“…Although a strong association between those characteristics and reduced dimorphism in body mass, canine size and skeletal dimensions has been shown for many primate taxa (Kay et al, 1988;Plavcan, 1993;Ford, 1994;Smith and Jungers, 1997), there are taxa in which the relationship is less clear (Milton, 1985;Kappeler, 1990;Lindenfors and Tullberg, 1998), has not been thoroughly examined (e.g., Pithecia), or has been evaluated relying on small collections of museum specimens or wild specimens of uncertain provenance and\or unknown sex and age (e.g., Aotus, Callicebus). Studies on larger sample sizes of sexually dimorphic free-ranging polygynous and polyandrous primates have illustrated some of the problems of assuming average population measurements from small samples of any particular location (Goldizen et al, 1988;Altmann et al, 1993;Jablonski and Ruliang, 1995;Turner et al, 1997;Schmid and Kappeler, 1998;Pochron and Wright, 2003;Johnson et al, 2005;Glander, 2006).Behavioral reconstructions of early hominins are regularly based on the observed behavior and morphology of extant primates (Plavcan and Van Schaik, 1997;Lovejoy, 2009;Takai et al, 2009;Gettler, 2010) and the taxonomic classification of fossils is influenced by our understanding of between and within population variation in the extent of sexual dimorphism, as well as possible changes in body size and dimorphism with latitude (Reno et al, 2003;Plavcan et al, 2005). In other words, our understanding of early hominin behavior and taxonomy will benefit from answering the following questions: What is the range of variation in sexually dimorphic physical traits of extant primates?…”