The DOI matches its Crossref record; 170 of the 170 references it cites were found in a registry or an index.
Shrinking body sizes in response to warming: explanations for the temperature–size rule with special emphasis on the role of oxygen
Open accessAbstract
Body size is central to ecology at levels ranging from organismal fecundity to the functioning of communities and ecosystems. Understanding temperature‐induced variations in body size is therefore of fundamental and applied interest, yet thermal responses of body size remain poorly understood. Temperature–size (T–S) responses tend to be negative (e.g. smaller body size at maturity when reared under warmer conditions), which has been termed the temperature–size rule (TSR). Explanations emphasize either physiological mechanisms (e.g. limitation of oxygen or other resources and temperature‐dependent resource allocation) or the adaptive value of either a large body size (e.g. to increase fecundity) or a short development time (e.g. in response to increased mortality in warm conditions). Oxygen limitation could act as a proximate factor, but we suggest it more likely constitutes a selective pressure to reduce body size in the warm: risks of oxygen limitation will be reduced as a consequence of evolution eliminating genotypes more prone to oxygen limitation. Thus, T–S responses can be explained by the ‘Ghost of Oxygen‐limitation Past’, whereby the resulting (evolved) T–S responses safeguard sufficient oxygen provisioning under warmer conditions, reflecting the balance between oxygen supply and demands experienced by ancestors. T–S responses vary considerably across species, but some of this variation is predictable. Body‐size reductions with warming are stronger in aquatic taxa than in terrestrial taxa. We discuss whether larger aquatic taxa may especially face greater risks of oxygen limitation as they grow, which may be manifested at the cellular level, the level of the gills and the whole‐organism level. In contrast to aquatic species, terrestrial ectotherms may be less prone to oxygen limitation and prioritize early maturity over large size, likely because overwintering is more challenging, with concomitant stronger end‐of season time constraints. Mechanisms related to time constraints and oxygen limitation are not mutually exclusive explanations for the TSR. Rather, these and other mechanisms may operate in tandem. But their relative importance may vary depending on the ecology and physiology of the species in question, explaining not only the general tendency of negative T–S responses but also variation in T–S responses among animals differing in mode of respiration (e.g. water breathers versus air breathers), genome size, voltinism and thermally associated behaviour (e.g. heliotherms).
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The Evolution of Life-histories
Benton, T. G., & Stearne, S. C. (1993) · The Journal of Animal Ecology · doi:10.2307/5403 · Cited by 12,228
Pianka, E. R. (1970) · The American Naturalist · doi:10.1086/282697 · Cited by 3,640
Temperature and Organism Size—A Biological Law for Ectotherms?
Atkinson, D. (1994) · Advances in Ecological Research · doi:10.1016/s0065-2504(08)60212-3 · Cited by 2,424
Self-citationThe Population Consequences of Life History Phenomena
Cole, L. C. (1954) · The Quarterly Review of Biology · doi:10.1086/400074 · Cited by 2,093
Global warming benefits the small in aquatic ecosystems
Daufresne, M., Lengfellner, K., & Sommer, U. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0902080106 · Cited by 1,686
Diversity and the Coevolution of Competitors, or the Ghost of Competition Past
Connell, J. H. (1980) · Oikos · doi:10.2307/3544421 · Cited by 1,555
The Evolution of Body Size: What Keeps Organisms Small?
Blanckenhorn, W. U. (2000) · The Quarterly Review of Biology · doi:10.1086/393620 · Cited by 1,277
Declining body size: a third universal response to warming?
Gardner, J. L., Peters, A., Kearney, M. R., Joseph, L., & Heinsohn, R. (2011) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2011.03.005 · Cited by 1,224
H., P. (2001) · Naturwissenschaften · doi:10.1007/s001140100216 · Cited by 1,160
Dynamic Energy Budget Theory for Metabolic Organisation
Kooijman, B. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9780511805400 · Cited by 1,153
Temperature, Growth Rate, and Body Size in Ectotherms: Fitting Pieces of a Life-History Puzzle
Angilletta, M. J. (2004) · Integrative and Comparative Biology · doi:10.1093/icb/44.6.498 · Cited by 1,011
Physiological plasticity increases resilience of ectothermic animals to climate change
Seebacher, F., White, C. R., & Franklin, C. E. (2015) · Nature Climate Change · doi:10.1038/nclimate2457 · Cited by 998
Guzy, R. D., & Schumacker, P. T. (2006) · Experimental Physiology · doi:10.1113/expphysiol.2006.033506 · Cited by 881
Size, temperature, and fitness: three rules
Kingsolver, J. G., & Huey, R. B. (2021) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/jtzc-v174 · Cited by 837
Why are organisms usually bigger in colder environments? Making sense of a life history puzzle
Atkinson, D., & Sibly, R. M. (1997) · Trends in Ecology & Evolution · doi:10.1016/s0169-5347(97)01058-6 · Cited by 808
Self-citationCoincidence, coevolution, or causation? DNA content, cellsize, and the C‐value enigma
GREGORY, T. R. (2001) · Biological Reviews · doi:10.1111/j.1469-185x.2000.tb00059.x · Cited by 730
Shrinking of fishes exacerbates impacts of global ocean changes on marine ecosystems
Cheung, W. W. L., Sarmiento, J. L., Dunne, J., Frölicher, T. L., Lam, V. W. Y., Deng Palomares, M. L., Watson, R., & Pauly, D. (2013) · Nature Climate Change · doi:10.1038/nclimate1691 · Cited by 720
The Temperature‐Size Rule in Ectotherms: Simple Evolutionary Explanations May Not Be General
Angilletta, Jr., & Dunham, A. E. (2003) · The American Naturalist · doi:10.1086/377187 · Cited by 708
Bergmann and Converse Bergmann Latitudinal Clines in Arthropods: Two Ends of a Continuum?
