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Majority rule: adaptation and the long-term dynamics of species

Published online by Cambridge University Press:  08 April 2016

Geerat J. Vermeij  and
Gregory P. Dietl
Geerat J. Vermeij
Affiliation:
Department of Geology, University of California at Davis, One Shields Avenue, Davis, California 95616. E-mail: [email protected]
Gregory P. Dietl
Affiliation:
Department of Geology and Geophysics, Yale University, Post Office Box 208109, New Haven, Connecticut 06520. E-mail: [email protected]
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Extract

Where do species that become important players in ecosystems evolve? This simple yet crucial question must be answered if we want to understand how the biosphere is rejuvenated following a crisis. We cannot simply assume that the environments in which we find fossil remains of a given species, or living populations of a species, are the environments in which that species evolved. Take the most obvious example: Fossil human skeletons have been unearthed by the hundreds in North America, but all available evidence points to a human origin in Africa. We can often identify the general geographic origins of species and clades thanks to fossil occurrences and the application of phylogenetic techniques; but can we do likewise for more ecological aspects of the environment? Advances in population biology and in paleobiology now permit us to outline a hypothesis of the circumstances most favorable to the evolution of abundant, widespread, or ecologically powerful species, those with adaptations that are selectively advantageous across many environments, and large short-term and long-term effects in ecosystems.

Type
Matters of the Record
Information
Paleobiology , Volume 32 , Issue 2 , Spring 2006 , pp. 173 - 178
Copyright
Copyright © The Paleontological Society 

