Digging energetics in the South American rodent Ctenomys talarum (Rodentia, Ctenomyidae)

2002 ◽  
Vol 80 (12) ◽  
pp. 2144-2149 ◽  
Author(s):  
Facundo Luna ◽  
C Daniel Antinuchi ◽  
Cristina Busch
Keyword(s):  
Metabolic Rate ◽  
Energy Cost ◽  
Resting Metabolic Rate ◽  
Energetic Cost ◽  
Soil Conditions ◽  
Natural Soil ◽  
Subterranean Rodents ◽  
South American ◽  
Ctenomys Talarum ◽  
The Cost

Ctenomys is the most speciose among subterranean rodents. There are few studies on energetics of Ctenomys, and none of them have focused on the energetics of digging. The present study aims to quantify the energetic cost of burrowing in Ctenomys talarum in natural soil conditions and to compare the energetics data with those reported for other subterranean rodents. Digging metabolic rate (DMR) in gravelly sand for C. talarum was 337.4 ± 65.9 mL O2·h–1 (mean ± SD). No differences in DMR were detected between sexes. Moreover, DMR was 295.9% of resting metabolic rate. In terms of a cost of burrowing model, the mass of soil removed per distance burrowed (Msoil) in gravelly sand was 44.5 ± 6.7 g·cm–1. Coefficients of the equation that related the energy cost of constructing a burrow segment of length S and Msoil(Eseg/Msoil) were Ks = 0.33 ± 0.32 J·g–1, which is the energy cost of shearing 1 g of soil, and Kp = 0.0055 ± 0.0042 J·g–1·cm–1, which is the energy cost of pushing 1 g of soil 100 cm. Regarding the cost of burrowing model, our data showed that C. talarum has the lowest DMR in gravelly sand among unrelated subterranean rodents analyzed. Moreover, despite C. talarum feeding aboveground, the foraging economics was similar that of to other rodents.

scholarly journals The energetic cost of mounting an immune response for Pallas’s long-tongued bat (Glossophaga soricina)

PeerJ ◽  
2018 ◽  
Vol 6 ◽  
pp. e4627 ◽  
Author(s):  
Lucia V. Cabrera-Martínez ◽  
L. Gerardo Herrera M. ◽  
Ariovaldo P. Cruz-Neto
Keyword(s):  
Immune Response ◽  
Metabolic Rate ◽  
Total Energy ◽  
Body Mass ◽  
Energy Cost ◽  
Resting Metabolic Rate ◽  
Energetic Cost ◽  
Body Mass Change ◽  
Glossophaga Soricina ◽  
Immune Challenges

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.

scholarly journals The energetic costs of mounting an immune response in Pallas’s long-tongued bat (Glossophaga soricina)

2017 ◽  
Author(s):  
Lucia Cabrera-Martinez ◽  
L. Gerardo Herrera M. ◽  
Ariovaldo Cruz Neto
Keyword(s):  
Immune Response ◽  
Metabolic Rate ◽  
Body Mass ◽  
Energy Cost ◽  
Feeding Habits ◽  
Resting Metabolic Rate ◽  
Energetic Cost ◽  
Body Mass Change ◽  
Glossophaga Soricina ◽  
Total Daily Energy Expenditure

Activation of immune response has been long assumed to be an energy-costly process but direct measures of changes in metabolic rate after eliciting immune response disputes the universality of this assertion. The acute phase response (APR) is the first line of defense of the vertebrate immune system against pathogens and is thought to be energetically costly. Measures of APR energetic cost in birds are higher than in rodents suggesting that this response is less expensive and important for mammals. However, large increase in metabolic rate after APR activation measured in a piscivorous bat species (Myotis vivesi) suggests that immune response is unusually costly for bats. Here we quantified the energetic cost and body mass change associated with APR in the nectarivorous Pallas’s long-tongued bat Glossophaga soricina and compared with values previously measured for piscivorous bats and other vertebrates. APR activation implied an energy cost for G. soricina as indicated by a short-term decrease in body mass and an increase in resting metabolic rate (RMR). However, the increase in RMR was far from the large increase detected in piscivorous bats and it was similar to the highest values measured in birds. Caloric cost of APR represented only 2% of the total daily energy expenditure estimated for G. soricina. Overall our results suggest that the costs of APR for bats may vary interespecifically probably in relation to feeding habits. 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 the animal´s energy budget.

