scholarly journals The Field Metabolic Rate, Water Turnover, and Feeding and Drinking Behavior of a Small Avian Desert Granivore During a Summer Heatwave

2019 ◽  
Vol 10 ◽  
Author(s):  
Christine Elizabeth Cooper ◽  
Philip Carew Withers ◽  
Laura Leilani Hurley ◽  
Simon Charles Griffith

2009 ◽  
Vol 57 (1) ◽  
pp. 23 ◽  
Author(s):  
A. J. Munn ◽  
T. J. Dawson ◽  
S. R. McLeod ◽  
D. B. Croft ◽  
M. B. Thompson ◽  
...  

Sustainable management of pastures requires detailed knowledge of total grazing pressure, but this information is critically lacking in Australia’s rangelands where livestock co-occur with large herbivorous marsupials. We present the first comparative measure of the field metabolic rate (an index of food requirement) of Australia’s largest marsupial, the red kangaroo (Macropus rufus), with that of domestic sheep (Ovis aries; merino breed). We tested the assumption that the grazing pressure of red kangaroos is equivalent to 0.7 sheep, and show this to be a two-fold overestimation of their contribution to total grazing. Moreover, kangaroos had extraordinarily lower rates of water turnover, being only 13% that of sheep. Consequently, our data support arguments that the removal of kangaroos may not markedly improve rangeland capacity for domestic stock. Furthermore, given the low resource requirements of kangaroos, their use in consumptive and non-consumptive enterprises can provide additional benefits for Australia’s rangelands than may occur under traditional rangeland practices.



Mammal Review ◽  
2003 ◽  
Vol 33 (3-4) ◽  
pp. 295-301 ◽  
Author(s):  
ROY K. WINSTANLEY ◽  
WILLIAM A. BUTTEMER ◽  
GLEN SAUNDERS


1995 ◽  
Vol 16 (1) ◽  
pp. 47-54 ◽  
Author(s):  
S.D. Bradshaw ◽  
P.C. Withers

AbstractRates of turnover of water, energy and sodium were measured for free-ranging thorny devils (Moloch horridus), which are myrmecophagous agamid lizards, in a semi-arid Western Australian habitat. There were significant differences in body water content and water turnover rate (WTR) measurements for cool, wet, average and hot periods, although the field metabolic rate (FMR) and sodium turnover (NaTR) rate did not differ significantly between weather conditions. The thorny devil had a substantially lower field WTR during dry periods (10-15 ml kg-1 d-1) than expected for semi-arid and arid lizards, although the WTR was higher in wet conditions (30-35 ml kg-1 d-1). The field metabolic rate of thorny devils (0.134 ml CO2 g-1 h-1) was only slightly less than that expected for a semi-arid/lizard (0.178 ml CO2 g-1 h-1), despite the apparently slothful nature of the thorny devil. The sodium turnover rate of the thorny devil (1.5-2.5 mmol kg-1 d-1) was within the range reported for other semi-arid/arid lizards. The field metabolic rate of the thorny devils suggests that they consume about 750 ants per day. The ratio of water to energy turnover measured for thorny devils in the field (0.11 ml H2O kj-1) was the same as that predicted from the composition of ants and their digestibility by thorny devils (0.11 ml H2O kj-1). However, the ratios of sodium-to-energy turnover (30 μmol Na+ kj-1) and sodium-to-water turnover (277 μmol ml H2O-1) were substantially higher than expected ratios (10 and 89 respectively).



