No description available.

Thesis (M.Sc.) - Carleton University, 2008. / Includes bibliographical references (p. 138-145). Also available in electronic format on the Internet.

Thesis (Ph. D.)--University of Wisconsin--Madison, 1959. / Typescript. Abstracted in Dissertation abstracts, v. 20 (1959) no. 2, p. 450. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 89-93).

Competition from non-crop vegetation decreases the productivity of conifer plantations across Canada. The objectives of this research were: (1) to develop reliable indices of perennial, interspecific competition; (2) to compare the responses of black spruce and jack pine seedlings to tree and brush competition in northern Ontario; and (3) to identify the silvicultural implications of the responses. An examination of potential components of a competition index considered measures based on hemispherical photographs, fractal geometry, stand maps, and mensurational data from 360 seedling-centred plots for each of the two crop species. Reliable competition indices should be simple formulations which include horizontal and vertical dimensions and which express the amount of competition relative to the size of the seedling. The optimum index was found to be the area of competing canopy on hemispherical photographs, relative to the seedling leaf area. An alternate index, requiring no elaborate equipment, was the sum of the competing stem volumes (relative to the seedling stem volume) of the largest competitor in each quadrant surrounding the seedling. Comparisons of crop tree responses were made using functional growth analysis, replacing the conventional time axis with a competition axis. The relationship between growth and competition was adequately modelled with a power exponential composite function. Jack pine and bare root stock of both species maintained superior growth despite greater sensitivities to competition, compared to black spruce and container stock, respectively. Thus, jack pine or bare root stock of black spruce would outperform the alternatives if tending were delayed, but competition should be removed in all cases to capture the maximum growth potential. The rate of growth decline in response to competition was consistently greatest at the lowest competition levels, indicating that no beneficial effect on growth was provided by a light cover of non-crop vegetation. Allometric analyses indicated that black spruce had a greater morphological plasticity than jack pine. At high competition levels black spruce allocated more biomass to branches and foliage, at the expense of stem and roots. Jack pine demonstrated no such adjustment in allocation pattern, but followed a strategy of stress avoidance through sustained high growth rates. / Forestry, Faculty of / Graduate

Relationships between jack pine dwarf mistletoe (Arceuthobium americanum Nutt. ex Engelm.) and Armillaria root disease (Armillaria ostoyae (Romagn.) Herink) were examined to determine how these two disease agents contribute to jack pine (Pinus banksiana Lamb.) decline and mortality in the Belair Provincial Forest, Manitoba, Canada. The incidence and extent of Armillaria root disease was strongly related to tree vigor. Dwarf mistletoe infection did not affect either the incidence of Armillaria or the mean percentage of root system colonization within vigorous, declining, and dead classes of trees. However, field observations and other analyses indicate that dwarf mistletoe was primary responsible for jack pine decline and mortality. In dwarf mistletoe mortality centers, Armillaria appeared to act opportunistically, extensively colonizing only the stressed trees. Analysis of distributions of percent Armillaria colonization revealed that rapid root system colonization occurred just prior to, or at the time of tree death.

<p> The analysis of six jack pine populations along a north-south transect through the MacKenzie River Valley in the Northwest Territories revealed no significant latitudinal trends in cone and seed morphometric measurements. In attempting to determine whether any variations may be environmentally induced, Radial Growth Rates were, 1)compared between sites. and 2), were correlated with morphometric measurements. No significant results were produced. In correlating trait measurements between sites and between one another in order to determine whether migration may be producing trends, again no significant relatlonships were obtained. A comparison of jack pine with the similar species lodgepole pine suggests that if the same factors controlling the migration of lodgepole pine also control jack pine migration, wing loading should be less in more recent populations. However, this study indicates no significant results in this respect. It is suggested, however, that a further sampling south along the latitudinal transect may produce significant results.</p> / Thesis / Candidate in Philosophy

No description available.

