scholarly journals The scaling and temperature dependence of vertebrate metabolism

2005 ◽  
Vol 2 (1) ◽  
pp. 125-127 ◽  
Author(s):  
Craig R White ◽  
Nicole F Phillips ◽  
Roger S Seymour
Keyword(s):  
Body Size ◽  
Metabolic Rate ◽  
Temperature Dependence ◽  
Body Mass ◽  
Standard Metabolic Rate ◽  
Power Scaling ◽  
Scaling Exponents ◽  
Magnitude Variation ◽  
Over 40 Years

Body size and temperature are primary determinants of metabolic rate, and the standard metabolic rate (SMR) of animals ranging in size from unicells to mammals has been thought to be proportional to body mass ( M ) raised to the power of three-quarters for over 40 years. However, recent evidence from rigorously selected datasets suggests that this is not the case for birds and mammals. To determine whether the influence of body mass on the metabolic rate of vertebrates is indeed universal, we compiled SMR measurements for 938 species spanning six orders of magnitude variation in mass. When normalized to a common temperature of 38 °C, the SMR scaling exponents of fish, amphibians, reptiles, birds and mammals are significantly heterogeneous. This suggests both that there is no universal metabolic allometry and that models that attempt to explain only quarter-power scaling of metabolic rate are unlikely to succeed.

Energetic costs of digestion in Australian crocodiles

2011 ◽  
Vol 59 (6) ◽  
pp. 416 ◽  
Author(s):  
C. M. Gienger ◽  
Christopher R. Tracy ◽  
Matthew L. Brien ◽  
S. Charlie Manolis ◽  
Grahame J. W. Webb ◽  
...  
Keyword(s):  
Body Size ◽  
Metabolic Rate ◽  
Body Mass ◽  
Rapid Growth ◽  
Metabolic Response ◽  
Standard Metabolic Rate ◽  
Specific Dynamic Action ◽  
Energetic Costs ◽  
Resting Metabolism ◽  
Crocodylus Porosus

We measured standard metabolic rate (SMR) and the metabolic response to feeding in the Australian crocodiles, Crocodylus porosus and C. johnsoni. Both species exhibit a response that is characterised by rapidly increasing metabolism that peaks within 24 h of feeding, a postfeeding metabolic peak (peak O2) of 1.4–2.0 times SMR, and a return to baseline metabolism within 3–4 days after feeding. Postfeeding metabolism does not significantly differ between species, and crocodiles fed intact meals have higher total digestive costs (specific dynamic action; SDA) than those fed homogenised meals. Across a more than 100-fold range of body size (0.190 to 25.96 kg body mass), SMR, peak O2, and SDA all scale with body mass to an exponent of 0.85. Hatchling (≤1 year old) C. porosus have unexpectedly high rates of resting metabolism, and this likely reflects the substantial energetic demands that accompany the rapid growth of young crocodilians.

scholarly journals Body size and temperature effects on standard metabolic rate for determining metabolic scope for activity of the polychaete Hediste (Nereis) diversicolor

PeerJ ◽  
2018 ◽  
Vol 6 ◽  
pp. e5675 ◽  
Author(s):  
Helena Lopes Galasso ◽  
Marion Richard ◽  
Sébastien Lefebvre ◽  
Catherine Aliaume ◽  
Myriam D. Callier
Keyword(s):  
Oxygen Consumption ◽  
Body Size ◽  
Metabolic Rate ◽  
Growth Rates ◽  
Reaction Rate ◽  
Specific Growth ◽  
Standard Metabolic Rate ◽  
Metabolic Scope ◽  
Specific Growth Rates ◽  
Arrhenius Temperature

Considering the ecological importance and potential value of Hediste diversicolor, a better understanding of its metabolic rate and potential growth rates is required. The aims of this study are: (i) to describe key biometric relationships; (ii) to test the effects of temperature and body size on standard metabolic rate (as measure by oxygen consumption) to determine critical parameters, namely Arrhenius temperature (TA), allometric coefficient (b) and reaction rate; and (iii) to determine the metabolic scope for activity (MSA) of H. diversicolor for further comparison with published specific growth rates. Individuals were collected in a Mediterranean lagoon (France). After 10 days of acclimatization, 7 days at a fixed temperature and 24 h of fasting, resting oxygen consumption rates (VO2) were individually measured in the dark at four different temperatures (11, 17, 22 and 27 °C) in worms weighing from 4 to 94 mgDW (n = 27 per temperature). Results showed that DW and L3 were the most accurate measurements of weight and length, respectively, among all the metrics tested. Conversion of WW (mg), DW (mg) and L3 (mm) were quantified with the following equations: DW = 0.15 × WW, L3 = 0.025 × TL(mm) + 1.44 and DW = 0.8 × L33.68. Using an equation based on temperature and allometric effects, the allometric coefficient (b) was estimated at 0.8 for DW and at 2.83 for L3. The reaction rate (VO2) equaled to 12.33 µmol gDW−1 h−1 and 0.05 µmol mm L3−1 h−1 at the reference temperature (20 °C, 293.15 K). Arrhenius temperature (TA) was 5,707 and 5,664 K (for DW and L3, respectively). Metabolic scope for activity ranged from 120.1 to 627.6 J gDW−1 d−1. Predicted maximum growth rate increased with temperature, with expected values of 7–10% in the range of 15–20 °C. MSA was then used to evaluate specific growth rates (SGR) in several experiments. This paper may be used as a reference and could have interesting applications in the fields of aquaculture, ecology and biogeochemical processes.

