1972
DOI: 10.1007/bf00693633
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Aerobic and anaerobic metabolism during activity in the lizardDipsosaurus dorsalis

Abstract: Summary. 1. Oxygen consumption and lactate content of the lizard Dipsosaurus dorsalis were determined under standard conditions and for a bout of maximal activity induced by a 2-min period of electrical stimulation. Observations were made between 25 ~ and 45 ~ C.2. Maximal aerobic scope, 2.27 cm a 02/(g• occurred at 40~ (Figs. 2, 4). The increase in oxygen consumption during activity at the various temperatures between 25 ~ and 45~ represented 7-to 17-fold of corresponding resting levels.3. Lactate content of … Show more

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Cited by 116 publications
(52 citation statements)
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“…First, this muscle exhibits low activity of LDH in comparison with truly specialized glycolytic muscles in ectotherms (for example: Baldwin et al, 1995; Bennett and . Specialization for digging in amphisbaenians Dawson, 1972;Mendiola et al, 1991;Miller et al, 1993;Somero and Childress, 1980). Indeed, the glycolytic capacity of the longissimus dorsi of L. microcephalum is somewhat lower than that of the white portion of leg muscles associated with locomotion in some lizards (Bennett and Dawson, 1972;Garland et al, 1987;Gleeson, 1983), snakes (Wilkinson and Nemeth, 1989) and crocodiles (Baldwin et al, 1995).…”
Section: Discussionmentioning
confidence: 99%
“…First, this muscle exhibits low activity of LDH in comparison with truly specialized glycolytic muscles in ectotherms (for example: Baldwin et al, 1995; Bennett and . Specialization for digging in amphisbaenians Dawson, 1972;Mendiola et al, 1991;Miller et al, 1993;Somero and Childress, 1980). Indeed, the glycolytic capacity of the longissimus dorsi of L. microcephalum is somewhat lower than that of the white portion of leg muscles associated with locomotion in some lizards (Bennett and Dawson, 1972;Garland et al, 1987;Gleeson, 1983), snakes (Wilkinson and Nemeth, 1989) and crocodiles (Baldwin et al, 1995).…”
Section: Discussionmentioning
confidence: 99%
“…This 'metabolic theory of ecology' has grown into a discipline of its own, emanating from the legendary astronomer Harlow Shapley's observation that walking speed in ants increased directly and predictably with temperature to the point that air temperature could be predicted to within 1°C from ant walking speed alone (Huey and Kingsolver, 2011) [see also Shapley (Shapley, 1966), cited in Huey and Kingsolver (Huey and Kingsolver, 2011)]. This close relationship between metabolic physiology, metabolic rate and temperature also applies in ectothermic reptiles (Bennett, 1982;Bennett and Dawson, 1976;Beyer and Spotila, 1994;Zari, 1991). This suggests that with increasing temperature comes an inevitable increase in metabolic rate and mitochondrial activity, and with that an increased production of reactive oxygen species (ROS), perhaps even at the cost of a reduced lifespan (Hollingsworth, 1969;Farmer and Sohal, 1987).…”
Section: Introductionmentioning
confidence: 99%
“…Aerobic metabolism provides only a portion of the total energy used to sustain high levels of activity in lizards, and most of the available energy is derived from anaerobic metabolism (Bennett and Dawson, 1972;Bennett and Licht, 1972; but see Bennett, 1991 for a review). The relative proportion of aerobic and anaerobic pathways is however an important factor in these animals, and can be used for understating how the metabolic balance between two pathways influences muscle function.…”
Section: Enzyme Activities On Hindlimb and Head Musclesmentioning
confidence: 99%