Heart rate and energy expenditure in resting and running Svalbard and Norwegian reindeer

1984 ◽  
Vol 246 (6) ◽  
pp. R963-R967 ◽  
Author(s):  
K. J. Nilssen ◽  
H. K. Johnsen ◽  
A. Rognmo ◽  
A. S. Blix
Keyword(s):  
Heart Rate ◽  
Energy Expenditure ◽  
Metabolic Rate ◽  
Ambient Temperature ◽  
High Arctic ◽  
O2 Consumption ◽  
Ambient Temperatures ◽  
Svalbard Reindeer ◽  
The Relationship ◽  
Cost Of Transportation

The purpose of this study was to determine whether a convenient relationship could be found between heart rate (HR) and energy expenditure at rest and during running in the high arctic Svalbard reindeer (SR) and the subarctic Norwegian reindeer (NR). Measurements of HR and energy expenditure (O2 consumption) were made at different ambient temperatures, at rest, and during running at different speeds during both summer and winter. Cost of transportation (Science 177: 222-228, 1972) was 3.56 and 2.67 J X g-1 X km-1 in SR and NR, respectively. The y-intercept value obtained for NR was close to the predicted value (J. Exp. Biol. 97: 1-22, 1982), whereas that of SR was much lower. In NR the relationship between HR and energy expenditure at running speeds from 0 to 9.2 km X h-1 is, regardless of ambient temperature (in the -30 to +10 degrees C range), described by the following equations: y = 8.04x + 48.70, r = 0.92, n = 27 (summer); and y = 7.48x + 31.20, r = 0.95, n = 52 (winter). In SR, the corresponding equations were y = 7.60x + 49.20, r = 0.94, n = 29 (summer); and y = 8.90x + 32.10, r = 0.96, n = 44 (winter), where y is HR (beats X min-1) and x is metabolic rate (W X kg-1).

Ambient temperature effects on physiological traits of white-tailed deer

1975 ◽  
Vol 53 (6) ◽  
pp. 679-685 ◽  
Author(s):  
J. B. Holter ◽  
W. E. Urban Jr. ◽  
H. H. Hayes ◽  
H. Silver ◽  
H. R. Skutt
Keyword(s):  
Heart Rate ◽  
Body Temperature ◽  
Energy Expenditure ◽  
Ambient Temperature ◽  
Temperature Effects ◽  
Temperature Changes ◽  
Wind Chill ◽  
Ambient Temperatures ◽  
Energy Equilibrium ◽  
Body Energy

Six adult white-tailed deer (Odocoileus virginianus borealis) were exposed to 165 periods of 12 consecutive hours of controlled constant ambient temperature in an indirect respiration calorimeter. Temperatures among periods varied from 38 to 0 (summer) or to −20C (fall, winter, spring). Traits measured were energy expenditure (metabolic rate), proportion of time spent standing, heart rate, and body temperature, the latter two using telemetry. The deer used body posture extensively as a means of maintaining body energy equilibrium. Energy expenditure was increased at low ambient temperature to combat cold and to maintain relatively constant body temperature. Changes in heart rate paralleled changes in energy expenditure. In a limited number of comparisons, slight wind chill was combatted through behavioral means with no effect on energy expenditure. The reaction of deer to varying ambient temperatures was not the same in all seasons of the year.

The effect of treadmill slope on the relationship between heart rate and energy expenditure in cattle walking on treadmills

1986 ◽  
Vol 106 (3) ◽  
pp. 433-436 ◽  
Author(s):  
Jennifer C. Sneddon
Keyword(s):  
Heart Rate ◽  
Energy Expenditure ◽  
Ambient Temperature ◽  
Bos Taurus ◽  
Regression Line ◽  
Bos Indicus ◽  
Live Weight ◽  
Percentage Increase ◽  
The Relationship ◽  
Working Heart

SummaryTwo steers (Bos indicus and Bos indicus x Bos taurus) were acclimatized to an ambient temperature of 30 °C before working at this temperature on two treadmills (gradients 0 and 6°) for 2 h (one on each treadmill) whilst carrying a load equivalent to 10% of body weight. The study was then repeated at an ambient temperature of 15 °C. The effect of variation between animals, ambient temperature and rate of energy expenditure were tested on the linear regression model EEw = A PHR + B (where EEw is the energy expenditure (w/kg0·75) and PHR is the percentage increase of working heart rate over resting heart rate).Animal and ambient temperature had no significant effect on the model. The gradient of the regression line was significantly greater (P < 0·01) when the animals were expending energy at the higher rate (about 30 W/kg live weight0·75) than when they were expending energy at the lower rate (about 14 W/kg live weight0·75).

scholarly journals Heart rate and energy expenditure of incubating wandering albatrosses: basal levels, natural variation, and the effects of human disturbance

