See you later: roost fidelity of the “Boomerang Bats”, Artibeus lituratus (Olfers, 1818) (Mammalia, Chiroptera)

Carolina Blefari  Batista; Alan Deivid Pereira; Guilherme de Toledo Figueiredo; Isaac Passos de Lima

doi:10.5433/1679-0367.2024v45n1p27

Autores/as

Carolina Blefari Batista Universidade Federal de Goiás - UFG https://orcid.org/0000-0002-5927-8184
Alan Deivid Pereira Universidade Estadual do Paraná - Unespar https://orcid.org/0000-0002-3182-2344
Guilherme de Toledo Figueiredo Universidade Estadual do Norte do Paraná - UENP https://orcid.org/0000-0002-8020-9829
Isaac Passos de Lima Universidade Federal Rural do Rio de Janeiro https://orcid.org/0000-0002-5684-5067

DOI:

https://doi.org/10.5433/1679-0367.2024v45n1p27

Palabras clave:

Chiroptera, Female, Aggregation, Roost ecology

Resumen

Animals exhibit sociability behaviors and spatial use patterns that are important for species survival. Bats are animals that exhibit complex patterns of aggregation of individuals, which can vary according to sex and age. Aggregation can be explained by active or passive mechanisms. In this behavioural note, we report a group of female Artibeus lituratus in the reproductive stage that exhibits aggregation behavior supporting the active mechanism hypothesis. The females returned to the same roost, for two reproductive season, maintaining the aggregation with the same individuals with which the social bonds were already established.

Descargas

Los datos de descargas todavía no están disponibles.

Biografía del autor/a

Carolina Blefari Batista, Universidade Federal de Goiás - UFG

PhD in Biological Sciences from the Universidade Estadual de Londrina (UEL), Londrina, Paraná, Brazil. Postdoctoral student in the Department of General Biology of the Institute of Biological Sciences (ICB) of the Universidade Federal de Goiás (UFG), Goiânia, Goiás.

Alan Deivid Pereira, Universidade Estadual do Paraná - Unespar

PhD in Biological Sciences from the Universidade Estadual de Londrina (UEL), Londrina, Paraná, Brazil. Collaborating Professor at the Universidade Estadual do Paraná (Unespar), União da Vitória, Paraná

Guilherme de Toledo Figueiredo, Universidade Estadual do Norte do Paraná - UENP

PhD in Biological Sciences from the Universidade Estadual de Londrina (UEL), Londrina, Paraná, Brazil. Professor at the Center for Human Sciences and Education at the Universidade Estadual do Norte do Paraná (UENP), Jacarezinho, Paraná

Isaac Passos de Lima, Universidade Federal Rural do Rio de Janeiro

PhD in Animal Biology from the Universidade Federal Rural do Rio de Janeiro (UFRRJ), Seropédica, Rio de Janeiro, Brazil. Associate Researcher at the Mastozoology Laboratory of the Institute of Biological and Health Sciences (ICBS) at the Universidade Federal Rural do Rio de Janeiro (UFRRJ), Seropédica, Rio de Janeiro

Citas

Allen GM. Bats. Massachusetts: Harvard University Press; 1939.

Barclay RMR, Harder LD. Life histories of bats: lifein the slow lane. In: Kunz TH, Fenton MB, editors. Ecology. Chicago: University of Chicago Pres; 2003. p. 209-53.

Batista CB, Reis NR, Rezende MI. Nutritional content of bat-consumed fruits in a forest fragment in Southern Brazil. Braz J Biol. 2017;77(2):244-50. doi: 10.1590/1519-6984.10115. DOI: https://doi.org/10.1590/1519-6984.10115

Berger-Tal O, Polak T, Oron A, Lubin Y, Kotler BP, Saltz D. Integrating animal behavior and conservation biology: a conceptual framework. Behav Ecol. 2011;22:236-9. doi: 10.1093/beheco/arq224. DOI: https://doi.org/10.1093/beheco/arq224

Bonaccorso RJ, Arends A, Genoud M, Cantoni D, Morton T. Thermal ecology of moustached and ghost-faced bats (Mormoopidae) in Venezuela. J Mammal. 1992;73:365-78. doi: 10.2307/1382071. DOI: https://doi.org/10.2307/1382071

