Kochia scoparia (L.) Schrad. has had limited use as a forage crop during the past fifteen. years in parts of the western United States, Canada, and Argentina. Erickson and Moxon (1947) reported kochia* to be a good emergency feed for sheep and cattle during dry years in South Dakota. Salguero (1946) said that this species could be utilized in Argentina as silage or pasturage if harvested before flowering. Bell, et al. (1952) in Saskatoon, Canada studied this species in a comparison with other introduced plants and reported that it seemed to have desirable nutrient characteristics for livestock roughage. Plummer (1949) reported beef cattle in Ephraim, Utah had eaten and gained normally on kochia hay.

Hogfish (Lachnolaimus maximus; Walbaum 1792) from Southeast Florida were aged using sectioned otoliths and growth rates were calculated using the von Bertalanffy growth equation. The samples were collected from Broward County (n=209); other regions of Southeast Florida (n=18), the Florida Keys (n=35) and Bahamas (n=43). Growth rates were determined for each of these areas and were then compared to previously reported growth rates from other regions including the eastern Gulf of Mexico and Florida Keys. There was significant separation at the 95% confidence level between growth rates from each reagion. The average maximum fork length increased, from the Florida Keys (336mm) to Southeast Florida (414-mm) by 78-mm. However, the annual survival rate was the same (S=61%) between these two regions and the maximum age of Southeast Florida (age 12) was still half that of the previously reported eastern Gulf (age 23). Broward County was divided into three reef zones each at different depths (5-m, 10-m, and 20-m) and growth rate and survival rate were compared between zones. Results showed a decrease in maximum fork length with reef depth (857-mm, 420-mm, 352-mm), as well as an increase in mean age (age 3, 4, 5), maximum age (9, 10, 12), and survival (42%, 65%, 73%), respectively. The decrease in observed growth rate of an area as a whole (e.g. Florida Keys) may represent an example of Lee’s phenomena caused by increased top-down selective fishing pressure. However, the growth rates of individual hogfish are most likely a result of differences in habitat and food resource availability. This study provides baseline age and growth information for hogfish in Southeast Florida prior to the recent changes to the fishery regulations, which will help fisheries management better understand the effects of alternative management strategies.

京都大学 / 0048 / 新制・課程博士 / 博士(農学) / 甲第20421号 / 農博第2206号 / 新制||農||1047(附属図書館) / 学位論文||H29||N5042(農学部図書室) / 京都大学大学院農学研究科森林科学専攻 / (主査)教授 吉村 剛, 教授 梅澤 俊明, 教授 本田 与一 / 学位規則第4条第1項該当 / Doctor of Agricultural Science / Kyoto University / DFAM

This thesis investigates fatigue crack growth rate behavior in the threshold and near-threshold regimes for a Ti-6Al-4V (STOA) alloy using two proposed ASTM procedures- (1) load-shedding (LS) using a larger load-shed rate than the current ASTM Standard E647 load-reduction (LR) test procedure, and (2) compression pre-cracking constant-amplitude (CPCA) or load-increasing (CPLI) and load-shedding (CPLS). Tests were conducted at a low stress ratio (R = 0.1) on compact C(T) specimens of two different widths (W = 51 and 76 mm) and threshold fatigue crack growth rates were generated. These test data were compared to previous test data produced from the same batch of material using the current LR and the CPCA test procedure. While no test procedure provided an exact representation of the threshold value (?Kth), the compression pre-cracking (CP) procedures were the most promising. The LR, LS, and CPLS test procedures were influenced by prior loading-history and various crack-closure mechanisms, leading to higher ?Kth values and slower crack growths in the threshold regime. The LS tests (at shed-rates of -0.08,-0.32, and -0.95 mm-1) generated ?Kth values that were 15% to 32% higher than the estimated threshold stress-intensity factor range (?*Kth)R=0.1. The CP test procedures are a more accurate alternative for developing near-threshold and threshold fatigue crack growth rates. The CPLS test procedure produced a ?Kth value that was 10% higher than (?*Kth)R=0.1. LR and LS tests produced different ?Kth values as a function of the specimen width for the given load ratio. The CP test procedures produced consistent crack growth rates over the same range of ?K values examined, independent of the specimen width. Further research is required for developing test procedure(s) capable of providing a more definitive representation of the ?Kth value and closureree fatigue crack growth rates in the threshold regime.

