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. 2017 Jan 24;7(6):1663-1673.
doi: 10.1002/ece3.2695. eCollection 2017 Mar.

Conservative whole-organ scaling contrasts with highly labile suborgan scaling differences among compound eyes of closely related Formica ants

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Conservative whole-organ scaling contrasts with highly labile suborgan scaling differences among compound eyes of closely related Formica ants

Craig D Perl et al. Ecol Evol. .

Abstract

Static allometries determine how organ size scales in relation to body mass. The extent to which these allometric relationships are free to evolve, and how they differ among closely related species, has been debated extensively and remains unclear; changes in intercept appear common, but changes in slope are far rarer. Here, we compare the scaling relationships that govern the structure of compound eyes of four closely related ant species from the genus Formica. Comparison among these species revealed changes in intercept but not slope in the allometric scaling relationships governing eye area, facet number, and mean facet diameter. Moreover, the scaling between facet diameter and number was conserved across all four species. In contrast, facet diameters from distinct regions of the compound eye differed in both intercept and slope within a single species and when comparing homologous regions among species. Thus, even when species are conservative in the scaling of whole organs, they can differ substantially in regional scaling within organs. This, at least partly, explains how species can produce organs that adhere to genus wide scaling relationships while still being able to invest differentially in particular regions of organs to produce specific features that match their ecology.

Keywords: evolutionary allometry; facet; static allometry; wood ant.

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Figures

Figure 1
Figure 1
Phylogeny of Formica sp. Species used in this study are highlighted in black, whereas other species are in gray. Scale bar indicates nucleotide substitutions per site. Modified from Goropashnaya et al. (2012)
Figure 2
Figure 2
Scaling relationships in the four species of Formica as derived from linear mixed‐effect models. (a) Allometry of facet number per eye as a function of rear left femur length (a proxy of body size). (b) Allometry of mean facet diameter as a function of rear femur length. (c) Allometry of eye area as a function of rear femur length. (d) Scaling of mean facet diameter as a function of number of facets per eye among the four species of Formica. Colored lines are individual regressions for species, when significant differences exist among species. A single black regression line indicates no significant difference between species, which are analyzed with a common slope
Figure 3
Figure 3
Hierarchical cluster analysis of facet number, mean facet diameter, and species after dimension reduction using principle component analysis (PCA). Clusters are defined with different colors, while different species are represented with different shapes
Figure 4
Figure 4
Intra‐eye facet diameter scaling within species as derived from linear mixed‐effect models. Comparison of the scaling of mean facet diameters in different regions of the compound eyes from (a) Formica fusca; (b) Formica lugubris; (c) Formica sanguinea; (d) Formica rufa
Figure 5
Figure 5
Intra‐eye facet diameter scaling among species as derived from linear mixed‐effect models. Comparison of the scaling of mean facet diameters from homologous regions of the compound eyes of the four Formica species. Mean facet diameter scaling of (a) the anterior region; (b) the dorsal region; (c) the posterior region; (d) the ventral region. Colored lines are individual regressions for species, when significant differences exist among species. A single black regression line indicates no significant difference between species, which are analyzed with a common slope

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