Flight metabolic rate variation and its consequences on muscle metabolic machinery

2016 ◽  
Author(s):  
Charles Darveau
2009 ◽  
Vol 55 (2) ◽  
pp. 130-135 ◽  
Author(s):  
A. McGaughran ◽  
G.P. Redding ◽  
M.I. Stevens ◽  
P. Convey

2010 ◽  
Vol 56 (1) ◽  
pp. 57-64 ◽  
Author(s):  
A. McGaughran ◽  
P. Convey ◽  
G.P. Redding ◽  
M.I. Stevens

2020 ◽  
Vol 375 (1793) ◽  
pp. 20190146 ◽  
Author(s):  
Jacob D. Gardner ◽  
Michel Laurin ◽  
Chris L. Organ

Genome size has long been hypothesized to affect the metabolic rate in various groups of animals. The mechanism behind this proposed association is the nucleotypic effect, in which large nucleus and cell sizes influence cellular metabolism through surface area-to-volume ratios. Here, we provide a review of the recent literature on the relationship between genome size and metabolic rate. We also conduct an analysis using phylogenetic comparative methods and a large sample of extant vertebrates. We find no evidence that the effect of genome size improves upon models in explaining metabolic rate variation. Not surprisingly, our results show a strong positive relationship between metabolic rate and body mass, as well as a substantial difference in metabolic rate between endothermic and ectothermic vertebrates, controlling for body mass. The presence of endothermy can also explain elevated rate shifts in metabolic rate whereas genome size cannot. We further find no evidence for a punctuated model of evolution for metabolic rate. Our results do not rule out the possibility that genome size affects cellular physiology in some tissues, but they are consistent with previous research suggesting little support for a direct functional connection between genome size and basal metabolic rate in extant vertebrates. This article is part of the theme issue ‘Vertebrate palaeophysiology’.


2015 ◽  
Vol 282 (1802) ◽  
pp. 20142232 ◽  
Author(s):  
Enrique Rodríguez ◽  
Jean-Michel Weber ◽  
Benoît Pagé ◽  
David W. Roubik ◽  
Raul K. Suarez ◽  
...  

Patterns of metabolic rate variation have been documented extensively in animals, but their functional basis remains elusive. The membrane pacemaker hypothesis proposes that the relative abundance of polyunsaturated fatty acids in membrane phospholipids sets the metabolic rate of organisms. Using species of tropical orchid bees spanning a 16-fold range in body size, we show that the flight muscles of smaller bees have more linoleate (%18 : 3) and stearate (%18 : 0), but less oleate (%18 : 1). More importantly, flight metabolic rate (FlightMR) varies with the relative abundance of 18 : 3 according to the predictions of the membrane pacemaker hypothesis. Although this relationship was found across large differences in metabolic rate, a direct association could not be detected when taking phylogeny and body mass into account. Higher FlightMR, however, was related to lower %16 : 0, independent of phylogeny and body mass. Therefore, this study shows that flight muscle membrane composition plays a significant role in explaining diversity in FlightMR, but that body mass and phylogeny are other factors contributing to their variation. Multiple factors are at play to modulate metabolic capacity, and changing membrane composition can have gradual and stepwise effects to achieve a new range of metabolic rates. Orchid bees illustrate the correlated evolution between membrane composition and metabolic rate, supporting the functional link proposed in the membrane pacemaker hypothesis.


Obesity ◽  
2007 ◽  
Vol 15 (3) ◽  
pp. 600-606 ◽  
Author(s):  
Sarah L. Johnston ◽  
Donna M. Souter ◽  
Bert J. Tolkamp ◽  
Iain J. Gordon ◽  
Andrew W. Illius ◽  
...  

2019 ◽  
Author(s):  
Jacob D. Gardner ◽  
Michel Laurin ◽  
Chris L. Organ

AbstractGenome size has long been hypothesized to affect metabolic rate in various groups of animals. The mechanism behind this proposed association is the nucleotypic effect, in which large nucleus and cell sizes influence cellular metabolism through surface area-to-volume ratios. Here, we provide a review of the recent literature on the relationship between genome size and metabolic rate. We also conduct an analysis using phylogenetic comparative methods and a large sample of extant vertebrates. We find no evidence that the effect of genome size improves upon models in explaining metabolic rate variation. Not surprisingly, our results show a strong positive relationship between metabolic rate and body mass, as well as a substantial difference in metabolic rate between endothermic and ectothermic vertebrates, controlling for body mass. The presence of endothermy can also explain elevated rate shifts in metabolic rate whereas genome size cannot. We further find no evidence for a punctuated model of evolution for metabolic rate. Our results do not rule out the possibility that genome size affects cellular physiology in some tissues, but they are consistent with previous research suggesting little support for a direct functional connection between genome size and basal metabolic rate in extant vertebrates.


2018 ◽  
Vol 35 ◽  
pp. 1-6 ◽  
Author(s):  
Ana Paula Fabio-Braga ◽  
Wilfried Klein

Basal metabolic rate (BMR) represents the lowest level of metabolic activity capable to sustain homeostasis in an endotherm and is an important tool to compare metabolic rates of different species. Echimyidae is the most specious family within caviomorph rodents, however, little is known about the biology of its species, such as Trinomys setosus (Desmarest, 1817) and Clyomys bishopi (Ávila-Pires & Wutke, 1981), a ground and an underground dwelling echimyid, respectively. The ambient temperature and circadian effects on metabolic rate were evaluated through closed-system respirometry for these two species, as well as the circadian effects on CO2 production and respiratory exchange ratio (RER). Trinomys setosus and C. bishopi showed the lowest metabolic rates (0.56 ± 0.02 mLO2.h-1.g-1 and 0.53 ± 0.03 mLO2.h-1.g-1, respectively) at 32 °C and during the light phase. Under laboratory conditions, T. setosus showed metabolic rate variation compatible with nocturnal activity, whereas C. bishopi activity cycle remains unclear. Both species showed BMR lower than expected by allometric regressions for rodents.


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