The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Beyond Thermal Performance Curves: Modeling Time-Dependent Effects of Thermal Stress on Ectotherm Growth Rates
Abstract
Thermal performance curves have been widely used to model the ecological responses of ectotherms to variable thermal environments and climate change. Such models ignore the effects of time dependence-the temporal pattern and duration of temperature exposure-on performance. We developed and solved a simple mathematical model for growth rate of ectotherms, combining thermal performance curves for ingestion rate with the temporal dynamics of gene expression and protein production in response to high temperatures to predict temporal patterns of growth rate in constant and diurnally fluctuating temperatures. We used the model to explore the effects of heat shock proteins on larval growth rates of Manduca sexta. The model correctly captures two empirical patterns for larval growth rate: first, maximal growth rate and optimal temperature decline with increasing duration of temperature exposure; second, mean growth rates decline with time in diurnally fluctuating temperatures at higher mean temperatures. These qualitative results apply broadly to cases where proteins or other molecules produced in response to high temperatures reduce growth rates. We discuss some of the critical assumptions and predictions of the model and suggest potential extensions and alternatives. Incorporating time-dependent effects will be essential for making more realistic predictions about the physiological and ecological consequences of temperature fluctuations and climate change.
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Cites
Impacts of climate warming on terrestrial ectotherms across latitude
Deutsch, C. A., Tewksbury, J. J., Huey, R. B., Sheldon, K. S., Ghalambor, C. K., Haak, D. C., & Martin, P. R. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709472105 · Cited by 3,840
Erosion of Lizard Diversity by Climate Change and Altered Thermal Niches
Sinervo, B., Méndez-de-la-Cruz, F., Miles, D. B., Heulin, B., Bastiaans, E., Villagrán-Santa Cruz, M., Lara-Resendiz, R., Martínez-Méndez, N., Calderón-Espinosa, M. L., Meza-Lázaro, R. N., et al. (2010) · Science · doi:10.1126/science.1184695 · Cited by 1,902
Novel climates, no‐analog communities, and ecological surprises
Williams, J. W., & Jackson, S. T. (2007) · Frontiers in Ecology and the Environment · doi:10.1890/070037 · Cited by 1,736
Global analysis of thermal tolerance and latitude in ectotherms
Sunday, J. M., Bates, A. E., & Dulvy, N. K. (2011) · Proceedings of the Royal Society B: Biological Sciences · doi:10.1098/rspb.2010.1295 · Cited by 1,300
Why tropical forest lizards are vulnerable to climate warming
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
Cited by
Thermal biology of mosquito‐borne disease
Mordecai, E. A., Caldwell, J. M., Grossman, M. K., Lippi, C. A., Johnson, L. R., Neira, M., Rohr, J. R., Ryan, S. J., Savage, V., Shocket, M. S., et al. (2019) · Ecology Letters · doi:10.1111/ele.13335 · Cited by 746
Evolution of heat‐shock protein expression underlying adaptive responses to environmental stress
Chen, B., Feder, M. E., & Kang, L. (2018) · Molecular Ecology · doi:10.1111/mec.14769 · Cited by 267
Kim, K. S., Chou, H., Funk, D. H., Jackson, J. K., Sweeney, B. W., & Buchwalter, D. B. (2017) · Journal of Experimental Biology · doi:10.1242/jeb.156919 · Cited by 37
Metadata
- Authors
- Kingsolver, J. G., & Woods, H. A.
- Venue
- The American Naturalist
- Publisher
- University of Chicago Press
- Published
- 2016-03
- Volume
- 187
- Issue
- 3
- Pages
- 283-294
- ISSN
- 0003-0147 (ISSN-L)
- 1537-5323
- OpenAlex
- W2284669351
- Cited by
- 208
- References
- 5
- FWCI
- 20.73
- Type
- journal article
- Language
- en
- Open access
- closed
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