYASHI et al., 1998) and in other birds, such as the white-tailed eagle (HOMBERGER; BRUSH, 1986), the cormorant (JACKOWIAK et al., 2006), the oriental scops owl, and the Japanese pigmy woodpecker (EMURA et al., 2009a and b), whose feeding habits depend on a more rigid and resistant tongue structure. In ratites, such as emus and ostriches, the tongue epithelium is not keratinized (CROLE; SOLEY, 2010; GUIMARAES et al., 2009; SANTOS et al., 2011). To compensate for this absence of the keratinized epithelium, saliva or mucous secretion is produced by the numerous salivary glands on both the dorsal and ventral parts of the tongue to protect the tongue in case of mechanical irritation (CROLE; SOLEY, 2009; SANTOS et al., 2011).

The structure of the tongue in birds has a direct correlation with the morphology of the beak (CAMPBELL; LACK, 1985; VOLLMERHAUS; SINOWATZ, 1992), and characteristics such as the epithelial cover and tongue skeleton are correlated with way food is captured and the feeding habits of the bird (MCLELLAND, 1979).

The triangular shape of the tongue of the Magellanic penguin showed a direct relationship with the shape of the lower jaw, taking up the whole cavity. This characteristics was also observed by Oliveira et al. (2011) in Spheniscus magllanicus and Kobayashi et al. (1998) in other four species of penguins: Spheniscus demersus, Pygoscelis papua, Spheniscus humboldti, and Eudyptes chrysolophus. The triangular shape with the pointed apex is considered the standard in omnivorous birds (GARDNER, 1927).

In birds such as ratites, which swallow the whole food, the tongue is rudimentary, taking up only 1/3 of the oral cavity, and does not follow the shape of the beak (GUIMARAES et al., 2009; JACKOWIAK; LUDWIG, 2008; SANTOS et al., 2011).

The presence of the cartilage in the tongue of the Magellanic penguin suggests that, besides having the structural function of maintaining the shape of the tongue (MCLELLAND, 1979), it makes up the hyobranchial system, which aids in the capture of the food, acting as a lever, pushing the food towards the back of the mouth for quick swallowing. This hyobranchial system in birds is not articulated with the cranium, enabling wide mobility, and it is the main contributor to the movement of the tongue (BONGA, 2000; KING; MCLELLAND, 1984).

In the tongue of the Magellanic penguin, as described in other penguin species (KOBAYASHI et al., 1998) it was possible to observe thin papillae with keratinized epithelium spread all over the surface of the organ. As the diet of the Magellanic penguins is mainly based on slippery animals, such as fish, cephalopods and shellfish (SCHIAVINI et al., 2005; YOFRE et al., 1983) lingual papillae have an important role in these animals, as they aid the apprehension of the food (MCLELLAND, 1979).

The presence of lingual papillae was already reported in other birds, such as the white-tailed eagle, the cormorant (HOMBERGER; BRUSH, 1986), oriental scops owl, and the Japanese pygmy woodpecker (EMURA et al., 2009a and b). However, the absence of these papillae was described in ratites, such as ostriches (GUIMARAES et al., 2009; JACKOWIAK; LUDWIG, 2008) and emus (CROLE; SOLEY, 2010; SANTOS et al., 2011).

In the tongue of the Magellanic and other penguin species (KOBAYASHI et al., 1998), only one type of lingual papillae was found, whose morphology is similar of filiform papillae described in aquatic mammals (KOBAYASHI et al., 1994). In this study, no gustative papillae were found, as has been reported for other species of penguins. However, when present in birds, these papillae may be spread not only in the tongue epithelium, but also in other regions of the oral cavity (GANCHROW; GANCHROW, 1985; REUTTER; WITT, 1993).

In our study the presence of salivary glands was not observed, as Kobayashi et al. (1998) in several species of penguins. However, Samar et al. (1995; 1999) observed the presence of salivary glands in the back of the tongue in the transition region with oropharynx and palate, in this same species. Thus, one may suggest that humidification of food commences from the oropharynx, which facilitates swallowing of food, which in penguins is swallowed whole.

In our study the presence of salivary glands was not observed, as Kobayashi et al. (1998) in several species of penguins. However, Samar et al. (1995; 1999) observed in this species the presence of salivary glands in the back of the tongue, in the transition region with oropharynx and palate. Thus, one may suggest that humidification of food commences from the oropharynx, which facilitates swallowing of food, which in penguins is swallowed whole.

Scanning electron microscopy results showed the sloughing of the epithelium in the dorsal surface of the tongue, which was more intense in the apex of the lingual papillae, due to the direct friction with the food. Sloughing of the epithelium was also observed in the dorsal surface of the tongue in emus (CROLE; SOLEY, 2010; SANTOS et al., 2011) and ostriches (GUIMARAES et al., 2009).

