The Round Top laccolith is considered to be one of the youngest laccoliths in a series of five known as the Sierra Blanca peaks, located in Hudspeth county, Texas. The laccolith is anomalous within the region in that it is peraluminous and enriched in HREEs, F, and U, and is comprised of intermingled discrete packages of various rhyolite types. The laccolith rhyolite varies in color from gray, purple, red, and tan, which combine locally to form distinct geometric mottled textures. The general composition of the rhyolite is 48-52% potassium feldspar, 28-30% quartz, 8-14% plagioclase feldspar, 4-5% annite biotite, 2-3% magnetite-hematite, 1% zircon, and 1% trace phases. The morphology of the trace phases suggests quenching of a late-stage volatile-rich vapor phase at the time of the laccolith formation. The rhyolite displays a wide array of unique mineralogical characteristics indicative to rapid emplacement and metastable crystallization conditions, including three-part quartz phenocrysts, hourglass sector-zoned potassium feldspars, and late-stage anhedral zircons. Unique accessory and trace phases include cassiterite, cerianite-(Ce), changbaiite, columbite, cryolite, tantalite, thorite, yttrofluorite, yttrocerite, and two unidentified minerals named (W) and (X). Initial alteration of the laccolith by high temperature volatile-rich vapor during the late stages of crystallization caused the partial dissolution of the feldspars and quartz. Subsequent quenching of this high temperature vapor phase produced the abundant interstitial, and pore filling REE-fluorides common to the laccolith. The variation in rhyolite color and the presence of the mottled textures are a direct result of partial oxidation of the laccolith by secondary fluids. The oxidizing fluids migrated within the laccolith along an extensive fracture network, altering the adjacent wallrock by oxidizing magnetite phenocrysts to hematite. The gray, purple, and red rhyolite types reflect an increase in turbidity caused by hematitic inclusions primarily within the pore spaces of the potassium feldspar portions of the groundmass. The tan rhyolite is locally restricted to the base of the laccolith and has been subjected to an intense degree of alteration independent of the other rhyolite types, primarily indicated by the conversion of feldspars to clay. Petrographic, microbeam, and geochemical studies have determined little variation in REE concentration between the three rhyolites of similar alteration intensity, but have indicated a depletion in LREEs within the more altered tan rhyolite. The average REE+Y content for the rhyolites sampled (n=11) ranges between 249 ppm and 518 ppm. The REE+Y concentrations between rhyolite samples of the same type show some variation, possibly indicating a correlation between alteration and REE+Y abundance and/or innate heterogeneity in the vapor phase during the initial laccolith formation. The magma emplaced at Round Top underwent a prolonged evolutionary process of fractionation/differentiation as evident by the unusual mineral assemblage and geochemical enrichment associated with the laccolith (e.g. extremely negative europium anomaly, and the positive La/Yb correlation). Future exploration for Round Top style REE-deposits should center within long-lived, tectonically active and complex regions where laccoliths are likely to exist. Specifically, exploration should focus on identifying the youngest laccolith in a felsic series, as this is the most likely to contain the greatest abundance of incompatible elements within the laccolithic group. The early alteration of feldspars by the high temperature vapor phase was crucial in the development of the REE+Y enrichment at Round Top. The feldspar dissolution provided abundant open pore space that was subsequently filled by the REE-fluorides. Thus, exploration should additionally seek laccoliths that have undergone a similar early alteration process, and expand to potential laccolith groups not yet exposed by erosional processes. / text

The Alnö Complex is a Late Precambrian alkaline and carbonatite intrusion (c. 30km2) into Early Proterozoic country rock that extends from the north east, to the north western shoulder of Alnö Island. Carbonatites are rare among volcanic provinces, with Oldoinyo Lengai of northern Tanzania being the only active carbonatite volcano in the world today. The high carbonate mineral volumes and rare earth element (REE) concentrations of carbonatites, in combination with the intrusive-extrusive nature of their suites contribute to the rarity of these rocks. Carbonatites, through their peculiar petrological and geochemical compositions, provide vital insights to the composition and condition of the Earth’s mantle. The genesis of the Alnö carbonatites and their relation to other lithological units at the complex is however, only partially understood. This stems from the epistemological division of carbonatites as having either a ‘magmatic’ or ‘reactive’ origin. This study focuses on sampled carbonatites from the Alnö Complex, employing an oxygen and carbon isotope approach on their native calcite, complemented with petrological and mineralogical methods in order to constrain petrogenesis. As a reference, oxygen and carbon isotope data of calcite from an earlier Alnö investigation as well as from an array of data from comparative alkaline complexes elsewhere are also discussed. The combined data and the derived findings support a scenario that is consistent with the ‘magmatic’ model wherein carbonatites have a primary mantle-derived origin, and prospectively stem from a parent magma akin to that of Oldoinyo Lengai, but have experienced a degree of silicate and sedimentary assimilation. The extraction of the Alnö carbonatites for their rare earth metals is a looming possibility due to the current volatility in the rare earth market. The risks and opportunities involved in this kind of natural resource extraction provide a context wherein sustainable development paradigms can be applied. The capacity of the Alnö environment to withstand the impact of development in the mining sector is discussed through a perspective of establishing a quarry, and quarry-related methods for rare earth extraction.

