Eocene–Oligocene extinction event

The Eocene–Oligocene extinction event, also called the Eocene-Oligocene transition or Grande Coupure (French for "great cut"), is the transition between the end of the Eocene and the beginning of the Oligocene, an extinction event and faunal turnover occurring between 33.9 and 33.4 million years ago[1] marked by large-scale extinction and floral and faunal turnover (although minor in comparison to the largest mass extinctions).[2] Most of the affected organisms were marine or aquatic in nature. They included the last of the ancient ungulates, the "condylarths".

E-OG
Marine extinction intensity during the Phanerozoic
%
Millions of years ago
Eocene–Oligocene extinction is labeled E–OG.

This was a time of major climatic change, especially cooling, not clearly caused by any single major impact or volcanic event.[3] Extended volcanic activity is one possible cause. Another speculation points to several large meteorite impacts near this time, including those of the Chesapeake Bay crater 40 km (25 mi) and the Popigai impact structure 100 km (62 mi) of central Siberia, which scattered debris perhaps as far as Europe. New dating of the Popigai meteor strengthens its association with the extinction.[4]

Causes

Glaciation

A leading model of climate cooling at this time predicts a decrease in atmospheric carbon dioxide, which slowly declined over the course of the Middle to Late Eocene.[5][6] Significant cooling took place in the final hundreds of thousands of years prior to the start of major Antarctic glaciation.[7] This cooling reached some threshold approximately 34 million years ago,[8][9][10] precipitating the formation of a large ice sheet in East Antarctica in response to falling carbon dioxide levels.[11][12] Though ephemeral ice sheets may have existed on the Antarctic continent during parts of the Middle and Late Eocene,[10] this interval of severe global cooling marked the beginning of permanent ice sheet coverage of Antarctica,[13][14] and thus the end of the greenhouse climate of the Early Palaeogene and the beginning of the Late Cenozoic Ice Age.[15]

Evidence points to the glaciation of Antarctica occurring in two steps, with the first step, the less pronounced and more modest step of the two, taking place at the Eocene-Oligocene boundary itself. This first step is referred to as EOT-1.[10] The Oligocene Oi-1 event, an oxygen isotope excursion that occurred around 33.55 million years ago,[16] was the second major pulse of Antarctic ice sheet formation.[10]

Effects on life

Grande Coupure

The Grande Coupure, or 'great break' in French,[17] with a major European turnover in mammalian fauna about 33.5 Ma, marks the end of the last phase of Eocene assemblages, the Priabonian, and the arrival in Europe of Asian species. The Grande Coupure is characterized by widespread extinctions and allopatric speciation in small isolated relict populations.[18] It was given its name in 1910 by the Swiss palaeontologist Hans Georg Stehlin,[19] to characterise the dramatic turnover of European mammalian fauna, which he placed at the Eocene–Oligocene boundary. A comparable turnover in Asian fauna has since been called the "Mongolian Remodelling".

The Grande Coupure marks a break between endemic European faunas before the break and mixed faunas with a strong Asian component afterwards. J. J. Hooker and his team summarized the break:[20]

"Pre-Grande Coupure faunas are dominated by the perissodactyl family Palaeotheriidae (distant horse relatives), six families of artiodactyls (cloven-hoofed mammals) (Anoplotheriidae, Xiphodontidae, Choeropotamidae, Cebochoeridae, Dichobunidae and Amphimerycidae), the rodent family Pseudosciuridae, the primate families Omomyidae and Adapidae, and the archontan family Nyctitheriidae.
"Post-Grande Coupure faunas include the true rhinoceros (family Rhinocerotidae), three artiodactyl families (Entelodontidae, Anthracotheriidae and Gelocidae) related respectively to pigs, hippos and ruminants, the rodent families Eomyidae, Cricetidae (hamsters) and Castoridae (beavers), and the lipotyphlan family Erinaceidae (hedgehogs). The speciose genus Palaeotherium plus Anoplotherium and the families Xiphodontidae and Amphimerycidae were observed to disappear completely.
"Only the marsupial family Herpetotheriidae, the artiodactyl family Cainotheriidae, and the rodent families Theridomyidae and Gliridae (dormice) crossed the faunal divide undiminished."