White spruce (<i>Picea glauca</i> (Moench) Voss), black spruce (<i>P. mariana</i> (Mill.) BSP), and jack pine (<i>Pinus banksiana</i> Lamb.) are dominant conifer trees within the boreal forest. Rising CO2 concentrations may create hotter and drier conditions in the Southern Boreal Forest of Canada, and have negative impacts on germination and regeneration of conifers. Conifers vary in their germination requirements and may have different responses to climate change. Experiments were conducted to access the germination potential, variability among collections, and to predict the ability of these conifers to germinate under future climatic conditions. Twelve collections of white spruce and black spruce and ten collections of jack pine seeds were collected from the Boreal Plain Ecozone of Saskatchewan. Seeds of all collections varied in their dormancy characteristics and dormancy breaking requirements because no single stratification or light treatment stimulated germination in all three species. Seed dormancy was greatest in white spruce and least in black spruce. Germination tests at 5, 10, 12.5, 15, 17.5, 20, 25, 30, and 35°C were used to develop thermal time models. Each species had unique temperatures for optimal germination ranging from 20°C in white spruce, 20-25°C in black spruce, and 25-30°C in jack pine. The speed of germination under similar temperature regimes was fastest for jack pine, intermediate for black spruce, and slowest for white spruce. The base temperature for white spruce decreased (r=0.63, P=0.03) with increasing June precipitation while that of jack pine tended to increase with latitude (r=0.60, P=0.07) and April precipitation (r=0.58, P=0.08). No environmental variables correlated with germination of black spruce. The Canadian Global Climate Model, version 2, with emission scenarios predicted future temperature and precipitation at the sites where seeds were collected. Using the base temperature for germination as a guideline, temperatures suitable for germination in the spring are predicted to advance by a few weeks to a month and a half earlier with increased concentrations of CO2. Moisture availability may, however, control seed germination at these sites. Overall, jack pine and black spruce might better adapt to increasing temperature because of their high germination temperatures (>30°C). Variation in most germination parameters existed among collections, suggesting this variability can be used to select seed sources for reforestation or assisted migration in a changing climate.

White spruce (<i>Picea glauca</i> (Moench) Voss), black spruce (<i>P. mariana</i> (Mill.) BSP), and jack pine (<i>Pinus banksiana</i> Lamb.) are dominant conifer trees within the boreal forest. Rising CO2 concentrations may create hotter and drier conditions in the Southern Boreal Forest of Canada, and have negative impacts on germination and regeneration of conifers. Conifers vary in their germination requirements and may have different responses to climate change. Experiments were conducted to access the germination potential, variability among collections, and to predict the ability of these conifers to germinate under future climatic conditions. Twelve collections of white spruce and black spruce and ten collections of jack pine seeds were collected from the Boreal Plain Ecozone of Saskatchewan. Seeds of all collections varied in their dormancy characteristics and dormancy breaking requirements because no single stratification or light treatment stimulated germination in all three species. Seed dormancy was greatest in white spruce and least in black spruce. Germination tests at 5, 10, 12.5, 15, 17.5, 20, 25, 30, and 35°C were used to develop thermal time models. Each species had unique temperatures for optimal germination ranging from 20°C in white spruce, 20-25°C in black spruce, and 25-30°C in jack pine. The speed of germination under similar temperature regimes was fastest for jack pine, intermediate for black spruce, and slowest for white spruce. The base temperature for white spruce decreased (r=0.63, P=0.03) with increasing June precipitation while that of jack pine tended to increase with latitude (r=0.60, P=0.07) and April precipitation (r=0.58, P=0.08). No environmental variables correlated with germination of black spruce. The Canadian Global Climate Model, version 2, with emission scenarios predicted future temperature and precipitation at the sites where seeds were collected. Using the base temperature for germination as a guideline, temperatures suitable for germination in the spring are predicted to advance by a few weeks to a month and a half earlier with increased concentrations of CO2. Moisture availability may, however, control seed germination at these sites. Overall, jack pine and black spruce might better adapt to increasing temperature because of their high germination temperatures (>30°C). Variation in most germination parameters existed among collections, suggesting this variability can be used to select seed sources for reforestation or assisted migration in a changing climate.

Thesis (Ph. D.)--Institute of Paper Chemistry, 1940. / Includes bibliographical references (p. 87-88).