Activity and diving metabolism correlate in Steller sea lion Eumetopias jubatus
By A. Fahlman, Rory P. Wilson, Caroline Svärd, D. Rosen, Andrew W. Trites. 2008
88 citations recorded by the source corpus.
Subfields: Ecology, Ocean Engineering
View Paper: https://www.semanticscholar.org/paper/50cbbab1c7444c1696f1fb08638f0a23abdb96bf
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In Ecology
In Ocean Engineering
Citations in the corpus
- Making overall dynamic body acceleration work: on the theory of acceleration as a proxy for energy expenditure (2011, methodology): “Few data are currently available for aquatic animals, and the exact shape of the relationship between ODBA and energy expenditure is unclear (Fahlman et al. 2008; Gleiss et al. 2010).”
- Estimated field metabolic rates and prey requirements of resident killer whales (2011, background): “Furthermore, for marine mammals, metabolic rates are further affected by dive depth and duration, activity, and swimming speed (Webb et al. 1998, Hurley and Costa 2001, Rosen and Trites 2002, Hastie et al. 2006, 2007, Fahlman et al. 2008, Williams and Noren 2009).”
- Derivation of body motion via appropriate smoothing of acceleration data (2008, background): “…in all 3 dimensional axes, has been shown to be strongly correlated with the rate of oxygen consumption (VO2) in great cormorants Phalacrocorax carbo, Linnaeus 1758 (Wilson et al. 2006), humans (Halsey et al. 2008), and a range of other species (Fahlman et al. 2008, Halsey et al. in press a,b).”
- Accelerometers can measure total and activity-specific energy expenditures in free-ranging marine mammals only if linked to time-activity budgets (2017, background): “This R2 is lower than values reported for other vertebrates measured in captivity/semi-captivity (0 47 for diving Steller sea lions, Fahlman et al. 2008; 0 84 in birds, Halsey et al. 2009a; 0 60 for swimming sharks, Gleiss et al. 2010; 0 56 for turtles, Halsey et al. 2011).”