Blanckenhorn, W. U. (2004) · Integrative and Comparative Biology · doi:10.1093/icb/44.6.413 · Cited by 682
Physiological Ecology: An Evolutionary Approach to Resource Use
Elliott, J. M., Townsend, C. R., & Calow, P. (1983) · The Journal of Animal Ecology · doi:10.2307/4613 · Cited by 669
Fish reproductive-energy output increases disproportionately with body size
Barneche, D. R., Robertson, D. R., White, C. R., & Marshall, D. J. (2018) · Science · doi:10.1126/science.aao6868 · Cited by 643
Principles of comparative respiratory physiology
Bernards, J. A. (1976) · European Journal of Obstetrics & Gynecology and Reproductive Biology · doi:10.1016/0028-2243(76)90013-7 · Cited by 605
Kozłowski, J. (1992) · Trends in Ecology & Evolution · doi:10.1016/0169-5347(92)90192-e · Cited by 565
Warming-induced reductions in body size are greater in aquatic than terrestrial species
Forster, J., Hirst, A. G., & Atkinson, D. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1210460109 · Cited by 535
Self-citationDell, A. I., Pawar, S., & Savage, V. M. (2014) · Journal of Animal Ecology · doi:10.1111/1365-2656.12081 · Cited by 480
Optimizing development time in a seasonal environment: The ?ups and downs? of clinal variation
Roff, D. (1980) · Oecologia · doi:10.1007/bf00346461 · Cited by 443
The correlation between rDNA copy number and genome size in eukaryotes
Prokopowich, C. D., Gregory, T. R., & Crease, T. J. (2003) · Genome · doi:10.1139/g02-103 · Cited by 441
The Effect of Flexible Growth Rates on Optimal Sizes and Development Times in a Seasonal Environment
Abrams, P. A., Leimar, O., Nylin, S., & Wiklund, C. (1996) · The American Naturalist · doi:10.1086/285857 · Cited by 432
Adult Size in Ectotherms: Temperature Effects on Growth and Differentiation
van der Have, T. M., & de Jong, G. (1996) · Journal of Theoretical Biology · doi:10.1006/jtbi.1996.0224 · Cited by 420
Climate warming and ectotherm body size – from individual physiology to community ecology
Ohlberger, J. (2013) · Functional Ecology · doi:10.1111/1365-2435.12098 · Cited by 406
CAVALIER-SMITH, T. (2005) · Annals of Botany · doi:10.1093/aob/mci010 · Cited by 396
Partridge, L., Barrie, B., Fowler, K., & French, V. (1994) · Evolution · doi:10.1111/j.1558-5646.1994.tb05311.x · Cited by 381
Reaction Norms for Age and Size at Maturity in Response to Temperature: A Puzzle for Life Historians
Berrigan, D., & Charnov, E. L. (1994) · Oikos · doi:10.2307/3545787 · Cited by 369
Latitudinal patterns in European ant assemblages: variation in species richness and body size
Cushman, J. H., Lawton, J. H., & Manly, B. F. J. (1993) · Oecologia · doi:10.1007/bf00649503 · Cited by 358
Warming temperatures and smaller body sizes: synchronous changes in growth of North Sea fishes
Baudron, A. R., Needle, C. L., Rijnsdorp, A. D., & Tara Marshall, C. (2014) · Global Change Biology · doi:10.1111/gcb.12514 · Cited by 350
Day, T., & Rowe, L. (2002) · The American Naturalist · doi:10.1086/338989 · Cited by 344
Verberk, W. C. E. P., Bilton, D. T., Calosi, P., & Spicer, J. I. (2011) · Ecology · doi:10.1890/10-2369.1 · Cited by 335
Self-citationBERGMANN SIZE CLINES: A SIMPLE EXPLANATION FOR THEIR OCCURRENCE IN ECTOTHERMS
Van Voorhies, W. A. (1996) · Evolution · doi:10.1111/j.1558-5646.1996.tb02366.x · Cited by 306
Oxygen permeability of phosphatidylcholine--cholesterol membranes.
