Weekly collections were conducted from May to December, 2007 (153 trap nights, total) in Denton, Texas, in and around large storm drains and overpass drainage facilities in residential and non-residential areas, using Centers for Disease Control (CDC) light traps and gravid traps. A total of 1964 mosquitoes were collected, representing 24 species within 6 genera: Aedes, Anopheles, Culiseta, Culex, Psorophora, and Uranotaenia. Culex was the most abundant genus, representing 75% of all mosquitoes collected; Aedes was the second most abundant, representing 12 % of all mosquitoes collected. Cx. quinquefasciatus was the dominant species collected via gravid traps; Cx. (Melanoconion) species were the dominant species collected via CDC light traps. Data of gravid traps and light traps were analyzed separately using nonparametric correlation analysis, comparing environmental data and physical characteristics to total abundance of mosquitoes. There was no significant correlation found when comparing the three dominant species collected in light traps (unidentified Cx. (Melanoconion) sp, Cx. quinquefasciatus, and Ae. vexans) to environmental characteristics and physical characteristics. Analysis of Cx. quinquefasciatus collected in gravid traps indicated no significant correlation between abundance, environmental data, and physical characteristics. Linear regression models were analyzed to determine if either environmental variables or physical characteristics of the …

The soil-nematode Caenorhabditis elegans survives oxygen deprivation (anoxia < 0.001 kPa of O2, 0% O2) by entering into a state of suspended animation during which cell cycle progression at interphase, prophase and metaphase stage of mitosis is arrested. I conducted cell biological characterization of embryos exposed to various anoxia exposure times, to demonstrate the requirement and functional role of spindle checkpoint gene san-1 during brief anoxia exposure. I conducted a synthetic lethal screen, which has identified genetic interactions between san-1, other spindle checkpoint genes, and the kinetochore gene hcp-1. Furthermore, I investigated the genetic and cellular mechanisms involved in anoxia-induced prophase arrest, a hallmark of which includes chromosomes docked at the nuclear membrane. First, I conducted in vivo analysis of embryos carried inside the uterus of an adult and exposed to anoxic conditions. These studies demonstrated that anoxia exposure prevents nuclear envelope breakdown (NEBD) in prophase blastomeres. Second, I exposed C. elegans embryos to other conditions of mitotic stress such as microtubule depolymerizing agent nocodazole and mitochondrial inhibitor sodium azide. Results demonstrate that NEBD and chromosome docking are independent of microtubule function. Additionally, unlike anoxia, exposure to sodium azide causes chromosome docking in prophase blastomeres but severely affects embryonic viability. …

The primary objectives of this project were: 1. to develop improved methods for extraction of DNA from human skeletal remains, 2. to improve STR profiling success of low-copy DNA samples by employing whole genome amplification to amplify the total pool of DNA prior to STR analysis, and 3. to improve STR profiling success of damaged DNA templates by using DNA repair enzymes to reduce the number/severity of lesions that interfere with STR profiling. The data from this study support the following conclusions. Inhibitory compounds must be removed prior to enzymatic amplification; either during bone section pretreatment or by the DNA extraction method. Overall, bleach outperformed UV as a pretreatment and DNA extraction using silica outperformed microconcentration and organic extraction. DNA repair with PreCR™ A outperformed both whole genome amplification and repair with PreCR™ T6. Superior DNA extraction results were achieved using the A6 PMB columns (20 ml capacity column with 6 layers of type A glass fiber filter), and DNA repair with PreCR™ A led to an overall improvement in profile quality in most cases, although whole genome amplification was unsuccessful. Rapid, robust DNA isolation, successful amplification of loci from the sample-derived DNA pool, and an elimination of DNA damage …