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ARTICLE IN PRESS<br />

6 N.D. Sheldon, N.J. Tabor / Earth-Science Reviews xxx (2009) xxx–xxx<br />

76% of original thickness given independent constraints on burial<br />

depth.<br />

The primary disadvantages to the approach of Sheldon <strong>and</strong><br />

Retallack (2001) are that it requires accurate soil taxonomy <strong>and</strong> that<br />

it requires a fairly accurate estimate of the burial overburden. Because<br />

the differences in compactibility among different soil orders can be<br />

fairly large (Fig. 4), accurate taxonomic identification is very<br />

important. Similarly, most of the compaction predicted by Eq. (4)<br />

occurs within burial depths of 4 km or less, with very little change<br />

among deeply buried paleosols. Thus, uncertainty in burial depth of<br />

even 500 m for shallowly buried paleosols would have a large effect on<br />

the calculated compaction.<br />

Fig. 4. Compactibility of different soil orders.<br />

To give one specific example, Retallack (1986) used ptygmatically<br />

folded clastic dikes in the ~2.2 Ga Hekpoort paleosol to estimate that it<br />

had been compacted to 67–73% of its original thickness. Sheldon <strong>and</strong><br />

Retallack (2001) used Eq. (4) <strong>and</strong> constants for a Vertisol (Retallack,<br />

1986; Driese et al., 2005) fromTable 2 to estimate compaction to 72–<br />

2.2.2. Ichnology<br />

A number of recent workers have begun integrating continental<br />

ichnology with studies of paleosols (e.g., Genise et al., 2004; Kirkl<strong>and</strong>,<br />

2006; Kraus <strong>and</strong> Hasiotis, 2006; Laza, 2006; Hamer et al., 2007a,b),<br />

<strong>and</strong> trace fossils have been key to underst<strong>and</strong>ing some early<br />

ecosystems (e.g., Feakes et al., 1989; Retallack <strong>and</strong> Feakes, 1987). A<br />

wide variety of animal <strong>and</strong> plant traces have been identified (e.g.,<br />

Hasiotis, 2004) that are useful in <strong>paleoenvironmental</strong> <strong>reconstruction</strong>s<br />

using paleosols. In particular, rhizolith or root trace density (Fig. 1D)<br />

<strong>and</strong> penetration depth have been used to underst<strong>and</strong> vegetation type<br />

<strong>and</strong> density (O'Geen <strong>and</strong> Busacca, 2001; Retallack, 2007) <strong>and</strong> to<br />

characterize the paleohydrological setting (Kraus <strong>and</strong> Hasiotis, 2006).<br />

In marine settings, a semi-quantitative ichnofabric index has been<br />

created (Droser <strong>and</strong> Bottjer, 1986) that looks at total bioturbation<br />

density. Attempts to apply this method to paleosols have been<br />

relatively rare <strong>and</strong> as Genise et al. (2004) point out, well-developed<br />

Fig. 5. Bioturbation index versus root size in paleosols. Data are from N.D. Sheldon <strong>and</strong> J.M.M. Hamer (unpublished). See text for discussion.<br />

Please cite this article as: Sheldon, N.D., Tabor, N.J., <strong>Quantitative</strong> <strong>paleoenvironmental</strong> <strong>and</strong> <strong>paleoclimatic</strong> <strong>reconstruction</strong> using paleosols, Earth-<br />

Science Reviews (2009), doi:10.1016/j.earscirev.2009.03.004

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