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Unlocking the secrets of kangaroo locomotor energetics: Postural adaptations underpin increased tendon stress in hopping kangaroos

Lauren H. Thornton, Taylor J.M. Dick, John R. Hutchinson, Glen A. Lichtwark, Craig P. McGowan, Jonas Rubenson, Alexis Wiktorowicz-Conroy, Christofer J. Clemente

Preprint posted on 8 February 2024 https://www.biorxiv.org/content/10.1101/2024.02.05.578950v1

Should we all be hopping like a kangaroo? @LivEvoBiomech , @SamRRCross and @james_charles90 review this exciting preprint: Unlocking the secrets of kangaroo locomotor energetics.

Selected by EMB EMB_Liv, James Charles, Roger Kissane

Categories: physiology, zoology

PreLight Authors

Samuel Cross, James Charles, Roger Kissane

Introduction

Terrestrial mammals generally experience higher metabolic rates the faster they run (1). Large to moderately sized macropods (kangaroos, wallabies) are known to decouple this relationship between locomotor speed and cost, as they are uniquely capable of hopping at greater speeds without incurring significantly higher energy expenditure (2; Figure 1). This ability is related to their capacity to generate greater stress in the Achilles tendon with speed, which in turn allows for improved storage of elastic strain energy and a greater contribution of tendinous recoil to total work performed at the ankle as they hop faster (3). However, while this phenomenon is well documented, its underlying mechanistic causes remain unclear.

Thornton et al., hypothesize that postural modulation (i.e. changing posture with speed) may provide a mechanism by which tendon stress can be increased. Unlike most mammals of comparable size, large macropods move with highly flexed lower limb postures where the ankle operates at a relatively low mechanical advantage (EMA) (Figure 2). A low MA should increase the stress on the tendon, allowing for greater storage of elastic strain energy. Therefore, they theorise that proportional reductions to MA with increasing speed may allow for increased tendon stress and elastic storage, which would facilitate the decoupling of energetic expenditure and movement velocity.

In this study, the authors generate 3D musculoskeletal models of kangaroos (Figure 2) and integrate 3D kinematics and force plate data from freely hopping kangaroos. These musculoskeletal models allow for quantitative analysis of kangaroo posture (Figure 2a) and EMA (Figure 2b) which are evaluated across differing speeds.

Figure 1: Energetic expenditure versus speed in terrestrial mammals. Most mammals (blue) show an increase in energy consumption with increasing speed, whereas the relationship is flat in macropods (red). Data is hypothetical/illustrative. (A) running mammals, from (1); (B) Red kangaroos, from (2).

 

Figure 2: Illustration of the kangaroo model (a) and the calculation of effective mechanical advantage (EMA) (b).

Key Findings

Kangaroo posture changes with speed

Thornton et al., showed that kangaroos change posture with increasing speed and body mass. However, while all limb joints became increasingly flexed with greater mass, increasing speed was associated only with localised flexion of the distal joints. This change in posture was found to decrease the leverage of the calves, causing MA to decrease with speed. Meanwhile, the forces within the ankle (the joint moment) increased with speed. These factors in combination led to relatively higher Achilles tendon stresses as kangaroos hopped faster.

Postural change increases elastic savings

Evaluation of work, or force generated over a certain distance, performed at the ankle found that while positive work (i.e. force produced during muscle contractions), increases with speed (similar to all other animals), kangaroos are also able to increase the negative work (i.e. force produced during muscle lengthening) performed. Typically, positive work is produced at the ankle during the push-off part of stance where the joints extend via muscle contractions, while the while negative work is generated at the start of stance, corresponding to the period where elastic energy is stored in the Achilles tendon as it lengthens. This increase in negative work with speed is an artefact of changing ankle posture, and allows for increased storage of elastic strain energy, which can be returned during the positive work phase replacing active (and metabolically costlier) muscle contractions. Because positive and negative work increased at equal rates with speed, the net work done about the ankle remained fairly constant irrespective of increasing speed. Thus, the authors conclude that postural modulation allows macropods to decouple locomotor cost and speed by improving elastic storage and utilisation (Figure 3).

Evolutionary implications for hopping

When compared to other mammals, the mechanical advantages used by kangaroos are disproportionately low for their body size. This means that even fairly marginal changes in mechanical advantage can lead to substantial increases in tendon stress and elastic storage. It illustrates a mechanistic difference between macropods and quadrupedal mammals, in which equivalent postural changes would incur only minimal increases in stress. However, such high tendon stresses present scaling challenges for macropods, as hopping at high speeds at large body sizes may dangerously approach or exceed the safety limit of the Achilles tendon. This suggests that the largest fossil kangaroos may have been incapable of gaits characteristic of their smaller-bodied contemporaries.

