This thesis examines the mineral suite of undeveloped heavy-mineral deposits in the Cretaceous of the Northern Mississippi Embayment and compares them to the developed deposits of the Atlantic Coastal Plain. The hypothesis presented here is that Cretaceous heavy-mineral deposits of the eastern Mississippi Embayment had the same provenance, the Appalachian Piedmont, as did the younger sediments of the U.S. Atlantic Coast. Kyanite/sillimanite and staurolite were recognized in all samples, and represent strong evidence for an Appalachian Provenance. Alternatively, the overall lack of epidote in the HM suite points away from a Mississippi River related provenance. The dominant heavy minerals found in the Mississippi Embayment samples are ilmenite, leucoxene, zircon, rutile, kyanite/sillimanite, staurolite, and monazite. This suite of heavy minerals compares favorably to those represented along the Atlantic Coastal Plane, and supports an Appalachian Provenance. Southwest trending Paleozoic paleovalleys were likely sedimentation pathways from the Appalachian region.

No description available.

The Morondava Basin is one of three Phanerozoic rift basins bordering the western coast of Madagascar. Sediments were first deposited in this basin during the initial stages of breakup of Gondwana in the Permian, sourced from the adjacent Precambrian basement terranes. Gondwana breakup resulted in several stages of subsidence, tilting, and uplift of Madagascar, the thermal history of which is recorded within the strata of the Morondava Basin. We have applied U-Pb detrital zircon techniques to investigating the sedimentation and transport patterns of Jurassic and Cretaceous strata. In order to reconstruct the thermal history of the Morondava Basin throughout the stages of rift basin development we have applied modelling of (U-Th)/He thermochronology data. Our models show a protracted cooling history influenced by multiple stages of uplift and subsidence occurring differentially across the basin. A furthered understanding of the Morondava Basin with respect to its development during Gondwana breakup has implications for oil exploration in the region.

<p>This dataset contains two datasets:</p> <p><br></p> <p>1) 16SI166 Bedrock Sample from the Ruby Range Batholith sampled by Steve Israel while he was at the Yukon Geological Survey and was Analyzed by Jim Crowely at Boise State University. Additional sheets show progression from LA-ICPMS methods to ID-TIMS and include CL imaging for individual grains</p> <p><br></p> <p>2) 09_CONG Tephra Sample from the Eastern Alaska Range that was dated as apart of the NG1 measured section. This sample was collected by Jeffrey Benowitz and analyzed by  Joshua Davies at the Département des sciences de la Terre et de l'atmosphère, Université du Québec à Montréal </p>

This thesis addresses various issues in U-Pb zircon geochronology, proposing new experimental protocols in conventional chemical abrasion-isotope dilution thermal ionization mass spectrometry or CA-(ID)-TIMS and developing a new method for Pb evaporation-condensation from zircon that allows high precision Pb-Pb age determination on Precambrian samples. Various experiments are also done on zircon to extract U-Pb information by in situ flux aided fusion methods and to optimize a better silica gel Pb-ionization activator. Radiation damage caused by U decay in zircon disrupts its ‘closed system’ behavior leading to the loss of daughter radiogenic Pb and resulting in inaccurate ages. A high temperature thermal annealing procedure has been proposed to prevent such Pb loss. Studies presented here have been carried out using Laser Raman Spectroscopy and Scanning Electron Microscopy to characterize radiation damage and effects of laboratory induced thermal annealing on such damage. Backscattered electron images reveal a variety of textures for ZrO2 overgrowths on zircon annealed at 1450oC. Highly damaged zircon produces finer polycrystalline aggregates (<5µm) than zircon with less damage. Raman spectroscopy indicates that crystals with different levels of radiation damage are only partially restored by annealing at 1000oC for 2–3 or 20 days. Annealing at 1450oC for 1 h results in partial breakdown of zircon but restores Raman peak widths and wave numbers. Raman spectra are much less sensitive to polarization angle for annealed highly damaged grains than for weakly damaged zircon showing that when highly damaged zircon is recrystallized, it becomes a polycrystalline aggregate that pseudomorphs the original single crystal. The whole grain Pb evaporation-condensation method is based on 206Pb-207Pb age analyses where zircon grains are pre-treated at 1450oC to drive out all disturbed Pb and then they are kept at 1600oC for an hour or two during which Pb atoms are evaporated out of the grain and deposited directly into a clean Savillex teflon vial or a wide Re filament. This technique allows the use of a 202Pb-205Pb double spike for precise isotopic fractionation correction. Examples are shown in which application of this technique to zircon from Precambrian samples has successfully yielded sub-million year age precisions.

