Endotherm Energetics - From a Scalable Individual-Based Model to Ecological Applications

1994 ◽  
Vol 42 (1) ◽  
pp. 125 ◽  
Author(s):  
WP Porter ◽  
JC Munger ◽  
WE Stewart ◽  
S Budaraju ◽  
J Jaeger

We outline a computer model of heat and mass transfer through flesh, fat and porous fur for endotherms of any dimensions. We then validate it with a series of laboratory studies. Finally, we explore applications of the model to Bergmann's rule, predicting the mouse-to-elephant curve, climate-disease-toxicant interactions, animal 'design' via genetic engineering and energetic constraints on community structure. As a first test of the model we present calculations and metabolic chamber measurements for mammals ranging in size from mice to Holstein calves. We then compare simultaneous measurements on deer mice, Peromyscus maniculatus, of oxygen consumption, doubly labelled water turnover and food consumption with calculations of metabolic rate using body temperature radio-telemetry as input to the endotherm model. The endotherm model derived in the Appendix requires data on allometry (body dimensions, surface area), fur properties, core temperature, air and radiant temperatures and wind speed. The model is useful for calculating energetic expenditure in different microclimates without the need for extensive physiological measurements in the laboratory. Model predictions of metabolic rate at 12-degrees-C and at 22-degrees-C were well correlated with each of the three empirical estimates. The model shows that the posture an animal assumes can influence measurements of metabolic rate. Model calculations of metabolic rate using postures ranging from a curled-up ball-like geometry to a sprawled-out, cylinder or ellipsoid geometry bracket all three sets of simultaneous empirical data taken on the same animals. Applications of the model show that it can be applied in a wide variety of circumstances to gain insight into physiological and ecological problems.

Biology Open ◽  
2021 ◽  
pp. bio.055475
Author(s):  
G. J. Sutton ◽  
J. A. Botha ◽  
J. R. Speakman ◽  
J. P. Y. Arnould

Understanding energy use is central to understanding an animal's physiological and behavioural ecology. However, directly measuring energy expenditure in free-ranging animals is inherently difficult. The doubly-labelled water (DLW) method is widely used to investigate energy expenditure in a range of taxa. Although reliable, DLW data collection and analysis is both financially costly and time consuming. Dynamic body acceleration (e.g. VeDBA) calculated from animal-borne accelerometers has been used to determine behavioural patterns, and is increasingly being used as a proxy for energy expenditure. Still its performance as a proxy for energy expenditure in free-ranging animals is not well established and requires validation against established methods. In the present study, the relationship between VeDBA and the at-sea metabolic rate calculated from DLW was investigated in little penguins (Eudyptula minor) using three approaches. Both in a simple correlation and activity-specific approaches were shown to be good predictors of at-sea metabolic rate. The third approach using activity-specific energy expenditure values obtained from literature did not accurately calculate the energy expended by individuals. However, all three approaches were significantly strengthened by the addition of mean horizontal travel speed. These results provide validation for the use of accelerometry as a proxy for energy expenditure and show how energy expenditure may be influenced by both individual behaviour and environmental conditions.


1991 ◽  
Vol 39 (3) ◽  
pp. 299 ◽  
Author(s):  
KA Nagy ◽  
SD Bradshaw ◽  
BT Clay

Field metabolic rates (FMRS) and water influx rates of free-living short-nosed bandicoots (Isoodon obesulus) were measured via the doubly labelled water technique. Bandicoots ranging in body mass from 775 to 1825 g (mean = 1230 g) had FMRS averaging 0.908 mL CO2 g-1 h-1, or 644 kJ d-1. This is about 2.7 times predicted basal metabolic rate. Water influx rates during the autumn measurement period were comparatively low, averaging 88.8 mL kg-1 d-1, or 103 mL d-1 for a 1230 g animal. Feeding rate (dry matter intake) was estimated to be 45 g d-1, assuming that the food was half invertebrates and half plant tissues (dry matter basis). Performed and metabolically produced water from the food can completely account for total water intake, indicating that bandicoots did not drink the rainwater or pond water that was available. The study population (estimated density = 0.63 bandicoots ha-1) consumed food at a rate of about 62 g fresh matter ha-1 d-1 (equivalent to 27 g dry matter or 605 kJ ha-1 d-1), which is similar to the food requirements of populations of small eutherian and marsupial insectivores in other habitats.


