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A Landscape Approach to Determining and Predicting Juvenile Coho Salmon (<i>Oncorhynchus kisutch</i>) Movement Timing and Growth Patterns Prior to Ocean EntryJohnson, Amelia Lee 29 August 2016 (has links)
Coho salmon (Oncorhynchus kisutch) rely on unique habitats during the winter season, which may dictate how much individuals may grow and when migration from freshwater rearing habitat to the ocean occurs. Here I analyze movement timing and growth patterns for coho salmon through a field-based study and a literature review. For the field portion, I examined hatchery-stocked juvenile coho salmon across four stream basins in the Russian River watershed, California to determine the relative importance of climate, landscape, and fish size metrics in predicting movement and growth patterns over a winter rearing and spring smolt outmigration time period (December 2014-June 2015). I observed three unique movement strategies: winter parr movement, spring smolt movement, and inter-tributary movement. Movement was predicted in relation to daily temperature and precipitation, followed by in-stream and upslope basin conditions in random forest modeling. Specifically, fish that moved later were associated with basins that contained higher productivity and low-gradient floodplain habitats, while fish that moved earlier came from streams that lacked invertebrate prey and had limited low-gradient rearing habitat. Fish size and timing of movement were the primary predictors of growth, with relatively larger fish in the spring growing faster than fish that were relatively smaller prior to winter. These relationships suggest that hatchery-release fish are still highly influenced by environmental conditions once released, especially in terms of initial seasonal movement, and that watershed conditions should be considered when utilizing hatchery-rearing programs to supplement wild fish populations.
In North America, coho salmon populations are distributed from Alaska through California, and may exhibit unique movement and growth patterns in relationship to population-scale vulnerability (Endangered Species Act listing), basin area, and availability and types of rearing habitat. For the second part of my thesis, I conducted a literature review to assess what factors are commonly considered in predicting movement and growth patterns for these fish, as well as the types (season and life stage) and number of movement strategies reported. Eighteen studies were summarized, of which sixteen identified unique movement strategies, ranging from one to four. Despite a wide range of basin areas and latitudes, winter parr and spring smolt movements were commonly observed, with authors primarily relating these behaviors to in-stream habitat and fish size metrics. Additionally, growth was linked positively and primarily with off-channel winter rearing, which may outweigh the importance of fish size in predicting growth when high quality rearing habitats are available during the winter season.
Recognizing movement timing diversity and its drivers can help recover threatened coho salmon populations. More widely distributed populations may have unique phenotypic expressions based on localized genetic and environmental interactions, increasing diversity and overall stability across the population, a concept known as the portfolio effect. Understanding fish-habitat relationships can aid recovery efforts by providing a framework of climatic and watershed conditions that support unique behaviors, even in already severely limited populations.
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Physiological response to challenge tests in six stocks of coho salmon Oncorhynchus kisutchMcGeer, James C. January 1990 (has links)
Coho salmon (Oncorhynchus kisutch) from six hatcheries operated by the Canadian Department of Fisheries and Oceans Salmonid Enhancement Project, were reared in a common facility and then subjected to a series of standardized challenge tests. Results suggest that there are genetically based differences in the response to stressful challenges among stocks of coho salmon from southern British Columbia. The challenge tests were: saltwater (30ppt); saltwater and an increase in temperature (30ppt and 4°C); high pH (9.4 and 10.0); low pH (3.55, 3.65, 3.75 and 4.1); thermal tolerance (1°C/h); and handling (30s netting). The measured parameters were plasma sodium and chloride ion concentrations for the saline and pH challenges, time to dysfunction in the thermal tolerance challenge and plasma glucose concentration in the handling challenge. No differences among stocks were found in responses to the high pH and thermal tolerance challenges. The Chehalis River stock had the smallest plasma ion increase in salt water but showed the largest plasma ion decrease in acidic waters. In some of the low pH challenges the Tenderfoot Creek stock showed less plasma ion loss than other stocks. The stock from Eagle River had the lowest plasma glucose concentration increase during handling challenges. The combined saltwater and temperature increase challenge demonstrated the cumulative effect that stressors can have. Sampling associated with the handling challenges revealed a diurnal fluctuation in resting plasma glucose concentrations.
The low pH and handling challenges showed that stock performance and the magnitude of the response observed varied with rearing conditions. Although there was some variation in the magnitude of the stock response to challenges between the two rearing conditions used, differences among stocks were consistent. When the response to all challenges were assembled into a relative challenge response profile (or performance profile), each stock was unique. / Land and Food Systems, Faculty of / Graduate
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