Water is an important limiting factor in the ecology of many animals, and even in rainforests, arboreal mammals, such as sloths, may have limited access to water sources. Here, we describe the spontaneous ingestion of water by a free-ranging three-toed sloth (Bradypus torquatus). The event occurred in the Ibura National Forest, in northeastern Brazil, where a sub-adult B. torquatus was monitored over three days in January, 2014. On the third day, the sloth was feeding on mature leaves and, at 16:22 h, it began raining heavily. Once the rain ceased, the sloth began to ingest the rainwater trickling down a vertical branch by licking it, and continued to ingest water for approximately 26 minutes. This behaviour indicates that the water was a valuable resource for this sloth, and sheds new light on the previous assumptions that these animals are able to satisfy their water requirements through their diet alone. This observation, together with an overview of the data on the ingestion of water by arboreal mammalian folivores, indicates that the direct ingestion of water may depend on specific local conditions, in particular, the availability of water sources, as well as the specific necessities of the mammal. As the lack of previous records of this behaviour in sloths is likely due to the cryptic behaviour of these animals, this finding highlights the importance of continuous, long-term behavioural monitoring for a more complete understanding of sloth ecology.
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Abreu, T.C.K., Rosa, C.A., Aximoff, I. & Passamani, M. (2017). New record of feeding behavior by the porcupine Coendou spinosus (F. Cuvier, 1823) in high-altitude grassland of the Brazilian Atlantic Forest. — Mammalia 81: 523-526.
Aguiar, L.M., Reis, N.R., Ludwig, G. & Rocha, V.J. (2003). Dieta, área de vida, vocalizações e estimativas populacionais de Alouatta guariba em um remanescente florestal no norte do estado do Paraná. — Neotrop. Primat. 11: 78.
Albuquerque, N.M., Silvestre, S.M., Cardoso, T.S., Ruiz-Esparza, J.M., Rocha, P.A., Beltrão-Mendes, R. & Ferrari, S.F. (2014). Capture of a common marmoset (Callithrix jacchus) by a capuchin monkey (Sapajus sp.) in the Ibura National Forest, Sergipe (Brazil). — Neotrop. Primat. 21: 218-221.
Altmann, J. (1974). Observational study of behavior: sampling methods. — Behaviour 49: 227-266.
Alvares, C.A., Stape, J.L., Sentelhas, P.C., Moraes, G., Leonardo, J. & Sparovek, G. (2013). Köppen’s climate classification map for Brazil. — Meteorol. Z. 22: 711-728.
Alvarez, S.J., Sanchez, A. & Carmona, M.M. (2004). Density, diet and habitat preference of the two-toed sloth Choloepus hoffmanni in an Andean Forest of Colombia. — Final Report, The Rufford Small Grant for Nature Conservation. Bogota, Colômbia, 13p.
Barreto, R.M.F. (2008). Uso do hábitat por preguiças-de-coleira Bradypus torquatus Illiger 1811, no sul da Bahia, Brasil. — Masters dissertation, Universidade Estadual Santa Cruz, Ilhéus.
Bauchop, T. & Martucci, R.W. (1968). Ruminant-like digestion of the langur monkey. — Science 161: 698-700.
Beltrão-Mendes, R., Cunha, M.A., Silva, C., Bastos, P.C.R., Ruiz-Esparza, J., Brandão, M.V., Rocha, P.A. & Ferrari, S.F. (2020). Non-volant mammals of the Ibura National Forest, northeastern Brazil. — Acta Sci. (Biol. Sci.) 42: e49958.
Bezerra, B.M., Souto, A.S., Halsey, L.G. & Schiel, N. (2008). Observation of brown-throated three-toed sloths: mating behaviour and the simultaneous nurturing of two young. — J. Ethol. 26: 175-178.
Bicca-Marques, J.C. (1992). Drinking behaviour in the black howler monkey (Alouatta caraya). — Folia Primatol. 58: 107-111.
