NOTES AND COMMENTS
Lateralized behavior in Guiana dolphins, Sotalia guianensis, at Pipa Beach, RN, Brazil
Casagrande, T.I; Lunardi, VO.II; Lunardi, DG.II,* * e-mail: firstname.lastname@example.org
IInstitute of Life Sciences, Universidade Federal de Alfenas UNIFAL, Alfenas, MG, Brazil
IIEvolutionary and Molecular Ecology Laboratory, Universidade Federal Rural do Semiárido UFERSA, Mossoró, RN, Brazil
Lateralized behavior patterns are those in which an animal shows a consistent preference for the use of one of the sides. The existence of population-level behavioral asymmetries in non-human species and their implications for the evolution of the brain are very controversial. In the last years, however, several studies have reported the existence of lateralization of brain functions among mammals, birds (see Walker, 1980), fishes, reptiles and amphibians (Bisazza et al., 1998).
In this study, we report data on possible behavioral asymmetries at the population level in Guiana dolphins, Sotalia guianensis van Bénéden, 1864, at Madeiro Bay, Pipa Beach (6° 13' S and 35° 04' W), southern of Rio Grande do Norte, Brazil. Our aim in this study was investigate whether Guiana dolphin individuals showed significant bias concerning direction of performance (right or left) in three active behavioral events. We studied three active behavior to test evidence of directional bias: (i) Breaching: the dolphin jumps out of the water, spinning on its longitudinal axis in one direction; (ii) Flippering: the dolphin raises one flipper (right or left) into the air and shows or slaps it on the water surface; and (iii) Tail slap: the dolphin hurls its tail out of the water. Only breaches and tail slaps to the right or to the left was included in this analysis. Data on these three active behaviors were recorded in the field from a land base, approximately 25 m above sea level, in January and February 2012. Using focal groups 2-minutes scan sampling method, the predominant group behavior was recorded as one of five mutually exclusive states: foraging, feeding, traveling, socializing and resting (Lunardi, 2011). Three size classes were used: adult, juvenile and calf (about ¾ and ½ of the body length of an adult animal, respectively). We tested data for significant directional bias using chi-squared tests. Analyses were performed with PASW 18 (SPSS Inc, Chicago, USA).
We observed 190 active behavioral events for 28 sampling days, for a total of 224 h of effort, in which dolphins were present for 148.4 hours. Only one of the three active behavioral events was lateralized: the majority of breaching events (63%) showed a bias to the right (χ2 = 10.7, df = 1, n = 157, p = 0.001). Flippering and tail slap events were rare (n = 23 and n = 10) and were not lateralized (χ2flippering = 2.1, df = 1, p = 0.14; χ2tail slap = 0.0, df = 1, p = 1). Lateralized events were observed only during three behavioral states: foraging, feeding and socializing. Although the foraging has been the predominant behavior according to the activity budget, lateralized events (breaching) were more common during the socializing (p < 0.001, Figure 1a). Groups composed solely of adults were more frequent throughout the study period, and the lateralized events followed this pattern, being more common in this type of group composition (Figure 1b).
Evidence of a population-level of lateralized behavior has been reported for several cetacean species as: humpback whales, Megaptera novaeangliae Borowski, 1781 (breaching, bottom-feeding and flipper slaps: Clapham et al., 1995), bottlenose dolphins, Tursiops truncatus Montagu, 1821 (visual lateralization: Yaman et al., 2003) and striped dolphins, Stenella coeruleoalba Meyen, 1833 (visual lateralization: Siniscalchi et al., 2012). Guiana dolphins also showed a bias to the right during the breaching. Thus, this study contributes to the growing evidence for behavioral laterality in cetaceans. Overall, our data suggest that Guiana dolphins exhibit some behavioral asymmetries at the population level, and possibly an asymmetry of somatosensory or a motor function, similar to other cetaceans.
Acknowledgements We thank to Maria Ercília Lunardi for her careful revision of English.
Received April 25, 2012
Accepted September 16, 2012
Distributed February 28, 2013
- BISAZZA, A., ROGERS, LJ. and VALLORTIGARA, G., 1998. The origins of cerebral asymmetry: A review of evidence of behavioural and brain lateralization in fishes, reptiles and amphibians. Neuroscience and Biobehavioral Reviews, vol. 22, n. 3, p. 411-426.
- CLAPHAM, PJ., LEIMKUHLER, E., GRAY, BK. and MATTILA, DK., 1995. Do humpback whales exhibit lateralized behaviour? Animal Behavior, vol. 50, n. 1, p. 73-82. http://dx.doi.org/10.1006/anbe.1995.0222
- LUNARDI, DG., 2011. Comportamento social de botos-cinza, Sotalia guianensis, na praia de Pipa, RN, Brasil: dinâmica, sequência, sincronia e respostas ao turismo de observação. Natal: Universidade Federal do Rio Grande do Norte. 151 p.
- SINISCALCHI, M., DIMATTEO, S., PEPE, AM., SASSO, R. and QUARANTA, A., 2012. Visual lateralization in wild striped dolphins (Stenella coeruleoalba) in response to stimuli with different degrees of familiarity. PloS ONE, vol. 7, e30001. http://dx.doi.org/10.1371/journal.pone.0030001
- WALKER, SF., 1980. Lateralization of functions in the vertebrate brain: A review. British Journal of Psychology, vol. 71, n. 3, p. 329-367. http://dx.doi.org/10.1111/j.2044-8295.1980.tb01750.x
- YAMAN, S., VON FERSEN, L., DEHNHARDT, G. and GÜNTÜRKÜN, O., 2003. Visual lateralization in the bottlenose dolphin (Tursiops truncatus): evidence for a population asymmetry? Behavioural Brain Research, vol. 142, n. 1-2, p. 109-114. http://dx.doi.org/10.1016/S0166-4328(02)00385-6
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