» Articles » PMID: 25861559

Sloths Like It Hot: Ambient Temperature Modulates Food Intake in the Brown-throated Sloth (Bradypus Variegatus)

Overview
Journal PeerJ
Date 2015 Apr 11
PMID 25861559
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Sloths are considered to have one of the lowest mass-specific metabolic rates of any mammal and, in tandem with a slow digestive rate, have been theorized to have correspondingly low rates of ingestion. Here, we show in a study conducted over five months, that three captive Bradypus variegatus (Brown-throated sloths) had a remarkably low mean food intake of 17 g kg(-1)day(-1) (SD 4.2). Food consumption was significantly affected by ambient temperature, with increased intake at higher temperatures. We suggest that the known fluctuation of sloth core body temperature with ambient temperature affects the rate at which gut fauna process digesta, allowing for increased rates of fermentation at higher temperatures. Since Bradypus sloths maintain a constantly full stomach, faster rates of fermentation should enhance digestive throughput, increasing the capacity for higher levels of food intake, thereby allowing increased energy acquisition at higher ambient temperatures. This contrasts with other mammals, which tend to show increased levels of food intake in colder conditions, and points to the importance of temperature in regulating all aspects of energy use in sloths.

Citing Articles

Metabolic skinflint or spendthrift? Insights into ground sloth integument and thermophysiology revealed by biophysical modeling and clumped isotope paleothermometry.

Deak M, Porter W, Mathewson P, Lovelace D, Flores R, Tripati A J Mamm Evol. 2025; 32(1):1.

PMID: 39822851 PMC: 11732909. DOI: 10.1007/s10914-024-09743-2.


Sloth metabolism may make survival untenable under climate change scenarios.

Cliffe R, Ewart H, Scantlebury D, Kennedy S, Avey-Arroyo J, Mindich D PeerJ. 2024; 12:e18168.

PMID: 39351373 PMC: 11441404. DOI: 10.7717/peerj.18168.


Nutritive Value and Degradation Kinetic Parameters of Three Plants for Feeding Schinz, In Vitro Evaluation.

Maximo I, Nascimento J, de Andrade G, Izidro J, de Albuquerque P, do Nascimento D Animals (Basel). 2024; 14(18).

PMID: 39335235 PMC: 11429112. DOI: 10.3390/ani14182645.


Fatal gastric amebiasis in a Linnaeus's two-toed sloth associated with infection.

Lee J, Braden M, Armien Medianero A, Uzal F, Li G, Paulsen D J Vet Diagn Invest. 2024; 36(6):915-920.

PMID: 39165089 PMC: 11529145. DOI: 10.1177/10406387241268315.


The behaviour and activity budgets of two sympatric sloths; and .

Cliffe R, Haupt R, Kennedy S, Felton C, Williams H, Avey-Arroyo J PeerJ. 2023; 11:e15430.

PMID: 37273542 PMC: 10234273. DOI: 10.7717/peerj.15430.


References
1.
Sikes R . 2016 Guidelines of the American Society of Mammalogists for the use of wild mammals in research and education. J Mammal. 2018; 97(3):663-688. PMC: 5909806. DOI: 10.1093/jmammal/gyw078. View

2.
Gillooly J, Brown J, WEST G, Savage V, Charnov E . Effects of size and temperature on metabolic rate. Science. 2001; 293(5538):2248-51. DOI: 10.1126/science.1061967. View

3.
Cliffe R, Avey-Arroyo J, Arroyo F, Holton M, Wilson R . Mitigating the squash effect: sloths breathe easily upside down. Biol Lett. 2014; 10(4):20140172. PMC: 4013704. DOI: 10.1098/rsbl.2014.0172. View

4.
Schwarm A, Ortmann S, Wolf C, Streich W, Clauss M . Passage marker excretion in red kangaroo (Macropus rufus), collared peccary (Pecari tajacu) and colobine monkeys (Colobus angolensis, C. polykomos, Trachypithecus johnii). J Exp Zool A Ecol Genet Physiol. 2009; 311(9):647-61. DOI: 10.1002/jez.552. View

5.
Pontzer H, Raichlen D, Gordon A, Schroepfer-Walker K, Hare B, ONeill M . Primate energy expenditure and life history. Proc Natl Acad Sci U S A. 2014; 111(4):1433-7. PMC: 3910615. DOI: 10.1073/pnas.1316940111. View