11 Supporting Online Material Calculation of pre-selection fitness function: Maternal fitness is calculated as the product of fecundity and survival, both of which are functions of egg mass. Empirical data was used to parameterize the coefficients (Fig. 1) of the maternal fitness function. The optimal egg size was estimated as the point where the first derivative of the maternal fitness function was equal to zero (0.16 g). To estimate the fitness cost of the observed decline in egg mass, we calculated the maternal fitness relationship for the YIAL salmon prior to the study period. We assumed that the initial (pre-selection) egg mass of 0.27 g was the optimal size in nature and that the fecundity - egg mass relationship was invariant over the study period, we then solved for the survival – egg mass relationship by setting the first derivative equal to zero at an egg mass of 0.27 g. The calculated (pre-selection) survival function is; Survival = 1.485(egg mass)0.923 and the resulting estimated (pre-selection) maternal fitness function is; Maternal Fitness = 2496(egg mass)0.923 - 4437(egg mass)1.923 These relationships are the same as those derived from the empirical data, except that the exponent in the survival function increased from 0.405 to a calculated 0.923 (the effect of this change is to reduce predicted survival and maternal fitness by approximately 55% for an egg of 0.20 g). Using the estimated pre-selection maternal fitness and survival relationships, the evolved egg mass of 0.20 g represents a reduction in egg survival of 24% and a reduction in 12 maternal fitness of 6%, if the fish were to be released into the wild (the reduction in maternal fitness is less than the reduction in egg survival due to changes in female fecundity). The dramatic reduction in predicted offspring survival and maternal fitness for the pre-selection relationships agree with expectations of lower fitness and survival under natural, or noncultured, conditions. Figure Caption (Supplemental Material) Figure S1: Changes in wet body mass (Kg ± 1 SE) over time for female YIAL chinook salmon. Body mass was measured prior to spawning (i.e. egg removal). No significant trend in body size was found (regression analysis; P > 0.15). Figure S2: Changes in female body length (mm; post-orbital to hypural plate) over time for the four Vancouver Island chinook salmon populations. Robertson Creek and Nahmint River data are for parents of fish used in hatchery rearing, Nanaimo River data are from dead fish collected in the river after spawning (M. Folkes, Department of Fisheries and Oceans, Canada, pers. comm.), and the Quinsam River data are for 5-yearold fish (mean age of maturation) collected in the river (www.dfo-mpo.gc.ca/csas/; Assessment of Campbell/Quinsam chinook salmon (Oncorhynchus tshawytscha) 2000/151). No significant trend in body length was found for any of the populations (regression analysis; P > 0.20).
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