SciELO - Scientific Electronic Library Online

 
vol.28 issue5Oviposition and post-embryonic development of Aglaoctenus lagotis (Araneae: Lycosidae)Reproductive plasticity of Hypostomus affinis (Siluriformes: Loricariidae) as a mechanism to adapt to a reservoir with poor habitat complexity author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

Share


Zoologia (Curitiba)

Print version ISSN 1984-4670

Zoologia (Curitiba, Impr.) vol.28 no.5 Curitiba Oct. 2011

https://doi.org/10.1590/S1984-46702011000500004 

BIOLOGY

 

Nesting of Phrynops geoffroanus (Testudines: Chelidae) on sandy beaches along the Upper Xingu River, Brazil

 

 

Paulo D. Ferreira JúniorI, 1; Rafael A. M. BalestraII; José R. MoreiraIII; Fábio de O. FreitasIII; Ana P. G. LustosaII; Rafael F. JorgeII; Artur J. de M. RosaIII; Antônio A. SampaioII; Aline S. GomesI

ICentro Universitário Vila Velha. Rua Comissário José Dantas de Melo 21, 29102-770 Vila Velha, ES, Brazil
IICentro Nacional de Pesquisa e Conservação de Répteis e Anfíbios. Rua 229, 95, Setor Leste Universitário, 74605-090 Goiânia, GO, Brazil
IIIEmbrapa Recursos Genéticos e Biotecnologia, Parque Estação Biológica. Avenida W5 Norte, Caixa Postal 02372, 70770-917 Brasília, DF, Brazil

 

 


ABSTRACT

This work presents the first data on incubation temperature of Phrynops geoffroanus (Schweigger, 1812) in a natural environment, and provides information on nest predation, hatching success and size of offspring born in the nests on sandy beaches along the Upper Xingu River. Thirty-one P. geoffroanus nests were found, of which eleven were completely predated, mainly by Cerdocyon thous (Linnaeus, 1766). Incubation was completed in nine out of the 17 nests protected by netting. The nests presented an average of 13.1 eggs and were distributed over the various geomorphological sectors of the nine sampled beaches. The size and weight of the hatchlings varied significantly between nests, and the incubation period in protected nests lasted for 76.5 days, less than reported for controlled incubation in the laboratory. Daily variation in incubation temperature in the three nests monitored for temperature was lower in those situated in fine sand sediments. Incubation temperature varied from 22 to 39 C and may have affected hatching success, which reached 60.8% in protected nests. Nest distribution in different geomorphological sectors indicated the plasticity of P. geoffroanus in terms of variation in nesting environment, which partly explains the species' broad geographical distribution.

Key words: Geoffroy's side-necked turtle; hatching success; incubation; nest predation; Xingu Indigenous Park.


 

 

Geoffroy's side-necked turtle, Phrynops geoffroanus (Schweigger, 1812), is the freshwater chelid turtle with the broadest geographical distribution in South America; it is found in all the main river basins (PRITCHARD & TREBBAU 1984, BALDO et al. 2007, VOGT 2008). Despite this broad distribution and common occurrence in the most varied aquatic environments (SOUZA 2005, RUEDA-ALMONACID et al. 2007), and although it is one of the most commonly found neotropical urban animals (SOUZA & ABE 2001, MARTINS et al. 2010) there are still taxonomic doubts about the occurrence of sub-species or cryptic species within the group. Some authors call the various occurrences of this freshwater turtle the "geoffroanus complex" (RHODIN & MITTERMEIER 1983, MCCORD et al. 2001, SOUZA 2005, VOGT 2008).

Egg-laying often takes place in shady areas and clay soils along the banks of rivers and lakes (MEDEM 1960). However, the females may migrate hundreds of meters from the river to lay eggs in open sites and among creeping vegetation (VOGT 2008). Although P. geoffroanus does not show gregarious behavior, its nests may be placed near one another (MEDEM 1960, VOGT 2008). Incubation is relatively prolonged, as with the other chelid turtles. There are no data available about incubation temperature in a natural environment, but in the laboratory embryonic development is viable at least between 25 and 32ºC (KARDON 1981, EWERT et al. 2004, LISBOA et al. 2004). It is worth noting that, unlike some turtle species, the sex of P. geoffroanus is genetically determined rather than being affected by environmental temperature during incubation (EWERT et al. 2004). Females lay eggs at least four times in any one reproductive season (VOGT 2008), and the nests may contain up to 30 spherical eggs, about 3 cm in diameter, with a hard shell (SOUZA et al. 2006, SOUZA & ABE 2001). The nests are generally shallow, not exceeding 20 cm in depth (MEDEM 1960).

