No description available.

Attenuation of uranium (U) and rare earth elements (REEs) has been observed in stream and wetland sediments, but the geochemical and mineralogical processes involved in sequestering these elements in natural systems are not well understood. The decommissioned Bicroft Uranium Mine near Bancroft, ON uses a modified stream and wetland system to reduce the concentrations of U and other metals in tailings pond effluent to levels below the Provincial Water Quality Objectives. The Bicroft Mine was operated from 1957 to 1963, and processed low-grade (~0.17 wt% U3O8), disseminated U hosted by pegmatite dykes in amphibolite gneiss, forming 2,284,421 tonnes of tailings, deposited into two tailings impoundments. The Bicroft site has since operated as a passively attenuating stream and wetland remediation system for 55 years, demonstrating the potential longevity and viability for long-term sequestration of U and REEs through natural attenuation. To identify U and REE hosts and their stability in the natural environment, colloids, tailings, stream and wetland sediments were analyzed using various methods, including tangential flow filtration (TFF), ICP-ES/MS, scanning electron microscopy, and synchrotron techniques (bulk and µXANES, µXRF, and µXRD). The results show that Fe- and Mn-oxyhydroxides, goethite, and birnessite are the main mineral hosts for U and REEs in both the colloids and sediments. In addition, detrital grains of U- and REE-bearing minerals were found >200 m downstream in colloids and wetland sediments, showing the potential for long range transport of colloids and particulates in the stream system. Seasonal influences on the stability of trace metals in sediments were observed, and may demonstrate the limitations of passively attenuating remediation systems as a viable method for attenuation. Changes in the redox state of the stream system were observed to influence the attenuation of U and REEs, however, changes in the redox state with depth in the wetland sediments were not observed, and showed no direct influence on the attenuation of U and REEs. The results of this study will help to develop better monitoring strategies for U tailings sites and should reduce the impacts of future U mining operations. / Thesis (Master, Geological Sciences & Geological Engineering) -- Queen's University, 2013-05-06 07:44:03.327

Ecological and evolutionary factors affecting threatened and endangered species may compromise a population’s ability to persist through time. Here, I determined how plant mating system, pollination biology, pollen source, habitat type, and white-tailed deer (Odocoileus virginianus) herbivory affected the persistence of a rare wetland endemic plant, Polemonium vanbruntiae (Eastern Jacob’s ladder). In contrast to several of the more common species of Polemonium, I found no pollen limitation in populations of P. vanbruntiae. The lack of pollen limitation was best explained by the capacity for P. vanbruntiae to self-fertilize. However, pollinators play an important role as inter- and intra-plant pollen vectors in this system because female reproductive fitness was greatly reduced when pollinators were excluded. These results support the reproductive assurance hypothesis, whereby the ability to self assures fertilization for plants in small populations. A mixed-mating strategy, including the ability for clonal reproduction, may explain the ability for this rare species to persist in small, fragmented populations. However, mixed mating strategies may incur both costs and benefits. The ability to self-fertilize may provide reproductive assurance that when pollinators and/or potential mates are scarce. Yet, selfing is potentially costly when the result is a reduction in offspring quantity and quality. I found that the relative performance of selfed offspring was lower than outcross offspring in terms of germination and offspring vigor. When pollen is received from a distant site, offspring exhibit heterosis with increased vigor in terms of more leaves, larger leaf area and height. Although I was unable to follow offspring survival to flowering, enhanced germination success and more vigorous growth suggest that gene flow among populations may increase plant vigor and enhance genetic variation within small, isolated populations of P. vanbruntiae. For long-lived organisms such as perennial plants, it is often difficult to determine which environmental factors will have the largest effects on long-term population dynamics. I incorporated the effects of habitat type and white-tailed deer herbivory into a population viability model for P. vanbruntiae to determine the effects of both habitat and herbivory on long-term ramet dynamics. Polemonium vanbruntiae ramets in wet meadow habitats are expected to increase at a faster rate than ramets in the forest seep habitats, but P. vanbruntiae is expected to increase over time in both habitat conditions. White-tailed deer preferentially browsed adult ramets, primarily those occurring in forest seep sites. Deer browsing significantly decreased the predicted population growth rate under stochastic conditions, although P. vanbruntiae ramets are expected to increase at a slow rate in the future under herbivore pressure. Herbivory also increased the extinction risk to a detectable level. Deer browsing shifted the potential for younger life histories stages to change future population growth. Instead, survival and stasis of large vegetative ramets became the vital rates having the largest potential impact on future population growth. Thus, active long-term management of deer populations appears necessary for the guaranteed persistence of populations of rare, endemic herbs such as P. vanbruntiae.

