Critical role of parasite-mediated trophic interactions for energy flow
and community dynamics
Abstract
Parasites form an integral part of food webs, however, mechanistic
insights into the role of parasites for energy flow and community
dynamics is currently limited by a lack of conceptual studies
investigating host-parasite interactions in a community context. In
aquatic systems, chytrids constitute a major group of fungal parasites
and their free-living infective stage (zoospores) forms a highly
nutritional food source to zooplankton. Consumption of zoospores can
create an energy pathway from otherwise inedible phytoplankton to
zooplankton (“mycoloop”). The impact of such parasite-mediated energy
pathways on community dynamics and energy transfer to higher trophic
levels is of high importance considering eutrophication and global
warming induced shifts to dominance of unfavourable prey such as
cyanobacteria. We theoretically investigated community dynamics and
energy transfer in a food web consisting of an edible-nonhost and an
inedible-host phytoplankton species, a fungal parasite, and a
zooplankton species grazing on edible phytoplankton and fungi. Food web
dynamics were investigated along a nutrient gradient for two cases: (1)
non-adaptive zooplankton species representative for filter feeders like
cladocerans and (2) zooplankton with the ability to actively adapt their
feeding preferences like many copepod species. For both feeding
strategies, the importance of the mycoloop for zooplankton increases
with nutrient availability. This increase is smooth for non-adaptive
consumers. For a consumer with an adaptive feeding preference, we
observe an abrupt shift from almost exclusive preference for edible
phytoplankton (dominant prey) at low nutrient levels to a strong
preference for parasitic fungi at high nutrient levels. The model
predicts that parasitic fungi can contribute up to 50% of the
zooplankton diet in nutrient rich environments, agreeing with empirical
observations on zooplankton gut content from eutrophic systems during
cyanobacterial blooms. Our findings highlight the role of
parasite-mediated energy pathway for predictions on energy flow and
community composition under environmental change.