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Community Replacement Pathways: What Do Fossil Sequences Reveal About Marine Ecosystem Transitions?

Published online by Cambridge University Press:  26 July 2017

William Miller III*
Affiliation:
Geology Department and Marine Laboratory, Humboldt State University, Arcata, California 95521
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Extract

Paleontologists have lavished much time and energy on description and explanation of large-scale patterns in the fossil record (e.g., mass extinctions, histories of monophyletic taxa, deployment of major biogeographic units), while paying comparatively little attention to biologic patterns preserved only in local stratigraphic sequences. Interpretation of the large-scale patterns will always be seen as the chief justification for the science of paleontology, but solving problems framed by long time spans and large areas is rife with tenuous inference and patterns are prone to varied interpretation by different investigators using virtually the same data sets (as in the controversy over ultimate cause of the terminal Cretaceous extinctions). In other words, the large-scale patterns in the history of life are the true philosophical property of paleontology, but there will always be serious problems in attempting to resolve processes that transpired over millions to hundreds-of-millions of years and encompassed vast areas of seafloor or landscape. By contrast, less spectacular and more commonplace changes in local habitats (often related to larger-scale events and cycles) and attendant biologic responses are closer to our direct experience of the living world and should be easier to interpret unequivocally. These small-scale responses are reflected in the fossil record at the scale of local outcrops.

Type
Research Article
Copyright
Copyright © 1990 Paleontological Society 

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References

Allen, T.F.H., and Starr, T.B. 1982. Hierarchy: Perspectives for Ecological Complexity. University of Chicago Press, Chicago, 310 p.Google Scholar
Bailey, R.H., and Tedesco, S.A. 1986. Paleoecology of a Pliocene coral thicket from North Carolina: an example of temporal change in community structure and function. Journal of Paleontology, 60:11591176.CrossRefGoogle Scholar
Connell, J.H. 1978. Diversity in tropical rain forests and coral reefs. Science, 199:13021310.CrossRefGoogle ScholarPubMed
Copper, P. 1988. Ecological succession in Phanerozoic reef ecosystems: is it real? Palaios, 3:136152.CrossRefGoogle Scholar
Davis, M.B. 1986. Climatic instability, time lags, and community disequilibrium, p. 269284. In Diamond, J. and Case, T. J. (eds.), Community Ecology. Harper and Row, New York.Google Scholar
Eldredge, N. 1985. Unfinished Synthesis: Biological Hierarchies and Modern Evolutionary Thought. Oxford University Press, New York, 237 p.Google Scholar
Eldredge, N., and Salthe, S. N. 1984. Hierarchy and evolution. Oxford Surveys in Evolutionary Biology, 1:182206.Google Scholar
Fagerstrom, J.A. 1987. The Evolution of Reef Communities. John Wiley, New York, 600 p.Google Scholar
Hoffman, A., and Narkiewicz, M. 1977. Developmental pattern of Lower to Middle Paleozoic banks and reefs. Neues Jahrbuch für Geologie und Paläontologie Monatshefte, 1977:272283.Google Scholar
Johnson, M.E. 1977. Succession and replacement in the development of Silurian brachiopod populations. Lethaia, 10:8393.CrossRefGoogle Scholar
Johnson, R.G. 1972. Conceptual models of benthic marine communities, p. 148159. In Schopf, T. J. M. (ed.), Models in Paleobiology. Freeman, Cooper and Co., San Francisco.Google Scholar
May, R.M. 1977. Thresholds and breakpoints in ecosystems with a multiplicity of stable states. Nature, 269:471477.CrossRefGoogle Scholar
Miller, K.B., Brett, C.E., and Parsons, K.M. 1988. The paleoecologic significance of storm-generated disturbance within a Middle Devonian muddy epeiric sea. Palaios, 3:3552.CrossRefGoogle Scholar
Miller, W. III. 1986a. Paleoecology of benthic community replacement. Lethaia, 19:225231.CrossRefGoogle Scholar
Miller, W. III. 1986b. The rise and fall of local ecosystems: toward a theory of community replacement. North American Paleontological Convention IV, Abstracts with Programs: A32.Google Scholar
Miller, W. III. 1986c. Community local history. Lethaia, 21:9596.CrossRefGoogle Scholar
Miller, W. III. This volume. Hierarchy, individuality and paleoecosystems.Google Scholar
Miller, W. III., and Du Bar, J.R. 1988. Community replacement of a Pleistocene Crepidula biostrome. Lethaia, 21:6778.CrossRefGoogle Scholar
Miller, W. III., and Metelman Alvis, L. 1986. Temporal change as an aspect of biogenic shell utilization and damage, Pleistocene of North Carolina, U.S.A. Palaeogeography, Palaeoclimatology, Palaeoecology, 56:197215.CrossRefGoogle Scholar
Rollins, H. B., and Donahue, J. 1975. Towards a theoretical basis of paleoecology: concepts of community dynamics. Lethaia, 8:255270.CrossRefGoogle Scholar
Rollins, H. B., Carothers, M., and Donahue, J. 1979. Transgression, regression and fossil community succession. Lethaia, 12: 89104.CrossRefGoogle Scholar
Rollins, H. B., West, R. R., and Busch, R. M. This volume. Hierarchical genetic stratigraphy and marine paleoecology.Google Scholar
Salthe, S. N. 1985. Evolving Hierarchical Systems: Their Structure and Representation. Columbia University Press, New York, 343 p.CrossRefGoogle Scholar
Underwood, A.J. 1986. What is a community?, p. 351367. In Raup, D. M. and Jablonski, D. (eds.), Patterns and Processes in the History of Life, Dahlem Konferenzen 1986. Springer-Verlag, Berlin.Google Scholar
Valentine, J.W. 1973. Evolutionary Paleoecology of the Marine Biosphere. Prentice-Hall, Englewood Cliffs, New Jersey, 511 pp.Google Scholar