No description available.

No description available.

This thesis examines the effect of spatial resolution on lithological and alteration mapping using remotely sensed multispectral data. The remotely sensed data were obtained by the Thematic Mapper (TM) and Airborne Thematic Mapper (ATM) over two areas in the Arabian Shield. These were the Mahd Adh Dhahab and Jabal Said areas. The ATM data had a nominal spatial resolution of 7.5m, 5m, and 2.5m. In order to compare these data sets it was necessary to correct for, sensor- and scene-related distortions. This was achieved by calibrating each data set and converting them to reflectance units using ground spectra with a similar spectral resolution obtained with the Barringer Hand Held Ratioing Radiometer (HHRR) . The ATM data were also corrected for X-track shading by normalising the brightness of each column to that of the centre column. The result of X-ray and laboratory spectral analysis of samples collected from the study areas, support the presence of characteristic minerals associated with the alteration zones. The corrected data were analysed by a variety of techniques in order to enhance the geological information present in the data. These included false colour compositing, decorrelating stretching and band ratioing. The latter two techniques proved most effective for discrimination and several additional geological units and areas were identified which had not been mapped previously. Results further indicate that the increased spatial resolution of the ATM data did not permit greater discrimination than the TM data. This suggests TM data should prove to be a cost-effective way of mapping and detection of alteration zones in the Arabian Shield.

No description available.

The primary goal of this research was the facilitation of cross-cultural communication between local Anishinaabe and settler communities within the context of the Rat Portage Common Ground Conservation Organization. Through the course of this study a combination of western cartographic conventions, phenomenological principles, and cultural asset mapping techniques have been applied. The original data discussed are the aggregation of three separate data collection initiatives. Each initiatives' individual results have been utilized in various ways to record, communicate, and verify the final research process and products. The research also sought to gain insight into the application of particular mapping methodologies to a phenomenological inquiry. The phenomenon under investigation was the place-based Anishinaabe cultural landscapes of the Common Ground Lands. While the employed mapping conventions were found to assist in realizing the phenomenological objectives of the research, it was also observed that phenomenology itself offered valuable insights into the act of mapping.

Thesis (Ph. D.)--University of Hawaii at Manoa, 2004. / Includes bibliographical references (leaves 147-159). / Also available by subscription via World Wide Web / xv, 159 leaves, bound ill. (some col.) 29 cm

Thesis (M.S.)--University of Hawaii at Manoa, 2005. / Includes bibliographical references (leaves 104-105). / vi, 105 leaves, bound ill. (some col.), col. maps 29 cm

After the initiation of the human genome sequencing project and the introduction of the field of ‘bioinformatics’, interest in human genetic diversity studies has been increased. Sequence diversity has helped define differences between genes and genomic regions that were previously unknown or difficult to determine. In this thesis I have undertaken to study sequence diversity in the human genome in three areas; 1) investigated diversity in the MHC as represented by the MICA alleles with respect to the known HLA alleles, 2) investigated the structure and diversity in the intergenic region from an MHC related (paralogous) genomic region and related the structural and diversity findings to the knowledge available on the MHC and the wider genome, and 3) described the identification of three and characterization of five new MHC class I polymorphic markers (Alu) and their polymorphic characteristics in worldwide populations and their associations with skin cancer. 1. Phylogenetic analysis of MICA alpha-domain (extracellular) sequences demonstrated relationships with HLA-B cross-reactive serogroups. The HLA-B and MICA loci are in linkage disequilibrium. The data indicated that MICA and HLA-B have evolved in concert from their common ancestors and that the transmembrane polymorphisms have arisen independently and more recently. 2. Sequence analysis of the CD1 genomic region confirmed the presence of five CD1 genes and revealed that there are four unrelated intergenic regions (IGRs). The IGRs are composed mostly of retroelements including five full-length L1 PA sequences and various pseudogenes. Genomic and phylogenetic analyses support the view that the human CD1 gene copies were duplicated prior to the evolution of primates and the bulk of the HLA class I genes found in humans. 3. Five polymorphic Alu insertions (POALINs) were identified (two from previous studies) and located within the 1.8 megabase of the MHC class I genomic region. All five POALINs are polymorphic, and are positively associated with the HLA-A and HLA-B alleles. The AluyHJ insertion was found most frequently associated with HLA-A1 or A24, AluyHG with HLA-A2, AluyHF with HLA-A2, A-10 or -A26 and AluyTF showed a marginal association with HLA-A29. The AluyMICB insertion was strongly associated with HLA-B17 (HLA-B57, HLA-B58) and HLA-B13. The presence of three Alu insertions (AluyHJ, AluyHG and AluyHF) was found in only one HLA class I haplotype (HLA-A1, -B57, -Cw6) in the 10th IHW cell lines. A novel positive association between the presence of AluyMICB and the ‘MICAdel/MICBnull/HLA-B48’ haplotype was determined. The AluyMICB insertion was also associated with at least three different MICB alleles (*0102, *0107N and *0105) and three different HLA-B alleles (B13, B48 and B57). Based on the analysis of associations between different polymorphic markers within the beta block, the MICB*0102 allele was inferred to be the ancestral form of the MICB*0105 and MICB*0107N alleles. The AluyMICB polymorphism can be used to further investigate haplotype relationship and consequently their lineage origins. Some of the MHC POALINs are haplospecific and associate strongly with certain groups of HLA class I alleles and MHC ancestral haplotypes. The AluyTF frequency was significantly associated with skin cancer (p<0.005). MICA gene diversity is derived from two different evolving paths, therefore one or the other alone cannot reliably mark an ancestral haplotype. The CD1 duplicons originated well before the HLA class I duplicons. The MHC POALINs provide new lineage and linkage markers for the fine mapping study of different haplotypes and variations in linkage groups across 1.8 Mb of the MHC class I region. The POALINs may also prove useful in investigating the origins and history of human populations and in determining the role of human genetic diversity in disease risk.

Thesis (Ph. D.)--University of Adelaide, Dept. of Genetics, 1984. / Includes bibliographical references (31 unnumbered leaves at end of vol).

Thesis (Ph.D.)--University of Texas at Dallas, 2007. / Includes vita. Includes bibliographical references (leaves 102-110)