Skip to main content Accessibility help
×
Hostname: page-component-8448b6f56d-c47g7 Total loading time: 0 Render date: 2024-04-19T02:06:33.575Z Has data issue: false hasContentIssue false

3 - Mass extinctions in plant evolution

Published online by Cambridge University Press:  18 December 2009

Scott L. Wing
Affiliation:
Department of Paleobiology, Smithsonian Institution, Washington, DC, USA
Paul D. Taylor
Affiliation:
Natural History Museum, London
Get access

Summary

INTRODUCTION

Mass extinctions generally are recognized as major features in the history of life. They sweep aside diverse, sometimes even dominant groups of organisms, freeing up resources that can then fuel the diversification and rise to dominance of lineages that survived the mass extinction. This view of the history of life has been developed in large part from the study of shelly marine animals, and to a lesser extent from studies of terrestrial vertebrates (e.g. Valentine, 1985). By compiling data on the stratigraphic ranges of genera and families of marine animals, palaeontologists have been able to recognize the ‘Big Five’ mass extinctions, occurring at the end of the Ordovician, in the Late Devonian and at the end of the Permian, Triassic and Cretaceous periods (e.g. Sepkoski, 1993; Chapters 1 and 5). Each of these episodes is a geologically sudden decrease in taxonomic diversity. Terrestrial vertebrates also show major declines in taxonomic diversity at the end of the Permian and at the end of the Cretaceous (Benton, 1993). In contrast, compilations of the stratigraphic ranges of species of land plants do not show major declines in diversity (Niklas et al., 1980, 1985; Niklas and Tiffney, 1994; Figure 3.1). The absence of major declines in the diversity of land plants as represented in these compilations of stratigraphic ranges has led to the suggestion that plants are more resistant to mass extinctions than animals (Niklas et al., 1980; Knoll, 1984; Traverse, 1988).

