Modelling the effect of varying metabolic rate and cardiac output on estimated tissue and blood O2 and CO2 levels in an extreme deep-diver, the goose-beaked whale (Ziphius cavirostris).
Andreas Fahlman, Gregory S Schorr, David A Sweeney, Brenda K Rone, Shannon N Coates, Austin S Allen, Lucia M Martín López, Susan M Jarvis, Erin A Falcone
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引用次数: 0
Abstract
High-resolution movement data from Cuvier's beaked, or goose-beaked whale (Ziphius cavirostris, hereafter Ziphius, n = 8) tag deployments (4.1-19.2 days) were used to estimate blood and tissue O2 and CO2 levels. Acceleration and magnetometry data were used to estimate the locomotion cost (LC) from the relationship between activity and the O2 consumption rate. We estimated that the diving metabolic rate (DMR) decreased with increasing dive duration, ranging from 6.18 mL O2 min-1 kg-1 for very short dives (<1.0 min) to 1.65 mL O2 min-1 kg-1 and 2.06 mL O2 min-1 kg-1 for intermediate (>17.5 and ≤33.3 min) and long dives (>33.3 min), respectively. The calculated aerobic dive limit (cADL), average behavioural ADL (bADL) and dynamic ADL (dADL) were 62.4, 61.3 (44.3-75.4) and 41.7 (2.0-102.5) min, respectively. Despite the physiological and metabolic adjustments assumed by the model, the muscle O2 ran out for many of the stereotypical long, deep dives exhibited by these animals. Based on the model results, we speculate that a large portion of the foraging dives in Ziphius are fuelled by alternative metabolic pathways, for example, phosphocreatine or glycolysis. A reliance on these alternative metabolic pathways during foraging may require long recovery periods, including primarily aerobic dives. Disturbing this normal dive pattern may disrupt this normal dive pattern, leading to behavioural and physiological changes that could cause trauma.
期刊介绍:
Experimental Physiology publishes research papers that report novel insights into homeostatic and adaptive responses in health, as well as those that further our understanding of pathophysiological mechanisms in disease. We encourage papers that embrace the journal’s orientation of translation and integration, including studies of the adaptive responses to exercise, acute and chronic environmental stressors, growth and aging, and diseases where integrative homeostatic mechanisms play a key role in the response to and evolution of the disease process. Examples of such diseases include hypertension, heart failure, hypoxic lung disease, endocrine and neurological disorders. We are also keen to publish research that has a translational aspect or clinical application. Comparative physiology work that can be applied to aid the understanding human physiology is also encouraged.
Manuscripts that report the use of bioinformatic, genomic, molecular, proteomic and cellular techniques to provide novel insights into integrative physiological and pathophysiological mechanisms are welcomed.