It was possible to observe, based on the results obtained in this study, that the tongue of the Magellanic penguin presented morphological similarities with other penguin species (Spheniscidae) (KOBAYASHI et al., 1998). In spite of sharing common characteristics with ratites (ostrich, rheas, emus, etc.), such as wings adapted to propulsion, the morphology of the tongue of these groups of birds were very different and adapted to the way of life and way food is captured in each species.

Conclusion

The structure of the tongue of the Magellanic penguin presented common characteristics described for other penguin species (Spheniscidae), being possible to observe the morphology of the organ is closely related to the dietary habits of these animals. Penguins, like other seabirds that feed on aquatic environment, present fairly lingual apparatus adapted to assist in obtaining and use of food.

Doi: 10.4025/actascibiolsci.v36i4.23168

References

BANNASCH, R. Morphologic-functional study of the locomotor system of penguins as a general model of movement in under-water flight. Gegenbaurs Morphologisches Jahrbuch, v. 132, n. 5, p. 645-679, 1986.

BINGHAM, M. The decline of Falkland Islands penguins in the presence of a commercial fishing industry. Revista Chilena de Historia Natural, n. 75, p. 805-818, 2002.

BONGA, C. A. Feeding in paleognathous birds, in feeding: form, function, and evolution in tetrapod vertebrates. San Diego: Academic Press, 2000.

CAMPBELL, B.; LACK, E. A dictionary of birds. London: Calton T& AD. Poyser, 1985.

CROLE, M. R.; SOLEY, J. T. Morphology of the tongue of the emu (Dromaius novaehollandiae). II. Histological features. Onderstepoort Journal Veterinary Research, v. 76, n. 4, p. 347-361, 2009.

CROLE, M. R.; SOLEY, J. T. Surface morphology of the emu (Dromaius novaehollandiae) tongue. Anatomia, Histologia Embryologia, v. 39, n. 4, p. 355-365, 2010.

EMURA, S.; OKUMURA, T.; CHEN, H. SEM studies on the connective tissue cores of the lingual papillae of the Northern goshawk (Accipiter gentilis). Acta Anatomica Nippon, v. 83, n. 3, p. 77-80, 2008a.

EMURA, S.; OKUMURA, T.; CHEN, H. Scanning electron microscopic study of the tongue in the peregrine falcon and common kestrel. Okajimas Folia Anatomica Japonica, v. 85, n. 1, p. 11-15, 2008b.

EMURA, S.; OKUMURA, T.; CHEN, H. Scanning electron microscopic study of the tongue in the oriental scops owl (Otus scops). Okajimas Folia Anatomica Japonica, v. 86, n. 1, p. 1-6, 2009a.

EMURA, S.; OKUMURA, T.; CHEN, H. Scanning electron microscopic study of the tongue in the Japanese pygmy woodpecker (Dendrocopos kizuki). Okajimas Folia Anatomica Japonica, v. 86, n. 1, p. 31-35, 2009b.

EMURA, S.; OKUMURA, T.; CHEN, H. Comparative studies of the dorsal surface of the tongue in three avian species by scanning electron microscopy. Okajimas Folia Anatomica Japonica, v. 86, n. 4, p. 111-115, 2010.

ERDOGAN, S.; IWASAKI, S. Function-related morphological characteristics and specialized structures of the avian tongue. Annals of Anatomy, v. 196, n. 2-3, p. 75-87, 2014.

ERDOGAN, S.; SAGSOZ, H.; AKBALIK, M. E. Anatomical and histological structure of the tongue and histochemical characteristics of the lingual salivary glands in the Chukar partridge (Alectoris chukar, Gray 1830). British Poultry Science, v. 53, n. 3, p. 307-315, 2012.

GANCHROW, D.; GANCHROW, J. R. Number and distribution of taste buds in the oral cavity of hatching chicks. Physiology and Behavior, v. 34, n. 6, p. 889-894, 1985.

GARDNER, L. L. On the tongue in birds. The Ibis, v. 69, n. 1, p. 185-196, 1927.

GUIMARAES, J. P; MARI, R. B.; CARVALHO, H. S.; WATANABE, I. Fine structure of the dorsal surface of ostrich's (Struthio camelus) tongue. Zoological Science, v. 26, n. 2, p. 153-156, 2009.

HARRISON, J. G. Tongue. In: THOMSON, A. L. (Ed.). A new dictionary of birds. London: Nelson, 1964. p. 398-399.

HILDEBRAND, M. Analysis of vertebrate structure. New York: J. Wiley and Son, 1974.

