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| Preface | |
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| Importance of Microvertebrate Sites, Sampling, Statistical Methods, and Taphonomy | |
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| Information from Microvertebrate Localities: Potentials and Limits | |
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| How Much Is Enough? A Repeatable, Efficient, and Controlled Sampling Protocol for Assessing Taxonomic Diversity and Abundance in Vertebrate Microfossil Assemblages | |
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| Taphonomic Issues Relating to Concentrations of Pedogenic Nodules and Vertebrates in the Paleocene and Miocene Gulf Coastal Plain: Examples from Texas and Louisiana, USA | |
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| Guild Analysis, Ecological and Faunal Analyses, Biodiversity, and Paleobiogeography | |
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| The Structure of Late Cretaceous (Late Campanian) Nonmarine Aquatic Communities: A Guild Analysis of Two Vertebrate Microfossil Localities in Dinosaur Provincial Park, Alberta, Canada | |
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| Vertebrate Paleoecology from Microsites, Talley Mountain, Upper Aguja Formation (Late Cretaceous), Big Bend National Park, Texas, USA | |
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| Terrestrial and Aquatic Vertebrate Paleocommunities of the Mesaverde Formation (Upper Cretaceous, Campanian) of the Wind River and Bighorn Basins, Wyoming, USA | |
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| Lack of Variability in Feeding Patterns of the Sauropod Dinosaurs Diplodocus and Camarasaurus (Late Jurassic, Western USA) with Respect to Climate as Indicated by Tooth Wear Features | |
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| Diversity of Latest Cretaceous (Late Maastrichtian) Small Theropods and Birds: Teeth from the Lance and Hell Creek Formations, USA | |
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| Small Theropod Teeth from the Lance Formation of Wyoming, USA | |
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| The First Serrated Bird Tooth | |
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| First Dinosaur Eggshells from Texas, USA: Aguja Formation (Late Campanian), Big Bend National Park | |
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| Review of the Albanerpetontidae (Lissamphibia), with Comments on the Paleoecological Preferences of European Tertiary Albanerpetontids | |
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| New Information on Frogs (Lissamphibia: Anura) from the Lance Formation (Late Maastrichtian) and Bug Creek Anthills (Late Maastrichtian and Early Paleocene), Hell Creek Formation, USA | |
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