Variation in Energy Expenditure among Black‐Legged Kittiwakes: Effects of Activity‐Specific Metabolic Rates and Activity Budgets

2003 ◽  
Vol 76 (3) ◽  
pp. 375-388 ◽  
Author(s):  
P. G. R. Jodice ◽  
D. D. Roby ◽  
R. M. Suryan ◽  
D. B. Irons ◽  
A. M. Kaufman ◽  
...  
Keyword(s):  
Energy Expenditure ◽  
Metabolic Rates ◽  
Activity Budgets

Metabolic Rate and Energy Expenditure of the Spiny Dogfish, Squalus acanthias

1978 ◽  
Vol 35 (6) ◽  
pp. 816-821 ◽  
Author(s):  
J. R. Brett ◽  
J. M. Blackburn
Keyword(s):  
Energy Expenditure ◽  
Metabolic Rate ◽  
Key Words ◽  
Swimming Performance ◽  
Squalus Acanthias ◽  
Spiny Dogfish ◽  
Metabolic Rates ◽  
Performance Curve ◽  
Power Performance ◽  
General Energy

The metabolic rate of spiny dogfish, Squalus acanthias, was determined in both a tunnel respirometer and a large, covered, circular tank (mass respirometer). Swimming performance was very poor in the respirometer, so that a power–performance curve could not be established. Instead, resting metabolic rates were determined, with higher rates induced by causing heavy thrashing (active metabolism). Routine metabolic rates were measured for the spontaneous activity characterizing behavior in the circular tank. For fish of 2 kg mean weight, the metabolic rates at 10 °C were 32.4 ± 2.6 SE (resting), 49.2 ± 5.0 SE (routine), and 88.4 ± 4.6 SE (active) mg O2∙kg−1∙h−1. Assuming that the routine rate represents a general energy expenditure in nature, this is equivalent to metabolizing about 3.8 kcal∙kg−1∙d−1 (15.9 × 103 J∙kg−1∙d−1). Key words: dogfish, metabolic rates, energetics, respiration

Energy expenditure during load carriage at high altitude

1981 ◽  
Vol 51 (1) ◽  
pp. 14-18 ◽  
Author(s):  
A. Cymerman ◽  
K. B. Pandolf ◽  
A. J. Young ◽  
J. T. Maher
Keyword(s):  
Energy Expenditure ◽  
High Altitude ◽  
Sea Level ◽  
Prediction Equation ◽  
Cycle Ergometer ◽  
Load Carriage ◽  
Metabolic Rates ◽  
Specific Exercise ◽  
Upper Limit ◽  
Predicted Values

To determine the applicability of a prediction equation for energy expenditure during load carriage at high altitude that was previously validated at sea level, oxygen uptake (Vo2) was determined in five young men at 4,300 m while they walked with backpack loads of 0, 15, and 30 kg at treadmill grades of 0,8, and 16% at 1.12 m.s-1 for 10 min. Mean +/- SE maximal Vo2, determined on the cycle ergometer, was 42.2 +/- 2.3 at sea level and 35.6 +/- 1.7 ml.kg-1 .min-1 at altitude. There were no significant differences in daily Vo2 at any specific exercise intensity on days 1, 5, and 9 of exposure, nor were there any differences in endurance times at the two most difficult exercise intensities. Endurance times for 15- and 30-kg loads at 16% grade were 7.3 and 4.2 min, respectively. Measured energy expenditure was compared with that predicted by the formula of Pandolf et al. (J. Appl. Physiol.: Respirat. Environ. Exercise Physiol. 43: 577–581, 1977) and found to be significantly different. The differences could be attributed to measurements at metabolic rates exceeding 730 W or 2.1 1.min-1 Vo2. These data indicate that the prediction equation can be used at altitude for exercise intensities not exceeding this upper limit. The observed deviations from predicted values at the high exercise intensities could possibly be attributed to the occurrence of appreciable oxygen deficits and the inability to achieve steady-state conditions.

scholarly journals Sugar Kelp (Saccharina latissima) Inhibits Hepatic Inflammation and Fibrosis with Increased Metabolic Rates in a Mouse Model of Diet-induced Nonalcoholic Steatohepatitis (OR24-08-19)

2019 ◽  
Vol 3 (Supplement_1) ◽  
Author(s):  
Mi-Bo Kim ◽  
Yoojin Lee ◽  
Minkyung Bae ◽  
Hyunju Kang ◽  
Siqi Hu ◽  
...  
Keyword(s):  
Physical Activity ◽  
Liver Fibrosis ◽  
Energy Expenditure ◽  
Mouse Model ◽  
Total Cholesterol ◽  
Nonalcoholic Steatohepatitis ◽  
Metabolic Rates ◽  
Metabolic Disturbances ◽  
Macrophage Marker ◽  
M1 Macrophage