Our Opinions

This article attempts to address a longstanding (and in our opinion, very interesting) question in evolutionary biomechanics/physiology. The ability of large macropods to defy what is otherwise a fairly universal relationship between speed and cost in running mammals has been discussed at length in the technical literature, but (to our knowledge) no succinct theory regarding underlying mechanical causes has thus far been demonstrated. We therefore appreciate the integrative approach taken by the authors, combining experimental data with musculoskeletal modelling, as well as incorporating a large body of analyses. In addition, there has also been a great deal of discussion about the energetic penalties of flexed postures in terrestrial vertebrates (a topic several of us are keenly interested in), so it was enjoyable to read about a reversal to this rule.

 

Figure 3: Summary figure from Thornton et al., illustrating how changes to posture and mechanical advantage can increase tendon stresses and elastic energy storage.

Questions for authors

  1. Throughout the study, the authors have used a mixture of macropodid taxa, and we wondered whether this may carry any further implications? For example, are there phylogenetic distinctions between red and grey kangaroos in any of the locomotor parameters reported here?
  2. How were the speeds allocated to the binning of Slow, Medium and Fast? Similarly with body mass, how were individuals classed as Small, Medium and Large?
  3. Are there any structural differences in the macropod Achilles tendon compared to other equally large mammals?
  4. Are there any further plans for the musculoskeletal models built for this study? Maybe some predictive simulations to further investigate the relationships between the Achilles tendon and locomotor cost, if muscle force-generating properties are available?

References

  1. Kram R. and Taylor, C. R. 1990. Energetics of running: a new perspective. Nature, 346, 265-267.
  2. Dawson, T. J. and Taylor, C. R. 1973. Energetic Cost of Locomotion in Kangaroos. Nature, 346, 313-314.
  3. Biewener, A. A., Konieczynski, D. D. and Baudinette, R. V. 1998. In Vivo Muscle Force–Length Behaviour During Steady-Speed Hopping in Tammar Wallabies. Journal of Experimental Biology, 201, 1681-1694.

 

Posted on: 25 March 2024

doi: https://doi.org/10.1242/prelights.36914

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Author's response

Lauren Thornton shared

Questions for authors

1) Throughout the study, the authors have used a mixture of macropodid taxa, and we wondered whether this may carry any further implications? For example, are there phylogenetic distinctions between red and grey kangaroos in any of the locomotor parameters reported here?

  • We did initially include species as a factor in the linear models, but it was not significant, so we removed it. Of the two reds we have, one is small and other is large.
  • I wrote a meta-analysis/review on the phylogenetic differences in bone, muscle and tendon physiology in macropods if you’re curious about the specific differences. (Thornton LH et al. (2021) Australian Journal of Zoology, 69(4), 136–157. doi:10.1071/ZO21048)

2) How were the speeds allocated to the binning of Slow, Medium and Fast? Similarly with body mass, how were individuals classed as Small, Medium and Large?

  • We organised the 100 trials by speed and divided into three groups of 33-34 trials, and organised the 16 kangaroos by mass and divided into three groups of 5-6 individuals. The number of trials per individual varies.
  • The groups are just for display purposes. E.g. the analysis tested peak joint angle vs speed, rather than checked if there was a difference in peak ankle between the slow and fast group.

3) Are there any structural differences in the macropod Achilles tendon compared to other equally large mammals?

  • In terms of material properties, no one has found anything that makes kangaroo tendon stand out from other mammals.
  • Kangaroo tendons might be a little thinner and they tend to be much longer than quadrupeds, which contributes to elastic storage because it depends on the tendon volume.
  • A bigger difference between kangaroos and quadrupeds is their muscle size – kangaroo calves are enormous. As macropod species increase in size, the increase in their muscle cross-sectional area (scales with positive allometry) far outstrips the increase in tendon CSA (scales more or less isometrically), i.e. muscle area to tendon area ratio, which is an indicator of how much stress the muscle-tendon unit can support, increases with size.
  • See the review for more information.

4) Are there any further plans for the musculoskeletal models built for this study? Maybe some predictive simulations to further investigate the relationships between the Achilles tendon and locomotor cost, if muscle force-generating properties are available?

  • We are currently writing that exact paper. We developed the model with the end goal of predictive simulations – these were successful and provided us with muscle parameters and metabolic cost for a range of speeds.
  • We also have a student creating a wallaby model. Wallabies carrying joeys have higher tendon stress but no increase in metabolic cost compared to unburdened wallabies (Baudinette, R. V., and A. A. Biewener. 1998. Young wallabies get a free ride. Nature (London) 395:653-654). We will replicate this study with our wallaby model and investigate whether the mechanism of constant metabolic cost with increasing loading is similar to what we observed with increasing speed.

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