Reproductive parameters, such as litter size, predation rate and hatching success, are important components in the species' life history and essential to management and conservation projects (SOUZA & VOGT 1994, CONGDON et al. 2000, FERREIRA JÚNIOR & CASTRO 2010). For neotropical freshwater turtles these parameters are little known (SOUZA et al. 2006), and for P. geoffroanus data on reproduction are mainly taken from captive individuals. This work presents the first data on incubation temperature in the natural environment and provides information on predation, hatching success and size of P. geoffroanus hatchling born in nests on sandy beaches along the Upper Xingu River, in the Parque Indígena do Xingu (Xingu Indigenous Park), state of Mato Grosso, Brazil.

 

MATERIAL AND METHODS

The Parque Indígena do Xingu, the first indigenous territory recognized by the Brazilian government in 1961, covers about 30,000 km2 and is a good example of well preserved forest. In recent years deforestation has increased in the area surrounding the Park, motivated by the expanding frontiers of agriculture and livestock grazing. This has made the Park a particularly important area in which to study P. geoffroanus in a natural environment. The region is situated in a transition zone between the Cerrado and the Amazon biome, so the monitored laying sites are often covered by sparse bushy herbaceous vegetation that provides little shade. These areas may be classified within the common Cerrado types as grassland, wet campo, savannah woodland, and gallery forest.

During the period of low water, from June to October, sand-bars known as beaches appear along the principal rivers of the Amazon basin. These are used as a nesting area by numerous species of turtle, especially those of the genus Podocnemis. In the Xingu Indigenous Park the beaches are formed in point bars made up of sandy sediments. In some beaches the stretches downstream and near the internal bank of the channel made by this point bar may have a centimetric to decimetric clay-silt layer that covers the sandy sediments.

The area monitored in this project includes nine consecutive beaches that lie along 13 km of river (from 11º55'49.34"S, 53º32'56.16"W to 11º59'08.19"S; 53º28'12.62"W). The edges and banks of the rivers and lakes were not monitored, and the nests were only searched for on beaches (Fig. 1).

Three nests located on beaches 4 (11º56'03.67"S, 53º31'04.83"W), 5 (11º56'58.03"S, 53º30'21.58"W) and 6 (11º56'38.12"S, 53º29'32.19"W) were monitored with dataloggers (Ibuttons Maxim DSG1921G), which recorded the temperature every 60 min during incubation. The dataloggers were inserted among the eggs at the center of the nest. The nests were protected with wire netting to prevent predation, which is intense in the area. The net was made of metal wire, 2 cm mesh, with 40 cm diameter, covering the nest completely. The possible influence of the netting on the nest temperature was not evaluated. After hatching, the hatchlings were measured (margin of error ± 0.01 mm) at the height of the shell, at the straight carapace length and width; they were weighed (± 0.1 g) and released into an internal lagoon on beach 5. On hatching, 100 g of sediments were collected from each nest to evaluate the texture characteristics in the egg-laying areas. The sediments were sieved and the granulometric fractions were classified into pebble, granule, very coarse sand, coarse sand, medium sand, fine sand, very fine sand and mud (FOLK 1974). To calculate the height of the nest in relation to the river level a CST Berger (± 1 cm) was used and the daily variations in river level were monitored with a limnetic ruler. October 3rd was adopted as the reference date for comparison of height of nests where eggs had been laid on different days and beaches. On this day the Xingu River reached its lowest level during the 2010 reproductive season.

Variation in size and weight of the hatchling and in the incubation temperature of the monitored nests was analyzed using a Kruskal-Wallis One Way Analysis of Variance on Ranks with an a posteriori Dunn test.

 

RESULTS

In October, when the wet season begins, the lowest parts of the beaches are flooded, often submerging the nests of Podocnemis unifilis (Troschel, 1848), which are common in these parts. In the study area within the Xingu National Park, P. unifilis nests in almost every parts of the beach. Phrynops geoffroanus shares the nesting areas with P. unifilis, with overlap in the sites. The large size of the beaches and the low nest density, however, prevents females from destroying other nests while they are laying eggs.

