Loose sheets comprise of profiles of the Oligocene. / Bibliography: leaves 89-158. / 158, [60] leaves, [16] leaves of plates : ill., maps ; 30 cm. + seven charts (some folded) / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / This study investigates a late Eocene to Miocene succession of diverse mid-latitude assemblages of foraminifera from carbonates and calcareous muds and sands on the southern Australian margin. It contrasts foraminiferal profiles from the restricted St. Vincent and Murray Basins with the Otway Basin that is more exposed to oceanic conditions. / Thesis (Ph.D.)--University of Adelaide, Dept. of Geology and Geophysics, 1995

published_or_final_version / Earth Sciences / Doctoral / Doctor of Philosophy

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).

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Orientador: Rosemarie Rohn Davies / Banca: Norberto Morales / Banca: Maria Gabriela Castillo Vincentelli / Resumo: O paleocânion de Regência é reconhecido em subsuperfície da bacia do Espírito Santo, localizado nas proximidades da foz do Rio Doce (ES), originado no Cretáceo e preenchido até meados do Eoceno. Dados de 31 seções sísmicas, 29 poços e marcadores bioestratigráficos (definidos por nanofósseis calcários) substanciaram a elaboração de modelos geológicos que aprimoram o conhecimento sobre a evolução do paleocânion. Os resultados incluem correlações estratigráficas, interpretações de feições estruturais e das principais superfícies estratigráficas no âmbito das formações Mariricu, São Mateus, Regência e Urucutuca, assim como seções esquemáticas transversais e longitudinais do paleocânion, mapas de contorno estrutural dos topos litoestratigráficos e de contorno morfológico do paleocânion. Estas informações foram integradas em detalhe para discutir sua origem, o preenchimento e os fatores de controle. Desde o início, o paleocânion foi estruturado por falhas no embasamento. Próximo ao topo da Formação Mariricu, de idade aptiana, já há indícios de uma extensa calha rasa. O paleocânion é dividido pela Zona de Charneira Cedro-Rio Doce (ZCCRD), que é um sistema de falhas normais de direção praticamente N-S. A morfologia e a largura do paleocânion também foram controladas por diversas falhas normais menores nos blocos proximal e distal à ZCCRD, originadas no embasamento, ainda ativas quase até o final do preenchimento do paleocânion, com direção principalmente SO-NE. Falhas normais também ... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Santo Basin, located near to the mouth of the Doce River (State of Espírito Santo, Southeast Brazil), carved from the Cretaceous and filled up to the mid Eocene. Data of 31 seismic sections, 29 wells and biostratigraphic markers (of calcareous nannofossils) have substantiated the conception of geological models that improve the awareness concerning the paleocanyon evolution. The results include stratigraphic correlations, structural geology interpretations and stratigraphic surfaces determination within the Mariricu, São Mateus, Regência and Urucutuca formations, as well as schematic transversal and longitudinal sections of the paleocanyon, structural contour maps of the lithostratigraphic tops and morphologic contour map of the paleocanyon. These information were integrated in detail to promote discussion about the origin, the filling and the controls of the paleocanyon development. Since the beginning, the structure was related to faults in the basement. The first long shallow channel is evidenced near the top of the Aptian Mariricu Formation. The paleocanyon is divided into a proximal block and a distal one by an almost N-S system of normal faults designated as Cedro-Rio Doce Fault Zone (CRDFZ). In both blocks, the morphology and width of the paleocanyon were also controlled by several smaller normal faults with main SW-NE direction, originated in the basement, still moving until the almost complete fill of the paleocanyon, with main direction SW-NE. Normal faults were als... (Complete abstract click electronic access below) / Mestre

The fossiliferous sediments of the Hueso and Tapiado formations exposed in the Vallecito Creek-Fish Creek section (VCFC) of the Anza-Borrego Desert (ABD) span the boundary between Blancan and Irvingtonian North American Land Mammal 'Ages.' Historically, the determination of the Blancan-Irvingtonian (B-I) boundary in the VCFC proved problematic. A new study to determine the B-I boundary in the VCFC revealed data inaccuracies in both published works and curatorial records of the mammal and other vertebrate fossils from the ABD. Most individual inaccuracies were minor, but an accumulation of over 50 years of multiple inaccuracies had significant effects on local and regional biostratigraphic and biochronologic correlations. A detailed investigation of the inaccurate data resulted in recognition of 17 types of error, with at least five sources. The two most prominent sources of error are those derived from publication and curation protocols. Examination of over 150 publications and in-house faunal lists produced over 830 taxonomic names and format variants, for 110 mammalian taxa identified from the ABD and VCFC. Approximately 50% of the taxonomic identifications were previously published without voucher catalogue numbers or fossil descriptions. A critical review of the taxonomic assignments resulted in an updated faunal list of ABD terrestrial Mammalia, including 110 taxonomic names, 66 unqualified genera, and 46 unqualified species. A supplemental list of 'retired' taxa includes 178 previously published or listed taxonomic names and format variants. The 4.5 km sequence of originally superposed sediments within VCFC is now tilted at 23 degrees and exposed in plan view. This exposure was captured in both aerial photos and satellite imagery. GIS layers of the Geomagnetic Polarity Time Scale and individual collecting localities are readily superposed onto the stratigraphic images. When united with the faunal database, GIS maps of biostratigraphic data facilitate detection and correction of data errors. Resulting corrected maps show highest and lowest stratigraphic occurrences of taxa, as well as geographic clustering of taxonomic groups, outlining possible paleohabitats. As a result of data improvement and GIS display, the local B-I boundary currently is best estimated by the presence of Ovibovini at >1.42 Ma. / text