scholarly journals Field Metabolic Rate, Water Flux and Food Consumption by Free-Living Silky Anteaters (Cyclopes didactylus) in Panama

Edentata ◽  
2012 ◽  
Vol 13 (1) ◽  
pp. 61-65
Author(s):  
Kenneth A. Nagya ◽  
G. Gene Montgomery
1988 ◽  
Vol 36 (2) ◽  
pp. 159 ◽  
Author(s):  
R Gales ◽  
B Green ◽  
C Stahel

Levels of circulating triglycerides and cholesterol in moulting little penguins in Tasmania were measured before, and throughout the moult. Levels at the initiation of moult were similar to those in breeding birds but increased by 2.5 times (triglycerides) and 1.8 times (cholesterol) during the moult. Water flux rates and field metabolic rate (FMR) were measured throughout moult with tritiated and doubly labelled water. TBW ranged from 54 to 70% body weight and increased during moult. Water influx rates were significantly correlated with rate of weight change. Mean FMR of moulting little penguins was 657 kJ kg-' day-', or 1.5 times basal metabolic rate (BMR), and there was no difference between sites or sexes. The water influx rates of birds foraging immediately after moult were 11 times higher than in moulting birds. The energy required to sustain a moulting little penguin is 15% higher than that required for a resting, non-moulting penguin. Although the cost of moult is elevated above BMR, the main energetic expense is met during the pre-moult foraging period when birds must consume enough food to ensure that they lay down sufficient fat reserves to sustain the moult.


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.


1995 ◽  
Vol 43 (1) ◽  
pp. 1 ◽  
Author(s):  
JB Williams ◽  
D Bradshaw ◽  
L Schmidt

Spinifex pigeons (Geophaps plumifera) are one of the few avian species that have evolved the capacity to reside in the hot and dry regions of central and north-western Australia. Previous investigation has revealed that their basal metabolic rate (BMR) equals only 68% of allometric prediction. In this study, we addressed the hypothesis that these birds have a reduced field metabolic rate (FMR) and water influx as a result of their lowered BMR. We measured the FMR and water flux of free-living spinifex pigeons by means of the doubly labelled water method. Although body mass of free-living male and female pigeons differed significantly, with males weighing on average 90.8 +/- 7.7 g (+/- s.d.) and females 80.2 +/- 5.6 g, FMR was statistically indistinguishable between sexes. For sexes combined, FMR averaged 139.9 mL CO2 h-1, or 73.5 kJ day-1, a value 38.7% of allometric expectation. These data support the hypothesis that spinifex pigeons have a markedly reduced FMR, probably, in part, the result of a depressed BMR compared with other birds of similar size. Our phylogenetic analysis of the BMR of pigeons lacked sufficient data to determine whether a reduced BMR in Australian pigeons was the consequence of ecological adaptation or phylogenetic constraint. Water influx ranged from 2.5 to 39.0 mL day-1 and averaged 18.4 mL day-1. Of the total water intake, 83.5% came from drinking; their food, seeds, supplied about 4%. Maintenance metabolism, energy allocated to basal plus thermoregulatory metabolism, accounted for about 67% of the average FMR, indicating that the activity requires relatively low energy expenditure in these birds.


1990 ◽  
Vol 38 (1) ◽  
pp. 1 ◽  
Author(s):  
WJ Foley ◽  
JC Kehl ◽  
KA Nagy ◽  
IR Kaplan ◽  
AC Borsboom

Water flux and metabolic rate were measured using a low-level, doubly-labelled water technique in eight free-living greater gliders, Petauroides volans which were maintaining constant body masses at about 1 kg in eucalypt forest near Maryborough, Queensland. Mean water influx was 88.0�3.2 mL d-' and mean metabolic rate was 25.1 L C02 d-' or 520 kJ d-'. These arboreal folivores have field metabolic rates and water influx rates that are 96% and 71% respectively of those predicted for a herbivorous marsupial of their body mass. Assuming that faecal energy losses were 43% of gross energy intakes and that urinary energy losses were 15% of digestible energy intakes, the gross energy intake of the animals was about 1130 kJ d-'. Animals would need to eat between 45 and 50 g of dry matter daily to satisfy these energy requirements. Based on these results, a preliminary energy budget for greater gliders has been proposed.


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