Bonvicino, C.R. (1989). Ecologia e comportamento de Alouatta belzebul (Primates: Cebidae) na Mata Atlântica. — Rev. Nordest. Biol. 6: 149-179.
Britton, S.W. (1941). Form and function in the sloth. — Q. Rev. Biol. 16: 13-34.
Cassano, C.R. (2006). Ecologia e conservação da preguiça-de-coleira (Bradypus torquatus Illiger, 1811) no sul da Bahia. — Master dissertation, Universidade Estadual de Santa Cruz, Ilhéus.
Cassano, C.R., Kierulff, M.C.M. & Chiarello, A.G. (2011). The cacao agroforests of the Brazilian Atlantic forest as habitat for the endangered maned sloth Bradypus torquatus. — Mammal. Biol. 76: 243-250.
Castro-Vásquez, L., Meza, M., Plese, T. & Moreno-Mora, S. (2010). Activity patterns, preference and use of floristic resources by Bradypus variegatus in a tropical dry forest fragment, Santa Catalina, Bolívar, Colombia. — Edentata 11: 62-69.
Chagas, R.R.D., Souza-Alves, J.P., Jerusalinsky, L. & Ferrari, S.F. (2009). New records of Bradypus torquatus (Pilosa: Bradypodidae) from southern Sergipe, Brazil. — Edentata 10: 21-24.
Chapman, C. (1988). Patterns of foraging and range use by three species of Neotropical primates. — Primates 29: 177-194.
Chew, R.M. (1961). Water metabolism of desert-inhabiting vertebrates. — Biol. Rev. 36: 1-28.
Chiarello, A.G. (1992). Dieta, padrão de atividades e área de vida de um grupo de bugios (Alouatta fusca) na Reserva de Santa Genebra, Campinas, SP. — Masters dissertation, Universidade Estadual de Campinas.
Chiarello, A.G. (1998a). Activity budgets and ranging patterns of the Atlantic forest maned sloth Bradypus torquatus (Xenarthra: Bradypodidae). — J. Zool. 246: 1-10.
Chiarello, A.G. (1998b). Diet of the Atlantic forest maned sloth Bradypus torquatus (Xenarthra: Bradypodidae). — J. Zool. 246: 11-19.
Chiarello, A.G. (2008). Sloth ecology: an overview of field studies. — In: The biology of the Xenarthra (Vizcaíno, S.F. & Loughry, W.J., eds). University Press of Florida, Gainesville, FL, p. 269-280.
Chiarello, A.G., Passamani, M. & Zortéa, M. (1997). Field observations on the thin-spined porcupine, Chaetomys subspinosus (Rodentia; Echimyidae). — Mammalia 61: 29-36.
Chiarello, A.G., Chivers, D.J., Bassi, C., Maciel, M.A.F., Moreira, L.S. & Bazzalo, M. (2004). A translocation experiment for the conservation of maned sloths, Bradypus torquatus (Xenarthra, Bradypodidae). — Biol. Conserv. 118: 421-430.
Cliffe, R.N., Haupt, R.J., Avey-Arroyo, J.A. & Wilson, R.P. (2015). Sloths like it hot: ambient temperature modulates food intake in the brown-throated sloth (Bradypus variegatus). — PeerJ 3: e875.
Cliffe, R.N., Scantlebury, D.M., Kennedy, S.J., Avey-Arroyo, J.A., Mindich, D. & Wilson, R.P. (2018). The metabolic response of the Bradypus sloth to temperature. — PeerJ 6: e5600.
Clifton, I.D. (2010). High koala mortality associated with low browse moisture in tropical environments. — Austral. Mammal. 32: 157-159.
Coelho, A.M., Bramblett, C.A., Quick, L.B. & Bramblett, S.S. (1976). Resource availability and population density in primates: a socio-bioenergetic analysis of the energy budgets of Guatemalan howler and spider monkeys. — Primates 17: 63-80.