Subczynski, W. K., Hyde, J. S., & Kusumi, A. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.12.4474 · Cited by 297
Body-size shifts in aquatic and terrestrial urban communities
Merckx, T., Souffreau, C., Kaiser, A., Baardsen, L. F., Backeljau, T., Bonte, D., Brans, K. I., Cours, M., Dahirel, M., Debortoli, N., et al. (2018) · Nature · doi:10.1038/s41586-018-0140-0 · Cited by 296
Horne, C. R., Hirst, A. G., & Atkinson, D. (2015) · Ecology Letters · doi:10.1111/ele.12413 · Cited by 272
Self-citationBergmann's rule; a concept cluster?
Watt, C., Mitchell, S., & Salewski, V. (2010) · Oikos · doi:10.1111/j.1600-0706.2009.17959.x · Cited by 268
A RELATIONSHIP BETWEEN DNA CONTENT, NUCLEAR VOLUME, AND MINIMUM MITOTIC CYCLE TIME
Hof, J. V., & Sparrow, A. H. (1963) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.49.6.897 · Cited by 263
The Temperature‐Size Rule in Ectotherms: May a General Explanation Exist after All?
Walters, R. J., & Hassall, M. (2006) · The American Naturalist · doi:10.1086/501029 · Cited by 261
Evolution caused by extreme events
Grant, P. R., Grant, B. R., Huey, R. B., Johnson, M. T. J., Knoll, A. H., & Schmitt, J. (2017) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2016.0146 · Cited by 258
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
How Rearing Temperature Affects Optimal Adult Size in Ectotherms
Sibly, R. M., & Atkinson, D. (1994) · Functional Ecology · doi:10.2307/2390073 · Cited by 238
Self-citationCan Optimal Resource Allocation Models Explain Why Ectotherms Grow Larger in Cold?
Kozlowski, J. (2004) · Integrative and Comparative Biology · doi:10.1093/icb/44.6.480 · Cited by 234
The lost generation hypothesis: could climate change drive ectotherms into a developmental trap?
Van Dyck, H., Bonte, D., Puls, R., Gotthard, K., & Maes, D. (2015) · Oikos · doi:10.1111/oik.02066 · Cited by 230
From cells to colonies: at what levels of body organization does the ‘temperature‐size rule’ apply?
Atkinson, D., Morley, S. A., & Hughes, R. N. (2006) · Evolution & Development · doi:10.1111/j.1525-142x.2006.00090.x · Cited by 224
Self-citationFish body sizes change with temperature but not all species shrink with warming
Audzijonyte, A., Richards, S. A., Stuart-Smith, R. D., Pecl, G., Edgar, G. J., Barrett, N. S., Payne, N., & Blanchard, J. L. (2020) · Nature Ecology & Evolution · doi:10.1038/s41559-020-1171-0 · Cited by 219
The fallacy of the average: on the ubiquity, utility and continuing novelty of Jensen's inequality
Denny, M. (2017) · Journal of Experimental Biology · doi:10.1242/jeb.140368 · Cited by 218
Bergmann’s Rule in Ectotherms: A Test Using Freshwater Fishes
Belk, M. C., & Houston, D. D. (2002) · The American Naturalist · doi:10.1086/343880 · Cited by 198
Cell size and the concept of wasteful and frugal evolutionary strategies
Szarski, H. (1983) · Journal of Theoretical Biology · doi:10.1016/s0022-5193(83)80002-2 · Cited by 196
Crill, W. D., Huey, R. B., & Gilchrist, G. W. (1996) · Evolution · doi:10.1111/j.1558-5646.1996.tb02361.x · Cited by 193
Kaiser, A., Klok, C. J., Socha, J. J., Lee, W.-K., Quinlan, M. C., & Harrison, J. F. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611544104 · Cited by 192 · cited 1×
“Larger species likely prevent progressive oxygen limitation with increasing body size by having greatly increased tracheal dimensions and these do appear to set upper limits to the size that insects may attain (Kaiser et al., 2007).”
