Hostname: page-component-586b7cd67f-rcrh6 Total loading time: 0 Render date: 2024-11-23T21:08:58.806Z Has data issue: false hasContentIssue false

Sexual dimorphism of structures showing indeterminate growth: tusks of American mastodons (Mammut americanum)

Published online by Cambridge University Press:  08 April 2016

Kathlyn M. Smith
Affiliation:
Department of Geological Sciences and Museum of Paleontology, University of Michigan, Ann Arbor, Michigan 48109-1005. E-mail: [email protected]
Daniel C. Fisher
Affiliation:
Department of Geological Sciences and Museum of Paleontology, University of Michigan, Ann Arbor, Michigan 48109-1005. E-mail: [email protected]

Abstract

Documenting sexual dimorphism for structures that exhibit indeterminate growth can be more difficult than for structures exhibiting determinate growth. Most proboscidean tusks are ever-growing structures that change size and shape throughout life. Sexual dimorphism is pronounced in tusks of mature individuals, but the external form of tusks offers no clear evidence of maturation, and it is difficult to distinguish a young male's tusk from that of an older female. Thus, with previous approaches, knowledge of age was often required to assess sex from tusk measurements. This study examines sexual dimorphism of American mastodon (Mammut americanum) tusks through principal components analysis to determine which aspects of tusk form contribute most strongly to the variance among measurements and to explore the relationship between tusk form and individual age and sex. Twenty-one mastodon tusks from the Great Lakes region were evaluated in two analyses, the first focusing on geometrically distinct aspects of tusk form and the second adding measurements that reflect ontogenetic changes in a single aspect of morphology (circumference). Both analyses separated mastodons by sex (PC-I) and sorted them by age (PC-II). The distribution of tusks on the PC-II versus PC-I plane provides better discrimination of sex than univariate or bivariate methods because tusks of similar size and opposite sex appear near opposite ends of an age spectrum. The second analysis enhances sorting by age, thereby clarifying assessment of sex. This work contributes to studies of mastodon paleobiology by presenting a reliable method for assessing the sex of an individual from tusk measurements without requiring independent knowledge of age.

Type
Articles
Copyright
Copyright © The Paleontological Society 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Literature Cited