Thirty-one P. geoffroanus nests were found on nine beaches along the Xingu River during the 2010 reproductive season. Eleven nests (35.5%) were completely predated; of these, one was predated by ants, five were predated before being protected by netting, five were completely predated by the crabeating fox, Cerdocyon thous (Linnaeus, 1766), after being covered by netting. This fox's tracks were sighted relatively frequently and one individual of the species was seen circling the nests of

P. geoffroanus and P. unifilis. Predation of the nests by C. thous was identified based on footprints and claw marks along the edges of the nests situated in clay silt substrate. The eggs in one nest did not present any sign of embryo development. One nest that was found after partial predation was then protected and incubation was completed. Eight nests were identified after hatching, when hatchlings and their tracks were found. Two protected nests were flooded and all the embryos died. Out of the 17 protected nests, 10 completed incubation.

The mean hatchling weight (9.1 ± 1.4 g; range = 6 to 11.5), length of the carapace (38.3 ± 2 mm; range = 31.5 to 41.3), width of carapace (30.1 ± 1.83 mm; range = 24.7 to 33.6), and height of shell (13.9 ± 1.06 mm; range = 11.3 to 16.1) were calculated for the 83 individuals from the 10 protected nests in the Xingu Indigenous Park. The nests presented a mean of 13.1 ± 2.38 eggs (n = 10; range = 9 to 17 eggs). The size (length of the carapace: Kruskal-Wallis, H5.56 = 22.8; p < 0.001; width of carapace: H5.56= 33.8; p < 0.001; height of shell: H5.56 = 13.7; p < 0.001) and the weight of hatchlings (Kruskal-Wallis, H5.56 = 43.1; p < 0.001) varied significantly between nests.

Hatching success was considered to be the relationship between the number of hatchlings and the total number of eggs containing an embryo; in the 10 protected nests it was 60.8 ± 37.5% (range of 0 to 100%). The duration of incubation, considered as the period, in days, which passed between laying and first hatching, was 76.5 ± 9.65 days for six protected nests (range between 65 and 94 days). The daily variation in incubation temperature in three monitored nests (Tab. I) was lowest in the nest situated in sediments classified as well selected fine sand (D50 = 164 ¼m) and differed significantly from the nests found in well selected medium sand (D50 = 305 ¼m and D50 = 289 ¼m) (Kruskal-Wallis, H = 118.6; p < 0.001).

The mean maximum height of the nests, in relation to the Xingu River level, was 211 ± 60.1 cm (n = 10; range 144 to 219 cm). The nests were situated mainly in the upper parts of the beaches, within open areas near the transition to vegetation. In this transition belt, the soil frequently has a sandy-silt layer, several centimeters deep and with a crisp consistency, over which creeping vegetation grows. The nests in this belt were normally found only after predation, because it is difficult to preserve and notice tracks and other signs of excavation in the sandy silt.

 

DISCUSSION

The open sandy beaches of the Xingu River presented a low density of nests, which suggests that P. geoffroanus nests in these places may occur in a secondary manner, subsidiary to other nesting sites, such as along the edges of rivers, creeks and lakes (MEDEM 1960, SOUZA & ABE 2001). The nests are found distributed throughout the various geomorphological sectors of the beaches, as occurs with P. unifilis, which lays eggs on the same beaches. The nests were found on the open beach, at the river's edge and in the belt between the beach and the adjacent vegetation (e.g. gallery forest and typical savannah woodland).

Phrynops geoffroanus lays its eggs in synchrony with the variation in level of the Xingu River, as do other species of Amazonian turtles, such as Podocnemis expansa (Schweigger, 1812) (ALHO & PÁDUA 1982, FERREIRA JÚNIOR & CASTRO 2006, 2010), Podocnemis sextuberculata (Cornalia, 1849) (PEZZUTI & VOGT 1999) and P. unifilis (FERREIRA JÚNIOR & CASTRO 2010). When nesting occurs on the beaches, the duration of incubation should be compatible with the low water period, and hatching should take place before the beaches flood. The length of time that P. geoffroanus incubates on the Xingu River is less than durations recorded in the laboratory, which were between 115 and 186 days (LISBOA et al. 2004); between 156 and 173 days (KARDON 1981); between 206 and 319 days (GUIX et al. 1989) and between 149 and 331 days (Flavio de B. Molina, unpubl. data). These durations would be incompatible with incubation on the Xingu River, since at the beginning of October the river level started to rise, flooding the beaches. VOGT (2008) suggested that the incubation period of P. geoffroanus varies according to temperature and humidity, which control embryo diapause and aestivation (DOODY et al. 2001). In natural surroundings, under a fluctuating daily temperature regime, embryo diapause would not take place. If it did, it would have a slight effect on incubation, allowing this to be shorter and the embryos to develop without being flooded. The shorter duration of incubation associated with the low water period in the Xingu River allows P. geoffroanus incubation to take place in open areas of the beaches, with little or no risk of flooding and drowning the young.