The Grenville orogeny was a protracted (~200 m.y.) series of “hot” magmatic- metamorphic events that contributed to the growth of the Laurentian margin in the late Mesoproterozoic. The granites contain remarkably high Zr content, lack xenocrysts, and become zircon saturated at high temperatures, which are all unusual for felsic magmas. The “hot Grenville granite” hypothesis is tested and use of high-Zr granitoids as potential zones of crustal magma generation through: U-Pb geochronology and cathodoluminescence imaging to assess inherited zircon components; quantitative modeling of zircon crystallization history using rhyolite-MELTS; and Ti-in-zircon thermometry. U-Pb zircon ages for two samples from the Virginia Blue Ridge are 1168 ± 25 Ma (2209 ppm Zr; Tzr = 1032°C) and 1050 ± 13 Ma (918 ppm Zr; Tzr = 898°C). A sample from the NJ – Hudson Highlands has been dated at 1018 ± 11 Ma (1238 ppm Zr; Tzr = 960°C). These samples produce crystallization histories that range over higher temperatures (983–1060°C) than colder, low-Zr counterparts and contain Ti concentrations of 2 to 86 ppm. This analytical approach will further the understanding of zircon’s utility and limitations as a proxy in granite petrogenesis, and constrain thermal models that produced uncommon lithospheric conditions that led to widespread hot granite production at a unique period in Earth history.

Ce travail présente une étude multi-échelle et multi-technique sur la caractérisation des oxy-hydroxydes de fer dans trois types de gisements d’uranium et leur encaissant. Le choix des sites d’études s’est porté sur un gisement de type roll front : Zoovch Ovoo dans le bassin crétacé de East Gobi (Mongolie) ; un autre de type tectono-lithologique : Akola/Ebba dans le bassin de Tim Mersoï (Niger) et enfin un type discordance protérozoïque : Kiggavik en bordure du bassin du Thelon (Canada). Une nouvelle approche a été mise en œuvre pour caractériser les oxy-hydroxydes de fer sur échantillons macroscopiques : la spectroscopie infrarouge de terrain en utilisant le spectromètre ASD TerraSpec®. À partir d’indices originaux calculés sur les spectres, il a été possible à la fois de caractériser les oxy-hydroxydes de fer ; seules l’hématite et la goethite ont été identifiées dans les parties oxydées des différents fronts uranifères, et de visualiser les différentes zonations d’altération le long des fronts redox. De plus, la partie visible du spectre a été utilisée pour quantifier la couleur des échantillons à travers les paramètres des systèmes ITS (Intensité – Teinte – Saturation) et de Munsell. L’étude des paramètres de couleurs a permis d’identifier une teinte spécifique pour les échantillons minéralisés étudiés : un mélange de jaune et de rouge (2,5 à 10 YR en notation de Munsell). A l’échelle des cristaux, les oxy-hydroxydes de fer ont été caractérisés par la spectroscopie micro-Raman. Cette étude a permis de mettre en évidence une différence de cristallinité des cristaux d’hématite dans les différents gisements. D’un point de vue morphologique, les cristaux de goethite du gisement de Zoovch Ovoo, seul oxy-hydroxyde de fer authigène décrit dans ce front, sont maclés en forme d’étoile à six branches, ce qui témoigne d’une cristallisation de basse température, comparé aux gisements du Niger et de Kiggavik. Cette cristallisation est principalement contrôlée par la disponibilité des ions Feᴵᴵᴵ dans le fluide, libérés par la dissolution de la pyrite en milieu oxydant et le pH. D’un point de vue chimique, les oxy-hydroxydes de fer enregistrent le passage du fluide uranifère de part leur teneur eu uranium. Et d’autre part la composition en éléments en trace qui marque la typologie du gisement, par exemple de la teneur en zirconium dans les oxy-hydroxydes de fer provenant du gisement du Niger, source d’origine volcanique. Cette typicité de la mobilité du zirconium est particulièrement bien exprimée dans les fronts uranifères d’Ebba par la précipitation de cristaux authigènes de zircon contemporains de la pechblende. Les données minéralogiques et géochimiques obtenues dans ce travail sur le gisement de Zoovch Ovoo permettent de proposer un modèle original pour sa formation : l’uranium n’a pas précipité massivement en amont du front puisqu’il n’y a pas d’auréole d’irradiation observable en cathodoluminescence dans les minéraux détritiques dans la zone oxydée. L’uranium a précipité lorsque l’eau oxydante a rencontré un faciès sédimentaire ayant un pouvoir réducteur assez fort pour permettre la réduction de l’uranium. La précipitation a lieu dans un endroit particulier de la formation : un paléo-lac où la matière organique et la pyrite sont abondantes. / This work presents a multi-scale and a multi-technical study for the characterization of iron oxi-hydroxides in three uranium-type deposits and host rock. The choice of sites has focused on a roll front deposit: Zoovch Ovoo in a Cretaceous basin of East Gobi (Mongolia); a tectonic-lithological type: Akola/Ebba in Tim Mersoï basin (Niger) and a Proterozoic unconformity type: Kiggavik in Thelon basin (Canada). A new approach has been implemented to characterize the iron oxi-hydroxides on macroscopic samples: field infrared spectroscopy using the ASD TerraSpec® spectrometer. From the original indexes calculated on the spectra, it was possible both to characterize the iron oxi-hydroxides; only hematite and goethite were identified in the different parts of oxidized uranium fronts, and visualize the alteration zonation along the redox front. In addition, the visible part of spectrum was used to quantify the color of samples through the IHS system parameters (Intensity – Hue – Saturation) and the Munsell system. The color setting of the study identified a specific hue for mineralized samples studied: a mixture of yellow and red (2.5 to 10YR in Munsell notation). At the crystals scale, the iron-hydroxides were characterized by µ-Raman spectroscopy. The study highlighted a difference in crystallinity of hematite crystals in different fields. From a morphological point of view, the crystals of goethite in the Zoovch Ovoo deposit, is only authigenic iron oxi-hydroxides described in this uranium front, are twinned in the form of six-pointed star, reflecting a low crystallization temperature, compared to Niger and Kiggavik deposits. This crystallization is mainly controlled by the availability of Feᴵᴵᴵ ions in the fluid, released by pyrite dissolution in an oxidizing environment and pH. From a chemical point of view, iron oxi-hydroxides record the fluid passage owing their uranium content. Secondly, the composition in trace elements marks the type of deposit, for example zirconium content in oxi-hydroxides from Niger deposit, volcanic source. This typical mobility of zirconium is particularly expressed in the uranium front in Ebba deposit by the precipitation of authigenic crystals of zircon contemporary of pitchblende. The mineralogical and geochemical data obtained in this work on the Zoovch Ovoo deposit (Mongolia) allow us to propose an original model for its formation: uranium did not precipitate massively in upstream edge of front, because not radiation halo is visible in cathodoluminescence in detrital minerals in the oxidized area. Uranium precipitated when the oxidizing water met with sedimentary facies having a fairly strong reducing power to allow uranium reduction. The precipitation occurs in a particular location of the formation: paleo-lake where organic matter and pyrite are abundant.