It has been suggested that this was caused by climate change associated with the earliest polar glaciations[21] and a major fall in sea levels, or by competition with taxa dispersing from Asia. However, few argue for an isolated single cause. Other possible causes are related to the impact of one or more large bolides in northern hemisphere at Popigai, Toms Canyon and Chesapeake Bay. Improved correlation of northwest European successions to global events[20] confirms the Grande Coupure as occurring in the earliest Oligocene, with a hiatus of about 350 millennia prior to the first record of post-Grande Coupure Asian immigrant taxa.

An element of the paradigm of the Grande Coupure was the apparent extinction of all European primates at the Coupure. However, the 1999 discovery[22] of a mouse-sized early Oligocene omomyid, reflecting the better survival chances of small mammals, undercut the Grand Coupure paradigm.

Evidence in the world's ocean current system indicates an abrupt cooling from 34.1 to 33.6 Ma across the Eocene–Oligocene boundary at 33.9 Ma. The remarkable cooling period in the ocean is correlated with pronounced mammalian faunal replacement within continental Asia as well. The Asian biotic reorganization events are comparable to the Grande Coupure in Europe and the Mongolian Remodeling of mammalian communities.[23] The global cooling is also correlated with marked drying conditions in low-latitudes Asia.[24]

In the marine realm, the frequency of drilling in recovery faunas, especially among bivalves, was drastically higher than in assemblages before the extinction event, a phenomenon attributed to a high extinction rate among escalated prey taxa with highly evolved defences against predators.[25] Veneroid bivalves experienced a short-term size increase during the biotic recovery.[26] Orthophragminid foraminifera disappeared in the extinction event; in Alpine carbonates, bryozoan facies show an expansion in response to the loss of orthophragminids.[27]

Some sites contain evidence that the Eocene–Oligocene extinction was not a sudden event but a prolonged biotic transition drawn out over as much as 6 million years. Localities near Eugene, Oregon, record a plant extinction 33.4 Ma and a marine invertebrate turnover 33.2 Ma; both of these turnovers post-date the supposed extinction event by hundreds of thousands of years.[28]