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2004

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Alvarez, L. W., Alvarez, W., Asaro, F. and Michel, H. V., 1980. Extraterrestrial cause for the Cretaceous–Tertiary extinctions. Science 208: 1095–108CrossRefGoogle Scholar
Benton, M. J. (Ed.) 1993. The Fossil Record, 2nd edn. London: Chapman and Hall
Claeys, P., Kiessling, W. and Alvarez, W., 2002. Distribution of Chicxulub ejecta at the Cretaceous–Tertiary boundary. In: C. Koeberl and K. G. MacLeod (Eds.), Catastrophic events and mass extinctions: impacts and beyond. Geological Society of America Special Paper 356: 55–68
Clark, J. S., Fastie, C., Hurtt, G.et al., 1998. Reid's paradox of rapid plant migration. BioScience 48: 13–24CrossRefGoogle Scholar
Clyde, W. C. and Gingerich, P. D., 1998. Mammalian community response to the latest Paleocene thermal maximum: an isotaphonomic study in the northern Bighorn Basin, Wyoming. Geology 26: 1011–10142.3.CO;2>CrossRefGoogle Scholar
Collinson, M. E., Boulter, M. C. and Holmes, P. L., 1993. Magnoliophyta (‘Angiospermae’). In: M. J. Benton (Ed.), The Fossil Record, 2nd edn. London: Chapman & Hall, pp. 809–841
Crane, P. and Lidgard, S., 1989. Angiosperm diversification and paleolatitudinal gradients in Cretaceous floristic diversity. Science 246: 675–678CrossRefGoogle ScholarPubMed
Crepet, W. L. and Nixon, K. C., 1998. Fossil Clusiaceae from the late Cretaceous (Turonian) of New Jersey and implications regarding the history of bee pollination. American Journal of Botany 85: 1122–1133CrossRefGoogle ScholarPubMed
Crouch, E. M., 2001. Environmental change at the time of the Paleocene–Eocene biotic turnover. Laboratory of Palaeobotany and Palynology Contributions Series 14: 1–216Google Scholar
Crouch, E. M., Heilmann-Clausen, C., Brinkhuis, H.et al., 2001. Global dinoflagellate event associated with the late Paleocene thermal maximum. Geology 29: 315–3182.0.CO;2>CrossRefGoogle Scholar
Crouch, E. M. and Visscher, H., 2003. Terrestrial vegetation from across the Initial Eocene Thermal Maximum at the Tawanui marine section, New Zealand. In: S. L. Wing, P. D. Gingerich, B. Schmitz and E. Thomas (Eds.), Causes and consequences of early Paleogene warm climates. Geological Society of America Special Paper 369: 351–364
Dickens, G. R., Castillo, M. M. and Walker, J. C. G., 1997. A blast of gas in the latest Paleocene: simulating first-order effects of massive dissociation of oceanic methane hydrate. Geology 25: 259–2622.3.CO;2>CrossRefGoogle ScholarPubMed
DiMichele, W. A. and Aronson, R. B. 1992. The Pennsylvanian–Permian vegetational transition: a terrestrial analogue to the onshore–offshore hypothesis. Evolution 46: 807–824CrossRefGoogle ScholarPubMed
DiMichele, W. A. and Phillips, T. L., 1996. Climate change, plant extinctions, and vegetational recovery during the middle–late Pennsylvanian transition: the case of tropical peat-forming environments in North America. In: M. L. Hart, (Ed.), Biotic Recovery from Mass Extinctions. London: Geological Society of London, pp. 201–221
Edwards, D. and Wellman, C., 2000. Embryophytes on land: the Ordovician to Lochkovian (lower Devonian) record. In: P. G. Gensel and D. Edwards (Eds.), Plants Invade the Land. New York: Columbia University Press, pp. 3–28
Erwin, D. H., Bowring, S. A. and Yugan, J., 2002. End-Permian mass extinctions: a review. In: C. Koeberl and K. G. MacLeod (Eds.), Catastrophic events and mass extinctions: impacts and beyond. Geological Society of America Special Paper 356: 363–383
Frederiksen, N. O., 1972. The rise of the Mesophytic flora. Geoscience and Man 4: 17–28CrossRefGoogle Scholar
Frederiksen, N. O. 1994. Paleocene floral diversities and turnover events in eastern North America and their relation to diversity models. Review of Palaeobotany and Palynology 82: 225–238CrossRefGoogle Scholar
Gingerich, P. D., 1989. New earliest Wasatchian mammalian fauna from the Eocene of northwestern Wyoming: composition and diversity in a rarely sampled high-floodplain assemblage. University of Michigan Papers on Paleontology 28: 1–97Google Scholar
Harrington, G. J., 2003. Geographic patterns in the floral response to Paleocene–Eocene warming. In: S. L. Wing, P. D. Gingerich, B. Schmitz, and E. Thomas, E. (Eds.), Causes and consequences of early Paleogene warm climates. Geological Society of America Special Paper 369: 381–394
Hildebrand, A. R., Penfield, G. T., Kring, D. A.et al., 1991. Chicxulub Crater: a possible Cretaceous/Tertiary boundary impact crater on the Yucatan Peninsula, Mexico. Geology 19: 867–8712.3.CO;2>CrossRefGoogle Scholar