Abstract Objectives We investigated whether consumption of sugar kelp, an edible brown seaweed, can attenuate metabolic disturbances and nonalcoholic steatohepatitis (NASH) in a mouse model of NASH with evident liver fibrosis. Methods Male C57BL/6 J mice were fed a low-fat control (LF; 6% fat by wt), a high-fat/high-sucrose/high-cholesterol control (HF; 34% fat, 34% sucrose, 2.0% cholesterol by wt), or a HF containing sugar kelp (HF-Kelp; 6.0% dried sugar kelp powder by wt) for 14 weeks. Blood chemistry as well as biochemical, molecular, and histological analyses were conducted in the liver and epididymal white adipose tissue (eWAT). Metabolic rates, energy expenditure, and physical activity of mice were determined using indirect calorimetry Results Body weight of mice fed HF-Kelp was significantly lower than that of HF group. Compared to LF, HF significantly increased serum total cholesterol and glucose, which were decreased by kelp. In the liver, HF-Kelp group showed decreases in weight, triglycerides, total cholesterol, and steatosis compared with HF-fed mice. Also, kelp decreased hepatic expression of a macrophage marker F4/80 and an M1 macrophage marker CD11c. Mice fed HF-Kelp also exhibited decreased liver fibrosis as evidenced by less expression of fibrogenic genes and collagen accumulation than those of HF group. In eWAT, HF-Kelp diet reduced weight and adipocyte size compared with HF control. While HF-Kelp diet increased mRNA abundance of peroxisome proliferator activated receptor γ, it decreased the expression of collagen type VI alpha 1 chain, F4/80, CD11c, and tumor necrosis factor α, in eWAT. Oxygen consumption, carbon dioxide production, energy expenditure, and physical activity were significantly higher in HF-Kelp group than HF. Conclusions Kelp consumption markedly prevented weight gain, fat accumulation, inflammation, and fibrosis in the liver and eWAT of mice with NASH. The health benefits of kelp were accompanied by increased metabolic rates, energy expenditure, and physical activity. Therefore, kelp may be consumed to prevent obesity-associated metabolic disturbances and NASH. Funding Sources This study was supported by USDA Hatch.

scholarly journals Specific metabolic rates of major organs and tissues across adulthood: evaluation by mechanistic model of resting energy expenditure

2010 ◽  
Vol 92 (6) ◽  
pp. 1369-1377 ◽  
Author(s):  
ZiMian Wang ◽  
Zhiliang Ying ◽  
Anja Bosy-Westphal ◽  
Junyi Zhang ◽  
Britta Schautz ◽  
...  
Keyword(s):  
Energy Expenditure ◽  
Mechanistic Model ◽  
Resting Energy Expenditure ◽  
Metabolic Rates ◽  
Resting Energy

scholarly journals Activity-specific metabolic rates for diving, transiting, and resting at sea can be estimated from time-activity budgets in free-ranging marine mammals

2017 ◽  
Vol 7 (9) ◽  
pp. 2969-2976 ◽  
Author(s):  
Tiphaine Jeanniard-du-Dot ◽  
Andrew W. Trites ◽  
John P. Y. Arnould ◽  
John R. Speakman ◽  
Christophe Guinet
Keyword(s):  
Marine Mammals ◽  
Metabolic Rates ◽  
Activity Budgets ◽  
Time Activity ◽  
Free Ranging

Metabolic strategies for winter survival by Svalbard reindeer

1993 ◽  
Vol 71 (9) ◽  
pp. 1787-1792 ◽  
Author(s):  
L. C. Cuyler ◽  
N. A. Øritsland
Keyword(s):  
Energy Expenditure ◽  
Metabolic Rate ◽  
Energy Requirement ◽  
Resting Metabolic Rate ◽  
Thermal Conductance ◽  
Activity Budget ◽  
Survival Strategies ◽  
Metabolic Rates ◽  
Energy Expenditures ◽  
Svalbard Reindeer

Lying and standing metabolic rates were determined for two tame Svalbard reindeer while the animals were in their winter lethargic state during January and February. Mean nonfasting metabolic rates for the 59-kg animals were 1.25 W∙kg−1 for lying and 1.64 W∙kg−1 for standing at rest. So the metabolic rate for standing at rest was about 1.3 times the lying resting metabolic rate (RMR). For Svalbard reindeer the lying RMR was 66–78% of the values for other reindeer/caribou, and was 78–89% of the predicted value. The standing RMR was 44–88% of the values from other reindeer/caribou. Total body thermal conductance was 1.95 ± 0.17 W∙°C−1 for lying and 3.08 ± 0.77 W∙°C−1 for standing at rest. The daily energy expenditure during winter was estimated to be about 9654 kJ∙day−1 or 112 W, and was 1.5 times Kleiber's predicted basal metabolic rate. By remaining lying 45% of the time rather than 35% Svalbard reindeer may conserve the equivalent of about 15 days' energy requirement over the winter. With locomotion at 2% of the winter daily activity budget, the Svalbard reindeer conserve about 21 days' energy expenditure, more than that if locomotion were 8.2% of the budget as in caribou (Boertje 1985). Thus, their low energy expenditures for lying and standing and their sedentary activity budget may be considered energy-saving and survival strategies. It is possible that disturbances, which cause the animals to increase activity, may have a detrimental effect on their overall winter energy balance.

