Thesis (Ph. D.)--University of Wisconsin--Madison, 1961. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.

Genic data from two chromosomal races of Geomys bursarius from a contact zone in central Texas indicated that the two races possessed distinct gene pools which would define them as separate species. Data from proteins encoded from 21 loci in this study substantiated this hypothesis. A pattern of alternately fixed alleles at the ADH-l, MDH-2, LDH-l, and IDH-1 loci with no apparent gene flow in zones of contact strongly suggested that these two races should be designated as separate species. Levels of heterozygosity and high FST values indicate that genomic structuring within Geomys is most heavily influenced by high levels of inbreeding and low migration rates. Fossorial rodents were suggested to undergo speciation primarily through parapatric means.

Genetic variation was analyzed for populations of seven taxa comprising four cytotypes of the Geomys bursarius chromosome complex, including G. b. major, G. b. knoxjonesi, and the Edwards Plateau taxa, G. b. llanensis and G. b. texensis. Genetic relationships of the Edwards Plateau gophers with other taxa and between themselves were examined. Genetic similarity, number of fixed allelic differences, and ectoparasite distribution indicate the Edwards Plateau gophers are a distinct gene pool. Isolation of the Edwards Plateau taxa precludes contact zone analysis. However, genetic differentiation is typical of that between other species of Geomys, and the Edwards Plateau taxa should be recognized as G. texensis. Distributions of allelic frequencies indicate little justification in retaining the subspecific status of the Edwards Plateau forms.

Electrophoretic techniques were utilized for the demonstration of variation in 22 proteins from 24 natural populations of four species ( G. bursarius, G. pinetis, G. arenarius and G. personatus ) of the Geomys complex of pocket gophers. Of the 24 structural loci , 19 were considered to be polymorphic. Five of the six esterases contributed greatested to the polymorphism while non-esterase proteins generally showed low values. In the GeoMys complex of pocket gophers in this study,selection appeared to be the most important influence on genetic structure with some evidence of random drift in two of the four species. Populations of G. arenarius and G. personatus had the highest average interspecific genetic similarities to G. bursarius and . pinetis was the most divergent. Biochemical evidence supports the phylogeny of Geomys based on morphological and fossil data.

The Baird’s pocket gopher (Geomys breviceps) is a solitary, fossorial rodent found throughout areas of Texas, Arkansas, Oklahoma, and Louisiana. Research focusing on the population genetics of pocket gophers and other species with limited vagility and isolated populations is lacking. Through the use of mitochondrial and microsatellite data, a series of population genetic analyses were completed to better understand the population structure and gene flow among a series of G. breviceps localities. Pocket gophers were captured from five localities in the Brazos Valley and used in this study. Due to the lack of microsatellite loci available for G. breviceps, 10 loci were created for use in this study. Overall estimates from the population genetic analyses showed high levels of gene flow amongst nearby localities with decreasing levels as distance between localities increased. Findings suggest that 2-3 localities located within 2 km of each other function as one genetic cluster thus showing 3-4 total genetic clusters total in this study. Results also suggest that the Baird’s pocket gopher is capable of moving at least 2 km, but further analyses should be completed to better understand dispersal distance.

A new subspecies of the plains pocket gopher (Geomys bursarius ozarkensis), located in the Ozark Mountains of north central Arkansas, was recently described by Elrod et al. (2000). Current range for G. b. ozarkensis was established, habitat preference was assessed by analyzing soil samples, vegetation and distance to stream and potential pocket gopher habitat within the current range was identified. A census technique was used to estimate a total density of 3, 564 pocket gophers. Through automobile and aerial survey 51 known fields of inhabitance were located extending the range slightly. Soil analyses indicated loamy sand as the most common texture with a slightly acidic pH and a broad range of values for other measured soil parameters and 21 families of vegetation were identified. All inhabited fields were located within an average of 107.2m from waterways and over 1,600 hectares of possible suitable habitat was identified.

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.