Cork, S.J., Hume, I.D. & Dawson, T.J. (1983). Digestion and metabolism of a natural foliar diet (Eucalyptus punctata) by an arboreal marsupial, the koala (Phascolarctos cinereus). — J. Comp. Physiol. 153: 181-190.
Davies, A.G., Bennett, E.L. & Waterman, P.G. (1988). Food selection by two South-east Asian colobine monkeys (Presbytis rubicunda and Presbytis melalophos) in relation to plant chemistry. — Biol. J. Linn. Soc. 34: 33-56.
Decker, B.S. (1994). Effects of habitat disturbance on the behavioral ecology and demographics of the Tana River red colobus (Colobus badius rufomitratus). — Int. J. Primatol. 15: 703.
Degabriele, R. & Dawson, T.J. (1979). Metabolism and heat balance in an arboreal marsupial, the koala (Phascolarctos cinereus). — J. Comp. Physiol. B: Bioch. Syst. Environm. Physiol. 134: 293-301.
Dias, P.A.D., Rangel-Negrín, A., Coyohua-Fuentes, A. & Canales-Espinosa, D. (2014). Factors affecting the drinking behavior of black howler monkeys (Alouatta pigra). — Primates 55: 1-5.
Ellis, W., Melzer, A., Clifton, I. & Carrick, F. (2010). Climate change and the koala Phascolarctos cinereus: water and energy. — Austral. Zool. 35: 369-377.
Ellis, W., Melzer, A., Green, B., Newgrain, K., Hindell, M.A. & Carrick, F.N. (1995). Seasonal-variation in water flux, field metabolic-rate and food-consumption of free-ranging koalas (Phascolarctos cinereus). — Austral. J. Zool. 43: 59-68.
Falconi, N., Vieira, E.M., Baumgarten, J., Faria, D. & Giné, G.A.F. (2015). The home range and multi-scale habitat selection of the threatened maned three-toed sloth (Bradypus torquatus). — Mammal. Biol. 80: 431-439.
Ferrari, S.F. (1991). An observation of western black spider monkeys, Ateles paniscus chamek, utilizing an arboreal water source. — Biotropica 23: 307-308.
Foley, W.J., Engelhardt, W.V. & Charles-Dominique, P. (1995). The passage of digesta, particle size, and in vitro fermentation rate in the three-toed sloth Bradypus tridactylus (Edentata: Bradypodidae). — J. Zool. 236: 681-696.
Gaulin, S.J., Knight, D.H. & Gaulin, C.K. (1980). Local variance in Alouatta group size and food availability on Barro Colorado Island. — Biotropica 12: 137-143.
Gilbert, K. & Stouffer, P.C. (1989). Use of a ground water source by mantled howler monkeys (Alouatta palliata). — Biotropica 21: 380.
Gilmore, D.P., Da-Costa, C.P. & Duarte, D.P.F. (2000). An update on the physiology of two-and three-toed sloths. — Braz. J. Med. Biol. Res. 33: 129-146.
Gilmore, D.P., Duarte, D.P.F. & Costa, C.P. (2008). The physiology of two- and three-toed sloths. — In: The biology of the Xenarthra (Vizcaíno, S.F. & Loughry, W.J., eds). University Press of Florida, Gainesville, p. 130-142.
Giné, G.A.F. (2009). Ecologia e comportamento do ouriço–preto (Chaetomys subspinosus, Olfers 1818) em fragmentos de Mata Atlântica do município de Ilhéus, sul da Bahia. — Doctoral dissertation, Universidade de São Paulo.
Giné, G.A.F., Cassano, C.R., Almeida, S.S. & Faria, D. (2015). Activity budget, pattern and rhythm of maned sloths (Bradypus torquatus): responses to variations in ambient temperature. — Mammal. Biol. 80: 459-467.
Giné, G.A.F., Duarte, J.M.B. & Faria, D. (2010). Feeding ecology of a selective folivore, the thin-spined porcupine (Chaetomys subspinosus) in the Atlantic forest. — J. Mammal. 91: 931-941.
