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Early Pottery
Early Pottery
Early Pottery
is considerably less complex, even in comparison Finally, these early Ediacaran burrows dem- 20. A. G. Collins, J. H. Lipps, J. W. Valentine, Paleobiology
with later Ediacaran burrows from northwest onstrate very early grazing activity by eumeta- 26, 47 (2000).
21. G. M. Narbonne, J. D. Aitken, Palaeontology 33, 945
Canada (21) and Australia (22). Conspicuously zoans. The grazing behavior is facilitated by a (1990).
absent are parallel meanders and three-dimensional low-amplitude sinusoidal search pattern and the 22. M. L. Droser, J. G. Gehling, S. Jensen, in Evolving Form
avoidance that appeared later in the Ediacaran ability to leave one sedimentary lamination for and Function: Fossils and Development, D. E. G. Briggs,
(21). Nevertheless, sinusoidal grazing probably another. Evidence of active backfilling of the Ed. (Peabody Museum of Natural History, New Haven, CT,
2005), pp. 125–138.
marks the advent of more sophisticated grazing burrow is important, as well as the ability to pass 23. G. D. Love et al., Nature 457, 718 (2009).
behaviors and is in itself evidence of early bur- sediment around or through the body and com- 24. A. C. Maloof et al., Nat. Geosci. 3, 653 (2010).
rowing adaptation. pact it in the animal’s wake, which was a crucial 25. G. M. Narbonne, Annu. Rev. Earth Planet. Sci. 33, 421
These findings extend the fossil record of advancement for infaunal life-styles. These be- (2005).
26. D. E. Canfield, S. W. Poulton, G. M. Narbonne, Science
bilaterian eumetazoans at least 30 million years havioral characteristics, though primitive, are clear- 315, 92 (2007).
backward to the early Ediacaran, a time con- ly derived from earlier animal ancestors. 27. K. A. McFadden et al., Proc. Natl. Acad. Sci. U.S.A. 105,
sistent with the youngest ages for the appearance 3197 (2008).
of bilaterians predicted by molecular clock analy- References and Notes 28. Y. Shen, T. Zhang, P. F. Hoffman, Proc. Natl. Acad. Sci.
1. S. B. Hedges, J. E. Blair, M. L. Venturi, J. L. Shoe, U.S.A. 105, 7376 (2008).
ses (2, 3). The molecular clock dates for the
BMC Evol. Biol. 4, 2 (2004). 29. L. M. Och, G. A. Shields-Zhou, Earth Sci. Rev. 110, 26 (2012).
Eumetazoa-sponge divergence have also been cor- 2. K. J. Peterson, N. J. Butterfield, Proc. Natl. Acad. 30. M. Gingras et al., Nat. Geosci. 4, 372 (2011).
roborated by the recently reported body fossil Sci. U.S.A. 102, 9547 (2005).
evidence of sponges from the Trezona Formation 3. K. J. Peterson, J. A. Cotton, J. G. Gehling, D. Pisani, Acknowledgments: This work was supported by Natural
Philos. Trans. R. Soc. B 363, 1435 (2008). Sciences and Engineering Research Council (NSERC) of
(Australia), immediately below the Marinoan-aged 4. J.-Y. Chen et al., Science 305, 218 (2004). Canada Discovery Grants to K.O.K., M.K.G., and L.M.H.;
Elatina Formation (635.2 Ma), and lipid bio- 5. D. Condon et al., Science 308, 95 (2005). by a Comisión Sectorial de Investigación Científica–UdelaR
markers suggestive of Demosponges in strata 6. T. Huldtgren et al., Science 334, 1696 (2011). Grant (“El Ediacarano en Uruguay y su importancia en el
P
MA 02318, USA.
ceramic container forms—differs consid- period (1) in its technological demands and in *To whom correspondence should be addressed. E-mail:
erably from the baked clay figurines or its significance both in subsistence activities, in- obaryos@fas.harvard.edu
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