Faculty Opinions recommendation of Metabolic rate and body size are linked with perception of temporal information.

2013 ◽  
Author(s):  
Kevin Lafferty
Keyword(s):  
Body Size ◽  
Metabolic Rate ◽  
Temporal Information

scholarly journals Metabolic rate and body size are linked with perception of temporal information

2013 ◽  
Vol 86 (4) ◽  
pp. 685-696 ◽  
Author(s):  
Kevin Healy ◽  
Luke McNally ◽  
Graeme D. Ruxton ◽  
Natalie Cooper ◽  
Andrew L. Jackson
Keyword(s):  
Body Size ◽  
Metabolic Rate ◽  
Temporal Information

scholarly journals Changes in body temperature influence the scaling of and aerobic scope in mammals

2006 ◽  
Vol 3 (1) ◽  
pp. 100-103 ◽  
Author(s):  
James F Gillooly ◽  
Andrew P Allen
Keyword(s):  
Body Size ◽  
Metabolic Rate ◽  
Size Dependence ◽  
Maximal Activity ◽  
Scaling Exponent ◽  
Temperature Influence ◽  
Aerobic Scope ◽  
Metabolic Scope ◽  
Single Power ◽  
Maximum Metabolic Rate

Debate on the mechanism(s) responsible for the scaling of metabolic rate with body size in mammals has focused on why the maximum metabolic rate ( ) appears to scale more steeply with body size than the basal metabolic rate (BMR). Consequently, metabolic scope, defined as /BMR, systematically increases with body size. These observations have led some to suggest that and BMR are controlled by fundamentally different processes, and to discount the generality of models that predict a single power-law scaling exponent for the size dependence of the metabolic rate. We present a model that predicts a steeper size dependence for than BMR based on the observation that changes in muscle temperature from rest to maximal activity are greater in larger mammals. Empirical data support the model's prediction. This model thus provides a potential theoretical and mechanistic link between BMR and .

Respiratory Exchange and Body Size in the Aldabra Giant Tortoise

1971 ◽  
Vol 55 (3) ◽  
pp. 651-665 ◽  
Author(s):  
G. M. HUGHES ◽  
R. GAYMER ◽  
MARGARET MOORE ◽  
A. J. WOAKES
Keyword(s):  
Body Weight ◽  
Body Size ◽  
Metabolic Rate ◽  
Relative Proportion ◽  
The Body ◽  
O2 Consumption ◽  
Weight Range ◽  
Testudo Hermanni ◽  
The Mean ◽  
Good Agreement

1. The O2 consumption and CO2 release of nine giant tortoises Testudo gigantea (weight range 118 g-35·5 kg) were measured at a temperature of about 25·5°C. Four European tortoises Testudo hermanni (weight range 640 g-2·16 kg) were also used. The mean RQ values obtained were 1·01 for T. gigantea and 0·97 for T. hermanni. These values were not influenced by activity or size. 2. The data was analysed by plotting log/log regression lines relating body weight to O2 consumption. Both maximum and minimum metabolic rates recorded for each individual T. gigantea showed a negative correlation with body weight. For active rates the relation was O2 consumption = 140·8W0·97, whereas for inactive animals O2 consumption = 45·47W0·82. 3. The maximum rates were obtained from animals that were observed to be active in the respirometer and the minimum rates from animals that remained quiet throughout. The scope for activity increased with body size, being 82 ml/kg/h for animals of 100 g and 103 ml/kg/h for 100 kg animals. The corresponding ratio between maximum and minimum rates increases from about 2 to 6 for the same weight range. 4. Values for metabolic rate in T. hermanni seem to be rather lower than in T. gigantea. Analysis of the relative proportion of the shell and other organs indicates that the shell forms about 31% of the body weight in adult T. hermanni but only about 18% in T. gigantea of similar size. The shell is not appreciably heavier in adult T. gigantea (about 20%). 5. Data obtained for inactive animals is in good agreement with results of other workers using lizards and snakes. Previous evidence suggesting that chelonians show no reduction in metabolic rate with increasing size is not considered to conflict with data obtained in the present work.

