scholarly journals Determinants of climbing energetic costs in humans

2021 ◽  
Author(s):  
Elaine E. Kozma ◽  
Herman Pontzer
Keyword(s):  
Body Size ◽  
Energy Expenditure ◽  
Body Mass ◽  
Anatomical Variation ◽  
Negligible Effect ◽  
Energetic Cost ◽  
Energetic Costs ◽  
Cost Of Transport ◽  
Specific Cost ◽  
Limb Proportions

Previous studies in primates and other animals have shown that mass specific cost of transport (J kg−1 m−1) for climbing is independent of body size across species, but little is known about within-species allometry of climbing costs or the effects of difficulty and velocity. Here, we assess the effects of velocity, route difficulty, and anatomical variation on the energetic cost of climbing within humans. Twelve experienced rock climbers climbed on an indoor wall over a range of difficulty levels and velocities, with energy expenditure measured via respirometry. We found no effect of body mass or limb proportions on mass-specific cost of transport among subjects. Mass-specific cost of transport was negatively correlated with climbing velocity. Increased route difficulty was associated with slower climbing velocities and thus higher costs, but there was no statistically significant effect of route difficulty on energy expenditure independent of velocity. Finally, human climbing costs measured in this study were similar to published values for other primates, suggesting arboreal adaptations have a negligible effect on climbing efficiency.

Speed, stride frequency and energy cost per stride: how do they change with body size and gait?

1988 ◽  
Vol 138 (1) ◽  
pp. 301-318 ◽  
Author(s):  
N. C. Heglund ◽  
C. R. Taylor
Keyword(s):  
Body Size ◽  
Body Mass ◽  
Energy Cost ◽  
Reaction Force ◽  
Stride Frequency ◽  
Energetic Cost ◽  
Published Data ◽  
Frequency Change ◽  
Cost Of Locomotion ◽  
The Cost

In this study we investigate how speed and stride frequency change with body size. We use this information to define ‘equivalent speeds’ for animals of different size and to explore the factors underlying the six-fold difference in mass-specific energy cost of locomotion between mouse- and horse-sized animals at these speeds. Speeds and stride frequencies within a trot and a gallop were measured on a treadmill in 16 species of wild and domestic quadrupeds, ranging in body size from 30 g mice to 200 kg horses. We found that the minimum, preferred and maximum sustained speeds within a trot and a gallop all change in the same rather dramatic manner with body size, differing by nine-fold between mice and horses (i.e. all three speeds scale with about the 0.2 power of body mass). Although the absolute speeds differ greatly, the maximum sustainable speed was about 2.6-fold greater than the minimum within a trot, and 2.1-fold greater within a gallop. The frequencies used to sustain the equivalent speeds (with the exception of the minimum trotting speed) scale with about the same factor, the −0.15 power of body mass. Combining this speed and frequency data with previously published data on the energetic cost of locomotion, we find that the mass-specific energetic cost of locomotion is almost directly proportional to the stride frequency used to sustain a constant speed at all the equivalent speeds within a trot and a gallop, except for the minimum trotting speed (where it changes by a factor of two over the size range of animals studied). Thus the energy cost per kilogram per stride at five of the six equivalent speeds is about the same for all animals, independent of body size, but increases with speed: 5.0 J kg-1 stride-1 at the preferred trotting speed; 5.3 J kg-1 stride-1 at the trot-gallop transition speed; 7.5 J kg-1 stride-1 at the preferred galloping speed; and 9.4 J kg-1 stride-1 at the maximum sustained galloping speed. The cost of locomotion is determined primarily by the cost of activating muscles and of generating a unit of force for a unit of time. Our data show that both these costs increase directly with the stride frequency used at equivalent speeds by different-sized animals. The increase in cost per stride with muscles (necessitating higher muscle forces for the same ground reaction force) as stride length increases both in the trot and in the gallop.

