TY - JOUR
T1 - Shrinking body sizes in response to warming
T2 - explanations for the temperature–size rule with special emphasis on the role of oxygen
AU - Verberk, Wilco C.E.P.
AU - Atkinson, David
AU - Hoefnagel, K. Natan
AU - Hirst, Andrew G.
AU - Horne, Curtis R.
AU - Siepel, Henk
N1 - Funding Information:
We thank Asta Audzijonyte and Aleksandra Walczyńska for providing thoughtful and constructive feedback, which was very helpful in improving our manuscript. W.C.E.P.V. gratefully acknowledges support from the Netherlands Organization for Scientific Research (NWO‐VIDI Grant 016.161.321). D.A., A.G.H. and C.R.H. were supported by NERC grant NE/P012183/2.
Funding Information:
We thank Asta Audzijonyte and Aleksandra Walczy?ska for providing thoughtful and constructive feedback, which was very helpful in improving our manuscript. W.C.E.P.V. gratefully acknowledges support from the Netherlands Organization for Scientific Research (NWO-VIDI Grant 016.161.321). D.A., A.G.H. and C.R.H. were supported by NERC grant NE/P012183/2.
Publisher Copyright:
© 2020 The Authors. Biological Reviews published by John Wiley & Sons Ltd on behalf of Cambridge Philosophical Society.
PY - 2021/2
Y1 - 2021/2
N2 - 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).
AB - 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).
KW - Bergmann's rule
KW - cell size
KW - climate warming
KW - gigantism
KW - growth trajectory
KW - hypoxia
KW - life-history trade-off
KW - phenotypic plasticity
KW - temperature–size rule
KW - thermal reaction norms
UR - https://www.scopus.com/pages/publications/85091313743
U2 - 10.1111/brv.12653
DO - 10.1111/brv.12653
M3 - Article
AN - SCOPUS:85091313743
SN - 1464-7931
VL - 96
SP - 247
EP - 268
JO - Biological Reviews
JF - Biological Reviews
IS - 1
ER -