The iron apatite mineralizations of northern Sweden are mainly situated in supracrustal rocks and are thought to have formed during approximately the same time as the major plutonic suites in northern Sweden. In this thesis the Malmberget iron apatite ore deposit have been compared to the Kiruna iron apatite ore deposit to see whether the role of hydrothermal processes are different between the two ore districts. Also, since it has proven problematic to distinguish between the different mafic and ultramafic members of the major plutonic suites in northern Sweden (i.e. the Haparanda suite (1.94-1.85 Ga), the Perthite-monzonite suite (PMS) (1.87 Ga) and the Edefors suite (1.80-1.79 Ga)), a second goal is to trace the distribution and distinguish between these suites. Major elements, REE and trace elements have been studied along with polished sections from the ores and oxygen isotopes of magnetites from the ore districts to trace the ore formation process and separate between suites. All ore districts display a close similarity in geochemistry between host rocks and magnetites, especially regarding the REE pattern. Oxygen isotopes show that samples from the Kiruna district plot exclusively at positive δ18O-values with the majority of them at values < 1‰. Samples from the Malmberget district display δ18O-values either close to the igenous range or at slightly negative values. However, samples that display very low or negative δ18O-values show signs of either high temperature hydrothermal alteration, oxidation or crustal contamination. The δ18O composition along with textural observations from the polished sections and geochemistry, points towards a magmatic origin for these deposits. No apparent evidence has been found to support a primary ore formation by hydrothermal process in any of the districts studied. Regarding the suites, normalized spider plot patterns of REEs and trace elements served as a basis for subdivision into groups by similarities in key identification parameters. Several patterns are characterized by a pronounced Eu-trough while the middle- to HREEs display a rather flat trend, criteria that are related to rocks from the Haparanda suite, while samples with positive Eu-anomaly (Eu/Eu* > 1) and a nearly flat trend from La to Pr with a marked positive peak at Sr and generally less enriched in LILE, are consistent with the Edefors suite. Also, the Edefors suite generally display low concentrations of both Th and U but are somewhat enriched in Sr with relation to Pr. No distinct geochemical features could help to separate between the Haparanda and the PMS suites.

La mobilisation des REE et de l’Hf par un fluide aqueux durant les processus métamorphiques HP-BT peut entraîner des perturbations dans la signature des protolithes et/ou dans les datations obtenues par les systèmes isotopiques Sm-Nd et Lu-Hf. L’étude couplée de la transition éclogite - amphibolite de la localité de Vårdalsneset (WGR, Norvège) et des coefficients de partage des REE et de l’Hf entre un fluide aqueux à NaCl ou à CO2 et le grenat pyrope (P = 3 GPa, T = 800°C) déterminés expérimentalement conduit à deux résultats majeurs. Tout d’abord, une différence d’échelle de mobilité entre les REE (mobiles à l’échelle décimétrique) et l’Hf (mobile à l’échelle du grain) est démontrée. Les signatures des protolithes restent cependant identifiables et les âges modèles Sm-Nd et Lu-Hf des métabasites ne sont pas perturbés, arguant d’une mobilité restreinte des REE. Ensuite; cette étude montre l’influence du CO2 dissous dans le fluide aqueux sur le partage fluide-roche des HREE. L'étude expérimentale indique que les HREE sont incompatibles dans le pyrope en présence d'un fluide à CO2. Ces résultats permettent d’expliquer l’appauvrissement en HREE sous l'effet de fluides à H2O-CO2 ou à CO2 des métabasites de Vårdalsneset. / REE and Hf mobility in aqueous fluids during HP-BT metamorphism can disturb magmatic signatures of protoliths and Sm-Nd and Lu-Hf dating. This study performed on both natural samples from Vårdalsneset (WGR, Norway) and experimental estimates of REE and Hf partition coefficients between aqueous fluid with NaCl or CO2 and pyrope (P = 3 GPa, T = 800°C) highlights two main results. Firstly, REE can be mobilized at the sample scale (tens of centimetres) whereas Hf is only mobilized at the grain scale. Magmatic signatures of protoliths are nevertheless recognizable and Nd and Hf model ages are not disturbed, that suggests slight mobility of REE. Secondly, an aqueous fluid with CO2 induces an incompatible behaviour of HREE in pyrope, which can explain the depletion in HREE of the metabasites of Vårdalsneset in presence of a H2O-CO2 or CO2 fluid.