scholarly journals The energetic costs of mounting an immune response in Pallas’s long-tongued bat (Glossophaga soricina)

2017 ◽  
Author(s):  
Lucia Cabrera-Martinez ◽  
L. Gerardo Herrera M. ◽  
Ariovaldo Cruz Neto
Keyword(s):  
Immune Response ◽  
Metabolic Rate ◽  
Body Mass ◽  
Energy Cost ◽  
Feeding Habits ◽  
Resting Metabolic Rate ◽  
Energetic Cost ◽  
Body Mass Change ◽  
Glossophaga Soricina ◽  
Total Daily Energy Expenditure

Activation of immune response has been long assumed to be an energy-costly process but direct measures of changes in metabolic rate after eliciting immune response disputes the universality of this assertion. The acute phase response (APR) is the first line of defense of the vertebrate immune system against pathogens and is thought to be energetically costly. Measures of APR energetic cost in birds are higher than in rodents suggesting that this response is less expensive and important for mammals. However, large increase in metabolic rate after APR activation measured in a piscivorous bat species (Myotis vivesi) suggests that immune response is unusually costly for bats. Here we quantified the energetic cost and body mass change associated with APR in the nectarivorous Pallas’s long-tongued bat Glossophaga soricina and compared with values previously measured for piscivorous bats and other vertebrates. APR activation implied an energy cost for G. soricina as indicated by a short-term decrease in body mass and an increase in resting metabolic rate (RMR). However, the increase in RMR was far from the large increase detected in piscivorous bats and it was similar to the highest values measured in birds. Caloric cost of APR represented only 2% of the total daily energy expenditure estimated for G. soricina. Overall our results suggest that the costs of APR for bats may vary interespecifically probably in relation to feeding habits. 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 the animal´s energy budget.

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.

Energy Expenditure of Level Overground Walking in Young Adults: Comparison With Prediction Equations

2021 ◽  
pp. 1-8
Author(s):  
Jingjing Xue ◽  
Shuo Li ◽  
Rou Wen ◽  
Ping Hong
Keyword(s):  
Young Adults ◽  
Energy Expenditure ◽  
Metabolic Rate ◽  
Energy Cost ◽  
Sports Medicine ◽  
Resting Metabolic Rate ◽  
Prediction Equations ◽  
Overground Walking ◽  
All Speeds ◽  
Walking Energy Cost

Background: The purpose of this study was to investigate the accuracy of the published prediction equations for determining level overground walking energy cost in young adults. Methods: In total, 148 healthy young adults volunteered to participate in this study. Resting metabolic rate and energy expenditure variables at speeds of 4, 5, and 6 km/h were measured by indirect calorimetry, walking energy expenditure was estimated by 3 published equations. Results: The gross and net metabolic rate per mile of level overground walking increased with increased speed (all P < .01). Females were less economical than males. The present findings revealed that the American College of Sports Medicine and Pandolf et al equations significantly underestimated the energy cost of overground walking at all speeds (all P < .01) in young adults. The percentage mean bias for American College of Sports Medicine, Pandolf et al, and Weyand et al was 12.4%, 16.8%, 1.4% (4 km/h); 21.6%, 15.8%, 7.1% (5 km/h); and 27.6%, 12%, 6.6% (6 km/h). Bland–Altman plots and prediction error analysis showed that the Weyand et al was the most accurate in 3 existing equations. Conclusions: The Weyand et al equation appears to be the most suitable for the prediction of overground walking energy expenditure in young adults.