京都大学 / 新制・課程博士 / 博士(理学) / 甲第24454号 / 理博第4953号 / 新制||理||1707(附属図書館) / 京都大学大学院理学研究科生物科学専攻 / (主査)教授 中野 伸一, 教授 木庭 啓介, 教授 中務 真人 / 学位規則第4条第1項該当 / Doctor of Science / Kyoto University / DGAM

Variation in somatic growth rates has interested biologists for decades because of the relationship between growth and other fitness-determining traits (i.e. fecundity, survival, and body size), and the corresponding effect of somatic growth on production of organisms humans use for food. The interaction between genetic variation in growth rates and environmentally induced variation in growth rates shows the pattern of growth across multiple environments (i.e. the reaction norm) that clarifies the history and potential future of evolutionary change in growth rates among populations. Theoretical predictions suggest variation in predator-induced mortality rates can influence mean growth rates and the shape of the reaction norm for growth. The adaptive growth hypothesis predicts that mean growth rates would evolve in response to environmental pressures, such as mortality rates, at different body sizes. Few studies, however, have focused on variation in reaction norms for growth in response to resource availability between high-predation and low-predation environments. We used juvenile Brachyrhaphis rhabdophora from high-predation and low-predation environments to test for variation in mean growth rates and for variation in reaction norms for growth at two levels of food availability in a common-environment experiment, and we compared field somatic growth rates in juveniles from the same two environments (high-predation and low-predation). In the common-environment experiment, mean growth rates did not differ between predation environments, but the interaction between predation environment and food level took the form of a crossing reaction norm for both growth in length and growth in mass. Fish from low-predation environments exhibited no significant variation in growth rate between high and low food amount treatments. In contrast, fish from high-predation environments exhibited wide variation in growth rates between low and high food treatments, with higher food availability resulting in higher growth rates. In the field, individuals in the high-predation environment grow at a faster rate than those in a low-predation environment at the smallest sizes (comparable to sizes in the common-environment experiment). These data provide no evidence for evolved differences in mean growth rates between predation environments. However, fish from high-predation environments exhibited greater plasticity in growth rates in response to resource availability suggesting that increased risk of predation could drive variation in food availability for prey and consequent selection for plasticity.

A new parametric model for the growth rate of turbulent mixing layers is proposed. A database of experimental and numerical mixing layer studies was extracted from the literature to support this effort. The domain of the model was limited to planar, spatial, nonreacting, free shear layers that were not affected by artificial mixing enhancement techniques. The model is split into two parts which were each tuned to optimally fit the database; equations for an incompressible growth rate were derived from the error function velocity profile, and a function for a compressibility factor was generalized from existing theory on the convective Mach number. The compressible model is supported by a detailed evaluation of the currently accepted models and practices, including error analysis of the convective Mach number derivation and a critical analysis of Slessor’s re-normalization technique which affected his 1998 compressibility parameter. Analysis of the database suggested that a distinction should be made between thickness definitions that are based on the velocity profile and those based on the density profile. Additionally, the accumulation of different normalization approaches throughout the literature was shown to have introduced non-physical variance in the trends. Resolution of this issue through a consistent normalization process has greatly improved the normality and scatter of the data and the goodness-of-fit of the models, resulting in R2 = 0.9856 for the incompressible model and R2 = 0.9004 for the compressible model.

Arbuscular mycorrhizal fungi (AMF) are a category of fungi that occupy virtually all of the Earth's soils. Their role as plant symbionts for nearly all land plants is well documented, where these fungi forms partnerships with plants through the root system. These relationships vary from mutualistic to parasitic and allow the exchange of nutrients between the partners via fungal hyphae that penetrate the cell walls of roots. However, many details of the nature of this symbiosis are not well understood, and the interaction between plants and AMF has been the subject of increased interest recently given the potential benefit to farming systems and natural ecosystems. This study evaluated the variability of mycorrhizal growth response (MGR) to inoculation by the common AMF species Rhizophagus intraradices in a diverse set of wild sunflower species (Helianthus), focusing on how changes in plant traits due to fungal colonization may determine the relative cost or benefit of AMF partnership for wild plants. Results indicate that the overall impacts of AMF colonization on plant growth rate are small, though MGR is correlated with AMF-driven shifts in leaf chlorophyll content. These findings suggest that relative changes in plant growth rate that result from AMF partnership are mediated by plant functional trait.

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