Burland TM, Wilmer JW. Seeing in the dark: Molecular approaches to the study of bat populations. Biological Reviews. 2001;76:389-409. doi: 10.1017/S1464793101005747. DOI: https://doi.org/10.1017/S1464793101005747

Campbell P, Akbar Z, Adnan AM, Kunz TH. Resource distribution and social structure in harem-forming Old World fruit bats: variations on a polygynous theme. Animal Behav. 2006;72:687-98. doi: 10.1016/j.anbehav.2006.03.002. DOI: https://doi.org/10.1016/j.anbehav.2006.03.002

Chaverri G, Kunz TH. Response of a bat specialist to the loss of a critical resource. PLoS ONE. 2011;6:e28821. doi: 10.1371/journal.pone.0028821. DOI: https://doi.org/10.1371/journal.pone.0028821

Davis W H, Hitchcock HB. Biology and migration of the bat, Myotis lucifugus, in New England. J Mammal. 1965;46(2):296e313. doi: 10.2307/1377850. DOI: https://doi.org/10.2307/1377850

Esbérard C. Diversidade de morcegos em área de Mata Atlântica regenerada no Sudeste do Brasil. Revista Brasileira de Zoociências. 2003;5(2):189-204.

Fenton MB, Rautenbach IL, Smith SE, Swanepoel CM, Grosell J, van Jaarsveld J. Raptors and bats: threats and opportunities. Animal Behav. 1994;48:9-18. doi: 10.1006/anbe.1994.1207. DOI: https://doi.org/10.1006/anbe.1994.1207

Fenton MB, Simmons N. Bats: a world of science and mystery. Chicago: The University of Chicago Press; 2014. DOI: https://doi.org/10.7208/chicago/9780226065267.001.0001

Fenton MB. Summer activity of Myotis lucifugus (Chiroptera:Vespertilionidae) at hibernacula in Ontario and Quebec. Can J Zool. 1969;47(4):597e602. doi: 10.1139/z69-103. DOI: https://doi.org/10.1139/z69-103

Frère CH, Krützen M, Mann J, Watson-Capps JJ, Tsai YJ, Patterson EM, et al. Home range overlap, matrilineal and biparental kinship drive female associations in bottlenose dolphins. Animal Behav. 2010;80 (3):481e486. doi: 10.1016/j.anbehav.2010.06.007. DOI: https://doi.org/10.1016/j.anbehav.2010.06.007

Garbino GST, Tavares VC. Roosting ecology of Stenodermatinae bats (Phyllostomidae): evolution of foliage roosting and correlated phenotypes. Mamm Rev. 2018;48(2):75-89. doi: 10.1111/mam.12114. DOI: https://doi.org/10.1111/mam.12114

Gomes MN, Uieda W, Latorre MDDD. Influence of sex differences in the same colony for chemical control of vampire Desmodus rotundus (Phyllostomidae) populations in the state of Sao Paulo, Brazil. Pesq Vet Bras. 2006;26:38-43. doi: 10.1590/S0100-736X2006000100008. DOI: https://doi.org/10.1590/S0100-736X2006000100008

Goodenough J, McGuire B, Jakob E. Perspectives on animal behaviour. 3rd ed. New York: Wiley; 2010.

Guedes PG, Silva SSP, Santos KS, Carneiro AMS, Lopes LS, Carvalho JF. Padrão reprodutivo, dieta e parasitologia de Artibeus lituratus (Olfers, 1818) (Mammalia, Chiroptera) em parques urbanos do município do rio de Janeiro (Rio de Janeiro, Brasil). Biotemas. 2020;33(2):1-16. doi: 10.5007/2175-7925.2020.e70047. DOI: https://doi.org/10.5007/2175-7925.2020.e70047

Kalka MB, Smith AR, Kalko EK. Bats limit arthropods and herbivory in a tropical forest. Science. 2008;320(5872):71. doi:10.1126/science.1153352. DOI: https://doi.org/10.1126/science.1153352

