Changing bodies, changing relationships? Heart rate as an indicator of the rate of oxygen consumption throughout the annual cycle of barnacle geese, Branta leucopsis

Author(s):  
Steven J. Portugal ◽  
Jon A. Green ◽  
Phill Cassey ◽  
Peter B. Frappell ◽  
Patrick J. Butler
2002 ◽  
Vol 205 (21) ◽  
pp. 3347-3356 ◽  
Author(s):  
S. Ward ◽  
C. M. Bishop ◽  
A. J. Woakes ◽  
P. J. Butler

SUMMARYWe tested the hypotheses that the relationship between heart rate(fH) and the rate of oxygen consumption(V̇O2) differs between walking and flying in geese and that fH and V̇O2 have a U-shaped relationship with flight speed. We trained barnacle geese Branta leucopsis (mean mass 2.1 kg) and bar-headed geese Anser indicus(mean mass 2.6 kg) to walk inside a respirometer on a treadmill and to fly in a wind tunnel with a respirometry mask at a range of speeds. We measured fH and V̇O2simultaneously during walking on the treadmill in five individuals of each species and in one bar-headed goose and four barnacle geese during flight in the wind tunnel. The relationships between fH and V̇O2 were significantly different between flying and walking. V̇O2 was higher,and the increment in V̇O2 for a given increase in fH was greater, for flying than for walking geese. The relationship between fH and V̇O2 of free-living barnacle geese during their natural migratory flights must differ from that measured in the wind tunnel, since the fH of wild migratory birds corresponds to values of V̇O2 that are unrealistically low when using the calibration relationship for our captive birds. Neither fH nor V̇O2 varied with flight velocity across the range of speeds over which the geese would fly sustainably.


1983 ◽  
Vol 104 (1) ◽  
pp. 193-201 ◽  
Author(s):  
B. Grubb ◽  
D. D. Jorgensen ◽  
M. Conner

Cardiovascular variables were studied as a function of oxygen consumption in the emu, a large, flightless ratite bird well suited to treadmill exercise. At the highest level of exercise, the birds' rate of oxygen consumption (VO2) was approximately 11.4 times the resting level (4.2 ml kg-1 min-1). Cardiac output was linearly related to VO2, increasing 9.5 ml for each 1 ml increase in oxygen consumption. The increase in cardiac output is similar to that in other birds, but appears to be larger than in mammals. The venous oxygen content dropped during exercise, thus increasing the arteriovenous oxygen content difference. At the highest levels of exercise, heart rate showed a 3.9-fold increase over the resting rate (45.8 beats min-1). The mean resting specific stroke volume was 1.5 ml per kg body mass, which is larger than shown by most mammals. However, birds have larger hearts relative to body mass than do mammals, and stroke volume expressed per gram of heart (0.18 ml g-1) is similar to that for mammals. Stroke volume showed a 1.8-fold increase as a result of exercise in the emus, but a change in heart rate plays a greater role in increasing cardiac output during exercise.


2000 ◽  
Vol 203 (8) ◽  
pp. 1383-1393
Author(s):  
M. Frederich ◽  
F.J. Sartoris ◽  
W.E. Arntz ◽  
H. Portner

Reptant decapod crustaceans are almost absent from the Southern Ocean south of the Antarctic Convergence. We tested the hypothesis that this may be due to the reduced ability of this group to regulate Mg(2+) levels in the haemolymph ([Mg(2+)](HL)). Mg(2+) acts as an anaesthetic in marine invertebrates and its level is higher in Reptantia (crabs such as Cancer spp., Chionoecetes spp., Maja spp., 30–50 mmol l(−)(1)) than in Natantia (prawns such as Pandalus spp., Palaemon spp., Crangon spp., 5–12 mmol l(−)(1)). We varied [Mg(2+)](HL) in three species of reptant decapod crustaceans, Carcinus maenas, Hyas araneus and Eurypodius latreillei, and investigated heart rate, the rate of oxygen consumption and levels of spontaneous and forced activity at different temperatures. The rate of oxygen consumption and heart rate increased significantly with reduction in [Mg(2+)](HL) over the entire temperature range investigated in E. latreillei. In H. araneus, an increase in metabolic and heart rates compared with control values was found only at temperatures below 2 degrees C. Forced and spontaneous activity levels increased significantly in the group of [Mg(2+)](HL)-reduced animals below 0 degrees C, at which control animals were mostly inactive. At a reduced [Mg(2+)](HL) of 5–12 mmol l(−)(1), which is the [Mg(2+)](HL) of caridean shrimps in the Southern Ocean, Q(10) and activation energy were reduced for all these variables and extended the temperature range over which physiological functions were maintained. We suggest that the high [Mg(2+)](HL) in Reptantia causes relaxation of the animals and reduces their scope for activity, especially at temperatures below 0 degrees C. The hypothesis that the synergistic effects of high [Mg(2+)](HL) and low temperature probably prevented the Reptantia from recolonizing the permanently cold water of polar areas is discussed.


