Foot pressure distribution in white rhinoceroses (Ceratotherium simum) during walking

Monash Biomedicine Discovery Institute, Department of Anatomy and Developmental Biology, Moving Morphology & Functional Mechanics Laboratory, Monash University, Clayton, Victoria, Australia
Department of Human Health Sciences, Kyoto University, Kyoto, Japan
Department of Comparative Biomedical Sciences, Structure and Motion Laboratory, Royal Veterinary College, Hatfield, United Kingdom
DOI
10.7287/peerj.preprints.27365v1
Subject Areas
Animal Behavior, Zoology
Keywords
Perissodactyla, biomechanics, osteopathology, gait, mechanobiology, locomotion
Copyright
© 2018 Panagiotopoulou et al.
Licence
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ Preprints) and either DOI or URL of the article must be cited.
Cite this article
Panagiotopoulou O, Pataky TC, Hutchinson JR. 2018. Foot pressure distribution in white rhinoceroses (Ceratotherium simum) during walking. PeerJ Preprints 6:e27365v1

Abstract

White rhinoceroses (Ceratotherium simum) are odd-toed ungulates that belong to the group Perissodactyla and are second only to elephants in terms of large body mass amongst extant tetrapods, making them fascinating studies for how large land animals support and move themselves. Rhinoceroses often are kept in captivity for protection from ivory poachers and for educational/touristic purposes, yet a detrimental side effect of captivity can be foot disease (i.e. enthesopathies and osteoarthritis around the phalanges). Foot diseases in large mammals are multifactorial, but locomotor biomechanics (e.g. pressures routinely experienced by the feet) surely can be a contributing factor. However, due to a lack of in vivo experimental data on rhinoceros foot pressures, our knowledge of locomotor performance and its links to foot disease is limited. The overall aim of this study was to characterize peak pressures and centre of pressure trajectories in white rhinoceroses during walking. We asked two major questions. First, are peak locomotor pressures the lowest around the fat pad and its lobes (as in the case of elephants)? Second, are peak locomotor pressures concentrated around the areas with the highest reported incidence of pathologies? Our results show a reduction of pressures around the fat pad and its lobes, which is potentially due to the material properties of the fat pad or the fact that our rhinoceros subjects avoided “heel” contact at impact. We also found an even and gradual concentration of foot pressures across all digits, which may be a by-product of the more horizontal foot roll-off during the stance phase. While our exploratory, descriptive sample precluded hypothesis testing, our study provides important new data on rhinoceros locomotion for future studies to build on, and thus impetus for improved implementation in the care of captive/managed rhinoceroses.

Author Comment

This is a submission to PeerJ for review.

Supplemental Information

Regional peak pressure data for all subjects and feet

Columns A-J show respectively the file name (A), subject ID (B), foot ID (C: left forefoot = 1; right forefoot = 2; left hindfoot = 3; right hindfoot = 4); ROI (D; also see Figure 1); peak pressure data in N cm-2 (E); walking speed in m s-1 (F); Shoulder height in metres (G); Froude number (H); Age (I; Adult=1; juvenile=2); Body mass estimate in kg (J; 1 = 2500; 2 = 1000). Some trials were excluded from further analyses due to being temporally incomplete. These are: [FORE LEFT: subject 1, trial 028_img001], [FORE RIGHT: subject 3, trial 033_img004; subject 3, trial 035_img003], HIND LEFT: subject 3, trial 010_img003], [HIND RIGHT: subject 3, trial 041_img006; subject 1, trial 001_img002; subject 1, trial 013_img005].

DOI: 10.7287/peerj.preprints.27365v1/supp-1

Image time series of the COP trajectories (light grey) for the left forefoot of subject 1 (010_img002 [A] and 027_img002 [B])

DOI: 10.7287/peerj.preprints.27365v1/supp-2

Image time series of the COP trajectories (light grey) for the left forefoot of subject 2 (trials 018_img005 [A], 021_img005 [B] and 031_img002 [C])

DOI: 10.7287/peerj.preprints.27365v1/supp-3

Image time series of the COP trajectories (light grey) for the right forefoot of subject 1 (trials 27_10_035_img002 [A] and 27_10_img002 [B])

DOI: 10.7287/peerj.preprints.27365v1/supp-4

Image time series of the COP trajectories (light grey) for the right forefoot of subject 2 (trials 004_img007 [A], 009_img006 [B], 011_img004 [C] and 033_img003 [D])

DOI: 10.7287/peerj.preprints.27365v1/supp-5

Image time series of the COP trajectories (light grey) for the left hindfoot of subject 1 (trials 27_10_038_img005 [A] and 014_img002 [B])

DOI: 10.7287/peerj.preprints.27365v1/supp-6

Image time series of the COP trajectories (light grey) for the left hindfoot of subject 2 (trial 026_img004)

DOI: 10.7287/peerj.preprints.27365v1/supp-7

Image time series of the COP trajectories (light grey) for the left hindfoot of subject 3 (trial 034_img003)

DOI: 10.7287/peerj.preprints.27365v1/supp-8

Image time series of the COP trajectories (light grey) for the right hindfoot of subject 1 (trials 27_10_037_img003 [A] and 032_img003 [B]) and subject 2 (trial 27_10_019_img001 [C])

DOI: 10.7287/peerj.preprints.27365v1/supp-9