Baird's pocket gopher (Geomys breviceps) is found in eastern Texas, eastern Oklahoma, central and western Arkansas, and western Louisiana. The cytochrome-b gene was sequenced and analyzed for 16 pocket gophers from throughout the range of the species. Similar phylogenetic trees were obtained using maximum-parsimony, maximum-likelihood, neighbor-joining, and Bayesian analyses. Two major clades were formed with northern individuals belonging to clade I and southern individuals belonging to clade II. G. b. sagittalis was paraphyletic in relation to G. b. breviceps in all analyses. Based on inconsistencies between the taxonomic classification and systematic relationships within Baird's pocket gopher, a taxonomic restructuring appears warranted.

This dissertation examines the ability of in vitro biotransformation assays to provide an indication of metabolic potential. The potential for xenobiotic compounds to bioconcentrate in aquatic organisms is expressed through the bioconcentration factor (BCF). The metabolic loss of ibuprofen, norethindrone and propranolol was measured using rainbow trout (Oncorhynchus mykiss) and channel catfish (Ictalurus punctatus) gill and liver S9 fractions, microsomes and cell suspensions. Metabolic transformation rates (kM) were extrapolated from in vitro intrinsic clearance of parent compound (CLm) and integrated into a refined BCF model. In general, CLm of test compounds was greater in liver S9 fractions and hepatocytes. However, the influence of hepatic metabolism on kM and BCF was limited by hepatic blood flow (20-25%) compared to gill blood flow (~100%). A significant difference was noted between BCF solely based on KOW and BCF including kM. These studies indicate that the inclusion of kM in BCF models can bring predicted bioconcentration estimates closer to in vivo values. Primary cell suspensions are preferred over subcellular fractions as cell suspensions possess both phase I and phase II enzyme activity. Further study was conducted on ibuprofen biotransformation pathways. As fish do not contain the same cytochrome P450 (CYP) 2C homologs known to …

Northern bobwhite populations have declined concurrent with global warming. The focal period of this study was the 12-d pre-incubation period, when bobwhite eggs remain in the nest without the thermal protection of the incubating parent. This study first established the storage and thermal limits of bobwhite eggs, then investigated how global warming may impact oviparous embryos and how bobwhite embryos react to acute and chronic doses of simulated drought temperatures during pre-incubation. First, the maximum storage limit of bobwhite eggs was determined by storing eggs ≤21 d and measuring hatching success and pH of egg albumen and yolk. Hatching success of stored eggs declined after 14 d, when yolk and albumen pH reached levels detrimental to embryonic development. Secondly, thermal limits were determined by exposing bobwhite eggs to hyperthermic temperatures (38-52 °C). Bobwhite embryos survived 50 °C for 1 h, 49 °C for 3 h and 46 °C for 6 h. Results indicate an adaptation to the naturally occurring temperature extremes that can occur in the bobwhite's southern range during pre-incubation. Subsequently, bobwhite eggs were exposed to either low constant (LC), low fluctuating (LF), high constant (HC), or high fluctuating (HF) temperatures during pre-incubation to determine if the nature of …

Polycyclic aromatic hydrocarbons (PAHs) are a well studied and diverse class of environmental toxicants. PAHs act via the aryl hydrocarbon receptor (AhR), and studies have suggested that PAHs may elicit neurological and estrogenic effects. Doses of PAHs between 50 to 150 ppm may elicit neurotoxicity in rodent models. The present study investigated the effects of naphthalene on in vivo steroidogenesis in Swiss Webster male mice, and in vitro neural function of Balb-C/ICR mice frontal cortex neurons. These data suggest that naphthalene may not elicit steroidogenic effects at concentrations ranging from 0.2 to 25 mg/kg/day, following a 7 day subcutaneous dosing regime. In addition, naphthalene may cause functional toxicity of frontal cortex neurons at concentrations of 32 to 160 ppm naphthalene.