ix, 131 leaves : ill. ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (Ph.D.1974)--University of Adelaide, Dept. of Zoology, 1974

ix, 131 leaves : ill. ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (Ph.D.1974)--University of Adelaide, Dept. of Zoology, 1974

The overall objective of this project was to investigate the effects of the symbiotic association of plants with vesicular - arbuscular mycorrhizal fungi on the intensity of intraspecific competition and its consequences on population structure I performed four main glasshouse experiments using a non - cultivated species, Rhodanthe chlorocephala ssp rosea, or a cultivated species, Trifolium subterraneum. I grew the plants at different plant densities, under different levels of resources ( phosphorus and / or light ), in environments with homogeneous and / or patchy distribution of phosphorus ( P ). In pots with homogeneous distribution of P, the addition of P to R. chlorocephala and mycorrhizal infection in T. subterraneum increased plant biomass of single plants. However, these beneficial effects were reduced by increasing plant density. Shading of plants of T. subterraneum did not generally alter these effects. Mycorrhizal symbiosis and the addition of P always increased the intensity of plant intraspecific competition. In trays with patchy or homogeneous distribution of P, mycorrhizal infection and patchy distribution of P increased the total biomass and size inequality of populations of plants of T. subterraneum. Individual biomass was determined by the local soil P concentration in patchy environments and by mycorrhizal infection in low density treatments. Mycorrhizal infection, but not patchy P distribution, increased relative competition intensity. Asymmetric or symmetric distribution of resources between plants will change these size hierarchies. The distinction between these two types of distributions has lead to two different models explaining the interaction between competition and size inequality ( degree to which the biomass is concentrated within a small fraction of the population &# 40 Weiner and Thomas 1986 ) ) the resource depletion and resource pre - emption models ( Weiner and Thomas 1986, Weiner 1988b ). In the first model ( resource depletion ) competition reduces the relative growth rate of all the individuals by the same proportion, reduces variance of growth rates and reduces variation in sizes. Thus, in this model resource acquisition is proportional to plant size ( Weiner 1990 ). This model is also called symmetric or two - sided competition and applies when competition for nutrients predominates. It predicts that at high density, plants will be smaller but the population will have less inequality than at low density ( Weiner and Thomas 1986 ). In the second model ( resource pre - emption ), competition increases the variation in relative growth rates and increases variation in sizes. Large plants obtain a more than proportional share of the resources ( relative to sizes ) ( Weiner 1990 ) and this increases their competitive ability which results in a positive feedback on plant size. This phenomenon is also called snowball cumulation, asymmetric or one - sided competition and it was observed only when competition for light was predominant ( Wilson 1988a ). This second model predicts that at high density plant populations will have more inequality than at low density ( Weiner and Thomas 1986 ). Although these two models are generally accepted, alternative analyses and recent experiments show that the degree of asymmetry of the interaction depends on the spatial and temporal distribution of the resource, the spatial distribution of the individuals in the population, neighbourhood competition and the mobility of the resource ( Huston 1986 ; Miller and Weiner 1989, Weiner 1990, Bonan 1991 ). Weiner ( 1990 ) suggested that if nutrients are distributed homogeneously and the uptake is proportional to root size, the competitive interaction will be more symmetric, whereas if patches with more nutrients can be reached by large individuals, asymmetric competition will predominate. This hypothesis has not been tested yet. Turner and Rabinowitz ( 1983 ) found that populations with an initial random spatial distribution of individuals had an unexpected increase in size inequality. My results emphasise that the main effects of mycorrhizas at the individual level cannot be expected to be apparent at the population level, because of the influence of density - dependent processes. However, infected individuals with a strong response to the symbiosis would have an advantage in situations of competition. This scenario can explain the maintenance of the symbiotic ability even under conditions such as dense populations, where there is no obvious advantage of the symbiosis at the population level. / Thesis (Ph.D.)--Department of Soil and Water, 1998.

Doctor of Philosophy / Dental caries continues to be a significant public health problem affecting mankind in many parts of the world. Microbial activities include the progressive localised destruction of teeth that without treatment, would eventually result in infection of the dental pulp and surrounding periapical tissues. Although the bacteria responsible for caries initiation and early caries progression have been extensively studied, the microbiology of dentine caries is reported to show considerable diversity and has not yet been fully identified. Few studies have analysed the microbiology of deep caries or examined the relationship between the microflora and the histopathy of chronic pulpits in symptomatic teeth. Matched carious dentine samples and dental pulps were obtained from teeth without evidence of periodontal disease but with coronal caries and symptoms of pulpits. Bacteria were cultured from the carious dentine samples under both anaerobic and microaerophilic conditions. Real-time polymerase chain reaction (PCR) technology was also used to identify and enumerate the bacteria. Development of the techniques for the efficient extraction of bacterial DNA from both Gram-negative and Gram-positive bacteria found in carious dentine was an essential prerequisite for molecular analysis. In addition, the dental pulps were processed and categorised into one of four groups on the basis of dominant pathology of the tissue (minimal inflammation, soft tissue degeneration, hard tissue degeneration, inflammatory degeneration). Analysis of the culture data indicated a predominance of Gram-positive bacteria, particularly lactobacilli, while Gram-negative bacteria were also present in significant numbers with Prevotella species the most numerous anaerobic group cultured. Real-time PCR indicated a greater anaerobic microbial load than that determined by colony counting. The total number of anaerobes detected by PCR was 41-fold greater, while Prevotella spp. and Fusobacterium ssp. were 82-fold and 2.4-fold greater respectively. PCR also identified the presence of Micromonas micros, Porphyromonas endodontalis and Porphyromonas gingivalis in 71%, 60% and 52% of carious dentine samples, respectively. Correlation matrices from the real-time PCR data revealed significant multiple associations involving Fusobacterium spp. in combination with P. endodontalis, M. micros and/or Prevotella in the tissue response categories of minimal inflammation, soft and hard disuse degeneration. A positive correlation was also observed between M. micros and P. endodontalis for the category of inflammatory degeneration of the dental pulp. These anaerobes have been strongly implicated in the endodontic infections that occur as sequelae to carious pulpitis. Accordingly, the data suggest that the presence of threshold levels of these bacteria in carious dentine may be indicative of irreversible pulpitis. Knowledge of the microbial predictors associated with irreversible pulpitis creates potential for the development of a diagnostic tool, and for restorative materials with antimicrobial properties.

Thesis (M.S. - Biological Sciences)--University of Arizona. / Includes bibliographical references.

Thesis (Ph. D.)--University of Adelaide, 1986. / Includes bibliographical references (p. [i.e. leaves ] 267-277).

Thesis (Ph. D.)--University of Auckland, 1990. / Includes bibliographical references.

Thesis (Ph. D.)--University of California, Davis, 2003. / Includes bibliographical references. Also issued online.

Thesis (Ph. D.)--University of Washington. / Bibliography: l. 138-143.

Thesis (Ph.D.)--McMaster University, 2002. / Advisor: Jurek Kolasa. Includes bibliographical references. Also available via World Wide Web.