The 'RMnO3': R = La, Nd, Pr, phases have been synthesised and characterised by a combination of electron probe microanalysis (EPMA), H2-reduction thermogravimetry (TG), x-ray (XRD) and neutron diffraction (ND). RMnO3 forms, at" 1400C, over the ranges: NdMn0, 95Oz to Nd0 88MnOz PrMn0.97O2 to Pr0 88MnOz LaMno 0.90Oz to La0.97MnOz Oxygen contents vary in air over the range 700 to 1400 C and can be varied further, either by high pressure Oz treatment or by reduction in H2. The structure of 'RMnO3' R = Nd, Pr is based on the GdFe03 structure with a Jahn-Teller distortion associated with the high proportion of Mn3+ ions present. The oxygen deficient 'LaMnOz' compositions also exhibit this structure consistent with earlier reports. By combining EPMA, TG, XRD and ND results various defect models describing the stoichiometry and structure of Mn-rich and R-rich, R = Nd, Pr compositions have been summarised. Both R = Nd and Pr systems exhibit very varied defect structures; depending on composition and heat treatment, vacancies can form on any one or any two of the three sublattices, R, Mn and O and the overall Mn oxidation state can include 2+, 3+ and 4+ contributions. For 'RMn03': R = La, Nd, Pr, data on their compositional ranges and defect crystal structures are presented in the form of novel phase diagram-defect structure maps from which the principal defect structure for a given stoichiometry can be easily obtained. The majority of the Pr-Sr-Mn-O pseudotemary phase diagram has been determined. EPMA was used to follow the progress of reaction and the conditions to achieve complete reaction established. Several solid solutions were evidenced, some previously unreported (3 - 6): 1) Pr1.xSrxMnO3 0[Special character omitted]x[Special character omitted]1.0 2) Pr1+xSr2.xMn2O7 0 [Special character omitted]x [Special character omitted] 0.4 3) SrxPr1-xO2 0[Special character omitted]x[Special character omitted]0.16 4) Sr1-xPrO3 0[Special character omitted]x[Special character omitted]0.15 5) Sr2.xMnxO4 6) Sr2.xPrxMnO4 The perovskite-like Pr1-xSrxMnO3 solid solution extends from PrMnOz to SrMnOz. The unit cell symmetry changes from orthorhombic to rhombohedral to tetragonal to cubic and finally to hexagonal as the Sr content increases. The limits of the Ruddlesden Popper (RP) n=2 Pr1+xSr2_xMn2O7 solid solution were determined: 0 [Special character omitted] x [Special character omitted] 0.4 and a tetragonal unit cell observed consistent with the literature. Synthesis of the RP compositions by solid state methods requires long heating times (up to 36 days) to produce homogeneous samples; qualitative EPMA of younger samples indicated an inhomogeneous distribution of Pr and Sr. Contrary to EPMA results, XRD of younger samples indicated that complete reaction had occurred and single phase compositions produced. It is suggested that the SrxPr1-.xO2 solid solution extends over the range 0 [Special character omitted] x [Special character omitted] 0.16 where similarly to the polymorphism of praseodymium oxides, compositions 0.03 [Special character omitted] x [Special character omitted]0.16 exhibit the cubic fluorite-type structure of Pr6O11 and x [Special character omitted] 0.03 is a mixture of cubic SrxPr1-xO2 and hexagonal SrxPr2.xO3. Perovskite-like SrPrO3 exhibits variable cation ratios; the Pr-rich boundary is Sr0.85PrOz. The lower Sr-rich boundary is yet to be identified. Similarly to 'RMnO3': R = La, Nd, Pr, the oxygen content of 'SrPrOz' is expected to vary. Therefore, various possible defect structures describing vacancies on the three sublattices, Sr, Pr and O could exist and charge compensation would be an interesting example of ionic and electronic mechanisms where Pr adopts the +4 and +3 oxidation states. Four layer hexagonal SrMnO3 exhibits variable Sr:Mn ratios but the solid solution limits are not yet known. The unreported Sr2-xPrxMnO4 solid solution has been observed but the solid solution limits are not yet known. The K2NiF4-type structure of Sr2Mn04 is retained at x = 0.75 and is expected to contain Mn3+ as Mn4+ is reduced to compensate Sr24 substitution by Pr3+.