scholarly journals Incubation temperature and physiological aging in the zebra finch

PLoS ONE ◽  
2021 ◽  
Vol 16 (11) ◽  
pp. e0260037
Author(s):  
Henrik H. Berntsen ◽  
Claus Bech
Keyword(s):  
Body Size ◽  
Oxidative Damage ◽  
Metabolic Rate ◽  
Body Mass ◽  
Basal Metabolic Rate ◽  
Incubation Temperature ◽  
Phenotypic Variability ◽  
Body Growth ◽  
Optimal Incubation

In birds, incubation temperature has received increased attention as an important source of phenotypic variability in offspring. A lower than optimal incubation temperature may negatively affect aspects of nestling physiology, such as body growth and energy metabolism. However, the long-term effects of sub-optimal incubation temperature on morphology and physiology are not well understood. In a previous study, we showed that zebra finches from eggs incubated at a low temperature (35.9°C) for 2/3 of the total incubation time suffered a lower post-fledging survival compared to individuals that had been incubated at higher temperatures (37.0 and 37.9°C). In the present study, we investigated whether these variations in incubation temperature could cause permanent long-lasting differences in body mass, body size, or basal metabolic rate. Furthermore, we tested whether the observed differences in survival between treatment groups would be reflected in the rate of physiological deterioration, assessed through oxidative damage and decreased metabolic rate with age (i.e. ‘metabolic aging’). Incubation temperature did not significantly affect embryonic or nestling body growth and did not influence final adult body mass or body size. Nor was there any long-term effect on basal metabolic rate. Birds from eggs incubated at the lowest temperature experienced an accumulation of oxidative damage with age, although this was not accompanied by an accelerated rate of metabolic aging. The present results suggest that the low survival in these birds was possibly mediated by increased oxidative stress, but independent of body growth and the basal metabolic rate.

scholarly journals Brain size varies with temperature in vertebrates

2014 ◽  
Author(s):  
James F Gillooly
Keyword(s):  
Body Size ◽  
Body Temperature ◽  
Metabolic Rate ◽  
Temperature Dependence ◽  
Aerobic Capacity ◽  
Brain Size ◽  
Metabolic Rates ◽  
Temperature Dependent ◽  
Spatial And Temporal Scales ◽  
Effects Of Temperature

The tremendous variation in brain size among vertebrates has long been thought to be related to differences in species’ metabolic rates. Species with higher metabolic rates can supply more energy to support the relatively high cost of brain tissue. And yet, while body temperature is known to be a major determinant of metabolic rate, the possible effects of temperature on brain size have scarcely been explored. Thus, here I explore the effects of temperature on brain size among diverse vertebrates (fishes,amphibians, reptiles, birds and mammals). I find that, after controlling for body size,brain size increases exponentially with temperature in much the same way asmetabolic rate. These results suggest that temperature-dependent changes in aerobic capacity, which have long been known to affect physical performance, similarly affect brain size. The observed temperature-dependence of brain size may explain observed gradients in brain size among both ectotherms and endotherms across broad spatial and temporal scales.

Intraspecific temperature dependence of the scaling of metabolic rate with body mass in fishes and its ecological implications

Oikos ◽  
2011 ◽  
Vol 121 (2) ◽  
pp. 245-251 ◽  
Author(s):  
Jan Ohlberger ◽  
Thomas Mehner ◽  
Georg Staaks ◽  
Franz Hölker
Keyword(s):  
Metabolic Rate ◽  
Temperature Dependence ◽  
Body Mass ◽  
Ecological Implications

Effect of sloughing and digestion on metabolic rate in the Australian carpet python, Morelia spilota imbricata

1999 ◽  
Vol 47 (6) ◽  
pp. 605 ◽  
Author(s):  
Graham G. Thompson ◽  
Philip C. Withers
Keyword(s):  
Metabolic Rate ◽  
Body Mass ◽  
Standard Metabolic Rate ◽  
Two Factors

The standard metabolic rate for juvenile carpet pythons, Morelia spilota imbricata, with a mean body mass of 129.6 g (range 57.7–253 g) increased from 6.75 ± 0.96 (s.e.) mL h–1 to 42.6 ± 12.40 (s.e.) mL h–1 in 48 h after ingesting mice equal to approximately 23% of their body mass, at a temperature of 30°C. Sloughing increased metabolic rate to approximately 146% of standard metabolic rate at 30°C. Metabolic rate is elevated before the eyes become opaque and other visual signs indicate that a slough is imminent. The implications of these two factors when measuring standard metabolic rate are discussed.

Sign in / Sign up

Export Citation Format

Share Document