Giné, G.A.F., Duarte, J.M.B., Motta, T.C.S. & Faria, D. (2012). Activity, movement and secretive behavior of a threatened arboreal folivore, the thin-spined porcupine, in the Atlantic forest of southern Bahia, Brazil. — J. Zool. 286: 131-139.
Giudice, A.M. & Mudry, M.D. (2000). Drinking behavior in the black howler monkey (Alouatta caraya). — Zoocriaderos 3: 11-19.
Glander, K.E. (1978). Drinking from arboreal water sources by mantled howling monkeys (Alouatta palliata Gray). — Folia Primatol. 29: 206-217.
Gouveia, S.F., Villalobos, F., Dobrovolski, R., Beltrão-Mendes, R. & Ferrari, S.F. (2014). Forest structure drives global diversity of primates. — J. Anim. Ecol. 83: 1523-1530.
Harrop, C.J.F. & Degabriele, R. (1976). Digestion and nitrogen metabolism in the koala, Phascolarctos cinereus. — Austral. J. Zool. 24: 201-215.
Hirsch, A. & Chiarello, A.G. (2012). The endangered maned sloth Bradypus torquatus of the Brazilian Atlantic forest: a review and update of geographical distribution and habitat preferences. — Mammal Rev. 42: 35-54.
Lara-Ruiz, P. & Chiarello, A.G. (2005). Life-history traits and sexual dimorphism of the Atlantic forest maned sloth Bradypus torquatus (Xenarthra: Bradypodidae). — J. Zool. 267: 63-73.
Lunney, D., Crowther, M.S., Wallis, I., Foley, W.J., Lemon, J., Wheeler, R., Madani, G., Orscheg, C., Griffith, J.E., Krockenberger, M., Retamales, M. & Stalenberg, E. (2012). Koalas and climate change: a case study on the Liverpool Plains, north-west New South Wales. — In: Wildlife and climate change: towards robust conservation strategies for Australian fauna (Lunney, D. & Hutchings, P., eds). Royal Zoological Society of New South Wales, Mosman, NSW, p. 150-168.
McNab, B.K. (1978). Energetics of arboreal folivores: physiological problems and ecological consequences of feeding on an ubiquitous food supply. — In: The ecology of arboreal folivores (Montgomery, G.G., ed.). Smithsonian University Press, Washington, DC, p. 153-162.
Mella, V.S., McArthur, C., Krockenberger, M.B., Frend, R. & Crowther, M.S. (2019). Needing a drink: rainfall and temperature drive the use of free water by a threatened arboreal folivore. — PLoS ONE 14: e0216964.
Mella, V.S., Orr, C., Hall, L., Velasco, S. & Madani, G. (2020). An insight into natural koala drinking behaviour. — Ethology 126: 858-863.
Mendel, F.C. (1985). Use of hands and feet of three-toed sloths (Bradypus variegatus) during climbing and terrestrial locomotion. — J. Mammal. 66: 359-366.
Mendes, S.L. (1989). Estudo ecológico de Alouatta fusca (Primates: Cebidae) na Estação Biológica de Caratinga, MG. — Rev. Nordest. Biol. 6: 71-104.
Meritt, D.A. (1985). The two-toed Hoffmann’s sloth, Choloepus hoffmanni Peters. — In: The evolution and ecology of armadillos, sloths, and vermilinguas (Montgomery, G.G., ed.). Smithsonian Institution Press, Washington, DC, p. 333-341.
Milton, K. (1979). Factors influencing leaf choice by howler monkeys: a test of some hypotheses of food selection by generalist herbivores. — Am. Nat. 114: 362-378.
Miranda, J.M., Moro-Rios, R.F., Bernardi, I.P. & Passos, F.C. (2005). Formas não usuais para a obtenção de água por Alouatta guariba clamitans em ambiente de floresta com Araucária no Sul do Brasil. — Neotrop. Primat. 13: 21-24.
