Energetic benefits and adaptations in mammalian limbs: Scale effects and selective pressures
Differences in limb size and shape are fundamental to mammalian morphological diversity; however, their relevance to locomotor costs has long been subject to debate. In particular, it remains unknown if scale effects in whole limb morphology could partially underlie decreasing mass-specific locomoto...
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Published in | Evolution Vol. 69; no. 6; pp. 1546 - 1559 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
United States
Blackwell Publishing Ltd
01.06.2015
Society for the Study of Evolution Oxford University Press |
Subjects | |
Online Access | Get full text |
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Summary: | Differences in limb size and shape are fundamental to mammalian morphological diversity; however, their relevance to locomotor costs has long been subject to debate. In particular, it remains unknown if scale effects in whole limb morphology could partially underlie decreasing mass-specific locomotor costs with increasing limb length. Whole fore- and hindlimb inertial properties reflecting limb size and shape—moment of inertia (MOI), mass, mass distribution, and natural frequency—were regressed against limb length for 44 species of quadrupedal mammals. Limb mass, MOI, and center of mass position are negatively allometric, having a strong potential for lowering mass-specific locomotor costs in large terrestrial mammals. Negative allometry of limb MOI results in a 40% reduction in MOI relative to isometry's prediction for our largest sampled taxa. However, fitting regression residuals to adaptive diversification models reveals that codiversification of limb mass, limb length, and body mass likely results from selection for differing locomotor modes of running, climbing, digging, and swimming. The observed allometric scaling does not result from selection for energetically beneficial whole limb morphology with increasing size. Instead, our data suggest that it is a consequence of differing morphological adaptations and body size distributions among quadrupedal mammals, highlighting the role of differing limb functions in mammalian evolution. |
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Bibliography: | istex:0233F38E0514F379274F849FFFE5F502F88896E2 ArticleID:EVO12675 ark:/67375/WNG-8WRW9WT4-9 Figure S1. Experimental setup to measure limb inertial properties. Tabel S1. Mammalian species sampled for our study. Tabel S2. Estimation of measurement error in our methodology to measure limb inertial properties. Tabel S3. Exponents predicted by geometric similarity for the inertial properties included in this study along with a short definition of each inertial property. Tabel S4. Phylogenies used to scale divergence times within the composite phylogeny. Tabel S5. Tests for phylogenetic signal when using GLS residuals. Tabel S6. Results of PGLS regressions estimating λ alongside other regression parameters. Tabel S7. Parameter estimates for single-rate Brownian motion and single-optimum Ornstein-Uhlenbeck models. Tabel S8. Parameter estimates for Brownian motion models based upon locomotor specializations. Tabel S9. Parameter estimates for Ornstein-Uhlenbeck models based upon locomotor specializations. Tabel S10. Parameter estimates for Brownian motion models based upon body size. Tabel S11. Parameter estimates for Ornstein-Uhlenbeck models based upon differences in body size. Tabel S12. Differences in the scaling of limb length, limb mass, and limb MOI between cursors (N = 25) and scansors (N = 7). SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0014-3820 1558-5646 1558-5646 |
DOI: | 10.1111/evo.12675 |