BackgroundAltitudinal body size clines: latitudinal effects associated with changing seasonality
Chown, S. L., & Klok, C. J. (2003) · Ecography · doi:10.1034/j.1600-0587.2003.03479.x · Cited by 188
Callier, V., & Nijhout, H. F. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1106556108 · Cited by 181
LATITUDINAL VARIATION IN LIFE-HISTORY TRAITS IN EURASIAN PERCH
Heibo, E., Magnhagen, C., & Vøllestad, L. A. (2005) · Ecology · doi:10.1890/04-1620 · Cited by 181
Audzijonyte, A., Barneche, D. R., Baudron, A. R., Belmaker, J., Clark, T. D., Marshall, C. T., Morrongiello, J. R., & van Rijn, I. (2019) · Global Ecology and Biogeography · doi:10.1111/geb.12847 · Cited by 180
Interactive Effects of Rearing Temperature and Oxygen on the Development of Drosophila melanogaster
Frazier, M. R., Woods, H. A., & Harrison, J. F. (2001) · Physiological and Biochemical Zoology · doi:10.1086/322172 · Cited by 177
Growth and Development Rates Have Different Thermal Responses
Forster, J., Hirst, A. G., & Woodward, G. (2011) · The American Naturalist · doi:10.1086/662174 · Cited by 176
Self-citationBody Size: The Structure and Function of Aquatic Ecosystems
(2007) · Cambridge University Press eBooks · doi:10.1017/cbo9780511611223 · Cited by 172
Life-history evolution under a production constraint
Brown, J. H., & Sibly, R. M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0608522103 · Cited by 171
The temperature‐size rule emerges from ontogenetic differences between growth and development rates
Forster, J., & Hirst, A. G. (2012) · Functional Ecology · doi:10.1111/j.1365-2435.2011.01958.x · Cited by 169
Self-citationThe Dynamic Nature of Eukaryotic Genomes
Parfrey, L. W., Lahr, D. J. G., & Katz, L. A. (2008) · Molecular Biology and Evolution · doi:10.1093/molbev/msn032 · Cited by 165
Studien über physiologische Ähnlichkeit VI. Wachstumsähnlichkeiten
Pütter, A. (1920) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf01755094 · Cited by 165
Gasping Fish and Panting Squids: Oxygen, Temperature and the Growth of Water-Breathing Animals
Pauly, D. F. (2010) · Cited by 164
Tropical fishes: patterns and propensities
PAULY, D. (1998) · Journal of Fish Biology · doi:10.1006/jfbi.1998.0810 · Cited by 164
New insights into the plasticity of gill structure
Nilsson, G. E., Dymowska, A., & Stecyk, J. A. W. (2012) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2012.07.012 · Cited by 161
Lefevre, S., McKenzie, D. J., & Nilsson, G. E. (2017) · Global Change Biology · doi:10.1111/gcb.13652 · Cited by 160
Adaptive sex-specific life history plasticity to temperature and photoperiod in a damselfly
Block, M. D., & Stoks, R. (2003) · Journal of Evolutionary Biology · doi:10.1046/j.1420-9101.2003.00581.x · Cited by 157
Environmental drivers of voltinism and body size in insect assemblages across Europe
Zeuss, D., Brunzel, S., & Brandl, R. (2016) · Global Ecology and Biogeography · doi:10.1111/geb.12525 · Cited by 156
Egg-Mass Size and Cell Size: Effects of Temperature on Oxygen Distribution
Woods, H. A. (1999) · American Zoologist · doi:10.1093/icb/39.2.244 · Cited by 151
Greenlee, K. J., & Harrison, J. F. (2003) · Journal of Experimental Biology · doi:10.1242/jeb.00767 · Cited by 140
Leiva, F. P., Calosi, P., & Verberk, W. C. E. P. (2019) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2019.0035 · Cited by 140
Self-citationDiamond, S. E., & Kingsolver, J. G. (2009) · The American Naturalist · doi:10.1086/648602 · Cited by 137
Respiratory control in aquatic insects dictates their vulnerability to global warming
Verberk, W. C. E. P., & Bilton, D. T. (2013) · Biology Letters · doi:10.1098/rsbl.2013.0473 · Cited by 136
Self-citationHarrison, J. F., Greenlee, K. J., & Verberk, W. C. E. P. (2017) · Annual Review of Entomology · doi:10.1146/annurev-ento-020117-043145 · Cited by 130
Self-citationDeBLOCK, M., & Stoks, R. (2008) · Ecological Entomology · doi:10.1111/j.1365-2311.2008.01024.x · Cited by 129