The ecology of dippers Cinclus cinclus (L.) in relation to stream acidity in upland Wales: time-activity budgets and energy expenditure

Oecologia ◽  
1990 ◽  
Vol 85 (2) ◽  
pp. 271-280 ◽  
Author(s):  
J. O'Halloran ◽  
S. D. Gribbin ◽  
Stephanie J. Tyler ◽  
S. J. Ormerod
Keyword(s):  
Energy Expenditure ◽  
Activity Budgets ◽  
Time Activity ◽  
Cinclus Cinclus

scholarly journals Reproductive energetics of adult male yellow-bellied marmots (Marmota flaviventris)

1995 ◽  
Vol 73 (10) ◽  
pp. 1791-1797 ◽  
Author(s):  
Carmen M. Salsbury ◽  
Kenneth B. Armitage
Keyword(s):  
Energy Expenditure ◽  
Metabolic Rate ◽  
Adult Male ◽  
Reproductive Investment ◽  
High Energy ◽  
Male Reproductive Success ◽  
Metabolic Rates ◽  
Marmota Flaviventris ◽  
Term Survival ◽  
Active Season

We examined the energy expenditure of adult male yellow-bellied marmots (Marmota flaviventris) and its relationship to various female-defense characteristics critical to male reproductive success. Resting metabolic rates of males were estimated in the laboratory via oxygen-consumption analysis, and field metabolic rates were estimated using a doubly labeled water technique. Male home-range size, number of females defended by males, dispersion of females in the habitat, and date into the active season were considered to be predictors of male energy expenditure in excess of maintenance costs (field metabolic rate minus resting metabolic rate). Energy expenditure was best explained by a defensibility index based on the number and dispersion of females defended; expenditure increased with number and dispersion of females. Energy expenditure increased with date into the active season. Environmental constraints on male activity during the mating season may have led to a shift in male reproductive investment to later in the season, when intruder pressure by conspecifics increased. No short-term survival costs were associated with high energy expenditure; males appeared to engage in reproductive behaviors congruent with their physiological capabilities.

scholarly journals Energetics of vertical kilometer foot races; is steeper cheaper?

2016 ◽  
Vol 120 (3) ◽  
pp. 370-375 ◽  
Author(s):  
Nicola Giovanelli ◽  
Amanda Louise Ryan Ortiz ◽  
Keely Henninger ◽  
Rodger Kram
Keyword(s):  
Energy Expenditure ◽  
Video Analysis ◽  
Vertical Velocity ◽  
Stride Length ◽  
Duty Factor ◽  
Stride Frequency ◽  
Ground Contact ◽  
Metabolic Rates ◽  
Metabolic Costs

Vertical kilometer foot races consist of a 1,000-m elevation gain in <5,000 m of overall distance, and the inclines of the fastest courses are ∼30°. Previous uphill locomotion studies have focused on much shallower angles. We aimed to quantify the metabolic costs of walking and running on very steep angles and to biomechanically distinguish walking from running. Fifteen runners (10 male, 5 female, 32.9 ± 7.5 yr, 1.75 ± 0.09 m, 64.3 ± 9.1 kg) walked and ran for 5 min at seven different angles (9.4, 15.8, 20.4, 24.8, 30.0, 35.0, and 39.2°) all at a fixed vertical velocity (0.35 m/s). We measured the metabolic rates and calculated the vertical costs of walking (Cwvert) and running (Crvert). Using video analysis, we determined stride frequency, stride length, and duty factor (fraction of stride that each foot is in ground contact). At all angles other than 9.4°, Cwvert was cheaper than Crvert (average −8.45 ± 1.05%; P < 0.001). Further, broad minima for both Cwvert and Crvert existed between 20.4 and 35.0° (average Cwvert 44.17 ± 0.41 J·kg−1·m−1 and average Crvert 48.46 ± 0.35 J·kg−1·m−1). At all angles and speeds tested, both walking and running involved having at least one foot on the ground at all times. However, in walking, stride frequency and stride length were ∼28% slower and longer, respectively, than in running. In conclusion, we found that there is a range of angles for which energy expenditure is minimized. At the vertical velocity tested, on inclines steeper than 15.8°, athletes can reduce their energy expenditure by walking rather than running.

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