Measuring the energy expenditure and water flux in free-ranging alpacas (Lama pacos) in the peruvian andes using the doubly labelled water technique

2007 ◽  
Vol 307A (12) ◽  
pp. 667-675 ◽  
Author(s):  
Alexander Riek ◽  
Leendert Van Der Sluijs ◽  
Martina Gerken
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.


Rangifer ◽  
2000 ◽  
Vol 20 (2-3) ◽  
pp. 211 ◽  
Author(s):  
Geir Gotaas ◽  
Eric Milne ◽  
Paul Haggarty ◽  
Nicholas J.C. Tyler

The doubly labelled water (DLW) method was used to measure total energy expenditure (TEE) in three male reindeer (Rangifer tarandus tarandus) aged 22 months in winter (February) while the animals were living unrestricted at natural mountain pasture in northern Norway (69°20'N). The concentrations of 2H and l8O were measured in water extracted from samples of faeces collecred from the animals 0.4 and 11.2 days after injection of the isotopes. Calculated rates of water flux and CO2-production were adjusted to compensate for estimated losses of 2H in faecal solids and in methane produced by microbial fermentation of forage in the rumen. The mean specific TEE in the three animals was 3.057 W.kg-1 (range 2.436 - 3.728 W.kg1). This value is 64% higher than TEE measured by the DLW method in four captive, non-pregnant adult female reindeer in winter and probably mainly reflects higher levels of locomotor activity in the free-living animals. Previous estimates of TEE in free-living Rangifer in winter based on factorial models range from 3.038 W.kg-1 in female woodland caribou (R. t. caribou) to 1.813 W.kg-1 in female Svalbard reindeer (R. t. platyrhynchus). Thus, it seems that existing factorial models are unlikely to overestimate TEE in reindeer/caribou: they may, instead, be unduly conservative. While the present study serves as a general validation of the factorial approach, we suggest that the route to progress in the understanding of field energetics in wild ungulates is via application of the DLW method.


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.


1988 ◽  
Vol 36 (3) ◽  
pp. 293 ◽  
Author(s):  
KA Nagy ◽  
AK Lee ◽  
RW Martin ◽  
MR Fleming

Field metabolic rates (FMRs) and rates of water flux in free-ranging fat-tailed dunnarts, Sminthopsis crassicaudata, were measured during spring (late October) using doubly labelled water. Feeding rates were estimated on the basis of water and energy fluxes. FMRs averaged 68.7 kJ d-' in adults (mean body mass= 16.6 g), and were 29.2 kJ d-' in juveniles (6.1 g). These FMRs are 6.6 times basal metabolic rate (BMR), and are much higher than the hypothetical maxima of four to five times BMR. Other dasyurid marsupials also have high FMR/BMR ratios, but so does a small petaurid marsupial. S. crassicaudata consumed 80-90% of its body mass in arthropods each day. The diet of arthropods apparently provided enough water for the animals to maintain water balance without drinking during this study.


1998 ◽  
Vol 80 (3) ◽  
pp. 263-272 ◽  
Author(s):  
P. Haggarty ◽  
J. J. Robinson ◽  
J. Ashton ◽  
E. Milne ◽  
C. L. Adam ◽  
...  

Energy expenditure was estimated using the doubly-labelled water (DLW) method in summer in five free-living adult, non-pregnant, non-lactating, red deer (Cervus elaphus) hinds (weight 107.3 (se 0.9) kg; age 6 (se 1) years) on lowland pasture under typical farming conditions. Climatic conditions were monitored throughout the experiment. Errors due to 2H losses in CH4 and faeces were calculated from previous estimates of stoichiometries. CH4 production, fractionated water loss, urinary N and O2 consumption were estimated using an iterative approach. The water flux (rH2O) in these animals consuming only fresh grass was 12 (se 0.5) kg/d, the CO2 production (rCO2) was 1271 (se 4.0) litres/d and the mean energy expenditure was 25 (se 0.8) MJ/d. There were no significant differences in the isotope distribution spaces and flux rates, rH2O, rCO2 or energy expenditure using the multi-point or two-point approaches to calculation. The DLW-derived energy expenditure of 25 MJ/d is approximately 20% higher than the recommended intake of 21 MJ/d for adult hinds kept outdoors (Adam, 1986) and, at 757 kJ/kg0.75 per d, one third higher than the value of 570 kJ/kg0.75 per d for stags penned indoors (Key et al. 1984).