Dynamics of photoconversion processes: the energetic cost of lifetime gain in photosynthetic and photovoltaic systems

2021 ◽  
Author(s):  
Robert Godin ◽  
James R. Durrant
Keyword(s):  
Kinetic Model ◽  
Solar Energy ◽  
Energy Conversion ◽  
Energy Cost ◽  
Energetic Cost ◽  
Photovoltaic Systems ◽  
Simple Kinetic Model ◽  
Energy Conversion Systems ◽  
Order Of Magnitude ◽  
The Cost

The energy cost of lifetime gain in solar energy conversion systems is determined from a breadth of technologies. The cost of 87 meV per order of magnitude lifetime improvement is strikingly close to the 59 meV determined from a simple kinetic model.

Resting and field metabolic rates of Awassi sheep and Baladi goats raised by Negev bedouin

2020 ◽  
Vol 158 (5) ◽  
pp. 431-437
Author(s):  
Michael Kam ◽  
Shaher El-Meccawi ◽  
Arieh Brosh ◽  
A. Allan Degen
Keyword(s):  
Metabolic Rate ◽  
Resting Metabolic Rate ◽  
Arid Areas ◽  
Metabolic Rates ◽  
Herbaceous Vegetation ◽  
Sheep And Goats ◽  
Awassi Sheep ◽  
Natural Pasture ◽  
Field Metabolic Rates ◽  
The Cost

AbstractSheep are grazers and goats are intermediate feeders. By employing O2 consumption and heart rate measurements, resting metabolic rate (RMR) and field metabolic rate (FMR) were determined in four male fat-tailed Awassi sheep (44.0 ± 3.94) and four male Baladi goats (35.5 ± 5.42 kg) that were co-grazing natural pasture in the Negev Desert. There were 67.7 ± 3.75 g DM/m2 of herbaceous vegetation biomass, which was rapidly becoming senescent and more fibrous. We hypothesized that FMR of these desert-adapted ruminants would be relatively low when compared to other sheep and goat breeds, as animals in arid areas tend to have low metabolic rates. Both sheep (n = 6) and goats (n = 6) foraged 71% of the allotted 11 h free-pasture period; however, sheep grazed more than goats (P < 0.001); whereas goats browsed more than sheep (P < 0.001). RMR was higher (P = 0.007) in sheep than in goats (529 ± 23.5 v. 474 ± 25.4 kJ/kg0.75 BW/d), but FMR did not differ between species (618 ± 55.7 v. 613 ± 115.2 kJ/kg0.75 BW/d). In addition, the cost of activities, as a proportion of FMR, did not differ between sheep and goats; FMR increased by 89 kJ/kg0.75 BW/d or 17% in sheep and by 138 kJ/kg0.75 BW/d or 29% in goats. In comparing FMRs of sheep and goats in this study with these species in other studies, differences were inconsistent and, therefore, our hypothesis was not supported.

scholarly journals Energy cost of NaCl transport in isolated gills of cutthroat trout

1999 ◽  
Vol 277 (3) ◽  
pp. R631-R639 ◽  
Author(s):  
John D. Morgan ◽  
George K. Iwama
Keyword(s):  
Oxygen Consumption ◽  
Energy Cost ◽  
Resting Metabolic Rate ◽  
Cutthroat Trout ◽  
Gill Tissue ◽  
Tissue Respiration ◽  
Nacl Transport ◽  
Oncorhynchus Clarki Clarki ◽  
The Cost ◽  
Total Tissue

Few studies have made direct estimates of the energy required for ion transport in gills of freshwater (FW) and seawater (SW) fish. Oxygen consumption was measured in excised gill tissue of FW-adapted cutthroat trout ( Oncorhynchus clarki clarki) to estimate the energy cost of NaCl transport in that osmoregulatory organ. Ouabain (0.5 mM) and bafilomycin A1 (1 μM) were used to inhibit the Na+-K+and H+ pumps, respectively. Both inhibitors significantly decreased gill tissue oxygen consumption, accounting for 37% of total tissue respiration. On a whole mass basis, the cost of NaCl uptake in the FW trout gill was estimated to be 1.8% of whole animal oxygen uptake. An isolated, saline-perfused gill arch preparation was also used to compare gill energetics in FW- and SW-adapted trout. The oxygen consumption of FW gills was significantly (33%) higher than SW gills. On a whole animal basis, total gill oxygen consumption in FW and SW trout accounted for 3.9 and 2.4% of resting metabolic rate, respectively. The results of both experiments suggest that the energy cost of NaCl transport in FW and SW trout gills represents a relatively small (<4%) portion of the animal’s total energy budget.