Bebej, R. M. 2009. Swimming mode inferred from skeletal proportions in the fossil pinnipeds Enaliarctous and Allodesmus (Mammalia, Carnivora). Journal of Mammalian Evolution 16:7797.CrossRefGoogle Scholar
Chapman, R. E., Galton, P. M., Sepkoski, J. J. Jr., and Wall, W. P. 1981. A morphometric study of the cranium of the pachycephalosaurid Stegoceras . Journal of Paleontology 55:608618.Google Scholar
Derocher, A. E., Andersen, M., and Wiig, Ø. 2005. Sexual dimorphism of polar bears. Journal of Mammalogy 86:895901.Google Scholar
Elder, W. H. 1970. Morphometry of elephant tusks. Zoologica Africana 5:143159.CrossRefGoogle Scholar
Fisher, D. C. 1996. Extinction of proboscideans in North America. Pp. 296315 in Shoshani, J. and Tassy, P., eds. The Proboscidea: evolution and palaeocology of elephants and their relatives. Oxford University Press, Oxford.Google Scholar
Fisher, D. C. 2001. Season of death, growth rates, and life history of North American mammoths. In West, D., ed. Proceedings of the International Conference on Mammoth Site Studies. Publications of Anthropology 22:121135.Google Scholar
Fisher, D. C. 2008. Taphonomy and paleobiology of the Hyde Park mastodon. In Allmon, W. D. and Nester, P. L., eds. Mastodon paleobiology, taphonomy, and paleoenvironment in the late Pleistocene of New York State: studies on the Hyde Park, Chemung, and North Java sites. Palaeontographica Americana 61:197290.Google Scholar
Fisher, D. C. 2009. Paleobiology and extinction of proboscideans in the Great Lakes region of North America. Pp. 5575 in Haynes, G., ed. American megafaunal extinctions at the end of the Pleistocene. Springer Science, New York.Google Scholar
Fisher, D. C., Beld, S. G., and Rountrey, A. N. 2008a. Tusk record of the North Java Mastodon. In Allmon, W. D. and Nester, P. L., eds. Mastodon paleobiology, taphonomy, and paleoenvironment in the late Pleistocene of New York state: studies on the Hyde Park, Chemung, and North Java sites. Palaeontographica Americana 61:417463.Google Scholar
Fisher, D. C., Rountrey, A. N., and Tedor, R. 2008b. Paleobiological analysis of a Holocene mammoth tusk, St. Paul, Pribilof Islands, Bering Sea. Journal of Vertebrate Paleontology 28(Suppl. to 3):77A.Google Scholar
Gingerich, P. D. 1981. Variation, sexual dimorphism, and social structure in the Early Eocene horse Hyracotherium (Mammalia, Perissodactyla). Paleobiology 7:443455.Google Scholar
Gingerich, P. D. 2000. Arithmetic or geometric normality of biological variation: an empirical test of theory. Journal of Theoretical Biology 204:201221.CrossRefGoogle ScholarPubMed
Gingerich, P. D. 2003. Land-to-sea transition in early whales: evolution of Eocene Archaeoceti (Cetacea) in relation to skeletal proportions and locomotion of living semi-aquatic mammals. Paleobiology 29:429454.Google Scholar
Holman, J. A., Fisher, D. C., and Kapp, R. O. 1986. Recent discoveries of fossil vertebrates in the lower peninsula of Michigan. Michigan Academician 28:431463.Google Scholar
Laws, R. M. 1966. Age criteria for the African elephant, Loxodonta a. africana . East African Wildlife Journal 4:137.CrossRefGoogle Scholar
Lee, P. C., and Moss, C. J. 1986. Early maternal investment in male and female African elephant calves. Behavioral Ecology and Sociobiology 18:353361.Google Scholar
Lee, P. C., and Moss, C. J. 1995. Statural growth in known-age African elephants (Loxodonta africana). Journal of the Zoological Society of London 236:2941.CrossRefGoogle Scholar
McLeod, M. I. 2005. Kendall: Kendall rank correlation and Mann-Kendall trend test. R package, Version 2.0. http://www.stats.uwo.ca/faculty/aim.Google Scholar
Mead, A. J. 2000. Sexual dimorphism and paleoecology in Teleoceras, a North American Miocene rhinoceros. Paleobiology 26:689706.2.0.CO;2>CrossRefGoogle Scholar
Mills, A. M. 2008. Passerines are sexually dimorphic in shape as well as size. Condor 110:354358.CrossRefGoogle Scholar
Pilgram, T., and Western, D. 1986. Inferring the sex and age of African elephants from tusk measurements. Biological Conservation 36:3952.CrossRefGoogle Scholar
Poole, J. H. 1987. Rutting behavior in African elephants: the phenomenon of musth. Behavior 102:283316.Google Scholar
Poole, J. H. 1994. Sex differences in the behavior of African elephants. Pp. 331346 in Short, R. V. and Balaban, E., eds. The differences between the sexes. Cambridge University Press, Cambridge.Google Scholar
R Development Core Team. 2006. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna. http://www.R-project.org.Google Scholar
Smith, K. M., and Fisher, D. C. 2007. Sexual dimorphism in tusks of Great Lakes-region American mastodons (Mammut americanum). Journal of Vertebrate Paleontology 27(Suppl. to 3):149A.Google Scholar
Smith, K. M., and Fisher, D. C. 2008. Tusk growth record of a female American mastodon (Mammut americanum) from southeastern New York State. Journal of Vertebrate Paleontology 28(Suppl. to 3):144A.Google Scholar
Zelditch, M. L., Swiderski, D. L., Sheets, H. D., and Fink, W. L. 2004. Geometric morphometrics for biologists: a primer. Elsevier Academic, San Diego.Google Scholar