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Publisher: Blackwell Publishing Ltd
Journal: Journal of Fish Biology
Languages: English
Types: Article
Subjects: teleosts, locomotion, Brief Communication, metabolism, Brief Communications, ecophysiology, fishes, aerobic scope

Classified by OpenAIRE into

mesheuropmc: complex mixtures, digestive system diseases
The rate at which active animals can expend energy is limited by their maximum aerobic metabolic rate (MMR). Two methods are commonly used to estimate MMR as oxygen uptake in fishes, namely during prolonged swimming or immediately following brief exhaustive exercise, but it is unclear whether they return different estimates of MMR or whether their effectiveness for estimating MMR varies among species with different lifestyles. A broad comparative analysis of MMR data from 121 fish species revealed little evidence of different results between the two methods, either for fishes in general or for species of benthic, benthopelagic or pelagic lifestyles.
  • The results below are discovered through our pilot algorithms. Let us know how we are doing!

    • Clark, T. D., Donaldson, M. R., Pieperhoff, S., Drenner, S. M., Lotto, A., Cooke, S. J., Hinch, S. G., Patterson, D. A. & Farrell, A. P. (2012). Physiological benefits of being small in a changing world: responses of coho salmon (Oncorhynchus kisutch) to an acute thermal challenge and a simulated capture event. PLoS One 7, e39079.
    • Clark, T. D., Sandblom, E. & Jutfelt, F. (2013). Aerobic scope measurements of fishes in an era of climate change: respirometry, relevance and recommendations. Journal of Experimental Biology 216, 2771 -2782.
    • Dupont-Prinet, A., Claireaux, G. & McKenzie, D. J. (2009). Effects of feeding and hypoxia on cardiac performance and gastrointestinal blood flow during critical speed swimming in the sea bass Dicentrarchus labrax. Comparative Biochemistry and Physiology A 154, 233 -240.
    • Farrell, A. P. (2016). Pragmatic perspective on aerobic scope: peaking, plummeting, pejus and apportioning. Journal of Fish Biology 88, 322 -343.
    • Fry, F. E. J. (1971). The effect of environmental factors on the physiology of fish. In Fish Physiology, Vol. VI (Hoar, W. S. & Randall, D. J., eds), pp. 1 -98. London: Academic Press.
    • Fu, S. J., Cao, Z. D., Peng, J. L. & Wang, Y. X. (2008). Is peak postprandial oxygen consumption positively related to growth rate and resting oxygen consumption in a sedentary catfish Silurus meridionalis? Journal of Fish Biology 73, 692 -701.
    • Garland, T. Jr. & Ives, A. R. (2000). Using the past to predict the present: confidence intervals for regression equations in phylogenetic comparative methods. American Naturalist 155, 346 -364.
    • Grafen, A. (1989). The phylogenetic regression. Philosophical Transactions of the Royal Society B 326, 119 -157.
    • Hinchliff, C. E., Smith, S. A., Allman, J. F., Burleigh, J. G., Chaudhary, R., Coghill, L. M., Crandall, K. A., Deng, J., Drew, B. T. & Gazis, R. (2015). Synthesis of phylogeny and taxonomy into a comprehensive tree of life. Proceedings of the National Academy of Sciences of the United States of America 112, 12764 -12769.
    • Jourdan-Pineau, H., Dupont-Prinet, A., Claireaux, G. & McKenzie, D. J. (2010). An investigation of metabolic prioritization in the European sea bass, Dicentrarchus labrax. Physiological and Biochemical Zoology 83, 68 -77.
    • Killen, S. S., Atkinson, D. & Glazier, D. S. (2010). The intraspecific scaling of metabolic rate with body mass in fishes depends on lifestyle and temperature. Ecology Letters 13, 184 -193.
    • Killen, S. S., Marras, S., Steffensen, J. F. & McKenzie, D. J. (2012). Aerobic capacity influences the spatial position of individuals within fish schools. Proceedings of the Royal Society B 279, 357 -364.
    • Killen, S. S., Mitchell, M. D., Rummer, J. L., Chivers, D. P., Ferrari, M. C. O., Meekan, M. G. & McCormick, M. I. (2014). Aerobic scope predicts dominance during early life in a tropical damselfish. Functional Ecology 28, 1367 -1376.
    • Killen, S. S., Glazier, D., Rezende, E. L., Clark, T. D., Atkinson, D., Willener, A. & Halsey, L. G. (2016). Ecological influences and physiological correlates of metabolic rates in teleost ifshes. American Naturalist 187, 592 -606.