Efficiency of uphill locomotion in nocturnal and diurnal lizards

1996 ◽  
Vol 199 (3) ◽  
pp. 587-592 ◽  
Author(s):  
C Farley ◽  
M Emshwiller
Keyword(s):  
Body Mass ◽  
Low Cost ◽  
Minimum Cost ◽  
Mechanical Work ◽  
Energetic Cost ◽  
Cost Of Transport ◽  
Unit Distance ◽  
Cost Of Locomotion ◽  
Average Body Mass ◽  
Average Body

Nocturnal geckos can walk on level ground more economically than diurnal lizards. One hypothesis for why nocturnal geckos have a low cost of locomotion is that they can perform mechanical work during locomotion more efficiently than other lizards. To test this hypothesis, we compared the efficiency of the nocturnal gecko Coleonyx variegatus (average body mass 4.2 g) and the diurnal skink Eumeces skiltonianus (average body mass 4.8 g) when they performed vertical work during uphill locomotion. We measured the rate of oxygen consumption when each species walked on the level and up a 50 slope over a range of speeds. For Coleonyx variegatus, the energetic cost of traveling a unit distance (the minimum cost of transport, Cmin) increased from 1.5 to 2.7 ml O2 kg-1 m-1 between level and uphill locomotion. For Eumeces skiltonianus, Cmin increased from 2.5 to 4.7 ml O2 kg-1 m-1 between level and uphill locomotion. By taking the difference between Cmin for level and uphill locomotion, we found that the efficiency of performing vertical work during locomotion was 37 % for Coleonyx variegatus and 19 % for Eumeces skiltonianus. The similarity between the 1.9-fold difference in vertical efficiency and the 1.7-fold difference in the cost of transport on level ground is consistent with the hypothesis that nocturnal geckos have a lower cost of locomotion than other lizards because they can perform mechanical work during locomotion more efficiently.

Energy expenditure is reduced in preobese 2-day Zucker fa/fa rats

1985 ◽  
Vol 249 (2) ◽  
pp. R262-R265 ◽  
Author(s):  
B. J. Moore ◽  
S. J. Armbruster ◽  
B. A. Horwitz ◽  
J. S. Stern
Keyword(s):  
Adipose Tissue ◽  
Oxygen Consumption ◽  
Body Size ◽  
Energy Expenditure ◽  
Body Mass ◽  
Early Age ◽  
Ambient Temperatures ◽  
Consumption Data ◽  
Brown Adipose ◽  
Rate Of Oxygen Consumption

The rate of oxygen consumption was measured in 2-day Zucker preobese (fa/fa), homozygous (Fa/Fa) lean, and lean rats of unknown genotype (Fa/?) over the ambient temperature range of 26-35 degrees C. Significant differences in body mass were found among the three groups at this early age, the preobese pups having the greatest body mass. To account for body mass differences, the oxygen consumption data were expressed in terms of metabolic body size (ml O2 consumed X g body mass-2/3 X h-1). This mass-independent rate of oxygen consumption was significantly lower in the preobese pups than in the homozygous lean (Fa/Fa) pups at both thermoneutral (33-34 degrees C) and cold (26-27 degrees C) ambient temperatures at which, respectively, minimal and maximal rates of oxygen consumption were observed. This reduction in energy expenditure occurs before the establishment of hyperphagia or decreased levels of activity in the preobese pups. These data support the view that attenuated energy expenditure is a significant contributor to the early development of obesity in the Zucker fatty rat and point to the possibility of defective brown adipose tissue-mediated thermogenesis in the preobese pup.

scholarly journals The fast and the frugal: Divergent locomotory strategies drive limb lengthening in theropod dinosaurs

2019 ◽  
Author(s):  
T. Alexander Dececchi ◽  
Aleksandra M. Mloszewska ◽  
Thomas R. Holtz ◽  
Michael B. Habib ◽  
Hans C.E. Larsson
Keyword(s):  
Body Size ◽  
Large Body ◽  
Limb Lengthening ◽  
Limb Length ◽  
Energetic Cost ◽  
Energetic Efficiency ◽  
Leg Length ◽  
Distal Limb ◽  
Cost Of Transport ◽  
The Impact

