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all geography including DSDP/ODP Sites and Legs
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Mammalian faunal change of the Miocene Dove Spring Formation, Mojave region, southern California, USA, in relation to tectonic history
Middle Miocene fire activity and C 4 vegetation expansion in the Barstow Formation, California, USA
THE INFLUENCE OF DEPOSITIONAL ENVIRONMENT AND BASIN HISTORY ON THE TAPHONOMY OF MAMMALIAN ASSEMBLAGES FROM THE BARSTOW FORMATION (MIDDLE MIOCENE), CALIFORNIA
FACIES, ENVIRONMENTS, AND FOSSIL PRESERVATION IN THE BARSTOW FORMATION, MOJAVE DESERT, CALIFORNIA
Feeding ecology and habitat preferences of top predators from two Miocene carnivore-rich assemblages
A new paleoprecipitation proxy based on soil magnetic properties: Implications for expanding paleoclimate reconstructions
Diversification of mammals from the Miocene of Spain
Diversity dynamics of mammals in relation to tectonic and climatic history: comparison of three Neogene records from North America
Flat latitudinal gradient in Paleocene mammal richness suggests decoupling of climate and biodiversity
Lateral trends in carbon isotope ratios reveal a Miocene vegetation gradient in the Siwaliks of Pakistan
CRITICAL ISSUES OF SCALE IN PALEOECOLOGY
Lothagam: The Dawn of Humanity in Eastern Africa
The multiple scales of biodiversity
A statistical assessment of last appearances in the Eocene record of mammals
Changes in sample size may confound interpretation of faunal change in the fossil record. The record of early Eocene mammals from the Wasatchian Land-Mammal Age in the Clark’s Fork Basin, Wyoming, shows a high correlation between the square root of sample size and species richness. This correlation suggests that Schankler’s (1980) Biohorizon A, a faunal turnover composed mainly of disappearances, is largely an artifact of sampling fluctuation. Within the interval of Biohorizon A, sample size drops from record high to record low values. Monte Carlo simulation of the drop in sample size across Biohorizon A demonstrates the role of sampling variation in producing artifacts of faunal change. The distribution of missing species resulting from the simulations provides a reliable estimate of the number of species that are likely to be missing at a specified sample size, even if they were present in the original population. Results of the simulations indicate that most of the 16 disappearances observed in the 200-m interval above Biohorizon A can be explained by low sample size alone. For each species that disappeared in the actual record, the frequency of absence in the simulations is a basis for comparing the likelihoods of two hypotheses: (1) that the species was present but not represented by fossils, and (2) that the species was absent Evaluation of the likelihood ratio for these hypotheses indicates that Arctodontomys wilsoni-A. nuptus, Phenacodus vortmani, and Homogalax n. sp.-H. semihians are the lineages most likely to have disappeared over the interval of low sample size. Reconsideration of the biostratigraphic correlation between the central Bighorn Basin and the Clark’s Fork Basin based on the first appearances of Homogalax protapirinus and Tetonius matthewi/steini supports a higher stratigraphic position for the interval corresponding to Biohorizon A in the Gark’s Fork Basin than its original placement.