Miranda, J.M. & Passos, F.C. (2004). Hábito alimentar de Alouatta guariba (Humboldt) (Primates, Atelidae) em Floresta de Araucária, Paraná, Brasil. — Rev. Bras. Zool. 21: 821-826.
Moreira, D.O., Leite, G.R., Siqueira, M.F., Coutinho, B.R., Zanon, M.S. & Mendes, S.L. (2014). The distributional ecology of the maned sloth: environmental influences on its distribution and gaps in knowledge. — PLoS ONE 9: e110929.
Moro-Rios, R.F., Serur-Santos, C.S., Miranda, J.M. & Passos, F.C. (2008). Obtenção de água por um grupo de Alouatta clamitans (Primates: Atelidae), em Floresta com Araucária: variações sazonais, sexo-etárias e circadianas. — Rev. Bras. Zool. 25: 558-562.
Moura Filho, A.G., Huggins, S.E. & Lines, S.G. (1983). Sleep and waking in the three-toed sloth, Bradypus tridactylus. — Comp. Biochem. Physiol. A: Physiol. 76: 345-355.
Nagy, K.A. & Martin, R.W. (1985). Field metabolic rate, water flux, food consumption and time budget of koalas, Phascolarctos cinereus (Marsupialia: Phascolarctidae) in Victoria. — Austral. J. Zool. 33: 655-665.
Nagy, K.A. & Montgomery, G.G. (1980). Field metabolic rate, water flux, and food consumption in three-toed sloths (Bradypus variegatus). — J. Mammal. 61: 465-472.
Neam, K.D. & Lacher Jr., T.E. (2015). Spatial distribution, resource use, and behavior of brown-throated sloths (Bradypus variegatus) in a multi-use landscape. — Edentata 46: 46-56.
Nicolson, S.W. (1980). Water balance and osmoregulation in Onymacris plana, a tenebrionid beetle from the Namib Desert. — J. Insect Physiol. 26: 315-320.
Novotny, V., Drozd, P., Miller, S.E., Kulfan, M., Janda, M., Basset, Y. & Weiblen, G.D. (2006). Why are there so many species of herbivorous insects in tropical rainforests?. — Science 313: 1115-1118.
Nowak, K. (2008). Frequent water drinking by Zanzibar red colobus (Procolobus kirkii) in a mangrove forest refuge. — Am. J. Primatol. 70: 1081-1092.
Nyakatura, J.A. (2012). The convergent evolution of suspensory posture and locomotion in tree sloths. — J. Mammal. Evol. 19: 225-234.
Oliveira, P.A. (2006). Ecologia de fêmeas de ouriço-preto Chaetomys subspinosus (Olfers 1818) (Rodentia: Erethizontidae) nas florestas de restinga do Parque Estadual Paulo César Vinha, Guarapari, Espírito Santo. — Master dissertation, Pontifícia Universidade Católica de Minas Gerais, Belo Horizonte.
Oliveira, P.A., Lima, R.B.S. & Chiarello, A.G. (2012). Home range, movements and diurnal roosts of the endangered thin-spined porcupine, Chaetomys subspinosus (Rodentia: Erethizontidae): in the Brazilian Atlantic Forest. — Mammal. Biol. 77: 97-107.
Passamani, M. (2010). Use of space and activity pattern of Sphiggurus villosus (F. Cuvier, 1823) from Brazil (Rodentia: Erethizontidae). — Mammal. Biol. 75: 455.
Pauli, J.N., Peery, M.Z., Fountain, E.D. & Karasov, W.H. (2016). Arboreal folivores limit their energetic output, all the way to slothfulness. — Am. Nat. 188: 196-204.
Queiroz, H.L. (1995). Preguiças e guaribas: os mamíferos folívoros arborícolas do Mamirauá. — Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), e Sociedade Civil Mamirauá, Brasília.