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References

Literature Cited

Amano, K., and Vermeij, G. J. 2003. Evolutionary adaptation and geographic spread of the Cenozoic buccinid genus Lirabuccinum in the North Pacific. Journal of Paleontology 77:863–872.Google Scholar
Amano, K., and Watanabe, M. 2001. Taxonomy and distribution of the Plio-Pleistocene Buccinum (Gastropoda: Buccinidae) in northeast Japan. Paleontological Research 5:215–226.Google Scholar
Ambrose, S. H. 2001. Paleolithic technology and human evolution. Science 291:1748–1753.Google Scholar
Benkman, C. W., Holimon, W. C., and Smith, J. W. 2001. The influence of a competitor on the geographic mosaic of coevolution between crossbills and lodgepole pine. Evolution 55:282–294.Google Scholar
Benkman, C. W., Parchman, T. L., Favis, A., and Siepielski, A. M. 2003. Reciprocal selection causes a coevolutionary arms race between crossbills and lodgepole pine. American Naturalist 162:182–194.Google Scholar
Briggs, J. C. 1966. Zoogeography and evolution. Evolution 20:282–289.Google Scholar
Brown, W. L. Jr. 1958. General adaptation and evolution. Systematic Zoology 7:157–168.Google Scholar
Collins, T. M., Frazer, K., Palmer, A. R., Vermeij, G. J., and Brown, W. M. 1996. Evolutionary history of northern hemisphere Nucella (Gastropoda: Muricidae): molecular, morphological, ecological, and paleontological evidence. Evolution 50:2287–2304.Google Scholar
Darlington, P. J. Jr. 1959. Area, climate, and evolution. Evolution 13:488–510.Google Scholar
Darwin, C. 1859. The origin of species by natural selection or the preservation of favored races in the struggle for life. Appleton, New York.Google Scholar
Eldredge, N., Thompson, J. N., Brakefield, P. M., Gavrilets, S., Jablonski, D., Jackson, J. B. C., Lenski, R. E., Lieberman, B. S., McPeek, M. A., and Miller, W. III. 2005. The dynamics of evolutionary stasis. In Vrba, E. S. and Eldredge, N., eds. Macroevolution: diversity, disparity, contingency. Paleobiology 31(Suppl. to No. 2):133–145.Google Scholar
Forde, S. E., Thompson, J. N., and Bohannan, B. J. M. 2004. Adaptation varies through space and time in a coevolving hostparasitoid interaction. Nature 431:841–844.Google Scholar
Futuyma, D. J. 1987. On the role of species in anagenesis. American Naturalist 130:465–473.Google Scholar
Gonzalez, A., and Holt, R. D. 2002. The inflationary effects of environmental fluctuations in source-sink systems. Proceedings of the National Academy of Sciences USA 99:14872–14877.Google Scholar
Gould, S. J. 1985. The paradigm of the first tier: an agenda for paleobiology. Paleobiology 11:2–12.CrossRefGoogle Scholar
Gould, S. J. 2002. The structure of evolutionary theory. Harvard University Press, Cambridge.Google Scholar
Herre, E. A. 1999. Laws governing species interactions? Encouragement and caution from figs and their associates. Pp. 209–237 in Keller, L., ed. Levels of selection in evolution. Princeton University Press, Princeton N.J.Google Scholar
Holt, R. D. 1996a. Adaptive evolution in source-sink environments: direct and indirect effects of density-dependence on niche evolution. Oikos 75:182–192.CrossRefGoogle Scholar
Holt, R. D. 1996b. Demographic constraints in evolution: towards unifying the evolutionary theories of senescence and niche conservatism. Evolutionary Ecology 10:1–11.CrossRefGoogle Scholar
Holt, R. D., and Gaines, M. S. 1992. Analysis of adaptation in heterogeneous landscapes: implications for the evolution of fundamental niches. Evolutionary Ecology 6:433–447.Google Scholar
Holt, R. D., and Gomulkiewicz, R. 1997. How does immigration influence local adaptation? A reexamination of a familiar paradigm. American Naturalist 149:563–572.Google Scholar
Holt, R. D., Barfield, M., and Gomulkiewicz, R. 2004. Temporal variation can facilitate niche evolution in harsh sink environments. American Naturalist 164:187–200.Google Scholar
Jackson, J. B. C. 1974. Biogeographic consequences of eurytopy and stenotopy among marine bivalves and their evolutionary significance. American Naturalist 108:541–560.Google Scholar
Kawecki, T. J. 2004. Ecological and evolutionary consequences of source-sink population dynamics. Pp. 387–414 in Hanski, I., and Gaggiotti, O. E., eds. Ecology, genetics, and evolution of metapopulations. Elsevier/Academic Press, New York.Google Scholar
Kohn, A. J. 1980. Conus kahiko, a new Pleistocene gastropod from Oahu, Hawaii. Journal of Paleontology 54:534–541.Google Scholar
Marquet, R. 1997. Pliocene gastropod faunas from Kallo (oost-Vlaanderen, Belgium)—Part 3. Caenogastropoda: Aporrhaidae to Muricidae, and Part 4. Buccinidae to Helicidae. Contributions to Tertiary and Quaternary Geology 34:69–149.Google Scholar
Marquet, R., Grigis, M., and Landau, B. M. 2002. Aporrhais dingdenensis, a new species from the Miocene of the North Sea Basin (Gastropoda, Caenogastropoda, Aporrhaidae). Basteria 66:149–161.Google Scholar
Moerdijk, P. W., and van Nieulande, F. A. D. 2000. Revision of Pliocene Glycymerididae (Mollusca, Bivalvia) from the North Sea Basin. Contributions to Tertiary and Quaternary Geology 37:3–21.Google Scholar
Solsona, M., Gili, C., and Martinell, J. 2000. Patterns of change in the biogeographic distribution of Atlanto-Mediterranean Aporrhaidae (Gastropoda) from the Neogene to the present. Palaeogeography, Palaeoclimatology, Palaeoecology 158:83–97.Google Scholar
Strauch, F. 1972. Phylogenese, Adaptation und Migration einiger nordischer mariner Molluskengenera (Neptunea, Panomya, Cyrtodaria und Mya). Abhandlungen der Senckenbergischen Naturforschenden Gesellschaft 531:1–211.Google Scholar
Templeton, A. R. 2002. Out of Africa again and again. Nature 416:45–51.Google Scholar
Thompson, J. N. 1994. The coevolutionary process. University of Chicago Press, Chicago.CrossRefGoogle Scholar
Thompson, J. N. 1998. The population biology of coevolution. Researches on Population Ecology 40:159–166.Google Scholar
Thompson, J. N. 1999a. Coevolution and escalation: are ongoing coevolutionary meanderings important? American Naturalist 153:S92–S93.Google Scholar
Thompson, J. N. 1999b. The evolution of species interactions. Science 284:2116–2118.Google Scholar
Thompson, J. N., and Cunningham, B. M. 2002. Geographic structure and dynamics of coevolutionary selection. Nature 417:735–738.Google Scholar
Vermeij, G. J. 1980. Drilling predation of bivalves in Guam: some paleoecological implications. Malacologia 19:329–334.Google Scholar
Vermeij, G. J. 1986. Survival during biotic crises: the properties and evolutionary significance of refuges. Pp. 231–246 in Elliott, D. K., ed. Dynamics of extinction. Wiley, New York.Google Scholar
Vermeij, G. J. 1987. Evolution and escalation: an ecological history of life. Princeton University Press, Princeton, N.J. Google Scholar
Vermeij, G. J. 1991. When biotas meet: understanding biotic interchange. Science 253:1099–1104.Google Scholar
Vermeij, G. J. 2002. The geography of evolutionary opportunity: hypothesis and two cases in gastropods. Integrative and Comparative Biology 42:935–940.Google Scholar
Vermeij, G. J. 2004. Nature: an economic history. Princeton University Press, Princeton, N.J. Google Scholar
Vermeij, G. J. 2005. Invasion as expectation: a historical fact of life. Pp. 315–339 in Sax, D. F., Stachowicz, J. J., and Gaines, S. D., eds. Species invasions: insights into ecology, evolution, and biogeography. Sinauer, Sunderland, Mass. Google Scholar