Trace element composition of archaeological artifacts is commonly used for provenance studies. Limestone has generally studied by geologists and there are a few researches done by various archaeological sciences. Although it is a common material for buildings and sculpture it is been thought that limestone used had not imported like marbles. Limestone figurines from Dat&ccedil / a/Emecik excavations are classified as Cypriote type, which was very popular through 6th century B.C. in the Mediterranean region. Since this type of figurines was found at Emecik numerously to determine its provenance was an important problem. Emecik figurines were examined for their some major, trace elements and REE compositions and results were compared with geological samples which were taken from a near by quarry. Inductively Coupled Plasma-Optical Emission Spectrometry (ICP-OES), Inductively Coupled Plasma-Mass Spectrometry (ICPMS) have been used for analysis. The methods have been optimized by using standard reference material NIST 1d, NCS DC 73306, and IGS40.

The Neoproterozoic was a time of major change in Earth’s surficial history, including a major rise in atmospheric oxygen, the first appearance of complex metazoan life, and a series of worldwide glaciations. A particular interesting element of these so called “snowball Earth” glacial deposits is the presence of iron formation, a distinctive Precambrian rock type that is largely absent from the post-Paleoproterozoic record. Despite being relatively poorly studied with respect to their geochemistry and sedimentology, Neoproterozoic iron formations are used to support many models for the record of oxygen concentrations of the Earth. The classical example of Neoproterozoic iron formation is the Rapitan iron formation of northwestern Canada. This hematite-jasper iron formation is associated with glaciogenic turbidites and diamictites. Despite being the archetype, the Rapitan iron formation has not been studied in the context of recent ideas about the Neoproterozoic. In this thesis, the stratigraphy, geochemistry, and basin architecture of the Rapitan iron formation are reassessed. Using the REE+Y and the redox-sensitive elements Mo and U, it is shown that the Rapitan iron formation was deposited in a partially restricted basin from biogenically reduced iron under variable redox conditions. Elemental Re and Mo isotopes further show that although oxic and ferruginous conditions predominated during deposition of the iron formation, a transition towards a sulfidic water column locally terminated deposition. Finally, regional stratigraphy and geochemistry show that the iron formation was preferentially deposited in deep, newly formed basins that were protected from significant siliciclastic sedimentation. These basins were delimited by inferred crustal-scale faults trending roughly perpendicular to the axis of the rift basin, and allowed significant changes in thickness and sedimentological character over short distances along strike. These factors help build an overall geotectonic regime under which Neoproterozoic iron formations were deposited: young, deep rift basins that had undergone marine incursion, and were intermittently sealed by an ice shelf, allowing for the generation of an anoxic, iron-rich water column. The absence of the Eu anomaly and the heavy Mo isotopic signature indicate that the open ocean was fully oxygenated at the time of Rapitan iron formation deposition, as opposed to ferruginous as previously suggested.

Carbonatites are unique and enigmatic magmatic rocks of unclear origin, with very specific mineralogy and geochemical properties. They are predominantly composed of magmatic calcite or other carbonate minerals (Le Bas 1987) and have low content of SiO2 (Le Maitre 2002). Origin of these peculiar magmas is still not clear but they appear to represent an important "window" into processes in Earth's mantle. They are considered either as residual melts from a fractionated carbonated nephelinite or melilitite (Gittins 1989; Gittins and Jago 1998), as immiscible fractions of CO2-saturated silicate melts (Freestone and Hamilton 1980; Amundsen 1987; Kjarsgaard and Hamilton 1988, 1989; Brooker and Hamilton 1990; Kjarsgaard and Peterson 1991; Church and Jones 1995; Lee and Wyllie 1997; Dawson 1998; Halama et al. 2005; Brooker and Kjarsgaard 2011), or as primary melts which are were generated from CO2-bearing peridotite through partial melting (Wallace and Green 1988; Sweeney 1994; Harmer and Gittins 1998; Harmer et al. 1998; Ying et al. 2004). Abundances of rare earth elements (REE) are often high in carbonatites because carbonatitic magmas can dissolve these elements much easily than silicate magmas (Nelson et al. 1988). Carbonatitic magma can also dissolve large quantities of Sr, Ba, P and mainly Zr and Nb,...