Relation between Metabolic Rate and Body Size in the Ovine Fetus

1987 ◽  
Vol 117 (6) ◽  
pp. 1181-1186 ◽  
Author(s):  
Alan W. Bell ◽  
Frederick C. Battaglia ◽  
Giacomo Meschia
Keyword(s):  
Body Size ◽  
Metabolic Rate ◽  
Ovine Fetus

A Note on Metabolic Rate Dependence on Body Size in Plants and Animals

2003 ◽  
Vol 221 (2) ◽  
pp. 301-307 ◽  
Author(s):  
ANASTASSIA M. MAKARIEVA ◽  
VICTOR G. GORSHKOV ◽  
BAI-LIAN LI
Keyword(s):  
Body Size ◽  
Metabolic Rate ◽  
Rate Dependence

Metabolic Rate of Female Rats as a Function of Age and Body Size

1956 ◽  
Vol 186 (1) ◽  
pp. 9-12 ◽  
Author(s):  
Max Kleiber ◽  
Arthur H. Smith ◽  
Theodore N. Chernikoff
Keyword(s):  
Body Weight ◽  
Body Size ◽  
Metabolic Rate ◽  
Age Groups ◽  
Female Rats ◽  
Standard Errors ◽  
Normal Female ◽  
Metabolic Rates ◽  
The Mean ◽  
Specific Unit

On the basis of 926 respiration trials, metabolic rates of normal female rats are presented as means of 42 different age groups from birth to 1000 days of age. The means with their standard errors are given for the metabolic rates per rat, per kilogram weight, per unit of the 2/3 power of body weight (surface), and per unit of the 3/4 power of body weight (inter specific unit of metabolic body size). A minimum of 72.6 Cal/kg.3/4 occurs between the ages of 200 and 300 days. An equation with two exponentials predicts the metabolic rate of rats from 77–1000 days of age with a standard deviation between prediction and observation of 2.2% of the mean.

scholarly journals Relationship of metabolic rate to body size in Orthoptera

2008 ◽  
Vol 17 (2) ◽  
pp. 301-306 ◽  
Author(s):  
Dennis J. Fielding ◽  
Linda S. DeFoliart
Keyword(s):  
Body Size ◽  
Metabolic Rate ◽  
Relationship Of

Why does metabolic rate scale with body size?/Allometric cascades

Nature ◽  
2003 ◽  
Vol 421 (6924) ◽  
pp. 714-714 ◽  
Author(s):  
Charles-A. Darveau ◽  
Raul K. Suarez ◽  
Russel D. Andrews ◽  
Peter W. Hochachka
Keyword(s):  
Body Size ◽  
Metabolic Rate

Body-size scaling of metabolic rate in the trilobite Eldredgeops rana

Paleobiology ◽  
2013 ◽  
Vol 39 (1) ◽  
pp. 109-122 ◽  
Author(s):  
Douglas S. Glazier ◽  
Matthew G. Powell ◽  
Travis J. Deptola
Keyword(s):  
Body Size ◽  
Metabolic Rate ◽  
Cell Size ◽  
The Body ◽  
Cell Multiplication ◽  
Compound Eyes ◽  
Metabolic Scaling ◽  
Size Scaling ◽  
Size Model ◽  
Facet Size

We infer the body-size scaling slope of metabolic rate in a trilobite by applying a cell-size model that has been proposed to explain metabolic scaling in living organisms. This application is especially tractable in fossil arthropods with well-preserved compound eyes because the number and size of eye facets appear to be useful proxies for the relative number and size of cells in the body. As a case study, we examined the ontogenetic scaling of facet size and number in a ∼390-Myr-old local assemblage of the trilobite Eldredgeops rana, which has well-preserved compound eyes and a wide body-size range. Growth in total eye lens area resulted from increases in both facet area and number in relatively small (presumably young) specimens, but only from increases in facet area in large (presumably more mature) specimens. These results suggest that early growth in E. rana involved both cell multiplication and enlargement, whereas later growth involved only cell enlargement. If the cell-size model is correct, then metabolic rate scaled allometrically in E. rana, and the scaling slope of log metabolic rate versus log body mass decreased from ∼0.85 to 0.63 as these animals grew. This inferred age-specific change in metabolic scaling is consistent with similar changes frequently observed in living animals. Additional preliminary analyses of literature data on other trilobites also suggest that the metabolic scaling slope was <1 in benthic species, but ∼1 in pelagic species, as has also been observed in living invertebrates. The eye-facet size (EFS) method featured here opens up new possibilities for examining the bioenergetic allometry of extinct arthropods.

Sign in / Sign up

Export Citation Format

Share Document