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Open Access Highly Accessed Research article

Integration, heterochrony, and adaptation in pedal digits of syndactylous marsupials

Vera Weisbecker1* and Maria Nilsson2

Author Affiliations

1 School of Biological, Earth and Environmental Sciences, University of New South Wales, UNSW/Sydney, NSW 2052, Australia

2 Lund University, Department of Cell and Organism Biology, Genetics, Division of Evolutionary Molecular Systematics, Sölvegatan 29, S-223 62 Lund, Sweden

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BMC Evolutionary Biology 2008, 8:160  doi:10.1186/1471-2148-8-160

Published: 25 May 2008

Abstract

Background

Marsupial syndactyly is a curious morphology of the foot found in all species of diprotodontian and peramelemorph marsupials. It is traditionally defined as a condition in which digits II and III of the foot are bound by skin and are reduced. Past treatments of marsupial syndactyly have not considered the implications of this unique morphology for broader issues of digit development and evolution, and the ongoing debate regarding its phylogenetic meaning lacks a broad empirical basis. This study undertakes the first interdisciplinary characterisation of syndactyly, using variance/covariance matrix comparisons of morphometric measurements, locomotor indices, ossification sequences, and re-assessment of the largely anecdotal data on the phylogenetic distribution of tarsal/metatarsal articulations and "incipient syndactyly".

Results

Syndactylous digits have virtually identical variance/covariance matrices and display heterochronic ossification timing with respect to digits IV/V. However, this does not impact on overall locomotor adaptation patterns in the syndactylous foot as determined by analysis of locomotor predictor ratios. Reports of incipient syndactyly in some marsupial clades could not be confirmed; contrary to previous claims, syndactyly does not appear to impact on tarsal bone arrangement.

Conclusion

The results suggest that marsupial syndactyly originates from a constraint that is rooted in early digit ontogeny and results in evolution of the syndactylous digits as a highly integrated unit. Although convergent evolution appears likely, syndactyly in Diprotodontia and Peramelemorpha may occur through homologous developmental processes. We argue that the term "syndactyly" is a misnomer because the marsupial condition only superficially resembles its name-giving human soft-tissue syndactyly.