This study analyzed the acute effect of water consumption on resting metabolic rate (RMR). It was hypothesized that water would have a small, nonclinically significant effect on RMR. Men and women ages 18–40 years participated in a crossover study in which each participant received a No Water and Water condition (order determined randomly) with a 7-day washout period between each condition. Both conditions began with visual analog scales to gauge hunger and thirst levels, urine spectrometry to quantify hydration status, and height and weight measurements. The No Water condition consisted of a 30-minute rest period followed by 45 minutes of RMR testing. The Water condition was identical except for the administration of 500 ml of purified water at 3 °C 10 minutes prior to the beginning of the RMR measurement. Resting metabolic rate testing was done via indirect calorimetry. There was not a condition-by-time difference in 24-hour resting energy expenditure, oxygen consumption, or metabolic equivalents when including all data points and controlling for nonlinearity (ps > 0.0682). There was a significant difference in respiratory quotient (RQ) (F = 13.73; p = 0.0006) with the No Water condition showing a slightly higher RQ than the Water condition. The nonlinear pattern was primarily driven by the first several minutes of testing. Accordingly, we completed analyses without the first 5 minutes of data. The results persisted; that is, there was no condition-by-time effect in 24-hour resting energy expenditure, oxygen consumption, or metabolic equivalents (ps > 0.2435). Further, the RQ remained significantly different (F = 10.57; ps > 0.0023); however, it was slightly higher in the Water condition. This study did not support our hypothesis that consumption of 500 ml of water would have a measurable effect on RMR and fuel utilization compared to not consuming water. Rather, this study replicates other studies that suggest there is not an acute measurable effect of water consumption on RMR. Nevertheless, one positive application of these findings is that water may be a suitable control in RMR studies. In addition, these results should not discourage overall water consumption for healthy functioning. Further, consumption of water-rich foods over time could be an effective strategy for weight management (as shown in other studies). Future studies could attempt to determine if larger volumes of water or different temperatures of water have an effect on RMR.

<p>Cilj istraživanja realizovanih u ovom radu, bio je je da se formalno opišu mogući pristupi transformacijama različitih opisa baza podataka iz jednog modela podataka u drugi i praktično provere kroz njihovu implementaciju u okviru jednog CASE alata, namenjenog projektovanju informacionih sistema i baza podataka. U skladu sa postavljenim ciljem definisan je metodološki pristup i softversko okruženje IIS*Ree koje omogućava visok nivo automatizacije procesa reinženjeringa informacionih sistema. Okruženje IIS*Ree, zasnovano na MDSD principima, kao krajnji rezultat generiše šemu baze podataka u izabranom ciljnom, konceptualnom ili implementacionom modelu podataka, kao i prototip aplikacije.</p> / <p>The goal of the research presented in this paper is to formally specify approaches to transformation of database specifications between different data models. The transformations are then to be implemented and tested using a CASE tool for modelling information systems and databases. Following this goal, a methodological approach is defined together with a software named IIS*Ree that provides a high level of automation of the information system reengineering process. The IIS*Ree software, developed in accordance to MDSD principles, generates database schemas specified in a target, conceptual or implementation data model, as well as application prototypes.</p>

La these s'integre dans la theorie des representations d'un groupe reductif fini. Un tel groupe est defini comme <b>G</b>^F, ou <b>G</b> est un groupe reductif connexe sur un corps algebriquement clos de caracteristique p>0 et F est un endomorphisme tel que l'ensemble des points fixes <b>G</b>^F est fini.<br />Dans cette situation, on obtient une famille de groupes finis en remplacant F par une puissance F^m. Cette idee joue un role important dans la theorie generale des groupes reductifs finis; elle est notamment developpee par Lusztig.<br />Dans le cas ou m=2, F agit comme un automorphisme sur <b>G</b>^F². On peut donc former le produit semi-direct de <b>G</b>^F² par F; la descente de Shintani definit alors une isometrie de l'espace des fonctions centrales sur la tranche <b>G</b>^F².F dans l'espace des fonctions centrales sur <b>G</b>^F. Le but de la these est d'etudier cette isometrie dans le cas des groupes de Suzuki et de Ree de type B₂ et G₂, definis par un endomorphisme F "tres tordu" (dans le sens que F n'est pas un endomorphisme de Frobenius). Ce dernier fait entraine un certain nombre de problemes au niveau de la theorie generale. Nous determinons donc explicitement la table des valeurs des fonctions centrales sur la tranche <b>G</b>^F².F.<br />Comme applications, nous pouvons explicitement determiner les valeurs propres associees par Lusztig aux representations unipotentes cuspidales du groupe de Suzuki et de Ree. Nous pouvons aussi verifier un certain nombre de conjectures dans la theorie des representations modulaires: conjecture de Broue, existence des ensembles basiques. Plus generalement, la determination des tables des caracteres des extensions cycliques rentre dans le projet de determiner les tables des caracteres de toutes les extensions des groupes finis simples.