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Taphonomic decoding of the paleobiological information locked in a lower Pleistocene assemblage of large mammals

Published online by Cambridge University Press:  08 April 2016

Paul Palmqvist  and
Alfonso Arribas
Paul Palmqvist
Affiliation:
Departamento de Geología y Ecología (Área de Paleontología), Facultad de Ciencias, Universidad de Málaga. 29071 Málaga, Spain. E-mail: [email protected]
Alfonso Arribas
Affiliation:
Museo Geominero, Instituto Geológico y Minero (I.G.M.E.), c/ Ríos Rosas, 23. 28003 Madrid, Spain. E-mail: [email protected]
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Abstract

The processes of fossilization have usually been perceived by paleontologists as destructive ones, leading to consecutive (and in most cases irretrievable) losses of paleobiological information. However, recent developments of conceptual issues and methodological approaches have revealed that the decrease in paleobiological information runs parallel to the gain of taphonomic information. This taphonomic imprinting often makes it possible to decode the fraction of paleobiological information that was lost during fossilization, and may also contribute new data for deciphering paleobiological information that was not originally preserved in the assemblage, such as paleoethology. A good example is the study of the macrovertebrate assemblage from the lower Pleistocene site at Venta Micena (Orce, southeastern Spain). Taphonomic analysis showed that the giant, short-faced hyenas (Pachycrocuta brevirostris) selectively transported ungulate carcasses and body parts to their maternity dens as a function of the mass of the ungulates scavenged. The fracturing of major limb bones in the dens was also highly selective, correlating with marrow content and mineral density. Important differences in bone-cracking intensity were related to which species the bones came from, which in turn biased the composition of the bone assemblage. The analysis of mortality patterns deduced for ungulate species from juvenile/adult proportions revealed that most skeletal remains were scavenged by the hyenas from carcasses of animals hunted by hypercarnivores, such as saber-tooths and wild dogs. Analytical study of the Venta Micena assemblage has unlocked paleobiological information that was lost during its taphonomic history, and has even provided paleobiological information that was not preserved in the original bone assemblage, such as the paleoethology of P. brevirostris, which differed substantially from modern hyenas in being a strict scavenger of the prey hunted by other carnivores.

Type
Articles
Information
Paleobiology , Volume 27 , Issue 3 , Summer 2001 , pp. 512 - 530
Copyright
Copyright © The Paleontological Society 