2002 ◽  
Vol 205 (4) ◽  
pp. 475-483 ◽  
Author(s):  
Henri Weimerskirch ◽  
Scott A. Shaffer ◽  
Geraldine Mabille ◽  
Julien Martin ◽  
Olivier Boutard ◽  
...  
Keyword(s):  
Heart Rate ◽  
Energy Expenditure ◽  
Metabolic Rate ◽  
Human Disturbance ◽  
Natural Variation ◽  
Metabolic Chamber ◽  
The Difference ◽  
Incubating Birds ◽  
The Individual ◽  
The Relationship

SUMMARYWe studied the changes in heart rate (HR) associated with metabolic rate of incubating and resting adult wandering albatrosses (Diomedea exulans) on the Crozet Islands. Metabolic rates of resting albatrosses fitted with external HR recorders were measured in a metabolic chamber to calibrate the relationship between HR and oxygen consumption (V̇O2) (V̇O2=0.074×HR+0.019, r2=0.567, P&lt;0.001, where V̇O2 is in ml kg–1 min–1 and HR is in beats min–1). Incubating albatrosses were then fitted with HR recorders to estimate energy expenditure of albatrosses within natural field conditions. We also examined the natural variation in HR and the effects of human disturbance on nesting birds by monitoring the changes in HR. Basal HR was positively related to the mass of the individual. The HR of incubating birds corresponded to a metabolic rate that was 1.5-fold (males) and 1.8-fold (females) lower than basal metabolic rate (BMR) measured in this and a previous study. The difference was probably attributable to birds being stressed while they were held in the metabolic chamber or wearing a mask. Thus, previous measurements of metabolic rate under basal conditions or for incubating wandering albatrosses are likely to be overestimates. Combining the relationship between HR and metabolic rate for both sexes, we estimate that wandering albatrosses expend 147 kJ kg–1 day–1 to incubate their eggs. In addition, the cost of incubation was assumed to vary because (i) HR was higher during the day than at night, and (ii) there was an effect of wind chill (&lt;0°C) on basal HR. The presence of humans in the vicinity of the nest or after a band control was shown to increase HR for extended periods (2–3 h), suggesting that energy expenditure was increased as a result of the disturbance. Lastly, males and females reacted differently to handling in terms of HR response: males reacted more strongly than females before handling, whereas females took longer to recover after being handled.

Energy expenditure by elite midget male ice hockey players in small-sided games

2017 ◽  
Vol 12 (4) ◽  
pp. 504-513 ◽  
Author(s):  
Charles-Mathieu Lachaume ◽  
François Trudeau ◽  
Jean Lemoyne
Keyword(s):  
Heart Rate ◽  
Oxygen Consumption ◽  
Energy Expenditure ◽  
Ice Hockey ◽  
Training Method ◽  
Hockey Players ◽  
Treadmill Testing ◽  
Effective Training ◽  
Relationship Of ◽  
The Relationship

The purpose of this study was to investigate the energy expenditure and heart rate responses elicited in elite male midget ice hockey players during small-sided games. Nine players (aged 15.89 ± 0.33 years) participated in the study. Maximal progressive treadmill testing in the laboratory measured the relationship of oxygen consumption ([Formula: see text]) to heart rate before on-ice assessments of heart rate during six different small-sided games: 1v1, 2v2, 2v2 with support player, 3v3 with support player, 3v3 with transitions, and 4v4 with two support players. Heart rate was recorded continuously in each game. 3v3 T small-sided game was the most intense for all four intensity markers. All six small-sided games reached 89% HRmax or more with heart rate peaks in active effort repetition. These findings demonstrate that such small-sided games are considered as high intensity games and are an effective training method for ice hockey players.

Effects of Television on Metabolic Rate: Potential Implications For Childhood Obesity

PEDIATRICS ◽  
1993 ◽  
Vol 91 (2) ◽  
pp. 281-286
Author(s):  
Robert C. Klesges ◽  
Mary L. Shelton ◽  
Lisa M. Klesges
Keyword(s):  
Energy Expenditure ◽  
Metabolic Rate ◽  
Television Viewing ◽  
Resting Energy Expenditure ◽  
Normal Weight ◽  
Laboratory Setting ◽  
Obese Children ◽  
Two Measures ◽  
The Relationship ◽  
Resting Energy

The effects of television viewing on resting energy expenditure (metabolic rate) in obese and normal-weight children were studied in a laboratory setting. Subjects were 15 obese children and 16 normal-weight children whose ages ranged from 8 to 12 years. All subjects had two measures of resting energy expenditure obtained while at rest and one measurement of energy expenditure taken while viewing television. Results indicated that metabolic rate during television viewing was significantly lower (mean decrease of 211 kcal extrapolated to a day) than during rest. Obese children tended to have a larger decrease, although this difference was not statistically significant (262 kcal/d vs 167 kcal/d, respectively). It was concluded that television viewing has a fairly profound lowering effect of metabolic rate and may be a mechanism for the relationship between obesity and amount of television viewing.

