First published online November 17, 2005
Journal of Experimental Biology 208, 4529-4547 (2005)
Published by The Company of Biologists 2005
doi: 10.1242/jeb.01903
Muscle fiber-type variation in lizards (Squamata) and phylogenetic reconstruction of hypothesized ancestral states
Kevin E. Bonine1,*,
Todd T. Gleeson2 and
Theodore Garland, Jr3
1 Department of Ecology and Evolutionary Biology, University of Arizona,
P.O. Box 210088 Tucson, AZ 85721, USA,
2 Department of Integrative Physiology, University of Colorado, Boulder, CO
80309, USA
3 Department of Biology, University of California Riverside, CA 92521,
USA

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Fig. 1. Hypothesized phylogenetic relationships for 24 species of lizard examined
in this study. See phylogeny section in the Materials and methods for
explanation. Branch lengths are arbitrary (as suggested by
Pagel, 1992 ).
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Fig. 2. Bivariate scatterplots of body and limb linear dimensions in relation to
body mass for 24 species of lizard (see
Fig. 1 for species codes),
using mean values reported in Table
1.
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Fig. 3. Proportion of fast-glycolytic fibers in the iliofibularis muscle
(Table 2) in relation to
hypothesized phylogenetic relationships among 24 lizard species (see
Fig. 1 for species codes).
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Fig. 4. Bivariate scatterplots of fiber-type proportion of the iliofibularis and
cross-sectional area of individual fibers in relation to body mass for 24
species of lizard (see Fig. 1
for species codes), using mean values reported in Tables
2 and
3.
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Fig. 5. Bivariate scatterplots of thigh and iliofibularis muscle properties in
relation to body mass (see Fig.
1 for species codes) for 23 species of lizard
(Dipsosaurus data not available for these variables), using mean
values from Tables 1 and
2.
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Fig. 6. (A) Proportion of fast twitch-glycolytic (FG) and fast twitch-oxidative
glycolytic (FOG) muscle fiber types in the iliofibularis in 24 species of
lizard (see Fig. 1 for species
codes). Across all 24 species, the correlation is r=0.940
(2-tailed, P<0.001). (B) Phylogenetically independent contrasts of
data presented in A, using topology and branch lengths shown in
Fig. 1 (number of independent
contrasts is always one less than the number of species). Correlation
(computed through origin)=0.886 (P<0.001). Deleting the
sand versus horned contrast reduces the magnitude of the correlation
to 0.794 (P<0.001).
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Fig. 7. Arbitrary branch lengths used for initial estimates of ancestral values (A;
following Pagel., 1992 ) and
after alteration based on standard errors for the proportional area of fast
twitch-oxidative glycolytic (FOG) fibers (B) or the proportional area of fast
twitch-glycolytic (FG) fibers in the iliofibularis (C). Topology is the same
as in Fig. 1. Refer to text and
Table 5 for numerical values of
reconstructed ancestral nodes and demonstration of how inclusion of standard
errors alters both node estimates and confidence intervals.
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Fig. 8. (A) Graphical depiction of reconstructed nodal values of fast-twitch
glycolytic (FG) fiber proportion during the evolution of the 24 lizard species
included in this study (see Fig.
1 for topology and branch lengths used). Confidence intervals
(95%) were calculated for selected nodes; root of all 24 species, origin of
Phrynosomatidae, and origin of Sceloporus group within
Phrynosomatidae. (B) Same as A, but for fast-twitch oxidative-glycolytic (FOG)
fiber proportion. The reconstructed ancestral nodes and confidence intervals
in each panel incorporate the standard errors for proportion measurements (see
Fig. 7; refer to text and
Table 5 for numerical
values).
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© The Company of Biologists Ltd 2005