Olson's Extinction

Olson's Extinction was a mass extinction that occurred 270 million years ago in the Early Guadalupian of the Permian period and which predated the Permian–Triassic extinction event.[1] Everett Olson noted that there was a hiatus and a sudden change in between the Early Permian and Middle/Late Permian faunas. Since then this event has been realized across many groups, including plants, marine invertebrates, and tetrapods.

Identification

The first evidence of extinction came when Everett C. Olson noted a hiatus between Early Permian faunas dominated by pelycosaurs and therapsid dominated faunas of the Middle and Late Permian. First considered to be a preservational gap in the fossil record, the event was originally dubbed 'Olson's Gap'.[2][3] To compound the difficulty in identifying the cause of the 'gap', researchers were having difficulty in resolving the uncertainty which exists regarding the duration of the overall extinction and about the timing and duration of various groups' extinctions within the greater process. Theories emerged which suggested the extinction was prolonged, spread out over a several million years[4] or that multiple extinction pulses preceded the Permian–Triassic extinction event.[1][5][6] The impact of Olson's Extinction amplified the effects of the Permian–Triassic extinction event and the final extinction killed off only about 80% of species alive at that time while the other losses occurred during the first pulse or the interval between pulses.

During the 1990s and 2000s researchers gathered evidence on the biodiversity of plants, marine organism and tetrapods that indicated an extinction pulse preceding the Permian–Triassic extinction event had a profound impact on life on land. On land Sahney and Benton showed that even discounting the sparse fossil assemblages from the extinction period, the event can be confirmed by the stages of time bracketing the event since well preserved sections of the fossil record from both before and after the event have been found and they referred to the event as 'Olson's Extinction'.[1] The 'Gap' was finally closed in 2012 when Michael Benton confirmed that the terrestrial fossil record of the Middle Permian is well represented by fossil localities in the American southwest and European Russia and that the gap is not an artifact of a poor rock record since there is no correlation between geological and biological records of the Middle Permian.[7]

Possible causes

There is no widely accepted theory for the cause of Olson's Extinction. Recent research has indicated that climate change may be a possible cause. Extreme environments were observed from the Permian of Kansas which resulted from a combination of hot climate and acidic waters particularly coincident with Olson’s Extinction.[8] Whether this climate change was a result of Earth's natural processes or exacerbated by another event is unknown.

Extinction patterns

On land

Plants

Plants showed large turnover in the Mid-Late Permian and into the Triassic. The duration of higher extinction rates (>60%) in land plants was about 23.4 Myr, starting from Olson's Extinction and into the early Middle Triassic.[9]

Tetrapods

The Permian was a time of rapid change for tetrapods; in particular there was a major changeover from faunas dominated by basal synapsids ("pelycosaurs”) and reptiliomorphs (Diadectes) to faunas dominated by therapsids (Dinocephalia, Anomodontia, Gorgonopsia, and Cynodontia) some of which were direct ancestors of mammals.[7] Edaphosauridae and Ophiacodontidae died out in an extinction event across the Kungurian/Roadian boundary, although Caseidae and Therapsida diversified.[10] In 2008 Sahney and Benton [1] confirmed that this was not just a turnover (gradual replacement of one faunal complex by another) but a real extinction event in which a significant drop in the biodiversity of tetrapods on a global scale and community level occurred.

In December 2011, the fossilized remains of the 'youngest' pelycosaur was described by Modesto et al. as from 260 million years ago in South Africa, the first evidence that one of these animals survived Olson’s Extinction.[11] This type of animal is called a disaster taxon, an organism that survives a major environmental disruption, perhaps forming the basis for a new adaptive radiation.