References

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  2. Ivany, Linda C.; Patterson, William P.; Lohmann, Kyger C. (2000). "Cooler winters as a possible cause of mass extinctions at the Eocene/Oligocene boundary" (PDF). Nature. 407 (6806): 887–890. Bibcode:2000Natur.407..887I. doi:10.1038/35038044. hdl:2027.42/62707. PMID 11057663. S2CID 4408282.
  3. Molina, Eustoquio; Gonzalvo, Concepción; Ortiz, Silvia; Cruz, Luis E. (2006-02-28). "Foraminiferal turnover across the Eocene–Oligocene transition at Fuente Caldera, southern Spain: No cause–effect relationship between meteorite impacts and extinctions". Marine Micropaleontology. 58 (4): 270–286. Bibcode:2006MarMP..58..270M. doi:10.1016/j.marmicro.2005.11.006.
  4. "Russia's Popigai Meteor Crash Linked to Mass Extinction". June 16, 2014.
  5. Villa, Giuliana; Fioroni, Chiara; Persico, Davide; Roberts, Andrew P.; Florindo, Fabio (20 December 2013). "Middle Eocene to Late Oligocene Antarctic glaciation/deglaciation and Southern Ocean productivity". Paleoceanography and Paleoclimatology. 29 (3): 223–237. doi:10.1002/2013PA002518. Retrieved 17 March 2023.
  6. Cappelli, C.; Bown, P. R.; Westerhold, T.; Bohaty, S. M.; De Riu, M.; Loba, V.; Yamamoto, Y.; Agnini, C. (15 November 2019). "The Early to Middle Eocene Transition: An Integrated Calcareous Nannofossil and Stable Isotope Record From the Northwest Atlantic Ocean (Integrated Ocean Drilling Program Site U1410)". Paleoceanography and Paleoclimatology. 34 (12): 1913–1930. Bibcode:2019PaPa...34.1913C. doi:10.1029/2019PA003686. S2CID 210245165. Retrieved 17 March 2023.
  7. Evans, David; Wade, Bridget S.; Henehan, Michael; Erez, Jonathan; Müller, Wolfgang (6 April 2016). "Revisiting carbonate chemistry controls on planktic foraminifera Mg / Ca: implications for sea surface temperature and hydrology shifts over the Paleocene–Eocene Thermal Maximum and Eocene–Oligocene transition". Climate of the Past. 12 (4): 819–835. Bibcode:2016CliPa..12..819E. doi:10.5194/cp-12-819-2016. Retrieved 5 April 2023.
  8. Hutchinson, David K.; Coxall, Helen K.; Lunt, Daniel J.; Steinthorsdottir, Margret; De Boer, Agatha M.; Baatsen, Michiel; Von der Heydt, Anna; Huber, Matthew; Kennedy-Asser, Alan T.; Kunzmann, Lutz; Ladant, Jean-Baptiste; Lear, Caroline H.; Moraweck, Karolin; Pearson, Paul N.; Piga, Emanuela; Pound, Matthew J.; Salzmann, Ulrich; Scher, Howie D.; Sijp, Willem P.; Śliwińska, Kasia K.; Wilson, Paul A.; Zhang, Zhongshi (28 January 2021). "The Eocene–Oligocene transition: a review of marine and terrestrial proxy data, models and model–data comparisons". Climate of the Past. 17 (1): 269–315. Bibcode:2021CliPa..17..269H. doi:10.5194/cp-17-269-2021. S2CID 234099337. Retrieved 17 March 2023.
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  13. Zachos, James C.; Quinn, Terrence M.; Salamy, Karen A. (1996-06-01). "High-resolution (104 years) deep-sea foraminiferal stable isotope records of the Eocene-Oligocene climate transition". Paleoceanography and Paleoclimatology. 11 (3): 251–266. Bibcode:1996PalOc..11..251Z. doi:10.1029/96PA00571. ISSN 1944-9186. Retrieved 17 March 2023.
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  17. also termed the MP 21 event.
  18. Called "dispersal-generated origination" in Hooker et al. 2004
  19. Stehlen, H.G. (1910). "Remarques sur les faunules de Mammifères des couches eocenes et oligocenes du Bassin de Paris". Bulletin de la Société Géologique de France. 4 (9): 488–520.
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  21. A major cooling event preceded the Grande Coupure, based on pollen studies in the Paris Basin conducted by Chateauneuf (J.J. Chateauneuf, 1980. "Palynostratigraphie et paleoclimatologie de l'Éocene superieur et de l'Oligocene du Bassin de Paris (France)" in Mémoires du Bureau de Recherches Géologiques et Minières, 116 1980).
  22. Köhler, M; Moyà-Solà, S (December 1999). "A finding of Oligocene primates on the European continent". Proceedings of the National Academy of Sciences of the United States of America. 96 (25): 14664–7. Bibcode:1999PNAS...9614664K. doi:10.1073/pnas.96.25.14664. ISSN 0027-8424. PMC 24493. PMID 10588762.
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  25. Kelley, Patricia H.; Hansen, Thor A. (4 April 1996). "Recovery of the naticid gastropod predator–prey system from the Cretaceous–Tertiary and Eocene–Oligocene extinctions". Geological Society, London, Special Publications. 102 (1): 373–386. Bibcode:1996GSLSP.102..373K. doi:10.1144/gsl.sp.1996.001.01.27. S2CID 129920064. Retrieved 16 April 2023.
  26. Lockwood, Rowan (1 January 2005). "Body size, extinction events, and the early Cenozoic record of veneroid bivalves: a new role for recoveries?". Paleobiology. 31 (4): 578–590. doi:10.1666/0094-8373(2005)031[0578:BSEEAT]2.0.CO;2. Retrieved 16 April 2023.
  27. Nebelsick, James H.; Rasser, Michael W.; Bassi, Davide (5 July 2005). "Facies dynamics in Eocene to Oligocene circumalpine carbonates". Facies. 51 (1–4): 197–217. doi:10.1007/s10347-005-0069-2. S2CID 140576829. Retrieved 10 May 2023.
  28. Retallack, Gregory J.; Orr, William N.; Prothero, Donald Ross; Duncan, Robert A.; Kester, Paul R.; Ambers, Clifford P. (1 July 2004). "Eocene–Oligocene extinction and paleoclimatic change near Eugene, Oregon". Geological Society of America Bulletin. 116 (7–8): 817–839. Bibcode:2004GSAB..116..817R. doi:10.1130/B25281.1. Retrieved 16 April 2023.
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