AbstractLimb length, cursoriality and speed have long been areas of significant interest in theropod paleobiology as locomotory capacity, especially running ability, is critical in not just in prey pursuit but also to avoid become prey oneself. One aspect that is traditionally overlooked is the impact of allometry on running ability and the limiting effect of large body size. Since several different non-avian theropod lineages have each independently evolved body sizes greater than any known terrestrial carnivorous mammal, ∼1000kg or more, the effect that such larger mass has on movement ability and energetics is an area with significant implications for Mesozoic paleoecology. Here using expansive datasets, incorporating several different metrics to estimate body size, limb length and running speed, to calculate the effects of allometry running We test both on traditional metrics used to evaluate cursoriality in non-avian theropods such as distal limb length, relative hindlimb length as well as comparing the energetic cost savings of relative hindlimb elongation between members of the Tyrannosauridae and more basal megacarnivores such as Allosauroids or Ceratosauridae. We find that once the limiting effects of body size increase is incorporated, no commonly used metric including the newly suggested distal limb index (Tibia + Metatarsus/ Femur length) shows a significant correlation to top speed. The data also shows a significant split between large and small bodied theropods in terms of maximizing running potential suggesting two distinct strategies for promoting limb elongation based on the organisms’ size. For small and medium sized theropods increased leg length seems to correlate with a desire to increase top speed while amongst larger taxa it corresponds more closely to energetic efficiency and reducing foraging costs. We also find, using 3D volumetric mass estimates, that the Tyrannosauridae show significant cost of transport savings compared to more basal clades, indicating reduced energy expenditures during foraging and likely reduced need for hunting forays. This suggests that amongst theropods while no one strategy dictated hindlimb evolution. Amongst smaller bodied taxa the competing pressures of being both a predator and a prey item dominant while larger ones, freed from predation pressure, seek to maximize foraging ability. We also discuss the implications both for interactions amongst specific clades and Mesozoic paleobiology and paleoecological reconstructions as a whole.

IS WALKING COSTLY FOR ANURANS? THE ENERGETIC COST OF WALKING IN THE NORTHERN TOAD BUFO BOREAS HALOPHILUS

1994 ◽  
Vol 197 (1) ◽  
pp. 165-178
Author(s):  
B Walton ◽  
C Peterson ◽  
A Bennett
Keyword(s):  
Oxygen Consumption ◽  
Body Mass ◽  
Minimum Cost ◽  
Aerobic Metabolism ◽  
Energetic Cost ◽  
Cost Of Transport ◽  
Bufo Boreas ◽  
Steady State Rate ◽  
Rate Of Oxygen Consumption ◽  
Locomotor Energetics

Locomotor mode and the maximal capacity for aerobic metabolism are thought to be co-adapted in anuran amphibians. Species that rely heavily on walking often have high capacities for aerobic metabolism relative to species that rely primarily on saltation. We tested the hypothesis of co-adaptation of gait and aerobic metabolism by investigating the locomotor energetics of Bufo boreas halophilus, a toad that walks, but does not hop. Rates of oxygen consumption during locomotion were measured in an enclosed variable-speed treadmill. The steady-state rate of oxygen consumption (V(dot)O2ss) increased linearly within a range of sustainable speeds [V(dot)O2ss (ml O2 g-1 h-1) = 0.93 x speed (km h-1) + 0.28]. The minimum cost of transport, Cmin (the slope of this relationship), varied significantly among individual toads. When expressed in units of oxygen consumed per distance travelled (ml O2 km-1), Cmin scaled isometrically with body mass: Cmin = 0.69mass1.07. Consequently, mass-specific Cmin (ml O2 g-1 km-1) was uncorrelated with body mass. Variation in Cmin was also unrelated to experimental temperature. Mass-specific Cmin estimates were similar to previous allometric predictions for terrestrial animals of similar size, which contrasts with previous findings for another toad species. Maximum rates of oxygen consumption measured in closed, rotating respirometers were significantly higher than the maximum rates achieved on the treadmill, but lower than those measured previously in other Bufo species. Our results indicate that walking is not necessarily a costly gait for toads and that high maximum rates of oxygen consumption are not associated with reliance on walking within the genus Bufo.