2016 ◽  
Vol 38 (4) ◽  
pp. 361 ◽  
Author(s):  
Adam J. Munn ◽  
Yohannes Alemseged ◽  
Catharina Vendl ◽  
Mathew Stewart ◽  
Keith Leggett

Details of the energy (food) requirements of domestic herbivores are essential for predicting grazing pressures and subsequent ecological impacts on rangelands. However, these details are lacking for some of the more recently introduced sheep breeds to Australia, such as the Dorper breed sheep, which are principally meat sheep, and it is uncertain how they compare with the traditional Merino, a wool-breed, sheep. We used the doubly labelled water method to compare the field metabolic rate and water turnover rate of Dorpers and Merinos grazing together in a small holding paddock in a typical rangeland environment. We found no significant differences in field metabolic rate (Dorpers 481 ± 125 kJ and Merinos 500 ± 109 kJ kg–0.73 day–1) or water turnover rate (Dorpers 397 ± 57 mL and Merinos 428 ± 50 mL kg–0.8 day–1). As such we conclude that under controlled conditions with limited movement and ready access to feed and water, dry sheep equivalent of 1 is appropriate for Dorpers (that is, one Dorper ewe had a grazing requirement equal to one standard, dry Merino wether). However, we also found that the field metabolic rate for Merinos under these conditions was only around half that measured in published studies for animals ranging freely in a large paddock system. This suggests that more work is needed to fully appreciate the energetic and grazing impacts of Dorpers versus Merinos under more realistic grazing conditions (e.g. large paddock systems) where feed and water are more spread. It also highlights limitations of the current dry sheep equivalent rating system, which has been derived from laboratory measures of sheep metabolic rates.



2003 ◽  
Vol 173 (8) ◽  
pp. 687-693 ◽  
Author(s):  
C. E. Cooper ◽  
P. C. Withers ◽  
S. D. Bradshaw


Author(s):  
Sonja Drack ◽  
Sylvia Ortmann ◽  
Nathalie Bührmann ◽  
Jutta Schmid ◽  
Ruth D. Heldmaier ◽  
...  


2013 ◽  
Vol 82 (5) ◽  
pp. 1009-1020 ◽  
Author(s):  
Lawrence N. Hudson ◽  
Nick J. B. Isaac ◽  
Daniel C. Reuman


2000 ◽  
Vol 203 (23) ◽  
pp. 3655-3665 ◽  
Author(s):  
D.P. Costa ◽  
N.J. Gales

The New Zealand sea lion, Phocarctos hookeri, is the deepest- and longest-diving sea lion. We were interested in whether the diving ability of this animal was related to changes in its at-sea and diving metabolic rates. We measured the metabolic rate, water turnover and diving behavior of 12 lactating New Zealand sea lions at Sandy Bay, Enderby Island, Auckland Islands Group, New Zealand (50 degrees 30′S, 166 degrees 17′E), during January and February 1997 when their pups were between 1 and 2 months old. Metabolic rate (rate of CO(2) production) and water turnover were measured using the (18)O doubly-labeled water technique, and diving behavior was measured with time/depth recorders (TDRs). Mean total body water was 66.0+/−1.1 % (mean +/− s.d.) and mean rate of CO(2) production was 0. 835+/−0.114 ml g(−)(1)h(−)(1), which provides an estimated mass-specific field metabolic rate (FMR) of 5.47+/−0.75 W kg(−)(1). After correction for time on shore, the at-sea FMR was estimated to be 6.65+/−1.09 W kg(−)(1), a value 5.8 times the predicted standard metabolic rate of a terrestrial animal of equal size. The mean maximum dive depth was 353+/−164 m, with a mean diving depth of 124+/−36 m. The mean maximum dive duration was 8.3+/−1.7 min, with an average duration of 3.4+/−0.6 min. The deepest, 550 m, and longest, 11.5 min, dives were made by the largest animal (155 kg). Our results indicate that the deep and long-duration diving ability of New Zealand sea lions is not due to a decreased diving metabolic rate. Individual sea lions that performed deeper dives had lower FMRs, which may result from the use of energetically efficient burst-and-glide locomotion. There are differences in the foraging patterns of deep and shallow divers that may reflect differences in surface swimming, time spent on the surface and/or diet. Our data indicate that, although New Zealand sea lions have increased their O(2) storage capacity, they do not, or cannot, significantly reduce their at-sea metabolic rates and are therefore likely to be operating near their physiological maximum.



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