Energy Metabolism of Dragonflies (Odonata: Anisoptera) at Rest and During Endothermic Warm-Up

1979 ◽  
Vol 83 (1) ◽  
pp. 79-94
Author(s):  
MICHAEL L. MAY

1. Energy metabolism at rest and during pre-flight warm-up was measured in a variety of anisopterous dragonflies. 2. Resting oxygen consumption was similar in its relation to body temperature (Tb) and body mass to that of other insects. At 30 °C, log M = 0.91 log m + 0.44, where M is metabolism (W) and m is body mass (kg). 3. Metabolism during warm-up was calculated both from measurements of Tb and from oxygen consumption. By the former method, log M = 1.01 log m + 2.22 at the maximum Tb attained during warm-up, and log M = 0.90 log m + 1.87 at Tb = 30 °C. Oxygen consumption measurements mostly gave values of M about 15% higher. 4. Total energy cost of warm-up is directly related to mass, thermal conductance and Tb at takeoff, and inversely related to warm-up rate.

1992 ◽  
Vol 262 (5) ◽  
pp. R771-R778 ◽  
Author(s):  
R. V. Baudinette ◽  
G. K. Snyder ◽  
P. B. Frappell

Rates of oxygen consumption and blood lactate levels were measured in tammar wallabies (Macropus eugenii) trained to hop on a treadmill. In addition, the work required to overcome wind resistance during forward locomotion was measured in a wind tunnel. Up to approximately 2.0 m/s, rates of oxygen consumption increased linearly with speed and were not significantly different from rates of oxygen consumption for a quadruped of similar body mass. Between 2.0 and 9.4 m/s, rates of oxygen consumption were independent of hopping speed, and between 3.9 and 7.9 m/s, the range over which samples were obtained, blood lactate levels were low (0.83 +/- 0.13 mmol.min-1.kg-1) and did not increase with hopping speed. The work necessary to overcome drag increased exponentially with speed but increased the energy cost of locomotion by only 10% at the average speed attained by our fast hoppers. Thus, during hopping, the energy cost of locomotion is effectively independent of speed. At rates of travel observed in the field, the estimated energy cost of transport in large macropods is less than one-third the cost for a quadruped of equivalent body mass. The energetic savings associated with this unique form of locomotion may have been an important physiological adaptation, enabling large macropods to efficiently cover the distances necessary to forage in the semiarid landscapes of Australia.


2003 ◽  
Vol 51 (6) ◽  
pp. 603 ◽  
Author(s):  
M. P. Ikonomopoulou ◽  
R. W. Rose

We investigated the metabolic rate, thermoneutral zone and thermal conductance of the eastern barred bandicoot in Tasmania. Five adult eastern barred bandicoots (two males, three non-reproductive females) were tested at temperatures of 3, 10, 15, 20, 25, 30, 35 and 40°C. The thermoneutral zone was calculated from oxygen consumption and body temperature, measured during the daytime: their normal resting phase. It was found that the thermoneutral zone lies between 25°C and 30°C, with a minimum metabolic rate of 0.51 mL g–1 h–1 and body temperature of 35.8°C. At cooler ambient temperatures (3–20°C) the body temperature decreased to approximately 34.0°C while the metabolic rate increased from 0.7 to 1.3 mL g–1�h–1. At high temperatures (35°C and 40°C) both body temperature (36.9–38.7°C) and metabolic rate (1.0–1.5 mL g–1 h–1) rose. Thermal conductance was low below an ambient temperature of 30°C but increased significantly at higher temperatures. The low thermal conductance (due, in part, to good insulation, a reduced body temperature at lower ambient temperatures, combined with a relatively high metabolic rate) suggests that this species is well adapted to cooler environments but it could not thermoregulate easily at temperatures above 30°C.


1965 ◽  
Vol 20 (3) ◽  
pp. 405-410 ◽  
Author(s):  
Hermann Pohl

Characteristics of cold acclimation in the golden hamster, Mesocricetus auratus, were 1) higher metabolic rate at -30 C, 2) less shivering when related to ambient temperature or oxygen consumption, and 3) higher differences in body temperature between cardiac area and thoracic subcutaneous tissues at all ambient temperatures tested, indicating changes in tissue insulation. Cold-acclimated hamsters also showed a rise in temperature of the cardiac area when ambient temperature was below 15 C. Changes in heat distribution in cold-acclimated hamsters suggest higher blood flow and heat production in the thoracic part of the body in the cold. The thermal conductance through the thoracic and lumbar muscle areas, however, did not change notably with lowering ambient temperature. Marked differences in thermoregulatory response to cold after cold acclimation were found between two species, the golden hamster and the thirteen-lined ground squirrel, showing greater ability to regulate body temperature in the cold in hamsters. hibernator; oxygen consumption— heat production; body temperature — heat conductance; muscular activity — shivering; thermoregulation Submitted on July 6, 1964