The Altiplano-Puna Volcanic Complex in the Central Andes is one of the youngest large silicic volcanic fields (LSVFs) in the world, erupting over 13,000 km³ of material during multiple supereruptions from 11 to 1 Ma. Understanding the timescales over which magma is stored in the crust prior to eruption is crucial to understanding the development of LSVFs such as the APVC. The residence time of a magma is defined as the time between magma formation and its eruption. While the eruption age of a volcanic system is generally well constrained through ⁴⁰Ar/³⁹Ar dating of sanidine and biotite crystals, determining the time of magma formation offers a bigger challenge. U-Pb dating of zircon—an early crystallizing, ubiquitous phase in silicic systems—is a commonly used method for determining the timing of magma formation. U-Pb zircon ages were collected for 16 ignimbrites representing the temporal and spatial distribution of the APVC. Zircon crystallization histories show significant overlap between eruptive centers of similar age separated by as much as 200 km. Ignimbrites erupted from the same multicyclic caldera show little relationship. This suggests that ignimbrites may share a deeper, regional source. Timescales of zircon crystallization for individual ignimbrites range from ~400 ka to more than 1 Ma, with little correlation with age or erupted volume. Ignimbrites with longer crystallization timescales frequently exhibit a stepped age distribution and highly variable U contents, suggesting that these ignimbrites likely formed in a very crystalline, low melt fraction environment while ignimbrites with short crystallization times and constrained U concentrations crystallized in high melt fraction systems. Zircon crystallization histories record periods of continuous zircon crystallization in the APVC that extend over 1.5-2 Ma pulses and correlate well with eruptive pulses recognized by previous studies. Overall, zircon crystallization histories of the magmas feeding ignimbrite eruptions in the APVC record long timescales of magmatic activity from a shared regional source, likely the Altiplano-Puna Magma Body currently detectable underlying the APVC. / Graduation date: 2012