Nonexercise movement in elderly compared with young people

2007 ◽  
Vol 292 (4) ◽  
pp. E1207-E1212 ◽  
Author(s):  
Ann M. Harris ◽  
Lorraine M. Lanningham-Foster ◽  
Shelly K. McCrady ◽  
James A. Levine
Keyword(s):  
Energy Expenditure ◽  
Lean Body Mass ◽  
Body Mass ◽  
The Elderly ◽  
Energetic Cost ◽  
Elderly Subjects ◽  
Older Individuals ◽  
Free Living ◽  
Healthy Elderly ◽  
Young Subjects

The association between free-living daily activity and aging is unclear because nonexercise movement and its energetic equivalent, nonexercise activity thermogenesis, have not been exhaustively studied in the elderly. We wanted to address the hypothesis that free-living nonexercise movement is lower in older individuals compared with younger controls matched for lean body mass. Ten lean, healthy, sedentary elderly and 10 young subjects matched for lean body mass underwent measurements of nonexercise movement and body posture over 10 days using sensitive, validated technology. In addition, energy expenditure was assessed using doubly labeled water and indirect calorimetry. Total nonexercise movement (acceleration arbitrary units), standing time, and standing acceleration were significantly lower in the elderly subjects; this was specifically because the elderly walked less distance per day despite having a similar number of walking bouts per day compared with the young individuals. The energetic cost of basal metabolic rate, thermic effect of food, total daily energy expenditure, and nonexercise activity thermogenesis were not different between the elderly and young groups. Thus, the energetic cost of walking in the elderly may be greater than in the young. Lean, healthy elderly individuals may have a biological drive to be less active than the young.

scholarly journals Dynamic body acceleration as a proxy to predict the cost of locomotion in bottlenose dolphins

2022 ◽  
Author(s):  
Austin S. Allen ◽  
Andrew J. Read ◽  
K. Alex Shorter ◽  
Joaquin Gabaldon ◽  
Ashley M. Blawas ◽  
...  
Keyword(s):  
Energy Expenditure ◽  
Marine Mammals ◽  
Bottlenose Dolphins ◽  
Activity Level ◽  
Energy Budgets ◽  
Activity Levels ◽  
Energetic Costs ◽  
Cetacean Species ◽  
Cost Of Transport ◽  
Body Acceleration

Estimates of the energetic costs of locomotion (COL) at different activity levels are necessary to answer fundamental eco-physiological questions and to understand the impacts of anthropogenic disturbance to marine mammals. We combined estimates of energetic costs derived from breath-by-breath respirometry with measurements of overall dynamic body acceleration (ODBA) from biologging tags to validate ODBA as a proxy for COL in trained common bottlenose dolphins (Tursiops truncatus). We measured resting metabolic rate (RMR); mean individual RMR was 0.71-1.42 times that of a similarly sized terrestrial mammal and agreed with past measurements which used breath-by-breath and flow-through respirometry. We also measured energy expenditure during submerged swim trials, at primarily moderate exercise levels. We subtracted RMR to obtain COL, and normalized COL by body size to incorporate individual swimming efficiencies. We found both mass-specific energy expenditure and mass-specific COL were linearly related with ODBA. Measurements of activity level and cost of transport (the energy required to move a given distance) improve understanding of the costs of locomotion in marine mammals. The strength of the correlation between ODBA and COL varied among individuals, but the overall relationship can be used at a broad scale to estimate the energetic costs of disturbance, daily locomotion costs to build energy budgets, and investigate the costs of diving in free-ranging animals where bio-logging data are available. We propose that a similar approach could be applied to other cetacean species.

scholarly journals Energy expenditure of soldiers in a warm humid climate

1972 ◽  
Vol 27 (2) ◽  
pp. 375-381
Author(s):  
M. F. Haisman
Keyword(s):  
Body Size ◽  
Energy Expenditure ◽  
Surface Area ◽  
Lean Body Mass ◽  
Body Mass ◽  
Individual Variation ◽  
Correlation Coefficients ◽  
Humid Climate ◽  
Uneven Terrain ◽  
Gross Energy

