No description available.

This thesis began as an investigation into evolution of the platypus family (Ornithorhynchidae, Monotremata), now known from both Australia and South America. The thesis broadened its scope with inclusion of non-ornithorhynchid Mesozoic monotremes from Lightning Ridge, NSW. This change in direction brought an unexpected result: a fossil mammal from Lightning Ridge investigated for this thesis (presumed to be monotreme: Flannery et al., 1995) appears to be a new and unique type of mammal. Specimens were procured through Queensland Museum (Riversleigh material); Australian Museum (Lightning Ridge material); and Museum of Victoria and the South Australian Museum (fossil ornithorhynchids). Specimens were examined under a light microscope and scanning electron microscope; specimens were photographed using light photography and a scanning electron microscope; and illustrations and reconstructions were done with a camera lucida microscope attachment and photographic references. Parsimony analysis utilised the computer programs PAUP and MacClade. Major conclusions: 1) analysis and reconstruction of the skull of the Miocene platypus Obdurodon dicksoni suggest this robust, large-billed platypus was a derived northern offshoot off the main line of ornithorhynchid evolution; 2) the well-preserved skull of Obdurodon dicksoni shows aspects of soft anatomy previously unknown for fossil ornithorhynchids; 3) two upper molars from Mammalon Hill (Etadunna Formation, late Oligocene, central Australia) represent a third species of Obdurodon; 4) the South American ornithorhynchid Monotrematum sudamericanum from the Paleocene of Argentina is very close in form to the Oligocene-Miocene Obdurodon species from Australia and should be considered congeneric; 5) a revised diagnosis of the lower jaw of the Early Cretaceous monotreme Steropodon galmani includes the presence of two previously undescribed archaic features: the probable presence of postdentary bones and a meckelian groove; 6) morphological evidence is presented supporting a separate family Steropodontidae; and 7) analysis of new fossil material for Kollikodon ritchiei suggests that this taxon is not a monotreme mammal as originally identified but is a basal mammal with close relationships to allotherian mammals (Morganucodonta; Haramiyida). Kollikodon is provisionally placed as basal allotherian mammal (Allotheria sensu Butler 2000) and is unique at the ordinal level, being neither haramiyid nor multituberculate. A new allotherian order ??? Kollikodonta ??? is proposed.

Thesis (Ph. D.)--University of Chicago, Department of Organismal Biology and Anatomy, June 2000. / Includes bibliographical references. Also available on the Internet.

Thesis (MPhil)--University of Stellenbosch, 2000. / ENGLISH ABSTRACT: The large mammal faunal sample, excavated since 1984 from the Late Pleistocene Klasies River main site, was studied. There are 27 species in eight genera represented. The bovids from the LBS member (110 000 years) and the Upper member (70 000 years) shows an increase in grazers relative to the fauna from the SAS member (100 000 years). This confirms previous research. The study of body part frequencies does not confirm the selective transport of the carcasses of larger bovids or that scavenging played an important role in the accumulation of the fauna. It is concluded that availability of marine mammals were the attraction of the locality and that all size classes of bovids were actively hunted and their carcasses returned to the site. KEYWORDS: Klasies River, Late Pleistocene, large mammal fauna, hunting. / AFRIKAANSE OPSOMMING: Die groot soogdier fauna van die Laat Pleistoseen vindplaas Klasies River main site, opgegrawe vanaf 1984, is bestudeer. Sewe-en-twintig spesies in agt genera is verteenwoordig. Die bokke van die LBS member (110 000 jare) en die Upper member (70 000 jare) toon 'n styging in grasvreters relatief tot dié van die SAS member (100 000 jare). Dit bevestig 'n vorige ondersoek. Die bestudering van ligaamsdeel frekwensies van alle groottes bokke bevestig nie dat selektiewe vervoer van groter bokkarkasse plaasgevind het nie, of dat aas 'n rol in die akkumulasie van die fauna gespeel het nie. Die gevolgtrekking is gemaak dat die teenwoordigheid van marine soogdiere die rede was vir die keuse van hierdie vindplaas was. Alle groottes bokke is doelbewus gejag en hulle karkasse is teruggebring na die vindplaas. SLEUTELWOORDE: Klasies River, Laat Pleistoseen, groot soogdiere, jag.