2004 ◽  
Vol 78 (2) ◽  
pp. 293-303 ◽  
Author(s):  
Z. Fuller ◽  
C. A. Maltin ◽  
E. Milne ◽  
G.S. Mollison ◽  
J. E. Cox ◽  
...  

AbstractEvaluations of the energy requirements of working animals have been confounded by the constraints of indirect calorimetric techniques (Cal). This study sought to investigate a non-restrictive methodology, the doubly labelled water (DLW; 2H218O) technique, for the measurement of energy expenditure in free ranging equids. Six pony geldings were intravenously injected with DLW in two sequential studies that permitted first, isotope equilibration and half-lives to be determined and then second, heat production (HP) to be measured simultaneously by DLW and traditional (Cal) techniques.In study 1, three animals were injected with DLW, three animals were untreated controls. Blood samples were collected every 30 min for 12 h and thereafter at 24 h intervals for 14 days. Isotopes equilibrated throughout the body water pool within 300 (2H) and 240 (18O) min and half-lives were 6.3 ± 0.6 days (2H) and 5.6 ± 0.4 days (18O).In study 2, HP was simultaneously determined by Cal and DLW over a 4-day period. Animals (no. = 6) were assigned to pairs and in successive weeks two ponies were injected with DLW and confined to metabolism chambers 12 h later. Cal HP was 0.51 ± 0.02 MJ/kg M0.75 per day compared with 0.48 ± 0.29 MJ/kg M0.75 per day estimated by DLW. Maintenance metabolizable energy intake was 0.53 ± 0.01 MJ/kg M0.75 per day (Cal) and 0.50 ± 0.01 MJ/kg M0.75 per day (DLW). Validation of the DLW technique may empower essential, systematic appraisal of energy requirements in unrestrained working horses.


2007 ◽  
Vol 80 (6) ◽  
pp. 635-642
Author(s):  
Daniel E. Crocker ◽  
Nathan Kofahl ◽  
Gary D. Fellers ◽  
Natalie B. Gates ◽  
Dorian S. Houser

1995 ◽  
Vol 16 (1) ◽  
pp. 55-66 ◽  
Author(s):  
Marcos Baez ◽  
Roland Vernet ◽  
Jacques Castanet

AbstractWater fluxes and daily energy expenditure (DEE) of Gallotia galloti, G. stehlini and G. atlantica, were estimated over a three-year period using the doubly-labelled water (DLW) method. Water influx varied little between seasons and between sexual categories. Juveniles tended to have higher water fluxes in spring in all three species; after a dry period the water turnover tended to decrease for all sexes in G. galloti and G. stehlini, whereas little variation was observed for G. atlantica. The average water influx, combined for all periods, was 46.27, 50.97 and 38.20 ml H2O.kg-1 d-1 for the three species respectively; only the last value differs significantly from the remaining two. The mean DEE, for all periods combined, were 189.7, 179.4 and 146.5 J g-1 d-1 for the three species respectively. As for water turnover, only the value for G. atlantica differed significantly. These data suggest that: G. atlantica may be better adaptated to maintain homeostasis during dry periods and that differences in interspecific DEE can also be explained by others factors than differences in habitat, climatic conditions, daily profiles of activity or body temperatures. We suspect that the incidence of intraspecific competition has more importance in G. atlantica than in the two other species.


1992 ◽  
Vol 70 (5) ◽  
pp. 1001-1006 ◽  
Author(s):  
R. P. Brown ◽  
R. S. Thorpe ◽  
J. R. Speakman

Within-island microgeographic variation in body size of the Gran Canarian skink, Chalcides sexlineatus, is described. Clear latitudinal patterns of variation were found for both males and females. Using Mantel tests we rejected within-island altitude-related ecological variation as the cause of the geographic variation, but found a significant relationship between body size and the pattern of lush–arid variation. Larger body size was found in populations from the lusher northern areas, and small body size in populations from the arid south. Studies with doubly labelled water showed higher energy expenditure per animal in a studied northern population than in a southern population, due to larger body size in the former. Mean mass-specific energy expenditure was found to be low in this species compared with other lizards, and did not differ significantly between populations (north, 150.1 J∙g−0.80∙d−1; south, 124.7 J∙g−0.80∙d−1). Mean mass-specific water fluxes were similar for lizards at both study sites (14.79 and 14.20 mL H2O∙kg−0.91∙d−1, respectively). Previous explanations invoking differences in water stress as the cause of variation in body size among populations of arid-zone lizards do not appear to be applicable to C. sexlineatus.


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