If an ancestral stem group repeatedly colonizes similar environments, developmental plasticity specific to that group should consistently give rise to similar phenotypes. Parallel selection on those similar phenotypes could lead to the repeated evolution of characteristic ecotypes, a property common to many adaptive radiations. A key prediction of this "flexible stem" model of adaptive radiation is that patterns of phenotypic divergence in derived groups should mirror patterns of developmental plasticity in their common ancestor. The threespine stickleback radiation provides an excellent opportunity to test this prediction because the marine form is representative of the ancestral stem group, which has repeatedly given rise to several characteristic ecotypes. We examined plasticity of several aspects of shape and trophic morphology in response to diets characteristic of either the derived benthic ecotype or the limnetic ecotype. When marine fish were reared on alternative diets, plasticity of head and mouth shape paralleled phenotypic divergence between the derived ecotypes, supporting the flexible stem model. Benthic and limnetic fish exhibited patterns of plasticity similar to those of the marine population; however, some differences in population means were present, as well as subtle differences in shape plasticity in the benthic population, indicating a role for genetic accommodation in this system.

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We investigated the relationship between reproduction in the threespine stickleback (Gasterosteus aculeatus) and parasitism by plerocercoids of the cestode Schistocephalus solidus in Walby Lake, Alaska, by quantifying stickleback reproduction and parasite infection using 1655 fish from four samples collected in 1990-1996. Stickleback in Walby Lake largely spawned during May and June as 2-year-olds in the second spring-summer after hatching, as was the case with other stickleback populations we studied in south-central Alaska. Contrary to an earlier hypothesis that S. solidus has been selected to delay its deleterious effects on threespine stickleback, i.e., limit its infection levels, until after the stickleback have reproduced, substantial levels of parasitic infection co-occurred with the stickleback reproductive period. Chi-squared analyses of individual samples suggested that in May, infected females were as capable of producing clutches of eggs as uninfected females but in June, S. solidus inhibited clutch production. An overall analysis, however, failed to support the hypothesis that the effect of S. solidus on clutch production differed between early and late periods of the spawning season. We concluded that S. solidus inhibits the ability of female stickleback in Walby Lake to produce a clutch, and that there was no differential effect on clutch production with season. Nonetheless, 77% of all infected females produced clutches. These results contrast with those of one study in which it was found only 9% of infected females became gravid (ripe) and another report that 23% of infected females were able to mature. We offer hypotheses for the co-occurrence of stickleback reproduction and substantial parasitism at the population level and for the ability of a large proportion of infected females to produce clutches. Our results suggest that the host-parasite relationship is more complex than was previously realized.

Parasites may cause fecundity reduction in their hosts via life-history strategies involving simple nutrient theft or manipulation of host energy allocation. Simple theft of nutrients incidentally reduces host energy allocation to reproduction, whereas manipulation is a parasite-driven diversion of energy away from host reproduction. We aimed to determine whether the diphyllobothriidean cestode parasite Schistocephalus solidus causes loss of fecundity in the threespine stickleback fish (Gasterosteus aculeatus) through simple nutrient theft or the manipulation of host energy allocation. In one stickleback population (Walby Lake, Matanuska-Susitna Valley, Alaska), there was no difference in the sizes and ages of infected and uninfected reproducing females. Lightly-and heavily-infected females produced clutches of eggs, but increasingly smaller percentages of infected females produced clutches as the parasite-to-host biomass ratio (PI) increased. Infected, clutch-bearing sticklebacks showed reductions in clutch size, egg mass, and clutch mass, which were related to increases in PI and reflected a reduction in reproductive parameters as growth in parasite mass occurs. The findings obtained for this population are consistent with the hypothesis of simple nutrient theft; however, populations of S. solidus in other regions may manipulate host energy allocation.

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