Digitized by Kansas Correctional Industries

Epidermolysis Bullosa simplex (EBS) is a rare genetic disorder that is typically inherited in an autosomal dominant fashion and affects approximately 1 out of 20 000 individuals. This disease is caused by mutations in either the KRT14, KRT5 or PLEC genes. These genes code for proteins involved in the formation of the cytoskeleton in basal keratinocytes, which form the basal layer of the epidermis. The cytoskeleton provides structural support to the basal keratinocytes and mutations in these genes cause cytoskeletal malformations, making these cells more susceptible to physical stress. This results in the cells undergoing lysis under trivial mechanical stress and causing the epidermis to detach from the dermis, the layer immediately below the epidermis. This leads to the primary symptom of EBS: the formation of blisters. The goal of this project is to recreate EBS in zebrafish using transgenesis and to create stable mutant transgenic line. In the future, high throughput drug screening will be done on mutant zebrafish embryos to find potential drug candidates that can alleviate the symptoms of EBS. To accomplish this, missense and deletion mutations in zebrafish krt5 cDNA using site-directed mutagenesis were performed. It was previously shown that mice models for this disease die shortly after birth and thus no stable mutant lines were able to be created. To ensure embryo survival and avoid a similar fate, mutant krt5 cDNA was expressed in non-essential tissue, such as the embryonic fin fold using a fin epithelial-specific enhancer named epi. These constructs were injected into one-cell stage zebrafish embryos, which were raised and screened for integration of the construct in their germ cells. While results from injected embryos were promising, mutant transgenic zebrafish did not demonstrate any blistering. In an attempt to induce blistering, mutant zebrafish embryos were placed under various environmental stressors known to worsen the symptoms of EBS. This was not successful. Expression of mutant keratin 5 in the basal epidermis of the entire embryo using the 2.3kb upstream region of the zebrafish krt5 gene to drive expression also did not yield any results. More investigations are needed to determine if it will be possible to use the zebrafish to model EBS.

No description available.

Abstract not available

Thesis (Ph. D.)--University of Texas at Austin, 2006. / Vita. Includes bibliographical references.

Brookhaven National Laboratory experiment E949 was designed to search for the rare K meson decay K⁺ → π⁺ , neutrino, and anti-neutrino, a decay sensitive to physics beyond the Standard Model. While previous data analyses dealt with the high π⁺ momentum region accessible for this reaction, this thesis concentrates on the lower range between 140 and 199 MeV/c. Analysis of this low π⁺ momentum region was performed to search for additional evidence of the process K⁺ → π⁺, neutrino, and anti-neutrino. A blind analysis technique was used to avoid bias when developing the selection criteria used to suppress the competing background processes. The blind analysis technique was based on identifying background sources a priori and only examining the signal region once all selection criteria and background estimates had been finalized. The background estimates were performed using a technique known as a "bifurcation method", which relied on using two uncorrelated selection criteria to suppress each background source. The analysis of an exposure of 1.71 x 10¹² K⁺ decays resulted in an observation of three events with an estimated background of 0.927 ± 0.168(stat.)⁺³²⁰-₀.₂₃₇(sys.) events and a single event sensitivity of (4.28 ± 0.43)x 10-¹⁰. Using a likelihood method, the three candidate events observed here were combine with the previous E787 and E949 results, yielding a branching ratio of ϐ(K⁺ → π⁺, neutrino, and anti-neutrino decay of (1.73+1.15-1.05) x 10⁻¹⁰ at the 68% confidence level. This branching ratio is consistent with the prediction of the Standard Model, (0.85 ± 0.07) x 10⁻¹⁰.