The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Cost and Benefits of Lizard Thermoregulation
Abstract
Lizards thermoregulate by behavioral and physiological adjustments. The resultant control over metabolic processes is generally assumed to be beneficial. However, these thermoregulatory adjustments have associated costs which, if extensive, make thermoregulation impractical. We extend this idea into an abstract mathematical, cost-benefit model of thermoregulation in lizards. Investigation of the model leads to a set of predictions which includes: (1) the physiologically optimal temperature is not always the ecologically optimal temperature; (2) thermoregulation is beneficial only when associated costs are low; (3) thermal specialists will normally thermoregulate more carefully than thermal generalists unless costs are high; and (4) lizards will thermoregulate more carefully if productivity of the habitat is increased or if exploitation competition is reduced. Data on lizards, where available, generally agree with these predicitions.
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Citations
Cites
Nonsynchronous Spatial Overlap of Lizards in Patchy Habitats
Schoener, T. W. (1970) · Ecology · doi:10.2307/1935376 · Cited by 1,745
Net Primary Productivity of Terrestrial Communities: Prediction from Climatological Data
Rosenzweig, M. L. (1968) · The American Naturalist · doi:10.1086/282523 · Cited by 858
Cowles, R. B., & Bogert, C. M. (1944) · Cited by 766
THERMOREGULATION IN REPTILES, A FACTOR IN EVOLUTION
Bogert, C. M. (1949) · Evolution · doi:10.1111/j.1558-5646.1949.tb00021.x · Cited by 661
Thermal Acclimation and Heat Resistance in Drosophila Species
Levins, R. (1969) · The American Naturalist · doi:10.1086/282616 · Cited by 353
Bartholomew, G. A., & Tucker, V. A. (1963) · Physiological Zoology · doi:10.1086/physzool.36.3.30152307 · Cited by 278
Observations on the Thermal Relations of Western Australian Lizards
Light, P., Dawson, W. R., Shoemaker, V. H., & Main, A. R. (1966) · Copeia · doi:10.2307/1440766 · Cited by 250
Some Niche Differences in Three Lesser Antillean Lizards of the Genus Anolis
Schoener, T. W., & Gorman, G. C. (1968) · Ecology · doi:10.2307/1936533 · Cited by 247
Ecology of Horned Lizards: A Review with Special Reference to Phrynosoma platyrhinos
Pianka, E. R., & Parker, W. S. (1975) · Copeia · doi:10.2307/1442418 · Cited by 243
Ecological Distribution in Anoline Lizards of Puerto Rico
Rand, A. S. (1964) · Ecology · doi:10.2307/1934922 · Cited by 232
DeWitt, C. B. (1967) · Physiological Zoology · doi:10.1086/physzool.40.1.30152438 · Cited by 209
Thermophilic Response Following Feeding in Certain Reptiles
Regal, P. J. (1966) · Copeia · doi:10.2307/1441092 · Cited by 165
On the Physiological Significance of the Preferred Body Temperatures of Reptiles
Dawson, W. R. (1975) · Ecological studies · doi:10.1007/978-3-642-87810-7_25 · Cited by 162
Hamilton, W. J. (1973) · Medical Entomology and Zoology · Cited by 151
A Field Study of Temperature Relations in the Galapagos Marine Iguana
Bartholomew, G. A. (1966) · Copeia · doi:10.2307/1441131 · Cited by 140
Solar Radiation through the Living Body Walls of Vertebrates with Emphasis on Desert Reptiles
Porter, W. P. (1967) · Ecological Monographs · doi:10.2307/1942325 · Cited by 134
The Ecology of Moloch horridus (Lacertilia: Agamidae) in Western Australia
Pianka, E. R., & Pianka, H. D. (1970) · Copeia · doi:10.2307/1441978 · Cited by 124
Regulation of Body Temperature in the Blue-Tongued Lizard
Hammel, H. T., Caldwell, F. T., & Abrams, R. M. (1967) · Science · doi:10.1126/science.156.3779.1260 · Cited by 119
Activity Cycle and Thermoregulation in the Australian Gecko Gehyra variegata
Bustard, H. R. (1967) · Copeia · doi:10.2307/1441885 · Cited by 108
Ballinger, R. Ε., Marion, K. R., & Sexton, O. J. (1970) · Ecology · doi:10.2307/1933660 · Cited by 72
Some Aspects of the Thermal Ecology of Puerto Rican Anoline Lizards
Heatwole, H., Lin, T.-H., Villalon, E., Muniz, A., & Matta, A. (1969) · Journal of Herpetology · doi:10.2307/1563225 · Cited by 67
Critical Thermal Tolerances and Heating and Cooling Rates of Lizards from Diverse Habitats
Kour, E. L., & Hutchison, V. H. (1970) · Copeia · doi:10.2307/1441644 · Cited by 64
Rand, A. S., & Humphrey, S. S. (1968) · Proceedings of the United States National Museum · doi:10.5479/si.00963801.125-3658.1 · Cited by 59
Temperature Responses and Ecological Relations of Two Bornean Lizards
Inger, R. F. (1959) · Ecology · doi:10.2307/1929930 · Cited by 56
Habitat Specificity in Three Sympatric Species of Ameiva (Reptilia: Teiidae)
Hillman, P. E. (1969) · Ecology · doi:10.2307/1933903 · Cited by 55
Thermal Ecology of Anoline Lizards: Temperate versus Tropical Strategies
Clark, D. R., & Kroll, J. C. (1974) · The Southwestern Naturalist · doi:10.2307/3669786 · Cited by 48
Reproductive influences on behavioral thermoregulation in the lizard, Sceloporus cyanogenys
Garrick, L. D. (1974) · Physiology & Behavior · doi:10.1016/0031-9384(74)90072-9 · Cited by 45
Cited by
Temperature as an Ecological Resource
MAGNUSON, J. J., CROWDER, L. B., & MEDVICK, P. A. (1979) · American Zoologist · doi:10.1093/icb/19.1.331 · Cited by 1,091
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
Self-citationPhysiological Consequences of Habitat Selection
Huey, R. B. (1991) · The American Naturalist · doi:10.1086/285141 · Cited by 914
Self-citationDissolved oxygen and fish behavior
Kramer, D. L. (1987) · Environmental Biology of Fishes · doi:10.1007/bf00002597 · Cited by 616
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., & Slatkin, M.
- Venue
- The Quarterly Review of Biology
- Publisher
- University of Chicago Press
- Published
- 1976-09
- Volume
- 51
- Issue
- 3
- Pages
- 363-384
- ISSN
- 0033-5770 (ISSN-L)
- 1539-7718
- OpenAlex
- W2046736242
- Cited by
- 1,084
- References
- 27
- FWCI
- 12.08
- Type
- journal article
- Language
- en
- Open access
- closed
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