2009 ◽  
Vol 87 (10) ◽  
pp. 956-964 ◽  
Author(s):  
Michael J. Sheriff ◽  
J. R. Speakman ◽  
L. Kuchel ◽  
S. Boutin ◽  
M. M. Humphries

The hypothesis that cold air temperatures (Ta) constrain the metabolic diversity of high-latitude endotherms is based on the observation among birds and mammals that mean field metabolic rate (FMR) increases, whereas the variability of FMR decreases, from the warm tropics to the cold poles. However, there is a paucity of FMR measurements from above 60° latitude and below 0 °C. We measured the daily energy expenditure of a high-latitude population of free-ranging snowshoe hares ( Lepus americanus Erxleben, 1777) in Yukon, Canada, in winter (Ta-mean = –16.4 °C) and in autumn (Ta-mean = 0.5 °C). Doubly labelled water measures of FMR were approximately 20% lower in winter than in autumn, and were a similar, low multiple of resting metabolic rate in both seasons (2.04 and 1.94, respectively). The mass-corrected FMR of snowshoe hares in winter was only half the value predicted by extrapolating the relationship between FMR and Ta > 0 to –16.4 °C. These results contribute to an emerging pattern of a reversal in the relationship between FMR and Ta in free-ranging mammals from negative above 0 °C to positive below 0 °C. We refer to the positive, low Ta portion of this relationship as the cold shoulder, and suggest that it may reflect the general necessity for free-ranging mammals to use behavioural and (or) physiological means to conserve energy during long winters when cold conditions coincide with resource scarcity.


1999 ◽  
Vol 77 (9) ◽  
pp. 1474-1485 ◽  
Author(s):  
Paul G Jensen ◽  
Peter J Pekins ◽  
James B Holter

For northern white-tailed deer (Odocoileus virginianus) fawns, the energetic cost of thermoregulation (HcE) during severe winters can result in substantial catabolism of body-tissue reserves. The heat increment of feeding (HiE) has the potential to offset thermoregulatory energy expenditure that would otherwise require the catabolism of these reserves. During winters 1996 and 1997, we conducted 18 fasting and 18 on-feed heat-production trials using indirect respiration calorimetry in a metabolic chamber. Nonlinear regression analysis was used to estimate the lower critical temperatures (Tlc) and determine the fasting metabolic rate (FMR) and resting metabolic rate (RMR). Resulting models were used to calculate HiE, HcE, and percent substitution of HiE for HcE. For fawns fed a natural browse diet, estimated FMR and RMR were 352 and 490 kJ·kg body mass (BM)-0.75·d-1, respectively; this 40% increase in thermoneutral heat production reduced Tlc from -0.8 to -11.2°C between the fasted and fed states, respectively, and reduced HcE by 59% for fed fawns. For fawns fed a concentrate diet, estimated FMR and RMR were 377 and 573 kJ·kg BM-0.75·d-1, respectively. Level of browse intake had a significant effect on RMR andTlc. RMR was 12% higher for fawns on a high versus a low level of intake, and estimated Tlc was -15.6 and -5.8°C, respectively. Our data indicate that the energetic cost of thermoregulation is probably a minor portion of the energy budget of a healthy fawn consuming natural forage.


Author(s):  
Enric Vilar ◽  
Sivakumar Sridharan ◽  
Jonathan Wong ◽  
Jocelyn Berdeprado ◽  
Ken Farrington

1994 ◽  
Vol 72 (11) ◽  
pp. 1967-1972 ◽  
Author(s):  
Donald W. Thomas ◽  
Kathy Martin ◽  
Hélène Lapierre

We measured background 2H and 18O abundances and field metabolic rate (FMR) for White-tailed Ptarmigan (Lagopus leucurus) above 3600 m elevation in the Colorado Rocky Mountains between May and July. 18O abundances ranged from 1982.4 to 2018.6 ppm [Formula: see text], while 2H abundance ranged from 142.8 to 154.0 ppm [Formula: see text]. Mean 2H abundance followed closely (−0.3 ppm deviation) the level predicted by Tatner's empirical model relating 2H and ambient temperature. However, 18O was more enriched than predicted (+3.4 ppm), which may reflect 18O fractionation in the plant diet. FMR, measured by means of the doubly labelled water method, ranged from 206.4 to 442.7 kJ/d and was not related to body mass. However, for males, FMR was significantly and positively related to age. Because of high variation in background isotope levels, the use of mean 2H and 18O background abundances instead of individual backgrounds would introduce a mean error of 7.1% (range −8.9 to +11.4%) in calculations of CO2 production and FMR.


