Most organisms must simultaneously find enough food for themselves while trying not to become food for some other organism. Previous field experiments have shown that larvae of Enallagma and Ischnura species are able to coexist in the littoral zones of lakes because they resolve this growth/predation risk trade‐off differently: Ischnura species grow more quickly than Enallagma species, but Ischnura species suffer higher mortality rates than Enallagma. We performed a series of laboratory studies to explore the mechanistic basis for the difference in growth between the genera. When held in complete isolation and with unlimited food, larvae of a number of Enallagma species that coexist with fish accumulated mass at much faster rates than Ischnura species. This difference in isolation was due to the fish‐lake Enallagma simply ingesting more food. In contrast, when held in the presence of other damselflies or a fish predator, Ischnura had significantly higher growth rates than Enallagma species from fish lakes. All species decreased the amount of food they ingested in the presence of the fish predator as compared to when fish were absent, which resulted in decreased growth in the presence of the predator for all species. However, the interspecific differences in growth rate were due primarily to differences in the abilities of the species to convert ingested food into their own biomass; in the presence of fish, comparably sized larvae ingested nearly identical amounts of food, but Ischnura larvae grew faster because they converted significantly more ingested food into their own biomass than did larvae of Enallagma species from fish lakes. This difference in conversion efficiency between the genera was not apparent when larvae were raised in complete isolation. These results indicate that Enallagma and Ischnura species differ in physiological stress responses to the presence of predators, and this difference may facilitate the coexistence of Enallagma and Ischnura species in the field.
Most organisms must simultaneously find enough food for themselves while trying not to become food for some other organism. Previous field experiments have shown that larvae of Enallagma and Ischnura species are able to coexist in the littoral zones of lakes because they resolve this growth/predation risk trade-off differently: Ischnura species grow more quickly than Enallagma species, but Ischnura species suffer higher mortality rates than Enallagma. We performed a series of laboratory studies to explore the mechanistic basis for the difference in growth between the genera. When held in complete isolation and with unlimited food, larvae of a number of Enallagma species that coexist with fish accumulated mass at much faster rates than Ischnura species. This difference in isolation was due to the fish-lake Enallagma simply ingesting more food. In contrast, when held in the presence of other damselflies or a fish predator, Ischnura had significantly higher growth rates than Enallagma species from fish lakes. All species decreased the amount of food they ingested in the presence of the fish predator as compared to when fish were absent, which resulted in decreased growth in the presence of the predator for all species. However, the interspecific differences in growth rate were due primarily to differences in the abilities of the species to convert ingested food into their own biomass; in the presence of fish, comparably sized larvae ingested nearly identical amounts of food, but Ischnura larvae grew faster because they converted significantly more ingested food into their own biomass than did larvae of Enallagma species from fish lakes. This difference in conversion efficiency between the genera was not apparent when larvae were raised in complete isolation. These results indicate that Enallagma and Ischnura species differ in physiological stress responses to the presence of predators, and this difference may facilitate the coexistence of Enallagma and Ischnura species in the field.
Given a trade-off between offspring size and number and an advantage to large size in competition, theory predicts that the offspring size that maximizes maternal fitness will vary with the level of competition that offspring experience. Where the strength of competition varies, selection should favor females that can adjust their offspring size to match the offspring's expected competitive environment. We looked for such phenotypically plastic maternal effects in the least killifish, Heterandria formosa, a livebearing, matrotrophic species. Long-term field observations on this species have revealed that some populations experience relatively constant, low densities, whereas other populations experience more variable, higher densities. We compared sizes of offspring born to females exposed during brood development to either low or high experimental densities, keeping the per capita food ration constant. We examined plastic responses to density for females from one population that experiences high and variable densities and another that experiences low and less-variable densities. We found that, as predicted, female H. formosa produced larger offspring at the higher density. Unexpectedly, we found similar patterns of plasticity in response to density for females from both populations, suggesting that this response is evolutionarily conserved in this species.
We explored whether a variation in predation and habitat complexity between conspecific populations can drive qualitatively different numerical dynamics in those populations. We considered two disjunct populations of the least killifish, Heterandria formosa, that exhibit long-term differences in density, top fish predator species, and dominant aquatic vegetation. Monthly censuses over a 3-year period found that in the higher density population, changes in H. formosa density exhibited a strong negative autocorrelation structure: increases (decreases) at one census tended to be followed by decreases (increases) at the next one. However, no such correlation was present in the lower density population. Monthly census data also revealed that predators, especially Lepomis sp., were considerably more abundant at the site with lower H. formosa densities. Experimental studies showed that the predation by Lepomis gulosus occurred at a much higher rate than predation by two other fish and two dragonfly species, although L. gulosus and L. punctatus had similar predation rates when the amount of vegetative cover was high. The most effective predator, L. gulosus, did not discriminate among life stages (males, females, and juveniles) of H. formosa. Increased predation rates by L. gulosus could keep H. formosa low in one population, thereby eliminating strong negative density-dependent regulation. In support of this, changes in H. formosa density were positively correlated with changes in vegetative cover for the population with a history of lower density, but not for the population with a history of higher density. Our results are consistent with the hypothesis that the observed differences among natural populations in numerical abundance and dynamics are caused in part by the differences in habitat complexity and the predator community.