Hotton, C. L., 2002. Palynology of the Cretaceous–Tertiary boundary in central Montana: evidence for extraterrestrial impact as a cause of the terminal Cretaceous extinctions. In: J. H. Hartman, K. R. Johnson and D. J. Nichols (Eds.), The Hell Creek Formation and the Cretaceous–Tertiary boundary in the northern Great Plains: an integrated continental record of the end of the Cretaceous. Geological Society of America Special Paper 361: 473–502
Jackson, S. T. and Overpeck, J. T., 2000. Responses of plant populations and communities to environmental changes of the Late Quaternary. Paleobiology 26: 194–220CrossRefGoogle Scholar
Jaramillo, C. A. and Dilcher, D. L., 2000. Microfloral diversity patterns of the late Paleocene–Eocene interval in Colombia. Geology 28: 815–8182.0.CO;2>CrossRefGoogle Scholar
Johnson, K. R., 1992. Leaf-fossil evidence for extensive floral extinction at the Cretaceous–Tertiary boundary, North Dakota, USA. Cretaceous Research 13: 91–117CrossRefGoogle Scholar
Johnson, K. R. 2002. Megaflora of the Hell Creek and lower Fort Union Formations in the western Dakotas: vegetational response to climate change, the Cretaceous-Tertiary boundary event, and rapid marine transgression. In: J. H. Hartman, K. R. Johnson and D. J. Nichols (Eds.), The Hell Creek Formation and the Cretaceous–Tertiary boundary in the northern Great Plains: an integrated continental record of the end of the Cretaceous. Geological Society of America Special Paper 361: 329–392
Johnson, K. R. and Hickey, L. J., 1990. Megafloral change across the Cretaceous/Tertiary boundary in the northern Great Plains and Rocky Mountains, U.S.A. In: V. L. Sharpton and P. D. Ward (Eds.), Global catastrophes in earth history: an interdisciplinary conference on impacts, volcanism, and mass mortality. Geological Society of America Special Paper 247: 433–444
Johnson, K. R., Nichols, D., Attrep, M. J. and Orth, C., 1989. High-resolution leaf-fossil record spanning the Cretaceous–Tertiary boundary. Nature 340: 708–711CrossRefGoogle Scholar
Jolley, D. W., 1998. Palynostratigraphy and depositional history of the Palaeocene Ormesby/Thanet depositional sequence set in southeastern England and its correlation with continental West Europe. Review of Palaeobotany and Palynology 99: 265–315CrossRefGoogle Scholar
Kelly, D. C., Bralower, T. J. and Zachos, J. C., 1998. Evolutionary consequences of the latest Paleocene thermal maximum for tropical planktonic foraminifera. Palaeogeography, Palaeoclimatology, Palaeoecology 141: 139–161CrossRefGoogle Scholar
Kenrick, P. and Crane, P. R., 1997. The Origin and Early Diversification of Land Plants: a Cladistic Study. Washington: Smithsonian Institution Press
Kerp, H., 2000. The modernization of landscapes during the late Paleozoic–early Mesozoic. In: R. A. Gastaldo and W. A. DiMichele (Eds.), Terrestrial ecosystems, a short course. The Paleontological Society Papers 6: 79–113
Knoll, A. H., 1984. Patterns of extinction in the fossil record of vascular plants. In: M. H. Nitecki (Ed.), Extinctions. Chicago: The University of Chicago Press, pp. 21–68
Lidgard, S. and Crane, P., 1990. Angiosperm diversification and Cretaceous floristic trends: a comparison of palynofloras and leaf macrofloras. Paleobiology 16: 77–93CrossRefGoogle Scholar
Lomax, B. H., Beerling, D. J., Upchurch, G. R. Jr and Otto-Bliesner, B. L., 2000. Terrestrial ecosystem responses to global environmental change across the Cretaceous–Tertiary boundary. Geophysical Research Letters 27: 2149–2152CrossRefGoogle Scholar
Looy, C. V., Brugman, W. A., Dilcher, D. L. and Visscher, H., 1999. The delayed resurgence of equatorial forests after the Permian–Triassic ecologic crisis. Proceedings of the National Academy of Science 96: 13857–13862CrossRefGoogle ScholarPubMed
Lupia, R., Lidgard, S. and Crane, P. R., 1999. Comparing palynological abundance and diversity: implications for biotic replacement during the Cretaceous angiosperm radiation. Paleobiology 25: 305–340CrossRefGoogle Scholar
Magallon, S., Crane, P. R. and Herendeen, P. S., 1999. Phylogenetic pattern, diversity, and diversification of eudicots. Annals of the Missouri Botanical Garden 86: 297–372CrossRefGoogle Scholar
Nichols, D. J. and Fleming, R. F., 1990. Plant microfossil record of the terminal Cretaceous event in the western United States and Canada. In: V. L. Sharpton and P. D. Ward (Eds.), Global catastrophes in earth history: an interdisciplinary conference on impacts, volcanism, and mass mortality. Geological Society of America Special Paper 247: 445–456