The average incubation temperature in the nests was within the limits recorded in laboratory work, where incubation lasted longer (KARDON 1981, GUIX et al. 1989, LISBOA et al. 2004). Daily temperature variation influences the duration of incubation (GEORGES et al. 1994, 2004) and there may be a relationship between temperature and the shorter incubation time observed in the natural nests of P. geoffroanus along the Xingu. The shallowness of the nests and the wide temperature variations led to extremes in temperature, which reached 22 and 39 C, and this may have affected hatching success. The distribution of the nests in various geomorphological sectors indicates great plasticity in P. geoffroanus, in terms of nesting environment. As sex determination of P. geoffroanus is genetic (EWERT et al. 2004) the species is free of incubation temperature's influence on the gender of its young, and may therefore make use of a greater variety of nesting sites.

The size of the litter and the dimensions and weight of young born on these beaches are similar to what has been described in other environments, such as the sandy beaches of the Guaporé River (VOGT 2008), clay riverbanks (MEDEM 1960) and urban rivers and creeks in areas changed by humans (SOUZA & ABE 2001). However, when only the beaches of the Xingu River are evaluated, it can be observed that the size and weight of the young differ between nests, and the incubation temperature is also influenced by nesting site. There is a well established connection between the effects of humidity and temperature on the phenotype of turtle hatchlings (PACKARD 1999, HEWAVISENTHI & PARMENTER 2001, FERREIRA JÚNIOR et al. 2007, BUJES & VERRASTRO 2009). More detailed studies are necessary to understand how environmental characteristics influence humidity and temperature, and how the fluctuating daily temperature regime (GEORGES et al. 2004) affects embryo development and hatchling phenotype in P. geoffroanus. As the species presents a wide geographical range with various ecological characteristics (SOUZA 2005), physiographic characteristics may play an important role in reproductive aspects, being reflected in population structure (SOUZA & ABE 2001).

The availability and type of predator are important components in reproductive success, mainly for freshwater turtles, which undergo the most critical moment of their lives in incubation. SCHNEIDER et al. (2009) reported predation of 92% (n = 39) of nests of P. geoffroanus by Tupinambis teguixin (Linnaeus, 1758) in the Guaporé River. FERREIRA JÚNIOR et al. (2010) reported predation of 97% of nests of P. unifilis by birds in the Javaés River. In the Xingu Indigenous Park, 26% of the nests (n = 31) completed incubation without any type of protection, and the main predator was C. thous. In this area there is no hunting pressure on P. geoffroanus, which is not consumed by the indigenous population. Capture may take place occasionally, and the animal is sometimes kept as a pet in indigenous villages. The high predation rate on nests shows the importance of preserving the nesting areas (CONGDON et al. 2000) and, even more, the adult chelids along the Upper Xingu River.

This work presents data on the reproductive biology and incubation period of P. geoffroanus in its natural environment in the headwaters of the Xingu River basin. The incubation period in natural surroundings was shorter than in the laboratory. It remains to be investigated if this reduced incubation time is due to the genetic variation of the populations that were compared with those in laboratory experiments, taken from different areas in the broad distribution range of this species, or if they arise from local physiographic parameters. Only with further data obtained in natural habitats in other regions within the species' range will it be possible to make comparisons within the species as a whole.

 

ACKNOWLEDGEMENTS

The authors acknowledge the financial support of Petrobras Ambiental and the management of resources invested in this work by Funcredi. FUNAI provided the permits allowing access to the Xingu Indigenous Park. ICMBio and IBAMA granted the Authorization to Carry out Activities for Scientific Purposes, number 16226-4/2010, within SISBIO. We thank the Kamayurá indigenous community from Morená village in the Xingu Indigenous Park.