The age of the Bridgerian/Uintan boundary has been regarded as one of the most important outstanding problems in North American Land Mammal “Age” (NALMA) biochronology. The Bridger Basin in southwestern Wyoming preserves one of the best stratigraphic records of the faunal boundary as well as the preceding Bridgerian NALMA. In this dissertation, I first developed a chronological framework for the Eocene Bridger Formation including the age of the boundary, based on a combination of magnetostratigraphy and U-Pb ID-TIMS geochronology. Within the temporal framework, I attempted at making a regional correlation of the boundary-bearing strata within the western U.S., and also assessed the body size evolution of three representative taxa from the Bridger Basin within the context of Early Eocene Climatic Optimum. Integrating radioisotopic, magnetostratigraphic and astronomical data from the early to middle Eocene, I reviewed various calibration models for the Geological Time Scale and intercalibration of 40Ar/39Ar data among laboratories and against U-Pb data, toward the community goal of achieving a high precision and well integrated Geological Time Scale. In Chapter 2, I present a magnetostratigraphy and U-Pb zircon geochronology of the Bridger Formation from the Bridger Basin in southwestern Wyoming. The ~560 meter composite section spans from the lower Bridger B to the Bridger E, including the Bridgerian/Uintan NALMA boundary in the uppermost part of the section. Analysis of samples from 90 sites indicates two paleomagnetic reversals that are correlated to an interval spanning Chrons C22n, C21r, and C21n by comparison to the Geomagnetic Polarity Time Scale (GPTS). This correlation places the Bridgerian/Uintan faunal boundary within Chron C21n, during the initial cooling phase following the peak of the Early Eocene Climatic Optimum. Based on the bio- and magnetostratigraphic correlation, I provide correlation of other Bridgerian/Uintan boundary-bearing sections to the GPTS, demonstrating that in the western North America, the Bridgerian/Uintan boundary occurs everywhere in Chron C21n. In addition, U-Pb zircon geochronological analyses were performed on three ash beds from the Bridger Formation. High-precision U-Pb dates were combined with the paleomagnetic polarity data of the same ash beds as well as the integrative chronostratigraphy of the basin to assess prior calibration models for the Eocene part of the GPTS. The data from the Bridger Formation indicate that the Option 3 age model of Westerhold et al. (2008) best reconciles the geochronological data from all of the ash beds except for one. Thus I favor this Option 3 model, which indicates the ages of 56.33 Ma and 66.08 Ma for the Paleocene-Eocene Thermal Maximum and Cretaceous/Paleogene boundary, respectively. In Chapter 3, the body size evolution of three mammalian taxa from the Bridgerian NALMA was analyzed within the context of Bergmann’s Rule, which poses a correlation between the size of endotherms and climate (latitude). The Bridgerian NALMA is from a time of global cooling following the peak of the Early Eocene Climatic Optimum, thus according to Bergmann’s Rule, the Bridgerian mammals are expected to increase in size. This hypothesis is tested among Notharctus, Hyopsodus, and Orohippus, using the size of molar dentition as a proxy for their body size. These taxa represent three different ecomorphs, and I investigated if these taxa showed a pattern of body size change consistent with the prediction made by Bergmann’s Rule, and how their ecological adaptation may have affected their response to the climate change. Prior to analyzing the body size evolution, specimens of Notharctus and Hyopsodus were identified to species based on dental characters. This practice differs from previous studies in which species identification relied on relative size of the individuals and stratigraphic levels of origin. Within the new framework of morphologically determined species identification, five species of Notharctus were recognized, among which, N. pugnax, N. robustior and N. sp. indet. exhibited statistically significant body size increase in the time span of interest. Based on morphological analyses of Hyopsodus dentition, I recognized five species. Dentition-based body size analysis showed that H. lepidus and H. despiciens exhibited a statistically significant change towards larger size within the sampled interval. When analyzed at the generic level, a statistically significant increase was observed for both Notharctus and Hyopsodus. Finally, a genus-level analysis of Orohippus showed a lack of statistically significant size increase over the study interval. Thus, among the three taxa from the Bridgerian, Bergmann’s Rule is supported by Notharctus and Hyopsodus, at least at the genus level, but not by Orohippus, although the patterns are more variable at the intraspecific level. In Chapter 4, 40Ar/39Ar dates were obtained from sanidines from the middle Eocene Henrys Fork tuff and Upper Carboniferous Fire Clay tonstein, with the goal of making highly precise measurements of these two samples, keyed to the Fish Canyon monitor standard. Analytically, both samples were well characterized, as had been shown previously. The irradiation disk was arranged such that there would have been control from the Fish Canyon surrounding each of the unknown pits. However, due to several complications in the lab during the course of the experiment, only the analyses from one run disk (Disk 677) were of the quality needed for the goals of the study. As a result, the Fish Canyon sanidine standards that were irradiated near the center of the irradiation disk had to be discarded, and thus, the neutron fluence could not be mapped out precisely across the entire disk. The 40Ar/39Ar age relative to Fish Canyon sanidines is 47.828 ± 0.205 Ma and 311.937 ± 1.282 Ma for the Henrys Fork tuff and Fire Clay tonstein, respectively (1σ, including error on the age of the monitor). Because the ages were both offset about the same amount, I explored the option of using the U-Pb ID-TIMS ages of the Henrys Fork tuff and Fire Clay tonstein to test the agreement in the chronometers. The Henrys Fork tuff was dated at 48.260 ± 0.107 Ma (1σ, including error on the age of the monitor) using the Fire Clay sanidines and assuming its age is the U-Pb zircon age. The Fire Clay tonstein was dated at 314.593 ± 0.699 Ma (1σ, including error on the age of the monitor), using the Henrys Fork sanidines and assuming its age is the U/Pb zircon age. Although the complications encountered render these data unpublishable, they show great promise as the ages of each sanidine sample, tied to the other ash using the other ash’s U-Pb age, give results that are in close agreement between the two chronometers on the same sample (e.g., 314.593 ± 0.699 Ma vs. 314.554 ± 0.020 Ma at 1σ for sanidine and zircon respectively from the Fire Clay tonstein, and 48.260 ± 0.107 Ma vs. 48.265 ± 0.008 Ma 1σ for sanidine and zircon respectively from the Henrys Fork tuff).

