Land Mammal Faunas of North America Rise and Fall During the Early Eocene Climatic Optimum

Climatic warming at the beginning of the Early Eocene Climatic Optimum (EECO) resulted in major increases in plant diversity and habitat complexity reflective of temporally unique, moist, paratropical conditions from about 53–50 Ma in the Western Interior of North America. In the early part of the EECO, mammalian faunal diversity increased at both local and continental scales in conjunction with a major increase in tropicality resulting from mean annual temperatures reaching 23 ̊C and mean annual precipitation approaching 150 cm/yr. A strong episode of taxonomic origination (high number of first appearances) in the latest Wasatchian and earliest Bridgerian Land Mammal Ages apparently was in response to these greatly diversified floral and habitat associations along with increasing temperature and precipitation. This is in contrast to a similar increase in first appearances at the beginning of the Wasatchian (Paleocene-Eocene Thermal Maximum, or PETM) that can be traced instead to climate-induced transcontinental immigration. In the later part of the EECO, from Br-1b–Br-3, climatic deterioration resulted in a major loss of faunal diversity at both continental and local levels, apparently mirroring climatic deterioration. Relative abundance shifted from diverse, evenly distributed communities to much less diverse, skewed distributions dominated by the condylarth Hyopsodus. Evolutionary innovation through the 53–50 Ma interval included a modest overall increase in body size and increased efficiency in carnivory and folivory as reflected by within-lineage patterns of evolution. Rather than being “optimum,” the EECO engendered the greatest episode of mammalian faunal turnover of the first 15 million years of the Cenozoic era, with both first and last appearances at their highest levels. Both the PETM and EECO faunas were climatically shaped.

[1]  A. Chew Paleoecology of the early Eocene Willwood mammal fauna from the central Bighorn Basin, Wyoming , 2009, Paleobiology.

[2]  A. Carroll,et al.  Capture of high-altitude precipitation by a low-altitude Eocene lake, western U.S. , 2008 .

[3]  R. E. Heinrich,et al.  Earliest Eocene Miacidae (Mammalia: Carnivora) from Northwestern Wyoming , 2008, Journal of Paleontology.

[4]  D. Boyer,et al.  Cranial Morphology of a Pantolestid Eutherian Mammal from the Eocene Bridger Formation, Wyoming, USA: Implications for Relationships and Habitat , 2007, Journal of Mammalian Evolution.

[5]  K. Beard,et al.  RODENTS OF THE FAMILY CYLINDRODONTIDAE (MAMMALIA) FROM THE EARLIEST EOCENE OF THE TUSCAHOMA FORMATION, MISSISSIPPI , 2007 .

[6]  P. Gingerich,et al.  Paleocene-Eocene Land Mammals From Three New Latest Clarkforkian And Earliest Wasatchian Wash Sites At Polecat Bench In the Northern Bighorn Basin, Wyoming , 2006 .

[7]  M. Woodburne,et al.  “South American” Marsupials from the Late Cretaceous of North America and the Origin of Marsupial Cohorts , 2005, Journal of Mammalian Evolution.

[8]  S. Wing,et al.  Oxygen isotope and paleobotanical estimates of temperature and δ18O–latitude gradients over North America during the early Eocene , 2004 .

[9]  P. Gingerich,et al.  Systematics and Phylogeny of Late Paleocene and Early Eocene Palaeoryctinae (Mammalia, Insectivora) from the Clarks Fork and Bighorn Basins, Wyoming , 2004 .

[10]  Kirk R. Johnson,et al.  Overview of the Late Cretaceous, early Paleocene, and early Eocene megafloras of the Denver Basin, Colorado , 2003 .

[11]  J. Zachos,et al.  Carbon and oxygen isotope records from Paleosols spanning the Paleocene-Eocene boundary, Bighorn Basin, Wyoming , 2003 .

[12]  P. Gingerich Mammalian responses to climate change at the Paleocene-Eocene boundary: Polecat Bench record in the northern Bighorn Basin, Wyoming , 2003 .

[13]  P. Gingerich,et al.  Marine-terrestrial linkages at the Paleocene-Eocene boundary , 2003 .

[14]  Kirk R. Johnson 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 , 2002 .

[15]  D. Froehlich Quo vadis eohippus? The systematics and taxonomy of the early Eocene equids (Perissodactyla) , 2002 .

[16]  G. Harrington Impact of Paleocene/Eocene Greenhouse Warming on North American Paratropical Forests , 2001 .

[17]  G. Gunnell,et al.  Basin Margins, Biodiversity, Evolutionary Innovation, and the Origin of New Taxa , 2001 .

[18]  P. Gingerich,et al.  OVERVIEW OF MAMMALIAN BIOSTRATIGRAPHY IN THE PALEOCENE-EOCENE FORT UNION AND WILLWOOD FORMATIONS OF THE BIGHORN AND CLARKS FORK BASINS , 2001 .

[19]  P. Gingerich,et al.  MAMMALIAN COMMUNITY RESPONSE TO THE LATEST PALEOCENE THERMAL MAXIMUM : AN ISOTAPHONOMIC STUDY IN THE NORTHERN BIGHORN BASIN, WYOMING , 1998 .

[20]  G. Gunnell Wasatchian-Bridgerian (Eocene) paleoecology of the western interior of North America: changing paleoenvironments and taxonomic composition of omomyid (Tarsiiformes) primates. , 1997, Journal of human evolution.

[21]  P. Gingerich Early Eocene Teilhardina Brandti: Oldest Omomyid Primate from North America , 1993 .

[22]  Michael Foote,et al.  Rarefaction analysis of morphological and taxonomic diversity , 1992, Paleobiology.

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

[24]  P. Gingerich New Earliest Wasatchian Mammalian Fauna from the Eocene of Northwestern Wyoming: Composition and Diversity in a Rarely Sampled High-Floodplain Assemblage , 1989 .

[25]  Philip D. Gingerich,et al.  Cranial Anatomy and Evolution of Early Tertiary Plesiadapidae (Mammalia, Primates) , 1977 .

[26]  T. Fleming Numbers of Mammal Species in North and Central American Forest Communities , 1973 .

[27]  Charles Lewis Gazin,et al.  A further study of the lower Eocene mammalian faunas of southwestern Wyoming , 1962 .