    • Lee, C. G., Farrell, A. P., Lotto, A., Hinch, S. G. & Healey, M. C. (2003). Excess post-exercise oxygen consumption in adult sockeye (Oncorhynchus nerka) and coho (O. kisutch) salmon following critical speed swimming. Journal of Experimental Biology 206, 3253 -3260.
    • Lefevre, S. (2016). Are global warming and ocean acidification conspiring against marine ectotherms? A meta-analysis of the respiratory effects of elevated temperature, high CO2 and their interaction. Conservation Physiology 4, cow009.
    • Martins, E. P. & Hansen, T. F. (1997). Phylogenies and the comparative method: a general approach to incorporating phylogenetic information into the analysis of interspecific data. American Naturalist 149, 646 -667.
    • Metcalfe, N. B., Van Leeuwen, T. E. & Killen, S. S. (2016). Does individual variation in metabolic phenotype predict fish behaviour and performance? Journal of Fish Biology 88, 298 -321.
    • Michonneau, F., Brown, J. & Winter, D. (2016). rotl, an R package to interact with the Open Tree of Life data. PeerJ Preprints 4, e1471v1473.
    • Norin, T. & Clark, T. D. (2016). Measurement and relevance of maximum metabolic rate in ifshes. Journal of Fish Biology 88, 122 -151.
    • Paradis, E., Claude, J. & Strimmer, K. (2004). APE: analyses of phylogenetics and evolution in R language. Bioinformatics 20, 289 -290.
    • Peake, S. J. & Farrell, A. P. (2004). Locomotory behaviour and post-exercise physiology in relation to swimming speed, gait transition and metabolism in free-swimming smallmouth bass (Micropterus dolomieu). Journal of Experimental Biology 207, 1563 -1575.
    • Peake, S. J. & Farrell, A. P. (2006). Fatigue is a behavioural response in respirometer-confined smallmouth bass. Journal of Fish Biology 68, 1742 -1755.
    • Pörtner, H. O. & Farrell, A. P. (2008). Physiology and climate change. Science 322, 690 -692.
    • Reidy, S. P., Nelson, J. A., Tang, Y. & Kerr, S. R. (1995). Post-exercise metabolic rate in Atlantic cod and its dependence upon the method of exhaustion. Journal of Fish Biology 47, 377 -386.
    • Roche, D. G., Binning, S. A., Bosiger, Y., Johansen, J. L. & Rummer, J. L. (2013). Finding the best estimates of metabolic rates in a coral reef fish. Journal of Experimental Biology 216, 2103 - 2110.
    • Rodgers, G., Tenzing, P. & Clark, T. D. (2016). Experimental methods in aquatic respirometry: the importance of mixing devices and accounting for background respiration. Journal of Fish Biology 88, 65 -80.
    • Rummer, J. L., Binning, S. A., Roche, D. G. & Johansen, J. L. (2016). Methods matter: considering locomotory mode and respirometry technique when estimating metabolic rates of ifshes. Conservation Physiology 4, cow008.
    • Scarabello, M., Heigenhauser, G. & Wood, C. (1992). Gas exchange, metabolite status and excess post-exercise oxygen consumption after repetitive bouts of exhaustive exercise in juvenile rainbow trout. Journal of Experimental Biology 167, 155 -169.
    • Scott, C. (2005). Misconceptions about aerobic and anaerobic energy expenditure. Journal of the International Society of Sports Nutrition 2, 32 - 37.
    • Sooafini, N. M. & Hawkins, A. D. (1982). Energetic costs at different levels of feeding in juvenile cod, Gadus morhua L. Journal of Fish Biology 21, 577 -592.
    • Sooafini, N. & Priede, I. (1985). Aerobic metabolic scope and swimming performance in juvenile cod, Gadus morhua L. Journal of Fish Biology 26, 127 - 138.
    • Steffensen, J. (1989). Some errors in respirometry of aquatic breathers: how to avoid and correct for them. Fish Physiology and Biochemistry 6, 49 -59.
    • Svendsen, J. C., Tudorache, C., Jordan, A. D., Steffensen, J. F., Aarestrup, K. & Domenici, P. (2010). Partition of aerobic and anaerobic swimming costs related to gait transitions in a labriform swimmer. Journal of Experimental Biology 213, 2177 -2183.
    • Svendsen, M. B. S., Bushnell, P. G. & Steffensen, J. F. (2016). Design and setup of intermittent-flow respirometry system for aquatic organisms. Journal of Fish Biology 88, 26 - 50.
    • Zhang, W., Cao, Z.-D. & Fu, S.-J. (2012). The effects of dissolved oxygen levels on the metabolic interaction between digestion and locomotion in Cyprinid fishes with different locomotive and digestive performances. Journal of Comparative Physiology B 182, 641 -650.
    • Froese, R. & Pauly, D. (2008). FishBase. Available at www.fishbase.org
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