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References

Literature Cited

Anyonge, W. 1993. Body mass in large extant and extinct carnivores. Journal of Zoology 231:339–350.Google Scholar
Anyonge, W. 1996. Locomotor behaviour in Plio-Pleistocene sabretooth cats: a biomechanical analysis. Journal of Zoology 238:395–413.CrossRefGoogle Scholar
Arribas, A. 1999. Análisis y modelización de la tafonomía del yacimiento de Venta Micena (Orce, Granada) y su estudio comparativo con otras localidades españolas del Plio-Pleistoceno continental. Ph.D. dissertation. Universidad Complutense de Madrid, Madrid.Google Scholar
Arribas, A., and Palmqvist, P. 1998. Taphonomy and paleoecology of an assemblage of large mammals: hyenid activity in the lower Pleistocene site at Venta Micena (Orce, Guadix-Baza Basin, Granada, Spain). Géobios 31(Suppl.):3–47.Google Scholar
Arribas, A., and Palmqvist, P. 1999. On the ecological connection between sabretooths and hominids: faunal dispersal events in the lower Pleistocene and a review of the evidence for the first human arrival in Europe. Journal of Archaeological Science 26:571–585.Google Scholar
Behrensmeyer, A. K. 1978. Taphonomic and ecologic information from bone weathering. Paleobiology 4:150–162.CrossRefGoogle Scholar
Behrensmeyer, A. K. 1991. Terrestrial vertebrate accumulations. Pp. 291–327in Allison, P. A. and Briggs, D. E. G., eds. Taphonomy: releasing the data locked in the fossil record. Plenum, New York.Google Scholar
Behrensmeyer, A. K., and Dechant Boaz, D. E. 1980. The recent bones of Amboseli Park, Kenya, in relation to East African Paleoecology. Pp. 72–93in Behrensmeyer, and Hill, 1980.Google Scholar
Behrensmeyer, A. K., and Hill, A. P., eds. 1980. Fossils in the making: vertebrate taphonomy and paleoecology. University of Chicago Press, Chicago.Google Scholar
Behrensmeyer, A. K., and Hook, R. W. 1992. Paleoenvironmental contexts and taphonomic modes. Pp. 15–136in Behrensmeyer, A. K., Damuth, J. D., DiMichele, W. A., Potts, R., Sues, H. D., and Wing, S. L., eds. Terrestrial ecosystems through time: evolutionary paleoecology of terrestrial plants and animals. University of Chicago Press, Chicago.Google Scholar
Behrensmeyer, A. K., and Kidwell, S. M. 1985. Taphonomy's contributions to paleobiology. Paleobiology 11:105–119.Google Scholar
Brain, C. K. 1980. Some criteria for the recognition of bone-collecting agencies in African caves. Pp. 108–130in Behrensmeyer, and Hill, 1980.Google Scholar
Brain, C. K. 1981. The hunters or the hunted: an introduction to African cave taphonomy. University of Chicago Press, Chicago.Google Scholar
Brink, J. W. 1997. Fat content in leg bones of Bison bison, and applications to archaeology. Journal of Archaeological Science 24:259–274.Google Scholar
Bunn, J. T. 1982. Meat-eating and human evolution: studies on the diet and subsistence patters of Plio-Pleistocene hominids in East Africa. Ph.D. dissertation. University of California, Berkeley.Google Scholar
Calder, W. A. 1984. Size, function, and life history. Harvard University Press, Cambridge.Google Scholar
Cutler, A. H., Behrensmeyer, A. K., and Chapman, R. E. 1999. Environmental information in a recent bone assemblage: roles of taphonomic processes and ecological change. Palaeogeography, Palaeoclimatology, Palaeoecology 149:359–372.Google Scholar
Damuth, J. 1982. Analysis of the preservation of community structure in assemblages of fossil mammals. Paleobiology 8:434–446.Google Scholar
Damuth, J., and MacFadden, B. J., eds. 1990. Body size in mammalian paleobiology: estimation and biological implications. Cambridge University Press, Cambridge.Google Scholar
De Renzi, M. 1997. Taphonomic information and paleobiological information: a wrong dilemma? Cuadernos de Geología Ibérica 23:183–208.Google Scholar
Emerson, A. M. 1990. Archaeological implications of variability in the economic anatomy of Bison bison. Ph.D. dissertation. Washington State University, Pullman.Google Scholar