HOMBERGER, D. G.; BRUSH, A. H. Functional morphological and biochemical correlations of the keratinized structure in the African Grey parrot, Psittaccus erithacus. Zoomorphology, v. 106, n. 2, p. 103-114, 1986.

HOMBERGER, D. G.; MEYERS, R. A. Morphology of the lingual apparatus of the domestic chicken, Gallus gallus, with special attention to the structure of the fasciae. American Journal of Anatomy, v. 186, n. 3, p. 217-257, 1989.

IUCN-International Union for Conservation of Nature and Natural Resources. Red list of threatened species. 2011. Available from: <http://www.iucnredlist.org/>. Access on: Feb., 2014.

IWASAKI, S. Evolution of the structure and function of the vertebrate tongue. Journal of Anatomy, v. 201, n. 1, p. 1-13, 2002.

JACKOWIAK, H.; LUDWIG, M. Light and scanning electron microscopic study of the structure of the ostrich (Strutio camelus). Zoological Science, v. 25, n. 2, p. 188-194, 2008.

JACKOWIAK, H.; ANDRZEJEWSKI, W.; GODYNICKI, S. Light and scanning electron microscopic study of the tongue in the cormorant Phalacrocorax carbo (Phalacrocoracidae, Aves). Zoological Science, v. 23, n. 2, p. 161-167, 2006.

KING, A. S.; MCLELLAND, J. Digestive system, in Birds--their structure and function. 2nd ed. London: Bailliere Tindall, 1984.

KOBAYASHI, K., KUMAKURA, M.; YOSHIMURA, K.; INATOMI, M.; ASAMI, T. Fine structure of the tongue and lingual papillae of the penguin. Archivum Histologicum Cytologicum, v. 61, n. 1, p. 37-46, 1998.

KOBAYASHI, K.; KUMAKURA, M.; YOSHIMURA, K. Stereo structure of the connective tissue cores of the lingual papillae in the steller sea lion. Journal of Electron Microscopy, v. 43, p. 246, 1994.

KOENIG, H. E.; LIEBIG, H. G. Anatomie und propadeutik des geflugels. Lehrbuch und Farbatlas fur Studium und Praxis. New York: Schattauer Stuttgart, 2001.

MADER, A.; SANDER, M.; CASA, J. R. Ciclo sazonal de mortalidade do pinguim-de-magalhaes, Spheniscus magellanicus influenciado por fatores antropicos e climaticos na costa do Rio Grande do Sul, Brasil. Revista Brasileira de Ornitologia, v. 18, n. 3, p. 228-233, 2010.

MCLELLAND, J. Digestive system. In: KING, A. S.; MCLELLAND, J. (Ed.). Form and function in birds. London: Academic Press, 1979. p. 69-181.

MCLELLAND, J. Digestive system. In: KING, A. S.; MCLELLAND, J. (Ed.). A color atlas of avian anatomy. Aylesbury: Wolfe Publishing Ltd., 1990. p. 47-49.

MURAKAMI, T. A revised tannic-osmium method for noncoated scanning electron microscope specimens. Archivum Histologicum Japonicum, v. 36, p. 189-193, 1974.

NICKEL, R.; SCHUMMER, A.; SEIFERLE, E. Anatomy of the Domestic Birds. Berlin; Hamburg: Verlag Paul Parey, 1977.

OHTANI, O. Three dimensional organization of the connective tissue fibers of the human pancreas: a scanning electron microscopy study of NaOH treated tissues. Archivum Histologicum Japonicum, v. 50, n. 5, p. 557-566, 1987.

OLIVERA, R. P. N.; SANTOS, B. G.; DUARTE, B. R.; NOGUEIRA, C. H. O.; SILVEIRA, L. S.; BARBOSA, L. A.; RODRIGUES, A. B. F. Morfologia, topografia e distribuicao das papilas linguais em pinguim-de-magalhaes (Spheniscus magellanicus). PUBVET, v. 5, n. 7, Ed. 154, Art. 1040, 2011. Available from: <http://www.pubvet.com.br/artigos_det.asp?artigo=926>. Acces on: Aug. 14, 2014.

OZETI, N.; WAKE, D. B. The morphology and evolution of the tongue and associated structures in salamanders and newts (Family Salamandridae). Copeia, v. 1961, n. 1, p. 91-123, 1969.

PARCHAMI, A.; DEHKORDI, R. A. F.; BAHADORAN, S. Fine structure of the dorsal lingual epithelium of the common quail (Coturnix coturnix). World Applied Sciences Journal, v. 10, n. 10, p. 1185-1189, 2010a.

PARCHAMI, A.; DEHKORDI, R. A. F.; BAHADORAN, S. Scanning electron microscopy of the tongue in the golden eagle Aquila chrysaetos (Aves: Falconiformes: Accipitridae). World Journal of Zoology, v. 5, n. 4, p. 257-263, 2010b.

