Correlated terrestrial and marine evidence for global climate changes before mass extinction at the Cretaceous–Paleogene boundary

Terrestrial climates near the time of the end-Cretaceous mass extinction are poorly known, limiting understanding of environmentally driven changes in biodiversity that occurred before bolide impact. We estimate paleotemperatures for the last ≈1.1 million years of the Cretaceous (≈66.6–65.5 million years ago, Ma) by using fossil plants from North Dakota and employ paleomagnetic stratigraphy to correlate the results to foraminiferal paleoclimatic data from four middle- and high-latitude sites. Both plants and foraminifera indicate warming near 66.0 Ma, a warming peak from ≈65.8 to 65.6 Ma, and cooling near 65.6 Ma, suggesting that these were global climate shifts. The warming peak coincides with the immigration of a thermophilic flora, maximum plant diversity, and the poleward range expansion of thermophilic foraminifera. Plant data indicate the continuation of relatively cool temperatures across the Cretaceous–Paleogene boundary; there is no indication of a major warming immediately after the boundary as previously reported. Our temperature proxies correspond well with recent pCO2 data from paleosol carbonate, suggesting a coupling of pCO2 and temperature. To the extent that biodiversity is correlated with temperature, estimates of the severity of end-Cretaceous extinctions that are based on occurrence data from the warming peak are probably inflated, as we illustrate for North Dakota plants. However, our analysis of climate and facies considerations shows that the effects of bolide impact should be regarded as the most significant contributor to these plant extinctions.

[1]  S. Dworkin,et al.  Paleosol barometer indicates extreme fluctuations in atmospheric CO2 across the Cretaceous-Tertiary boundary , 2002 .

[2]  Kirk R. Johnson,et al.  A Tropical Rainforest in Colorado 1.4 Million Years After the Cretaceous-Tertiary Boundary , 2002, Science.

[3]  D. Beerling,et al.  An atmospheric pCO2 reconstruction across the Cretaceous-Tertiary boundary from leaf megafossils , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[4]  D. Jablonski Survival without recovery after mass extinctions , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[5]  G. Keller,et al.  High stress late Maastrichtian paleoenvironment: inference from planktonic foraminifera in Tunisia , 2002 .

[6]  Peter Wilf,et al.  Impact of the terminal Cretaceous event on plant–insect associations , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[7]  R. Norris,et al.  Deep-sea paleotemperature record of extreme warmth during the Cretaceous , 2002 .

[8]  J. Raine,et al.  Indication of Global Deforestation at the Cretaceous-Tertiary Boundary by New Zealand Fern Spike , 2001, Science.

[9]  K. Miller,et al.  Paleobiogeography of Pseudotextularia elegans during the latest Maastrichtian global warming event , 2001 .

[10]  N. Pitman,et al.  Habitat-related error in estimating temperatures from leaf margins in a humid tropical forest. , 2001, American journal of botany.

[11]  Philip M. Novack-Gottshall,et al.  Effects of sampling standardization on estimates of Phanerozoic marine diversification , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[12]  P. Fullagar,et al.  Evidence for a small (∼0.000 030) but resolvable increase in seawater 87Sr/86Sr ratios across the Cretaceous-Tertiary boundary , 2001 .

[13]  D. Pearson,et al.  Palynologically calibrated vertebrate record from North Dakota consistent with abrupt dinosaur extinction at the Cretaceous-Tertiary boundary , 2001 .

[14]  M. Foote Origination and extinction components of taxonomic diversity: general problems , 2000, Paleobiology.

[15]  Y. Gallet,et al.  Cosmic markers, 40Ar/39Ar dating and paleomagnetism of the KT sections in the Anjar Area of the Deccan large igneous province , 2000 .

[16]  K. M. Gregory-Wodzicki,et al.  Relationships between leaf morphology and climate, Bolivia: implications for estimating paleoclimate from fossil floras , 2000, Paleobiology.

[17]  R. Hoffmann,et al.  Dinosaur abundance was not declining in a “3 m gap” at the top of the Hell Creek Formation, Montana and North Dakota , 2000 .

[18]  P. Wilf Late Paleocene–early Eocene climate changes in southwestern Wyoming: Paleobotanical analysis , 2000 .

[19]  J. Self‐Trail,et al.  Synchroneity of the K-T oceanic mass extinction and meteorite impact: Blake Nose, western North Atlantic , 1999 .

[20]  S. Manchester,et al.  Estimation of temperature and precipitation from morphological characters of dicotyledonous leaves. , 1998, American journal of botany.

[21]  G. Keller,et al.  Abrupt deep-sea warming at the end of the Cretaceous , 1998 .

[22]  M. Kučera,et al.  Terminal Cretaceous warming event in the mid-latitude South Atlantic Ocean: evidence from poleward migration of Contusotruncana contusa (planktonic foraminifera) morphotypes , 1998 .

[23]  P. Wilf When are leaves good thermometers? A new case for Leaf Margin Analysis , 1997, Paleobiology.

[24]  K. Gregory Are paleoclimate estimates biased by foliar physiognomic responses to increased atmospheric CO2 , 1996 .

[25]  D. Greenwood,et al.  Eocene continental climates and latitudinal temperature gradients , 1995 .

[26]  P. N. Shukla,et al.  Impact did not trigger Deccan volcanism: Evidence from Anjar K/T Boundary intertrappean sediments , 1995 .

[27]  J. A. Wolfe PALEOCLIMATIC ESTIMATES FROM TERTIARY LEAF ASSEMBLAGES , 1995 .

[28]  S. Kamo,et al.  U–Pb ages of single shocked zircons linking distal K/T ejecta to the Chicxulub crater , 1993, Nature.

[29]  D. Greenwood,et al.  Fossils and fossil climate: the case for equable continental interiors in the Eocene , 1993 .

[30]  Kirk R. Johnson Leaf-fossil evidence for extensive floral extinction at the Cretaceous-Tertiary boundary, North Dakota, USA , 1992 .

[31]  K. Caldeira,et al.  Carbon dioxide emissions from Deccan volcanism and a K/T boundary greenhouse effect. , 1990, Geophysical research letters.

[32]  L. Hickey,et al.  Megafloral change across the Cretaceous/Tertiary boundary in the northern Great Plains and Rocky Mountains, U.S.A. , 1990 .

[33]  J. A. Wolfe Palaeobotanical evidence for a marked temperature increase following the Cretaceous/Tertiary boundary , 1990 .

[34]  Kirk R. Johnson,et al.  High-resolution leaf-fossil record spanning the Cretaceous/Tertiary boundary , 1989, Nature.

[35]  J. A. Wolfe,et al.  Vegetation, climatic and floral changes at the Cretaceous-Tertiary boundary , 1986, Nature.

[36]  J. S. Gilmore,et al.  Disruption of the Terrestrial Plant Ecosystem at the Cretaceous-Tertiary Boundary, Western Interior , 1984, Science.

[37]  J. Erez,et al.  Experimental paleotemperature equation for planktonic foraminifera , 1983 .

[38]  J. Hutchison Turtle, crocodilian, and champsosaur diversity changes in the Cenozoic of the north-central region of western United States , 1982 .

[39]  B. Malmgren Biostratigraphy of planktic Foraminifera from the Maastrichtian white chalk of Sweden , 1982 .

[40]  L. W. Alvarez,et al.  Extraterrestrial Cause for the Cretaceous-Tertiary Extinction , 1980, Science.

[41]  V. Krassilov CLIMATIC CHANGES IN EASTERN ASIA AS INDICATED BY FOSSIL FLORAS. II. LATE CRETACEOUS AND DANIAN , 1975 .