This study developed a robust technique for the assessment of morphometric differences among overwintering northern fish populations. Arctic charr were sampled soon before the freeze-up and just after ice break-up at two subarctic Quebec lakes. A homogenous sample of 397 fish was used. Regression analyses of the length-weight relationships and their derived condition indices were insufficient, due to their inherent limitations, to recognize the differences between sampling groups. A series of multivariate analyses (canonical, stepwise and discriminant analysis), based on eleven morphometric characters of the fish, provided a better assessment. The analysis recognized the distinctions between sampling groups, correctly classified 70-100% of the fish into their appropriate groupings, and indicated that body height measured at the anal opening was the most discriminatory variable. Landmark variables related to shape differences were effective in discriminating fish according to their lake of origin, whereas length and weight variables, which closely reflected the size differences, were better at distinguishing seasonal changes. The study provides a simple, efficient assessment method based on phenotypic variations to explain different survival strategies, and the associated life history traits, adopted by fish.

Thesis (M.S.)--Virginia Polytechnic Institute and State University, 1992. / Vita. Abstract. Includes bibliographical references (leaves 43-45). Also available via the Internet.

Thesis (Ph. D.)--Brigham Young University Dept. of Chemical Engineering, 2005. / Includes bibliographical references (p. 155-163).

Th. doct.--Lettres. / Bibliogr. p. 245-247. Index.

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The catalytic effect of potassium on the rate of CO₂ gasification of a bituminous coal char and a pure carbon substrate is investigated. The gasification rate depends on both the catalyst concentration (K/C atomic ratio) and the internal porous structure of the solid. For low values of the K/C atomic ratio, the initial gasification rate (mg carbon gasified per initial gram carbon per min) increases sharply with the addition of catalyst; at higher values, the rate profile levels off. The sharp increase in rate is due to the activation of reaction sites while the plateau is attributed to the saturation of the surface with active sites. The variation of the instantaneous gasification rate (based on remaining carbon) with carbon conversion at various initial K/C ratios is studied. The important reasons for the change in rate are the change in the solid surface area, the loss of active sites, the loss of catalyst by vaporization and the change in the K/C ratio due to carbon depletion. The loss of catalyst from the pure carbon substrate by vaporization is also determined. The extent of this loss depends primarily on the reaction start-up procedure. Temperature programmed experiments show that under inert atmospheres, both KOH and K₂CO₃ react with carbon to give a reduced form of the catalyst which appears to be a prerequisite for the rapid vaporization of potassium. The effect of catalyst loss on both the initial gasification rate and the variation in rate with conversion is determined. The reaction mechanism is studied by a temperature and concentration programmed reaction technique. The proposed redox mechanism contains three surface complexes: -CO₂K, -COK and -CK. The oxide groups are the intermediates during C/CO₂ gasification. The completely reduced form, -CK, is the end product of catalyst reduction and is the precursor for K loss. The stoichiometries of these surface groups are confirmed by oxygen and potassium balance.

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Pyrolysis is the thermo-chemical degradation of biomass in an oxygen-free environment to product liquid, gaseous, and solid co-products. The liquid co-product, known as bio-oil, can be used as a transportation fuel. The gaseous co-product, known as synthesis gas, can be used to power the pyrolysis reactor or other machinery. The solid co-product, known as bio-char, has been studied as an amendment to enhance soil physical and chemical properties and nutrient status. Although previous publications have described the beneficial effects of pyrolysis bio-char on soil physical and chemical properties, relatively little has been published on the recovery of mineral nutrients from pyrolysis co-products. This work quantified the recovery of feedstock nutrients (P, K, Ca, and Mg) and micronutrients (Na, Zn, Fe, Cu, and Mn) from pyrolysis co-products from various feedstocks using three distinct pyrolysis reactor designs. The reactors comprised a laboratory-scale fixed-bed reactor and two fluidized-bed reactors located in College Station, TX and Wyndmoor, PA. Nutrient recoveries, on a feedstock basis, were calculated for a comparison of reactor efficiencies. In addition to nutrient recoveries, physical and chemical properties of input biomass and of bio-char generated by each reactor were characterized through ultimate and proximate analyses. For the fixed-bed reactor, results revealed variation among feedstocks for the recoveries of feedstock sources of macronutrients and Na, Fe, and Cu in pyrolysis co-products. Variation among species was also detected for the recoveries of feedstock sources of P, K, Ca, Mg, and Fe in pyrolysis co-products for samples pyrolyzed using the Wyndmoor reactor. For the College Station reactor, recoveries of feedstock sources of P, K, Ca, and Mg in pyrolysis co-products did not vary among species, but Zn did vary. Ultimate and proximate analyses of biomass and bio-chars generated by the three reactors revealed variation among species. Additionally, the results showed that the recovery of feedstock nutrients varied by reactor design. Statistical analysis revealed high correlations and linear relationships between the recovery of nutrients and reactor mass and energy efficiency and feedstock fiber properties.