What drives chytrid infections in newt populations? Associations with substrate, temperature, and shade.

The pathogenic chytrid fungus Batrachochytrium dendrobatidis (Bd) is considered responsible for the population declines and extinctions of hundreds of amphibian species worldwide. The panzootic was likely triggered by human-assisted spread, but once the pathogen becomes established in a given region, its distribution is probably determined by local drivers. To assess the relative importance of potential drivers of infection in red-spotted newts (Notophthalmus viridescens), we measured Bd levels in 16 populations throughout central Pennsylvania. Infected individuals were detected in all but four populations, indicating that Bd is widespread in this region. We quantified local factors hypothesized to influence Bd, and found that infection levels were best predicted by the proportion of the pond substrate consisting of leaf litter or vegetation, along with a significant effect of water temperature. Bd infection in amphibians is temperature-dependent, and one possible explanation of the apparent substrate effect is that tree cover and vegetation provide shade, reducing the availability of shallow, warm-water patches in which newts might reduce or clear Bd infections. Alternatively, leaf litter and emergent vegetation might increase Bd infection more directly, perhaps by providing substrates for environmental growth of the fungus. We also observed a curvilinear relationship between Bd load and snout-vent length (a proxy for age), hinting that newts might develop acquired resistance to Bd infection. Though correlational, these results add to a growing body of evidence suggesting that environmental temperature is an important driver of Bd infection dynamics.

Parasitism in a community context: trait-mediated interactions with competition and predation.

Predation and competition can induce important density- and trait-mediated effects on species, with implications for community stability. However, interactions of these factors with parasitism remain understudied. Here we investigate interactions among competition, predation and parasitism by crossing tadpole density (Bufo americanus), presence of a caged predator (Notophthalmus viridescens), and Echinostoma trivolvis trematodes, experimentally partitioning their effects on tadpole exposure and susceptibility to infection. Predation did not affect E. trivolvis infection but accelerated tadpole development and growth, and decreased activity. The presence of E. trivolvis caused the opposite effects on these three responses and reduced tadpole survival. High conspecific density reduced tadpole survival, growth, and development, and increased tadpole activity. Effects of predation and parasitism on activity were only evident at low tadpole density. High-density mesocosms also had twice the number of E. trivolvis infections as low-density mesocosms, despite a lack of evidence for stress-induced immunomodulation. Instead, this effect was explained by high density delaying tadpole development, which increased both the duration of exposure to cercariae and susceptibility to infection, because tadpoles spent more time in highly susceptible early stages. These results highlight the importance of accounting for trait-mediated effects, host plasticity, and exposure vs. susceptibility in parasite ecology.