Ewer, R. F. 1973. The carnivores. Cornell University Press, Ithaca, N.Y.Google Scholar
Fernández-López, S. 1991. Taphonomic concepts for a theoretical biochronology. Revista Española de Paleontología 6:37–49.Google Scholar
Fosse, P. 1996. La grotte n° 1 de Lunel-Viel (Hérault, France): repaire d'hyènes du Pléistocène moyen. Etude taphonomique du matériel osseux. Paleo 8:47–81.Google Scholar
Hill, A. P. 1981. A modern hyena den in Amboseli National Park, Kenya. Pp. 137–138in Pan-African Congress on Prehistory and Quaternary Studies, Proceedings.Google Scholar
Kerbis Peterhans, J. C., and Kolska-Horwitz, L. 1992. A bone assemblage from a striped hyaena (Hyaena hyaena) den in Negev Desert, Israel. Israel Journal of Zoology 37:225–245.Google Scholar
Kidwell, S. M., and Bosence, D. W. J. 1991. Taphonomy and time-averaging of marine shelly faunas. Pp. 116–209in Allison, P. A. and Briggs, D. E. G., eds. Taphonomy: releasing the data locked in the fossil record. Plenum, New York.Google Scholar
Kidwell, S. M., and Flessa, K. W. 1995. The quality of the fossil record: populations, species, and communities. Annual Reviews of Ecology and Systematics 26:269–299.Google Scholar
Klein, R. G., and Cruz-Uribe, K. 1984. The analysis of animal bones from archaeological sites. University of Chicago Press, Chicago.Google Scholar
Kruuk, H. 1972. The spotted hyena: a study of predation and social behavior. University of Chicago Press, Chicago.Google Scholar
Leakey, L. N., Milledge, S. A. H., Leakey, S. M., Edung, J., Haynes, P., Kiptoo, D. K., and McGeorge, A. 1999. Diet of striped hyaena in northern Kenya. African Journal of Ecology 37:314–326.CrossRefGoogle Scholar
Lewis, M. E. 1997. Carnivoran paleoguilds of Africa: implications for hominid food procurement strategies. Journal of Human Evolution 32:257–288.CrossRefGoogle ScholarPubMed
Lyman, R. L. 1994. Vertebrate taphonomy. Cambridge University Press, Cambridge.Google Scholar
Maguire, J. M., Pemberton, D., and Collet, M. H. 1980. The Makapansgat Limeworks grey breccia: hominids, hyaenas, hystricids or hillwash? Palaeontologia Africana 23:75–98.Google Scholar
Marean, C. W. 1989. Sabertooth cats and their relevance for early hominid diet and evolution. Journal of Human Evolution 18:559–582.Google Scholar
Marean, C. W., and Ehrhardt, C. L. 1995. Paleoanthropological and paleoecological implications of the taphonomy of a sabretooth's den. Journal of Human Evolution 29:515–547.Google Scholar
Martin, L. D., Babiarz, J. P., Naples, V. L., and Hearst, J. 2000. Three ways to be a saber-toothed cat. Naturwissenschaften 87:41–44.CrossRefGoogle ScholarPubMed
Martin, R. E. 1999. Taphonomy: a process approach. Cambridge Paleobiology Series, No. 4. Cambridge University Press, Cambridge.Google Scholar
Martínez-Navarro, B., and Palmqvist, P. 1995. Presence of the African machairodont Megantereon whitei (Broom, 1937) (Felidae, Carnivora, Mammalia) in the lower Pleistocene site of Venta Micena (Orce, Granada, Spain), with some considerations on the origin, evolution and dispersal of the genus. Journal of Archaeological Science 22:569–582.Google Scholar
Martínez-Navarro, B., and Palmqvist, P. 1996. Presence of the African saber-toothed felid Megantereon whitei (Broom, 1937) (Mammalia, Carnivora, Machairodontidae) in Apollonia-1 (Mygdonia basin, Macedonia, Greece). Journal of Archaeological Science 23:869–872.Google Scholar
Mills, M. G. L. 1989. The comparative behavioral ecology of hyenas: the importance of diet and food dispersion. Pp. 125–142in Gittleman, J. L., ed. Carnivore behavior, ecology, and evolution. Chapman and Hall, London.Google Scholar
Outram, A., and Rowley-Conwy, P. 1998. Meat and marrow utility indices for horse (Equus). Journal of Archaeological Science 25:839–849.Google Scholar
Palmqvist, P., and Arribas, A. 2001. An overview of the taphonomy and paleoecology of the assemblage of large mammals preserved in lower Pleistocene deposits from Venta Micena (Guadix-Baza basin, Spain). Paleontologia i Evolució 32–33:37–58.Google Scholar