Summary 1. Amphibians are in decline, and the disease chytridiomycosis, caused by the chytrid fungus Batrachochytrium dendrobatidis (Bd), has been repeatedly implicated throughout the world. This chytrid reproduces via an infectious, motile zoospore stage that remains viable for weeks in the water column. 2. Daphnia is a keystone zooplankton grazer in intact freshwater ecosystems, whose importance to amphibians may be overlooked. As an efficient grazer, Daphnia can suppress chytrid epidemics by consuming zoospores and may therefore play a role in Bd infection dynamics. Daphnia may also have important effects on tadpoles by mediating the properties of pond food webs. We tested the role of Daphnia in outdoor mesocosms containing the tadpoles of red‐legged frogs (Rana aurora) infected with Bd. We also tested the ability of Daphnia to filter Bd from the water column in laboratory microcosms. 3. In the water of microcosms, Daphnia dramatically decreased the number of Bd genomic equivalents detectable using quantitative PCR. Bd genomic equivalents fell below the limit of detection at very high (>1 Daphnia mL−1) Daphnia densities. 4. In mesocosms, Daphnia was critical to the development of tadpoles: in the presence of Daphnia, tadpoles were twofold heavier at metamorphosis than in their absence. Daphnia and Bd interacted to affect the tadpole survival: survival was highest in the presence of Daphnia and in the absence of Bd. We were unable to detect an effect of Daphnia on the transmission of Bd in mesocosms. However, Bd transmission among the tadpoles in mesocosms was unexpectedly low, limiting our power to detect an effect of Daphnia on transmission. 5. Tadpole dissection showed that tadpoles also consumed large numbers of Daphnia. Current models of mesocosm food webs that assume no predation by tadpoles on zooplankton therefore probably overlook important features of both natural and experimental systems.
Conservation strategies depend on our understanding of the ecosystem and community dynamics. To date, such understanding has focused mostly on predator-prey and competitor interactions. It is increasingly clear, however, that parasite-host interactions may represent a large, and important, component of natural communities. The need to consider multiple factors and their synergistic interactions if we are to elucidate the contribution of anthropogenic factors to loss in biodiversity is exemplified by research into present-day amphibian declines. Only recently has the role of factors such as trematode parasite infections been incorporated into studies of the population and community dynamics of aquatic systems. We argue that this is due, at least in part, to difficulties faced by aquatic ecologists in sifting through the complex systematics that pervade the parasite literature. We note that two trematode species are of dominant importance with regard to North American larval anuran communities, and provide in this review a clear explanation of how to distinguish between the infective stages of these two parasites. We describe the general biology and life history of these parasites, as well as what is known about their effect on larval anurans, and the interactive effects of environmental stressors (typically anthropogenic in nature) and parasites on larval anurans. We hope that this review will convince the reader of the potential importance of these parasites to aquatic communities in general, and to amphibian communities specifically, and will also provide the information necessary for aquatic ecologists to more frequently consider the role of these parasites in their studies of aquatic ecology.
Sex-determining systems are remarkably diverse and may evolve rapidly. Polygenic sex-determination systems are predicted to be transient and evolutionarily unstable, yet examples have been reported across a range of taxa. Here, we provide the first direct evidence of polygenic sex determination in Tigriopus californicus, a harpacticoid copepod with no heteromorphic sex chromosomes. Using genetically distinct inbred lines selected for male- and female-biased clutches, we generated a genetic map with 39 SNPs across 12 chromosomes. Quantitative trait locus mapping of sex ratio phenotype (the proportion of male offspring produced by an F2 female) in four F2 families revealed six independently segregating quantitative trait loci on five separate chromosomes, explaining 19% of the variation in sex ratios. The sex ratio phenotype varied among loci across chromosomes in both direction and magnitude, with the strongest phenotypic effects on chromosome 10 moderated to some degree by loci on four other chromosomes. For a given locus, sex ratio phenotype varied in magnitude for individuals derived from different dam lines. These data, together with the environmental factors known to contribute to sex determination, characterize the underlying complexity and potential lability of sex determination, and confirm the polygenic architecture of sex determination in T. californicus.
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