Temperature-size rule is mediated by thermal plasticity of critical size inDrosophila melanogaster
Ghosh, S. M., Testa, N. D., & Shingleton, A. W. (2013) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2013.0174 · Cited by 129
Genome size diversity in the family Drosophilidae
Gregory, T. R., & Johnston, J. S. (2008) · Heredity · doi:10.1038/hdy.2008.49 · Cited by 127
Verberk, W. C. E. P., & Atkinson, D. (2013) · Functional Ecology · doi:10.1111/1365-2435.12152 · Cited by 126
Self-citationThermal performance of fish is explained by an interplay between physiology, behaviour and ecology
Neubauer, P., & Andersen, K. H. (2019) · Conservation Physiology · doi:10.1093/conphys/coz025 · Cited by 126
Robb, T., & Abrahams, M. V. (2003) · Journal of Fish Biology · doi:10.1046/j.1095-8649.2003.00097.x · Cited by 125
Fishing and temperature effects on the size structure of exploited fish stocks
Tu, C., Chen, K., & Hsieh, C. (2018) · Scientific Reports · doi:10.1038/s41598-018-25403-x · Cited by 119
Large but uneven reduction in fish size across species in relation to changing sea temperatures
van Rijn, I., Buba, Y., DeLong, J. P., Kiflawi, M., & Belmaker, J. (2017) · Global Change Biology · doi:10.1111/gcb.13688 · Cited by 117
Temperature‐size relations from the cellular‐genomic perspective
Hessen, D. O., Daufresne, M., & Leinaas, H. P. (2012) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12006 · Cited by 116
Amphipod crustacean size spectra: new insights in the relationship between size and oxygen
Chapelle, G., & Peck, L. S. (2004) · Oikos · doi:10.1111/j.0030-1299.2004.12934.x · Cited by 112
Hirst, A. G., Glazier, D. S., & Atkinson, D. (2014) · Ecology Letters · doi:10.1111/ele.12334 · Cited by 112
Self-citationKammenga, J. E., Doroszuk, A., Riksen, J. A. G., Hazendonk, E., Spiridon, L. N., Petrescu, A., Tijsterman, M., Plasterk, R. H. A., & Bakker, J. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030034 · Cited by 107
Kooijman, S. A. L. M., & Troost, T. A. (2007) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/j.1469-185x.2006.00006.x · Cited by 104
Seibel, B. A., & Deutsch, C. A. (2020) · Journal of Experimental Biology · doi:10.1242/jeb.210492 · Cited by 103
Klok, C. J., & Harrison, J. F. (2013) · Integrative and Comparative Biology · doi:10.1093/icb/ict075 · Cited by 102
Alfsnes, K., Leinaas, H. P., & Hessen, D. O. (2017) · Ecology and Evolution · doi:10.1002/ece3.3163 · Cited by 99
Is the temperature-size rule mediated by oxygen in aquatic ectotherms?
Hoefnagel, K. N., & Verberk, W. C. E. P. (2014) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2014.12.003 · Cited by 98
Self-citationThe Cold-Water Connection: Bergmann’s Rule in North American Freshwater Fishes
Rypel, A. L. (2013) · The American Naturalist · doi:10.1086/674094 · Cited by 97
Cooler butterflies lay larger eggs: developmental plasticity versus acclimation
Fischer, K., Eenhoorn, E., Bot, A. N. M., Brakefield, P. M., & Zwaan, B. J. (2003) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2003.2470 · Cited by 92
Greenberg, S., & Ar, A. (1996) · Journal of Insect Physiology · doi:10.1016/s0022-1910(96)00071-6 · Cited by 91
Fischer, K., & Fiedler, K. (2002) · Evolutionary Ecology · doi:10.1023/a:1020271600025 · Cited by 88
Latitudinal shifts in body size of Enallagma cyathigerum (Odonata)
Johansson, F. (2003) · Journal of Biogeography · doi:10.1046/j.1365-2699.2003.00796.x · Cited by 88
Why might they be giants? Towards an understanding of polar gigantism
Moran, A. L., & Woods, H. A. (2012) · Journal of Experimental Biology · doi:10.1242/jeb.067066 · Cited by 88
Henry, J. R., & Harrison, J. F. (2004) · Journal of Experimental Biology · doi:10.1242/jeb.01189 · Cited by 88
Calboli, F. C. F., Gilchrist, G. W., & Partridge, L. (2003) · Evolution · doi:10.1111/j.0014-3820.2003.tb01548.x · Cited by 88
A global synthesis of seasonal temperature–size responses in copepods
Horne, C. R., Hirst, A. G., Atkinson, D., Neves, A., & Kiørboe, T. (2016) · Global Ecology and Biogeography · doi:10.1111/geb.12460 · Cited by 88