No description available.

Thesis (Ph. D.)--California Institute of Technology, 1943. / No collective t.p.; titles transcribed from individual title pages. Includes bibliographical references.

No description available.

This project examines small mammal faunas from cave sites in south-west England and south Wales. The aims are threefold: To examine the rapid environmental changes taking place in the Late Pleistocene and early Holocene: To understand the processes by which small mammal remains were deposited in the caves examined: To demonstrate the value of small mammal studies as an archaeological tool. All identifiable small mammal remains from twelve selected sites are listed. Ten of the sites are new material. As the species examined here are seldom exploited by humans, the small mammals provide a record of the past environment unaffected by human selection of particular species, as might be the case in larger mammal assemblages. An examination of possible agents of accumulation is provided for each site to identify any bias introduced by prey selection. Reconstructions of the environment local to each cave at the time of deposition are offered. The evidence provided by the small mammals is related to the archaeological findings from each cave, to demonstrate the effect of human habitation of cave sites on the depositional and post-depositional processes shown by the microfauna. The environmental evidence provided by the study reflects a wider landscape rather than merely the immediate surroundings of the cave, and so gives a basis for human exploitation patterns in the area accessible from the cave. Reconstructions of the ecological mosaics formed by the rapidly changing climate of the period and the topographic variation around the cave sites are provided, demonstrating the potential complexity of the environment in which the humans and other fauna of the period existed. It is hoped that this will encourage archaeologists to look beyond the general division of environmental boundaries in this period, and to examine the local variation in habitat availability and use.

The Sucker Creek Formation exposures at Devils Gate in southeastern Oregon have yielded a significant small mammal fauna of at least thirty small mammal taxa from five stratigraphic horizons. The mammal-bearing portion of the Devils Gate section is more than 200 m thick. Fossil mammals occur in lacustrine and marginal lacustrine deposits lower in the section and occur in overbank and paleosol deposits higher in the section. ⁴⁰Ar/³⁹Ar single-crystal laser-fusion dates on three Devils Gate ashes shows that the age of the mammal-bearing sequence at Devils Gate spans the late early Barstovian land-mammal age with possible overlap into the late Barstovian, as currently defined. Duration of the entire mammal-bearing portion of the Devils Gate section was less than a million years. Both a new ash date from the type section and biostratigraphic correlations between Devils Gate and the type section support considerable temporal overlap between the two exposures. The Devils Gate Local Fauna includes several new taxa: a phyllostomatid bat; two "flying squirrels", Petauristodon sp. A and Petauristodon sp. B; and an eomyid rodent, Leptodontomys sp. A. Several fossil occurrences represent the first record of a taxon in the northern Great Basin and/or in the Barstovian land-mammal age, including: Blackia sp., Schaubeaumys grangeri, Protospermophilus quatalensis, and Pseudadjidaumo stirtoni. The Stagestop locality produced two new taxa, Copemys sp. aff C. esmeraldensis and Mystipterus sp. The Stagestop local fauna is Clarendonian in age. Concretions are an important source of fossil mammals in exposures of the Sucker Creek Formation. Geochemical analyses show that concretions formed through a complex interaction between bone and surrounding volcaniclastic material. Although some superficial bone was consumed during concretion diagenesis, concretion development reduced the chance of prolonged chemical and physical destruction of bone during later soil development. The broad ecological diversity of small mammals recovered from Devils Gate supports an interpretation of the local paleoecology as a mosaic of grassland, forest, and pond/lake-bank environments. Sequential small mammal faunas across a prominent ash event show a generally stable composition with no pronounced ecomorphic differences in pre- and post-volcanic disturbance intervals. Therefore, small mammals do not show analogous ecological patterns to disturbance-driven plant successions in the Sucker Creek Formation. I infer that the local ecosystem recovered from volcanic blasts at a temporal scale below the resolution of time-averaged, post-disturbance paleosols.