Kerth G, Kiefer A, Trappmann C, Weishaar M. High gene diversity at swarming sites suggests hot spots for gene flow in the endangered Bechstein’s bat. Conserv Genet. 2003;4:491-9. doi: 10.1023/A:1024771713152. DOI: https://doi.org/10.1023/A:1024771713152

Kerth G, Morf L. Behavioural and genetic data suggest that Bechstein’s bats predominantly mate outside the breeding habitat. Ethology. 2004;110:987-99. doi: 10.1111/j.1439-0310.2004.01040.x. DOI: https://doi.org/10.1111/j.1439-0310.2004.01040.x

Kerth G, Perony N, Schweitzer F. Bats are able to maintain long-term social relationships despite the high fission-fusion dynamics of their groups. Proc Royal Soc B. 2011;278(1719):2761-7. doi: 10. 1098/ rspb. 2010. 2718. DOI: https://doi.org/10.1098/rspb.2010.2718

Kerth G. Causes and consequences of sociality in bats. BioScience. 2008;58(8):737-46. doi: 10.1641/B580810. DOI: https://doi.org/10.1641/B580810

Kunz TH, Hood WR. Parental care and postnatal growth in the Chiroptera. In: Krutzsch PH, Creighton EG, editors. Reproductive biology of bats. New York: Academic Press; 2000. p. 415-68. DOI: https://doi.org/10.1016/B978-012195670-7/50011-4

Kunz TH. Roosting ecology of bats. In: Kunz TH, editor. Ecology of bats. New York: Plenum Press; 1982. p. 1-55. DOI: https://doi.org/10.1007/978-1-4613-3421-7_1

Lewis SE. Roost fidelity of bats: a review. J Mammal. 1995;76:481-96. doi: doi.org/10.2307/1382357. DOI: https://doi.org/10.2307/1382357

Lopes EV, Anjos LA. Composição da avifauna do campus da Universidade Estadual de Londrina, norte do Paraná, Brasil. Rev Bras Zool. 2006;23(1):145-56. doi: 10.1590/S0101-81752006000100006. DOI: https://doi.org/10.1590/S0101-81752006000100006

McCracken GF, Bradbury JW. Social organization and kinship in the polygynous bat Phyllostomus hastatus. Behav Ecol Sociobiol. 1981;8:1-34. doi: 10.1007/BF00302840. DOI: https://doi.org/10.1007/BF00302840

McCracken GF, Wilkinson GS. Bat mating systems. In: Crichton EG, Krutzsch PH, editors. Reproductive biology of bats. San Diego: Academic Press; 2000. p. 321-62. DOI: https://doi.org/10.1016/B978-012195670-7/50009-6

Santana SE, Dial TO, Eiting TP, Alfaro ME. Roosting ecology and the evolution of pelage markings in bats. PLoS ONE. 2011;6:e25845. doi: 10.1371/journal.pone.0025845. DOI: https://doi.org/10.1371/journal.pone.0025845

Silveira M. A vegetação do Parque EstadualMata dos Godoy. In: Torezan JM, organizador. Ecologia do Parque Estadual Matado Godoy. Londrina: Itedes, 2006. p. 19-27.

Sunga J, Webber KMR, Humber J, Rodrigues B, Broders HG. Roost fidelity partially explains maternity roosting association patterns in Myotis lucifugus. Animal Behav. 2022;194. doi: 10.1016/j.anbehav.2022.09.008. DOI: https://doi.org/10.1016/j.anbehav.2022.09.008

Vicente RF. O Parque Estadual Mata dosGodoy. In: Torezan JM, organizador. Ecologia do Parque Estadual Mata dos Godoy. Londrina: Itedes; 2006. p. 13-8.

Voss RS, Fleck DW, Strauss RE, Velazco PM, Simmons NB. Roosting ecology of Amazonian bats: evidence for guild structure in hyperdiverse mammalian communities. Am Mus Novit. 2016;3870:1-43. doi: 10.1206/3870.1. DOI: https://doi.org/10.1206/3870.1

Wilkinson GS. Reciprocal food sharing in the vampire bat. Nature. 1984;308:181-4. doi:10.1038/308181a0. DOI: https://doi.org/10.1038/308181a0