Self-citationA guided tour of large genome size in animals: what we know and where we are heading
Dufresne, F., & Jeffery, N. W. (2011) · Chromosome Research · doi:10.1007/s10577-011-9248-x · Cited by 86
Czarnołęski, M., Kozłowski, J., Dumiot, G., Bonnet, J., Mallard, J., & Dupont‐Nivet, M. (2008) · Journal of Experimental Biology · doi:10.1242/jeb.013169 · Cited by 83
Perrin, N. (1988) · Functional Ecology · doi:10.2307/2389399 · Cited by 83
Grasshopper ontogeny in relation to time constraints: adaptive divergence and stasis
Berner, D., & Blanckenhorn, W. U. (2005) · Journal of Animal Ecology · doi:10.1111/j.1365-2656.2005.01028.x · Cited by 83
Individual state controls temperature dependence in a butterfly ( Lasiommata maera )
Gotthard, K., Nylin, S., & Wiklund, C. (2000) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2000.1042 · Cited by 82
Miller, G. A., Clissold, F. J., Mayntz, D., & Simpson, S. J. (2009) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2009.1030 · Cited by 81
Horne, C. R., Hirst, A. G., & Atkinson, D. (2017) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2017.0238 · Cited by 80
Self-citationNew spicular skeletons in Turbellaria, and the occurrence of spicules in marine meiofauna1
Rieger, R. M., & Sterrer, W. E. (2009) · Journal of Zoological Systematics & Evolutionary Research · doi:10.1111/j.1439-0469.1975.tb00509.x · Cited by 79
Latitudinal insect body size clines revisited: a critical evaluation of the saw-tooth model
Kivelä, S. M., Välimäki, P., Carrasco, D., Mäenpää, M. I., & Oksanen, J. (2011) · Journal of Animal Ecology · doi:10.1111/j.1365-2656.2011.01864.x · Cited by 77
Shape shifting predicts ontogenetic changes in metabolic scaling in diverse aquatic invertebrates
Glazier, D. S., Hirst, A. G., & Atkinson, D. (2015) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2014.2302 · Cited by 76
Self-citationThe relationship between genome size, development rate, and body size in copepods
Wyngaard, G. A., Rasch, E. M., Manning, N. M., Gasser, K., & Domangue, R. J. (2005) · Hydrobiologia · doi:10.1007/s10750-004-9521-5 · Cited by 75
Temperature‐associated upper limits to body size in terrestrial poikilotherms
Makarieva, A. M., Gorshkov, V. G., & Li, B. (2005) · Oikos · doi:10.1111/j.1600-0706.2005.14095.x · Cited by 74
Trexler, J. C., Travis, J., & Trexler, M. (1990) · Evolution · doi:10.1111/j.1558-5646.1990.tb04286.x · Cited by 71
Flies developed small bodies and small cells in warm and in thermally fluctuating environments.
Czarnołęski, M., Cooper, B. S., Kierat, J., & Angilletta, M. J. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.083535 · Cited by 69
Ecological emergence of thermal clines in body size
Édeline, É., Lacroix, G., Delire, C., Poulet, N., & Legendre, S. (2013) · Global Change Biology · doi:10.1111/gcb.12299 · Cited by 68
Experimental demonstration of a ‘rate–size’ trade-off governing body size optimization
DeLong, J. P. (2012) · Evolutionary ecology research · Cited by 67
Horne, C. R., Hirst, A. G., & Atkinson, D. (2017) · Functional Ecology · doi:10.1111/1365-2435.13031 · Cited by 67
Self-citationCallier, V., Shingleton, A. W., Brent, C. S., Ghosh, S. M., Kim, J. K., & Harrison, J. F. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.093120 · Cited by 66
Ellis, L. L., Huang, W., Quinn, A. M., Ahuja, A., Alfrejd, B., Gomez, F. E., Hjelmen, C. E., Moore, K. L., Mackay, T. F. C., Johnston, J. S., et al. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004522 · Cited by 65
Parsons, S., & Joern, A. (2013) · Oecologia · doi:10.1007/s00442-013-2785-6 · Cited by 64
Buckley, L. B., Nufio, C. R., Kirk, E. M., & Kingsolver, J. G. (2015) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2015.0441 · Cited by 59
Walczyńska, A., Łabęcka, A. M., Sobczyk, M., Czarnołęski, M., & Kozłowski, J. (2014) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2014.11.002 · Cited by 59
