Apparatus for measuring oxygen consumption of small animals

1961 ◽  
Vol 16 (5) ◽  
pp. 923-925 ◽  
Author(s):  
John Haldi ◽  
Winfrey Wynn ◽  
Harold Breding
1959 ◽  
Vol 38 (4) ◽  
pp. 899-902 ◽  
Author(s):  
Lowell W. Charkey ◽  
Paul A. Thornton

1942 ◽  
Vol 19 (2) ◽  
pp. 168-175
Author(s):  
R. J. WHITNEY

1. A size factor is demonstrated for the oxygen consumption at 14.5° C. of four species of fresh-water Turbellaria obtained from different habitats. 2. For three of the species studied (Polycelis cornuta, Crenobia alpina and Planaria polychroa) small animals were found to have a higher oxygen consumption per unit weight than large ones. In the case of Polycelis nigra small animals were shown to have a lower oxygen consumption per unit weight than large ones. 3. The adherence of the size factor to the surface law of Rubner is discussed. Only Crenobia alpina satisfies the theoretical requirements of the law, and in this species it is shown that the size factor is practically unchanged when the oxygen consumptions are determined at 7.0° C. instead of 14.5° C.


Author(s):  
John R. B. Lighton

This chapter describes the theory and practical applications of coulometric respirometry. Coulometric respirometry is probably the most accurate method for measuring oxygen consumption rates. It is ideal for small animals and has the dual advantages of high sensitivity and the fact that the oxygen in the organism’s environment is not depleted, allowing measurements to continue for long periods in many cases. The technique works by maintaining a constant pressure in a sealed system by electrolytically producing oxygen at the same rate at which an enclosed organism consumes it.


1980 ◽  
Vol 86 (1) ◽  
pp. 9-18 ◽  
Author(s):  
C. RICHARD TAYLOR ◽  
NORMAN C. HEGLUND ◽  
THOMAS A. McMAHON ◽  
TODD R. LOONEY

The energetic cost of generating muscular force was studied by measuring the energetic cost of carrying loads in rats, dogs, humans, and horses for loads ranging between 7 and 27% of body mass. Oxygen consumption increased in direct proportion to mass supported by the muscles, i.e. V OO2,L/VOO2/mL/m = 1.01 ± S.D. ± 0.017, where VOO2,L is the oxygen consumption of the animal running with a load, VOO2 is the oxygen consumption at the same speed without a load, mL, is the mass of the animal plus the load, and m is the mass of the animal. Stride frequency, average number of feet on the ground over an integral number of strides, the time of contact of each foot relative to the other feet, and the average vertical acceleration during the contact phase were not measurably changed by the loads used in our experiments. From these observations we conclude that the average accelerations of the centre of mass of the animal are not changed by carrying the loads, and that muscular force developed by the animal increases in direct proportion to the load. It follows that the rate of energy utilization by muscles of an animal as it runs along the ground at any particular speed is nearly directly proportional to the force exerted by its muscles. The energetic cost of generating force over an interval of time (∫ F dt) increases markedly with running speed. An important consequence of the direct proportionality between increased oxygen consumption and mass of the load is that small animals expend much more energy to generate a given force at a given speed than large animals.


1932 ◽  
Vol 95 (1) ◽  
pp. 73-78
Author(s):  
J.E. Davis ◽  
H.B. van Dyke

1990 ◽  
Vol 149 (1) ◽  
pp. 307-317 ◽  
Author(s):  
R. J. Full ◽  
A. Tullis

Small animals use more metabolic energy per unit mass than large animals to run on a level surface. If the cost to lift one gram of mass one vertical meter is constant, small animals should require proportionally smaller increases in metabolic cost to run uphill. To test this hypothesis on very small animals possessing an exceptional capacity for ascending steep gradients, we measured the metabolic cost of locomotion in the cockroach, Periplaneta americana, running at angles of 0, 45 and 90 degrees to the horizontal. Resting oxygen consumption (VO2rest) was not affected by incline angle. Steady-state oxygen consumption (VO2ss) increased linearly with speed at all angles of ascent. The minimum cost of locomotion (the slope of the VO2ss versus speed function) increased with increasing angle of ascent. The minimum cost of locomotion on 45 and 90 degrees inclines was two and three times greater, respectively, than the cost during horizontal running. The cockroach's metabolic cost of ascent greatly exceeds that predicted from the hypothesis of a constant efficiency for vertical work. Variations in stride frequency and contact time cannot account for the high metabolic cost, because they were independent of incline angle. An increase in the metabolic cost or amount of force production may best explain the increase in metabolic cost. Small animals, such as P. americana, can easily scale vertical surfaces, but the energetic cost is considerable.


Sign in / Sign up

Export Citation Format

Share Document