Palmqvist, P., Martínez-Navarro, B., and Arribas, A. 1996. Prey selection by terrestrial carnivores in a lower Pleistocene paleocommunity. Paleobiology 22:514–534.Google Scholar
Palmqvist, P., Arribas, A., and Martínez-Navarro, B. 1999. Ecomorphological analysis of large canids from the lower Pleistocene of southeastern Spain. Lethaia 32:75–88.Google Scholar
Peters, R. H. 1983. The ecological implications of body size. Cambridge University Press, Cambridge.Google Scholar
Rawn-Schatzinger, V. 1992. The scimitar cat Homotherium serum Cope: osteology, functional morphology, and predatory behavior. Illinois State Museum Reports of Investigations 47:1–80.Google Scholar
Richardson, P. R. K. 1980. Carnivore damage to antelope bones and its archaeological implications. Palaeontologia Africana 23:109–125.Google Scholar
Saunders, J. J., and Dawson, B. K. 1998. Bone damage patterns produced by extinct hyena, Pachycrocuta brevirostris (Mammalia: Carnivora) at the Haro River Quarry, Northwestern Pakistan. In Yomida, Y., Flynn, L. J., and Jacobs, L. L., eds. Advances in vertebrate paleontology and geochronology. National Science Museum Monographs 14:215–242. Tokyo.Google Scholar
Schaller, G. B. 1972. The Serengeti lion: a study of predator-prey relations. University of Chicago Press, Chicago.Google Scholar
Shipman, P. 1981. Life history of a fossil: an introduction to taphonomy and paleoecology. Harvard University Press, Cambridge.Google Scholar
Skinner, J. D., and Van Aarde, R. J. 1981. The distribution and ecology of the brown hyaena Hyaena brunnea and spotted hyaena Crocuta crocuta in the central Namib Desert. Madoqua 12:231–239.Google Scholar
Skinner, J. D., and Van Aarde, R. J. 1991. Bone collecting by brown hyaenas Hyaena brunnea in the central Namib Desert, Namibia. Journal of Archaeological Science 18:513–523.Google Scholar
Skinner, J. D., Davis, S., and Ilani, G. 1980. Bone collecting by striped hyenas, Hyena hyena, in Israel. Palaeontologia Africana 23:99–104.Google Scholar
Skinner, J. D., Henschel, J. R., and Van Jaarsveld, A. S. 1986. Bone-collecting habits of spotted hyenas Crocuta crocuta in the Kruger National Park. South African Journal of Zoology 21:303–308.Google Scholar
Skinner, J. D., Van Aarde, R. J., and Goss, R. A. 1995. Space and resource use by brown hyaenas Hyaena brunnea in the central Namib Desert. Journal of Zoology 237:123–131.Google Scholar
Skinner, J. D., Haupt, M. A., Hoffmann, M., and Dott, H. M. 1998. Bone collecting by brown hyaenas Hyaena brunnea in the Namib desert: rate of accumulation. Journal of Archaeological Science 25:69–71.Google Scholar
Turner, A., and Antón, M. 1996. The giant hyena, Pachycrocuta brevirostris (Mammalia, Carnivora, Hyaenidae). Géobios 29:455–468.Google Scholar
Turner, A., and Antón, M. 1998. Climate and evolution: implications of some extinction patterns in African and European machairodontine cats of the Plio-Pleistocene. Estudios Geológicos 54:209–230.Google Scholar
Van Valkenburgh, B. 1990. Skeletal and dental predictors of body mass in carnivores. Pp. 181–205in Damuth, and MacFadden, 1990.Google Scholar
Voorhies, M. R. 1969. Taphonomy and population dynamics of the early Pliocene vertebrate fauna, Knox County, Nebraska. Contributions to Geology University of Wyoming, Special Paper No. 1.Google Scholar
Vrba, E. S. 1980. The significance of bovid remains as indicators of environment and predation patterns. Pp. 247–271in Behrensmeyer, and Hill, 1980.Google Scholar
Western, D. 1979. Size, life history and ecology in mammals. African Journal of Ecology 17:185–204.Google Scholar
Western, D. 1980. Linking the ecology of past and present mammal communities. Pp. 41–54in Behrensmeyer, and Hill, 1980.Google Scholar
Wilson, M. V. H. 1988. Taphonomic processes: information loss and information gain. Geoscience Canada 15:131–148.Google Scholar