Fossil record II: Temporal sequencing

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Temporal Sequences

Maggie Koopman and Erik Hoffmann

0.0

Now!

1.0

First hard parts

First multicellular

2.0

First eukaryotes

3.0

4.0

First life!

The beginning!

Time is on my side

1.5 billion years

The Outcrop

Sometimes you have a lot to work with...

The Outcrop

...and sometimes you don’t!

The Outcrop

Dooley et al., 2004

No crystalline rocks

• No absolute dating

• Imprecise age calibration

2 meters = 10 yrs or 10 million?

Dooley et al., 2004

The Outcrop

Unconformities

• Stratigraphic gaps caused by non-deposition or erosion

• The bigger the time window, the bigger and more frequent the gaps will be

Dooley et al., 2004

The Outcrop

Cover

• Prevents examination

• vegetation

• loose sediment/soil

• snow/ice/permafrost

The (so-so) Outcrop

Constant Motion

100 km

Modified from Tibert et al., 2003.

No Outcrop!

• Resolution depends on depositional rates

– High rates allow high resolution

– Low rates allow low resolution

– Negative rates erase the record

• Not all environments are created equal!

Schindel, 1982

Dooley et al., 2004

Gingerich, 1983

Limitations

• Preservable hard parts only!

• Morphological change only!

Limitations cont.

• Can’t detect fine changes.

• Small directional changes followed by reversals show up as variability within the population

Geary et al., 2002

Punctuated Equilibrium

• Long periods (relative to species durations) of morphological stasis coupled with brief periods of very rapid morphological change

• Stasis does NOT mean nothing is happening

• Changes in soft parts

• Changes in tolerances/behaviors

• Small directional morphological change followed by doubling back

Biases

• Lineage (size, hard parts, frequency)

• Location (range, availability)

• Temporal resolution ((sub)stage level)

• Character sets

• Usefulness/Interest

Does the fossil record need to be complete?

Can we work around the gaps?

Can we derive viable sequences from a spotty record?

Quality of the fossil record through time

M. J. Benton, M. A. Wills and R. Hitchin

What does this paper do?

• Offers evidence that the fossil record provides uniformly good documentation of past life.

Assesses the congruence between stratigraphy and phylogeny.

The Congruence Metrics

• Valid techniques for comparing large samples of cladograms to try to estimate variations in congruence between the fossil record for different groups of organisms and for different habitats

• RCI (relative completeness index)

• GER (gap ratio index)

• SCI (stratigraphic consistency index)

Depend on branching point estimates and calc. Of ghost ranges

Stratigraphic consistency index

(Huelsenbeck 1994)

• Fit of the record to the tree= proportion of the nodes that are stratigraphically consistent.

•Significance of the fit= generate a null distribution for SCI under the hyp. That the statigraphic fit is not better than expected at random.

Figure 2

• Hypothesis 1: congruence is better than random (bars to the left)

• Alternative hypothesis: congruence is worse than expected from a random model: direct conflict between data (bars to the right)

RCI SCI

Fig 1 a/b Benton et al 1999

What causes poor matching of age and clade data?

Bias in the metric

• Difference in quality of trees

• Difference in quality of fossil record

• Stratigraphic problems

• Taxonomy

• Sampling density

Molecular Clock Divergence Estimates and the Fossil Record of Cetartiodactyla

Jessica M. Theodor

J. Paleontology 78 (1), 2004, p 39-44

Why this paper?

• Ties molecular clocks to the fossil record

• Introduces cetaceans and hippopotamids

Molecular Clocks vs. the Fossil Record

• Artiodactyla/Cetacea split – 60 Ma

– Earliest fossil whales 53.5 Ma

– Earliest fossil artiodactyls 55 Ma

• Odontocete/Mysticete split – 34-35 Ma

– Rare at 34 Ma, good record ~30 Ma

• Hippopotamid/Cetacean split

– Earliest fossil whales 53.5 Ma

– Earliest fossil hippos 15.6-15.8 Ma

» Anthracotheres - ~43 Ma

• New study using one mitochondrial and one nuclear gene sequence

Boisserie et al., 2005

Take home messages

• The fossil record is necessary to calibrate molecular clocks (and refute the bad ones)

• The fossil record fills gaps in phylogenetic trees, allowing us to confirm evolutionary sequences

References

Benton, M.J., M.A. Wills, and R. Hitchin 2000, Nature. 403, 534-537

Benton, M.J. 2001, Proceedings of the Royal Society of London B. 268, 2123-2130

Boisserie, J.-R., F. Lihoreau, and M. Brunet 2005, Proceedings of the National Academy of Science 102

(5), 1537-1541

Dooley Jr., A.C., N.C. Fraser, and Z.-X. Luo 2004, Journal of Vertebrate Paleontology. 24 (2), 453-463

Geary, D.H., A.W. Staley, P. Muller, and I. Magyar 2002, Paleobiology. 28 (2), 208-221

Gingerich, P.D. 1983, Science. 222, 159-161

Gingerich, P.D. 1984, Science. 226, 995-996

Gingerich, P.D. 2002, Cetacean Evolution

Gould, S.J. 1984, Science. 226, 994-995

Huelsenbeck, J.P. 1994, Paleobiology. 20 (4), 470-483

Koch, C.F. 1978, Paleobiology. 4 (3), 367-372

Levinton, J., L. Dubb, and G.A. Wray 2004, Journal of Paleontology. 78 (1), 31-38

Lihoreau, F., and J.-R. Boisserie 2004, Journal of Vertebrate Paleontology 24 (Supp. 3), 83A

Rose, K. 2001, Science. 293, 2216-2217

Schindel, D. 1982, Paleobiology. 8 (4), 340-353

Schopf, T.J.M. 1982, Evolution. 36 (6), 1144-1157

Theodor, J.M. 2004, Journal of Paleontology. 78 (1), 39-44

Tibert, N.E., R.M. Leckie, J.G. Eaton, J.I. Kirkland, J.-P Colin, E.L. Leithold, and M.E. McCormick

2003, in Olson, H.C. and R.M. Leckie, eds., Micropaleontologic Proxies for Sea-Level Change and

Stratigraphic Discontinuities : SEPM Special Publication No. 75, 263-299

Wills, M.A. 1999, Systematic Biology. 48 (3), 559-58

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