Nichols, D. J. and Johnson, K. R., 2002. Palynology and microstratigraphy of Cretaceous–Tertiary boundary sections in southwestern North Dakota. In: J. H. Hartman, K. R. Johnson and D. J. Nichols (Eds.), The Hell Creek Formation and the Cretaceous–Tertiary boundary in the northern Great Plains: an integrated continental record of the end of the Cretaceous. Geological Society of America Special Paper 361: 95–144
Niklas, K. J., 1997. The Evolutionary Biology of Plants. University of Chicago Press: Chicago and London
Niklas, K. J. and Tiffney, B. H., 1994. The quantification of plant biodiversity through time. Philosophical Transactions of the Royal Society, London, Series B 345: 35–44CrossRefGoogle Scholar
Niklas, K. J., Tiffney, B. H. and Knoll, A. H., 1980. Apparent changes in the diversity of fossil plants. Evolutionary Biology 12: 1–89Google Scholar
Niklas, K. J., Tiffney, B. H. and Knoll, A. H. 1985. Patterns in vascular land plant diversification: an analysis at the species level. In: J. W. Valentine (Ed.), Phanerozoic Diversity Patterns: Profiles in Macroevolution. Princeton: Princeton University Press, pp. 97–128
Norris, R. D. and Firth, J. V., 2002. Mass wasting of Atlantic continental margins following the Chicxulub impact event. In: C. Koeberl and K. G. MacLeod (Eds.), Catastrophic events and mass extinctions: impacts and beyond. Geological Society of America Special Paper356: 79–95
O'Keefe, J. D. and Ahrens, T. J., 1989. Impact production of CO2 by the Cretaceous–Tertiary extinction bolide and the resultant heating of the Earth. Nature 338: 247–249CrossRefGoogle Scholar
Orth, C., Gilmore, J., Knight, J., Pillmore, C., Tschudy, R. and Fassett, J., 1981. An iridium abundance anomaly at the palynological Cretaceous–Tertiary boundary in northern New Mexico. Science 214: 1341–1342CrossRefGoogle ScholarPubMed
Page, C. N., 2002. Ecological strategies in fern evolution: a neopteridological overview. Review of Palaeobotany and Palynology 119: 1–33CrossRefGoogle Scholar
Pocknall, D. T., 1987. Paleoenvironments and age of the Wasatch Formation (Eocene), Powder River Basin, Wyoming. Palaios 2: 368–376CrossRefGoogle Scholar
Pollack, J. B., Toon, O. B., Ackerman, T. P., McKay, C. P. and Turco, R. P., 1983. Environmental effects of an impact-generated dust cloud: implications for the Cretaceous–Tertiary extinctions. Science 219: 287–289CrossRefGoogle ScholarPubMed
Pope, K. O., 2002. Impact dust not the cause of the Cretaceous–Tertiary mass extinction. Geology 30: 99–1022.0.CO;2>CrossRefGoogle Scholar
Pope, K. O., Baines, K. H., Ocampo, A. C. and Ivanov, B. A., 1994. Impact winter and the Cretaceous/Tertiary extinctions: results of a Chicxulub asteroid impact model. Earth and Planetary Science Letters 128: 719–725CrossRefGoogle Scholar
Rees, P. M., 2002. Land-plant diversity and the end-Permian mass extinction. Geology 30: 827–8302.0.CO;2>CrossRefGoogle Scholar
Retallack, G. J., 1995. Permian–Triassic life crisis on land. Science 267: 77–80CrossRefGoogle ScholarPubMed
Retallack, G. J., Veevers, J. J. and Morante, R., 1996. Global coal gap between Permian–Triassic extinction and Middle Triassic recovery of peat-forming plants. Geological Society of America Bulletin 108: 195–2072.3.CO;2>CrossRefGoogle Scholar
Rothwell, G. W., Grauvogel-Stamm, L. and Mapes, G., 2000. An herbaceous fossil conifer: gymnospermous ruderals in the evolution of Mesozoic vegetation. Palaeogeography, Palaeoclimatology, Palaeoecology 156: 139–145CrossRefGoogle Scholar
Rowley, D., Raymond, A., Parrish, J., Lottes, A., Scotese, C. and Ziegler, A., 1985. Carboniferous paleogeographic, phytogeographic, and paleoclimatic reconstructions. International Journal of Coal Geology 5: 7–42CrossRefGoogle Scholar
Rull, V., 1999. Palaeofloristic and palaeovegetational changes across the Paleocene/Eocene boundary in northern South America. Review of Palaeobotany and Palynology 107: 83–95CrossRefGoogle Scholar
Schultz, P. H. and D'Hondt, S., 1996. Cretaceous–Tertiary (Chicxulub) impact angle and its consequences. Geology 24: 963–9672.3.CO;2>CrossRefGoogle Scholar
Sepkoski, J. J. Jr, 1993. Ten years in the library: new data confirm paleontological patterns. Paleobiology 19: 43–51CrossRefGoogle ScholarPubMed
Shen-Miller, J., Mudgett, M. B., Schopf, J. W., Clarke, S. and Berger, R. 1995. Exceptional seed longevity and robust growth: ancient sacred lotus from China. American Journal of Botany 82: 1367–1380CrossRefGoogle Scholar
Strother, P. K., 2000. Cryptospores: the origin and early evolution of the terrestrial flora. In: R. A. Gastaldo and W. A. DiMichele (Eds.), Phanerozoic terrestrial ecosystems. The Paleontological Society Special Papers 6: 3–20
