scholarly journals Energy Expenditure of Free-Ranging Chicks of the Cape GannetMorus capensis

2015 ◽  
Vol 88 (4) ◽  
pp. 406-415 ◽  
Author(s):  
René A. Navarro ◽  
Ralf H. E. Mullers ◽  
Haro A. J. Meijer ◽  
Les G. Underhill
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.


2002 ◽  
Vol 75 (1) ◽  
pp. 3-18 ◽  
Author(s):  
M. J. Donohue ◽  
D. P. Costa ◽  
E. Goebel ◽  
G. A. Antonelis ◽  
J. D. Baker

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Tiphaine Jeanniard-du-Dot ◽  
Andrew W. Trites ◽  
John P. Y. Arnould ◽  
John R. Speakman ◽  
Christophe Guinet

Copeia ◽  
2006 ◽  
Vol 2006 (1) ◽  
pp. 129-136 ◽  
Author(s):  
Patrick G. R. Jodice ◽  
Deborah M. Epperson ◽  
G. HenkVisser

2011 ◽  
Vol 8 (3) ◽  
pp. 347-350 ◽  
Author(s):  
Claudia A. F. Wascher ◽  
Brigitte M. Weiß ◽  
Walter Arnold ◽  
Kurt Kotrschal

In group-living vertebrates, reliable social allies play a decisive role in dealing with stressors. For example, support by social allies is known to dampen glucocorticoid responses. It remains unknown, however, how social embedding affects the sympatho-adrenergic axis as indicated by heart rate (HR) in non-human animals. We studied the relationships between HR, pair-bond status and distance from the pair-partner in twenty-five free-ranging greylag geese ( Anser anser ) in a natural social environment. In three individuals, we investigated HR responses following partner loss. Overall, we found a context- and sex-dependent difference in HR between paired and unpaired individuals, paired males having a lower HR during agonistic encounters, and unpaired females having a lower HR during resting. Also, in paired females HR increased with increasing distance from the partner. Our data suggest that HR is modulated by pair-bond status in greylag geese in a context- and sex-dependent manner, which may be representative for social vertebrates in general. Despite the low sample size, the present study indicates that proper social embedding may optimize an individual's physiological investment in the social domain. This reduces individual energy expenditure and may benefit health and reproductive success.


1995 ◽  
Vol 350 (1332) ◽  
pp. 119-131 ◽  

As heart rate ( f H ) can be used to determine the energy expenditure of black-browed albatrosses ( Diomedea melanophrys ) (Bevan et al. 1994), data loggers - recording f H and abdominal temperature ( T ab ) -were implanted into free-ranging black-browed albatrosses breeding at South Georgia. Five birds also had salt water switches (sws) attached to one leg to record when the birds were on the water, and two others had satellite transmitters attached to their back to determine the birds’ position at sea. The birds were released into their natural environment and recaptured, on average, 23 days later when the data loggers were removed. The f H data were then converted into estimates of energy expenditure (ee) using a previously derived equation. The mean EE during incubation and brooding were 2.22 and 2.42 W kg -1 , respectively. When the birds were foraging at sea, EE increased to between 4.63 and 5.80 W kg -1 , depending on the phase of the reproductive cycle. As the birds spent approximately the same length of time at the nest and at sea during incubation and brooding, the overall mean ee during these phases were 3.63 and 3.54 W kg -1 respectively. These rates are significantly lower than that during the chick-rearing phase when a high level of foraging EE is maintained almost continuously. By combining information from the sws with the f H data, it was possible to determine the EE of the birds when on the water (5.77 W kg -1 ) and when flying (6.21 W kg -1 ). These values are approximately twice the estimated basal metabolic rate (BMR) for the species. The energy costs of flight are half previous values, estimated using the doubly labelled water technique, because of the previous assumption that birds on the water have an EE equivalent to BMR. When the birds were on the nest, T ab was 39.3 + 0.4 °C and this changed very little with time. However, when they were at sea, T ab showed large variations, depending on the behaviour of the bird. Information from the sws indicated that all large drops (> 0.5 °C) in Tab occurred when the birds were on water. The mean minimum value reached was 32.5 + 2.0 °C. It is likely that ingestion of prey or water are the major causes of this decrease. This is the first study to have used f H extensively to determine the EE of a free-ranging marine bird. The advantages of using this technique are that data can be obtained over long durations with high resolution, permitting the EE of different activities to be estimated.


Rangifer ◽  
2000 ◽  
Vol 20 (2-3) ◽  
pp. 59 ◽  
Author(s):  
Paul Haggarty

When natural diets meet an animal's requirement for energy, other essential nutrients will usually be supplied in amounts at least sufficient for survival. Knowledge of the energy requirements of free ranging species under typical conditions are important in assessing both their nutritional needs and their ecological impact. The doubly labelled water (DLW) method is currently the most promising objective field methodology for estimating free living energy expenditure but expenditure is only equal to the energy requirement when an animal is in energy balance. Reproduction and seasonal cycles of fat deposition and utilization represent significant components of the energy budget of arctic ungulates but the information gained in the course of a typical DLW study may be used to estimate processes such as milk output and fat storage and mobilization in order to predict requirements from expenditure. The DLW method has been exhaustively validated under highly controlled conditions and the introduction of innovations such as faecal sampling for the estimation of body water isotopic enrichment, the availability of appropriate correction factors and stoichiometrics for known sources of error, and iterative calculation of unknown parameters, have produced a methodology suitable for use in truly free ranging species. The few studies carried out so far in arctic ungulates indicate that previous predictions have generally underestimated the true level of expenditure, that there is considerable between animal variation in the level of expenditure and that this is largely determined by physical activity. The disadvantages of the DLW methodology are that it remains expensive and the isotope analysis is technically demanding. Furthermore, although DLW can provide an accurate value for free living energy expenditure, it is often important to have information on the individual components of expenditure, for example the relative contribution of physical activity and thermoregulatory thermogenesis, in order to interpret the values for overall expenditure. For these reasons the most valuable use of the DLW method in the field may be to validate factorial models and other approaches so that they may be used with confidence. Additional important information on the energy exchanges of free ranging animals may be obtained from other stable isotope methodologies. In addition to the use of the isotopes 2H and lsO in the DLW method, natural variations in the abundance of "C and 15N in the arctic environment may be exploited to study diet selection in truly free living arctic ungulates.


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