The northeast African continental margin of the Western Desert of Egypt is host to a complexly deformed series of Phanerozoic basins. Substantial sedimentary deposition (~5 km) and basin formation resulted from regional deformation due to continental collision and repeated rifting and inversion cycles. Limited sedimentary exposure and exploration has prevented elucidation of Phanerozoic basin evolution, particularly in the Paleozoic. Previous studies of the region have largely relied upon sedimentary analysis, gravity, and 2D/3D seismic data. This study, in contrast, has employed extensive use of detrital zircon (U-Th)/He thermochronology (n=1004) from 17 wells in conjunction with 3D seismic, well log correlation, and heat flow data to elucidate a spatiotemporally comprehensive tectonic and stratigraphic model. The detrital zircon thermochronometric data provides new evidence that the lower Paleozoic, Carboniferous, and Mesozoic stratigraphic sequences of the Western Desert represent thermally distinct, tectonically controlled sequences with independent thermal evolutions. The lower Paleozoic sequence has been partially thermally reset, reaching temperatures of ~140-170 ̊C. Partial resetting is noted throughout the region and reached its thermal maximum in the Permo-Triassic, synchronous with onset of Neotethyan rifting. The Carboniferous sequence has not been thermally reset, with exposure to temperatures no greater than ~140 ̊C and reaching thermal maximum presently. Carboniferous (U-Th)/He ages have dominant input from short-lag-time zircons (exhumation to deposition) and indicate the stratigraphic sequence was proximally sourced. The proximal sourcing is likely from transmitted stress and fault reactivation in Egypt during the Hercynian Orogeny that caused fault block exhumation and erosional unroofing. Sediment was shed from uplifted fault blocks that formed the eastern boundary of the Carboniferous sequence. The Mesozoic sequence has not been thermally reset, reaching temperatures no greater than ~120 ̊C and presently reaching thermal maximum. Localized areas with stacking of lower Paleozoic, Carboniferous, and Mesozoic sequences likely bury the lower Paleozoic to abnormally deep depths (~7 km) and elevated temperatures of ~200 ̊C. Evidence from faulting relationships, basin controlling structures, and heat flow data indicate that N-S trending basement structures may define a region of crustal transition between the Archean-Paleoproterozoic Saharan Metacraton and the juvenile Arabian-Nubian Shield. / text

This thesis addresses various issues in U-Pb zircon geochronology, proposing new experimental protocols in conventional chemical abrasion-isotope dilution thermal ionization mass spectrometry or CA-(ID)-TIMS and developing a new method for Pb evaporation-condensation from zircon that allows high precision Pb-Pb age determination on Precambrian samples. Various experiments are also done on zircon to extract U-Pb information by in situ flux aided fusion methods and to optimize a better silica gel Pb-ionization activator. Radiation damage caused by U decay in zircon disrupts its ‘closed system’ behavior leading to the loss of daughter radiogenic Pb and resulting in inaccurate ages. A high temperature thermal annealing procedure has been proposed to prevent such Pb loss. Studies presented here have been carried out using Laser Raman Spectroscopy and Scanning Electron Microscopy to characterize radiation damage and effects of laboratory induced thermal annealing on such damage. Backscattered electron images reveal a variety of textures for ZrO2 overgrowths on zircon annealed at 1450oC. Highly damaged zircon produces finer polycrystalline aggregates (<5µm) than zircon with less damage. Raman spectroscopy indicates that crystals with different levels of radiation damage are only partially restored by annealing at 1000oC for 2–3 or 20 days. Annealing at 1450oC for 1 h results in partial breakdown of zircon but restores Raman peak widths and wave numbers. Raman spectra are much less sensitive to polarization angle for annealed highly damaged grains than for weakly damaged zircon showing that when highly damaged zircon is recrystallized, it becomes a polycrystalline aggregate that pseudomorphs the original single crystal. The whole grain Pb evaporation-condensation method is based on 206Pb-207Pb age analyses where zircon grains are pre-treated at 1450oC to drive out all disturbed Pb and then they are kept at 1600oC for an hour or two during which Pb atoms are evaporated out of the grain and deposited directly into a clean Savillex teflon vial or a wide Re filament. This technique allows the use of a 202Pb-205Pb double spike for precise isotopic fractionation correction. Examples are shown in which application of this technique to zircon from Precambrian samples has successfully yielded sub-million year age precisions.