Sweet, A. R., 2001. Plants, a yardstick for measuring the environmental consequences of the Cretaceous–Tertiary boundary event. Geoscience Canada 28: 127–138Google Scholar
Sweet, A. R., Braman, D. R. and Lerbekmo, J. F., 1999. Sequential palynological changes across the composite Cretaceous–Tertiary (K–T) boundary claystone and contiguous strata, western Canada and Montana, USA. Canadian Journal of Earth Sciences 36: 743–768CrossRefGoogle Scholar
Traverse, A., 1988. Plant evolution dances to a different beat: plant and animal evolutionary mechanisms compared. Historical Biology 1: 277–301CrossRefGoogle Scholar
Tschudy, R., Pillmore, C., Orth, C., Gilmore, J. and Knight, J., 1984. Disruption of the terrestrial plant ecosystem at the Cretaceous–Tertiary boundary, Western Interior. Science 225: 1030–1032CrossRefGoogle ScholarPubMed
Twitchett, R. J., Looy, C. V., Morante, R., Visscher, H. and Wignall, P. B., 2001. Rapid and synchronous collapse of marine and terrestrial ecosystems during the end-Permian biotic crisis. Geology 29: 351–3542.0.CO;2>CrossRefGoogle Scholar
Vajda, V., Raine, J. I. and Hollis, C. J., 2001. Indication of global deforestation at the Cretaceous–Tertiary boundary by New Zealand fern spike. Science 294: 1700–1702CrossRefGoogle ScholarPubMed
Valentine, J. W. 1985. Phanerozoic Diversity Patterns: Profiles in Macroevolution. Princeton: Princeton University Press
Visscher, H., Brinkhuis, H., Dilcher, D. L.et al., 1996. The terminal Paleozoic fungal event: evidence of terrestrial ecosystem destabilization and collapse. Proceedings of the National Academy of Sciences 93: 2155–2158CrossRefGoogle Scholar
Wing, S. L., 1998. Late Paleocene–early Eocene floral and climatic change in the Bighorn Basin, Wyoming. In: W. Berggren, M. P. Aubry and S. Lucas (Eds.), Late Paleocene–Early Eocene Biotic and Climatic Events. New York: Columbia University Press, pp. 380–400
Wing, S. L. 2000. Evolution and expansion of flowering plants. In: R. A. Gastaldo and W. A. DiMichele (Eds.), Terrestrial ecosystems, a short course. The Paleontological Society Papers 6: 209–232
Wing, S. L. and Harrington, G. J., 2001. Floral response to rapid warming in the earliest Eocene and implications for concurrent faunal change. Paleobiology 27: 539–5622.0.CO;2>CrossRefGoogle Scholar
Wing, S. L., Gingerich, P. D., Schmitz, B. and Thomas, E. (Eds.) 2003a. Causes and consequences of early Paleogene warm climates. Geological Society of America Special Paper 369, 624 pp
Wing, S. L., Harrington, G. J., Bowen, G. J. and Koch, P. L., 2003b. Floral change during the Initial Eocene Thermal Maximum in the Powder River Basin, Wyoming. In: S. L. Wing, P. D. Gingerich, B. Schmitz and E. Thomas (Eds.), Causes and consequences of early Paleogene warm climates. Geological Society of America Special Paper 369: 425–440
Wolbach, W. S., Gilmour, I., Anders, E., Orth, C. J. and Brooks, R. R., 1988. Global fire at the Cretaceous–Tertiary boundary. Nature 334: 665–669CrossRefGoogle Scholar
Wolfe, J. A., 1990. Palaeobotanical evidence for a marked temperature increase following the Cretaceous–Tertiary boundary. Nature 343: 153–156CrossRefGoogle Scholar
Wolfe, J. A. 1991. Palaeobotanical evidence for a June ‘impact winter’ at the Cretaceous/Tertiary boundary. Nature 352: 420–423CrossRefGoogle Scholar
Wolfe, J. A. and Upchurch, G. R. Jr, 1986. Vegetation, climatic and floral changes at the Cretaceous–Tertiary boundary. Nature 324: 148–152CrossRefGoogle Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

  • Mass extinctions in plant evolution
    • By Scott L. Wing, Department of Paleobiology, Smithsonian Institution, Washington, DC, USA
  • Edited by Paul D. Taylor, Natural History Museum, London
  • Book: Extinctions in the History of Life
  • Online publication: 18 December 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511607370.004
Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

  • Mass extinctions in plant evolution
    • By Scott L. Wing, Department of Paleobiology, Smithsonian Institution, Washington, DC, USA
  • Edited by Paul D. Taylor, Natural History Museum, London
  • Book: Extinctions in the History of Life
  • Online publication: 18 December 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511607370.004
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Mass extinctions in plant evolution
    • By Scott L. Wing, Department of Paleobiology, Smithsonian Institution, Washington, DC, USA
  • Edited by Paul D. Taylor, Natural History Museum, London
  • Book: Extinctions in the History of Life
  • Online publication: 18 December 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511607370.004
Available formats
×