1. Energy expenditure determinations have been made on thirty-two soldiers newly arrived in the warm humid climate of southern Malaya. Ergometer cycling was investigated as well as everyday activities such as lying, sitting, riding in a trunck, abultions, buildings a jungle camp and walking with loads over four different routes.2. The inter-individual variation in the gross energy expenditure (kcal/min and kJ/min) of each activity has been compared with the variation in energy expenditure standardized for body-weight, surface area and lean body mass. Standardization for body size did not consistently or effectively reduce the coefficients of variation of energy expenditure.3. The gross energy expenditure of most activities was significantly correlated with bodyweight, surface area or lean body mass but the correlation coefficients were not of a high order, suggesting that less than 41% of the inter-individual variation in energy expenditure was accounted for by variation in body size.4. The energy expenditure of walking at various speeds over both firm and uneven terrain was related to the square of the walking speed and the total weight of the man and his equipment (correlation coefficients 0.89–0.92, P < 0.001).

Energy and protein requirements for molt in the king penguin Aptenodytes patagonicus

1994 ◽  
Vol 266 (4) ◽  
pp. R1182-R1188 ◽  
Author(s):  
Y. Cherel ◽  
J. B. Charrassin ◽  
E. Challet
Keyword(s):  
Energy Expenditure ◽  
Total Energy ◽  
Body Mass ◽  
Dry Mass ◽  
Total Energy Expenditure ◽  
Energetic Cost ◽  
Energetic Efficiency ◽  
Composition Analysis ◽  
Epidermal Structure ◽  
Fasting Duration

Adult king penguins annually fast ashore for 1 mo for molting. By the end of molt, they have lost 44% of their prefasting body mass. About 18% of new feather synthesis occurs at sea, thus reducing both nutrient requirement and fasting duration. Plumage synthesis continues during the first 3 wk of fasting. Loss of old feathers occurs between day 12 and day 21 of the molt, and it is associated with a peak in daily body mass loss. The dry mass of epidermal structure synthesized during molt is 395 g. Body composition analysis indicates that fat oxidation accounts for 85% of total energy expenditure. The proportion for protein is 15%, a value twofold higher than during the breeding (nonmolting) fast. The mean energy expenditure is also 21% higher during the molting fast (3.04 W/kg). Compared with other birds, the energetic cost of feather synthesis is the lowest in king penguins (85 kJ/g) and consequently the energetic efficiency is the highest (25%). Changes in tissue composition during molt show that integument is the main lipid source (72% of the lipid loss) and thus the main source of energy (61% of the total energy expenditure). The integument and the pectoral muscles play a major role in molting protein metabolism, providing 20 and 57%, respectively, of the total protein needs for feather synthesis and/or energy expenditure. This result emphasizes the role of integument as a protein source, because the large premolting muscle hypertrophy is not sufficient to account for the totality of the protein cost of molt.

Energetics of swimming of a sea turtle

1976 ◽  
Vol 64 (1) ◽  
pp. 1-12 ◽  
Author(s):  
H. D. Prange
Keyword(s):  
Oxygen Consumption ◽  
Body Mass ◽  
Water Channel ◽  
Chelonia Mydas ◽  
Sea Turtle ◽  
Energetic Cost ◽  
Cost Of Transport ◽  
Ascension Island ◽  
Fat Stores ◽  
The Cost

Young (mean mass 735 g) green turtles (Chelonia mydas) were able to swim in a water channel at sustained speeds between 0–14 and 0–35 m.s-1. Oxygen consumption at rest was was 0–07 l.kg-1.h-1; at maximum swimming speed oxygen consumption was 3–4 times greater than at rest for a given individual. In comparison with other animals of the same body mass the cost of transport for the green turtle (0.186lO2.kg-1.km-1) is less than that for flying birds but greater than that for fish. From drag measurements it was calculated that the aerobic efficiency of swimming was between 1 and 10%; the higher efficiencies were found at the higher swimming speeds. Based upon the drag calculations for young turtles, it is estimated that adult turtles making the round-trip breeding migration between Brazil and Ascension Island (4800 km) would require the equivalent of about 21% of their body mass in fat stores to account for the energetic cost of swimming.

Sign in / Sign up

Export Citation Format

Share Document