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      Ontogeny and ecological significance of metabolic rates in sea turtle hatchlings

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          Abstract

          Background

          Sea turtle hatchlings must avoid numerous predators during dispersal from their nesting beaches to foraging grounds. Hatchlings minimise time spent in predator-dense neritic waters by swimming almost continuously for approximately the first 24 h post-emergence, termed the ‘frenzy’. Post-frenzy, hatchling activity gradually declines as they swim in less predator-dense pelagic waters. It is well documented that hatchlings exhibit elevated metabolic rates during the frenzy to power their almost continuous swimming, but studies on post-frenzy MRs are sparse.

          Results

          We measured the frenzy and post-frenzy oxygen consumption of hatchlings of five species of sea turtle at different activity levels and ages to compare the ontogeny of mass-specific hatchling metabolic rates. Maximal metabolic rates were always higher than resting metabolic rates, but metabolic rates during routine swimming resembled resting metabolic rates in leatherback turtle hatchlings during the frenzy and post-frenzy, and in loggerhead hatchlings during the post-frenzy. Crawling metabolic rates did not differ among species, but green turtles had the highest metabolic rates during frenzy and post-frenzy swimming.

          Conclusions

          Differences in metabolic rate reflect the varying dispersal stratagems of each species and have important implications for dispersal ability, yolk consumption and survival. Our results provide the foundations for links between the physiology and ecology of dispersal of sea turtles.

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          Most cited references70

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          Anthropogenic causes of jellyfish blooms and their direct consequences for humans: a review

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            Aerobic scope measurements of fishes in an era of climate change: respirometry, relevance and recommendations.

            Measurements of aerobic scope [the difference between minimum and maximum oxygen consumption rate ( and , respectively)] are increasing in prevalence as a tool to address questions relating to fish ecology and the effects of climate change. However, there are underlying issues regarding the array of methods used to measure aerobic scope across studies and species. In an attempt to enhance quality control before the diversity of issues becomes too great to remedy, this paper outlines common techniques and pitfalls associated with measurements of , and aerobic scope across species and under different experimental conditions. Additionally, we provide a brief critique of the oxygen- and capacity-limited thermal tolerance (OCLTT) hypothesis, a concept that is intricately dependent on aerobic scope measurements and is spreading wildly throughout the literature despite little evidence for its general applicability. It is the intention of this paper to encourage transparency and accuracy in future studies that measure the aerobic metabolism of fishes, and to highlight the fundamental issues with assuming broad relevance of the OCLTT hypothesis.
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              What causes intraspecific variation in resting metabolic rate and what are its ecological consequences?

              Individual differences in the energy cost of self-maintenance (resting metabolic rate, RMR) are substantial and the focus of an emerging research area. These differences may influence fitness because self-maintenance is considered as a life-history component along with growth and reproduction. In this review, we ask why do some individuals have two to three times the 'maintenance costs' of conspecifics, and what are the fitness consequences? Using evidence from a range of species, we demonstrate that diverse factors, such as genotypes, maternal effects, early developmental conditions and personality differences contribute to variation in individual RMR. We review evidence that RMR is linked with fitness, showing correlations with traits such as growth and survival. However, these relationships are modulated by environmental conditions (e.g. food supply), suggesting that the fitness consequences of a given RMR may be context-dependent. Then, using empirical examples, we discuss broad-scale reasons why variation in RMR might persist in natural populations, including the role of both spatial and temporal variation in selection pressures and trans-generational effects. To conclude, we discuss experimental approaches that will enable more rigorous examination of the causes and consequences of individual variation in this key physiological trait.
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                Author and article information

                Contributors
                christopher.r.gatto@gmail.com
                Journal
                Front Zool
                Front Zool
                Frontiers in Zoology
                BioMed Central (London )
                1742-9994
                5 February 2022
                5 February 2022
                2022
                : 19
                : 6
                Affiliations
                [1 ]GRID grid.1002.3, ISNI 0000 0004 1936 7857, School of Biological Sciences, , Monash University, ; 25 Rainforest Walk, Clayton, VIC 3800 Australia
                [2 ]GRID grid.466960.b, ISNI 0000 0004 0601 127X, NOAA Fisheries, , Pacific Islands Fisheries Science Center, ; Honolulu, HI USA
                [3 ]GRID grid.17091.3e, ISNI 0000 0001 2288 9830, Centre for Comparative Medicine, , The University of British Columbia, ; Vancouver, BC Canada
                Author information
                http://orcid.org/0000-0003-1946-5791
                Article
                451
                10.1186/s12983-022-00451-2
                8818257
                35123495
                501af879-5402-4d4b-8fb9-2e30b30645e4
                © The Author(s) 2022

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 10 December 2021
                : 25 January 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100013814, Great Barrier Reef Marine Park Authority;
                Award ID: Reef Guardian Grant
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2022

                Animal science & Zoology
                oxygen consumption,metabolism,sea turtle,ontogeny,life history,aerobic scope
                Animal science & Zoology
                oxygen consumption, metabolism, sea turtle, ontogeny, life history, aerobic scope

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