The DOI matches its Crossref record; 95 of the 95 references it cites were found in a registry or an index.
Oxygen- and capacity-limited thermal tolerance: bridging ecology and physiology
Open accessAbstract
Observations of climate impacts on ecosystems highlight the need for an understanding of organismal thermal ranges and their implications at the ecosystem level. Where changes in aquatic animal populations have been observed, the integrative concept of oxygen- and capacity-limited thermal tolerance (OCLTT) has successfully characterised the onset of thermal limits to performance and field abundance. The OCLTT concept addresses the molecular to whole-animal mechanisms that define thermal constraints on the capacity for oxygen supply to the organism in relation to oxygen demand. The resulting ‘total excess aerobic power budget’ supports an animal's performance (e.g. comprising motor activity, reproduction and growth) within an individual's thermal range. The aerobic power budget is often approximated through measurements of aerobic scope for activity (i.e. the maximum difference between resting and the highest exercise-induced rate of oxygen consumption), whereas most animals in the field rely on lower (i.e. routine) modes of activity. At thermal limits, OCLTT also integrates protective mechanisms that extend time-limited tolerance to temperature extremes – mechanisms such as chaperones, anaerobic metabolism and antioxidative defence. Here, we briefly summarise the OCLTT concept and update it by addressing the role of routine metabolism. We highlight potential pitfalls in applying the concept and discuss the variables measured that led to the development of OCLTT. We propose that OCLTT explains why thermal vulnerability is highest at the whole-animal level and lowest at the molecular level. We also discuss how OCLTT captures the thermal constraints on the evolution of aquatic animal life and supports an understanding of the benefits of transitioning from water to land.
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Cites
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The complex drivers of thermal acclimation and breadth in ectotherms
Rohr, J. R., Civitello, D. J., Cohen, J. M., Roznik, E. A., Sinervo, B., & Dell, A. I. (2018) · Ecology Letters · doi:10.1111/ele.13107 · Cited by 293
Sound physiological knowledge and principles in modeling shrinking of fishes under climate change
Pauly, D., & Cheung, W. W. L. (2018) · Global Change Biology · doi:10.1111/gcb.13831 · Cited by 257
Agyekum, T. P., Botwe, P. K., Arko-Mensah, J., Issah, I., Acquah, A. A., Hogarh, J. N., Dwomoh, D., Robins, T. G., & Fobil, J. N. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18147255 · Cited by 164
Hvas, M., Morin, A., Johansen, I. B., & Vågseth, T. (2025) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2025.104231 · Cited by 11
Hypoxia and warming are associated with reductions in larval bivalve abundance in a tropical lagoon
Weinstock, J., & Collin, R. (2021) · Marine Ecology Progress Series · doi:10.3354/meps13630 · Cited by 8
Metadata
- Authors
- Pörtner, H.-O., Bock, C., & Mark, F. C.
- Venue
- Journal of Experimental Biology
- Publisher
- The Company of Biologists
- Published
- 2017-08-01
- Volume
- 220
- Issue
- 15
- Pages
- 2685-2696
- ISSN
- 0022-0949 (ISSN-L)
- 1477-9145
- OpenAlex
- W2743646195
- Cited by
- 655
- References
- 95
- FWCI
- 31.46
- Type
- journal article
- Language
- en
- Open access
- bronze
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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