Compensatory effect of the heat increment of feeding on thermoregulation costs of white-tailed deer fawns in winter

1999 ◽  
Vol 77 (9) ◽  
pp. 1474-1485 ◽  
Author(s):  
Paul G Jensen ◽  
Peter J Pekins ◽  
James B Holter
Keyword(s):  
Metabolic Rate ◽  
Heat Production ◽  
Resting Metabolic Rate ◽  
Energetic Cost ◽  
Critical Temperatures ◽  
Metabolic Chamber ◽  
Heat Increment Of Feeding ◽  
Heat Increment ◽  
Minor Portion ◽  
A Minor

For northern white-tailed deer (Odocoileus virginianus) fawns, the energetic cost of thermoregulation (HcE) during severe winters can result in substantial catabolism of body-tissue reserves. The heat increment of feeding (HiE) has the potential to offset thermoregulatory energy expenditure that would otherwise require the catabolism of these reserves. During winters 1996 and 1997, we conducted 18 fasting and 18 on-feed heat-production trials using indirect respiration calorimetry in a metabolic chamber. Nonlinear regression analysis was used to estimate the lower critical temperatures (Tlc) and determine the fasting metabolic rate (FMR) and resting metabolic rate (RMR). Resulting models were used to calculate HiE, HcE, and percent substitution of HiE for HcE. For fawns fed a natural browse diet, estimated FMR and RMR were 352 and 490 kJ·kg body mass (BM)-0.75·d-1, respectively; this 40% increase in thermoneutral heat production reduced Tlc from -0.8 to -11.2°C between the fasted and fed states, respectively, and reduced HcE by 59% for fed fawns. For fawns fed a concentrate diet, estimated FMR and RMR were 377 and 573 kJ·kg BM-0.75·d-1, respectively. Level of browse intake had a significant effect on RMR andTlc. RMR was 12% higher for fawns on a high versus a low level of intake, and estimated Tlc was -15.6 and -5.8°C, respectively. Our data indicate that the energetic cost of thermoregulation is probably a minor portion of the energy budget of a healthy fawn consuming natural forage.

Body temperature and standard metabolic rate of the female viviparous lizard Eremias multiocellata during reproduction

2012 ◽  
Vol 90 (1) ◽  
pp. 79-84 ◽  
Author(s):  
Feng Yue ◽  
Xiao-Long Tang ◽  
De-Jiu Zhang ◽  
Xue-Feng Yan ◽  
Ying Xin ◽  
...  
Keyword(s):  
Body Temperature ◽  
Metabolic Rate ◽  
Ambient Temperature ◽  
Energy Cost ◽  
Energy Requirement ◽  
Standard Metabolic Rate ◽  
The Body ◽  
Energetic Cost ◽  
Pregnant Females ◽  
Eremias Multiocellata

The body temperature (Tb) and standard metabolic rate (SMR) of female Eremias multiocellata Günther, 1872, a viviparous lizard, were measured at 25, 30, and 35 °C during pregnancy and after parturition to assess energy requirement of reproduction. The results showed that the Tbs of female lizards were slightly higher than actual ambient temperature in the 25 and 30 °C groups, while they were slightly lower than ambient temperature in the 35 °C group. Ambient temperature significantly affected SMR and gestation period of females. Energy requirement was constant in nonpregnant females, whereas it was increased in pregnant females. The maximal estimates of maintenance costs of pregnancy (MCP) were 4.219, 4.220, and 4.448 mg CO2·min–1, which accounted for 19.40%, 14.15%, and 12.32% of the total metabolic rate in the 25, 30, and 35 °C group, respectively. The results indicated the MCP was an important component of total energy cost for the lizard E. multiocellata and the MCP in this lizard incurs a relative fixed energetic cost irrespective of ambient temperature.

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