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By John Ya-Otto, Ole Gjerstad, Michael Mercer

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Bioi. Rev. 41:587-640. ]. 1975a. Allometry in Primates, with emphasis on scaling and the evolution of the brain. In: F. ) Approaches to Primate Paleobiology. pp. 244-292. Karger, Basel. Gould, S. J. 1975b. On the scaling of tooth size in mammals. Am. Zool. 15:351-362. Gould, S. J. 1989. A developmental constraint in Cerion, with comments on the definition and interpretation of constraint in evolution. Evolution 43:516-539. , and Lewontin, R. C. 1979. The Spandrels of San Marco and the Panglossion Paradigm: A critique of the adaptationist programme.

The application of functional morphology to evolutionary studies. TREE 11: 124-129. Galis, F. 1999. Why do almost all mammals have seven cervical vertebrae? ]. Exp. Zool. (Mol. Dev. ) 285:19-26. Gans, C. 1963. Functional analysis within a single adaptive radiation. Proc. XIV Congr. Zool. 3:278-282. Garland, T. , and Adolph, S. C. 1994. Why not to do two-species comparative studies: limitations on inferring adaptation. Physiol. Zool. 67:797-828. Garland, T. and Ives, A. R. 2000. Using the past to predict the present: confidence intervals for regression equations and phylogenetic comparative methods.

Because of the latter concern, multiple cases of independent evolution of a trait-function association in living taxa provide the strongest evidence for attribution of the same function to that trait in a fossil. Once function has been established for the fossil taxon, further evaluation of a hypothesis of adaptation relies on experimental observations of extant taxa and biomechanical arguments. We also should acknowledge that some details of function (such as muscle firing patterns) can never be verified for fossils.

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