1965 ◽  
Vol 20 (1) ◽  
pp. 46-50 ◽  
Author(s):  
D. H. Kang ◽  
P. K. Kim ◽  
B. S. Kang ◽  
S. H. Song ◽  
S. K. Hong

Rectal temperature and oxygen consumption were determined in the ama while diving during the summer and winter. In addition, a dietary survey and a physical-fitness test were conducted. The average rectal temperature fell to 35.3 C after 45 min of work in summer (water temp., 22–26 C) and to 34.8 C after 30 min of work in winter (water temp., 10–13 C). The lowest rectal temperature was 33.2 C in summer and 34.3 C in winter. Vo2 increased to nearly 1 liter/min in summer and to 1.4 liter/min in winter. One can calculate that the total extra energy expenditure for diving work is approximately 1,000 kcal/day in both winter and summer. The actual dietary survey showed that the total caloric intake of the ama is 3,000 kcal/day in both summer and winter, which exceeds the daily requirement for nondiving women of comparable age by 1,000 kcal. The protein intake was not different between summer and winter. Physical fitness, as judged by the score of Harvard step-up test, was significantly better in the ama than in the control in both summer and winter. Moreover, physical fitness was poorer in winter as compared to summer in the control, whereas it was excellent throughout a year in the ama. cold stress; physical fitness Submitted on January 15, 1964


2006 ◽  
Vol 290 (4) ◽  
pp. R881-R891 ◽  
Author(s):  
Roee Gutman ◽  
Itzhak Choshniak ◽  
Noga Kronfeld-Schor

Golden spiny mice, which inhabit rocky deserts and do not store food, must therefore employ physiological means to cope with periods of food shortage. Here we studied the physiological means used by golden spiny mice for conserving energy during food restriction and refeeding and the mechanism by which food consumption may influence thermoregulatory mechanisms and metabolic rate. As comparison, we studied the response to food restriction of another rocky desert rodent, Wagner’s gerbil, which accumulates large seed caches. Ten out of 12 food-restricted spiny mice (resistant) were able to defend their body mass after an initial decrease, as opposed to Wagner’s gerbils ( n = 6). Two of the spiny mice (nonresistant) kept losing weight, and their food restriction was halted. In four resistant and two nonresistant spiny mice, we measured heart rate, body temperature, and oxygen consumption during food restriction. The resistant spiny mice significantly ( P < 0.05) reduced energy expenditure and entered daily torpor. The nonresistant spiny mice did not reduce their energy expenditure. The gerbils’ response to food restriction was similar to that of the nonresistant spiny mice. Resistant spiny mice leptin levels dropped significantly ( n = 6, P < 0.05) after 24 h of food restriction, and continued to decrease throughout food restriction, as did body fat. During refeeding, although the golden spiny mice gained fat, leptin levels were not correlated with body mass ( r2 = 0.014). It is possible that this low correlation allows them to continue eating and accumulate fat when food is plentiful.


1976 ◽  
Vol 86 (3) ◽  
pp. 471-473 ◽  
Author(s):  
M. Van Kampen

SummaryThe energy cost of nesting activity and oviposition of hens in different environments has been determined.The oxygen consumption of hens on a wire floor reached a peak during the last 15 min before oviposition. However, the oxygen uptake of hens accustomed to a litter floor had fallen to a minimum at this time.The energy cost of expelling the egg is minimal. There is a good correlation between the locomotor activity and the heat production.The variations in heat production and body temperature on different types of floors are explicable by the differences in nesting activity.


1989 ◽  
Vol 37 (6) ◽  
pp. 685 ◽  
Author(s):  
PC Withers ◽  
KC Richardson ◽  
RD Wooller

Euthermic honey possums have a higher body temperature (Tb), basal metabolic rate and wet thermal conductance than other marsupials of similar mass. Honey possums enter torpor when cold-stressed and deprived of food. The pattern of decline in body temperature and oxygen consumption during torpor generally resembles that of other heterothermic endotherms. The duration of torpor bouts in honey possums was about 10 h; torpor bouts longer than one day were not observed. The Tb declined during torpor to within 1-2�C of ambient temperature (Ta>5�C) and oxygen consumption rate declined dramatically. The minimal body temperature (Tb,min) measured for torpid honey possums was about 5�C, because Tb was regulated at about 5�C by honey possums torpid at Ta<5�C, by an elevation of oxygen consumption rate. Previous studies of small marsupials have delineated two basic patterns of torpor: (1) shallow (Tb,min>10-15�C) and short-term torpor cycles (e.g. in dasyurids); (2) deep (Tb,min<10�C) and multi-day torpor cycles (e.g. in burramyids). Honey possums appear to have a third pattern of deep (Tb,min=5�C) but short-term torpor. The ecological reasons for this pattern of deep torpor and the apparent absence of multi-day torpor in honey possums may be related to their nectarivorous diet and lack of extensive fat stores.