1996 ◽  
Vol 44 (5) ◽  
pp. 445 ◽  
Author(s):  
WW Weathers ◽  
DC Paton ◽  
RS Seymour

Field metabolic rate (FMR) and water influx of New Holland honeyeaters (Phylidonyris novaehollandiae), eastern spinebills (Acanthorhynchus tenuirostris) and a crescent honeyeater (P. pyrrhoptera) were measured by the doubly labelled water technique. New Holland honeyeaters had just finished breeding and were beginning their summer moult. They ranged in mass from 15.4 to 21.0 g (mean = 17.3 g, n = 12) and had FMRs averaging 8.8 mt CO2 g(-1) h(-1) or 77.6 kJ day(-1), which was 2.8 times their measured basal metabolic rate (BMR). Their water influx rate averaged 10.7 mL day(-1). Eastern spinebills were still feeding young and had yet to begin moulting. They ranged in mass from 8.0 to 10.7 g (mean = 9.7 g, n = 6), had FMRs averaging 10.9 mL CO2 g(-1) h(-1) or 52.9 kJ day(-1) (2.5 times their measured BMR), and had an average water influx rate of 8.7 mL day(-1). FMR and water influx of a single 14.6-g crescent honeyeater, which was in late primary moult, were 75.9 kJ day(-1) (2.7 times measured BMR) and 12.5 mL day(-1). The FMR of New Holland honeyeaters varied inversely with mean standard operative temperature (T-es) calculated for values of T-es below 20 degrees C as follows: FMR (kJ day(-1)) = 134 - 5.47 T-es (n = 12, r(2) = 0.52). Honeyeater FMRs were much lower than would be predicted allometrically for hummingbirds of the same mass, reflecting the honeyeaters' low-cost foraging tactic of consuming nectar while perched.


2014 ◽  
Vol 281 (1783) ◽  
pp. 20140180 ◽  
Author(s):  
Victor M. Ortega-Jimenez ◽  
Nir Sapir ◽  
Marta Wolf ◽  
Evan A. Variano ◽  
Robert Dudley

Animal fliers frequently move through a variety of perturbed flows during their daily aerial routines. However, the extent to which these perturbations influence flight control and energetic expenditure is essentially unknown. Here, we evaluate the kinematic and metabolic consequences of flight within variably sized vortex shedding flows using five Anna's hummingbirds feeding from an artificial flower in steady control flow and within vortex wakes produced behind vertical cylinders. Tests were conducted at three horizontal airspeeds (3, 6 and 9 m s −1 ) and using three different wake-generating cylinders (with diameters equal to 38, 77 and 173% of birds' wing length). Only minimal effects on wing and body kinematics were demonstrated for flight behind the smallest cylinder, whereas flight behind the medium-sized cylinder resulted in significant increases in the variances of wingbeat frequency, and variances of body orientation, especially at higher airspeeds. Metabolic rate was, however, unchanged relative to that of unperturbed flight. Hummingbirds flying within the vortex street behind the largest cylinder exhibited highest increases in variances of wingbeat frequency, and of body roll, pitch and yaw amplitudes at all measured airspeeds. Impressively, metabolic rate under this last condition increased by up to 25% compared with control flights. Cylinder wakes sufficiently large to interact with both wings can thus strongly affect stability in flight, eliciting compensatory kinematic changes with a consequent increase in flight metabolic costs. Our findings suggest that vortical flows frequently encountered by aerial taxa in diverse environments may impose substantial energetic costs.


1995 ◽  
Vol 9 (2) ◽  
pp. 151 ◽  
Author(s):  
I. L. Boyd ◽  
A. J. Woakes ◽  
P. J. Butler ◽  
R. W. Davis ◽  
T. M. Williams

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