 

LITERATURE CITED

ALHO, C.J.R. & L.F.M. PÁDUA. 1982. Sincronia entre o regime de vazante do rio e o comportamento de nidificação da tartaruga da Amazônia Podocnemis expansa (Testudinata: Pelomedusidae). Acta Amazonica 12 (2): 323-326.         [ Links ]

BALDO, D.; P. MARTINEZ; J.M. BOERIS & A.R. GIRAUDO. 2007. Reptilia, Chelonii, Chelidae, Phrynops geoffroanus Schweigger, 1812 and Mesoclemmys vanderhaegei (Bour, 1973): Distribution extension, new country record, and new province records in Argentina. Check List 3 (4): 348-352.         [ Links ]

BUJES, C.S. & L. VERRASTRO. 2009. Nest temperature, incubation time, hatching, and emergence in the Hilaire's Side-Necked Turtle (Phrynops hilarii). Herpetological Conservation and Biology 4 (3): 306-312.         [ Links ]

CONGDON, J.D.; R.D. NAGLE; O.M. KINNEY; M. OSENTOSKI; H.W. AVERY; C.R.S. VAN LOBEN & D.W. TINCKLE. 2000. Nesting ecology and embryo mortality: implications for hatchling success and demography of Blanding's turtles (Emydoidea Blandingii). Chelonian Conservation and Biology 3 (4): 569-579.         [ Links ]

DOODY, J.S.; A. GEORGES; J.E. YOUNG; M.D. PAUZA; A.L. PEPPER; R.L. ALDERMAN & M.A. WELSH. 2001. Embryonic aestivation and emergence behaviour in the pig-nosed turtle, Carettochelys insculpta. Canadian Journal of Zoology 79 (6): 1062-1072. doi: 10.1139/cjz-79-6-1062.         [ Links ]

EWERT, M.A.; C.R. ETCHEBERGER & C.E. NELSON. 2004. Turtle sexdetermination modes and TSD patterns, and some TSD patterns correlates, p. 21-32. In: N. VALENZUELA & V.A. LANCE (Eds). Temperature-dependent sex determination in vertebrates. Washington, DC, Smithsonian Books, 194p.         [ Links ]

FERREIRA JÚNIOR, P.D. & P.T.A. CASTRO. 2006. Geological characteristics of the nesting areas of the giant Amazon river turtle (Podocnemis expansa) in the Crixás-Açu river in Goiás State, Brazil. Acta Amazonica 36 (2): 249-258.         [ Links ]

FERREIRA JÚNIOR, P.D. & P.T.A. CASTRO. 2010. Nesting ecology of Podocnemis expansa (Schweigger, 1812) and Podocnemis unifilis (Troschel, 1848) (Testudines, Podocnemididae) in the Javaés River, Brazilian Journal of Biology 70 (1): 85-94. doi: 10.1590/S1519-69842010000100012.         [ Links ]

FERREIRA JÚNIOR, P.D.; A.Z. CASTRO & P.T.A. CASTRO. 2007. The importance of nidification environment in the Podocnemis expansa and Podocnemis unifilis phenotypes (Testudines: Podocnemididae). South American Journal of Herpetology 2 (1): 39-46.         [ Links ]

FOLK, R.L. 1974. Petrology of Sedimentary Rocks. Austin, Hemphill Publication Company, 182p.         [ Links ]

GEORGES, A.; C. LIMPUS & R. STOUTJESDIJK. 1994. Hatchling sex in the marine turtle Caretta caretta is determined by proportion of development at a temperature, not daily duration of exposure. Journal of Experimental Zoology 270 (3): 432-444.         [ Links ]

GEORGES, A.; S. DOODY; K. BEGGS. & J. YOUNG. 2004. Thermal models of TSD under laboratory and field conditions, p. 79-89. In: N. VALENZUELA & V.A. LANCE (Eds). Temperaturedependent sex determination in vertebrates. Washington, DC, Smithsonian Books, 194p.         [ Links ]

GUIX, J.C.; M. SALVATTI; M.A. PERONI & J.S. LIMA-VERDE 1989. Aspectos da reprodução de Phrynops geoffroanus (Schweigger, 1812) em cativeiro (Testudines, Chelidae). Grupo Estudos Ecológicos Série Documentos 1 (1): 1-19.         [ Links ]

HEWAVISENTHI, S. & J.C. PARMENTER. 2000. Hydric environment and sex determination in the flatback turtle (Natator depressus Garman) (Chelonia: Cheloniidae). Australian Journal of Zoology 48 (6): 653-659.         [ Links ]

KARDON, A. 1981. Captive reproduction in Geoffroy's side-necked turtle, Phrynops geoffroanus geoffroanus. International Zoo Yearbook 21 (1): 71-72. doi: 10.1111/j.1748-1090.1981. tb01947.x         [ Links ]