1965 ◽  
Vol 20 (3) ◽  
pp. 398-404 ◽  
Author(s):  
Hermann Pohl ◽  
J. Sanford Hart

In the thirteen-lined ground squirrel, Citellus tridecemlineatus, the maintenance of body temperature and oxygen consumption in the cold is improved by acclimation to 18 and 6 C in the laboratory. Heat production at -30 C was greater in animals acclimated to 6 C, whether or not they had been previously hibernating, than in squirrels kept at 28 C. Oxygen consumption was correlated to body weight0.41. This relationship was not significantly affected by changes in ambient temperature. Local heat flow from the dorsal thorax was similar at a given temperature in all acclimation groups but the thermal conductance was greater and the cardiac-subcutaneous temperature difference was smaller in squirrels acclimated to 6 and 18 C. Although shivering was equally high in warm- and cold-acclimated ground squirrels in the cold, nonshivering thermogenesis occurred in curarized cold-acclimated animals exposed to cold or injected with noradrenaline. The results of the study suggest that ground squirrels are regularly exposed to temperatures in their natural habitat which induce considerable cold acclimation. oxygen consumption—heat production; body temperature—heat conductance; muscular activity Submitted on July 6, 1964


PeerJ ◽  
2018 ◽  
Vol 6 ◽  
pp. e4627 ◽  
Author(s):  
Lucia V. Cabrera-Martínez ◽  
L. Gerardo Herrera M. ◽  
Ariovaldo P. Cruz-Neto

The acute phase response (APR) is the first line of defense of the vertebrate immune system against pathogens. Mounting an immune response is believed to be energetically costly but direct measures of metabolic rate during immune challenges contradict this assumption. The energetic cost of APR for birds is higher than for rodents, suggesting that this response is less expensive for mammals. However, the particularly large increase in metabolic rate after APR activation for a piscivorous bat (Myotis vivesi) suggests that immune response might be unusually costly for bats. Here we quantified the energetic cost and body mass change associated with APR for the nectarivorous Pallas’s long-tongued bat (Glossophaga soricina). Activation of the APR resulted in a short-term decrease in body mass and an increase in resting metabolic rate (RMR) with a total energy cost of only 2% of the total energy expenditure estimated for G. soricina. This increase in RMR was far from the large increase measured for piscivorous bats; rather, it was similar to the highest values reported for birds. Overall, our results suggest that the costs of APR for bats may vary interspecifically. Measurement of the energy cost of vertebrate immune response is limited to a few species and further work is warranted to evaluate its significance for an animal’s energy budget.


1987 ◽  
Vol 130 (1) ◽  
pp. 137-153 ◽  
Author(s):  
ROBERT J. FULL

Arthropods possess spectacular diversity in locomotor design. Yet it is not clear what unique constraints, if any, variation in design imposes on mechanics, metabolic energy cost or endurance during terrestrial locomotion. In the present study metabolic energy cost and endurance on a treadmill are measured for an arthropod, the eight-legged sideways travelling ghost crab, Ocypode quadrata (Fabricius). In a second paper the mechanics of locomotion are determined during walking and running over a force plate. Severe limitations in O2 uptake during exercise are not inherent in the design of a crab's O2 transport system, which consists of gills and an open circulatory system. The ghost crab's capacity to elevate oxygen consumption (VOO2) rapidly is correlated with a lesser dependence on anaerobic sources than observed in other crab species. Accelerated glycolysis contributed at the onset of submaximal exercise, before O2 uptake adjustments were completed, but played only a minor role during steady-state exercise. O. quadrata elevated VOO2 6–4- to 8-fold above resting rates. The ghost crab's maximal oxygen consumption (VOO2max) was not different from that of an ectothermic vertebrate of the same body mass and temperature, such as a lizard, that uses lungs and a closed circulatory system. The minimum metabolic energy necessary to move 1 g of crab 1 km (Cmin) decreased as a function of body mass and age. Cmin was comparable to that predicted for vertebrates of a similar body mass and, therefore, appears to be relatively independent of locomotor design. This is consistent with the hypothesis that a similarity in the energetic properties of muscle and elastic structures may result in similar metabolic costs of locomotion. Endurance capacity did not increase with body mass, as predicted from interspecific comparisons of mammals and lizards. Instead, endurance capacity correlated with the speed at which oxygen consumption was maximal. Mean endurance capacity for ghost crabs was similar to that found for lizards, but was far less than the values predicted for mammals. Ghost crabs could only sustain a slow walk. Running at speeds 20 times faster is possible for short periods, but not without the aid of anaerobic metabolism.


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