Santana, J.P., Rocha, P.A., Oliveira, E.V.S., Prata, A.P.N. & Ribeiro, A.S. (2018). Phenological patterns of zoochoric shrub and tree species in two areas of Ibura National Forest, Northeastern Brazil. — Neotrop. Biol. Conserv. 13: 212-223. https://doi.org/10.4013/nbc.2018.133.04
Santana, J.P., Rocha, P.A., Silva, T.R., Ribeiro, A.S. & Prata, A.P.N. (2017). Floristic characterization of Ibura National Forest, Sergipe, Brazil. — Biosci. J. 33: 447-464.
Schmidt-Nielsen, K. (1964). Desert animals: physiological problems of heat and water. — Clarendon Press, Oxford.
Serio-Silva, J.C. & Rico-Gray, V. (2000). Use of a stream by Mexican howler monkeys. — Southwest. Nat. 45: 332-333.
Silva, S.M., Clozato, C.L., Moraes-Barros, N. & Morgante, J.S. (2013). Towards a standard framework to describe behaviours in the common-sloth (Bradypus variegatus Schinz, 1825): novel interactions data observed in distinct fragments of the Atlantic forest, Brazil. — Braz. J. Biol. 73: 527-531.
Souto-Lima, R.B., Oliveira, P.A. & Chiarello, A.G. (2010). Diet of the thin-spined porcupine (Chaetomys subspinosus): an Atlantic forest endemic threatened with extinction in southeastern Brazil. — Mammal. Biol. 75: 538-546.
Starin, E.D. (2002). Drinking observations in Temminck’s red colobus. — Folia Primatol. 73: 137.
Steinmetz, S. (2001). Drinking by howler monkeys (Alouatta fusca) and its seasonality at the Intervales State Park, São Paulo, Brazil. — Neotrop. Primat. 9: 111-112.
Sullivan, B.J., Baxter, G.S. & Lisle, A.T. (2003). Low-density koala (Phascolarctos cinereus) populations in the Mulgalands of southwest Queensland. III. Broad-scale patterns of habitat use. — Wildl. Res. 30: 583-591.
Sunquist, M.E. & Montgomery, G.G. (1973). Activity patterns and rates of movement of two-toed and three-toed sloths (Choloepus hoffmanni and Bradypus infuscatus). — J. Mammal. 54: 946-954.
Urbani, B. & Bosque, C. (2007). Feeding ecology and postural behaviour of the three-toed sloth (Bradypus variegatus flaccidus) in northern Venezuela. — Mammal. Biol. 72: 321-329.
Weir, J.T. & Schluter, D. (2007). The latitudinal gradient in recent speciation and extinction rates of birds and mammals. — Science 315: 1574-1576.
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Water is an important limiting factor in the ecology of many animals, and even in rainforests, arboreal mammals, such as sloths, may have limited access to water sources. Here, we describe the spontaneous ingestion of water by a free-ranging three-toed sloth (Bradypus torquatus). The event occurred in the Ibura National Forest, in northeastern Brazil, where a sub-adult B. torquatus was monitored over three days in January, 2014. On the third day, the sloth was feeding on mature leaves and, at 16:22 h, it began raining heavily. Once the rain ceased, the sloth began to ingest the rainwater trickling down a vertical branch by licking it, and continued to ingest water for approximately 26 minutes. This behaviour indicates that the water was a valuable resource for this sloth, and sheds new light on the previous assumptions that these animals are able to satisfy their water requirements through their diet alone. This observation, together with an overview of the data on the ingestion of water by arboreal mammalian folivores, indicates that the direct ingestion of water may depend on specific local conditions, in particular, the availability of water sources, as well as the specific necessities of the mammal. As the lack of previous records of this behaviour in sloths is likely due to the cryptic behaviour of these animals, this finding highlights the importance of continuous, long-term behavioural monitoring for a more complete understanding of sloth ecology.
| All Time | Past 365 days | Past 30 Days | |
|---|---|---|---|
| Abstract Views | 1467 | 271 | 10 |
| Full Text Views | 55 | 5 | 0 |
| PDF Views & Downloads | 83 | 10 | 0 |