In the water

Sharks

Using data on chondrichthyan diversity, Koot showed that despite variability in the Permian–Triassic fossil record, the Lopingian is adequate in completeness, specifically, range-through genus diversity is not significantly correlated with the number of taxonomic occurrences. Genus diversity declined from the mid-Guadalupian following an increasing extinction rate, which intensified throughout the Lopingian. This supports a combined overall extinction as a result of the end-Guadalupian and Late Permian events.[12]

Recovery

Fauna did not recover fully from Olson's Extinction before the impact of the Permian-Triassic extinction event. Estimates of recovery time vary, where some authors indicated recovery was prolonged, lasting 30 million years into the Triassic.[1]

Several important events took place during Olson's Extinction, most notably the origin of therapsids, a group that includes the evolutionary ancestors of mammals. Further research on the recently identified primitive therapsid of the Xidagou Formation (Dashankou locality) in China of Roadian age may provide more information on this topic.[13]

References

  1. 1 2 3 4 5 Sahney, S.; Benton, M.J. (2008). "Recovery from the most profound mass extinction of all time" (PDF). Proceedings of the Royal Society: Biological. 275 (1636): 759–65. doi:10.1098/rspb.2007.1370. PMC 2596898Freely accessible. PMID 18198148.
  2. Lucas, S. G. (2004). "A global hiatus in the Middle Permian tetrapod fossil record" (PDF). Stratigraphy. 1: 47–64.
  3. Ivakhnenko, M. F. (2005). "Comparative survey of Lower Permian tetrapod faunas of eastern Europe and South Africa". Paleontological Journal. 39 (1): 66–71.
  4. Ward PD, Botha J, Buick R, De Kock MO, Erwin DH, Garrison GH, Kirschvink JL & Smith R (2005). "Abrupt and Gradual Extinction Among Late Permian Land Vertebrates in the Karoo Basin, South Africa". Science. 307 (5710): 709–714. Bibcode:2005Sci...307..709W. doi:10.1126/science.1107068. PMID 15661973.
  5. Retallack, G.J.; Metzger, C.A.; Greaver, T.; Jahren, A.H.; Smith, R.M.H.; Sheldon, N.D. (2006). "Middle-Late Permian mass extinction on land". Bulletin of the Geological Society of America. 118 (11–12): 1398–1411. Bibcode:2006GSAB..118.1398R. doi:10.1130/B26011.1.
  6. Rampino MR, Prokoph A & Adler A (2000). "Tempo of the end-Permian event: High-resolution cyclostratigraphy at the Permian–Triassic boundary". Geology. 28 (7): 643–646. Bibcode:2000Geo....28..643R. doi:10.1130/0091-7613(2000)28<643:TOTEEH>2.0.CO;2. ISSN 0091-7613.
  7. 1 2 Benton, M.J. (2012). "No gap in the Middle Permian record of terrestrial vertebrates". Geology. 40: 339–342. doi:10.1130/g32669.1.
  8. Zambito J.J. IV.; Benison K.C (2013). "Extreme high temperatures and paleoclimate trends recorded in Permian ephemeral lake halite". Geology. 41: 587–590. doi:10.1130/G34078.1.
  9. Xiong, C.; Wang, Q. (2011). "Permian–Triassic land-plant diversity in South China: Was there a mass extinction at the Permian/Triassic boundary?". Paleobiology. 37 (1): 157–167. doi:10.1666/09029.1.
  10. Brocklehurst, N.; Kammerer, C. F.; Fröbisch, J. (2013). "The early evolution of synapsids, and the influence of sampling on their fossil record". Paleobiology. 39 (3): 470–490. doi:10.1666/12049.
  11. Sean P. Modesto; Roger M. H. Smith; Nicolás E. Campione & Robert R. Reisz (2011). "The last "pelycosaur": a varanopid synapsid from the Pristerognathus Assemblage Zone, Middle Permian of South Africa". Naturwissenschaften. 98: 1027–34. doi:10.1007/s00114-011-0856-2. PMID 22009069.
  12. Koot, M.B. 2013. Effects of the late Permian mass extinction on chondrichthyan palaeobiodiversity and distribution patterns
  13. Liu, J.; Rubidge, B; Li, J. (2009). "New basal synapsid supports Laurasian origin for therapsids" (PDF). Acta Palaeontologica Polonica. 54 (3): 393–400. doi:10.4202/app.2008.0071.

Further reading

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