LISBOA, C.S.; S. CHINEN & F.B. MOLINA. 2004. Influência da temperatura no período de incubação dos ovos de Phrynops geoffroanus (Testudines, Chelidae). Arquivos do Instituto Biológico 71 (Supl.): 390-393.         [ Links ]

MARTINS, F.I.; F.L. SOUZA, & H.T.M. COSTA. 2010. Feeding habits of Phrynops geoffroanus (Chelidae) in an urban river in Central Brazil. Chelonian Conservation and Biology 9 (2): 294-297. doi: 10.2744/CCB-0809.1         [ Links ]

MEDEM, F. 1960. Informe sobre reptiles colombianos (V). Observaciones sobre la distribucion geografica y ecologia de la tortuga Phrynops geoffroana ssp. en Colombia. Novedades Colombianas 1 (5): 291-300.         [ Links ]

MCCORD, W.P.; M. JOSEPH-OUNI & W.W. LAMAR. 2001. A taxonomic reevaluation of Phrynops (Testudines: Chelidae) with the description of two new genera and a new species of Batrachemys. Revista de Biología Tropical 49 (2): 715-764.         [ Links ]

PACKARD, G.C. 1999. Water relations of chelonian eggs and embryos: is wetter better? American Zoologist 39 (2): 289-303.         [ Links ]

PEZZUTI, J.C.B. & R.C. VOGT. 1999. Nesting ecology of Podocnemis sextuberculata (Testudines, Pelomedusidae) in the Japurá River, Amazonas, Brazil. Chelonianian Conservation and Biology 3 (3): 419-424.         [ Links ]

PRITCHARD, P.C.H. & P. TREBBAU. 1984. The turtles of Venezuela. Oxford, Society for the Study of Amphibians and Reptiles, 403p.         [ Links ]

RHODIN, A.G.J. & R.A. MITTERMEIER. 1983. Description of Phrynops williamsi, a new species of Chelid turtle of the South American P. geoffroanus complex, p. 58-73. In: A.G.J. RHODIN & K. MIYATA (Eds). Advances in herpetology and evolutionary biology. Essays in honor of E.E. Williams. Cambridge, Museum of Comparative Zoology, 725p.         [ Links ]

RUEDA-ALMONACID, J.V.; J.L. CARR; R.A. MITTERMEIER; J.V. RODRÍGUEZMAHECHA; R.B. MAST; R.C. VOGT; A.G.J. RHODIN; J. OSSA-VELÁSQUEZ; J.N. RUEDA & C.G. MITTERMEIER. 2007. Las tortugas y los cocodrilianos de los países andinos del Trópico. Bogotá, Colombia, Conservación Internacional, 537p.         [ Links ]

SCHNEIDER, L.; C.R. FERRARA. & R.C. VOGT. 2009. Phrynops geoffroanus (Geofroy's Side Necked Turtle) nest predation. Herpetological Review 40: 436.         [ Links ]

SOUZA, F.L. 2005. Geographical distribution patterns of South American side-necked turtles (Chelidae), with emphasis on Brazilian species. Revista Española de Herpetología 19 (1): 33-46.         [ Links ]

SOUZA, F.L. & A.S. ABE. 2001. Population structure and reproductive aspects of the freshwater turtle, Phrynops geoffroanus, inhabiting an urban river in southeastern Brazil. Studies on Neotropical Fauna and Environment 36 (1): 57-62. doi: 10.1076/snfe.36.1.57.8887.         [ Links ]

SOUZA, F.L.; G.R. GIRALDELLI & T.A. MARTINS. 2006. Reproductive aspects of Brazilian side-necked-turtles (Chelidae). Boletin de la Asociacion Herpetologica Española 17 (1): 28-34.         [ Links ]

SOUZA, R.R. & R.C. VOGT. 1994. Incubation temperature influences sex and hatchling size in the neotropical turtle Podocnemis unifilis. Journal of Herpetology 28 (4): 453-464.         [ Links ]

VOGT, R.C. 2008. Tartarugas da Amazônia. Lima, Peru, Gráfica Biblos, 104p.         [ Links ]

 

 

Submitted: 25.VI.2011; Accepted: 13.VIII.2011.

 

 

Editorial responsibility: Diego Astúa de Moraes
1 Corresponding author. E-mail: pdfj@hotmail.com

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License