The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Evolution of Resistance to High Temperature in Ectotherms
Abstract
Body temperature influences the performance and fitness of ectotherms. How thermal sensitivity responds to selection for resistance to high temperature is broadly relevant in evolutionary physiology and also has practical implications. We review several complementary approaches to studying the evolution of thermal sensitivity. First, we analyze comparative data that illustrate the historical evolution of thermal sensitivity of locomotion in iguanid lizards. Taxa that experience high body temperatures in nature have evolved high optimal temperatures for sprinting. Critical thermal maxima are co-adapted with optimal temperatures but not with critical thermal minima. Thus some but not all aspects of thermal sensitivity are co-adapted. Second, we describe selection experiments that help reveal potential genetic constraints on the future evolution of thermal sensitivity in Drosophila. Thermal sensitivity responds rapidly both to laboratory natural selection and artificial selection, and tolerance of extreme high temperature appears genetically correlated with performance at intermediate temperature. Third, applying a recent model by Lynch and Lande, we describe how the shape of thermal performance curves may affect evolutionary responses of thermal sensitivity to a gradual shift in the thermal environment. Our theoretical predictions depend crucially on the relationship between the genetic variation in optimal temperature and the performance breadth. If genetic variation is independent of breadth, then populations with an intermediate value of performance breadth will tolerate the greatest rate of environmental change. Moreover, if a trade-off exists between maximum performance and breadth of performance, then thermal specialists will be favored over thermal generalists in a rapidly changing environment. On the other hand, if genetic variation increases with increasing breadth, then populations of thermal generalists will tolerate the greatest rates of environmental change.
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Cites
Phylogenies and the Comparative Method
Felsenstein, J. (1985) · The American Naturalist · doi:10.1086/284325 · Cited by 9,793
The Comparative Method: Moving Beyond Qualitative and Quantitative Strategies
Ragin, C. C. (2014) · doi:10.1525/9780520957350 · Cited by 2,130
EVOLUTIONARY QUANTITATIVE GENETICS: HOW LITTLE DO WE KNOW?
Barton, N. H., & Turelli, M. (1989) · Annual Review of Genetics · doi:10.1146/annurev.ge.23.120189.002005 · Cited by 686
Cited by
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Self-citationThe physiology of life history trade-offs in animals
Zera, A. J., & Harshman, L. G. (2001) · Annual Review of Ecology and Systematics · doi:10.1146/annurev.ecolsys.32.081501.114006 · Cited by 1,577
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Huey, R. B., Deutsch, C. A., Tewksbury, J. J., Vitt, L. J., Hertz, P. E., Álvarez Pérez, H. J., & Garland, T. (2009) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2008.1957 · Cited by 962
Self-citationPhysiological Diversity in Insects: Ecological and Evolutionary Contexts
Chown, S. L., & Terblanche, J. S. (2006) · Advances in Insect Physiology · doi:10.1016/s0065-2806(06)33002-0 · Cited by 573
Calosi, P., Bilton, D. T., Spicer, J. I., Votier, S. C., & Atfield, A. (2010) · Journal of Animal Ecology · doi:10.1111/j.1365-2656.2009.01611.x · Cited by 332
Metadata
- Authors
- Huey, R. B., & Kingsolver, J. G.
- Venue
- The American Naturalist
- Publisher
- University of Chicago Press
- Published
- 1993-07
- Volume
- 142
- Pages
- S21-S46
- ISSN
- 0003-0147 (ISSN-L)
- 1537-5323
- OpenAlex
- W2088422888
- Cited by
- 491
- References
- 3
- FWCI
- 8.63
- Type
- journal article
- Language
- en
- Open access
- closed
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