Evaluation of alternative hypotheses to explain temperature-induced life history shifts in Daphnia
Weetman, D. (2004) · Journal of Plankton Research · doi:10.1093/plankt/fbh013 · Cited by 59
Why adult mayflies ofCloeon dipterum(Ephemeroptera:Baetidae) become smaller as temperature warms
Sweeney, B. W., Funk, D. H., Camp, A. A., Buchwalter, D. B., & Jackson, J. K. (2018) · Freshwater Science · doi:10.1086/696611 · Cited by 57
Copepod development rates in relation to genome size and 18S rDNA copy number
White, M. M., & McLaren, I. A. (2000) · Genome · doi:10.1139/g00-048 · Cited by 54
Weber, M. J., Brown, M. L., Wahl, D. H., & Shoup, D. E. (2015) · Ecosphere · doi:10.1890/es14-00435.1 · Cited by 51
Woods, H. A. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.089698 · Cited by 51
Levy, R. C., Kozak, G. M., Wadsworth, C. B., Coates, B. S., & Dopman, E. B. (2014) · Journal of Evolutionary Biology · doi:10.1111/jeb.12562 · Cited by 50
Patterns of genome size in the copepoda
Wyngaard, G. A., & Rasch, E. M. (2000) · Hydrobiologia · doi:10.1023/a:1003855322358 · Cited by 49
Aguilar‐Alberola, J. A., & Mesquita‐Joanes, F. (2014) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2014.02.016 · Cited by 49
Local adaptation reduces the metabolic cost of environmental warming
Moffett, E. R., Fryxell, D. C., Palkovacs, E. P., Kinnison, M. T., & Simon, K. S. (2018) · Ecology · doi:10.1002/ecy.2463 · Cited by 49
Rollinson, N., & Rowe, L. (2018) · Evolution · doi:10.1111/evo.13458 · Cited by 48
Body temperature, rate of biosynthesis, and evolution of genome size.
Xia, X. (1995) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a040260 · Cited by 47
Food Availability Alters the Effects of Larval Temperature on Aedes aegypti Growth
Padmanabha, H., Bolker, B. M., Lord, C. C., Rubio, C., & Lounibos, L. P. (2011) · Journal of Medical Entomology · doi:10.1603/me11020 · Cited by 46
Dufresne, F., & Hebert, P. D. N. (1998) · Ecoscience · doi:10.1080/11956860.1998.11682481 · Cited by 45
Predictions of seasonal natural mortality rates in a copepod population using life-history theory
Myers, R., & Runge, J. (1983) · Marine Ecology Progress Series · doi:10.3354/meps011189 · Cited by 44
Scharf, I., Galkin, N., & Halle, S. (2015) · Evolutionary Biology · doi:10.1007/s11692-014-9298-z · Cited by 43
Dispersal potential impacts size clines of grasshoppers across an elevation gradient
Levy, R. A., & Nufio, C. R. (2014) · Oikos · doi:10.1111/oik.01615 · Cited by 41
Hoefnagel, K. N., de Vries, E. H. J., Jongejans, E., & Verberk, W. C. E. P. (2018) · Ecology and Evolution · doi:10.1002/ece3.3933 · Cited by 41
Self-citation‘Optimal thermal range’ in ectotherms: Defining criteria for tests of the temperature-size-rule
Walczyńska, A., Kiełbasa, A., & Sobczyk, M. (2016) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2016.06.006 · Cited by 40
Critical PO2 is size-independent in insects: implications for the metabolic theory of ecology
Harrison, J. F., Klok, C. J., & Waters, J. S. (2014) · Current Opinion in Insect Science · doi:10.1016/j.cois.2014.08.012 · Cited by 39
Similar nucleus numbers among copepods
McLaren, I. A., & Marcogliese, D. J. (1983) · Canadian Journal of Zoology · doi:10.1139/z83-095 · Cited by 37
Hemmer‐Brepson, C., Replumaz, L., Romestaing, C., Voituron, Y., & Daufresne, M. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.096172 · Cited by 37
Fryxell, D. C., Hoover, A. N., Alvarez, D. A., Arnesen, F. J., Benavente, J. N., Moffett, E. R., Kinnison, M. T., Simon, K. S., & Palkovacs, E. P. (2020) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2020.0608 · Cited by 35
Loisel, A., Isla, A., & Daufresne, M. (2019) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2019.07.029 · Cited by 34
van de Pol, I. L. E., Flik, G., & Verberk, W. C. E. P. (2020) · PLoS ONE · doi:10.1371/journal.pone.0229468 · Cited by 34
Self-citationBruijning, M., ten Berge, A. C. M., & Jongejans, E. (2018) · Functional Ecology · doi:10.1111/1365-2435.13192 · Cited by 33