1975 ◽  
Vol 63 (1) ◽  
pp. 193-206
Author(s):  
P. N. Claridge ◽  
I. C. Potter

1. The standard rate of oxygen consumption, ventilatory frequency and heart rate of adult Lampetra fluviatilis were measured during the light phase of the photoperiod and at times corresponding to various stages in the upstream migration. 2. All three parameters increased during the spawning run but only in mature individuals were significant differences found between the sexes. 3. The regression coefficients for the logarithmic relationship between oxygen consumption and body weight of immature animals were 0.912 and 0.925 at 9.5 and 16 degrees C respectively. 4. Both the standard rate of oxygen consumption and the amount of oxygen taken up during activity increased greatly during the hours of darkness. 5. Oxygen consumption, ventilatory frequency and, to a lesser extent, heart rate increased significantly at 9.5 degrees C over the 100–20% range of saturation with air. 6. Below 20% saturation with air, lampreys no longer remained attached by their oral disc for prolonged periods and the ventilatory frequency rose even more rapidly to reach a maximum of 175 beats/min at 12.5%. Exposure to 7.5% resulted in death within 5–8 h.


2001 ◽  
Vol 204 (12) ◽  
pp. 2133-2144 ◽  
Author(s):  
G. Froget ◽  
P. J. Butler ◽  
Y. Handrich ◽  
A. J. Woakes

SUMMARY The use of heart rate to estimate field metabolic rate has become a more widely used technique. However, this method also has some limitations, among which is the possible impact that several variables such as sex, body condition (i.e. body fat stores) and/or inactivity might have on the relationship between heart rate and rate of oxygen consumption. In the present study, we investigate the extent to which body condition can affect the use of heart rate as an indicator of the rate of oxygen consumption. Twenty-two breeding king penguins (Aptenodytes patagonicus) were exercised on a variable-speed treadmill. These birds were allocated to four groups according to their sex and whether or not they had been fasting. Linear regression equations were used to describe the relationship between heart rate and the rate of oxygen consumption for each group. There were significant differences between the regression equations for the four groups. Good relationships were obtained between resting and active oxygen pulses and an index of the body condition of the birds. Validation experiments on six courting king penguins showed that the use of a combination of resting oxygen pulse and active oxygen pulse gave the best estimate of the rate of oxygen consumption V̇O2. The mean percentage error between predicted and measured V̇O2 was only +0.81% for the six birds. We conclude that heart rate can be used to estimate rate of oxygen consumption in free-ranging king penguins even over a small time scale (30min). However, (i) the type of activity of the bird must be known and (ii) the body condition of the bird must be accurately determined. More investigations on the impact of fasting and/or inactivity on this relationship are required to refine these estimates further.


2002 ◽  
Vol 205 (16) ◽  
pp. 2511-2517 ◽  
Author(s):  
G. Froget ◽  
Y. Handrich ◽  
Y. Le Maho ◽  
J.-L. Rouanet ◽  
A. J. Woakes ◽  
...  

SUMMARY This study investigated whether exposure to low ambient temperature could be used as an alternative to exercise for calibrating heart rate (fH)against rate of oxygen consumption(V̇O2) for subsequent use of fH to estimate V̇O2 in free-ranging animals. Using the relationship between the oxygen pulse (OP, the amount of oxygen used per heart beat) and an index of body condition (or nutritional index, NI), a relationship between fH and V̇O2 was established for resting king penguins exposed to a variety of environmental temperatures. Although there was a small but significant increase in the OP above and below the lower critical temperature (-4.9°C), there was no difference in the relationship obtained between the OP and body condition (NI)obtained above or below the lower critical temperature. These results were then compared with those obtained in a previous study in which the relationship between fH and V̇O2 had been established for king penguins during steady-state exercise. The relationship between OP and NI in the present study was not significantly different from the relationship between resting OP and NI in the previous study. However, the relationship was different from that between active OP and NI. We conclude that, at least for king penguins, although thermoregulation does not affect the relationship between resting OP and NI, temperature cannot be used as an alternative to exercise for calibrating fH against V̇O2 for subsequent use of fH to estimate V̇O2 in free-ranging animals.


2001 ◽  
Vol 204 (3) ◽  
pp. 395-407 ◽  
Author(s):  
T. Dawson

Scaling laws governing the cardiovascular system of mammals are discussed in the present review in a manner emphasizing their experimental basis. Specific attention is given to the well-known experimental laws requiring the rate of oxygen consumption and the heart rate of mammals to vary with body mass raised to the powers 3/4 and −1/4, respectively. This review involves reconsideration and further discussion of the previous work of the writer in which these and other scaling relationships were developed from fundamental considerations. The predicted scaling laws remain unchanged from the earlier work, but alternative assumptions leading to the laws are used so as to provide additional insight. The scaling laws are shown to have their origin in the basic design of the cardiovascular system and in the basic processes involved in its working. Modification of the design assumptions of the system to account for known differences in the relative heart masses of mammals and birds is shown to lead to the scaling laws for rate of oxygen consumption and heart rate of birds.


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