PUTZ, K.; INGHAM, R. J.; SMITH, J. G. Satellite tracking of the winter migration of Magellanic penguins (Spheniscus magellanicus) breeding in the Falkland Islands. Journal of Ornithology, v. 142, n. 4, p. 614-622, 2000.

REECE, W. O. Physiology of domestic animals. 2nd ed. Baltimore, Philadelphia, London, Paris, Bangkok, Buenos Aires, Hong Kong, Munich, Sydney, Tokyo and Wroclaw: Williams and Wilkins, 1996.

REUTTER, K.; WITT, M. Morphology of vertebrate taste organs and their nerve supply. In: SIMON, S. A.; ROPER, S. D. (Ed.). Mechanisms of taste transduction. London and Tokyo: CRC Press, 1993. p. 29-82.

ROOS, A. L. Pinguins-de-magalhaes (Spheniscus magellanicus) no Nordeste: migrantes ou errantes? Boletim Eletronico do CEMAVE, v. 1, n. 2, s/p., 2008.

SAMAR, M. E.; AVILA, R. E.; FABRO, S. P; CENTURION, C. Structural and cytochemical study of salivar glands in the Magellanic penguin Spheniscus magellanicus and the kelp gull Larus dominicanus. Marine Ornithology, v. 23, n. 2, p. 153-157, 1995.

SAMAR, M. E.; AVILA, R. E.; FABRO, S. P; PORFIRIO, V; ESTEBAN, F. J.; PEDROSA, J. A.; PEINADO, M. A. Histochemical study of magellanic penguin (Spheniscus magellanicus) minor salivary glands during postnatal growth. The Anatomical Records, v. 254, n. 2, p. 298-306, 1999.

SANTOS, T. C.; FUKUDA, K. Y.; GUIMARAES, J. P.; OLIVEIRA, M. F.; MIGLINO, M. A.; WATANABE, I. Light and scanning electron microscopy study of the tongue in Rhea americana. Zoological Science, v. 28, n. 1, p. 41-46, 2011.

SCHIAVINI, A.; YORIO, P; GANDINI, P; REY, A. R.; BOERSMA, P D. Los pinguinos de las costas Argentinas: estado poblacional y conservacion. Hornero, v. 20, n. 1, p. 5-23, 2005.

SILVA FILHO, R. P.; RUOPPOLO, V. Sphenisciformes (Pinguim). In: CUBAS, Z. S.; SILVA, J. C. R.; CATAO-DIAS, J. L. (Ed.). Tratado de animais selvagens medicina veterinaria. Sao Paulo: Roca, 2007. p. 309-323.

STOKES, D. L.; BOERSMA, P D.; DAVIS, L. S. Satellite tracking of Magellanic Penguin migration. Condor, v. 100, p. 376-38, 1998.

STURKIE, P. D. Sturkie's Avian Pysiology. 5th ed. San Diego, London, Boston, New York, Sydney, Tokyo and Toronto: Academic Press, 2000.

VOLLMERHAUS, B.; SINOWATZ, F. Verdauungsapparat. In: NICKEL, R.; SCHUMMER, E.; SEIFERLE, E. (Ed.). Anatomie der vogel. Parey and Berlin: Lehrbuch der anatomie der haustiere, 1992. p. 188-223.

WATANABE, I.; YAMADA, E. The fine structure of lamellated nerve endings found in the rat gingiva. Archivum Histologicum Japonicum, v. 46, n. 6, p. 173-182, 1983.

YOFRE, A. E.; NAROVSKY, T.; PALERMO, M. A.; MARCHETTI, B. El pinguino de Magallanes. Fauna Argentina 1. Buenos Aires: Centro Editor de America Latina, 1983.

Received on March 3, 2014.

Accepted on July 23, 2014.

Juliana Placido Guimaraes (1) *, Renata de Britto Mari (2), Alfredo Le Bas (3) and Maria Angelica Miglino (4)

(1) Programa de Pos-graduacao em Sustentabilidade de Ecossistemas Costeiros e Marinhos, Universidade Santa Cecilia, Oswaldo Cruz, 277, 11045-907, Santos, Sao Paulo, Brazil. (2) Universidade Estadual Paulista, Campus Experimental do Litoral Paulista, Sao Vicente, Sao Paulo, Brazil. (3) Secao de Fisiologia e Nutricao, Faculdade de Ciencias, Universidade da Republica, Montevideo, Uruguay. (4) Departamento de Cirurgia, Faculdade de Medicina Veterinaria e Zootecnia, Universidade de Sao Paulo, Sao Paulo, Brazil. * Author for correspondence. E-mail: jpgrbm@yahoo.com.br
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