Seasonal time constraints do not explain exceptions to the temperature size rule in ectotherms
Cabanita, R., & Atkinson, D. (2006) · Oikos · doi:10.1111/j.2006.0030-1299.14708.x · Cited by 32
Self-citationSlow development as an evolutionary cost of long life
Lind, M. I., Chen, H., Meurling, S., Gil, A. C. G., Carlsson, H., Zwoinska, M. K., Andersson, J., Larva, T., & Maklakov, A. A. (2017) · Functional Ecology · doi:10.1111/1365-2435.12840 · Cited by 31
Multiple effects of temperature, photoperiod and food quality on the performance of a pine sawfly
Kollberg, I., Bylund, H., Schmidt, A., Gershenzon, J., & Björkman, C. (2013) · Ecological Entomology · doi:10.1111/een.12005 · Cited by 29
Dormancy cues alter insect temperature–size relationships
Clemmensen, S. F., & Hahn, D. A. (2014) · Oecologia · doi:10.1007/s00442-014-3094-4 · Cited by 29
Low Temperature and Polyploidy Result in Larger Cell and Body Size in an Ectothermic Vertebrate
Hermaniuk, A., Rybacki, M., & Taylor, J. R. E. (2016) · Physiological and Biochemical Zoology · doi:10.1086/684974 · Cited by 29
Horne, C. R., Hirst, A. G., Atkinson, D., Almeda, R., & Kiørboe, T. (2019) · Oikos · doi:10.1111/oik.06016 · Cited by 28
Self-citationDittrich, C., Drakulić, S., Schellenberg, M., Thein, J., & Rödel, M. (2016) · Canadian Journal of Zoology · doi:10.1139/cjz-2015-0168 · Cited by 27
Jeffery, N. W., Yampolsky, L. Y., & Gregory, T. R. (2016) · Genome · doi:10.1139/gen-2016-0128 · Cited by 25
Arendt, J. (2014) · Journal of Evolutionary Biology · doi:10.1111/jeb.12554 · Cited by 24
Body size response to warming: time of the season matters in a tephritid fly
Xi, X., Wu, X., Nylin, S., & Sun, S. (2015) · Oikos · doi:10.1111/oik.02521 · Cited by 24
Hypoxia induces calpain activity and degrades SMAD2 to attenuate TGFβ signaling in macrophages
Cui, W., Zhou, J., Dehne, N., & Brüne, B. (2015) · Cell & Bioscience · doi:10.1186/s13578-015-0026-x · Cited by 20
Ejsmond, M. J., McNamara, J. M., Søreide, J. E., et al. (2018) · Functional Ecology · doi:10.1111/1365-2435.13191 · Cited by 19
van der Have, T. M. (2008) · doi:10.18174/121943 · Cited by 17
Implications of hypoxia tolerance for wetland refugia use in Lake Nabugabo, Uganda
Reid, A. J., Farrell, M. J., Luke, M. N., & Chapman, L. J. (2013) · Ecology Of Freshwater Fish · doi:10.1111/eff.12036 · Cited by 14
Banas, N. S., & Campbell, R. (2016) · Marine Ecology Progress Series · doi:10.3354/meps11873 · Cited by 14
Reconsidering the Oxygen–Temperature Hypothesis of Polar Gigantism: Successes, Failures, and Nuance
Woods, H. A., & Moran, A. L. (2020) · Integrative and Comparative Biology · doi:10.1093/icb/icaa088 · Cited by 14
Kivelä, S. M., Viinamäki, S., Keret, N., Gotthard, K., Hohtola, E., & Välimäki, P. (2017) · Journal of Experimental Biology · doi:10.1242/jeb.166157 · Cited by 7
Antoł, A., Labecka, A. M., Horváthová, T., Zieliński, B., Szabla, N., Vasko, Y., Pecio, A., Kozłowski, J., & Czarnoleski, M. (2020) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2020.102600 · Cited by 7
Cited by
‘Aerobic scope protection’ reduces ectotherm growth under warming
Jutfelt, F., Norin, T., Åsheim, E. R., Rowsey, L. E., Andreassen, A. H., Morgan, R., Clark, T. D., & Speers‐Roesch, B. (2021) · Functional Ecology · doi:10.1111/1365-2435.13811 · Cited by 115
Sinai, N., Glos, J., Mohan, A. V., Lyra, M. L., Riepe, M., Thöle, E., Zummach, C., & Ruthsatz, K. (2022) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2022.103233 · Cited by 45
Metadata
- Authors
- Verberk, W. C. E. P., Atkinson, D., Hoefnagel, K. N., Hirst, A. G., Horne, C. R., & Siepel, H.
- Venue
- Biological Reviews
- Publisher
- Wiley
- Published
- 2020-09-22
- Volume
- 96
- Issue
- 1
- Pages
- 247-268
- ISSN
- 0006-3231 (ISSN-L)
- 1464-7931
- 1469-185X
- OpenAlex
- W3087646956
- Cited by
- 363
- References
- 170
- FWCI
- 3.16
- Type
- journal article
- Language
- en
- Open access
- hybrid
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.