scholarly journals Validating accelerometry-derived proxies of energy expenditure using the doubly-labelled water method in the smallest penguin species

Biology Open ◽  
2021 ◽  
pp. bio.055475
Author(s):  
G. J. Sutton ◽  
J. A. Botha ◽  
J. R. Speakman ◽  
J. P. Y. Arnould
Keyword(s):  
Energy Expenditure ◽  
Metabolic Rate ◽  
Energy Use ◽  
Travel Speed ◽  
Specific Energy Expenditure ◽  
Doubly Labelled Water ◽  
Data Collection And Analysis ◽  
Behavioural Patterns ◽  
Free Ranging ◽  
The Relationship

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.

Parasympathetic influence on heart rate in euthermic and hibernating ground squirrels.

1995 ◽  
Vol 198 (4) ◽  
pp. 931-937 ◽  
Author(s):  
M B Harris ◽  
W K Milsom
Keyword(s):  
Heart Rate ◽  
Ambient Temperature ◽  
Parasympathetic Nervous System ◽  
Ground Squirrels ◽  
Relative Role ◽  
Body Temperatures ◽  
Inotropic Effects ◽  
Ambient Temperatures ◽  
Isolated Hearts ◽  
C 32

The relative role of the parasympathetic nervous system during deep hibernation is enigmatic. Conflicting hypotheses exist, and both sides draw support from investigations of vagal influence on the heart. Recent studies have shown cardiac chronotropic and inotropic effects of parasympathetic stimulation and inhibition in isolated hearts and anesthetized animals at hibernating body temperatures. No studies, however, have demonstrated such occurrences in undisturbed deeply hibernating animals. The present study documents respiratory-related alterations in heart rate during euthermia and hibernation at ambient temperatures of 15, 10 and 5 degrees C mediated by parasympathetic influence. During quiet wakefulness, euthermic squirrels breathed continuously and exhibited a 29% acceleration in heart rate during inspiration. During deep undisturbed hibernation, at 15, 10 and 5 degrees C ambient temperature, animals exhibited an episodic breathing pattern and body temperatures were slightly above ambient temperature. At each temperature, heart rate during the respiratory episode was greater than that during the apnea. The magnitude of this ventilatory tachycardia decreased with ambient temperature, being 108% at 15 degrees C, 32% at 10 degrees C and 11.5% at 5 degrees C. Animals exposed to 3% CO2 at 5 degrees C, which significantly increased ventilation, still exhibited an 11.7% increase in heart rate during breathing. Thus, the magnitude of the ventilation tachycardia was independent of the level of ventilation, at least over the range studied. Inhibition of vagus nerve conduction at 5 degrees C was achieved using localized nerve block. This led to an increase in apneic heart rate and abolished the ventilatory tachycardia.(ABSTRACT TRUNCATED AT 250 WORDS)

Thermoregulation of African and European Honeybees during Foraging, Attack, and Hive Exits and Returns

1979 ◽  
Vol 80 (1) ◽  
pp. 217-229 ◽  
Author(s):  
HEINRICH BERND
Keyword(s):  
Metabolic Rate ◽  
Ambient Temperature ◽  
Heat Loss ◽  
Warm Up ◽  
Ambient Temperatures ◽  
Thoracic Temperature

1. While foraging, attacking, or leaving or returning to their hives, both the African and European honeybees maintained their thoracic temperature at 30 °C or above, independent of ambient temperature from 7 to 23 °C (in shade). 2. Thoracic temperatures were not significantly different between African and European bees. 3. Thoracic temperatures were significantly different during different activities. Average thoracic temperatures (at ambient temperatures of 8–23 °C) were lowest (30 °C) in bees turning to the hive. They were 31–32 °C during foraging, and 36–38 °C in bees leaving the hive, and in those attacking. The bees thus warm up above their temperature in the hive (32 °C) before leaving the colony. 4. In the laboratory the bees (European) did not maintain the minimum thoracic temperature for continuous flight (27 °C) at 10 °C. When forced to remain in continuous flight for at least 2 min, thoracic temperature averaged 15 °C above ambient temperature from 15 to 25 °C, and was regulated only at high ambient temperatures (30–40 °C). 5. At ambient temperatures &gt; 25 °C, the bees heated up during return to the hive, attack and foraging above the thoracic temperatures they regulated at low ambient temperatures to near the temperatures they regulated during continuous flight. 6. In both African and European bees, attack behaviour and high thoracic temperature are correlated. 7. The data suggest that the bees regulate thoracic temperature by both behavioural and physiological means. It can be inferred that the African bees have a higher metabolic rate than the European, but their smaller size, which facilitates more rapid heat loss, results in similar thoracic temperatures.

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